<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Parasitology">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>10</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2015</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Cloning and Expression of Recombinant Plasmid Containing P36/LACK Gene of Leishmania infantum Iranian Strain</title>
    <FirstPage>164</FirstPage>
    <LastPage>170</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Saloomeh</FirstName>
        <LastName>Shirali</LastName>
        <affiliation locale="en_US">Dept. of Biology, Faculty of Basic science, Ahvaz branch, Islamic Azad University, Ahvaz, Iran AND Dept. of Parasitology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Hamidreza</FirstName>
        <LastName>Haddadzadeh</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mehdi</FirstName>
        <LastName>Mohebali</LastName>
        <affiliation locale="en_US">Dept. of Medical Parasitology and Mycology, School of Public health, Tehran University of Medical Sciences, Iran AND Center for Research of Endemic Parasites of Iran (CREPI), Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Bahram</FirstName>
        <LastName>Kazemi</LastName>
        <affiliation locale="en_US">Cellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran AND Dept. of Biotechnology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Narges</FirstName>
        <LastName>Amini</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background:There are several methods, such as vaccination, to control visceral leishmaniasis. Although there is no efficient vaccine, it seem DNA vaccination with stimulates both cellular and humoral immunity apparently is the best way. The aim of this study was cloning and expression of LACK gene, a 36kD protein, as a can-didate protein for vaccination against Iranian L.infantum.
Methods:Iranian strain of L. infantum [MCAN/IR/07/Moheb-gh] was used as a template for PCR to amplify LACK gene. The LACK gene was cloned in pTZ57R/T vector and after confirmation it was digested by restriction enzymes (BamH1) and cloned in pcDNA3.1 expression vector. Recombinant plasmid was extracted and analyzed by sequencing, restriction digestion analysis and PCR reac-tion. The pc- LACK recombinant plasmid was purified from transformed E.coli (DH5&#x3B1;) and its expression was analyzed by SDS-PAGE and Western blot.
Results:The results of sequencing, restriction digestion analysis and PCR reaction revealed that LACK gene was cloned correctly in pcDNA3.1 vector and the results of SDS PAGE and Western blot emphasized that LACK protein of Iranian L. in-fantum is a well-expressed protein.
&#xA0;Conclusion:We amplified, cloned and expressed Iranian L. infantum LACK genes successfully.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/336</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/336/463</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>10</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2015</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">An Annotated Checklist of the Human and Animal Entamoeba (Amoebida: Endamoebidae) Species- A Review Article</title>
    <FirstPage>146</FirstPage>
    <LastPage>156</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>Hooshyar</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, School of Medicine, Kashan University of Medical Sciences, Kashan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Parvin</FirstName>
        <LastName>Rostamkhani</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, School of Medicine, Kashan University of Medical Sciences, Kashan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mostafa</FirstName>
        <LastName>Rezaeian</LastName>
        <affiliation locale="en_US">Dept. of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran AND Center for Research of Endemic Parasite of Iran (CREPI), Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background:The number of valid of pathogen and non-pathogen species of Entamoeba has continuously increased in human and animals. This review is per-formed to provide an update list and some summarized information on Entamoeba species, which were identified up to the 2014.
Methods:We evaluated the Entamoeba genus with a broad systematic review of the literature, books and electronic databases until February 2014. The synonyms, hosts, pathogenicity and geographical distribution of valid species were considered and recorded. Repeated and unrelated cases were excluded. 
Results:Totally 51 defined species of Entamoeba were found and arranged by the number of nuclei in mature cyst according to Levin's grouping. Seven of these spe-cies within the 4 nucleate mature cysts group and 1 species with one nucleate ma-ture cyst are pathogen. E. histolytica, E. invadence, E. rananrum and E. anatis causes lethal infection in human, reptiles, amphibians and brides respectively, four species causes non-lethal mild dysentery. The other species were non-pathogen and are important to differential diagnosis of amoebiasis.
Conclusion:There are some unknown true species of Entamoeba that available information on the morphology, hosts, pathogenicity and distribution of them are still very limited and more considerable investigation will be needed in order to clarify the status of them.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/338</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/338/461</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>10</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2015</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Hoarseness as the Presenting Symptom of Visceral Leishmaniasis with Muco-Cutaneous Lesions: A Case Report</title>
    <FirstPage>296</FirstPage>
    <LastPage>300</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>Mortazavi</LastName>
        <affiliation locale="en_US">Dept. of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mehdi</FirstName>
        <LastName>Mohebali</LastName>
        <affiliation locale="en_US">Dept. of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran AND Center for Research of Endemic Parasites of Iran (CREPI), Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Yasaman</FirstName>
        <LastName>Taslimi</LastName>
        <affiliation locale="en_US">Molecular Immunology and Vaccine Research Laboratory, Pasteur Institute of Iran, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Pardis</FirstName>
        <LastName>Sadeghipour</LastName>
        <affiliation locale="en_US">Molecular Immunology and Vaccine Research Laboratory, Pasteur Institute of Iran, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mahsa</FirstName>
        <LastName>Ansari</LastName>
        <affiliation locale="en_US">Dept. of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Kambiz</FirstName>
        <LastName>Kamyab</LastName>
        <affiliation locale="en_US">Department of Pathology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Marjan</FirstName>
        <LastName>Talebi</LastName>
        <affiliation locale="en_US">Dept. of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Ali</FirstName>
        <LastName>Khamesipour</LastName>
        <affiliation locale="en_US">Skin and Leprosy Research Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">&#xA0;
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Herein, a 28-year-old man with hoarseness, skin and oral lesions is presented. At the time of admission, the patient had an erythematous plaque on his chin near his lower lip and an erythematous-violaceous plaque on his palate near the open-ing of the pharynx and 20 kg weight lost in last one year. The biopsy of his skin lesions by hematoxylin and eosin staining revealed an infiltration of the dermis by lymphoplasma and histiocytic cells with a loose granuloma formation sugges-tive of leishmaniasis. Biopsy of mucosal lesions revealed Leishman bodies in dermis. PCR was performed on the specimens of skin, bone marrow, mucosa, and saliva, the results were positive. The pathogenic agent was identified as Leishmania major by the nested PCR. Serologic tests including direct agglutination test (DAT) and indirect immunofluorescence test (IFAT) were positive with high titers of anti-L. infantum antibodies (1:102400 versus 1:800, respectively), indicative of visceral involvement. The patient responded to a combination of miltefosine and meglumine antimoniate (Glucantime&#xAE;). Visceral involvement due to L. major is rarely reported. To the best of our knowledge, probably hoarseness due to L. major has not been previously reported from Iran.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/319</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/319/493</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>10</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2015</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">The First Identification of Encephalitozoon cuniculi Infection in an Animal Care Worker in Turkey</title>
    <FirstPage>280</FirstPage>
    <LastPage>528</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Ahmet</FirstName>
        <LastName>Carhan</LastName>
        <affiliation locale="en_US">Dept. of Medical Biology, Faculty of Medicine, Y&#x131;ld&#x131;r&#x131;m Beyaz&#x131;t University, Ankara, Turkey.</affiliation>
      </Author>
      <Author>
        <FirstName>Ozcan</FirstName>
        <LastName>Ozkan</LastName>
        <affiliation locale="en_US">Experimental Research and Application Center, Drug and Medical Devices Agency, Ankara, Turkey.</affiliation>
      </Author>
      <Author>
        <FirstName>Ethem</FirstName>
        <LastName>Ozkaya</LastName>
        <affiliation locale="en_US">Ozkaya Medical Center, Ankara, Turkey.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: As a zoonotic pathogen, Encephalitozoon cuniculi is a cause of serious disease in animals and people. The present study was to evaluate the health status examination of this seropositive animal care worker in our pre-vious study.
Methods:Blood samples were taken from five workers. CIA test was ap-plied to detect antibodies against E. cuniculi in blood serum. The indirect immunofluorescence antibody test was used as confirmation test. Seroposi-tive worker had a complete medical examination.
Results:Only one worker was found to be seropositive according to the results of the serological test. Sera positive to E. cuniculi was confirmed with IFAT and spores were detected in the urine sample of the worker. The worker was treated with albendazole.
Conclusion:Rabbits should be examined routinely for the presence of anti-E. cuniculi antibody. People working with laboratory animal should avoid contact with urine and faeces of infected or pay attention to personal hy-giene.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/322</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/322/486</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>10</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2015</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Anti-Toxoplasma Activity of 2-(Naphthalene-2-&#x3B3;lthiol)-1H Indole</title>
    <FirstPage>171</FirstPage>
    <LastPage>180</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Qasem</FirstName>
        <LastName>Asgari</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, Shiraz University of Medical Sciences, Shiraz, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>Keshavarz</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mostafa</FirstName>
        <LastName>Rezaeian</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>Sadeghpour</LastName>
        <affiliation locale="en_US">Medicinal and Natural Products Chemistry Research Center, Shiraz University of Medical Sciences, Shiraz, Iran AND Dept. of Medicinal Chemistry of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Ramin</FirstName>
        <LastName>Miri</LastName>
        <affiliation locale="en_US">Medicinal and Natural Products Chemistry Research Center, Shiraz University of Medical Sciences, Shiraz, Iran AND Dept. of Medicinal Chemistry of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Hossein</FirstName>
        <LastName>Motazedian</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, Shiraz University of Medical Sciences, Shiraz, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background:This study was undertaken to evaluate the viability, infectivity and immunity of Toxoplasma gondii tachyzoites exposed to 2-(naphthalene-2-ylthio)-1H-indole.
&#xA0;Methods:Tachyzoites of RH strain were incubated in various concentrations of 2- (naphthalene-2-ylthio)-1H-indole (25-800&#x3BC;M) for 1.5 hours. Then, they were stained by PI and analyzed by Fluorescence-activated cell sorting (FACS). To eval-uate the infectivity, the tachyzoites exposed to the different concentrations of the compound were inoculated to 10 BALB/c mice groups. For Control, parasites ex-posed to DMSO (0.2% v/v) were also intraperitoneally inoculated into two groups of mice. The immunity of the exposed tachyzoites was evaluated by inoculation of the na&#xEF;ve parasite to the survived mice.
Results:The LD50 of 2-(naphthalene-2-ylthio)-1H-indole was 57 &#x3BC;mol. The lon-gevity of mice was dose dependent. Five mice out of group 400&#x3BC;mol and 3 out of group 800&#x3BC;mol showed immunization to the parasite.
&#xA0;Conclusion:Our findings demonstrated the toxoplasmocidal activity of the com-pound. The presence of a well-organized transporter mechanism for indole com-pounds within the parasite in conjunction with several effective mechanisms of these compounds on Toxoplasma viability would open a window for production of new drugs and vaccines.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/335</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/335/464</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>10</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2015</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Current Status of Acanthamoeba in Iran: A Narrative Review Article</title>
    <FirstPage>157</FirstPage>
    <LastPage>163</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Maryam</FirstName>
        <LastName>Niyyati</LastName>
        <affiliation locale="en_US">Dept. of Medical Parasitology and Mycology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mostafa</FirstName>
        <LastName>Rezaeian</LastName>
        <affiliation locale="en_US">Dept. of Medical Parasitology and Mycology, School of Public health, Tehran University of Medical Sciences, Tehran, Iran AND Center for Research of Endemic Parasites of Iran (CREPI), Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Backgrund:Free-living amoebae belonging to the genus Acanthamoeba have an environmental distribution. Amoebic keratitis due to these protozoan parasites continue to rise in Iran and worldwide. In Iran, there are various researches regard-ing both morphological and molecular identification of Acanthamoeba spp. in envi-ronmental and clinical samples. However, there is no thorough review about Acan-thamoeba genotypes and their distribution in environmental sources such as water, dust and biofilm in Iran. Besides, according to increasing cases of Amoebic kerati-tis in the region awareness regarding the pathogenic potential of these sight-threatening amoebae is of utmost importance.
&#xA0;Methods:We conducted a thorough review based on the database sources such as MEDLINE, PubMed and Google scholar. No restrictions were placed on study date, study design or language of publication. We searched all valuable and relevant information considering the occurrence of the Acanthamoeba in both environmental and clinical samples.
Results:According to our thorough review Acanthamoeba belonging to T4 geno-type is the most prevalent type strain in environmental and clinical samples in sev-eral regions in Iran and worldwide, however, there are reports regarding Acan-thamoeba belonging to other genotypes such as T2, T3, T5, T6 and T11 and the mentioned point could leads us to more researches with the goal of presenting the real genotype dominance of Acanthamoeba and related disease in the country.
Conclusion:Overall, the present review will focus on present status of genotypes of Acanthamoeba in Iran during recent years.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/337</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/337/498</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>10</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2015</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Regurgitations in a Lamb with Acute Coenurosis-A case Report</title>
    <FirstPage>301</FirstPage>
    <LastPage>305</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Evi</FirstName>
        <LastName>Ioannidou</LastName>
        <affiliation locale="en_US">Clinic of Farm Animals, School of Health Sciences, Faculty of Veterinary Medicine, Aristotle University of Thessaloniki, Greece.</affiliation>
      </Author>
      <Author>
        <FirstName>Dimitra</FirstName>
        <LastName>Psalla</LastName>
        <affiliation locale="en_US">Laboratory of Pathology, School of Health Sciences, Faculty of Veterinary Medicine, Aristotle University of Thessaloniki, Greece.</affiliation>
      </Author>
      <Author>
        <FirstName>Elias</FirstName>
        <LastName>Papadopoulos</LastName>
        <affiliation locale="en_US">Laboratory of Parasitology and Parasitic Diseases, School of Health Sciences, Faculty of Veterinary Medicine, Aristotle University of Thessaloniki, Greece.</affiliation>
      </Author>
      <Author>
        <FirstName>Anastasia</FirstName>
        <LastName>Diakou</LastName>
        <affiliation locale="en_US">Laboratory of Parasitology and Parasitic Diseases, School of Health Sciences, Faculty of Veterinary Medicine, Aristotle University of Thessaloniki, Greece.</affiliation>
      </Author>
      <Author>
        <FirstName>Vasiliki</FirstName>
        <LastName>Papanikolopoulou</LastName>
        <affiliation locale="en_US">Clinic of Farm Animals, School of Health Sciences, Faculty of Veterinary Medicine, Aristotle University of Thessaloniki, Greece.</affiliation>
      </Author>
      <Author>
        <FirstName>Harilaos</FirstName>
        <LastName>Karatzias</LastName>
        <affiliation locale="en_US">Clinic of Farm Animals, School of Health Sciences, Faculty of Veterinary Medicine, Aristotle University of Thessaloniki, Greece.</affiliation>
      </Author>
      <Author>
        <FirstName>Zoe S</FirstName>
        <LastName>Polizopoulou</LastName>
        <affiliation locale="en_US">Laboratory of Clinical Diagnosis, School of Health Sciences, Faculty of Veterinary Medicine, Aristotle University of Thessaloniki, Greece.</affiliation>
      </Author>
      <Author>
        <FirstName>Nektarios D</FirstNamegy, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hakimeh</FirstName>
        <LastName>ZALI</LastName>
        <affiliation locale="en_US">Proteomics Research Center, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mostafa</FirstName>
        <LastName>REZAEIAN</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Abolfazl</FirstName>
        <LastName>GOLESTANI</LastName>
        <affiliation locale="en_US">Department of Biochemistry, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Bagher</FirstName>
        <LastName>MOLAEI RAD</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>04</Month>
        <Day>25</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: The aim of this research was to compare excretory-secretory and somatic extract materials of Fasciola hepatica and F. gigantica to detect protein maps of two species.
&#xD;

Methods: Twenty infected livers were collected from sheep in industrial slaughterhouse in Tehran, 2017-2019. Worms were detached from bile ducts, then recognized according to morphologic and morphometric criteria. After three times washing, worms were incubated in RPMI culture media and excretory-secretory products were collected. Worms were crushed and homogenized for preparation of somatic extract. Two Dimensional Electrophoresis gels were accomplished for both excretory-secretory material and somatic extracts. Gels were scanned with densitometer and analyzed with Same Spots software and protein spots were identified with Expasy database.
&#xD;

Results: For both excretory-secretory products and somatic extract, protein spots were appeared with two-dimensional electrophoresis technique. Quantitative analysis showed 40 and 28 protein spots for excretory-secretory of F. hepatica and F. gigantica respectively. For somatic extract 19 and 12 protein spots were recognized for F. hepatica and F. gigantica in that order.
&#xD;

Conclusion: The rate of expression of some proteins were more in F. hepatica while expression of other proteins was high in F. gigantica. The expression of protease enzyme was higher in F. gigantica than F. hepatica. These data could be considered for biochemical differentiation of Fasciola species and subsequently to design and prepare of antigens for diagnosis/vaccine development.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/2108</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/2108/961</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>23</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Esophageal Infection of Spirocerca lupi with Vulpes rueppellii in Yazd Province, Iran: Case Report</title>
    <FirstPage>482</FirstPage>
    <LastPage>486</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Seyed Mohammad</FirstName>
        <LastName>HOSEINI</LastName>
        <affiliation locale="en_US">Department of Pathobiology, Babol Branch, Islamic Azad University, Babol, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hooman</FirstName>
        <LastName>RONAGHI</LastName>
        <affiliation locale="en_US">Department of Microbiology, Faculty of Specialized Veterinary Science, Science and Research Branch, Islamic Azad University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Bahram Ali</FirstName>
        <LastName>ZAHERI</LastName>
        <affiliation locale="en_US">Department of Environmental Protection Semnan, Semnan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Amir  Hossein</FirstName>
        <LastName>MOSHREFI</LastName>
        <affiliation locale="en_US">Young Researchers and Elite Club, Babol Branch, Islamic Azad University, Babol, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Ali</FirstName>
        <LastName>ADIBI</LastName>
        <affiliation locale="en_US">Department of Environmental Protection Semnan, Semnan, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>09</Month>
        <Day>22</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2018</Year>
        <Month>05</Month>
        <Day>21</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Spirocerca lupi is an international nematode of Canine and wild carnivores. The generic clinical symptoms are regurgitation, vomiting, and pursiness. The parasite usually procreates nodular masses in the esophagus and pectoral aorta. On July 2014, a four-month male sandy fox was found accidentally killed on the road in Bafgh City, Southeast of Yazd, Yazd Province, Iran during necropsy, referring to esophagus, parasites were collected from esophagus and transmissive up to 70% of alcohol. Parasites were recognized as S. lupi. After clarification of lactophenol and staining, the nematodes were recognized as S. lupi according to key guidelines of Taylor. Besides, the tissue samples were isolated from esophagus wall - the appendix site of nematode for histopathological investigation - so they were transmissive up to 10% of buffered formalin and stained with haematoxylin and eosin. Microscopic diagnoses in esophagus were included epithelial destruction, wall thickening, inflammatory cells infiltration, necrosis and vascular thrombosis. With the author&#x2019;s knowledge, this is the first report and histopathological investigation of S. lupi in sandy fox.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/1785</web_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Detection of Spiked Fasciola hepatica Eggs in Stool Specimens Using LAMP Technique</title>
    <FirstPage>387</FirstPage>
    <LastPage>393</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Sahar</FirstName>
        <LastName>GHODSIAN</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Soheila</FirstName>
        <LastName>ROUHANI</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Shirzad</FirstName>
        <LastName>FALLAHI</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Seyyed Javad</FirstName>
        <LastName>SEYYED-TABAEI</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Niloofar</FirstName>
        <LastName>TAGHIPOUR</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>02</Month>
        <Day>24</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Fascioliasis is one of the most important food-borne worm disease caused by Fasciola sp. Parasitological diagnosis is more difficult due to the low parasite burden and a few eggs shedding of helminths. Therefore, it will be valuable to development of simple, fast and reliable diagnostic tests for detection of human and animal fascioliasis.
&#xD;

Methods: Infected liver collected from abattoir in Tehran, Iran in 2017. F. hepatica eggs were detached from the uterus of worms under a stereo microscope. Various numbers of eggs were spiked to 200 mgr. of negative feces samples. DNA was extracted and then target regions (nuclear IGS) were amplified by LAMP assay using six primers. Fecal specimens without egg and DNA of other helminths were used as negative controls. F. hepatica sample which confirmed by morphologic criteria and PCR- RFLP was used as positive control.
&#xD;

Results: LAMP products by using SYBR Green I could detect even a single egg in fecal samples which was visible by change of color from orange to green. There was no cross amplification by other helminths including; Taenia saginata, Dicrosolium dendriticum and F. gigantica.
&#xD;

Conclusion: LAMP seems a rapid, sensitive, cost-effective technique for detection of human fascioliasis.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/2008</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/2008/962</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>23</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Gluteal Hydatid Cyst: A Case Report</title>
    <FirstPage>487</FirstPage>
    <LastPage>491</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mirsalim</FirstName>
        <LastName>SEYEDSADEGHI</LastName>
        <affiliation locale="en_US">Department of Surgery, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Jaffar</FirstName>
        <LastName>GHOBADI</LastName>
        <affiliation locale="en_US">Department of Emergency Medicine, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Negin</FirstName>
        <LastName>HAGHSHENAS</LastName>
        <affiliation locale="en_US">Department of Anesthesiology, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Afshin</FirstName>
        <LastName>HABIBZADEH</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>04</Month>
        <Day>10</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2018</Year>
        <Month>11</Month>
        <Day>21</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Hydatid cyst caused by Echinococcus granulosus usually involves lung and liver but can appear in other organs. We report a 29-yr-old woman presented to Fatemi Hospital, Ardabil, Iran in 2017 with progressive painful swelling of the left gluteus which in imaging showed hydatid cyst. The cyst was successfully en blocked and the patient was discharged on albendazole treatment with no recurrence in the symptoms during the first week, first and second months after surgery follow-up and in the final visit at third months. In the endemic regions, the possibility of hydatid cysts should be considered in differential diagnosis of any cystic mass.&#xA0;</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/2081</web_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Evaluation of Morphine with Imiquimod as Opioid Growth  Factor Receptor or Nalmefene as Opioid Blocking Drug on Leishmaniasis Caused by Leishmania major in Vitro</title>
    <FirstPage>394</FirstPage>
    <LastPage>403</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Javad</FirstName>
        <LastName>JABARI</LastName>
        <affiliation locale="en_US">Department of Parasitology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Fatemeh</FirstName>
        <LastName>GHAFFARIFAR</LastName>
        <affiliation locale="en_US">Department of Parasitology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>John</FirstName>
        <LastName>HORTON</LastName>
        <affiliation locale="en_US">Tropical Projects, Hitchin, UK</affiliation>
      </Author>
      <Author>
        <FirstName>Abdolhosein</FirstName>
        <LastName>DALIMI</LastName>
        <affiliation locale="en_US">Department of Parasitology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Zohreh</FirstName>
        <LastName>SHARIFI</LastName>
        <affiliation locale="en_US">Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>02</Month>
        <Day>04</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: In this research, the effect of morphine on promastigotes and amastigotes of Leishmania major has been investigated in the presence of nalmefene as a blocking opioid drug and imiquimod as an opioid growth factor receptor.
&#xD;

Methods: This study was conducted at Tarbiat Modares University, Tehran, Iran in 2015-2018. Morphine with different concentration (0.1, 1, 10 and 100 1&#xB5;g/ml) alone and with imiquimod (0.01, 0.1 and 1&#xB5;g/ml) and nalmefene (0.1, 1 and 10 &#xB5;g/ml) on promastigotes and amastigotes in macrophages and also the percentage of infected macrophages was investigated. For evaluation of the apoptosis, we used flow cytometry method. The effect of imiquimod and nalmefene on glucantime and amphotericin B as current drugs for treatment of leishmaniasis was evaluated too.
&#xD;

Results: The effect of morphine on promastigotes and amastigotes has a reverse relationship with its concentration. The results of flow cytometry for drug-treated promastigotes revealed that apoptosis and necrosis did not increase markedly relative to the control group. A combination of morphine and imiquimod in concentrations of 0.05, 5 and 5 &#xB5;g/ml had a pronounced effect on reduction and prevention of macrophage infection with amastigotes. Morphine at a concentration of 0.1 &#xB5;g/ml plays the role of adjunctive treatment. In amastigote assay we found the better results in group that get glucantime 25 &#xB5;g/ml+ imiquimod 0.5 &#xB5;g/ml.
&#xD;

Conclusion: This effect is strengthened with imiquimod and weakened with nalmefene. Using high dose morphine and nalmefene had reverse effects. They suppress immune system and had no controlling effect in macrophages amastigote infection and reduction of promastigotes.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/1987</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/1987/963</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>23</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Combined Albenazole-Praziquantel Treatment in Recurrent Brain Echinococcosis: Case Report</title>
    <FirstPage>492</FirstPage>
    <LastPage>496</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Tomislava</FirstName>
        <LastName>SKUHALA</LastName>
        <affiliation locale="en_US">University Hospital for Infectious Diseases &#x201C;Fran Mihaljevi&#x107;&#x201D;, Zagreb, Croatia</affiliation>
      </Author>
      <Author>
        <FirstName>Vladimir</FirstName>
        <LastName>TRKULJA</LastName>
        <affiliation locale="en_US">Department of Pharmacology, School of Medicine, Zagreb University, Zagreb, Croatia</affiliation>
      </Author>
      <Author>
        <FirstName>Mislav</FirstName>
        <LastName>RUNJE</LastName>
        <affiliation locale="en_US">TAPI Research and Development Analytics, Pliva Croatia, Zagreb, Croatia</affiliation>
      </Author>
      <Author>
        <FirstName>Mirjana</FirstName>
        <LastName>BALEN-TOPI&#x106;</LastName>
        <affiliation locale="en_US">University Hospital for Infectious Diseases &#x201C;Fran Mihaljevi&#x107;&#x201D;, Zagreb, Croatia</affiliation>
      </Author>
      <Author>
        <FirstName>Dalibor</FirstName>
        <LastName>VUKELI&#x106;</LastName>
        <affiliation locale="en_US">University Hospital for Infectious Diseases &#x201C;Fran Mihaljevi&#x107;&#x201D;, Zagreb, Croatia</affiliation>
      </Author>
      <Author>
        <FirstName>Bo&#x161;ko</FirstName>
        <LastName>DESNICA</LastName>
        <affiliation locale="en_US">University Hospital for Infectious Diseases &#x201C;Fran Mihaljevi&#x107;&#x201D;, Zagreb, Croatia</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>23</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">We present a 40-year-old woman with a history of relapsing echinococcosis who had undergone a number of surgical procedures for cyst removal (right pulmectomy, cardiac surgery and 6 subsequent brain surgeries and two gamma knife procedures) and was admitted to University Hospital for Infectious Diseases &#x201C;Fran Mihaljevi&#x107;&#x201D;, Zagreb, Croatia in 2014 for pre-operative medical treatment of brain hydatidosis in the right parietal region. We aimed to attain a high cyst albendazole sulphoxide (ASO) concentration in order to achieve a more pronounced protoscolex inactivation and a high serum ASO concentration (reflecting the tissue concentrations) to reduce the risk of disease recurrence. The patient was treated with a higher dose of albendazole (15 mg/kg/day for 4 wk) that we had found effective in patients with liver hydatidosis, and combined with praziquantel over the last 14 d at a dose that is typically used to treat neurocysticercosis with an intention to improve ASO bioavailability. Neither serum nor cerebrospinal fluid concentrations on day 10 apparently differed from those on day 24 indicating a lack of an effect of praziquantel on ASO bioavailability. Intra-cystic ASO concentration was below the lower limit of quantification, but above the limit of detection. After the 7th episode of the disease and combined albendazole-praziquantel and surgery treatment, the patient achieved a 3-year remission. With the apparent lack of a meaningful pharmacokinetic praziquantel-albendazole interaction, this is most likely ascribable to the use of a higher albendazole dose than previously.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/2674</web_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Epidemiological Study of Equine Piroplasmosis (Theileria equi and Babesia caballi) by Microscopic Examination and Competitive-ELISA in Erbil Province North-Iraq</title>
    <FirstPage>404</FirstPage>
    <LastPage>412</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Khalid Jabar</FirstName>
        <LastName>AZIZ</LastName>
        <affiliation locale="en_US">Department of Animal Resources, College of Agricultural Engineering Sciences, Salahaddin University-Erbil, Erbil, Iraq</affiliation>
      </Author>
      <Author>
        <FirstName>Lokman Taib Omer</FirstName>
        <LastName>AL-BARWARY</LastName>
        <affiliation locale="en_US">Department of Microbiology and Pathology, College of Veterinary Medicine, University of Duhok, Duhok, Iraq</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>06</Month>
        <Day>11</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Equine piroplasmosis is a major tick-borne disease that can lead to serious health problems and economic losses in horse industry. The aim of the study is to determine the prevalence of Theileria equi and Babesia caballi in different species of Equus namely (Horse, mule, donkey and pony) by Giemsa stained blood films and competitive ELISA.
&#xD;

Methods: This study was conducted at various geographic areas of Erbil governorate.&#xA0; A total of 349 blood samples from equine (209 horses, 62 mule, 57 donkey and 21 ponies) were collected to estimate the prevalence rate of Theileria equi and Babesia caballi by using Giemsa stained blood smear and competitive ELISA.
&#xD;

Results: The overall prevalence rates were (10.6%) consisting of (8.3%), (1.7%) and (0.6) for T. equi, B. caballi and both infection respectively by Giemsa stained blood smears, and the rate was 38.97%, consisting of 20.9% for T. equi, 11.2% for B. caballi and 6.9% for both infection by cELISA. Seroprevalence rate of T. equi was significantly higher (P &lt; 0.001) than that B. caballi in equids. There was also a significant difference associated between age (P &lt; 0.01), activity (P &lt; 0.01), management (P &lt; 0.001) and tick infestation (P &lt; 0.001), but neither the type of equids nor the gender was significant differences associated with prevalence rate.
&#xD;

Conclusion: The present study concluded that the equine piroplasmosis is a vital infection distributed among the equine in Erbil province North of Iraq. Thus a better control programme should be implemented to contain and control the prevalence of the disease within the area.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/2176</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/2176/964</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Esophageal-Crop Capillariasis and Proventriculus Ventriculus Hystrichisiasis in a Migratory Duck (Anas crecca)</title>
    <FirstPage>413</FirstPage>
    <LastPage>420</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mohammad Javad</FirstName>
        <LastName>GHARAGOZLOU</LastName>
        <affiliation locale="en_US">Department of Pathology, School of Veterinary Medicine, University of Tehran, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Iraj</FirstName>
        <LastName>MOBEDI</LastName>
        <affiliation locale="en_US">Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Reza</FirstName>
        <LastName>AGHAEBRAHIMI  SAMANI</LastName>
        <affiliation locale="en_US">Department of Pathology, School of Veterinary Medicine, University of Tehran, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Fariba</FirstName>
        <LastName>TAGHIZADEH</LastName>
        <affiliation locale="en_US">Field Practitioner Veterinarian, Babol, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Gholamreza</FirstName>
        <LastName>MOWLAVI</LastName>
        <affiliation locale="en_US">Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>03</Month>
        <Day>11</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: The aim of the present study was to study pathological and parasitological characteristics of simultaneous capillariasis and hystrichiasis in a diseased Anas crecca captured in Mazandaran Province of Iran on Oct 2016.
&#xD;

Methods: Parasitology and histopathology techniques were used to detect the parasites of the carcass of the captive common teal.
&#xD;

Results: Macroscopically, severe chronic inflammatory reactions and nodular or granuloma formation and irregular thickening of the affected wall of the esophagus, crop, proventrculus and ventriculus were observed. Microscopically, apart from the chronic inflammatory reactions and granuloma formation, in the paraffin sections stained with Harris Hematoxyline and Eosin technique, the characteristics of the mature female and male Capillaria spp.&#xA0; and their barrel-shaped operculated embryonated eggs were found within the tunnels burrowed by the nematode in the hyperplastic stratified squamous epithelium of the inflamed crop and distal portion of the esophagus. The mature female Hystrichis spp. containing oval-shaped, embryonated non-operculated eggs and male parasite were found within the labyrinthus spaces formed in the submucosa granulomas of the ventriculus and proventriculus.
&#xD;

Conclusion: Based on the parasitological and pathological studies, the species of the nematode parasites were identified as Capillaria (Thominx) contorta and Hystrichis. tricolor.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/1544</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/1544/965</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Situation and Cercarial Infection of Freshwater Mollusk from Sirindhorn Reservoir, Ubon Ratchathani Province, Thailand</title>
    <FirstPage>421</FirstPage>
    <LastPage>429</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Surat</FirstName>
        <LastName>HARUAY</LastName>
        <affiliation locale="en_US">Community Health Program, Faculty of Public Health, Ubon Ratchathani Rajabhat University, Ubon Ratchathani, Thailand</affiliation>
      </Author>
      <Author>
        <FirstName>Supawadee</FirstName>
        <LastName>PIRATAE</LastName>
        <affiliation locale="en_US">One Health Research Unit, Faculty of Veterinary Sciences, Mahasarakham University, Maha Sarakham, Thailand</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>07</Month>
        <Day>06</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Most of trematodes need snails to complete their life cycles. Consequently freshwater snails are served as intermediate hosts of many parasites worldwide. There is a lack of report on snail diversity and parasitic infection in snails in Sirindhorn Reservoir, Ubon Ratchathani province, Thailand.
&#xD;

Methods: Mollusk diversity and trematode cercariae infections were investigated in snails from 120 sampling sites surround Sirindhorn Reservoir from April 2018 to June 2018. Mollusk species were identified based on their shell morphology. The presence of cercariae infections in snails was examined by cercarial shedding methods. The interaction between snail species was analyzed by the correlation method.
&#xD;

Results: Overall, 2076 mollusks were collected which comprised six species of snails and two species of bivalves. Snail species were identified as Bithynia siamensis goniomphalos, Anentome helena, Filopaludina sumatrensis spiciosa, F. martensi martensi, F. martensi munensis and Pomacea canaliculata. The overall rate of trematode cercariae infection was 1.69% (35/2,076). The cercariae found infecting snails were Cercariaeum cercaria, Virgulate cercaria, Cotylomicrocercous cercaria and Furcocercous cercaria. The most common snails found was the assassin snail, A. helena, which showed the negative relationship among other species interactions.
&#xD;

Conclusion: This finding indicated infection with animal&#x2019;s parasites in snails in this area are common, besides, we found many species of snails in Sirindhorn Reservoir are potentially be the host of parasite in animal and human.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/2236</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/2236/966</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Toxoplasma gondii in Aborted Fetuses of Sheep in Ardebil Area, North-West of Iran</title>
    <FirstPage>430</FirstPage>
    <LastPage>435</LastPage>
rse, prognosis and choice of treatment are differing from species; differentiation of species is critical. The present study was aimed to detect the parasite species using the PCR-RFLP method.

Methods: A total of 130 Giemsa-Stained slides from suspected Cutaneous leishmaniasis (CL) patients were examined under a light microscope at&#xD7;1000. DNA from each slide was extracted PCR method was undertaken with HSP70 genes and the PCR products were digested with a restriction enzyme HaeIII (BsuR1). The study was conducted in the laboratory of Zahedan University of Medical Sciences in the Sistan and Baluchestan Province, southeastern Iran in 2015.

Results: From 130 suspected samples, 59 (45.3%) were positive by the microscopic examination, meanwhile 64 (49.2%) were positive by PCR-RFLP, Leishmania species were recognized, and L. tropica was introduced as predominant species in current study.
Conclusion: PCR-RFLP is a valuable technique for distinguish of Leishmania species. Furthermore, anthroponotic CL is the dominant cause of CL in Sistan and Baluchestan Province.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/1348</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/1348/626</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>11</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Microscopic and Molecular Detection of Cryptosporidium andersoni and Cryptosporidium xiaoi in Wastewater Samples of Tehran Prov-ince, Iran</title>
    <FirstPage>499</FirstPage>
    <LastPage>506</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Kareem</FirstName>
        <LastName>HATAM-NAHAVANDI</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran AND Department of Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran AND Infectious Diseases and Tropical Medicine Research Center, Zahedan University of Medical Sciences, Zahedan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mehdi</FirstName>
        <LastName>MOHEBALI</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran AND Center for Research of Endemic Parasites of Iran (CREPI), Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Amir-Hossein</FirstName>
        <LastName>MAHVI</LastName>
        <affiliation locale="en_US">Department of Environmental Health Engineering, School of Public Health, Tehran, Iran AND Center for Water Quality Research, Institute for Environmental Research (IER), Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>KESHAVARZ</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran AND Center for Research of Endemic Parasites of Iran (CREPI), Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hamid-Reza</FirstName>
        <LastName>NAJAFIAN</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hamed</FirstName>
        <LastName>MIRJALALI</LastName>
        <affiliation locale="en_US">Foodborne and Waterborne Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran AND Gastroenterology and Liver Disease Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Sasan</FirstName>
        <LastName>REZAEI</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mostafa</FirstName>
        <LastName>REZAEIAN</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran AND Center for Research of Endemic Parasites of Iran (CREPI), Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: As a waterborne pathogen, Cryptosporidium is one of the most common causes of gastroenteritis in human and hoofed livestock animals. This study aimed to investigate the distribution of Cryptosporidium spp. in human and livestock wastewaters in Iran, by the 18S rRNA sequence analysis.

Methods: A total of 54 raw wastewater samples collected from three urban treatment plants and two slaughterhouses during 2014-2015 in Tehran, Iran. The presence of the Cryptosporidium oocysts was assessed by immunofluorescence with monoclonal antibodies. To characterize the oocysts at the molecular level, the 18S rRNA gene of Cryptosporidium was PCR amplified and sequenced.

Results: Of the 54 wastewater samples examined, 34 (62.9%) were positive for Cryptosporidium oocysts using the IFA. Of these, 70.5% (24/34) were positive by PCR, that 91.6% (22/24) were successfully sequenced. The species of C. andersoni (95.4%) and C. xiaoi (4.6%) were detected in livestock wastewater samples.
Conclusion: C. andersoni was the major Cryptosporidium sp. found in the aquatic environmental wastewater samples. The high rate of detection of C. andersoni in domestic wastewater was probably the result of the predominancy of this species in cattle herds in Iran. The current study is the first report of C. xiaoi in Iran.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/1349</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/1349/627</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>11</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Molecular Characterization of Trichomonas vaginalis Strains Based on Identifying Their Probable Variations in Asymptomatic Patients</title>
    <FirstPage>507</FirstPage>
    <LastPage>514</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Adel</FirstName>
        <LastName>SPOTIN</LastName>
        <affiliation locale="en_US">Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran AND Department of Parasitology and Mycology, Faculty of Medicine, Tabriz University of  Medical Sciences, Tabriz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Sanaz</FirstName>
        <LastName>TAGHIZADEH EGHTEDAR</LastName>
        <affiliation locale="en_US">Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran AND Department of Parasitology and Mycology, Faculty of Medicine, Tabriz University of  Medical Sciences, Tabriz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Abbas</FirstName>
        <LastName>SHAHBAZI</LastName>
        <affiliation locale="en_US">Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran AND Department of Parasitology and Mycology, Faculty of Medicine, Tabriz University of  Medical Sciences, Tabriz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Asghar</FirstName>
        <LastName>SALEHPOUR</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, Faculty of Medicine, Tabriz University of  Medical Sciences, Tabriz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Seddigheh</FirstName>
        <LastName>SARAFRAZ</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, Faculty of Medicine, Tabriz University of  Medical Sciences, Tabriz, Iran AND East Azerbaijan Province Health Center, Tabriz Health Center, Tabriz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Seyyed Ali</FirstName>
        <LastName>SHARIATZADEH</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, Faculty of Medicine, Tabriz University of  Medical Sciences, Tabriz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mahmoud</FirstName>
        <LastName>MAHAMI-OSKOUEI</LastName>
        <affiliation locale="en_US">Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran AND Department of Parasitology and Mycology, Faculty of Medicine, Tabriz University of  Medical Sciences, Tabriz, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: The aim of this study was to identify the Trichomonas vaginalis strains/haplotypes based on identifying their probable variations in asymptomatic patients referred to Tabriz health centers, northwestern Iran.

Methods: Sampling was taken from 50-suspected women to T. vaginalis in northwestern Iran. The obtained samples were smeared and cultured. Fifty DNA samples were extracted, amplified and identified by nested polymerase chain reaction and PCR-RFLP of actin gene using two endonuclease enzymes: MseI and RsaI. To reconfirm, the amplicons of actin gene were directly sequenced in order to identify the strains/haplotypes.

Results: PCR-RFLP patterns, sequencing and phylogenetic analyses revealed definitely the presence of the G (n=22; 73.4%) and E (n=8; 26.6%) strains. Multiple alignments findings of genotype G showed five haplotypes and two amino acid substitutions in codons 192 and 211 although, no remarkable unique haplotype was found in genotype E.

Conclusion: The accurate identification of T. vaginalis strains based on discrimination of their unknown haplotypes particularly those which are impacted on protein translation should be considered in parasite status, drug resistance, mixed infection with HIV and monitoring of asymptomatic trichomoniasis in the region.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/1350</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/1350/628</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>11</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Anti-inflammatory Potentials of Excretory/Secretory (ES) and Somatic Products of Marshallagia marshalli on Allergic Airway Inflammation in BALB/c Mice</title>
    <FirstPage>515</FirstPage>
    <LastPage>526</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Sima</FirstName>
        <LastName>PARANDE SHIRVAN</LastName>
        <affiliation locale="en_US">Dept. of Pathobiology, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hassan</FirstName>
        <LastName>BORJI</LastName>
        <affiliation locale="en_US">Dept. of Pathobiology, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ahmadreza</FirstName>
        <LastName>MOVASSAGHI</LastName>
        <affiliation locale="en_US">Dept. of Pathobiology, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammadreza</FirstName>
        <LastName>KHAKZAD</LastName>
        <affiliation locale="en_US">Zakaria Research Center, Faculty of Medicine, Islamic Azad University, Mashhad Branch, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hamidreza</FirstName>
        <LastName>FARZIN</LastName>
        <affiliation locale="en_US">Razi Vaccine and Serum Research Institute, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohsen</FirstName>
        <LastName>MALEKI</LastName>
        <affiliation locale="en_US">Dept. of Pathobiology, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Alireza</FirstName>
        <LastName>HAGHPARAST</LastName>
        <affiliation locale="en_US">Dept. of Pathobiology, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Inverse relationship between helminths infection and immune-mediated diseases has inspired researchers to investigate therapeutic potential of helminths in allergic asthma. Helminth unique ability to induce immunoregulatory responses has already been documented in several experimental studies. This study was designed to investigate whether excretory/secretory (ES) and somatic products of Marshallagia marshalli modulate the development of ovalbumin-induced airway inflammation in a mouse model.

Methods: This study was carried out at the laboratories of Immunology and Parasitology of Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran during spring and summer 2015. Allergic airway inflammation was induced in mice by intraperitoneal (IP) injection with ovalbumin (OVA). The effects of ES and somatic products of M. marshalli were analyzed by inflammatory cell infiltration in bronchoalveolar lavage fluid (BALF), pathological changes and IgE response.

Results: Treatment with ES and somatic products of M. marshalli decreased cellular infiltration into BALF when they were administered during sensitization with allergen. Pathological changes were decreased in helminth-treated group, as demonstrated by reduced inflammatory cell infiltration, goblet cell hyperplasia, epithelial lesion and smooth muscle hypertrophy. However, no significant differences were observed in IgE serum levels, cytokines and eosinophil counts between different groups.
Conclusion: This study provides new insights into anti-inflammatory effects of ES and somatic products of M. marshalli, during the development of non-eosinophilic model of asthma. Further study is necessary to characterize immunomodulatory molecules derived from M. marshalli as a candidate for the treatment of airway inflammation.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/1351</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/1351/629</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>11</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Prevalence of Strongyloides stercoralis and Other Intestinal  Parasites among Institutionalized Mentally Disabled Individuals in Rasht, Northern Iran</title>
    <FirstPage>527</FirstPage>
    <LastPage>533</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Amin</FirstName>
        <LastName>SAEIDINIA</LastName>
        <affiliation locale="en_US">Student Research Committee, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ilnaz</FirstName>
        <LastName>TAVAKOLI</LastName>
        <affiliation locale="en_US">Student Research Committee, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Reza</FirstName>
        <LastName>NAGHIPOUR</LastName>
        <affiliation locale="en_US">Department of Social Medicine, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Behnaz</FirstName>
        <LastName>RAHMATI</LastName>
        <affiliation locale="en_US">Department of Microbiology, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>GHAVAMI LAHIJI</LastName>
        <affiliation locale="en_US">Student Research Committee, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Omid</FirstName>
        <LastName>SALKHORI</LastName>
        <affiliation locale="en_US">Student Research Committee, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Keyhan</FirstName>
        <LastName>ASHRAFI</LastName>
        <affiliation locale="en_US">Department of Microbiology, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran AND Research Center for Fascioliasis and Parasitic Diseases, Guilan University of Medical Sciences, Rasht, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: We aimed to determine the status of strongyloidiasis in mentally disabled population in the institutional places in Rasht City, the capital of Guilan Province, northern Iran.

Methods: This cross-sectional study was conducted in 8 institutions for mentally retarded population in Rasht in 2013. Before collecting the samples, a questionnaire was filled out for each participant by an expert person. A single&#xA0; stool sample was obtained from each of the 173 subjects and examined using direct wet mount, formalin-ether concentration technique and agar plate culture method.&#xA0;

Results: A total of 173 mentally disabled individuals aged 2-57 (25.69&#xB1;11.56) yr old were studied. Stool examination showed that 51 (29.5%) cases were infected with at least one parasite. Of 173 studied cases only 10 (5.8%) individuals were infected with pathogenic parasites, of which 2 (1.2%) cases were infected with Strongyloides stercoralis and 8 (4.6%) with Giardia lamblia. On the other hand, 42 (24.3%) of the studied population were infected with non-pathogenic intestinal protozoa such as Blastocystis hominis (n=29, 16.8%), Entamoeba coli (n=16, 9.2%) and Endolimax nana (n=4, 2.3%). Mixed protozoal infections were observed in 8 (4.6%) individuals.
Conclusion: The prevalence rate of S. stercoralis in mentally disabled individuals in Rasht was somewhat higher than those of normal population of the province. The same picture was seen when the prevalence of G. lamblia and non-pathogenic protozoa in normal and mentally disabled populations were compared.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/1352</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/1352/630</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>11</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Expression of Pro-inflammatory Genes in Lesions and Neutrophils during Leishmania major Infection in BALB/c Mice</title>
    <FirstPage>534</FirstPage>
    <LastPage>541</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Soheyla</FirstName>
        <LastName>AKHZARI</LastName>
        <affiliation locale="en_US">Dept. of Laboratory Sciences, School of Veterinary Sciences, Bu-Ali Sina University, Hamadan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>REZVAN</LastName>
        <affiliation locale="en_US">Dept. of Laboratory Sciences, School of Veterinary Sciences, Bu-Ali Sina University, Hamadan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Masoud</FirstName>
        <LastName>ZOLHAVARIEH</LastName>
        <affiliation locale="en_US">Dept. of Laboratory Sciences, School of Veterinary Sciences, Bu-Ali Sina University, Hamadan, Iran AND Dept. of Clinical Sciences, Faculty of Para-Veterinary Sciences, Bu-Ali Sina University, Hamedan, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2016</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Leishmaniasis is a worldwide disease prevalent in tropical and sub- tropical countries in the world. Characterization of inflammatory responses produced in cutaneous leishmaniasis has not yet been completed.

Methods: The specific primers were designed for ten pro-inflammatory genes including CCL4, CCL3, TNF-&#x3B1;, IL-1&#x3B1;, IL-12P35, IL-12P40, CCL5, CCR5, IL-1&#x3B2; and IFN- &#x3B3; and their expression were assessed and compared using RT-PCR in the lesion and peripheral blood neutrophils in Leishmania infected BALB/c mice.

Results: None of the pro-inflammatory genes was expressed in the healthy tissue and except IFN-&#x3B3; others were down-regulated by the parasite in the lesion in untreated mice. In mice treated with anti-Leishmanial drugs, the expression of the pro-inflammatory genes restarted. The figure of pro-inflammatory gene expression in neutrophils was different was from the lesions in treated and untreated mice.
Conclusion: Leishmania is capable to suppress the expression of pro-inflammatory genes in the lesions but not in neutrophils. The expression of TNF-&#x3B1; in the lesions and down-regulation of IL-1&#x3B2; in neutrophils could be accounted as an indication for healing of cutaneous leishmaniasis. The results open a new window on characterization of Leishmani