<?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>9</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2014</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Emerging Intestinal Microsporidia Infection in HIV(+)/AIDS Patients in Iran: Microscopic and Molecular Detection</title>
    <FirstPage>149</FirstPage>
    <LastPage>154</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Hamed</FirstName>
        <LastName>Mirjalali</LastName>
        <affiliation locale="en_US">Dept. of Medical Parasitology and Mycology, School of Public Health, 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>Hossein</FirstName>
        <LastName>Mirhendi</LastName>
        <affiliation locale="en_US">Dept. of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Rashid</FirstName>
        <LastName>Gholami</LastName>
        <affiliation locale="en_US">Dept. of Infectious Diseases, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>Keshavarz</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>Ahmad Reza</FirstName>
        <LastName>Meamar</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, School of Medicine, Iran 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">Background: Species of Microsporidia have been known as opportunistic obli-gate intracellular parasites particularly in immunocompromised patients. Enterocyto-zoon bieneusi is one of most prevalent intestinal microsporida parasites in HIV+/AIDS patients. In this study, intestinal microsporidia infection was deter-mined in HIV+/AIDS patients using microscopic and molecular methods. 
&#xD;
Methods: Stool samples were collected from HIV+/AIDS patients during 12 months. All of the stool specimens washed with PBS (pH: 7.5). Slim slides were prepared from each sample and were examined using light microscope with 1000X magnification. DNA extraction carried out in microscopic positive samples. DNA amplification and genus/species identification also performed by Nested-PCR and sequencing techniques. 
&#xD;
Results: From 81 stool samples, 25 were infected with microsporidia species and E. bieneusi were identified in all of positive samples. No Encephalitozoon spp. was identified in 81 collected samples using specific primers. 
&#xD;

Conclusion: E. bieneusi is the most prevalent intestinal microsporidia in immuno-compromised patients of Iran. On the other hand, Nested-PCR using specific pri-mers for ssu rRNA gene is an appropriate molecular method for identification of E. bieneusi.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/419</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/419/325</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>9</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2014</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">An Analysis of Clinical Characteristics of Strongyloides stercoralis in 70 indigenous patients in Iran</title>
    <FirstPage>155</FirstPage>
    <LastPage>162</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Meysam</FirstName>
        <LastName>Sharifdini</LastName>
        <affiliation locale="en_US">Department 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>Eshrat Beigom</FirstName>
        <LastName>Kia</LastName>
        <affiliation locale="en_US">Department 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>Keyhan</FirstName>
        <LastName>Ashrafi</LastName>
        <affiliation locale="en_US">Dept. of Medical Microbiology, School of Medicine, Gilan University of Medical Sciences, Rasht, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mostafa</FirstName>
        <LastName>Hosseini</LastName>
        <affiliation locale="en_US">Department of Biostatistics and Epidemiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>Mirhendi</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>Mehdi</FirstName>
        <LastName>Mohebali</LastName>
        <affiliation locale="en_US">Department 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>Bahare</FirstName>
        <LastName>Kamranrashani</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>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Clinical manifestations of Strongyloides stercoralis are variable from asymptomatic to hyperinfection and devastating disseminated infections. Hereby, clinical characteristics of a large series of Iranian strongyloidiasis indigenous cases are described.
&#xD;

Methods: The records of people referred to the Helminthological Diagnostic La-boratory of School of Public Health, Tehran University of Medical Sciences and School of Medicine, Gilan University of Medical Sciences, during 2009-2013 were reviewed. For those patients that were infected with S. stercoralis and their clinical manifestations and demographic data were available (70 cases) a checklist was pre-pared and data analyzed.
&#xD;

Results: Forty-three patients (61.4%) were male and 27 (38.6%) female. Gastroin-testinal, cutaneous and pulmonary symptoms were present in 71.4%, 25.7%, and 15.7% of patients, respectively. None of them had larva currens eruption. Eosino-philia was the most prevalent reason for suspicious on S. stercoralis, but the mean was lower in elderly patients. Hyperinfection were recorded in 8 patients (11.4%), and 2 cases had disseminated infection.
&#xD;

Conclusion: Eosinophilia is common both in asymptomatic and symptomatic cas-es of strongyloidiasis, but the mean tend to lower with increase in age.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/418</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/418/326</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>9</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2014</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Canine Babesiosis in China Caused by Babesia gibsoni: A Molecular Approach</title>
    <FirstPage>163</FirstPage>
    <LastPage>168</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Da-Wei</FirstName>
        <LastName>Yao</LastName>
        <affiliation locale="en_US">College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, China.</affiliation>
      </Author>
      <Author>
        <FirstName>Jing-Ya</FirstName>
        <LastName>Jiang</LastName>
        <affiliation locale="en_US">College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, China.</affiliation>
      </Author>
      <Author>
        <FirstName>Ze-Zhong</FirstName>
        <LastName>Yu</LastName>
        <affiliation locale="en_US">YuXi Agriculture Vocation-Technical College, Yuxi, Yunnan, China.</affiliation>
      </Author>
      <Author>
        <FirstName>Dong-Qin</FirstName>
        <LastName>Yao</LastName>
        <affiliation locale="en_US">College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, China.</affiliation>
      </Author>
      <Author>
        <FirstName>De-Ji</FirstName>
        <LastName>Yang</LastName>
        <affiliation locale="en_US">College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, China.</affiliation>
      </Author>
      <Author>
        <FirstName>Yan-Bing</FirstName>
        <LastName>ZhAO</LastName>
        <affiliation locale="en_US">College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, China.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: To provide a point of reference to study the epidemiology and clin-ical expression of canine babesiosis in China.
&#xD;

Methods: A total of 30 dogs infected with canine babesiosis were evaluated by mean of clinical history, physical examination, hematological, restriction fragment length polymorphism of PCR products (PCR-RFLP) and sequencing analysis.
&#xD;

Result: The most prevalent clinical abnormalities were lethargy (100%), anorexia (100%), pale or icteric mucous membranes (80%), fever (70%) and dark urine (70%). Hematology parameters revealed that anemia and thrombocytopenia were the major abnormalities in blood of dogs infected with canine babesia. The results of PCR-RFLP and sequencing analysis indicated that B. gibsoni was the main species responsible for canine babesiosis cases at the time of the study in Nanjing, China.
&#xD;

Conclusions: The results provide valuable information for better understanding of the epidemiology of canine babesiosis in China.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/417</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/417/327</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>9</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2014</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Epidemiology, Sero-Diagnosis and Therapeutic Studies on Nematodes Infection in Balochi Range-Sheep at District Quetta, Balochistan, Pakistan</title>
    <FirstPage>169</FirstPage>
    <LastPage>180</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Abdul</FirstName>
        <LastName>Razzaq</LastName>
        <affiliation locale="en_US">Animal Sciences Research Program, Balochistan Agricultural Research and Development Centre, PARC, Brewery Road, Quetta, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Kamran</FirstName>
        <LastName>Ashraf</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, University of Veterinary and Animal Sciences, Lahore, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Azhar</FirstName>
        <LastName>Maqbool</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, University of Veterinary and Animal Sciences, Lahore, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Muhammad</FirstName>
        <LastName>Islam</LastName>
        <affiliation locale="en_US">International Centre for Agriculture Research in Dry Areas (ICARDA), National Agricultural Research Centre, Islamabad, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Abdul</FirstName>
        <LastName>Hanan</LastName>
        <affiliation locale="en_US">Range and Forestry Research Program, Balochistan Agricultural Research and Development Centre, PARC, Brewery Road, Quetta, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Mian Muhammad</FirstName>
        <LastName>Awais</LastName>
        <affiliation locale="en_US">Dept. of Pathobiology, Sub campus Jhang, University of Veterinary and Animal Sciences, Lahore, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Munir Ahmad</FirstName>
        <LastName>Khetran</LastName>
        <affiliation locale="en_US">Crop Sciences Research Program, Balochistan Agricultural Research and Development Centre, PARC, Brewery Road, Quetta, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Saadullah</FirstName>
        <LastName>Jan</LastName>
        <affiliation locale="en_US">Centre for Advance Studies in Vaccinology and Bacteriology, University of Balochistan, Quetta, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Muhammad</FirstName>
        <LastName>Shafee</LastName>
        <affiliation locale="en_US">Centre for Advance Studies in Vaccinology and Bacteriology, University of Balochistan, Quetta, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Muhammad</FirstName>
        <LastName>Essa</LastName>
        <affiliation locale="en_US">Diseases Investigation Lab. Livestock and Dairy Development Department, Quetta, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Hamdullah</FirstName>
        <LastName>Kakar</LastName>
        <affiliation locale="en_US">Dairy Farm, Livestock and Dairy Development Department, Quetta, Pakistan.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">&#xA0;
&#xD;
&#xD;
&#xD;
&#xD;
&#xD;

Background:Among the infectious organisms of parasitic origin, gastrointestinal nematodes are very important as they have been reported worldwide. The main aim of the present research study to highlight the annual epidemiological contributing factors associated with the prevalence of gastrointestinal nematodes and their control in sheep.
&#xD;

Methods:A total 1200 faecal samples (100 per month) were collected from farmers holding Balochi-sheep (either sexes, 1-5 years old) during January-December 2012 and analyzed to determine the prevalence of nematodes based on microscopy and ELISA based diagnostic assay. Therapeutic efficacies of different synthetic and herbal medicines against these nematodes were assessed by field trials.
&#xD;

Results:Results showed that 23.92% Balochi-sheep were infected with nematodes. Five nematodes infections were recorded with highest prevalence of Haemonchus (7.75%) fol-lowed by Nematodirus (7.58%), Strongyloides (4.42%), Trichostrongylus (2.33%) and Trichuris (1.83%). The younger and older ewes (one and five years) presented higher nematodes prevalence with peak during March/April and August/September. Haemonchus and Tri-churis positive samples based on coprological examination were also showed 92-100% positive sensitivity for these nematodes by the ELISA. Sheep treated with Ivermectin showed higher reduction (97.76%) in nematode egg counts followed by Atreefal deedan (96.42%) and Oxfendazole (95.44%), respectively.
&#xD;

Conclusion:The gastro-intestinal nematodes are prevalent in all age and either sex of Balochi-sheep with peak during summer. The ELISA based diagnosis is more accurte. The synthetic and herbal products are very effective against sheep nematodes.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/416</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/416/328</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>9</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2014</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Seroprevalence of Toxoplasma gondii Infections in Pregnant Women in Gorgan City, Golestan Province, Northern Iran-2012</title>
    <FirstPage>181</FirstPage>
    <LastPage>187</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mitra</FirstName>
        <LastName>Sharbatkhori</LastName>
        <affiliation locale="en_US">Department of Medical Parasitology &amp; Mycology, School of Medicine, Golestan University of Medical Sciences, Gorgan, Iran AND Infectious Diseases Research Center, Golestan University of Medical Sciences, Gorgan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Yusef</FirstName>
        <LastName>Dadi Moghaddam</LastName>
        <affiliation locale="en_US">Social Security Organization, Gonbad, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Abdol Sattar</FirstName>
        <LastName>Pagheh</LastName>
        <affiliation locale="en_US">Toxoplasmosis Research Center, Mazandaran University of Medical Sciences, Sari, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Rasool</FirstName>
        <LastName>Mohammadi</LastName>
        <affiliation locale="en_US">Department of Epidemiology, School of Public Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Haleh</FirstName>
        <LastName>Hedayat Mofidi</LastName>
        <affiliation locale="en_US">School of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Saeedeh</FirstName>
        <LastName>Shojaee</LastName>
        <affiliation locale="en_US">Department of Medical Parasitology &amp; Mycology, School of Public Health, 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: Toxoplasma gondii is one of the most prevalent parasites of human and warm- blooded animals. Toxoplasmosis is important especially in two groups: pregnant women and immunocompromised patients. If women acquire the primary infection during the pregnancy, it would be life threatening or re-mains severe disorders for the fetus. This study was performed to evaluate the seroprevalence of T. gondii infection in pregnant women referred to Health Cen-ter in Gorgan City, Golestan Province, northern Iran.
&#xD;

Methods: Serum samples were collected from pregnant women referred to Health Center in Gorgan City, south eastern Caspian Sea. Anti- Toxoplasma IgG and IgM antibodies were determined by commercially ELISA kits and the rela-tion of infection with socio-demographic and risk factors such as age, education, occupation, cat ownership, soil contact and some other factors was studied.
&#xD;

Results: From 555 tested sera of pregnant women referred to Health Center in Gorgan, 39.8% had IgG antibodies against T. gondii and 3.4% were positive for IgM antibodies. A significant correlation was seen between T. gondii infection with age and soil contact.
&#xD;

Conclusion: About 60% of pregnant women in Gorgan City are seronegative against T. gondii, so they should considered as at risk persons.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/415</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/415/329</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Parasitology</JournalTitle>
      <Issn>1735-7020</Issn>
      <Volume>9</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2014</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Paleoparasitological Findings from Rodent Coprolites Dated At 500 CE Sassanid Era in Archeological Site of Chehrabad(Douzlakh), Salt Mine Northwestern Iran</title>
    <FirstPage>188</FirstPage>
    <LastPage>193</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Gholamreza</FirstName>
        <LastName>Mowlavi</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>Mahsasadat</FirstName>
        <LastName>Makki</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>Iraj</FirstName>
        <LastName>Mobedi</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>Adauto</FirstName>
        <LastName>Araujo</LastName>
        <affiliation locale="en_US">Escola Nacional de Sa&#xFA;de P&#xFA;blica, Funda&#xE7;&#xE3;o Oswaldo Cruz, Rio de Janeiro, RJ, Brasil (Brazilian Shool of Public Health, Oswaldo Cruz Foundation).</affiliation>
      </Author>
      <Author>
        <FirstName>Abolfazl</FirstName>
        <LastName>Aali</LastName>
        <affiliation locale="en_US">Archaeological Museum of Zanjan, Zanjan, Iran.</affiliation>
      </Author>
    >
        <LastName>Giadinis</LastName>
        <affiliation locale="en_US">Clinic of Farm Animals, School of Health Sciences, Faculty of Veterinary Medicine, Aristotle University of Thessaloniki, Greece.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">&#xA0;
&#xD;
&#xD;
&#xD;
&#xD;
&#xD;

Coenurosis is a disease of the central nervous system in sheep, caused by Coenurus cerebralis, the larval stage of Multiceps multiceps, which inhabits the small intestine of Canidae. A case of regurgitations in a 2.5 month old lamb with acute coenurosis is being reported. The lamb was presented with a sudden onset of ataxia and re-gurgitations for 10 days. The post-mortem examination revealed 4 immature C. cerebralis cysts between 0.5 and 1.5 cm in diameter located in the brainstem and cerebellum, and histopathological examination revealed multifocal pyogranuloma-tous meningoencephalitis, so a diagnosis of acute coenurosis was established. Thus, acute coenurosis should be included in the differential diagnosis of regurgi-tations in lambs.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/318</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/318/494</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">Soil Contamination with Toxocara Spp. Eggs in Public Parks of Mashhad and Khaf, North East of Iran</title>
    <FirstPage>286</FirstPage>
    <LastPage>2899</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Fariba</FirstName>
        <LastName>Berenji</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Abdul Ghayoum</FirstName>
        <LastName>Movahedi Rudy</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Abdolmajid</FirstName>
        <LastName>Fata</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mousa</FirstName>
        <LastName>Tavassoli</LastName>
        <affiliation locale="en_US">Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mojtaba</FirstName>
        <LastName>Mousavi Bazaz</LastName>
        <affiliation locale="en_US">Dept. of Community Medicine, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Ghodratolah</FirstName>
        <LastName>Salehi Sangani</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Toxocariasis is an important disease caused by the larvae of parasitic worms such as Toxocara canis and T. cati. Public parks can be the source of toxocariasis for small children. This survey was conducted to de-termine the prevalence of Toxocara spp. ova in parks of Mashhad and Khaf northeastern Iran.
Methods:In this descriptive cross-sectional study, performed in November 2011 to June 2012, overall, 340 soil samples were collected from 39 parks of Mashhad and 29 parks in Khaf city. Flotation method and direct smear were used, and the samples were evaluated using a light microscope. The results were analyzed using SPSS version 19 and Chi-square test.
Results:In the evaluation of 195 and 145 soil samples, 18 (9.2%) and 16 cases (11.3%) of contamination with Toxocara spp. eggs were detected, re-spectively.
Conclusion:Although the prevalence of Toxocara eggs in soil samples was low, parks can be a source of Toxocara infection of children in these areas.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/321</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/321/488</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">Occurrence of Potentially Pathogenic Bacterial-Endosymbionts in Acanthamoeba Spp</title>
    <FirstPage>181</FirstPage>
    <LastPage>188</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 AND Cellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mahyar</FirstName>
        <LastName>Mafi</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>Ali</FirstName>
        <LastName>Haghighi</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>Mojdeh</FirstName>
        <LastName>Hakemi Vala</LastName>
        <affiliation locale="en_US">Dept. of Medical Microbiology, School of Medicine, Shahid Beheshti 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:Acanthamoeba- bacteria interactions enable pathogenic bacteria to tolerate harsh conditions and lead to transmission to the susceptible host. The present study was aimed to address the presence of bacterial endosymbionts of Acanthamoeba isolated from recreational water sources of Tehran, Iran. To the best of our knowledge this is the first study regarding occurrence of bacteria in environmental canthamoeba spp. in Iran.
Methods:A total of 75 samples of recreational water sources were collected. Samples were cultured on non- nutrient agar 1.5% plates. Positive Acanthamoeba &#xA0;spp. were axenically grown. DNA extraction and PCR reaction was performed using JDP1-2 primers. All positive samples of Acanthamoeba were examined for the presence of endosymbionts using staining and molecular methods. The PCR products were then sequenced in order to determine the genotypes of Acan-thamoeba and bacteria genera.
Results:Out of 75 samples, 16 (21.3%) plates were positive for Acanthamoeba according to the morphological criteria. Molecular analysis revealed that Acan-thamoeba belonged to T4 and T5 genotypes. Five isolates (35.7%) were positive for bacterial endosymbionts using staining method and PCR test. Sequencing of PCR products confirmed the presence of Pseudomonas aeruginosa and Agrobacterium tumefasiens.
Conclusion:The presence of Acanthamoeba bearing pathogenic endosymbionts in water sources leads us to public health issues including improved sanitation and decontamination measures in recreational water sources in order to prevent amoebae-related infection. To the best of our knowledge this is the first report regarding the isolation of A. tumefasiens from Acanthamoeba in Iran and world-wide.&#xA0;</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/334</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/334/466</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">Seroprevalence of Encephalitozoon cuniculi in Humans and Rabbits in China</title>
    <FirstPage>290</FirstPage>
    <LastPage>295</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Yaoqian</FirstName>
        <LastName>Pan</LastName>
        <affiliation locale="en_US">College of Animal Science and Henan Higher Education Engineering Technology Research Center for Animal Diseases Control and Residues Supervision, Henan Institute of Science and Technology, Xinxiang, Henan, PR China.</affiliation>
      </Author>
      <Author>
        <FirstName>Shuai</FirstName>
        <LastName>Wang</LastName>
        <affiliation locale="en_US">College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, 210095, PR China.</affiliation>
      </Author>
      <Author>
        <FirstName>Xingyou</FirstName>
        <LastName>Liu</LastName>
        <affiliation locale="en_US">College of Animal Science and Henan Higher Education Engineering Technology Research Center for Animal Diseases Control and Residues Supervision, Henan Institute of Science and Technology, Xinxiang, Henan, PR China.</affiliation>
      </Author>
      <Author>
        <FirstName>Ruizhen</FirstName>
        <LastName>Li</LastName>
        <affiliation locale="en_US">College of Animal Science and Henan Higher Education Engineering Technology Research Center for Animal Diseases Control and Residues Supervision, Henan Institute of Science and Technology, Xinxiang, Henan, PR China.</affiliation>
      </Author>
      <Author>
        <FirstName>Yuqian</FirstName>
        <LastName>Sun</LastName>
        <affiliation locale="en_US">College of Animal Science and Henan Higher Education Engineering Technology Research Center for Animal Diseases Control and Residues Supervision, Henan Institute of Science and Technology, Xinxiang, Henan, PR China.</affiliation>
      </Author>
      <Author>
        <FirstName>Javaid Ali</FirstName>
        <LastName>Gadahi</LastName>
        <affiliation locale="en_US">College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, 210095, PR China AND Department of Veterinary Parasitology, Sindh Agriculture University, Tandojam, Pakistan.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Encephalitozoon cuniculi is a microsporidian parasite commonly found in rabbits that can infect humans, causing encephalitozoonosis. Our objective in this study was to evaluate the seroprevalence of this parasite in rabbits and humans in China.
Methods: Overall, 300 serum samples each from clinically healthy rabbit and hu-man were collected from three regions of China (Sichuan Province, Chongqing Municipality and Jilin Province) from January to September 2013 and tested for anti- E. Cuniculi antibodies using an ELISA.
Results: An overall seroprevalence of E. cuniculi was recorded as 56/300 (18.76%) and 29/300 (9.76%) in rabbit and human sera, respectively. The seropositivity of rabbit samples collected from Jilin province was 41%, which was significantly higher (P&lt;0.01) than Sichuan Province (9%) and Chongqing Municipality (6%). Three breeds of rabbit were used in the present study and antibody detection in Rex Rabbit was significantly (P&lt;0.01) higher than Japanese White and New Zea-land Rabbit. In human, Jilin province was more prevalent (18%) followed by Si-chuan Province (6%) and Chongqing Municipality (5%).
Conclusions The E. cuniculi was present and widespread among healthy rabbits and humans in China.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/320</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/320/491</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">Phylogenetic Study of Haemonchus Species from Iran Based On Morpho-Molecular Characterization</title>
    <FirstPage>189</FirstPage>
    <LastPage>196</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Behnam</FirstName>
        <LastName>Meshgi</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Faculty of Veterinary Medicine, University of Tehran, Iran (Center of Excellent of Ecosystem and Ultrastructural Changes of Helminthes).</affiliation>
      </Author>
      <Author>
        <FirstName>Fatemeh</FirstName>
        <LastName>Jalousian</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Faculty of Veterinary Medicine, University of Tehran, Iran (Center of Excellent of Ecosystem and Ultrastructural Changes of Helminthes).</affiliation>
      </Author>
      <Author>
        <FirstName>Zahra</FirstName>
        <LastName>Masih</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Faculty of Veterinary Medicine, University of Tehran, Iran (Center of Excellent of Ecosystem and Ultrastructural Changes of Helminthes).</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background:Haemonchosis has a negative effect on the farming industry throughout the world, especially in the tropic and sub-tropic countries. The present study was carried out to differentiate Haemonchus species from its main hosts in Iran, including sheep, goat and camel.
&#xA0;Methods:The identification took place based on the morphometrics of the spic-ules and molecular characters. Two hundred seventy adult male nematodes were collected from the abomasums of different ruminants (90 samples from each ani-mal) at the slaughterhouses from different localities in Iran. Samples were morpho-logically identified according to the spicules&#x2019; morphometric measurements. In the section on molecular study, 10 samples of each Haemonchus isolates were genetically examined. A simple PCR-restriction fragment length polymorphism (PCR-RFLP) assay of the second internal transcribed spacer of ribosomal DNA (ITS2-rDNA) were described to confirm the PCR results.
Results:PCR-RFLP profile obtained from the restriction enzyme HPa1 in H. con-tortus and H. longistipes indicated 1 (278 bp) and 2 (113 and 135 bp) different frag-ments, respectively. The morphological parameters clearly distinguish H. contortus from H. longistipes. Moreover, regarding the ITS2-rDNA, sequences of 295 bp and 314 bp were obtained from H. contortus and H. longistipes, respectively.
Conclusion:The genotypic results are in agreement with the phenotypic findings of both species.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/333</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/333/468</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">Cloning and Sequence Analysis of Recombinant Plasmodium vivax Merozoite Surface Protein 1 (PvMSP-142 kDa) In pTZ57R/T Vector</title>
    <FirstPage>197</FirstPage>
    <LastPage>205</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Hadi</FirstName>
        <LastName>Mirahmadi</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, Shahid Beheshti 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>Adel</FirstName>
        <LastName>Spotin</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Shirzad</FirstName>
        <LastName>Fallahi</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Niloofar</FirstName>
        <LastName>Taghipour</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Habibollah</FirstName>
        <LastName>Turki</LastName>
        <affiliation locale="en_US">Infectious and Tropical Diseases Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Seyyed Javad</FirstName>
        <LastName>Seyyed Tabaei</LastName>
        <affiliation locale="en_US">Dept. of Parasitology and Mycology, Shahid Beheshti 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:Haemonchosis has a negative effect on the farming industry throughout the world, especially in the tropic and sub-tropic countries. The present study was carried out to differentiate Haemonchus species from its main hosts in Iran, including sheep, goat and camel.
&#xA0;Methods:The identification took place based on the morphometrics of the spic-ules and molecular characters. Two hundred seventy adult male nematodes were collected from the abomasums of different ruminants (90 samples from each ani-mal) at the slaughterhouses from different localities in Iran. Samples were morpho-logically identified according to the spicules&#x2019; morphometric measurements. In the section on molecular study, 10 samples of each Haemonchus isolates were genetically examined. A simple PCR-restriction fragment length polymorphism (PCR-RFLP) assay of the second internal transcribed spacer of ribosomal DNA (ITS2-rDNA) were described to confirm the PCR results.
Results:PCR-RFLP profile obtained from the restriction enzyme HPa1 in H. con-tortus and H. longistipes indicated 1 (278 bp) and 2 (113 and 135 bp) different frag-ments, respectively. The morphological parameters clearly distinguish H. contortus from H. longistipes. Moreover, regarding the ITS2-rDNA, sequences of 295 bp and 314 bp were obtained from H. contortus and H. longistipes, respectively.
Conclusion:High similarity of cloned PvMSP-142 kDa gene in comparison to reference sequence and other sequences could be beneficial as a remarkable mo-lecular marker for serological diagnostic.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/332</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/332/469</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">Comparison of Scolicidal Effects of Amphotricin B, Silver Nanoparticles,_and Foeniculum vulgare Mill on Hydatid Cysts Protoscoleces</title>
    <FirstPage>206</FirstPage>
    <LastPage>212</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mohammad Reza</FirstName>
        <LastName>Lashkarizadeh</LastName>
        <affiliation locale="en_US">Dept. of Surgery and the Research Center for Tropical and Infectious diseases, Kerman University of Medical Sciences, Kerman, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Keivan</FirstName>
        <LastName>Asgaripour</LastName>
        <affiliation locale="en_US">Dept. of Surgery and the Research Center for Tropical and Infectious diseases, Kerman University of Medical Sciences, Kerman, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Ebrahim</FirstName>
        <LastName>Saedi Dezaki</LastName>
        <affiliation locale="en_US">Research Center for Hydatid Disease in Iran, Kerman University of Medical Sciences, Kerman, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Majid</FirstName>
        <LastName>Fasihi Harandi</LastName>
        <affiliation locale="en_US">Research Center for Hydatid Disease in Iran, Kerman University of Medical Sciences, Kerman, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">&#xA0;
&#xD;
&#xD;
&#xD;
&#xD;
Background:Haemonchosis has a negative effect on the farming industry throughout the world, especially in the tropic and sub-tropic countries. The present study was carried out to differentiate Haemonchus species from its main hosts in Iran, including sheep, goat and camel.
&#xA0;Methods:The identification took place based on the morphometrics of the spic-ules and molecular characters. Two hundred seventy adult male nematodes were collected from the abomasums of different ruminants (90 samples from each ani-mal) at the slaughterhouses from different localities in Iran. Samples were morpho-logically identified according to the spicules&#x2019; morphometric measurements. In the section on molecular study, 10 samples of each Haemonchus isolates were genetically examined. A simple PCR-restriction fragment length polymorphism (PCR-RFLP) assay of the second internal transcribed spacer of ribosomal DNA (ITS2-rDNA) were described to confirm the PCR results.
Results:PCR-RFLP profile obtained from the restriction enzyme HPa1 in H. con-tortus and H. longistipes indicated 1 (278 bp) and 2 (113 and 135 bp) different frag-ments, respectively. The morphological parameters clearly distinguish H. contortus from H. longistipes. Moreover, regarding the ITS2-rDNA, sequences of 295 bp and 314 bp were obtained from H. contortus and H. longistipes, respectively.
Conclusion:High similarity of cloned PvMSP-142 kDa gene in comparison to reference sequence and other sequences could be beneficial as a remarkable mo-lecular marker for serological diagnostic.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/331</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/331/470</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">Abnormalities of Endocytosis, Phagocytosis, and Development Process in Dictyostelium Cells That Over-Express Acanthamoeba castellanii Metacaspase Protein</title>
    <FirstPage>213</FirstPage>
    <LastPage>229</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Entsar</FirstName>
        <LastName>Saheb</LastName>
        <affiliation locale="en_US">Dept. of Biology, College of Sciences, University of Baghdad, Baghdad, Iraq.</affiliation>
      </Author>
      <Author>
        <FirstName>Wendy</FirstName>
        <LastName>Trzyna</LastName>
        <affiliation locale="en_US">Dept. of Biological Sciences, Marshall University, Huntington, West Virginia, USA.</affiliation>
      </Author>
      <Author>
        <FirstName>Katherine</FirstName>
        <LastName>Maringer</LastName>
        <affiliation locale="en_US">Dept. of Biology, College of Science and Mathematics, University of Arkansas at Little Rock, Arkansas, USA.</affiliation>
      </Author>
      <Author>
        <FirstName>John</FirstName>
        <LastName>Bush</LastName>
        <affiliation locale="en_US">Dept. of Biology, College of Science and Mathematics, University of Arkansas at Little Rock, Arkansas, USA.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background:Acanthamoeba castellanii forms a resistant cyst that protects the para-site against the host&#x2019;s immune response. Acanthamoeba Type-I metacaspase (Acmcp) is a caspase-like protein that has been found to be expressed during the encysta-tions. Dictyostelium discoideum is an organism closely related to Acanthamoeba useful for studying the molecular function of this protozoan caspase-like protein. 
Methods:The full length of Acmcp and a mutated version of the same gene, which lacks the proline rich N-terminal region (Acmcp-dpr), were cloned into the pDneo2a-GFP vector separately. The pDneo2a-GFP-Acmcp and pDneo2a-GFP-Acmcp-dpr were electro-transfected into wild type D. discoideum cells to create cell lines that over-expressed Acmcp or Acmcp-dpr.
Results:Both cell lines that over-expressed Acmcp and Acmcp-dpr showed a sig-nificant increase in the fluid phase internalization and phagocytosis rate compared to the control cells. Additionally, the cells expressing the Acmcp-dpr mutant were unable to initiate early development and failed to aggregate or form fruiting bodies under starvation conditions, whereas Acmcp over-expressing cells showed the op-posite phenomena. Quantitative cell death analysis provided additional support for these findings.
&#xA0;Conclusion:Acmcp is involved in the processes of endocytosis and phagocytosis. In addition, the proline rich region in Acmcp is important for cellular development in Dictyostelium. Given its important role in the development process, metacaspase protein is proposed as a candidate drug target against infections caused by A. castel-lanii.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/330</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/330/471</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 Use of Recombinant 31 kDa Antigens of Trichinella spiralis for Serodiagnosis of Experimental Trichinellosis</title>
    <FirstPage>230</FirstPage>
    <LastPage>237</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Li</FirstName>
        <LastName>Wang</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Medical College, Zhengzhou University, P. R. China.</affiliation>
      </Author>
      <Author>
        <FirstName>Xiang Yu</FirstName>
        <LastName>Tian</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Medical College, Zhengzhou University, P. R. China.</affiliation>
      </Author>
      <Author>
        <FirstName>Ge Ge</FirstName>
        <LastName>Sun</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Medical College, Zhengzhou University, P. R. China.</affiliation>
      </Author>
      <Author>
        <FirstName>Ruo Dan</FirstName>
        <LastName>Liu</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Medical College, Zhengzhou University, P. R. China.</affiliation>
      </Author>
      <Author>
        <FirstName>Li Na</FirstName>
        <LastName>Liu</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Medical College, Zhengzhou University, P. R. China.</affiliation>
      </Author>
      <Author>
        <FirstName>Xi</FirstName>
        <LastName>Zhang</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Medical College, Zhengzhou University, P. R. China.</affiliation>
      </Author>
      <Author>
        <FirstName>Peng</FirstName>
        <LastName>Jiang</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Medical College, Zhengzhou University, P. R. China.</affiliation>
      </Author>
      <Author>
        <FirstName>Zhong Quan</FirstName>
        <LastName>Wang</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Medical College, Zhengzhou University, P. R. China.</affiliation>
      </Author>
      <Author>
        <FirstName>Jing</FirstName>
        <LastName>Cui</LastName>
        <affiliation locale="en_US">Dept. of Parasitology, Medical College, Zhengzhou University, P. R. China.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background:We have previously reported that a 31 kDa protein was screened from the excretory-secretory (ES) proteins of Tichinella spiralis muscle larvae (ML) by immunoproteomics using early infection sera, and the gene encoding a 31 kDa protein from T. spiralis was cloned and expressed in an E. coli expression system. In this study, the recombinant 31 kDa antigens were used for detection of anti- Trichinella antibodies in serum of experimentally infected mice by ELISA.
&#xA0;Methods:Anti-Trichinella IgG antibodies in sera of mice infected with Trichinella were assayed by ELISA with recombinant 31 kDa antigens, and its sensitivity and specificity were compared with ELISA with ES antigen.
Results:The sensitivity and specificity of ELISA with recombinant antigens was 96.67% (29/30) and 96.87% (62/64), compared with 100% (30/30) and 98.44% (63/64) of ELISA with ES antigens was (P&#xFF1E;0.05). In heavily, moderately and lightly infected mice (500, 300 and 100 larvae/mouse), anti-Trichinella antibodies were firstly detected by ELISA with recombinant antigens at 8, 12 and 14 dpi, re-spectively; then increased rapidly with a detection rate of 100% respectively at 28, 22 and 30 dpi. While the antibodies were firstly detected by ELISA with ES anti-gens at 10, 8 and 10 dpi, respectively, the antibody positive rate reached 100% at 14, 12 and 22 dpi, respectively.
Conclusion:The recombinant 31 kDa antigens of T. spirali had a good sensitivity and sp <LastName>FALLAH</LastName>
        <affiliation locale="en_US">Department of Clinical Biochemistry, School of Medicine, Iran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Abdoulreza</FirstName>
        <LastName>ESTEGHAMATI</LastName>
        <affiliation locale="en_US">Research Center of Pediatric Infectious Diseases, Institute of Immunology and Infectious Diseases, Iran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>MASOUMI-ASL</LastName>
        <affiliation locale="en_US">Research Center of Pediatric Infectious Diseases, Institute of Immunology and Infectious Diseases, Iran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>09</Month>
        <Day>16</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>06</Month>
        <Day>19</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Trichomonas vaginalis is a prevalent sexually transmitted infection cause trichomoniasis. In this study prevalence and genotype of Iranian isolates of T. vaginalis infected (dsRNA) viruses were evaluated by PCR-RFLP and obtained patterns were then confirmed by sequence analysis and genotype of these Iranian isolates confirmed again.
&#xD;

Methods: Ten strains of T.vaginalis were collected from 1700 vaginal samples of women referred to hospitals associated with Iran University of Medical Sciences in Tehran, Iran during Feb 2016 to Jul 2017, evaluated in points of infection to T. vaginalis Virus (TVV-1) were used in a PCR-RFLP. All of ten isolates of T. vaginalis were examined by designed nested PCR for actin gene and then digestion patterns of three endonuclease enzymes of HindII, MseI and RsaI were evaluated and genotype of these isolates was defined.
&#xD;

Results: By combination of fragments pattern of three enzymes of HindII, RsaI and MseI, three genotypes were found; six genotypes E, two genotypes G and two genotypes I. The most dominant genotypes were genotype E. Among four TVV infected isolates two genotype E, one genotype G and one genotype I were found, however among six uninfected T. vaginalis isolates to TVV-1, all of three genotypes were also found.
&#xD;

Conclusion: Three genotypes E, G and I in T. vaginalis infected with dsRNA isolates were found, however, these three genotypes in T. vaginalis without virus were also observed. Further study is needed to evaluate genotypes of T. vaginalis, which infected virus in more great T. vaginalis population.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/1758</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/1758/957</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>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>06</Month>
        <Day>18</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Metabolomics Based Study of the Antileishmanial Activity of Xanthium strumarium Leaf Extract on Promastigotes Phases of Leishmania major by Proton NMR Spectroscopy</title>
    <FirstPage>258</FirstPage>
    <LastPage>268</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>AHMADI</LastName>
        <affiliation locale="en_US">Metabolomics Laboratory, Department of Biochemistry, Pasteur Institute of Iran, Tehran, Iran  AND Department of Biological Sciences, Payam Noor University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ziba</FirstName>
        <LastName>AKBARI</LastName>
        <affiliation locale="en_US">Metabolomics Laboratory, Department of Biochemistry, Pasteur Institute of Iran, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mahbobeh</FirstName>
        <LastName>ALIKHANI</LastName>
        <affiliation locale="en_US">Metabolomics Laboratory, Department of Biochemistry, Pasteur Institute of Iran, Tehran, Iran AND	Department of Biological Sciences, Payam Noor University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Reza</FirstName>
        <LastName>HAJHOSSIANI</LastName>
        <affiliation locale="en_US">Department of Biological Sciences, Payam Noor University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Zahra</FirstName>
        <LastName>ZAMANI</LastName>
        <affiliation locale="en_US">Metabolomics Laboratory, Department of Biochemistry, Pasteur Institute of Iran, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>ARJMAND</LastName>
        <affiliation locale="en_US">Metabolomics Laboratory, Department of Biochemistry, Pasteur Institute of Iran, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>05</Month>
        <Day>20</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>06</Month>
        <Day>18</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Xanthium strumarium L. is extensively used as a traditional herb to treat many diseases and is also known as a source of phytochemicals. It has been used traditionally to treat trypanosomiasis, malaria fever, eczema, cancer, ulcer, fever, herpes headache, and skin lesion such as leishmaniasis. In this preliminary study, nuclear magnetic resonance (NMR)-metabolomics approaches was used to evaluate the inhibitory effects and metabolic alterations caused by leaf extract of X. strumarium on the stationary phases of promastigotes in Leishmania major.
&#xD;

Methods: The promastigotes were cultured in Biochemistry Laboratory at Pasteur Institute of Iran in 2017, stationary phases were obtained from 5 to 6 day-old cultures and treated with different concentrations of the plant&#x2019;s extract. Antileishmanial activity was assayed by MTT method and cell metabolites were extracted. 1H NMR spectroscopy was applied, and outliers were separated using multivariate statistical analysis.
&#xD;

Results: The most affected metabolic pathways in the experimental groups were limited to amino sugar and nucleotide sugar metabolism, cyanoamino acid metabolism, starch and sucrose metabolism, butanoate metabolism, and galactose metabolism.
&#xD;

Conclusion: The ethanolic leaf extract of X. strumarium is a potent growth inhibitor of Leishmania major and can affect vital metabolic pathways of Leishmania promastigotes. The assay provided new perspectives on the development of novel treatment strategies for leishmanial activity derived from natural products.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/2138</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/2138/941</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>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>06</Month>
        <Day>18</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">In Vitro and in Vivo Scolicidal Activities of Holothuria leucospilota Extract and CeO2 Nanoparticles against Hydatid Cyst</title>
    <FirstPage>269</FirstPage>
    <LastPage>279</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Safa</FirstName>
        <LastName>ARYAMAND</LastName>
        <affiliation locale="en_US">Cellular and Molecular Research Center, Department of Medical Parasitology and Mycology, Urmia University of Medical Sciences, Urmia, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Shahram</FirstName>
        <LastName>KHADEMVATAN</LastName>
        <affiliation locale="en_US">Cellular and Molecular Research Center, Department of Medical Parasitology and Mycology, Urmia University of Medical Sciences, Urmia, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Khosrow</FirstName>
        <LastName>HAZRATI TAPPEH</LastName>
        <affiliation locale="en_US">Cellular and Molecular Research Center, Department of Medical Parasitology and Mycology, Urmia University of Medical Sciences, Urmia, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Behnam</FirstName>
        <LastName>HESHMATIAN</LastName>
        <affiliation locale="en_US">Department of Physiology, Urmia University of Medical Sciences, Urmia, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ali</FirstName>
        <LastName>JELODAR</LastName>
        <affiliation locale="en_US">Department of Medical Parasitology, Jondishapur University of Medical Sciences, Ahvaz, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>10</Month>
        <Day>10</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2018</Year>
        <Month>05</Month>
        <Day>21</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: We aimed to investigate the scolicidal effects of Holothuria leucospilota extract and CeO2 nanoparticles against protoscoleces of hydatid cysts in-vitro and in-vivo.
&#xD;

Methods: Hydatid cysts were collected from, Urmia slaughterhouses between years 2016-2017 and the hydatid fluid aspirated from the fertile cysts. Various concentration of H. leucospilota extract, CeO2 NPs and combination of CeO2-NPs/H. leucospilota were used for 10-60 min to evaluate the viability of protoscoleces by 0.1% eosin method. CASPASE -3 activity measured for assessment of cell apoptosis in treated protoscoleces. BALB/c mice were infected intraperitoneally with 2000 viable protoscoleces and treated daily for 4 wk by intragastrical inoculation with H. leucospilota, CeO2 NPs, combination of CeO2 NPs/H. leucospilota and Albendazole. Cyst development was macroscopically analyzed.
&#xD;

Results: H. leucospilota extract and combination of CeO2 NPs/H. leucospilota have potent scolicidal activity at concentration of 20 mg/ml and 15 mg/ml after 60 min treatment. Maximum caspase-3 activity was observed when protoscoleces expose with H. leucospilota and combination H. leucospilota &amp; CeO2 NPs. After treatment of cyst infected mice with extract and CeO2 NPs, combination of CeO2 NPs/H leucospilota and albendazole, a significant decrease in number of cysts, size and volume of cyst (P&lt;0.05) was observed.
&#xD;

Conclusion: This result shows an antihydatic and scolicidal effects of H. leucospilota extract and CeO2 NPs.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/1820</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/1820/942</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>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>06</Month>
        <Day>18</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Evaluation of Three Different Laboratory Methods for Identification of Pneumocystis jirovecii Pneumonia (PCP) among HIV Positive Asymptomatic Prisoners</title>
    <FirstPage>280</FirstPage>
    <LastPage>287</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Shohreh</FirstName>
        <LastName>AZIMI</LastName>
        <affiliation locale="en_US">Department of Microbiology, Karaj Branch, Islamic Azad University, Karaj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Azar</FirstName>
        <LastName>SABOKBAR</LastName>
        <affiliation locale="en_US">Department of Microbiology, Karaj Branch, Islamic Azad University, Karaj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Amir</FirstName>
        <LastName>BAIRAMI</LastName>
        <affiliation locale="en_US">Department of Medical Parasitology and Mycology, School of Medicine, Alborz University of Medical Sciences, Karaj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Javad</FirstName>
        <LastName>GHARAVI</LastName>
        <affiliation locale="en_US">Department of Medical Parasitology and Mycology, School of Medicine, Alborz University of Medical Sciences, Karaj, Iran AND Department of Parasitology, School of Allied Medicine, Iran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>08</Month>
        <Day>28</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2018</Year>
        <Month>01</Month>
        <Day>15</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Pneumocystis jirovecii pneumonia (PCP) remains a leading cause of mortality among HIV-infected patients. The aim of study was to find out P. jirovecii in versatile group of HIV-positive patients prisoners.
&#xD;

Methods: Overall, 102 HIV positive patients from Ghezel Hesar Prison, Karaj, Iran from October 2016 to March 2017 without any respiratory symptoms were selected with different medication histories against HIV and PCP. Microscopic and molecular (qualitative real-time PCR) examination were applied on sputum specimens and serological investigation (&#x3B2;-D-glucan assay for fungal diseases) carried out on patient&#x2019;s sera.
&#xD;

Results: Only 3 and 1 patients were positive for PCP by microscopic and molecular testing, respectively. Twenty-four (23.5%) and 78 (76.5%) out of 102 patients were seropositive and seronegative for fungi disease, respectively. Seropositive patients were older than seronegative subjects (P&lt;0.001). Most of seropositive individuals showed less mean value of CD4 counts compared to seronegative group (P&lt;0.001). Of 54 patients who were under HIV therapy, 13 were seropositive compared to 11 out of 24 seropositives who were no adhere to treatment (P&lt;0.001). In terms of prophylactic antibiotic therapy against PCP, of 24 patients who received prophylaxis, 3 (12.5%) and 21 (87.5%) were seropositive and seronegative, respectively (P&lt;0.001). On the contrary, among 78 patients who did not receive prophylaxis, 21 (27%) and 57 (73%) belonged to seropositive and seronegative patients, respectively (P&lt;0.001).
&#xD;

Conclusion: There was no strong evidence for PCP infection/disease among symptomless, HIV positive patients. According to their mean CD4 counts, the hypothesis for being negative in a majority of applied tests would be the absence of severe immunosuppression in the patients.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/1740</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/1740/943</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>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>06</Month>
        <Day>18</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Echinococcus granulosus sensu stricto in Livestock and Human in Hamadan, Western Iran</title>
    <FirstPage>288</FirstPage>
    <LastPage>296</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>MATINI</LastName>
        <affiliation locale="en_US">Department of Medical Parasitology and Mycology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>FALLAH</LastName>
        <affiliation locale="en_US">Department of Medical Parasitology and Mycology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Amir Hossein</FirstName>
        <LastName>MAGHSOOD</LastName>
        <affiliation locale="en_US">Department of Medical Parasitology and Mycology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Massoud</FirstName>
        <LastName>SAIDIJAM</LastName>
        <affiliation locale="en_US">Department of Molecular Medicine and Genetics, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Majid</FirstName>
        <LastName>FASIHI HARANDI</LastName>
        <affiliation locale="en_US">Research Center for Hydatid Disease in Iran, Kerman University of Medical Sciences, Kerman, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>04</Month>
        <Day>07</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>06</Month>
        <Day>18</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Cystic echinococcosis, a major public health and economic concern, is a zoonotic helminth infection with worldwide distribution. This study was conducted to investigate the genetic characteristics of hydatid cysts isolated from human and livestock in Hamadan region, western Iran during 2016-2017.
&#xD;

Methods: Ten human hydatid cysts and 40 animal hydatid cysts including 32 sheep, 5 cattle and 3 goats were genotyped by PCR amplification of two mitochondrial genes, cox1 and nad1. Genetic identification of the isolates was performed by using bioinformatics software and mtDNA nucleotide sequences of the parasite, available in GenBank database.
&#xD;

Results: The PCR amplification was successfully carried out on 50 hydatid cyst isolates and then the nucleotide sequencing was conducted. The sequence analysis of the samples found that the isolates belonged to E. granulosus sensu stricto including G1 (42/50, 84%), G2 (4/50, 8%) and G3 (4/50, 8%) genotype. The G1 genotype was detected in human (8/10, 80%), sheep (26/32, 81%), cattle (5/5, 100%) and goat (3/3, 100%) hydatid cysts. The G2 and G3 genotypes were found only in sheep and human isolates. Alignment analysis of the cox1 and nad1 gene sequences revealed thirteen and ten sequence types, respectively.
&#xD;

Conclusion: G1 was the prevailing genotype of E. granulosus in the area and dog-sheep transmission cycle should be considered when implementing hydatidosis control programs. In addition, high genetic diversity was detected among the hydatid cyst isolates.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/2074</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/2074/944</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>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>06</Month>
        <Day>19</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">First Molecular Survey on Anaplasma phagocytophilum Revealed High Prevalence in Rural Dogs from Khuzestan Province, Iran</title>
    <FirstPage>297</FirstPage>
    <LastPage>302</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>HAMIDINEJAT</LastName>
        <affiliation locale="en_US">Department of Parasitology, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Somayeh</FirstName>
        <LastName>BAHRAMI</LastName>
        <affiliation locale="en_US">Department of Parasitology, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Bahman</FirstName>
        <LastName>MOSALANEJAD</LastName>
        <affiliation locale="en_US">Department of Clinical Sciences, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Sharareh</FirstName>
        <LastName>PAHLAVAN</LastName>
        <affiliation locale="en_US">Department of Parasitology, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>08</Month>
        <Day>20</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2018</Year>
        <Month>05</Month>
        <Day>21</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Anaplasmosis due to Anaplasma phagocytophilum is an important tick-borne zoonotic disease, which affects dogs, horses, cattle and human as well. This study aimed to probe the existence of this organism by means of molecular biology techniques for the first time in rural dogs of Khuzestan province, Southwestern Iran.
&#xD;

Methods: During Sep 2014 to Apr 2015 blood samples of 103 apparently healthy rural dogs (60 males) were collected for A. phagocytophilum detection by light microscopical examination of Giemsa stained slides and Nested PCR on a fragment of 16S rRNA gene.
&#xD;

Results: From the examined slides, 11.65% were positive for A. morulae while 57.28% of infection was revealed by Nested PCR method. There was no statistical difference between ages and sexes of dogs and infection in molecular survey of A. phagocytophilum.
&#xD;

Conclusion: Molecular prevalence of A. phagocytophilum was noticeably high. It may cause the incidence of disease in human population.</abstract>
    <web_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/view/1739</web_url>
    <pdf_url>https://ijpa.tums.ac.ir/index.php/ijpa/article/download/1739/945</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>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2019</Year>
        <Month>06</Month>
        <Day>19</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Epidemiological Studies on Porcine Trichinellosis in Five States of North East India</title>
    <FirstPage>303</FirstPage>
    <LastPage>309</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Gohain Barua</FirstName>
        <LastName>ACHEENTA</LastName>
        <affiliation locale="en_US">Department of Veterinary Public Health, College of Veterinary Science, Assam Agricultural University, Guwahati-781022, Assam, India</affiliation>
      </Author>
      <Author>
        <FirstName>Chutia Pawan</FirstName>
 