Articles

Phylogenetic Location of the Spirometra Sparganum Isolates from China, Based on Sequences of 28S rDNA D1

Abstract

Background: The phylogenetic location of Chinese Spirometra sparganum isolates remains unclear. The aim of this study was to explore the phylogenetic location of the Spirometra sparganum isolates from China.

Methods: The 28S ribosomal DNA (rDNA) D1 sequences of 14 Spirometra sparganum isolates collected from thirteen locations in China were analyzed by using Neighbor-Joining (NJ), maximum parsimony (MP) and Bayesian inference (BI),respectively. To investigate the deep variance of 28S rDNA D1 region among included species, the secondary structure of 28S rDNA D1 region was also calculated using the program RNA structure.

Results: The genus Spirometra as a monophyletic group was evidenced by two inference methods (MP and BI). All sequences within the genus Spirometra had a bulge of a cytosine residue (Bulge C) in the stem 13 of the secondary structure model of 28S rRNA D1 region. Varietal sites in sequences from all thirteen Chinese isolates were appeared in loops. In loops, adenine was the most abundant base(averagely 41.9%) followed by guanine (averagely 30.0%), and cytosine (averagely 15.1%). In stems, the average percentage of G + C (58.3%) was higher than the percentage of A + T (41.7%).

Conclusion: The „Bulge C‟ in the stem 13 of the 28S rDNA D1 secondary structure could be as a suitable mark to identify the Spirometra species

Fukushima T, Yamane Y. How does the sparganosis occur? Parasitol Today. 1999;15:124.

Nithiuthai S, Anantaphruti MT, Waikagul J, Gajadhar A. Waterborne zoonotic helminthiases. Vet Parasitol. 2004;126:167–193.

Magnino S, Colin P, Dei-Cas E, Madsen M, McLauchlin J, Nöckler K, Maradona MP, Tsigarida E, Vanopdenbosch E, Van Peteghem C. Biological risks associated with consumption of reptile products. Int J Food Microbiol. 2009;134:163–175.

Shirakawa K, Yamasaki H, Ito A, Miyajima H. Cerebral sparganosis: the wandering lesion. Neurology. 2010;74:180.

Cui J, Lin XM, Zhang HW, Xu BL, Wang ZQ. Sparganosis, Henan Province, central China. Emerg Infect Dis. 2011;17:146–147.

Hu DD, Cui J, Wang L, Liu LN, Wei T, ZQ. Immunoproteomic analysis of the excretorysecretory proteins from Spirometra mansoni sparganum. Iran J Parasitol. 2013;8:408–416.

Wiwanitkit V. A review of human sparganosis in Thailand. Int J Infect Dis. 2005;9:312–316.

Lee SU, Huh S, Sohn WM. Molecular phylogenic location of the Plagiorchis muris (Digenea, Plagiorchiidae) based on sequences of partial 28S rDNA and mitochondrial cytochrome c oxidase subunit I. Korean J Parasitol. 2004;42:71–75.

Lee SU, Chun HC, Huh S. Molecular phylogeny of parasitic Platyhelminthes based on sequences of partial 28S rDNA D1 and mitochondrial cytochrome c oxidase subunit I. Korean J Parasitol. 2007;45:181–189.

Olson PD, Littlewood DTJ, Bray RA, Mariaux J. Interrelationships and Evolution of the Tapeworms (Platyhelminthes: Cestoda). Mol Phylogenet Evol. 2001;19:443–467.

Brabec J, Kuchta R, Scholz T. Paraphyly of the Pseudophyllidea (Platyhelminthes: Cestoda): Circumscription of monophyletic clades based on phylogenetic analysis of ribosomal RNA. Int J Parasitol. 2006;36:1535–1541.

Waeschenbach A, Webster BL, Bray RA, Littlewood DTJ. Added resolution among ordinal level relationships of tapeworms (Platyhelminthes: Cestoda) with complete small and large subunit nuclear ribosomal RNA genes. Mol Phylogenet Evol. 2007;45:311–325.

Crease TJ, Colbourne JK. The unusually long small-subunit ribosomal RNA of the Crustacean, Daphnia pulex: sequence and predicted secondary structure. J Mol Evol. 1998;46:307–313.

Hwang UW, Ree HI, Kim W. Evolution of hypervariable regions, V4 and V7, of insect 18S rRNA and their phylogenetic implications. Zoolog Sci. 2000;17:111–121.

Zhao YE, Wang ZH, Xu Y, Wu LP, Hu L. Secondary structure prediction for complete rDNA sequences (18S, 5.8S, and 28S rDNA) of Demodex folliculorum, and comparison of divergent domains structures across Acari. Exp Parasitol. 2013;135:370–381.

Gillespie JJ, Yoder MJ, Wharton RA. Predicted secondary structure for 28S and 18S rRNA from Ichneumonoidea (Insecta: Hymenoptera: Apocrita): impact on sequence alignment and phylogeny estimation. J Mol Evo. 2005;61:114–137.

Pepato AR, da Rocha CE, Dunlop JA. Phylogenetic position of the acariform mites: sensitivity to homology assessment under total evidence. BMC Evol Biol 2010;10:235.

Higgins DG, Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, Valentin F, Wallace IM, Wilm A, Lopez R, Thompson JD, Gibson TJ. Clustal W and clustal X version 2.0. Bioinformatics. 2007;23:2947–2948.

Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S. MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011;28:2731–2739.

Xia XH, Xie ZH. DAMBE: Data analysis in molecular biology and evolution. J Hered. 2001;92:371–373.

Xia XH, Xie ZH, Salemi M, Chen L, Wang Y. An index of substitution saturation and its application. Mol Phylogenet Evol. 2003;26:1–7.

Swofford DL. Phylogenetic Analysis Using Parsimony (PAUP) and Other Methods. Version 4.0b10. Sinauer Associates, Sunderland, MA. 2003.

Posada D, Crandall KA. MODELTEST: testing the model of DNA substitution. Bioinformatics. 1998;14:817–818.

Ronquist F, Huelsenbeck JP. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003;19:1572–1574.

Mathews DH, Disney MD, Childs JL, Schroeder SJ, Zuker M, Turner DH. Incorporating chemical modification constraints into a dynamic programming algorithm for prediction of RNA secondary structure. Proc Natl Acad Sci USA. 2004;101:7287–7292.

van Knippenberg PH, Formenoy LJ, Heus HA. Is there a special function for U : G basepairs in ribosomal RNA? Biochimica et Biophysica Acta. 1990;1050:14–17.

De Rijk P, Wuyts J, De Wachter R. RnaViz 2: an improved representation of RNA secondary structure. Bioinformatics. 2003;19:299–300.

Dai RS, Liu GH, Song HQ, Lin RQ, Yuan ZG, Li MW, Huang SY, Liu W, Zhu XQ. Sequence variability in two mitochondrial DNA regions and internal transcribed spacer among three cestodes infecting animals and humans from China. J Helminthol. 2012;86:245–251.

Liu W, Liu GH, Li F, He DS, Wang T, Sheng XF, Zeng DL, Yang FF, Liu Y. Sequence variability in three mitochondrial DNA regions of Spirometra erinaceieuropaei spargana of human and animal health significance. J Helminthol. 2012;86:271–275.

Bogitsch BJ, Carter CE, Oeltmann TN. Human parasitology, 3rd ed. Academic, New York, NY. 2005.

Roberts LS, Janovy J Jr, Gerald D. Foundations of Parasitology, 8th ed. McGraw-Hill, New York. 2009.

Springer MS, Douzery E. Secondary structure and patterns of evolution among mammalian mitochondrial 16S rRNA molecules. J Mol Evol. 1996;43:357–373.

Burk A, Douzery E, Springer MS. The Secondary Structure of Mammalian Mitochondrial 16S rRNA Molecules: Refinements Based on a Comparative Phylogenetic Approach. J Mamm Evol. 2000;9:225–252.

Files
IssueVol 9 No 3 (2014) QRcode
SectionArticles
Keywords
28S ribosomal DNA Diphyllobothrium Molecular phylogeny Secondary structure Spirometra

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
1.
Zhang X, Cui J, Liu LN, Wei T, Jiang P, Wang ZQ. Phylogenetic Location of the Spirometra Sparganum Isolates from China, Based on Sequences of 28S rDNA D1. Iran J Parasitol. 1;9(3):319-328.