Background Oncomelania hupensis is the unique intermediate host of Schistosoma japonicum, which causes schistosomiasis endemic in the Far East, and especially in mainland China. O. hupensis largely determines the parasite's geographical range. How O. hupensis's genetic diversity is distributed geographically in mainland China has never been well examined with DNA sequence data. Methodology/Principal Findings In this study we investigate the genetic variation among O. hupensis from different geographical origins using the combined complete internal transcribed spacer 1 (ITS1) and ITS2 regions of nuclear ribosomal DNA. 165 O. hupensis isolates were obtained in 29 localities from 7 provinces across mainland China: lake/marshland and hill regions in Anhui, Hubei, Hunan, Jiangxi and Jiangsu provinces, located along the middle and lower reaches of Yangtze River, and mountainous regions in Sichuan and Yunnan provinces. Phylogenetic and haplotype network analyses showed distinct genetic diversity and no shared haplotypes between populations from lake/marshland regions of the middle and lower reaches of the Yangtze River and populations from mountainous regions of Sichuan and Yunnan provinces. The genetic distance between these two groups is up to 0.81 based on Fst, and branch time was estimated as 2–6 Ma. As revealed in the phylogenetic tree, snails from Sichuan and Yunnan provinces were also clustered separately. Geographical separation appears to be an important factor accounting for the diversification of the two groups of O. hupensis in mainland China, and probably for the separate clades between snails from Sichuan and Yunnan provinces. In lake/marshland and hill regions along the middle and lower reaches of the Yangtze River, three clades were identified in the phylogenetic tree, but without any obvious clustering of snails from different provinces. Conclusions O. hupensis in mainland China may have considerable genetic diversity, and a more complex population structure than expected. It will be of significant importance to consider the genetic diversity of O. hupensis when assessing co-evolutionary interactions with S. japonicum.
References
[1]
Davis GM, Zhang Y, Guo YH, Spolsky CM (1995) Population genetics and systematic status of Oncomelania hupensis (Gastropoda: Pomatiopsidae) throughout China. Malacologia 37: 133–156.
[2]
Liu YY, Lou TK, Wang YX, Zhang WZ (1981) Subspecific differentiation of oncomelanid snails. Acta Zootaxonomica Sinica 6: 253–267 (In Chinese).
[3]
Wilke T, Davis GM, Chen C-E, Zhou X-N, Zeng XP (2000) Oncomelania hupensis (Gastropoda: Rissooidea) in eastern China: molecular phylogeny, population structure, and ecology. Acta Trop 77: 215–227. doi: 10.1016/S0001-706X(00)00143-1
[4]
Davis GM, Zhang Y, Xu XJ, Yang XX (1999) Allozyme analyses test the taxonomic relevance of ribbing in Chinese Oncomelania (Gastropoda: Rissoacea: Pomatiopsidae). Malacologia 41: 297–317.
[5]
Hadidjaja P, Sudomo M (1976) Some aspects on the ecology and biology of Oncomelania hupensis lindoensis. Southeast Asian J Trop Med Public Health 7: 227–232.
[6]
Kajihara N, Horimi T, Minai M, Hosaka Y (1979) Field assessment of B-2 as a new molluscicide for the control of Oncomelania nosophora. Jpn J Med Sci Biol 32: 225–228.
[7]
Yasuraoka K, Santos AT Jr, Blas BL, Tanaka H, Matsuda H, et al. (1989) Schistosomiasis on Bohol Island, Philippines, with special emphasis on the successful discovery of new habitats of the vector snail, Oncomelania quadrasi, and area-wide mollusciciding. Jpn J Exp Med 59: 149–155.
[8]
Lo CT, Lee KM (1995) Schistosoma japonicum, zoophilic strain, in Oncomelania hupensis chiui and O. h. formosana: miracidial penetration and comparative histology. J Parasitol 81: 708–713. doi: 10.2307/3283959
[9]
Ross AG, Sleigh AC, Li Y, Davis GM, Williams GM, et al. (2001) Schistosomiasis in the People's Republic of China: prospects and challenges for the 21st century. Clin Microbiol Rev 14: 270–295. doi: 10.1128/CMR.14.2.270-295.2001
[10]
Zhou XN, Wang LY, Chen MG, Wu XH, Jiang QW, et al. (2005) The public health significance and control of schistosomiasis in China – then and now. Acta Trop 96: 96–105. doi: 10.1016/j.actatropica.2005.07.005
[11]
Zhou YB, Jiang QW, Zhao GM, Yuan HC (2007) Subspecies differentiation of Oncomelania hupensis from mainland China. Chin J Schisto Control 19: 485–487 (In Chinese).
[12]
Zhou YB, Yang MX, Zhao GM, Wei JG, Jiang QW (2007) Oncomelania hupensis (Gastropoda: Rissooidea), intermediate host of Schistosoma japonicum in China: genetics and molecular phylogeny based on amplified fragment length polymorphisms. Malacologia 49: 367–382. doi: 10.4002/0076-2997-49.2.367
[13]
Zhou YB, Zhao GM, Wei JG, Jiang QW (2007) Spatial genetic correlation analyses of Schistosoma japonicum intermediate hosts within Oncomelania hupensis (Gastropoda: Rissooidea) from mainland China based on amplified fragment length polymorphisms. Fudan Univ J Med Sci 34: 207–212 (In Chinese).
[14]
Li SZ, Wang YX, Yang K, Liu Q, Wang Q, et al. (2009) Landscape genetics: the correlation of spatial and genetic distances of Oncomelania hupensis, the intermediate host snail of Schistosoma japonicum in mainland China. Geospat Health 3: 221–231.
[15]
Spolsky CM, Davis GM, Zhang Y (1996) Sequencing methodology and phylogenetic analysis: cytochrome b gene sequence reveals significant diversity in Chinese populations of Oncomelania (Gastropoda: Pomatiopsidae). Malacologia 38: 213–221.
[16]
Zhou XN, Hong QB, Sun LP, Xu Q, Lu AS, et al. (1995) Population genetics of Oncomelania spp. in mainland China. I. Genetic variation among populations of Oncomelania spp. Chin J Schisto Control 7: 67–71 (In Chinese).
[17]
Qian BZ, Kristensen TK, B?gh HO (1996) Allozyme variations among six populations of freshwater-snail Oncomelania hupensis in Zhejiang, China. Southeast Asian J Trop Med Public Health 27: 400–405.
[18]
Sambrook J, Fritsch EF, Maniatis T (2001) Molecular Cloning: A laboratory manual. NY: Cold Spring Harbor Laboratory Press.
[19]
Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1997) The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucl Acids Res 25: 4876–4882. doi: 10.1093/nar/25.24.4876
[20]
Galtier N, Gouy M, Gautier C (1996) SEAVIEW and PHYLO_WIN: two graphic tools for sequence alignment and molecular phylogeny. Comput Appl Biosci 12: 543–548. doi: 10.1093/bioinformatics/12.6.543
[21]
Rozas J, Sánchez-DelBarrio JC, Messeguer X, Rozas R (2003) DNAsp, DNA polymorphism analyses by the coalescent and other methods. Bioinformatics 19: 2496–2497. doi: 10.1093/bioinformatics/btg359
[22]
Excoffier L, Laval G, Schneider S (2005) Arlequin ver. 3.0: An integrated software package for population genetics data analysis. Evol Bioinform Online 1: 47–50.
[23]
Tajima F (1989) Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics 123: 585–595.
[24]
Fu YX (1997) Statistical test of neutrality of mutations against population growth, hitchhiking and background selection. Genetics 147: 915–925.
[25]
Swofford DL (2002) PAUP*. Phylogenetic analysis using parsimony (* and other methods). Version 4. Sunderland, MA: Sinauer.
[26]
Guindon S, Gascuel O (2003) A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol 52: 696–704. doi: 10.1080/10635150390235520
[27]
Posada D, Crandall KA (1998) MODELTEST: testing the model of DNA substitution. Bioinformatics 14: 817–818. doi: 10.1093/bioinformatics/14.9.817
[28]
Huelsenbeck JP, Ronquist F (2001) MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics 17: 754–755. doi: 10.1093/bioinformatics/17.8.754
[29]
Clement M, Posada D, Crandall KA (2000) TCS: a computer program to estimate gene genealogies. Mol Ecol 9: 1657–1659. doi: 10.1046/j.1365-294x.2000.01020.x
[30]
Tamura K, Dudley J, Nei M, Kumar S (2007) MEGA4: Molecular evolutionary genetics snalysis (MEGA) software version 4.0. Mol Biol Evol 24: 1596–1599. doi: 10.1093/molbev/msm092
[31]
Tajama F (1989) The effect of change in population size on DNA polymorphism. Genetics 123: 597–601.
[32]
Brandt M, Fischer-Blass B, Heinze J, Foitzik S (2007) Population structure and the co-evolution between social parasites and their hosts. Mol Ecol 16: 2063–2078. doi: 10.1111/j.1365-294X.2007.03300.x
[33]
Bargues MD, Marcilla A, Ramsey JM, Dujardin JP, Schofield CJ, et al. (2000) Nuclear rDNA-based molecular clock of the evolution of the Triatominae (Hemiptera: Reduviidae), vectors of Chagas disease. Mem Inst Oswaldo Cruz 95: 567–573. doi: 10.1590/S0074-02762000000400020
[34]
Wares JP (2001) Biogeography of Asterias: North Atlantic climate change and speciation. Biol Bull 201: 95–103. doi: 10.2307/1543530
[35]
DeJong RJ, Morgan JA, Paraense WL, Pointier JP, Amarista M, et al. (2001) Evolutionary relationships and biogeography of Biomphalaria (Gastropoda: Planorbidae) with implications regarding its role as host of the human blood fluke, Schistosoma mansoni. Mol Biol Evol 18: 2225–2239. doi: 10.1093/oxfordjournals.molbev.a003769
[36]
Wright S (1978) Evolution and genetics of populations. Volume 4. Variability within and among natural populations. Chicago: University of Chicago Press. 580 p.
[37]
Wilke T, Davis GM, Qiu DC, Spear RC (2006) Extreme mitochondrial sequence diversity in the intermediate schistosomiasis host Oncomelania hupensis robertsoni: another case of ancestral polymorphism? Malacologia 48: 143–157.
[38]
Nolan MJ, Cribb TH (2005) The use and implications of ribosomal DNA sequencing for the discrimination of digenean species. Adv Parasitol 60: 101–163. doi: 10.1016/S0065-308X(05)60002-4
[39]
Bargues MD, Mas-Coma S (2005) Reviewing lymnaeid vectors of fascioliasis by ribosomal DNA sequence analyses. J Helminthol 79: 257–267. doi: 10.1079/JOH2005297
[40]
Belbahri L, McLeod A, Paul B, Calmin G, Moralejo E, et al. (2008) Intraspecific and within-isolate sequence variation in the ITS rRNA gene region of Pythium mercuriale sp. nov. (Pythiaceae). FEMS Microbiol Lett 284: 17–27. doi: 10.1111/j.1574-6968.2008.01168.x
[41]
Jarne P, Théron A (2001) Genetic structure in natural populations of flukes and snails: a practical approach and review. Parasitology 123: 27–40. doi: 10.1017/s0031182001007715
[42]
Cross JH, Zaraspe G, Lu SK, Chiu KM, Hung HK (1984) Susceptibility of Oncomelania hupensis subspecies to infection with geographic strains of Schistosoma japonicum. Southeast Asian J Trop Med Public Health 15: 155–160.
[43]
He YX, Guo YH, Ni CH, Xia F, Liu HX, et al. (1990) Studies on the strain differences of Schistosoma japonicum in the mainland of China I. compatibility between schistosomes and their snail hosts. Chin J Parasitol Parasit Dis 8: 92–95.
[44]
Dong XQ, Feng XG, Dong Y, Xiong MT, Jiang H, et al. (2008) Epidemiological characteristics and control strategies of schistosomiasis in mountainous areas of Yunnan province. Chi J Schisto Control 20: 135–137 (in Chinese).
[45]
Utzinger J, Zhou XN, Chen MG, Bergquist R (2005) Conquering schistosomiasis in China: the long march. Acta Trop 96: 69–96. doi: 10.1016/j.actatropica.2005.08.004
[46]
Davis GM (1979) The origin and evolution of the Gastropod family Pomatiopsidae with emphasis on the Mekong River Triculinae. Academy of Natural Sciences of Philadelphia, Monograph 20: 1–120.
[47]
Attwood SW, Upatham ES, Meng XH, Qiu DC, Southgate VR (2002) The phylogeography of Asian Schistosoma (Trematoda: Schistosomatidae). Parasitology 125: 99–112. doi: 10.1017/S0031182002001981
[48]
Davis GM, Wilke T, Zhang Y, Xu X, Qiu C-P, et al. (1999) Snail-Schistosoma, Paragonimus interactions in China: population ecology, genetic diversity, coevolution and emerging diseases. Malacologia 41: 355–377.
[49]
Lockyer E, Olson PD, ?stergaard P, Rollinson D, Johnston DA, et al. (2003) The phylogeny of the Schistosomatidae based on three genes with emphasis on the interrelationships of Schistosoma Weinland, 1858. Parasitology 126: 203–224. doi: 10.1017/S0031182002002792
[50]
Shrivastava J, Qian BZ, McVean G, Webster JP (2005) An insight into the genetic variation of Schistosoma japonicum in mainland China using DNA microsatellite markers. Mol Ecol 14: 839–849. doi: 10.1111/j.1365-294X.2005.02443.x