Berger SA, 2011. Infectious Diseases of the Philippines. Gideon e-books, 379 pp. Available at: http://www.gideononline.com/ebooks/country/infectious-diseases-of-the-philippines/.
Berger SA, 2011. Schistosoma Japonicum: Global Status. Gideon e-books, 14 pp. Available at: http://www.gideononline.com/ebooks/disease/schistosoma-japonicum-global-status/.
Fernandez TJ Jr, Tarafder MR, Balolong E Jr, Joseph L, Willingham AL 3rd, Belisle P, Webster JP, Olveda RM, McGarvey ST, Carabin H, 2007. Prevalence of Schistosoma japonicum infection among animals in fifty villages of Samar Province, the Philippines. Vector Borne Zoonotic Dis 7: 147–155.
Tarafder MR, Balolong E Jr, Carabin H, Belisle P, Tallo V, Joseph L, Alday P, Gonzales RO, Riley S, Olveda R, McGarvey ST, 2006. A cross-sectional study of the prevalence of intensity of infection with Schistosoma japonicum in 50 irrigated and rain-fed villages in Samar Province, the Philippines. BMC Public Health 6: 61.
Hauswald AK, Remais JV, Xiao N, Davis GM, Lu D, Bale MJ, Wilke T, 2011. Stirred, not shaken: genetic structure of the intermediate snail host Oncomelania hupensis robertsoni in an historically endemic schistosomiasis area. Parasit Vectors 4: 206.
Zhao QP, Jiang MS, Littlewood DT, Nie P, 2010. Distinct genetic diversity of Oncomelania hupensis, intermediate host of Schistosoma japonicum in mainland China as revealed by ITS sequences. PLoS Negl Trop Dis 4: e611.
Davis GM, Wilke T, Zhang Y, Xu XJ, Qiu CP, Spolsky CM, Oiu DC, Li Y, Xia MY, Feng Z, 1999. Snail-Schistosoma, Paragonimus interaction in China: population ecology, genetic diversity, coevolution and emerging diseases. Malacologia 41: 355–377.
Webster JP, Davies CM, 2001. Coevolution and compatibility in the snail-schistosome system. Parasitology 123 (Suppl): S41–S56.
Webster JP, Shrivastava J, Johnson PJ, Blair L, 2007. Is host-schistosome coevolution going anywhere? BMC Evol Biol 7: 91.
Shi CH, Wilke T, Davis GM, Xia MY, Qiu CP, 2002. Population genetic, micro-phylogeography, ecology, and susceptibility to schistosome infection of Chinese Oncomelania hupensis hupensis (Gastropoda: Rissooidea: Pomatiopsidae) in the Miao river system. Malacologia 44: 333–347.
Hope M, McManus DP, 1994. Genetic variation in geographically isolated populations and subspecies of Oncomelania hupensis determined by a PCR-based RFLP method. Acta Trop 57: 75–82.
Okamoto M, Lo C-T, Tiu WU, Qui D-C, Hadidjaja P, Upatham S, Sugiyama H, Taguchi T, Hirai H, Saitoh Y, Habe S, Kawanaka M, Hirata M, Agatsuma T, 2003. Phylogenetic relationships of snails of the genera Oncomelania and Tricula inferred from the mitochondrial 12S rRNA gene. Jpn J Trop Med Hyg 31: 5–10.
Woodruff DS, Staub KC, Upatham ES, Viyanant V, Yuan HC, 1998. Genetic variation in Oncomelania hupensis: Schistosoma japonicum transmitting snails in China and the Philippines are distinct species. Malacologia 29: 347–361.
Viyanant V, Upatham ES, Blas BL, Yuan HC, 1987. Analysis of allozymes by electrofocusing in schistosome snail hosts (Oncomelania hupensis) from China and the Philippines. Malacol Rev 20: 91–96.
Woodruff DS, Carpenter MP, Upatham ES, Viyanant V, 1999. Molecular phylogeography of Oncomelania lindoensis (Gastropoda: Pomatiopsidae), the intermediate host of Schistosoma japonicum in Sulawesi. J Molluscan Stud 65: 21–31.
Slatkin M, Hudson RR, 1991. Pairwise comparisons of mitochondrial DNA sequences in stable and exponentially growing populations. Genetics 129: 555–562.
Librado P, Rozas J, 2009. DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Bioinformatics 25: 1451–1452.
Excoffier L, Lischer HE, 2010. Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. Mol Ecol Resour 10: 564–567.
Bandelt HJ, Forster P, Rohl A, 1999. Median-joining networks for inferring intraspecific phylogenies. Mol Biol Evol 16: 37–48.
Felsenstein J, 2005. PHYLIP (Phylogeny Inference Package) version 3.6. Distributed by the author. Seattle, WA: Department of Genome Sciences, University of Washington.
Thomas JA, Welch JJ, Lanfear R, Bromham L, 2010. A generation time effect on the rate of molecular evolution in invertebrates. Mol Biol Evol 27: 1173–1180.
Woodruff DS, Merenlender AM, Upatham ES, Viyanant V, 1987. Genetic variation and differentiation of three Schistosoma species from the Philippines, Laos, and Peninsular Malaysia. Am J Trop Med Hyg 36: 345–354.
Kiatsopit N, Sithithaworn P, Saijuntha W, Petney TN, Andrews RH, 2013. Opisthorchis viverrini: Implications of the systematics of first intermediate hosts, Bithynia snail species in Thailand and Lao PDR. Infect Genet Evol 14: 313–319.
Saijuntha W, Sithithaworn P, Wongkham S, Laha T, Pipitgool V, Tesana S, Chilton NB, Petney TN, Andrews RH, 2007. Evidence of a species complex within the food-borne trematode Opisthorchis viverrini and possible co-evolution with their first intermediate hosts. Int J Parasitol 37: 695–703.
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.
Li SZ, Wang YX, Yang K, Liu Q, Wang Q, Zhang Y, Wu XH, Guo JG, Bergquist R, Zhou XN, 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.
Zhou YB, Zhao GM, Jiang QW, 2008. Genetic variability of Schistosoma japonicum (Katsorada, 1904) intermediate hosts Oncomelania hupensis (Gredler, 1881) (Gastropoda: Rissooidea). Annal Zool 58: 881–889.
Zhao QP, Jiang MS, Dong HF, Nie P, 2012. Diversifiation of Schistosoma japonicum in mainland China revealed by mitochondrial DNA. PLoS Negl Trop Dis 6: e1503.
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Species and subspecies of the Oncomelania hupensis species complex are recognized as intermediate hosts of Schistosoma japonicum. Of these species and subspecies, O. quadrasi is distributed throughout the Philippines. This study used 12S ribosomal RNA sequences to explore the genetic structure of O. quadrasi populations in the Philippines. Three subspecies, O. h. hupensis, O. h. formosana, and O. h. chiui of this group were also examined. The phylogenetic tree and haplotypes network showed that O. quadrasi separated from the subspecies. Ten O. quadrasi haplotypes (Oq1–Oq10) clustered in relation to their geographic origin. Genetic differentiation (FST) and estimated gene flow (Nm) among populations showed significant differences, ranging from 0.556–1.000 to 0.00–0.74, respectively. Genetic differences among groups (FCT = 0.466), populations within a group (FSC = 0.727), and populations (FST = 0.854) were observed. These results indicate that the O. quadrasi populations in the Philippines have a substructure associated with their geographic origin.
Financial support: This study was supported by the Japan Society for the Promotion of Science (grant no. L-11566) and TRF-CHE-MSU (grant no. MRG5480009) to Weerachai Saijuntha.
Authors' addresses: Weerachai Saijuntha, Walai Rukhavej Botanical Research Institute, Mahasarakham University, Maha Sarakham, Thailand, E-mail: weerachai.s@msu.ac.th. Blanca Jarilla and Takeshi Agatsuma, Division of Environmental Health Sciences, Kochi Medical School, Nankoku, Japan, E-mails: blancajarilla@yahoo.com and agatsuma@kochi-u.ac.jp. Alvin K. Leonardo and Lydia R. Leonardo, College of Public Health, University of the Philippines, Manila, Philippines, E-mail: leonardolydia7@gmail.com. Louie S. Sunico, Municipal Health Office, Municipality of Gonzaga, Cagayan, Philippines, E-mail: HRMO_gonzaga@yahoo.com. Ross H. Andrews and Paiboon Sithithaworn, Department of Parasitology, and Liver Fluke and Cholangiocarcinoma Research Center, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand, E-mails: rhandrews@gmail.com and paib_sit@hotmail.com. Trevor N. Petney, Department of Ecology and Parasitology, Karlsruhe Institute of Technology, Karlsruhe, Germany, E-mail: petney@kit.edu. Masashi Kirinoki, Naoko Kato-Hayashi, and Yuichi Chigusa, Laboratory of Tropical Medicine and Parasitology, Dokkyo Medical University, Tochigi, Japan, E-mails: kirinoki@dokkyomed.ac.jp, nkato@dokkyo.med.ac.jp, and ychigusa@dokkyomed.ac.jp. Mihoko Kikuchi, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan, E-mail: mkikuchi@nagasaki-u.ac.jp.
Berger SA, 2011. Infectious Diseases of the Philippines. Gideon e-books, 379 pp. Available at: http://www.gideononline.com/ebooks/country/infectious-diseases-of-the-philippines/.
Berger SA, 2011. Schistosoma Japonicum: Global Status. Gideon e-books, 14 pp. Available at: http://www.gideononline.com/ebooks/disease/schistosoma-japonicum-global-status/.
Fernandez TJ Jr, Tarafder MR, Balolong E Jr, Joseph L, Willingham AL 3rd, Belisle P, Webster JP, Olveda RM, McGarvey ST, Carabin H, 2007. Prevalence of Schistosoma japonicum infection among animals in fifty villages of Samar Province, the Philippines. Vector Borne Zoonotic Dis 7: 147–155.
Tarafder MR, Balolong E Jr, Carabin H, Belisle P, Tallo V, Joseph L, Alday P, Gonzales RO, Riley S, Olveda R, McGarvey ST, 2006. A cross-sectional study of the prevalence of intensity of infection with Schistosoma japonicum in 50 irrigated and rain-fed villages in Samar Province, the Philippines. BMC Public Health 6: 61.
Hauswald AK, Remais JV, Xiao N, Davis GM, Lu D, Bale MJ, Wilke T, 2011. Stirred, not shaken: genetic structure of the intermediate snail host Oncomelania hupensis robertsoni in an historically endemic schistosomiasis area. Parasit Vectors 4: 206.
Zhao QP, Jiang MS, Littlewood DT, Nie P, 2010. Distinct genetic diversity of Oncomelania hupensis, intermediate host of Schistosoma japonicum in mainland China as revealed by ITS sequences. PLoS Negl Trop Dis 4: e611.
Davis GM, Wilke T, Zhang Y, Xu XJ, Qiu CP, Spolsky CM, Oiu DC, Li Y, Xia MY, Feng Z, 1999. Snail-Schistosoma, Paragonimus interaction in China: population ecology, genetic diversity, coevolution and emerging diseases. Malacologia 41: 355–377.
Webster JP, Davies CM, 2001. Coevolution and compatibility in the snail-schistosome system. Parasitology 123 (Suppl): S41–S56.
Webster JP, Shrivastava J, Johnson PJ, Blair L, 2007. Is host-schistosome coevolution going anywhere? BMC Evol Biol 7: 91.
Shi CH, Wilke T, Davis GM, Xia MY, Qiu CP, 2002. Population genetic, micro-phylogeography, ecology, and susceptibility to schistosome infection of Chinese Oncomelania hupensis hupensis (Gastropoda: Rissooidea: Pomatiopsidae) in the Miao river system. Malacologia 44: 333–347.
Hope M, McManus DP, 1994. Genetic variation in geographically isolated populations and subspecies of Oncomelania hupensis determined by a PCR-based RFLP method. Acta Trop 57: 75–82.
Okamoto M, Lo C-T, Tiu WU, Qui D-C, Hadidjaja P, Upatham S, Sugiyama H, Taguchi T, Hirai H, Saitoh Y, Habe S, Kawanaka M, Hirata M, Agatsuma T, 2003. Phylogenetic relationships of snails of the genera Oncomelania and Tricula inferred from the mitochondrial 12S rRNA gene. Jpn J Trop Med Hyg 31: 5–10.
Woodruff DS, Staub KC, Upatham ES, Viyanant V, Yuan HC, 1998. Genetic variation in Oncomelania hupensis: Schistosoma japonicum transmitting snails in China and the Philippines are distinct species. Malacologia 29: 347–361.
Viyanant V, Upatham ES, Blas BL, Yuan HC, 1987. Analysis of allozymes by electrofocusing in schistosome snail hosts (Oncomelania hupensis) from China and the Philippines. Malacol Rev 20: 91–96.
Woodruff DS, Carpenter MP, Upatham ES, Viyanant V, 1999. Molecular phylogeography of Oncomelania lindoensis (Gastropoda: Pomatiopsidae), the intermediate host of Schistosoma japonicum in Sulawesi. J Molluscan Stud 65: 21–31.
Slatkin M, Hudson RR, 1991. Pairwise comparisons of mitochondrial DNA sequences in stable and exponentially growing populations. Genetics 129: 555–562.
Librado P, Rozas J, 2009. DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Bioinformatics 25: 1451–1452.
Excoffier L, Lischer HE, 2010. Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. Mol Ecol Resour 10: 564–567.
Bandelt HJ, Forster P, Rohl A, 1999. Median-joining networks for inferring intraspecific phylogenies. Mol Biol Evol 16: 37–48.
Felsenstein J, 2005. PHYLIP (Phylogeny Inference Package) version 3.6. Distributed by the author. Seattle, WA: Department of Genome Sciences, University of Washington.
Thomas JA, Welch JJ, Lanfear R, Bromham L, 2010. A generation time effect on the rate of molecular evolution in invertebrates. Mol Biol Evol 27: 1173–1180.
Woodruff DS, Merenlender AM, Upatham ES, Viyanant V, 1987. Genetic variation and differentiation of three Schistosoma species from the Philippines, Laos, and Peninsular Malaysia. Am J Trop Med Hyg 36: 345–354.
Kiatsopit N, Sithithaworn P, Saijuntha W, Petney TN, Andrews RH, 2013. Opisthorchis viverrini: Implications of the systematics of first intermediate hosts, Bithynia snail species in Thailand and Lao PDR. Infect Genet Evol 14: 313–319.
Saijuntha W, Sithithaworn P, Wongkham S, Laha T, Pipitgool V, Tesana S, Chilton NB, Petney TN, Andrews RH, 2007. Evidence of a species complex within the food-borne trematode Opisthorchis viverrini and possible co-evolution with their first intermediate hosts. Int J Parasitol 37: 695–703.
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.
Li SZ, Wang YX, Yang K, Liu Q, Wang Q, Zhang Y, Wu XH, Guo JG, Bergquist R, Zhou XN, 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.
Zhou YB, Zhao GM, Jiang QW, 2008. Genetic variability of Schistosoma japonicum (Katsorada, 1904) intermediate hosts Oncomelania hupensis (Gredler, 1881) (Gastropoda: Rissooidea). Annal Zool 58: 881–889.
Zhao QP, Jiang MS, Dong HF, Nie P, 2012. Diversifiation of Schistosoma japonicum in mainland China revealed by mitochondrial DNA. PLoS Negl Trop Dis 6: e1503.
Past two years | Past Year | Past 30 Days | |
---|---|---|---|
Abstract Views | 228 | 167 | 5 |
Full Text Views | 349 | 7 | 0 |
PDF Downloads | 116 | 9 | 0 |