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dc.contributor.authorAgola, LE
dc.contributor.authorMburu, DN
dc.contributor.authorDeJong, RJ
dc.contributor.authorMungai, BN
dc.contributor.authorMuluvi, GM
dc.contributor.authorNjagi, EN
dc.contributor.authorLoker, ES
dc.contributor.authorMkoji, GM
dc.date.accessioned2013-12-04T12:36:23Z
dc.date.available2013-12-04T12:36:23Z
dc.date.issued2006
dc.identifier.citationInfect Genet Evol. 2006 Nov;6(6):484-90en_US
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/16675308
dc.identifier.urihttp://hdl.handle.net/11295/61755
dc.description.abstractGenetic diversity and population structure of seven populations of Schistosoma mansoni sampled in Kenya were assessed using five microsatellite markers. The mean number of alleles per locus, expected heterozygosity in Hardy-Weinberg equilibrium and pairwise F(ST) values ranged from 5.2 to 10.7, 0.5-0.8 and 3.6-27.3%, respectively. These data reveal that S. mansoni populations in Kenyan have relatively high levels of genetic diversity and is significantly differentiated. Our data combined with information on biogeography support the hypothesis that the strong genetic structure in Kenyan schistosomes is as a result of limited gene flow and large population sizes. Resistance to anthelminthics has not been reported among the Kenyan schistosomes, we hypothesize that this is probably due to the very little gene flow among populations, thereby limiting opportunities for the spread of rare alleles that might confer resistance to the drugs.en_US
dc.language.isoenen_US
dc.publisherKMAen_US
dc.titleMicrosatellite typing reveals strong genetic structure of Schistosoma mansoni from localities in Kenya.en_US
dc.typeArticleen_US


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