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Microsatellite analysis supports clonal propagation and reduced divergence of Trypanosoma vivax from asymptomatic to fatally infected livestock in South America compared to West Africa
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نویسنده
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garcia h.a. ,rodrigues a.c. ,rodrigues c.m.f. ,bengaly z. ,minervino a.h.h. ,riet-correa f. ,machado r.z. ,paiva f. ,batista j.s. ,neves l. ,hamilton p.b. ,teixeira m.m.g.
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منبع
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parasites and vectors - 2014 - دوره : 7 - شماره : 1
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چکیده
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Background: mechanical transmission of the major livestock pathogen trypanosoma vivax by other biting flies than tsetse allows its spread from africa to the new world. genetic studies are restricted to a small number of isolates and based on molecular markers that evolve too slowly to resolve the relationships between american and west african populations and,thus,unable us to uncover the recent history of t. vivax in the new world. methods. t. vivax genetic diversity,population structure and the source of outbreaks was investigated through the microsatellite multiloci (7 loci) genotype (mlgs) analysis in south america (47isolates from brazil,venezuela and french guiana) and west africa (12 isolates from the gambia,burkina faso,ghana,benin and nigeria). relationships among mlgs were explored using phylogenetic,principal component and structure analyses. results: although closely phylogenetically related,for the first time,genetic differences were detected between t. vivax isolates from south america (11 genotypes/47 isolates) and west africa (12 genotypes/12 isolates) with no mlgs in common. diversity was far greater across west africa than in south america,where genotypes from brazil (mlg1-6),venezuela (mlg7-10) and french guiana (mlg11) shared similar but not identical allele composition. no mlg was exclusive to asymptomatic (endemic areas) or sick (outbreaks in non-endemic areas) animals,but only mlgs1,2 and 3 were responsible for severe haematological and neurological disorders. conclusions: our results revealed closely related genotypes of t. vivax in brazil and venezuela,regardless of endemicity and clinical conditions of the infected livestock. the mlgs analysis from t. vivax across sa and wa support clonal propagation,and is consistent with the hypothesis that the sa populations examined here derived from common ancestors recently introduced from west africa. the molecular markers defined here are valuable to assess the genetic diversity,to track the source and dispersion of outbreaks,and to explore the epidemiological and pathological significance of t. vivax genotypes. © 2014 garcia et al.; licensee biomed central ltd.
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کلیدواژه
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Africa; Animal trypanosomosis; Clonal structure; Epidemiology; Microsatellite genotyping; Nagana; Outbreak; Pathology; South America
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آدرس
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departamento de parasitologia,instituto de ciências biomédicas,universidade de são paulo,são paulo,sp,brazil,departamento de patología veterinaria,facultad de ciencias veterinarias,universidad central de venezuela,maracay,aragua, Venezuela, departamento de parasitologia,instituto de ciências biomédicas,universidade de são paulo,são paulo,sp, Brazil, departamento de parasitologia,instituto de ciências biomédicas,universidade de são paulo,são paulo,sp, Brazil, centre international de recherche-développement sur l'elevage en zone subhumide (cirdes),bobo dioulasso, Burkina Faso, instituto de biodiversidade e floresta,universidade federal do oeste do pará,santarém,pará, Brazil, hospital veterinário,universidade federal de campina grande,patos,paraíba, Brazil, departamento de patologia,faculdade de veterinária,universidade estadual paulista julio de mesquita filho,jaboticabal,são paulo, Brazil, departamento de parasitologia veterinária,universidade federal do mato grosso do sul,campo grande,mato grosso do sul, Brazil, departamento de ciências animais,universidade federal rural do semi-árido,mossoró,rio grande do norte, Brazil, centro de biotecnologia,universidade eduardo mondlane,maputo,mozambique,department of veterinary tropical diseases,faculty of veterinary science,university of pretoria,pretoria, South Africa, biosciences,college of life and environmental sciences,university of exeter,exeter, United Kingdom, departamento de parasitologia,instituto de ciências biomédicas,universidade de são paulo,são paulo,sp, Brazil
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Authors
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