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Spatial distribution of African Animal Trypanosomiasis in Suba and Teso districts in Western Kenya
BACKGROUND: Studies on the epidemiology of African Animal Trypanosomiasis (AAT) rarely consider the spatial dimension of disease prevalence. This problem is confounded by use of parasitological diagnostic methods of low sensitivity in field surveys. Here we report a study combining highly sensitive...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2826354/ https://www.ncbi.nlm.nih.gov/pubmed/20205857 http://dx.doi.org/10.1186/1756-0500-3-6 |
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author | Thumbi, Samuel M Jung'a, Joseph O Mosi, Reuben O McOdimba, Francis A |
author_facet | Thumbi, Samuel M Jung'a, Joseph O Mosi, Reuben O McOdimba, Francis A |
author_sort | Thumbi, Samuel M |
collection | PubMed |
description | BACKGROUND: Studies on the epidemiology of African Animal Trypanosomiasis (AAT) rarely consider the spatial dimension of disease prevalence. This problem is confounded by use of parasitological diagnostic methods of low sensitivity in field surveys. Here we report a study combining highly sensitive and species specific molecular diagnostic methods, and Geographical information system (GIS) for spatial analysis of trypanosome infection patterns, to better understand its epidemiology. Blood samples from 44 and 59 animals randomly selected from Teso and Suba districts respectively were screened for trypanosomes using PCR diagnostic assays. Spatial distribution of the positive cases was mapped and average nearest neighbour analysis used to determine the spatial pattern of trypanosome cases detected. FINDINGS: Trypanosome prevalence of 41% and 29% in Suba and Teso districts respectively was observed. T. vivax infections were most prevalent in both areas. Higher proportions of T. brucei infections (12%) were observed in Suba, a known sleeping sickness foci compared with 2% in Teso. Average nearest neighbour analysis showed the pattern of trypanosome infections as random. An overlay with tsetse maps showed cases lying outside the tsetse infested areas, mostly being cases of T. vivax which is known to be transmitted both biologically by tsetse and mechanically by biting flies. CONCLUSION: These findings suggest a need to design control strategies that target not just the biological vector tsetse, but also the parasite in cattle in order to clear the possibly mechanically transmitted T. vivax infections. There is need to also review the accuracy of available tsetse maps. |
format | Text |
id | pubmed-2826354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28263542010-02-23 Spatial distribution of African Animal Trypanosomiasis in Suba and Teso districts in Western Kenya Thumbi, Samuel M Jung'a, Joseph O Mosi, Reuben O McOdimba, Francis A BMC Res Notes Short Report BACKGROUND: Studies on the epidemiology of African Animal Trypanosomiasis (AAT) rarely consider the spatial dimension of disease prevalence. This problem is confounded by use of parasitological diagnostic methods of low sensitivity in field surveys. Here we report a study combining highly sensitive and species specific molecular diagnostic methods, and Geographical information system (GIS) for spatial analysis of trypanosome infection patterns, to better understand its epidemiology. Blood samples from 44 and 59 animals randomly selected from Teso and Suba districts respectively were screened for trypanosomes using PCR diagnostic assays. Spatial distribution of the positive cases was mapped and average nearest neighbour analysis used to determine the spatial pattern of trypanosome cases detected. FINDINGS: Trypanosome prevalence of 41% and 29% in Suba and Teso districts respectively was observed. T. vivax infections were most prevalent in both areas. Higher proportions of T. brucei infections (12%) were observed in Suba, a known sleeping sickness foci compared with 2% in Teso. Average nearest neighbour analysis showed the pattern of trypanosome infections as random. An overlay with tsetse maps showed cases lying outside the tsetse infested areas, mostly being cases of T. vivax which is known to be transmitted both biologically by tsetse and mechanically by biting flies. CONCLUSION: These findings suggest a need to design control strategies that target not just the biological vector tsetse, but also the parasite in cattle in order to clear the possibly mechanically transmitted T. vivax infections. There is need to also review the accuracy of available tsetse maps. BioMed Central 2010-01-15 /pmc/articles/PMC2826354/ /pubmed/20205857 http://dx.doi.org/10.1186/1756-0500-3-6 Text en Copyright ©2010 Thumbi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Report Thumbi, Samuel M Jung'a, Joseph O Mosi, Reuben O McOdimba, Francis A Spatial distribution of African Animal Trypanosomiasis in Suba and Teso districts in Western Kenya |
title | Spatial distribution of African Animal Trypanosomiasis in Suba and Teso districts in Western Kenya |
title_full | Spatial distribution of African Animal Trypanosomiasis in Suba and Teso districts in Western Kenya |
title_fullStr | Spatial distribution of African Animal Trypanosomiasis in Suba and Teso districts in Western Kenya |
title_full_unstemmed | Spatial distribution of African Animal Trypanosomiasis in Suba and Teso districts in Western Kenya |
title_short | Spatial distribution of African Animal Trypanosomiasis in Suba and Teso districts in Western Kenya |
title_sort | spatial distribution of african animal trypanosomiasis in suba and teso districts in western kenya |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2826354/ https://www.ncbi.nlm.nih.gov/pubmed/20205857 http://dx.doi.org/10.1186/1756-0500-3-6 |
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