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Multiple evolutionary origins of Trypanosoma evansi in Kenya
Trypanosoma evansi is the parasite causing surra, a form of trypanosomiasis in camels and other livestock, and a serious economic burden in Kenya and many other parts of the world. Trypanosoma evansi transmission can be sustained mechanically by tabanid and Stomoxys biting flies, whereas the closely...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605091/ https://www.ncbi.nlm.nih.gov/pubmed/28880965 http://dx.doi.org/10.1371/journal.pntd.0005895 |
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author | Kamidi, Christine M. Saarman, Norah P. Dion, Kirstin Mireji, Paul O. Ouma, Collins Murilla, Grace Aksoy, Serap Schnaufer, Achim Caccone, Adalgisa |
author_facet | Kamidi, Christine M. Saarman, Norah P. Dion, Kirstin Mireji, Paul O. Ouma, Collins Murilla, Grace Aksoy, Serap Schnaufer, Achim Caccone, Adalgisa |
author_sort | Kamidi, Christine M. |
collection | PubMed |
description | Trypanosoma evansi is the parasite causing surra, a form of trypanosomiasis in camels and other livestock, and a serious economic burden in Kenya and many other parts of the world. Trypanosoma evansi transmission can be sustained mechanically by tabanid and Stomoxys biting flies, whereas the closely related African trypanosomes T. brucei brucei and T. b. rhodesiense require cyclical development in tsetse flies (genus Glossina) for transmission. In this study, we investigated the evolutionary origins of T. evansi. We used 15 polymorphic microsatellites to quantify levels and patterns of genetic diversity among 41 T. evansi isolates and 66 isolates of T. b. brucei (n = 51) and T. b. rhodesiense (n = 15), including many from Kenya, a region where T. evansi may have evolved from T. brucei. We found that T. evansi strains belong to at least two distinct T. brucei genetic units and contain genetic diversity that is similar to that in T. brucei strains. Results indicated that the 41 T. evansi isolates originated from multiple T. brucei strains from different genetic backgrounds, implying independent origins of T. evansi from T. brucei strains. This surprising finding further suggested that the acquisition of the ability of T. evansi to be transmitted mechanically, and thus the ability to escape the obligate link with the African tsetse fly vector, has occurred repeatedly. These findings, if confirmed, have epidemiological implications, as T. brucei strains from different genetic backgrounds can become either causative agents of a dangerous, cosmopolitan livestock disease or of a lethal human disease, like for T. b. rhodesiense. |
format | Online Article Text |
id | pubmed-5605091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56050912017-09-28 Multiple evolutionary origins of Trypanosoma evansi in Kenya Kamidi, Christine M. Saarman, Norah P. Dion, Kirstin Mireji, Paul O. Ouma, Collins Murilla, Grace Aksoy, Serap Schnaufer, Achim Caccone, Adalgisa PLoS Negl Trop Dis Research Article Trypanosoma evansi is the parasite causing surra, a form of trypanosomiasis in camels and other livestock, and a serious economic burden in Kenya and many other parts of the world. Trypanosoma evansi transmission can be sustained mechanically by tabanid and Stomoxys biting flies, whereas the closely related African trypanosomes T. brucei brucei and T. b. rhodesiense require cyclical development in tsetse flies (genus Glossina) for transmission. In this study, we investigated the evolutionary origins of T. evansi. We used 15 polymorphic microsatellites to quantify levels and patterns of genetic diversity among 41 T. evansi isolates and 66 isolates of T. b. brucei (n = 51) and T. b. rhodesiense (n = 15), including many from Kenya, a region where T. evansi may have evolved from T. brucei. We found that T. evansi strains belong to at least two distinct T. brucei genetic units and contain genetic diversity that is similar to that in T. brucei strains. Results indicated that the 41 T. evansi isolates originated from multiple T. brucei strains from different genetic backgrounds, implying independent origins of T. evansi from T. brucei strains. This surprising finding further suggested that the acquisition of the ability of T. evansi to be transmitted mechanically, and thus the ability to escape the obligate link with the African tsetse fly vector, has occurred repeatedly. These findings, if confirmed, have epidemiological implications, as T. brucei strains from different genetic backgrounds can become either causative agents of a dangerous, cosmopolitan livestock disease or of a lethal human disease, like for T. b. rhodesiense. Public Library of Science 2017-09-07 /pmc/articles/PMC5605091/ /pubmed/28880965 http://dx.doi.org/10.1371/journal.pntd.0005895 Text en © 2017 Kamidi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kamidi, Christine M. Saarman, Norah P. Dion, Kirstin Mireji, Paul O. Ouma, Collins Murilla, Grace Aksoy, Serap Schnaufer, Achim Caccone, Adalgisa Multiple evolutionary origins of Trypanosoma evansi in Kenya |
title | Multiple evolutionary origins of Trypanosoma evansi in Kenya |
title_full | Multiple evolutionary origins of Trypanosoma evansi in Kenya |
title_fullStr | Multiple evolutionary origins of Trypanosoma evansi in Kenya |
title_full_unstemmed | Multiple evolutionary origins of Trypanosoma evansi in Kenya |
title_short | Multiple evolutionary origins of Trypanosoma evansi in Kenya |
title_sort | multiple evolutionary origins of trypanosoma evansi in kenya |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605091/ https://www.ncbi.nlm.nih.gov/pubmed/28880965 http://dx.doi.org/10.1371/journal.pntd.0005895 |
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