Cargando…

A longitudinal two-year survey of the prevalence of trypanosomes in domestic cattle in Ghana by massively parallel sequencing of barcoded amplicons

BACKGROUND: Animal African Trypanosomiasis (AAT) is one of the most economically important diseases affecting livestock productivity in sub-Saharan Africa. The disease is caused by a broad range of Trypanosoma spp., infecting both wild and domesticated animals through cyclical and mechanical transmi...

Descripción completa

Detalles Bibliográficos
Autores principales: Ofori, Jennifer Afua, Bakari, Soale Majeed, Bah, Saikou, Kolugu, Michael Kojo, Aning, George Kwame, Awandare, Gordon Akanzuwine, Carrington, Mark, Gwira, Theresa Manful
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060370/
https://www.ncbi.nlm.nih.gov/pubmed/35442960
http://dx.doi.org/10.1371/journal.pntd.0010300
_version_ 1784698491261419520
author Ofori, Jennifer Afua
Bakari, Soale Majeed
Bah, Saikou
Kolugu, Michael Kojo
Aning, George Kwame
Awandare, Gordon Akanzuwine
Carrington, Mark
Gwira, Theresa Manful
author_facet Ofori, Jennifer Afua
Bakari, Soale Majeed
Bah, Saikou
Kolugu, Michael Kojo
Aning, George Kwame
Awandare, Gordon Akanzuwine
Carrington, Mark
Gwira, Theresa Manful
author_sort Ofori, Jennifer Afua
collection PubMed
description BACKGROUND: Animal African Trypanosomiasis (AAT) is one of the most economically important diseases affecting livestock productivity in sub-Saharan Africa. The disease is caused by a broad range of Trypanosoma spp., infecting both wild and domesticated animals through cyclical and mechanical transmission. This study aimed to characterize trypanosomes present in cattle at regular intervals over two years in an AAT endemic and a non-endemic region of Ghana. METHODOLOGY/PRINCIPAL FINDINGS: Groups of cattle at Accra and Adidome were selected based on their geographical location, tsetse fly density, prevalence of trypanosomiasis and the breed of cattle available. Blood for DNA extraction was collected at approximately four to five-week intervals over a two-year period. Trypanosome DNA were detected by a sensitive nested PCR targeting the tubulin gene array and massively parallel sequencing of barcoded amplicons. Analysis of the data was a semi-quantitative estimation of infection levels using read counts obtained from the sequencing as a proxy for infection levels. Majority of the cattle were infected with multiple species most of the time [190/259 (73%) at Adidome and 191/324 (59%) at Accra], with T. vivax being the most abundant. The level of infection and in particular T. vivax, was higher in Adidome, the location with a high density of tsetse flies. The infection level varied over the time course, the timings of this variation were not consistent and in Adidome it appeared to be independent of prophylactic treatment for trypanosome infection. Effect of gender or breed on infection levels was insignificant. CONCLUSIONS/SIGNIFICANCE: Most cattle were infected with low levels of several trypanosome species at both study sites, with T. vivax being the most abundant. The measurements of infection over time provided insight to the importance of the approach in identifying cattle that could suppress trypanosome infection over an extended time and may serve as reservoir.
format Online
Article
Text
id pubmed-9060370
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-90603702022-05-03 A longitudinal two-year survey of the prevalence of trypanosomes in domestic cattle in Ghana by massively parallel sequencing of barcoded amplicons Ofori, Jennifer Afua Bakari, Soale Majeed Bah, Saikou Kolugu, Michael Kojo Aning, George Kwame Awandare, Gordon Akanzuwine Carrington, Mark Gwira, Theresa Manful PLoS Negl Trop Dis Research Article BACKGROUND: Animal African Trypanosomiasis (AAT) is one of the most economically important diseases affecting livestock productivity in sub-Saharan Africa. The disease is caused by a broad range of Trypanosoma spp., infecting both wild and domesticated animals through cyclical and mechanical transmission. This study aimed to characterize trypanosomes present in cattle at regular intervals over two years in an AAT endemic and a non-endemic region of Ghana. METHODOLOGY/PRINCIPAL FINDINGS: Groups of cattle at Accra and Adidome were selected based on their geographical location, tsetse fly density, prevalence of trypanosomiasis and the breed of cattle available. Blood for DNA extraction was collected at approximately four to five-week intervals over a two-year period. Trypanosome DNA were detected by a sensitive nested PCR targeting the tubulin gene array and massively parallel sequencing of barcoded amplicons. Analysis of the data was a semi-quantitative estimation of infection levels using read counts obtained from the sequencing as a proxy for infection levels. Majority of the cattle were infected with multiple species most of the time [190/259 (73%) at Adidome and 191/324 (59%) at Accra], with T. vivax being the most abundant. The level of infection and in particular T. vivax, was higher in Adidome, the location with a high density of tsetse flies. The infection level varied over the time course, the timings of this variation were not consistent and in Adidome it appeared to be independent of prophylactic treatment for trypanosome infection. Effect of gender or breed on infection levels was insignificant. CONCLUSIONS/SIGNIFICANCE: Most cattle were infected with low levels of several trypanosome species at both study sites, with T. vivax being the most abundant. The measurements of infection over time provided insight to the importance of the approach in identifying cattle that could suppress trypanosome infection over an extended time and may serve as reservoir. Public Library of Science 2022-04-20 /pmc/articles/PMC9060370/ /pubmed/35442960 http://dx.doi.org/10.1371/journal.pntd.0010300 Text en © 2022 Ofori et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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
Ofori, Jennifer Afua
Bakari, Soale Majeed
Bah, Saikou
Kolugu, Michael Kojo
Aning, George Kwame
Awandare, Gordon Akanzuwine
Carrington, Mark
Gwira, Theresa Manful
A longitudinal two-year survey of the prevalence of trypanosomes in domestic cattle in Ghana by massively parallel sequencing of barcoded amplicons
title A longitudinal two-year survey of the prevalence of trypanosomes in domestic cattle in Ghana by massively parallel sequencing of barcoded amplicons
title_full A longitudinal two-year survey of the prevalence of trypanosomes in domestic cattle in Ghana by massively parallel sequencing of barcoded amplicons
title_fullStr A longitudinal two-year survey of the prevalence of trypanosomes in domestic cattle in Ghana by massively parallel sequencing of barcoded amplicons
title_full_unstemmed A longitudinal two-year survey of the prevalence of trypanosomes in domestic cattle in Ghana by massively parallel sequencing of barcoded amplicons
title_short A longitudinal two-year survey of the prevalence of trypanosomes in domestic cattle in Ghana by massively parallel sequencing of barcoded amplicons
title_sort longitudinal two-year survey of the prevalence of trypanosomes in domestic cattle in ghana by massively parallel sequencing of barcoded amplicons
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060370/
https://www.ncbi.nlm.nih.gov/pubmed/35442960
http://dx.doi.org/10.1371/journal.pntd.0010300
work_keys_str_mv AT oforijenniferafua alongitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT bakarisoalemajeed alongitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT bahsaikou alongitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT kolugumichaelkojo alongitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT aninggeorgekwame alongitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT awandaregordonakanzuwine alongitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT carringtonmark alongitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT gwiratheresamanful alongitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT oforijenniferafua longitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT bakarisoalemajeed longitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT bahsaikou longitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT kolugumichaelkojo longitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT aninggeorgekwame longitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT awandaregordonakanzuwine longitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT carringtonmark longitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons
AT gwiratheresamanful longitudinaltwoyearsurveyoftheprevalenceoftrypanosomesindomesticcattleinghanabymassivelyparallelsequencingofbarcodedamplicons