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Mapping brucellosis risk in Kenya and its implications for control strategies in sub-Saharan Africa
In Sub-Saharan Africa (SSA), effective brucellosis control is limited, in part, by the lack of long-term commitments by governments to control the disease and the absence of reliable national human and livestock population-based data to inform policies. Therefore, we conducted a study to establish t...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657468/ https://www.ncbi.nlm.nih.gov/pubmed/37980384 http://dx.doi.org/10.1038/s41598-023-47628-1 |
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author | Akoko, James M. Mwatondo, Athman Muturi, Mathew Wambua, Lillian Abkallo, Hussein M. Nyamota, Richard Bosire, Caroline Oloo, Stephen Limbaso, Konongoi S. Gakuya, Francis Nthiwa, Daniel Bartlow, Andrew Middlebrook, Earl Fair, Jeanne Ogutu, Joseph O. Gachohi, John Njenga, Kariuki Bett, Bernard |
author_facet | Akoko, James M. Mwatondo, Athman Muturi, Mathew Wambua, Lillian Abkallo, Hussein M. Nyamota, Richard Bosire, Caroline Oloo, Stephen Limbaso, Konongoi S. Gakuya, Francis Nthiwa, Daniel Bartlow, Andrew Middlebrook, Earl Fair, Jeanne Ogutu, Joseph O. Gachohi, John Njenga, Kariuki Bett, Bernard |
author_sort | Akoko, James M. |
collection | PubMed |
description | In Sub-Saharan Africa (SSA), effective brucellosis control is limited, in part, by the lack of long-term commitments by governments to control the disease and the absence of reliable national human and livestock population-based data to inform policies. Therefore, we conducted a study to establish the national prevalence and develop a risk map for Brucella spp. in cattle to contribute to plans to eliminate the disease in Kenya by the year 2040. We randomly generated 268 geolocations and distributed them across Kenya, proportionate to the area of each of the five agroecological zones and the associated cattle population. Cattle herds closest to each selected geolocation were identified for sampling. Up to 25 cattle were sampled per geolocation and a semi-structured questionnaire was administered to their owners. We tested 6,593 cattle samples for Brucella immunoglobulin G (IgG) antibodies using an Enzyme-linked immunosorbent assay (ELISA). We assessed potential risk factors and performed spatial analyses and prevalence mapping using approximate Bayesian inference implemented via the integrated nested Laplace approximation (INLA) method. The national Brucella spp. prevalence was 6.8% (95% CI: 6.2–7.4%). Exposure levels varied significantly between agro-ecological zones, with a high of 8.5% in the very arid zone with the lowest agricultural potential relative to a low of 0.0% in the agro-alpine zone with the highest agricultural potential. Additionally, seroprevalence increased with herd size, and the odds of seropositivity were significantly higher for females and adult animals than for males or calves. Similarly, animals with a history of abortion, or with multiple reproductive syndromes had higher seropositivity than those without. At the herd level, the risk of Brucella spp. transmission was higher in larger herds, and herds with a history of reproductive problems such as abortion, giving birth to weak calves, or having swollen testes. Geographic localities with high Brucella seroprevalence occurred in northern, eastern, and southern regions of Kenya all primarily characterized by semi-arid or arid agro-ecological zones dominated by livestock pastoralism interspersed with vast areas with mixed livestock-wildlife systems. The large spatial extent of our survey provides compelling evidence for the widespread geographical distribution of brucellosis risk across Kenya in a manner easily understandable for policymakers. Our findings can provide a basis for risk-stratified pilot studies aiming to investigate the cost-effectiveness and efficacy of singular and combined preventive intervention strategies that seek to inform Kenya’s Brucellosis Control Policy. |
format | Online Article Text |
id | pubmed-10657468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106574682023-11-18 Mapping brucellosis risk in Kenya and its implications for control strategies in sub-Saharan Africa Akoko, James M. Mwatondo, Athman Muturi, Mathew Wambua, Lillian Abkallo, Hussein M. Nyamota, Richard Bosire, Caroline Oloo, Stephen Limbaso, Konongoi S. Gakuya, Francis Nthiwa, Daniel Bartlow, Andrew Middlebrook, Earl Fair, Jeanne Ogutu, Joseph O. Gachohi, John Njenga, Kariuki Bett, Bernard Sci Rep Article In Sub-Saharan Africa (SSA), effective brucellosis control is limited, in part, by the lack of long-term commitments by governments to control the disease and the absence of reliable national human and livestock population-based data to inform policies. Therefore, we conducted a study to establish the national prevalence and develop a risk map for Brucella spp. in cattle to contribute to plans to eliminate the disease in Kenya by the year 2040. We randomly generated 268 geolocations and distributed them across Kenya, proportionate to the area of each of the five agroecological zones and the associated cattle population. Cattle herds closest to each selected geolocation were identified for sampling. Up to 25 cattle were sampled per geolocation and a semi-structured questionnaire was administered to their owners. We tested 6,593 cattle samples for Brucella immunoglobulin G (IgG) antibodies using an Enzyme-linked immunosorbent assay (ELISA). We assessed potential risk factors and performed spatial analyses and prevalence mapping using approximate Bayesian inference implemented via the integrated nested Laplace approximation (INLA) method. The national Brucella spp. prevalence was 6.8% (95% CI: 6.2–7.4%). Exposure levels varied significantly between agro-ecological zones, with a high of 8.5% in the very arid zone with the lowest agricultural potential relative to a low of 0.0% in the agro-alpine zone with the highest agricultural potential. Additionally, seroprevalence increased with herd size, and the odds of seropositivity were significantly higher for females and adult animals than for males or calves. Similarly, animals with a history of abortion, or with multiple reproductive syndromes had higher seropositivity than those without. At the herd level, the risk of Brucella spp. transmission was higher in larger herds, and herds with a history of reproductive problems such as abortion, giving birth to weak calves, or having swollen testes. Geographic localities with high Brucella seroprevalence occurred in northern, eastern, and southern regions of Kenya all primarily characterized by semi-arid or arid agro-ecological zones dominated by livestock pastoralism interspersed with vast areas with mixed livestock-wildlife systems. The large spatial extent of our survey provides compelling evidence for the widespread geographical distribution of brucellosis risk across Kenya in a manner easily understandable for policymakers. Our findings can provide a basis for risk-stratified pilot studies aiming to investigate the cost-effectiveness and efficacy of singular and combined preventive intervention strategies that seek to inform Kenya’s Brucellosis Control Policy. Nature Publishing Group UK 2023-11-18 /pmc/articles/PMC10657468/ /pubmed/37980384 http://dx.doi.org/10.1038/s41598-023-47628-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Akoko, James M. Mwatondo, Athman Muturi, Mathew Wambua, Lillian Abkallo, Hussein M. Nyamota, Richard Bosire, Caroline Oloo, Stephen Limbaso, Konongoi S. Gakuya, Francis Nthiwa, Daniel Bartlow, Andrew Middlebrook, Earl Fair, Jeanne Ogutu, Joseph O. Gachohi, John Njenga, Kariuki Bett, Bernard Mapping brucellosis risk in Kenya and its implications for control strategies in sub-Saharan Africa |
title | Mapping brucellosis risk in Kenya and its implications for control strategies in sub-Saharan Africa |
title_full | Mapping brucellosis risk in Kenya and its implications for control strategies in sub-Saharan Africa |
title_fullStr | Mapping brucellosis risk in Kenya and its implications for control strategies in sub-Saharan Africa |
title_full_unstemmed | Mapping brucellosis risk in Kenya and its implications for control strategies in sub-Saharan Africa |
title_short | Mapping brucellosis risk in Kenya and its implications for control strategies in sub-Saharan Africa |
title_sort | mapping brucellosis risk in kenya and its implications for control strategies in sub-saharan africa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657468/ https://www.ncbi.nlm.nih.gov/pubmed/37980384 http://dx.doi.org/10.1038/s41598-023-47628-1 |
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