Molecular epidemiology of Brucella species in mixed livestock-human ecosystems in Kenya.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
23 04 2021
Historique:
received: 29 09 2020
accepted: 09 04 2021
entrez: 24 4 2021
pubmed: 25 4 2021
medline: 10 11 2021
Statut: epublish

Résumé

Brucellosis, caused by several species of the genus Brucella, is a zoonotic disease that affects humans and animal species worldwide. Information on the Brucella species circulating in different hosts in Kenya is largely unknown, thus limiting the adoption of targeted control strategies. This study was conducted in multi-host livestock populations in Kenya to detect the circulating Brucella species and assess evidence of host-pathogen associations. Serum samples were collected from 228 cattle, 162 goats, 158 sheep, 49 camels, and 257 humans from Narok and Marsabit counties in Kenya. Information on age, location and history of abortion or retained placenta were obtained for sampled livestock. Data on age, gender and location of residence were also collected for human participants. All samples were tested using genus level real-time PCR assays with primers specific for IS711 and bcsp31 targets for the detection of Brucella. All genus positive samples (positive for both targets) were further tested with a speciation assay for AlkB and BMEI1162 targets, specific for B. abortus and B. melitensis, respectively. Samples with adequate quantities aggregating to 577 were also tested with the Rose Bengal Test (RBT). A total of 199 (33.3%) livestock and 99 (38.5%) human samples tested positive for genus Brucella. Animal Brucella PCR positive status was positively predicted by RBT positive results (OR = 8.3, 95% CI 4.0-17.1). Humans aged 21-40 years had higher odds (OR = 2.8, 95% CI 1.2-6.6) of being Brucella PCR positive compared to the other age categories. The data on detection of different Brucella species indicates that B. abortus was detected more often in cattle (OR = 2.3, 95% CI 1.1-4.6) and camels (OR = 2.9, 95% CI 1.3-6.3), while B. melitensis was detected more in sheep (OR = 3.6, 95% CI 2.0-6.7) and goats (OR = 1.7, 95% CI 1.0-3.1). Both B. abortus and B. melitensis DNA were detected in humans and in multiple livestock host species, suggesting cross-transmission of these species among the different hosts. The detection of these two zoonotic Brucella species in humans further underpins the importance of One Health prevention strategies that target multiple host species, especially in the multi-host livestock populations.

Identifiants

pubmed: 33893352
doi: 10.1038/s41598-021-88327-z
pii: 10.1038/s41598-021-88327-z
pmc: PMC8065124
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

8881

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/L019019/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 107753/A/15/Z
Pays : United Kingdom

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Auteurs

James M Akoko (JM)

Department of Biomedical Sciences and Technology, Maseno University, Kisumu, Kenya. jamesakoko@yahoo.com.
Biosciences Eastern and Central Africa-International Livestock Research Institute (BecA-ILRI) Hub KE, Nairobi, Kenya. jamesakoko@yahoo.com.
International Livestock Research Institute, Nairobi, Kenya. jamesakoko@yahoo.com.

Roger Pelle (R)

Biosciences Eastern and Central Africa-International Livestock Research Institute (BecA-ILRI) Hub KE, Nairobi, Kenya.

AbdulHamid S Lukambagire (AS)

Sokoine University of Agriculture, Morogoro, Tanzania.

Eunice M Machuka (EM)

Biosciences Eastern and Central Africa-International Livestock Research Institute (BecA-ILRI) Hub KE, Nairobi, Kenya.

Daniel Nthiwa (D)

Department of Biological Sciences, University of Embu, Embu, Kenya.

Coletha Mathew (C)

Sokoine University of Agriculture, Morogoro, Tanzania.

Eric M Fèvre (EM)

International Livestock Research Institute, Nairobi, Kenya.
Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.

Bernard Bett (B)

International Livestock Research Institute, Nairobi, Kenya.

Elizabeth A J Cook (EAJ)

International Livestock Research Institute, Nairobi, Kenya.
Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.

Doreen Othero (D)

Department of Public Health, Maseno University, Kisumu, Kenya.

Bassirou Bonfoh (B)

Centre Suisse de Recherches Scientifiques en Côte d'Ivoire, Abidjan, Côte d'Ivoire.

Rudovick R Kazwala (RR)

Sokoine University of Agriculture, Morogoro, Tanzania.

Gabriel Shirima (G)

Nelson Mandela African Institute of Science and Technology, Arusha, Tanzania.

Esther Schelling (E)

Vétérinaires Sans Frontières Suisse, Bern, Switzerland.

Jo E B Halliday (JEB)

Institute of Biodiversity, Animal Health and Comparative Medicine, College of Medical Veterinary and Life Sciences, University of Glasgow, Glasgow, G12 8QQ, UK.

Collins Ouma (C)

Department of Biomedical Sciences and Technology, Maseno University, Kisumu, Kenya.

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