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Serological detection of brucellosis among febrile, malaria-negative children and domesticated dogs in an urban African setting
BACKGROUND: Childhood brucellosis and malaria are co-endemic febrile illnesses in some sub-Saharan African countries. Malaria and brucellosis co-infection or brucellosis sole infections are often missed due to an over emphasis on malaria and the lack of appropriate diagnostic infrastructure. Brucell...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AOSIS
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564948/ https://www.ncbi.nlm.nih.gov/pubmed/33102165 http://dx.doi.org/10.4102/ajlm.v9i1.864 |
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author | Kalule, John B. Tomusange, Joseph Namatovu, Teddy |
author_facet | Kalule, John B. Tomusange, Joseph Namatovu, Teddy |
author_sort | Kalule, John B. |
collection | PubMed |
description | BACKGROUND: Childhood brucellosis and malaria are co-endemic febrile illnesses in some sub-Saharan African countries. Malaria and brucellosis co-infection or brucellosis sole infections are often missed due to an over emphasis on malaria and the lack of appropriate diagnostic infrastructure. Brucellosis in dogs is usually overlooked and yet there is extensive contact between humans and their pets. OBJECTIVE: This study investigated brucellosis in children and dogs using a confirmatory serological testing series that screens for three Brucella sp. METHODS: Residual blood samples from malaria smear-negative febrile children were collected and tested for Brucella sp and malaria parasite. During the same period, residual blood samples presented to a veterinary microbiology laboratory in the same area were tested for brucellosis using the same approach. RESULTS: A total of 105 human and 80 canine blood samples were tested for brucellosis antibodies. The seroprevalence of brucellosis was 22.86% (25/105) in children and 1.3% (1/80) in dogs using the Card, buffered acidified plate antigen, and standard plate agglutination tests but was 0% using the rivanol precipitation plate agglutination test. CONCLUSION: Given that brucellosis can be caused by both smooth and rough colony strains, there is a need to modify the current serological surveillance strategy (targeted at only Brucella abortus and other smooth colony Brucella strains) to figure out the relative contribution of rough colony Brucella strains (B. ovis and B. canis). Since Uganda is endemic for brucellosis there is a need to modify the brucellosis surveillance strategy. |
format | Online Article Text |
id | pubmed-7564948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AOSIS |
record_format | MEDLINE/PubMed |
spelling | pubmed-75649482020-10-22 Serological detection of brucellosis among febrile, malaria-negative children and domesticated dogs in an urban African setting Kalule, John B. Tomusange, Joseph Namatovu, Teddy Afr J Lab Med Original Research BACKGROUND: Childhood brucellosis and malaria are co-endemic febrile illnesses in some sub-Saharan African countries. Malaria and brucellosis co-infection or brucellosis sole infections are often missed due to an over emphasis on malaria and the lack of appropriate diagnostic infrastructure. Brucellosis in dogs is usually overlooked and yet there is extensive contact between humans and their pets. OBJECTIVE: This study investigated brucellosis in children and dogs using a confirmatory serological testing series that screens for three Brucella sp. METHODS: Residual blood samples from malaria smear-negative febrile children were collected and tested for Brucella sp and malaria parasite. During the same period, residual blood samples presented to a veterinary microbiology laboratory in the same area were tested for brucellosis using the same approach. RESULTS: A total of 105 human and 80 canine blood samples were tested for brucellosis antibodies. The seroprevalence of brucellosis was 22.86% (25/105) in children and 1.3% (1/80) in dogs using the Card, buffered acidified plate antigen, and standard plate agglutination tests but was 0% using the rivanol precipitation plate agglutination test. CONCLUSION: Given that brucellosis can be caused by both smooth and rough colony strains, there is a need to modify the current serological surveillance strategy (targeted at only Brucella abortus and other smooth colony Brucella strains) to figure out the relative contribution of rough colony Brucella strains (B. ovis and B. canis). Since Uganda is endemic for brucellosis there is a need to modify the brucellosis surveillance strategy. AOSIS 2020-09-30 /pmc/articles/PMC7564948/ /pubmed/33102165 http://dx.doi.org/10.4102/ajlm.v9i1.864 Text en © 2020. The Authors https://creativecommons.org/licenses/by/4.0/ Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License. |
spellingShingle | Original Research Kalule, John B. Tomusange, Joseph Namatovu, Teddy Serological detection of brucellosis among febrile, malaria-negative children and domesticated dogs in an urban African setting |
title | Serological detection of brucellosis among febrile, malaria-negative children and domesticated dogs in an urban African setting |
title_full | Serological detection of brucellosis among febrile, malaria-negative children and domesticated dogs in an urban African setting |
title_fullStr | Serological detection of brucellosis among febrile, malaria-negative children and domesticated dogs in an urban African setting |
title_full_unstemmed | Serological detection of brucellosis among febrile, malaria-negative children and domesticated dogs in an urban African setting |
title_short | Serological detection of brucellosis among febrile, malaria-negative children and domesticated dogs in an urban African setting |
title_sort | serological detection of brucellosis among febrile, malaria-negative children and domesticated dogs in an urban african setting |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564948/ https://www.ncbi.nlm.nih.gov/pubmed/33102165 http://dx.doi.org/10.4102/ajlm.v9i1.864 |
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