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Selection assisted by a BoLA-DR/DQ haplotype against susceptibility to bovine dermatophilosis
Bovine dermatophilosis is a severe skin infection of tropical ruminants inducing a severe loss in productivity and a 15% mortality rate. This disease is caused by the actinomycete bacterium Dermatophilus congolensis associated with the tick Amblyomma variegatum. Currently there are no prospects for...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3231761/ https://www.ncbi.nlm.nih.gov/pubmed/12927091 http://dx.doi.org/10.1186/1297-9686-35-S1-S193 |
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author | Maillard, Jean-Charles Berthier, David Chantal, Isabelle Thevenon, Sophie Sidibé, Issa Stachurski, Frederic Belemsaga, Désiré Razafindraïbé, Hanta Elsen, Jean-Michel |
author_facet | Maillard, Jean-Charles Berthier, David Chantal, Isabelle Thevenon, Sophie Sidibé, Issa Stachurski, Frederic Belemsaga, Désiré Razafindraïbé, Hanta Elsen, Jean-Michel |
author_sort | Maillard, Jean-Charles |
collection | PubMed |
description | Bovine dermatophilosis is a severe skin infection of tropical ruminants inducing a severe loss in productivity and a 15% mortality rate. This disease is caused by the actinomycete bacterium Dermatophilus congolensis associated with the tick Amblyomma variegatum. Currently there are no prospects for a vaccine, and acaricide or antibiotic control is hampered by the development of chemoresistance. Animal breeders have observed that dermatophilosis susceptibility seems to be determined genetically, and we previously identified a BoLA-DRB3-DQB class II haplotype marker for high (R(2 )= 0.96) susceptibility to the disease. With this marker, we developed a successful eugenic selection procedure for zebu Brahman cattle in Martinique (FWI). Over a period of five years, a marked reduction in disease prevalence, from 0.76 to 0.02 was achieved, and this low level has been maintained over the last two years. The selection procedure, based on a genetic marker system targeting the highly polymorphic BoLA locus, eliminates only those individuals which are at the highest risk of contracting the disease. In the present work, we discuss the properties of this system, including the "heterozygote advantage" and the "frequency dependence" theories, and examine their involvement in the biological mechanisms at the host/pathogen interface. We speculate on the exact role of the MHC molecules in the control of the disease, how the natural selection pressure imposed by the pathogens selectively maintains MHC diversity, and how our results can be practically applied for integrated control of dermatophilosis in developing countries. |
format | Online Article Text |
id | pubmed-3231761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32317612011-12-07 Selection assisted by a BoLA-DR/DQ haplotype against susceptibility to bovine dermatophilosis Maillard, Jean-Charles Berthier, David Chantal, Isabelle Thevenon, Sophie Sidibé, Issa Stachurski, Frederic Belemsaga, Désiré Razafindraïbé, Hanta Elsen, Jean-Michel Genet Sel Evol Research Bovine dermatophilosis is a severe skin infection of tropical ruminants inducing a severe loss in productivity and a 15% mortality rate. This disease is caused by the actinomycete bacterium Dermatophilus congolensis associated with the tick Amblyomma variegatum. Currently there are no prospects for a vaccine, and acaricide or antibiotic control is hampered by the development of chemoresistance. Animal breeders have observed that dermatophilosis susceptibility seems to be determined genetically, and we previously identified a BoLA-DRB3-DQB class II haplotype marker for high (R(2 )= 0.96) susceptibility to the disease. With this marker, we developed a successful eugenic selection procedure for zebu Brahman cattle in Martinique (FWI). Over a period of five years, a marked reduction in disease prevalence, from 0.76 to 0.02 was achieved, and this low level has been maintained over the last two years. The selection procedure, based on a genetic marker system targeting the highly polymorphic BoLA locus, eliminates only those individuals which are at the highest risk of contracting the disease. In the present work, we discuss the properties of this system, including the "heterozygote advantage" and the "frequency dependence" theories, and examine their involvement in the biological mechanisms at the host/pathogen interface. We speculate on the exact role of the MHC molecules in the control of the disease, how the natural selection pressure imposed by the pathogens selectively maintains MHC diversity, and how our results can be practically applied for integrated control of dermatophilosis in developing countries. BioMed Central 2003-06-15 /pmc/articles/PMC3231761/ /pubmed/12927091 http://dx.doi.org/10.1186/1297-9686-35-S1-S193 Text en Copyright ©2003 INRA, EDP Sciences |
spellingShingle | Research Maillard, Jean-Charles Berthier, David Chantal, Isabelle Thevenon, Sophie Sidibé, Issa Stachurski, Frederic Belemsaga, Désiré Razafindraïbé, Hanta Elsen, Jean-Michel Selection assisted by a BoLA-DR/DQ haplotype against susceptibility to bovine dermatophilosis |
title | Selection assisted by a BoLA-DR/DQ haplotype against susceptibility to bovine dermatophilosis |
title_full | Selection assisted by a BoLA-DR/DQ haplotype against susceptibility to bovine dermatophilosis |
title_fullStr | Selection assisted by a BoLA-DR/DQ haplotype against susceptibility to bovine dermatophilosis |
title_full_unstemmed | Selection assisted by a BoLA-DR/DQ haplotype against susceptibility to bovine dermatophilosis |
title_short | Selection assisted by a BoLA-DR/DQ haplotype against susceptibility to bovine dermatophilosis |
title_sort | selection assisted by a bola-dr/dq haplotype against susceptibility to bovine dermatophilosis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3231761/ https://www.ncbi.nlm.nih.gov/pubmed/12927091 http://dx.doi.org/10.1186/1297-9686-35-S1-S193 |
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