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Within-host evolution of Brucella canis during a canine brucellosis outbreak in a kennel

BACKGROUND: Little is currently known about Brucella evolution within the host during infection. The current study is the first to employ fine-scale genotyping on an isolate collection derived from a Brucella canis outbreak. Eight isolates of B. canis, cultured from different tissues of three dogs (...

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Autores principales: Gyuranecz, Miklós, Rannals, Brandy D, Allen, Christina A, Jánosi, Szilárd, Keim, Paul S, Foster, Jeffrey T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3637509/
https://www.ncbi.nlm.nih.gov/pubmed/23587163
http://dx.doi.org/10.1186/1746-6148-9-76
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author Gyuranecz, Miklós
Rannals, Brandy D
Allen, Christina A
Jánosi, Szilárd
Keim, Paul S
Foster, Jeffrey T
author_facet Gyuranecz, Miklós
Rannals, Brandy D
Allen, Christina A
Jánosi, Szilárd
Keim, Paul S
Foster, Jeffrey T
author_sort Gyuranecz, Miklós
collection PubMed
description BACKGROUND: Little is currently known about Brucella evolution within the host during infection. The current study is the first to employ fine-scale genotyping on an isolate collection derived from a Brucella canis outbreak. Eight isolates of B. canis, cultured from different tissues of three dogs (female, stud dog, puppy of another female) from a single kennel over three months were genetically characterized with a 15-marker multi-locus, variable-number tandem repeat (VNTR) analysis (MLVA) to assess the genetic relatedness of isolates and potential rapid mutational changes. RESULTS: MLVA discriminated among the otherwise indistinguishable isolates from different animals and from isolates collected at different time points within each host, with different VNTR alleles being detected at multiple dates and tissue sites. We suspect that all isolates cultured from the female, puppy, and stud dogs originated from the same strain, with subsequent rapid in vivo mutations. However, high mutation rates and apparent in several of the loci prevented making definitive epidemiological relationships among isolates. CONCLUSIONS: This investigation highlights the rapid in vivo genetic mutations of several VNTRs of B. canis over a short time period in the host and the emergence of alternate alleles. However, this work also suggests the challenges of using highly mutable VNTRs to infer epidemiological relationships of strains within a short duration outbreak.
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spelling pubmed-36375092013-04-27 Within-host evolution of Brucella canis during a canine brucellosis outbreak in a kennel Gyuranecz, Miklós Rannals, Brandy D Allen, Christina A Jánosi, Szilárd Keim, Paul S Foster, Jeffrey T BMC Vet Res Research Article BACKGROUND: Little is currently known about Brucella evolution within the host during infection. The current study is the first to employ fine-scale genotyping on an isolate collection derived from a Brucella canis outbreak. Eight isolates of B. canis, cultured from different tissues of three dogs (female, stud dog, puppy of another female) from a single kennel over three months were genetically characterized with a 15-marker multi-locus, variable-number tandem repeat (VNTR) analysis (MLVA) to assess the genetic relatedness of isolates and potential rapid mutational changes. RESULTS: MLVA discriminated among the otherwise indistinguishable isolates from different animals and from isolates collected at different time points within each host, with different VNTR alleles being detected at multiple dates and tissue sites. We suspect that all isolates cultured from the female, puppy, and stud dogs originated from the same strain, with subsequent rapid in vivo mutations. However, high mutation rates and apparent in several of the loci prevented making definitive epidemiological relationships among isolates. CONCLUSIONS: This investigation highlights the rapid in vivo genetic mutations of several VNTRs of B. canis over a short time period in the host and the emergence of alternate alleles. However, this work also suggests the challenges of using highly mutable VNTRs to infer epidemiological relationships of strains within a short duration outbreak. BioMed Central 2013-04-12 /pmc/articles/PMC3637509/ /pubmed/23587163 http://dx.doi.org/10.1186/1746-6148-9-76 Text en Copyright © 2013 Gyuranecz et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gyuranecz, Miklós
Rannals, Brandy D
Allen, Christina A
Jánosi, Szilárd
Keim, Paul S
Foster, Jeffrey T
Within-host evolution of Brucella canis during a canine brucellosis outbreak in a kennel
title Within-host evolution of Brucella canis during a canine brucellosis outbreak in a kennel
title_full Within-host evolution of Brucella canis during a canine brucellosis outbreak in a kennel
title_fullStr Within-host evolution of Brucella canis during a canine brucellosis outbreak in a kennel
title_full_unstemmed Within-host evolution of Brucella canis during a canine brucellosis outbreak in a kennel
title_short Within-host evolution of Brucella canis during a canine brucellosis outbreak in a kennel
title_sort within-host evolution of brucella canis during a canine brucellosis outbreak in a kennel
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3637509/
https://www.ncbi.nlm.nih.gov/pubmed/23587163
http://dx.doi.org/10.1186/1746-6148-9-76
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