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Identification of new IS711 insertion sites in Brucella abortus field isolates
BACKGROUND: Brucellosis is a zoonosis caused by Brucella spp., a group of highly homogeneous bacteria. The insertion sequence IS711 is characteristic of these bacteria, and occurs in variable numbers and positions, but always constant within a given species. This species-associated polymorphism is u...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3163539/ https://www.ncbi.nlm.nih.gov/pubmed/21813003 http://dx.doi.org/10.1186/1471-2180-11-176 |
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author | Mancilla, Marcos Ulloa, Marcos López-Goñi, Ignacio Moriyón, Ignacio María Zárraga, Ana |
author_facet | Mancilla, Marcos Ulloa, Marcos López-Goñi, Ignacio Moriyón, Ignacio María Zárraga, Ana |
author_sort | Mancilla, Marcos |
collection | PubMed |
description | BACKGROUND: Brucellosis is a zoonosis caused by Brucella spp., a group of highly homogeneous bacteria. The insertion sequence IS711 is characteristic of these bacteria, and occurs in variable numbers and positions, but always constant within a given species. This species-associated polymorphism is used in molecular typing and identification. Field isolates of B. abortus, the most common species infecting cattle, typically carry seven IS711 copies (one truncated). Thus far, IS711 transposition has only been shown in vitro and only for B. ovis and B. pinnipedialis, two species carrying a high number of IS711 copies, but never in other Brucella species, neither in vitro nor in field strains. RESULTS: We found several B. abortus strains isolated from milk and aborted fetuses that carried additional IS711 copies in two hitherto undescribed insertion sites: one in an intergenic region near to the 3' end of a putative lactate permease gene and the other interrupting the sequence of a marR transcriptional regulator gene. Interestingly, the second type of insertion was identified in isolates obtained repeatedly from the same herd after successive brucellosis outbreaks, an observation that proves the stability and virulence of the new genotype under natural conditions. Sequence analyses revealed that the new copies probably resulted from the transposition of a single IS711 copy common to all Brucella species sequenced so far. CONCLUSIONS: Our results show that the replicative transposition of IS711 can occur under field conditions. Therefore, it represents an active mechanism for the emergence of genetic diversity in B. abortus thus contributing to intra-species genetic polymorphism. |
format | Online Article Text |
id | pubmed-3163539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31635392011-08-30 Identification of new IS711 insertion sites in Brucella abortus field isolates Mancilla, Marcos Ulloa, Marcos López-Goñi, Ignacio Moriyón, Ignacio María Zárraga, Ana BMC Microbiol Research Article BACKGROUND: Brucellosis is a zoonosis caused by Brucella spp., a group of highly homogeneous bacteria. The insertion sequence IS711 is characteristic of these bacteria, and occurs in variable numbers and positions, but always constant within a given species. This species-associated polymorphism is used in molecular typing and identification. Field isolates of B. abortus, the most common species infecting cattle, typically carry seven IS711 copies (one truncated). Thus far, IS711 transposition has only been shown in vitro and only for B. ovis and B. pinnipedialis, two species carrying a high number of IS711 copies, but never in other Brucella species, neither in vitro nor in field strains. RESULTS: We found several B. abortus strains isolated from milk and aborted fetuses that carried additional IS711 copies in two hitherto undescribed insertion sites: one in an intergenic region near to the 3' end of a putative lactate permease gene and the other interrupting the sequence of a marR transcriptional regulator gene. Interestingly, the second type of insertion was identified in isolates obtained repeatedly from the same herd after successive brucellosis outbreaks, an observation that proves the stability and virulence of the new genotype under natural conditions. Sequence analyses revealed that the new copies probably resulted from the transposition of a single IS711 copy common to all Brucella species sequenced so far. CONCLUSIONS: Our results show that the replicative transposition of IS711 can occur under field conditions. Therefore, it represents an active mechanism for the emergence of genetic diversity in B. abortus thus contributing to intra-species genetic polymorphism. BioMed Central 2011-08-03 /pmc/articles/PMC3163539/ /pubmed/21813003 http://dx.doi.org/10.1186/1471-2180-11-176 Text en Copyright ©2011 Mancilla 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 Mancilla, Marcos Ulloa, Marcos López-Goñi, Ignacio Moriyón, Ignacio María Zárraga, Ana Identification of new IS711 insertion sites in Brucella abortus field isolates |
title | Identification of new IS711 insertion sites in Brucella abortus field isolates |
title_full | Identification of new IS711 insertion sites in Brucella abortus field isolates |
title_fullStr | Identification of new IS711 insertion sites in Brucella abortus field isolates |
title_full_unstemmed | Identification of new IS711 insertion sites in Brucella abortus field isolates |
title_short | Identification of new IS711 insertion sites in Brucella abortus field isolates |
title_sort | identification of new is711 insertion sites in brucella abortus field isolates |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3163539/ https://www.ncbi.nlm.nih.gov/pubmed/21813003 http://dx.doi.org/10.1186/1471-2180-11-176 |
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