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BMC Microbiol ; 11: 176, 2011 Aug 03.
Artigo em Inglês | MEDLINE | ID: mdl-21813003

RESUMO

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.


Assuntos
Brucella abortus/genética , Elementos de DNA Transponíveis , DNA Bacteriano/genética , Feto Abortado/microbiologia , Animais , Brucella abortus/isolamento & purificação , Brucelose Bovina/microbiologia , Bovinos , DNA Bacteriano/química , DNA Intergênico , Leite/microbiologia , Dados de Sequência Molecular , Mutagênese Insercional , Recombinação Genética , Proteínas Repressoras/genética , Análise de Sequência de DNA
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