Roles of genomic island 3 (GI-3) BAB1_0267 and BAB1_0270 open reading frames (ORFs) in the virulence of Brucella abortus 2308
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2014Metadata
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Ortiz Román, Luisa
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Roles of genomic island 3 (GI-3) BAB1_0267 and BAB1_0270 open reading frames (ORFs) in the virulence of Brucella abortus 2308
Abstract
One of the properties of bacteria is their capacity to acquire large fragments of genomic
DNA from other bacteria or to loose important parts of their own genome. Such fragments
include genomic islands (GIs); nine GIs are present in Brucella, including genomic island 3
(GI-3), present in B. abortus, B. melitensis and B. ovis. The GI-3 have 29 open reading frames
(ORFs) most of them with unknown function. Within the GI-3, the ORFs BAB1_0267
encodes a hypothetical protein sharing a SH3 domain and BAB1_270 a zinc-dependent
metallopeptidase. We have obtained deletion mutants for BAB1_0267 and BAB1_0270
ORFs present within GI-3, which have been named the D0267 and D0270, respectively; in
both cases the mutation did not affect the growth of bacteria. Both mutants were
evaluated with respect to their growth rates, their ability to invade and replicate in the
non-professional and professional phagocytes, HeLa and J774.A1 cells, respectively. Their
persistence in the spleens of mice was also evaluated. The mutants efficiently invaded
HeLa and J774.A1 cells but both mutants showed a decreased intracellular survival in
macrophages and HeLa cells 72 and 96 h post-infection, respectively, and were nondetected
in J774.A1 cells 120 h post infection. With respect to in vivo persistence D0267
was detected through the fourth week while D0270 decreased at 7 days disappearing the
second week. Our results indicated that deletion of BAB1_0267 and BAB1_270 are
necessary to establish an optimal infectious process in B. abortus 2308, having more effect
the deletion of ORF BAB1_0270. Therefore these ORFs, principally BAB1_0270 are
important virulent of B. abortus.
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Patrocinador
This work was supported by grant 1130093 from
‘‘Fondo Nacional de Investigacio´n Cientı´fica y Tecnolo´ gica’’
(FONDECYT), Chile. Luisa Ortiz-Roma´n was supported by a
fellowship from Agencia de Cooperacio´n Internacional de
Chile (AGCI). The authors thank Donald L. Court, PhD from
the National Cancer Institute for providing us the plasmid
pSIM7.
Identifier
URI: https://repositorio.uchile.cl/handle/2250/129473
DOI: dx.doi.org/10.1016/j.vetmic.2014.05.005
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Veterinary Microbiology 172 (2014) 279–284
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