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Brucella microti: the genome sequence of an emerging pathogen

BACKGROUND: Using a combination of pyrosequencing and conventional Sanger sequencing, the complete genome sequence of the recently described novel Brucella species, Brucella microti, was determined. B. microti is a member of the genus Brucella within the Alphaproteobacteria, which consists of medica...

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Autores principales: Audic, Stéphane, Lescot, Magali, Claverie, Jean-Michel, Scholz, Holger C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743711/
https://www.ncbi.nlm.nih.gov/pubmed/19653890
http://dx.doi.org/10.1186/1471-2164-10-352
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author Audic, Stéphane
Lescot, Magali
Claverie, Jean-Michel
Scholz, Holger C
author_facet Audic, Stéphane
Lescot, Magali
Claverie, Jean-Michel
Scholz, Holger C
author_sort Audic, Stéphane
collection PubMed
description BACKGROUND: Using a combination of pyrosequencing and conventional Sanger sequencing, the complete genome sequence of the recently described novel Brucella species, Brucella microti, was determined. B. microti is a member of the genus Brucella within the Alphaproteobacteria, which consists of medically important highly pathogenic facultative intracellular bacteria. In contrast to all other Brucella species, B. microti is a fast growing and biochemically very active microorganism with a phenotype more similar to that of Ochrobactrum, a facultative human pathogen. The atypical phenotype of B. microti prompted us to look for genomic differences compared to other Brucella species and to look for similarities with Ochrobactrum. RESULTS: The genome is composed of two circular chromosomes of 2,117,050 and 1,220,319 base pairs. Unexpectedly, we found that the genome sequence of B. microti is almost identical to that of Brucella suis 1330 with an overall sequence identity of 99.84% in aligned regions. The most significant structural difference between the two genomes is a bacteriophage-related 11,742 base pairs insert only present in B. microti. However, this insert is unlikely to have any phenotypical consequence. Only four protein coding genes are shared between B. microti and Ochrobactrum anthropi but impaired in other sequenced Brucella. The most noticeable difference between B. microti and other Brucella species was found in the sequence of the 23S ribosomal RNA gene. This unusual variation could have pleiotropic effects and explain the fast growth of B. microti. CONCLUSION: Contrary to expectations from the phenotypic analysis, the genome sequence of B. microti is highly similar to that of known Brucella species, and is remotely related to the one of O. anthropi. How the few differences in gene content between B. microti and B. suis 1330 could result in vastly different phenotypes remains to be elucidated. This unexpected finding will complicate the task of identifying virulence determinants in the Brucella genus. The genome sequence of B. microti will serve as a model for differential expression analysis and complementation studies. Our results also raise some concerns about the importance given to phenotypical traits in the definition of bacterial species.
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spelling pubmed-27437112009-09-15 Brucella microti: the genome sequence of an emerging pathogen Audic, Stéphane Lescot, Magali Claverie, Jean-Michel Scholz, Holger C BMC Genomics Research Article BACKGROUND: Using a combination of pyrosequencing and conventional Sanger sequencing, the complete genome sequence of the recently described novel Brucella species, Brucella microti, was determined. B. microti is a member of the genus Brucella within the Alphaproteobacteria, which consists of medically important highly pathogenic facultative intracellular bacteria. In contrast to all other Brucella species, B. microti is a fast growing and biochemically very active microorganism with a phenotype more similar to that of Ochrobactrum, a facultative human pathogen. The atypical phenotype of B. microti prompted us to look for genomic differences compared to other Brucella species and to look for similarities with Ochrobactrum. RESULTS: The genome is composed of two circular chromosomes of 2,117,050 and 1,220,319 base pairs. Unexpectedly, we found that the genome sequence of B. microti is almost identical to that of Brucella suis 1330 with an overall sequence identity of 99.84% in aligned regions. The most significant structural difference between the two genomes is a bacteriophage-related 11,742 base pairs insert only present in B. microti. However, this insert is unlikely to have any phenotypical consequence. Only four protein coding genes are shared between B. microti and Ochrobactrum anthropi but impaired in other sequenced Brucella. The most noticeable difference between B. microti and other Brucella species was found in the sequence of the 23S ribosomal RNA gene. This unusual variation could have pleiotropic effects and explain the fast growth of B. microti. CONCLUSION: Contrary to expectations from the phenotypic analysis, the genome sequence of B. microti is highly similar to that of known Brucella species, and is remotely related to the one of O. anthropi. How the few differences in gene content between B. microti and B. suis 1330 could result in vastly different phenotypes remains to be elucidated. This unexpected finding will complicate the task of identifying virulence determinants in the Brucella genus. The genome sequence of B. microti will serve as a model for differential expression analysis and complementation studies. Our results also raise some concerns about the importance given to phenotypical traits in the definition of bacterial species. BioMed Central 2009-08-04 /pmc/articles/PMC2743711/ /pubmed/19653890 http://dx.doi.org/10.1186/1471-2164-10-352 Text en Copyright © 2009 Audic 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
Audic, Stéphane
Lescot, Magali
Claverie, Jean-Michel
Scholz, Holger C
Brucella microti: the genome sequence of an emerging pathogen
title Brucella microti: the genome sequence of an emerging pathogen
title_full Brucella microti: the genome sequence of an emerging pathogen
title_fullStr Brucella microti: the genome sequence of an emerging pathogen
title_full_unstemmed Brucella microti: the genome sequence of an emerging pathogen
title_short Brucella microti: the genome sequence of an emerging pathogen
title_sort brucella microti: the genome sequence of an emerging pathogen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743711/
https://www.ncbi.nlm.nih.gov/pubmed/19653890
http://dx.doi.org/10.1186/1471-2164-10-352
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