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The genomic diversification of the whole Acinetobacter genus: origins, mechanisms, and consequences
M. Touchon, J. Cury, EJ. Yoon, L. Krizova, GC. Cerqueira, C. Murphy, M. Feldgarden, J. Wortman, D. Clermont, T. Lambert, C. Grillot-Courvalin, A. Nemec, P. Courvalin, EP. Rocha,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
NT14466
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
Directory of Open Access Journals
od 2009
Free Medical Journals
od 2009
PubMed Central
od 2009
Europe PubMed Central
od 2009
Open Access Digital Library
od 2009-01-01
Open Access Digital Library
od 2009-01-01
Open Access Digital Library
od 2009-01-01
Oxford Journals Open Access Collection
od 2009
ROAD: Directory of Open Access Scholarly Resources
od 2009
PubMed
25313016
DOI
10.1093/gbe/evu225
Knihovny.cz E-zdroje
- MeSH
- Acinetobacter genetika MeSH
- fylogeneze MeSH
- genom bakteriální genetika MeSH
- genomika metody MeSH
- rozptýlené repetitivní sekvence genetika MeSH
- sekvence CRISPR genetika MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
Bacterial genomics has greatly expanded our understanding of microdiversification patterns within a species, but analyses at higher taxonomical levels are necessary to understand and predict the independent rise of pathogens in a genus. We have sampled, sequenced, and assessed the diversity of genomes of validly named and tentative species of the Acinetobacter genus, a clade including major nosocomial pathogens and biotechnologically important species. We inferred a robust global phylogeny and delimited several new putative species. The genus is very ancient and extremely diverse: Genomes of highly divergent species share more orthologs than certain strains within a species. We systematically characterized elements and mechanisms driving genome diversification, such as conjugative elements, insertion sequences, and natural transformation. We found many error-prone polymerases that may play a role in resistance to toxins, antibiotics, and in the generation of genetic variation. Surprisingly, temperate phages, poorly studied in Acinetobacter, were found to account for a significant fraction of most genomes. Accordingly, many genomes encode clustered regularly interspaced short palindromic repeats (CRISPR)-Cas systems with some of the largest CRISPR-arrays found so far in bacteria. Integrons are strongly overrepresented in Acinetobacter baumannii, which correlates with its frequent resistance to antibiotics. Our data suggest that A. baumannii arose from an ancient population bottleneck followed by population expansion under strong purifying selection. The outstanding diversification of the species occurred largely by horizontal transfer, including some allelic recombination, at specific hotspots preferentially located close to the replication terminus. Our work sets a quantitative basis to understand the diversification of Acinetobacter into emerging resistant and versatile pathogens.
Broad Institute of Harvard and MIT Cambridge Massachusetts
Collection de l'Institut Pasteur Institut Pasteur Paris France
Laboratory of Bacterial Genetics National Institute of Public Health Prague Czech Republic
Microbial Evolutionary Genomics Institut Pasteur Paris France CNRS UMR3525 Paris France
Unité des Agents Antibactériens Institut Pasteur Paris France
Citace poskytuje Crossref.org
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