Evolution of a pathogen: a comparative genomics analysis identifies a genetic pathway to pathogenesis in Acinetobacter

• Published in: PloS one Vol. 8; no. 1; p. e54287
• Main Authors: Sahl, Jason W, Gillece, John D, Schupp, James M, Waddell, Victor G, Driebe, Elizabeth M, Engelthaler, David M, Keim, Paul
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 24.01.2013; Public Library of Science (PLoS)
• Subjects: Acinetobacter; Acinetobacter - classification; Acinetobacter - genetics; Acinetobacter - isolation & purification; Acinetobacter - pathogenicity; Acinetobacter baumannii; Acinetobacter baumannii - classification; Acinetobacter baumannii - genetics; Acinetobacter baumannii - isolation & purification; Acinetobacter baumannii - pathogenicity; Acinetobacter calcoaceticus; Acinetobacter Infections - microbiology; Antimicrobial agents; Bacterial Proteins - classification; Bacterial Proteins - genetics; Base Sequence; Biochemistry; Biofilms; Biological Evolution; Biology; Chromosome Mapping; Chromosomes, Bacterial - genetics; Conservation; Deoxyribonucleic acid; DNA; Epidemiology; Evolution; Evolutionary genetics; Gene regulation; Gene sequencing; Genes; Genetic aspects; Genetic testing; Genome, Bacterial; Genomes; Genomics; Genotypes; Health aspects; Hospitals; Humans; Infectious diseases; Medicine; Microbiology; Multilocus Sequence Typing; Nosocomial infection; Nosocomial infections; Pathogenesis; Pathogens; Phylogeny; RNA, Ribosomal, 16S - classification; RNA, Ribosomal, 16S - genetics; Transcription; Transcription (Genetics); Virulence; Virulence (Microbiology); Virulence factors; Virulence Factors - classification; Virulence Factors - genetics; United States > US; Arizona
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0054287

Acinetobacter baumannii is an emergent and global nosocomial pathogen. In addition to A. baumannii, other Acinetobacter species, especially those in the Acinetobacter calcoaceticus-baumannii (Acb) complex, have also been associated with serious human infection. Although mechanisms of attachment, persistence on abiotic surfaces, and pathogenesis in A. baumannii have been identified, the genetic mechanisms that explain the emergence of A. baumannii as the most widespread and virulent Acinetobacter species are not fully understood. Recent whole genome sequencing has provided insight into the phylogenetic structure of the genus Acinetobacter. However, a global comparison of genomic features between Acinetobacter spp. has not been described in the literature. In this study, 136 Acinetobacter genomes, including 67 sequenced in this study, were compared to identify the acquisition and loss of genes in the expansion of the Acinetobacter genus. A whole genome phylogeny confirmed that A. baumannii is a monophyletic clade and that the larger Acb complex is also a well-supported monophyletic group. The whole genome phylogeny provided the framework for a global genomic comparison based on a blast score ratio (BSR) analysis. The BSR analysis demonstrated that specific genes have been both lost and acquired in the evolution of A. baumannii. In addition, several genes associated with A. baumannii pathogenesis were found to be more conserved in the Acb complex, and especially in A. baumannii, than in other Acinetobacter genomes; until recently, a global analysis of the distribution and conservation of virulence factors across the genus was not possible. The results demonstrate that the acquisition of specific virulence factors has likely contributed to the widespread persistence and virulence of A. baumannii. The identification of novel features associated with transcriptional regulation and acquired by clades in the Acb complex presents targets for better understanding the evolution of pathogenesis and virulence in the expansion of the genus.