Email updates

Keep up to date with the latest news and content from BMC Microbiology and BioMed Central.

Open Access Highly Accessed Research article

Genome organization of epidemic Acinetobacter baumannii strains

Pier Paolo Di Nocera1*, Francesco Rocco1, Maria Giannouli2, Maria Triassi2 and Raffaele Zarrilli2*

Author Affiliations

1 Dipartimento di Biologia e Patologia Cellulare e Molecolare, Università Federico II, Via S. Pansini 5, 80131 Napoli, Italy

2 Dipartimento di Scienze Mediche Preventive, Sezione di Igiene, Università Federico II, Via S. Pansini 5, 80131 Napoli, Italy

For all author emails, please log on.

BMC Microbiology 2011, 11:224  doi:10.1186/1471-2180-11-224

Published: 10 October 2011

Abstract

Background

Acinetobacter baumannii is an opportunistic pathogen responsible for hospital-acquired infections. A. baumannii epidemics described world-wide were caused by few genotypic clusters of strains. The occurrence of epidemics caused by multi-drug resistant strains assigned to novel genotypes have been reported over the last few years.

Results

In the present study, we compared whole genome sequences of three A. baumannii strains assigned to genotypes ST2, ST25 and ST78, representative of the most frequent genotypes responsible for epidemics in several Mediterranean hospitals, and four complete genome sequences of A. baumannii strains assigned to genotypes ST1, ST2 and ST77. Comparative genome analysis showed extensive synteny and identified 3068 coding regions which are conserved, at the same chromosomal position, in all A. baumannii genomes. Genome alignments also identified 63 DNA regions, ranging in size from 4 o 126 kb, all defined as genomic islands, which were present in some genomes, but were either missing or replaced by non-homologous DNA sequences in others. Some islands are involved in resistance to drugs and metals, others carry genes encoding surface proteins or enzymes involved in specific metabolic pathways, and others correspond to prophage-like elements. Accessory DNA regions encode 12 to 19% of the potential gene products of the analyzed strains. The analysis of a collection of epidemic A. baumannii strains showed that some islands were restricted to specific genotypes.

Conclusion

The definition of the genome components of A. baumannii provides a scaffold to rapidly evaluate the genomic organization of novel clinical A. baumannii isolates. Changes in island profiling will be useful in genomic epidemiology of A. baumannii population.