Abstract

Acinetobacter baumannii is the source of numerous nosocomial infections in humans and therefore deserves close attention as multidrug or even pandrug resistant strains are increasingly being identified worldwide. Here we report the comparison of two newly sequenced genomes of A. baumannii. The human isolate A. baumannii AYE is multidrug resistant whereas strain SDF, which was isolated from body lice, is antibiotic susceptible. As reference for comparison in this analysis, the genome of the soil-living bacterium A. baylyi strain ADP1 was used. The most interesting dissimilarities we observed were that i) whereas strain AYE and A. baylyi genomes harbored very few Insertion Sequence elements which could promote expression of downstream genes, strain SDF sequence contains several hundred of them that have played a crucial role in its genome reduction (gene disruptions and simple DNA loss); ii) strain SDF has low catabolic capacities compared to strain AYE. Interestingly, the latter has even higher catabolic capacities than A. baylyi which has already been reported as a very nutritionally versatile organism. This metabolic performance could explain the persistence of A. baumannii nosocomial strains in environments where nutrients are scarce; iii) several processes known to play a key role during host infection (biofilm formation, iron uptake, quorum sensing, virulence factors) were either different or absent, the best example of which is iron uptake. Indeed, strain AYE and A. baylyi use siderophore-based systems to scavenge iron from the environment whereas strain SDF uses an alternate system similar to the Haem Acquisition System (HAS). Taken together, all these observations suggest that the genome contents of the 3 Acinetobacters compared are partly shaped by life in distinct ecological niches: human (and more largely hospital environment), louse, soil.

Highlights

  • Low-grade pathogens in humans, human-adapted Acinetobacter species mainly belong to the A. baumannii-A. calcoaceticus complex are of growing interest due to increased incidence of multidrug resistance (MDR) [1]

  • The GC-content of the three sequences is around 40%, a value corresponding to that reported for other members of the Acinetobacter genus

  • Like in the case of tRNAs, the missing rRNA cluster may have been lost during one of the numerous recombination events probably mediated by Insertion Sequences (ISs; see below)

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Summary

Introduction

Low-grade pathogens in humans, human-adapted Acinetobacter species mainly belong to the A. baumannii-A. calcoaceticus complex are of growing interest due to increased incidence of multidrug resistance (MDR) [1]. A. baumannii strains are isolated in up to 1% of nosocomial infections mostly from immunocompromised patients hospitalized in intensive care units. A. baumannii isolates are commonly found in clinical environment, Acinetobacters are mostly free-living saprophytes ubiquitously found in nature (soil, water, sewage). Acinetobacter species have been identified in small-size living organisms (body lice, fleas and ticks) that are potential vectors for infection transmission [2]. The genus Acinetobacter consists of strictly aerobic, Gramnegative coccobacillary rods, non-motile, catalase positive, oxidase negative and growing at 20u–30uC on usual laboratory culture media. G-proteobacteria classified as members of the genus Acinetobacter have a long history of taxonomic changes moving from the family Neisseriaceae to the family Moraxellaceae.

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