Acinetobacter baumannii has emerged as an important opportunistic pathogen worldwide, being responsible for large outbreaks for nosocomial infections, primarily in intensive care units. A. baumannii ATCC 19606(T) is the species type strain, and a reference organism in many laboratories due to its low virulence, amenability to genetic manipulation and extensive antibiotic susceptibility. We wondered if frequent propagation of A. baumannii ATCC 19606(T) in different laboratories may have driven micro- and macro-evolutionary events that could determine inter-laboratory differences of genome-based data. By combining Illumina MiSeq, MinION and Sanger technologies, we generated a high-quality whole-genome sequence of A. baumannii ATCC 19606(T). then performed a comparative genome analysis between A. baumannii ATCC 19606(T) strains from several research laboratories and a reference collection. Differences between publicly available ATCC 19606(T) genome sequences were observed, including SNPs, macro- and micro-deletions, and the uneven presence of a 52kb prophage belonging to genus Vieuvirus. Two plasmids, pMAC and p1ATCC19606, were invariably detected in all tested strains. The presence of a putative replicase. a replication origin containing four 22-mer direct repeats, and a toxin-antitoxin system implicated in plasmid stability were predicted by in silico analysis of p1ATCC19606, and experimentally confirmed. This work refines the sequence, structure and functional annotation of the A. baumannii ATCC 19606(T) genome, and highlights some remarkable differences between domesticated strains, likely resulting from genetic drift.

Genome diversity of domesticated Acinetobacter baumannii ATCC 19606T strains / Artuso, Irene; Lucidi, Massimiliano; Visaggio, Daniela; Capecchi, Giulia; Lugli, Gabriele Andrea; Ventura, Marco; Visca, Paolo. - In: MICROBIAL GENOMICS. - ISSN 2057-5858. - 8:1(2022), p. 1. [10.1099/mgen.0.000749]

Genome diversity of domesticated Acinetobacter baumannii ATCC 19606T strains

Lugli, Gabriele Andrea;Ventura, Marco;Visca, Paolo
2022-01-01

Abstract

Acinetobacter baumannii has emerged as an important opportunistic pathogen worldwide, being responsible for large outbreaks for nosocomial infections, primarily in intensive care units. A. baumannii ATCC 19606(T) is the species type strain, and a reference organism in many laboratories due to its low virulence, amenability to genetic manipulation and extensive antibiotic susceptibility. We wondered if frequent propagation of A. baumannii ATCC 19606(T) in different laboratories may have driven micro- and macro-evolutionary events that could determine inter-laboratory differences of genome-based data. By combining Illumina MiSeq, MinION and Sanger technologies, we generated a high-quality whole-genome sequence of A. baumannii ATCC 19606(T). then performed a comparative genome analysis between A. baumannii ATCC 19606(T) strains from several research laboratories and a reference collection. Differences between publicly available ATCC 19606(T) genome sequences were observed, including SNPs, macro- and micro-deletions, and the uneven presence of a 52kb prophage belonging to genus Vieuvirus. Two plasmids, pMAC and p1ATCC19606, were invariably detected in all tested strains. The presence of a putative replicase. a replication origin containing four 22-mer direct repeats, and a toxin-antitoxin system implicated in plasmid stability were predicted by in silico analysis of p1ATCC19606, and experimentally confirmed. This work refines the sequence, structure and functional annotation of the A. baumannii ATCC 19606(T) genome, and highlights some remarkable differences between domesticated strains, likely resulting from genetic drift.
2022
Genome diversity of domesticated Acinetobacter baumannii ATCC 19606T strains / Artuso, Irene; Lucidi, Massimiliano; Visaggio, Daniela; Capecchi, Giulia; Lugli, Gabriele Andrea; Ventura, Marco; Visca, Paolo. - In: MICROBIAL GENOMICS. - ISSN 2057-5858. - 8:1(2022), p. 1. [10.1099/mgen.0.000749]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2933420
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