Acinetobacter variabilis represents a diverse species with novel regions associated with antibiotic resistance and surface polysaccharides

<i>Acinetobacter variabilis</i> is an opportunistic pathogen found in both clinical and environmental settings with the potential to harbour and disseminate clinically significant antibiotic resistance genes. Here, we sequenced the complete genome of NGH-QLD-N1, an <i>A. variabilis</i> isolate recovered from a blood sample of a patient at Nambour General Hospital located on the Sunshine Coast region of Queensland, Australia. The assembly was used as a reference to assess the diversity in available <i>A. variabilis</i> genome sequences and investigate the genomic context of surface polysaccharide biosynthesis genes and antibiotic resistance determinants in relation to the priority pathogen, <i>Acinetobacter baumannii</i>. Phylogenetic analysis revealed substantial diversity in the species, with a distinct NGH-QLD-N1 subclade containing multiple strains with important resistance determinants. We identified a novel transposon related to the Tn<i>6022</i> family, designated Tn<i>6929</i>, that interrupted <i>comM</i> and identified multiple structural variants in <i>A. variabilis</i> genomes. Notably, some variants carried <i>bla</i> <sub>NDM</sub> and <i>aphA6</i> in ISAba14-bounded regions, suggesting acquisition from diverse bacterial hosts. We also identified several integrative conjugative elements (ICEs) variants integrated into the chromosomal <i>thyA</i> gene, which differed in backbone structure and resistance gene content from our previously described <i>A. baumannii</i> ICE. The capsule and outer core loci for surface carbohydrate structures also had similar arrangements to those found in <i>A. baumannii</i>. This study provides a new understanding of the diversity of mobile genetic elements and ICEs carrying resistance genes, and surface polysaccharides associated with virulence, across the <i>Acinetobacter</i> genus.

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Journal
Microbial Genomics
Published
2026-02-13
DOI
https://doi.org/10.1099/mgen.0.001643
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
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article

Acinetobacter variabilis represents a diverse species with novel regions associated with antibiotic resistance and surface polysaccharides

Johanna J. Kenyon, Eva Hatje, Mohammad Katouli, Lucy L. Patterson et al.
Microbial Genomics
Antibiotic Resistance in Bacteria
article

Acinetobacter variabilis represents a diverse species with novel regions associated with antibiotic resistance and surface polysaccharides

Johanna J. Kenyon, Eva Hatje, Mohammad Katouli, Lucy L. Patterson, Mehrad Hamidian
article en

Abstract

<i>Acinetobacter variabilis</i> is an opportunistic pathogen found in both clinical and environmental settings with the potential to harbour and disseminate clinically significant antibiotic resistance genes. Here, we sequenced the complete genome of NGH-QLD-N1, an <i>A. variabilis</i> isolate recovered from a blood sample of a patient at Nambour General Hospital located on the Sunshine Coast region of Queensland, Australia. The assembly was used as a reference to assess the diversity in available <i>A. variabilis</i> genome sequences and investigate the genomic context of surface polysaccharide biosynthesis genes and antibiotic resistance determinants in relation to the priority pathogen, <i>Acinetobacter baumannii</i>. Phylogenetic analysis revealed substantial diversity in the species, with a distinct NGH-QLD-N1 subclade containing multiple strains with important resistance determinants. We identified a novel transposon related to the Tn<i>6022</i> family, designated Tn<i>6929</i>, that interrupted <i>comM</i> and identified multiple structural variants in <i>A. variabilis</i> genomes. Notably, some variants carried <i>bla</i> <sub>NDM</sub> and <i>aphA6</i> in ISAba14-bounded regions, suggesting acquisition from diverse bacterial hosts. We also identified several integrative conjugative elements (ICEs) variants integrated into the chromosomal <i>thyA</i> gene, which differed in backbone structure and resistance gene content from our previously described <i>A. baumannii</i> ICE. The capsule and outer core loci for surface carbohydrate structures also had similar arrangements to those found in <i>A. baumannii</i>. This study provides a new understanding of the diversity of mobile genetic elements and ICEs carrying resistance genes, and surface polysaccharides associated with virulence, across the <i>Acinetobacter</i> genus.

Microbial GenomicsVol. 12(2)
University of Technology Sydney (AU), Griffith University (AU), Queensland University of Technology (AU), University of the Sunshine Coast (AU)
Life below water
Openalex Percentile: Top 53%
Antibiotic Resistance in Bacteria
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