GR13-type plasmids in Acinetobacter potentiate the accumulation and horizontal transfer of diverse accessory genes

Robert A Moran, Haiyang Liu, Emma L Doughty, Xiaoting Hua, Elizabeth A Cummins, Tomas Liveikis, Alan McNally, Zhihui Zhou, Willem van Schaik, Yunsong Yu

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Abstract

Carbapenem and other antibiotic resistance genes (ARGs) can be found in plasmids in Acinetobacter, but many plasmid types in this genus have not been well-characterized. Here we describe the distribution, diversity and evolutionary capacity of rep group 13 (GR13) plasmids that are found in Acinetobacter species from diverse environments. Our investigation was prompted by the discovery of two GR13 plasmids in A. baumannii isolated in an intensive care unit (ICU). The plasmids harbour distinct accessory genes: pDETAB5 contains blaNDM-1 and genes that confer resistance to four further antibiotic classes, while pDETAB13 carries putative alcohol tolerance determinants. Both plasmids contain multiple dif modules, which are flanked by pdif sites recognized by XerC/XerD tyrosine recombinases. The ARG-containing dif modules in pDETAB5 are almost identical to those found in pDETAB2, a GR34 plasmid from an unrelated A. baumannii isolated in the same ICU a month prior. Examination of a further 41 complete, publicly available plasmid sequences revealed that the GR13 pangenome consists of just four core but 1186 accessory genes, 123 in the shell and 1063 in the cloud, reflecting substantial capacity for diversification. The GR13 core genome includes genes for replication and partitioning, and for a putative tyrosine recombinase. Accessory segments encode proteins with diverse putative functions, including for metabolism, antibiotic/heavy metal/alcohol tolerance, restriction-modification, an anti-phage system and multiple toxin–antitoxin systems. The movement of dif modules and actions of insertion sequences play an important role in generating diversity in GR13 plasmids. Discrete GR13 plasmid lineages are internationally disseminated and found in multiple Acinetobacter species, which suggests they are important platforms for the accumulation, horizontal transmission and persistence of accessory genes in this genus.
Original languageEnglish
Article number000840
Number of pages14
JournalMicrobial Genomics
Volume8
Issue number6
DOIs
Publication statusPublished - 22 Jun 2022

Bibliographical note

Funding Information:
This work was undertaken as part of the DETECTIVE research project funded by the National Natural Science Foundation of China (81861138054, 82072313, 31970128), Zhejiang Province Medical Platform Backbone Talent Plan (2020RC075) and the Medical Research Council (MR/S013660/1). W.v.S was also supported by a Wolfson Research Merit Award (WM160092).

Funding Information:
information This work was undertaken as part of the DETECTIVE research project funded by the National Natural Science Foundation of China (81861138054, 82072313, 31970128), Zhejiang Province Medical Platform Backbone Talent Plan (2020RC075) and the Medical Research Council (MR/S013660/1). W.v.S was also supported by a Wolfson Research Merit Award (WM160092). Acknowledgements We are grateful to the doctors and nurses in the ICU for sample collection. We thank Professor Zhiyong Zong and his team for their careful teaching of sampling methods.

Publisher Copyright:
© 2022 The Authors.

Keywords

  • Acinetobacter
  • Microbial Genomics
  • dif modules
  • plasmids

ASJC Scopus subject areas

  • Epidemiology
  • Microbiology
  • Molecular Biology
  • Genetics

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