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May 3, 2026Frontiers in Bacteriology0 citationsOpen Access

Efflux-dominated resistome architecture and phylogeny-resistance decoupling in pharmaceutical effluent-associated Acinetobacter isolates

AIAswetha IyerRURiddhi UpadhyayPAPeriyasamy Ashokkumar

Key Points

  • This research aims to characterize the resistome of Acinetobacter isolates from pharmaceutical effluents and explore its relationship with phylogeny.
  • Whole-genome sequences were assembled and screened for antimicrobial resistance genes using CARD.
  • Core and accessory resistomes were defined, and phylogeny was analyzed using 16S rRNA analysis.
  • Isolates carried between 13–35 antimicrobial resistance (AMR) genes despite having a shared origin.
  • Efflux systems AdeIJK and AdeABC formed a conserved intrinsic core, while accessory genes showed variable distribution.
  • Resistome patterns did not strictly follow phylogeny, indicating dynamic gene acquisition.

Abstract

Aim This study aimed to characterise the resistome of Acinetobacter isolates from pharmaceutical effluents and assess its association with phylogeny. Methodology In this study, Whole-genome sequences were assembled and screened for Antimicrobial Resistance (AMR) genes using CARD. Core and accessory resistomes were defined, and phylogeny was inferred using 16S rRNA analysis. Results Isolates carried 13–35 AMR genes despite shared origin. Efflux systems (AdeIJK, AdeABC) formed a conserved intrinsic core, while accessory genes, including OXA-type carbapenemases, ESBLs, aminoglycoside- and sulfonamide-resistance genes, and qacEΔ1, were variably distributed. Resistome patterns did not strictly follow phylogeny. Interpretation Pharmaceutical effluents select for a conserved efflux-based resistance backbone while enabling dynamic acquisition of accessory genes via Horizontal Gene Transfer, highlighting the role of environmental pressure in multidrug resistance evolution.

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Cite This Study

Iyer et al. (2026) studied this question.

synapsesocial.com/papers/69f6e5ac8071d4f1bdfc6581https://doi.org/10.3389/fbrio.2026.1822309
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