Unraveling the impact and mechanism of antipyretic paracetamol on intergenera conjugative plasmid transfer

Environ Res. 2022 Dec;215(Pt 1):114263. doi: 10.1016/j.envres.2022.114263. Epub 2022 Sep 6.

Abstract

Antimicrobial resistance has been considered as a great threat to biosecurity and human health. And the transmission of antibiotic resistance genes (ARGs) by conjugated plasmid is a key factor in the prevalence of antimicrobial resistance. Paracetamol (PRC), one of nonopioid analgesics, is an extensively used antipyretic and mild analgesic worldwide available for numerous prescriptions. It was unclear whether PRC could promote the spread of ARGs. Here, it was demonstrated that PRC promoted intergenera conjugative plasmid transfer in an established conjugation model. Both donor and recipient strains treated by PRC emerged the variations of reactive oxygen species (ROS), SOS response and cell membrane permeability. Correspondingly, transcriptome analysis revealed that the gene expression involved in cell membrane permeability and SOS response was up-regulated significantly after PRC exposure. More directly, PRC also increased the expressions of conjugation related genes of trbG and trbP in donor. This study proved for the first time that PRC could enhance the intergenera conjugative plasmid transfer. Collectively, these findings manifested the potential threat associated with the existence of non-antibiotic substance PRC, which could provide an important insight into antimicrobial resistance spread.

Keywords: Antibiotic resistance genes; Intergenera conjugative plasmid transfer; Paracetamol; Reactive oxygen species; Transcriptome analysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetaminophen / pharmacology
  • Analgesics, Non-Narcotic*
  • Anti-Bacterial Agents
  • Antipyretics*
  • Gene Transfer, Horizontal
  • Genes, Bacterial
  • Humans
  • Plasmids / genetics
  • Reactive Oxygen Species

Substances

  • Analgesics, Non-Narcotic
  • Anti-Bacterial Agents
  • Antipyretics
  • Reactive Oxygen Species
  • Acetaminophen