4.7 Article

Paclitaxel and its derivative facilitate the transmission of plasmid-mediated antibiotic resistance genes through conjugative transfer

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 810, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2021.152245

Keywords

ARGs; Conjugative transfer; Plasmids; Paclitaxel; Mechanism

Funding

  1. National Natural Science Foundation of China [32172907, 32002331, 31872526]
  2. Jiangsu Agricultural Science and Technology Innovation Fund [CX(20)3091, CX(21)2010]
  3. China Postdoctoral Science Foundation [2019M651984, 2021T140579]
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  5. Young Elite Scientists Sponsorship Program by CAST [2020QNRC001]

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This study found that paclitaxel and its derivative docetaxel facilitated the conjugative transfer of resistance plasmids carrying multiple antibiotic resistance genes. The underlying mechanisms involved a series of cellular responses, including up-regulation of rpoS expression, activated SOS response, increased cell membrane permeability, and enhanced plasmid replication and mating pilus formation.
The rapid dissemination of antibiotic resistance by horizontal gene transfer (HGT) renders the global resistance crisis more tense and urgent as few effective antimicrobials are available to combat multidrug-resistant (MDR) pathogens at present. Conjugation is one of the most dominant and representative pathways of HGT. Antibiotic residue in environ-ment is recognized as an important accelerator for conjugal transfer, whereas the roles of non-antibiotic pharmaceuti-cals in this process are not fully understood. Here we found that environmentally relevant concentrations of paclitaxel as well as its derivative docetaxel, two commonly used anticancer drugs, remarkably facilitated the conjugative trans-fer of resistance plasmids carrying multiple antibiotic resistance genes (ARGs). The underlying mechanisms accounting for the enhanced conjugation were investigated by detecting the activity of RpoS regulon, membrane permeability, SOS response and gene expression of conjugative transfer systems. Our results showed that paclitaxel induced a series of cellular responses, including up-regulation of rpoS expression, activated SOS response, increased cell membrane per-meability, enhanced plasmid replication and mating pilus formation. Collectively, our data provide new insight on the roles of paclitaxel and its derivative in promoting the conjugal transfer of ARGs, highlighting the importance of good antimicrobial stewardship.

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