Biotransformation mechanism of Vibrio diabolicus to sulfamethoxazole at transcriptional level

J Hazard Mater. 2021 Jun 5:411:125023. doi: 10.1016/j.jhazmat.2020.125023. Epub 2021 Jan 2.

Abstract

Sulfamethoxazole (SMX) has attracted much attention due to its high probability of detection in the environment. Marine bacteria Vibrio diabolicus strain L2-2 has been proven to be able to transform SMX. In this study, the potential resistance and biotransformation mechanism of strain L2-2 to SMX, and key genes responses to SMX at environmental concentrations were researched. KEGG pathways were enriched by down-regulated genes including degradation of L-Leucine, L-Isoleucine, and fatty acid metabolism. Resistance mechanism could be concluded as the enhancement of membrane transport, antioxidation, response regulator, repair proteins, and ribosome protection. Biotransformation genes might involve in arylamine N-acetyltransferases (nat), cytochrome c553 (cyc-553) and acyl-CoA synthetase (acs). At the environmental concentration of SMX (0.1-10 μg/L), nat was not be activated, which meant the acetylation of SMX might not occur in the environment; however, cyc-553 was up-regulated under SMX stress of 1 μg/L, which indicated the hydroxylation of SMX could occur in the environment. Besides, the membrane transport and antioxidation of strain L2-2 could be activated under SMX stress of 10 μg/L. The results provided a better understanding of resistance and biotransformation of bacteria to SMX and would support related researches about the impacts of environmental antibiotics.

Keywords: Biotransformation; Resistance; Sulfamethoxazole; Transcriptome; Vibrio diabolicus strain L2–2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents
  • Biotransformation
  • Sulfamethoxazole*
  • Vibrio* / genetics

Substances

  • Anti-Bacterial Agents
  • Sulfamethoxazole

Supplementary concepts

  • Vibrio diabolicus