As(III) Exposure Induces a Zinc Scarcity Response and Restricts Iron Uptake in High-Level Arsenic-Resistant Paenibacillus taichungensis Strain NC1

Appl Environ Microbiol. 2022 May 10;88(9):e0031222. doi: 10.1128/aem.00312-22. Epub 2022 Apr 18.

Abstract

The Gram-positive bacterium Paenibacillus taichungensis NC1 was isolated from the Zijin gold-copper mine and shown to display high resistance to arsenic (MICs of 10 mM for arsenite in minimal medium). Genome sequencing indicated the presence of a number of potential arsenic resistance determinants in NC1. Global transcriptomic analysis under arsenic stress showed that NC1 not only directly upregulated genes in an arsenic resistance operon but also responded to arsenic toxicity by increasing the expression of genes encoding antioxidant functions, such as cat, perR, and gpx. In addition, two highly expressed genes, marR and arsV, encoding a putative flavin-dependent monooxygenase and located adjacent to the ars resistance operon, were highly induced by As(III) exposure and conferred resistance to arsenic and antimony compounds. Interestingly, the zinc scarcity response was induced under exposure to high concentrations of arsenite, and genes responsible for iron uptake were downregulated, possibly to cope with oxidative stress associated with As toxicity. IMPORTANCE Microbes have the ability to adapt and respond to a variety of conditions. To better understand these processes, we isolated the arsenic-resistant Gram-positive bacterium Paenibacillus taichungensis NC1 from a gold-copper mine. The transcriptome responding to arsenite exposure showed induction of not only genes encoding arsenic resistance determinants but also genes involved in the zinc scarcity response. In addition, many genes encoding functions involved in iron uptake were downregulated. These results help to understand how bacteria integrate specific responses to arsenite exposure with broader physiological responses.

Keywords: Paenibacillus; Paenibacillus taichungensis; arsenite; transcriptomic; zinc scarcity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arsenic* / metabolism
  • Arsenic* / toxicity
  • Arsenites* / metabolism
  • Arsenites* / toxicity
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Copper
  • Gold
  • Iron
  • Operon
  • Paenibacillus
  • Zinc

Substances

  • Arsenites
  • Bacterial Proteins
  • Gold
  • Copper
  • Iron
  • Zinc
  • Arsenic

Supplementary concepts

  • Paenibacillus taichungensis