The NarX-NarL two-component system regulates biofilm formation, natural product biosynthesis, and host-associated survival in Burkholderia pseudomallei

Sci Rep. 2022 Jan 7;12(1):203. doi: 10.1038/s41598-021-04053-6.

Abstract

Burkholderia pseudomallei is a saprophytic bacterium endemic throughout the tropics causing severe disease in humans and animals. Environmental signals such as the accumulation of inorganic ions mediates the biofilm forming capabilities and survival of B. pseudomallei. We have previously shown that B. pseudomallei responds to nitrate and nitrite by inhibiting biofilm formation and altering cyclic di-GMP signaling. To better understand the roles of nitrate-sensing in the biofilm inhibitory phenotype of B. pseudomallei, we created in-frame deletions of narX (Bp1026b_I1014) and narL (Bp1026b_I1013), which are adjacent components of a conserved nitrate-sensing two-component system. We observed transcriptional downregulation in key components of the biofilm matrix in response to nitrate and nitrite. Some of the most differentially expressed genes were nonribosomal peptide synthases (NRPS) and/or polyketide synthases (PKS) encoding the proteins for the biosynthesis of bactobolin, malleilactone, and syrbactin, and an uncharacterized cryptic NRPS biosynthetic cluster. RNA expression patterns were reversed in ∆narX and ∆narL mutants, suggesting that nitrate sensing is an important checkpoint for regulating the diverse metabolic changes occurring in the biofilm inhibitory phenotype. Moreover, in a macrophage model of infection, ∆narX and ∆narL mutants were attenuated in intracellular replication, suggesting that nitrate sensing contributes to survival in the host.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Benzopyrans / metabolism
  • Biofilms / growth & development*
  • Biological Products / metabolism*
  • Burkholderia pseudomallei / genetics
  • Burkholderia pseudomallei / growth & development
  • Burkholderia pseudomallei / metabolism*
  • Gene Expression Regulation, Bacterial
  • Host-Pathogen Interactions
  • Lactones / metabolism
  • Microbial Viability
  • Mutation
  • Nitrates / metabolism*
  • Nitrites / metabolism*
  • Transcription, Genetic

Substances

  • Bacterial Proteins
  • Benzopyrans
  • Biological Products
  • Lactones
  • Nitrates
  • Nitrites
  • malleilactone
  • bactobolin