Group A Streptococcus AdcR Regulon Participates in Bacterial Defense against Host-Mediated Zinc Sequestration and Contributes to Virulence

Infect Immun. 2020 Jul 21;88(8):e00097-20. doi: 10.1128/IAI.00097-20. Print 2020 Jul 21.

Abstract

Colonization by pathogenic bacteria depends on their ability to overcome host nutritional defenses and acquire nutrients. The human pathogen group A streptococcus (GAS) encounters the host defense factor calprotectin (CP) during infection. CP inhibits GAS growth in vitro by imposing zinc (Zn) limitation. However, GAS counterstrategies to combat CP-mediated Zn limitation and the in vivo relevance of CP-GAS interactions to bacterial pathogenesis remain unknown. Here, we report that GAS upregulates the AdcR regulon in response to CP-mediated Zn limitation. The AdcR regulon includes genes encoding Zn import (adcABC), Zn sparing (rpsN.2), and Zn scavenging systems (adcAII, phtD, and phtY). Each gene in the AdcR regulon contributes to GAS Zn acquisition and CP resistance. The ΔadcC and ΔrpsN.2 mutant strains were the most susceptible to CP, whereas the ΔadcA, ΔadcAII, and ΔphtD mutant strains displayed less CP sensitivity during growth in vitro However, the ΔphtY mutant strain did not display an increased CP sensitivity. The varied sensitivity of the mutant strains to CP-mediated Zn limitation suggests distinct roles for individual AdcR regulon genes in GAS Zn acquisition. GAS upregulates the AdcR regulon during necrotizing fasciitis infection in WT mice but not in S100a9-/- mice lacking CP. This suggests that CP induces Zn deficiency in the host. Finally, consistent with the in vitro results, several of the AdcR regulon genes are critical for GAS virulence in WT mice, whereas they are dispensable for virulence in S100a9-/- mice, indicating the direct competition for Zn between CP and proteins encoded by the GAS AdcR regulon during infection.

Keywords: Zn acquisition; bacterial pathogenesis; gene regulation; host nutritional immunity; streptococcus.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / immunology
  • Binding Sites
  • Binding, Competitive
  • Calgranulin B / genetics
  • Calgranulin B / immunology
  • Gene Expression Regulation
  • Host-Pathogen Interactions / genetics
  • Host-Pathogen Interactions / immunology*
  • Humans
  • Ion Transport
  • Leukocyte L1 Antigen Complex / genetics
  • Leukocyte L1 Antigen Complex / immunology*
  • Mice
  • Mice, Knockout
  • Protein Binding
  • Regulon*
  • Streptococcal Infections / immunology*
  • Streptococcal Infections / metabolism
  • Streptococcal Infections / microbiology
  • Streptococcal Infections / mortality
  • Streptococcus pyogenes / immunology
  • Streptococcus pyogenes / metabolism
  • Streptococcus pyogenes / pathogenicity*
  • Survival Analysis
  • Virulence
  • Zinc / immunology
  • Zinc / metabolism*

Substances

  • Bacterial Proteins
  • Calgranulin B
  • Leukocyte L1 Antigen Complex
  • S100A9 protein, mouse
  • Zinc