Spontaneous Loss of Virulence in Natural Populations of Listeria monocytogenes

Infect Immun. 2017 Oct 18;85(11):e00541-17. doi: 10.1128/IAI.00541-17. Print 2017 Nov.

Abstract

The pathogenesis of Listeria monocytogenes depends on the ability of this bacterium to escape from the phagosome of the host cells via the action of the pore-forming toxin listeriolysin O (LLO). Expression of the LLO-encoding gene (hly) requires the transcriptional activator PrfA, and both hly and prfA genes are essential for L. monocytogenes virulence. Here, we used the hemolytic activity of LLO as a phenotypic marker to screen for spontaneous virulence-attenuating mutations in L. monocytogenes Sixty nonhemolytic isolates were identified among a collection of 57,820 confirmed L. monocytogenes strains isolated from a variety of sources (0.1%). In most cases (56/60; 93.3%), the nonhemolytic phenotype resulted from nonsense, missense, or frameshift mutations in prfA Five strains carried hly mutations leading to a single amino acid substitution (G299V) or a premature stop codon causing strong virulence attenuation in mice. In one strain, both hly and gshF (encoding a glutathione synthase required for full PrfA activity) were missing due to genomic rearrangements likely caused by a transposable element. The PrfA/LLO loss-of-function (PrfA-/LLO-) mutants belonged to phylogenetically diverse clades of L. monocytogenes, and most were identified among nonclinical strains (57/60). Consistent with the rare occurrence of loss-of-virulence mutations, we show that prfA and hly are under purifying selection. Although occurring at a low frequency, PrfA-/LLO- mutational events in L. monocytogenes lead to niche restriction and open an evolutionary path for obligate saprophytism in this facultative intracellular pathogen.

Keywords: Listeria monocytogenes; genomics; hemolysis; spontaneous mutations; virulence.

MeSH terms

  • Amino Acid Substitution
  • Animals
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Bacterial Toxins / genetics*
  • Bacterial Toxins / metabolism
  • Biological Evolution
  • Cloning, Molecular
  • Erythrocytes / microbiology
  • Gene Expression Regulation, Bacterial*
  • Heat-Shock Proteins / genetics*
  • Heat-Shock Proteins / metabolism
  • Hemolysin Proteins / genetics*
  • Hemolysin Proteins / metabolism
  • Hemolysis
  • Humans
  • Listeria monocytogenes / classification
  • Listeria monocytogenes / genetics*
  • Listeria monocytogenes / growth & development
  • Listeria monocytogenes / pathogenicity*
  • Listeriosis / microbiology
  • Listeriosis / pathology
  • Mice
  • Mice, Inbred BALB C
  • Mutation*
  • Peptide Termination Factors / genetics*
  • Peptide Termination Factors / metabolism
  • Phylogeny
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Selection, Genetic
  • Severity of Illness Index
  • Virulence

Substances

  • Bacterial Proteins
  • Bacterial Toxins
  • Heat-Shock Proteins
  • Hemolysin Proteins
  • Peptide Termination Factors
  • PrfA protein, Listeria monocytogenes
  • Recombinant Proteins
  • hlyA protein, Listeria monocytogenes