beta-lactam antibiotics induce the SOS response and horizontal transfer of virulence factors in Staphylococcus aureus

J Bacteriol. 2006 Apr;188(7):2726-9. doi: 10.1128/JB.188.7.2726-2729.2006.

Abstract

Antibiotics that interfere with DNA replication and cell viability activate the SOS response. In Staphylococcus aureus, the antibiotic-induced SOS response promotes replication and high-frequency horizontal transfer of pathogenicity island-encoded virulence factors. Here we report that beta-lactams induce a bona fide SOS response in S. aureus, characterized by the activation of the RecA and LexA proteins, the two master regulators of the SOS response. Moreover, we show that beta-lactams are capable of triggering staphylococcal prophage induction in S. aureus lysogens. Consequently, and as previously described for SOS induction by commonly used fluoroquinolone antibiotics, beta-lactam-mediated phage induction also resulted in replication and high-frequency transfer of the staphylococcal pathogenicity islands, showing that such antibiotics may have the unintended consequence of promoting the spread of bacterial virulence factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ampicillin / pharmacology
  • Anti-Bacterial Agents / pharmacology*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Gene Expression Regulation, Bacterial
  • Gene Transfer, Horizontal / drug effects*
  • Penicillins / pharmacology
  • Rec A Recombinases / genetics
  • Rec A Recombinases / metabolism
  • SOS Response, Genetics / drug effects*
  • Serine Endopeptidases / genetics
  • Serine Endopeptidases / metabolism
  • Staphylococcus aureus / drug effects*
  • Staphylococcus aureus / genetics
  • Staphylococcus aureus / metabolism
  • Virulence Factors / genetics
  • Virulence Factors / metabolism*
  • beta-Lactams / pharmacology*

Substances

  • Anti-Bacterial Agents
  • Bacterial Proteins
  • LexA protein, Bacteria
  • Penicillins
  • Virulence Factors
  • beta-Lactams
  • Ampicillin
  • Rec A Recombinases
  • Serine Endopeptidases