Resistance determinants for β-lactam antibiotics in laboratory mutants of Streptococcus pneumoniae that are involved in genetic competence

Dorothea Zähner, Thorsten Grebe, Eric Guenzi, Jan Krau, Mark Der Van Linden, Kyla Terhune, Jeffry B. Stock, Regine Hakenbeck

Research output: Contribution to journalArticle

23 Scopus citations

Abstract

Laboratory mutants of Streptococcus pneumoniae resistant to either cefotaxime or piperacillin reveal defects in competence development independent of the selective β-lactam. A resistance determinant ciaH encoding a putative histidine kinase of a two-component signal-transducing system that is also involved in competence regulation was recently identified in cefotaxime-resistant mutants. We show now that the CiaH protein can be phosphorylated by ATP in vitro, and that it also phosphorylates the cognate response regulator CiaR. The mutant C306 containing the CiaH mutation Thr- 230-Pro is completely noncompetent. It does not release competence-inducing activity (competence factor) into the medium nor can such an activity be released from the cells. Competence in C306 cannot be induced upon addition of external competence factor, in contrast to the competence-defective piperacillin-resistant mutants P506 and P408. A novel resistance determinant cpoA specific for piperacillin was identified in piperacillin-resistant mutants. CpoA is responsible for the competence defect in P506 but not in P408. The results document a tight link between the action of β-lactams and competence development in the pneumococcus and confirm that the two β- lactams piperacillin and cefotaxime act via different primary targets.

Original languageEnglish (US)
Pages (from-to)187-191
Number of pages5
JournalMicrobial Drug Resistance
Volume2
Issue number2
DOIs
StatePublished - 1996

All Science Journal Classification (ASJC) codes

  • Microbiology
  • Immunology
  • Pharmacology
  • Microbiology (medical)

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