Distribution of the mosaic structured murM genes among natural populations of Streptococcus pneumoniae

S R Filipe1, E Severina, A Tomasz

  • 1Laboratory of Microbiology, The Rockefeller University, New York, New York 10021, USA.

Journal of Bacteriology
|November 14, 2000
PubMed

Insights

This study investigated the murM gene in Streptococcus pneumoniae, finding that most strains possess a common murMA sequence. However, a subset of penicillin-resistant strains exhibit a divergent murMB sequence, linked to altered peptidoglycan structure.

Area of Science:

  • Microbiology
  • Genetics
  • Molecular Biology

Background:

  • Streptococcus pneumoniae is a leading cause of bacterial infections.
  • Penicillin resistance in S. pneumoniae is a significant public health concern.
  • The murM gene plays a role in peptidoglycan biosynthesis, a target for antibiotics.

Purpose of the Study:

  • To investigate the presence and sequence variation of the murM gene in a diverse collection of Streptococcus pneumoniae isolates.
  • To correlate murM sequence types with penicillin resistance and peptidoglycan composition.

Main Methods:

  • Analysis of 814 genetically diverse S. pneumoniae strains, including penicillin-susceptible and resistant isolates.
  • DNA hybridization using murMA and murMB probes to differentiate murM sequence types.
  • High-pressure liquid chromatography (HPLC) analysis of peptidoglycan composition.
  • Complete sequencing of the murM gene in selected penicillin-resistant isolates.

Main Results:

  • The majority of S. pneumoniae strains (761/814) hybridized exclusively with the murMA probe.
  • A smaller group of penicillin-resistant strains (48/814) hybridized only with the murMB probe.
  • Strains hybridizing with murMB showed increased branched peptides in their peptidoglycan, suggesting altered cell wall synthesis.

Conclusions:

  • The murM gene exhibits significant sequence diversity in Streptococcus pneumoniae.
  • The divergent murMB allele is associated with penicillin resistance and altered peptidoglycan structure.
  • The findings suggest a possible common heterologous origin for the divergent murMB sequences.