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Presence of a small plasmid in clinical isolates of Streptococcus pneumoniae

A M Berry1, E M Glare, D Hansman

  • 1Microbiology Department, Adelaide Children's Hospital, Australia.

FEMS Microbiology Letters
|December 1, 1989
PubMed

Insights

A small plasmid, similar to the previously reported pDP1, was found in 8 clinical Streptococcus pneumoniae isolates. This discovery suggests pDP1 may be a useful cloning vector for S. pneumoniae research.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Genetics

Background:

  • Plasmids are extrachromosomal DNA elements that can confer advantageous traits to bacteria.
  • The characterization of plasmids in Streptococcus pneumoniae is crucial for understanding bacterial adaptation and developing novel genetic tools.
  • Previously, only one pneumococcal plasmid, pDP1, had been reported.

Purpose of the Study:

  • To investigate the presence and characteristics of plasmids in clinical isolates of Streptococcus pneumoniae.
  • To compare a newly detected plasmid with the known pneumococcal plasmid pDP1.
  • To assess the potential of pDP1 as a cloning vector for S. pneumoniae.

Main Methods:

  • Plasmid DNA isolation from a clinical isolate of Streptococcus pneumoniae.
  • Restriction mapping and DNA hybridization to compare plasmids.
  • Cloning of plasmid fragments into Escherichia coli using the pUC19 vector.
  • Screening of 500 clinical S. pneumoniae isolates using a DNA probe derived from pDP1.

Main Results:

  • A small (2.95 kb) plasmid was detected in a clinical isolate of Streptococcus pneumoniae.
  • The detected plasmid showed no apparent differences from pDP1 and hybridized strongly to it.
  • The pDP1 sequence was found in 8 out of 500 screened isolates, with no correlation to serotype, infection type, or drug resistance.
  • The plasmid pDP1 contains at least seven unique restriction sites, indicating potential for cloning.

Conclusions:

  • The plasmid pDP1 is present in a subset of clinical Streptococcus pneumoniae isolates.
  • The prevalence and distribution of pDP1 do not appear to be linked to specific serotypes, infection types, or antibiotic resistance.
  • The unique restriction sites within pDP1 suggest its utility as a potential cloning vector for genetic manipulation in S. pneumoniae.

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