Simultaneous detection and serotype identification of Streptococcus agalactiae using multiplex PCR and reverse line blot hybridization

J Med Microbiol. 2005 Dec;54(Pt 12):1133-1138. doi: 10.1099/jmm.0.46244-0.

Abstract

Streptococcus agalactiae (group B streptococcus, GBS) is an important cause of sepsis in neonates and their mothers, and the elderly and immunocompromised patients. Ongoing surveillance to monitor GBS serotype distribution is needed to guide the development and assess the feasibility of GBS conjugate vaccines. The authors previously developed a molecular serotype identification method based on serotype-specific PCR and partial sequencing of cps genes. In this study, a novel 10-primer pair multiplex PCR and reverse line blot (mPCR/RLB) hybridization assay was developed for simultaneous detection and serotype identification of all nine GBS serotypes. For all 316 GBS isolates tested the mPCR/RLB results corresponded with those of conventional serotyping and individual serotype-specific PCR, and the method was more convenient and practical than either alternative.

MeSH terms

  • Base Sequence
  • DNA Primers
  • Humans
  • Nucleic Acid Hybridization
  • Polymerase Chain Reaction / methods*
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Sensitivity and Specificity
  • Serotyping
  • Streptococcus agalactiae / classification*
  • Streptococcus agalactiae / genetics
  • Streptococcus agalactiae / isolation & purification*

Substances

  • DNA Primers