Aim-To develop a polymerase chain reaction (PCR) for the specific dete
ction of the C protein gene in strains of group B Streptococcus. Metho
ds-A single primer pair derived from the nucleotide sequence of the Ig
A binding beta antigen of the C protein complex permitted the specific
amplification of a 592 base pair DNA fragment from the C protein gene
. After 35 cycles of amplification this product could be detected by a
garose gel electrophoresis. Southern blot hybridisation confirmed that
this product was the C protein gene. Results-PCR detected the C prote
in gene in 75 (63%) of 119 strains of group B streptococci analysed. T
he product was not detected in other Gram positive organisms, showing
that this PCR assay was highly specific. The sensitivity of the assay
was satisfactory to a dilution of 1 in 10 000 of extracted DNA. Conclu
sions-The C protein of group B streptococci is associated with neonata
l sepsis. The specific detection of the C protein gene by PCR may help
identify which strains are likely to be associated with infection by
the organism.