AI Article Synopsis

  • Most newborn infections from group B streptococcus (GBS) are caused by capsular types Ia, Ib, or III, prompting the need for effective detection methods.
  • A real-time PCR technique was developed to quickly identify GBS and its capsular types from vaginal swabs taken from pregnant women at 36-39 weeks of gestation, yielding results in under 2 hours.
  • Testing of 1,226 samples showed that direct PCR demonstrated higher positivity rates and proved to be highly sensitive and specific compared to traditional culture methods, allowing timely treatment for potential GBS infections.

Article Abstract

Most group B streptococcus (GBS) infections in newborns are with capsular type Ia, Ib, or III. To prevent these infections more effectively, we developed a real-time PCR method to simultaneously detect GBS species and identify these 3 capsular types in vaginal swab samples from women at 36-39 weeks of gestation. DNA to be detected included those of the dltS gene (encoding a histidine kinase specific to GBS) and cps genes encoding capsular types. PCR sensitivity was 10 CFU/well for a 33-35 threshold cycle. Results were obtained within 2 h. Direct PCR results were compared with results obtained from cultures. Samples numbering 1226 underwent PCR between September 2008 and August 2012. GBS positivity rates by direct PCR and after routine culture were 15.7% (n = 192) and 12.6% (n = 154), respectively. Sensitivity and specificity of direct PCR relative to culture were 96.1% and 95.9%. Of GBS positive samples identified by PCR, capsular types determined directly by real-time PCR were Ia (n = 24), Ib (n = 32), and III (n = 26). Real-time PCR using our designed cycling probe is a practical, highly sensitive method for identification of GBS in pregnant carriers, allowing use of prophylactic intrapartum antibiotics in time to cover the possibility of unexpected premature birth.

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Source
http://dx.doi.org/10.1016/j.jiac.2014.08.024DOI Listing

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