TY - JOUR
T1 - Direct identification of Streptococcus agalactiae and capsular type by real-time PCR in vaginal swabs from pregnant women
AU - Morozumi, Miyuki
AU - Chiba, Naoko
AU - Igarashi, Yuko
AU - Mitsuhashi, Naoki
AU - Wajima, Takeaki
AU - Iwata, Satoshi
AU - Ubukata, Kimiko
N1 - Funding Information:
Our research was supported by a grant under the category “Research on Emerging and Re-emerging Infectious Diseases (number H22-013 )” from the Japanese Ministry of Health, Labour and Welfare (to Dr. K. Ubukata).
Publisher Copyright:
© 2014 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases.
PY - 2014/4/15
Y1 - 2014/4/15
N2 - 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.
AB - 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.
KW - Capsular type
KW - Pregnant women
KW - Real-time PCR
KW - Streptococcus agalactiae
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U2 - 10.1016/j.jiac.2014.08.024
DO - 10.1016/j.jiac.2014.08.024
M3 - Article
C2 - 25287153
AN - SCOPUS:84942081441
SN - 1341-321X
VL - 21
SP - 34
EP - 38
JO - Journal of Infection and Chemotherapy
JF - Journal of Infection and Chemotherapy
IS - 1
ER -