The Application of Realtime Fluorescence Quantitative PCR for Prenatal Screening of Group B Streptococcal Infections
Source: By:Changzhi Xu
DOI: https://doi.org/10.30564/jams.v2i3.669
Abstract:Objective: In the prenatal screening, several different methods were used to detect the presence of group B streptococcus (GBS) infection, in this assay, the diagnostic value and clinical signifcance of the application of realtime fluorescent PCR were explored. Methods: A total of 86 women with 35-37 weeks pregnancy were enrolled, vaginal secretion samples were collected. Fluorescence PCR, bacterial culture and gene sequencing were used to detect whether there was GBS infection, and the results obtained were compared and analyzed. Results: 10 subjects were detected to be positive for GBS by fluorescence PCR (the positive rate was 11.6%), however, only 4 cases were positive for GBS by bacterial culture method (the positive rate was 4.7%). There was a statistically signifcant difference in the positive rate between the two methods (P<0.01). Compared with the results of gene sequencing, the detection of GBS infection by fluorescence PCR has an accuracy of 95.2%, and the sensitivity was 90.9% with 100% specificity. Conclusion: The application of realtime fluorescence quantitative PCR for the detection of GBS infection is signifcantly better than the use of bacterial culture method. Compared with the gold standard method (gene sequencing method), its detection effciency, accuracy, sensitivity and specifcity are relatively high. In summary, PCR for prenatal screening of GBS is worthy of promotion in clinical practice.
References:[1] Rosen G H , Randis T M , Desai P V , et al. Group B Streptococcus and the vaginal microbiota[J]. The Journal of Infectious Diseases, 2017. [2] Gao K, Guan X, Zeng L, et al. An increasing trend of neonatal invasive multidrug-resistant group B streptococcus infections in southern China, 2011-2017[J]. Infection and Drug Resistance, 2018:2561-2569. [3] Rosa-Fraile M , Spellerberg B . Reliable Detection of Group B Streptococcus in the Laboratory Medicine[J]. Journal of Clinical Microbiology, 2017:JCM.00582-17. [4] Armistead B, Oler E, Waldorf K M, et al. The Double Life of Group B Streptococcus: Asymptomatic Colonizer and Potent Pathogen[J]. Journal of Molecular Biology, 2019. [5] Biringer K, K B B, Hasko M, et al. Streptococci group B in perinatology[J]. Ceska gynekologie /Ceska lekarska spolecnost J. Ev. Purkyne, 2010,75(5). [6] Wang X, Ma L K, Song Y N, et al. Rapid Group B streptococcus screening methods in late pregnancy and the maternal-neonatal outcomes[J]. National Medical Journal of China, 2016, 96(15). [7] Helali N E, Habibi F, Azria E, et al. Point-of-Care Intrapartum Group B Streptococcus Molecular Screening: Effectiveness and Costs[J]. Obstetrics & Gynecology, 2019, 133(2):276-281. [8] Ji W, Liu H, Jin Z, et al. Disease burden and antimicrobial resistance of invasive group B streptococcus among infants in China: a protocol for a national prospective observational study[J]. Bmc Infectious Diseases, 2017, 17(1):377. [9] Wang Y, Du Y, Miao X, et al. Risk factors and drug resistance in early-onset neonatal group B streptococcal disease[J]. Journal of Zhejiang University-science B, 2018, 19(12):973-978. [10] Guo Y, Deng X, Liang Y, et al. The draft genomes and investigation of serotype distribution, antimicrobial resistance of group B Streptococcus strains isolated from urine in Suzhou, China[J]. Annals of Clinical Microbiology and Antimicrobials, 2018, 17(1). [11] Guo D, Cao X, Li S, et al. Neonatal colonization of group B Streptococcus in China: Prevalence, antimicrobial resistance, serotypes, and molecular characterization[J]. American Journal of Infection Control,2018, 46(3).