:: Volume 26, Issue 2 (6-2018) ::
Journal of Ilam University of Medical Sciences 2018, 26(2): 37-44 Back to browse issues page
Detection of GBS(scpB gene) Carriers in Pregnant Women in Kermanshah By phenotypic and Colony PCR Methods
Sahra Behrvash1 , Fatemeh Keshavarzi * 2, Farshid Raeisi3
1- Dept of Biology, Kurdistan Science and Research Branch, Islamic Azad University, Sanandaj, Iran
2- Dept of Biology, Sanandaj Branch, Islamic Azad University, Sanandaj, Iran , gol.keshavarzi@gmail.com
3- Dept of Pathology, Faculty of Medicine, Kermanshah University of Medical Science, Kermanshah, Iran
Abstract:   (4797 Views)

Background: Group B Streptococcus (GBS) or agalactia is an important cause of infection among the early newborns. The bacterium is transmitted from mother to child and most often leads to infant death. The goal of this study was to detect GBS among clinical samples of pregnant women in Kermanshah province, using Colony PCR and standard microbiological culture and then to compare the phenotypic and genotypic methods against each other.
 
Materials & methods: One hundred cases aged at 30- 38 weeks of life were selected during 4 months from April 2014 on at health centers of Kermanshah province. The samples were taken from the women’s vaginal secretions and tested by standard culture using basic culture medium Todd- Hewitt broth, blood agar and Colony- PCR targeting scpB gene.
 
Findings: The results showed phenotypic test among 100 samples, 5 (5%) as carriers of group B streptococci, compared to 7 patients (7%) by Colony PCR test.
 
Conclusion & discussion: According to our study, the rate of GBS incidence is high in women of Kermanshah. Furthermore,   the Colony PCR method that eliminates DNA extraction process can be a rapid, reliable and low cost method to detect the carrier.

Keywords: group B Streptococcus (agalactia), Colony PCR, scp B gene
Full-Text [PDF 684 kb]   (3845 Downloads)    
Type of Study: Research |
Received: 2017/02/20 | Accepted: 2017/05/29 | Published: 2018/06/15



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Volume 26, Issue 2 (6-2018) Back to browse issues page