The application of multiplex PCR to detect seven different DNA targets in group B streptococci
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu hodnotící studie, časopisecké články, práce podpořená grantem
PubMed
22407941
PubMed Central
PMC3345335
DOI
10.1007/s12223-012-0108-7
Knihovny.cz E-zdroje
- MeSH
- bakteriální geny MeSH
- bakteriologické techniky metody normy MeSH
- DNA bakterií genetika MeSH
- DNA primery genetika MeSH
- dospělí MeSH
- kojenec MeSH
- lidé MeSH
- multiplexová polymerázová řetězová reakce metody normy MeSH
- plošný screening metody normy MeSH
- Streptococcus agalactiae klasifikace genetika izolace a purifikace MeSH
- Check Tag
- dospělí MeSH
- kojenec MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA bakterií MeSH
- DNA primery MeSH
Group B Streptococcus (GBS) causes severe infections in infants and in immunocompromised adults. GBS pathogenicity varies between and within serotypes, with considerable variation in genetic content between strains. For this reason, it is important to be able to carry out immediate and comprehensive diagnostics of these infections. Seven genes important for screening of GBS infection were detected: cfb gene encoding the CAMP factor presented in every GBS; the cps operon genes such as cps1aH, cps1a/2/3IJ, and cps5O specific for capsular polysaccharide types Ia, III, and V, respectively; macrolide resistance genes ermB and mefA/E; and the gbs2018 S10 region specific for ST17 hypervirulent clone. Standardization of multiplex PCR with the use of seven primer pairs was performed on 81 bacterial strains representing different GBS isolates (n = 75) and other Gram-positive cocci (n = 10). Multiplex PCR can be used as an effective screening method to detect different sequences important for the screening of GBS infection.
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