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Real-time PCR-based serotyping of Streptococcus agalactiae

Group B Streptococcus (GBS) is an encapsulated, gram-positive pathogen that is an important cause of neonatal invasive infections, including sepsis and meningitis. There are ten known GBS serotypes based on distinct capsule compositions (Ia, Ib, II-IX), and current candidate capsular polysaccharide...

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Autores principales: Breeding, Kathleen M., Ragipani, Bhavana, Lee, Kun-Uk David, Malik, Martin, Randis, Tara M., Ratner, Adam J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133537/
https://www.ncbi.nlm.nih.gov/pubmed/27910939
http://dx.doi.org/10.1038/srep38523
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author Breeding, Kathleen M.
Ragipani, Bhavana
Lee, Kun-Uk David
Malik, Martin
Randis, Tara M.
Ratner, Adam J.
author_facet Breeding, Kathleen M.
Ragipani, Bhavana
Lee, Kun-Uk David
Malik, Martin
Randis, Tara M.
Ratner, Adam J.
author_sort Breeding, Kathleen M.
collection PubMed
description Group B Streptococcus (GBS) is an encapsulated, gram-positive pathogen that is an important cause of neonatal invasive infections, including sepsis and meningitis. There are ten known GBS serotypes based on distinct capsule compositions (Ia, Ib, II-IX), and current candidate capsular polysaccharide conjugate vaccines target only a subset of these. Serotyping of GBS isolates is important for understanding local epidemiology and for monitoring for serotype replacement or capsular switching. However, serotyping generally requires either latex agglutination, multiplex PCR with analysis of band sizes, or analysis of whole genome sequences–all techniques that are either expensive or not widely available. Here we report the development of a robust real-time PCR assay for determining GBS serotypes. Using both a diverse reference set of strains encompassing all ten serotypes and a collection of clinical isolates, we demonstrate concordance between real-time PCR serotyping and latex agglutination. We propose that real-time PCR serotyping represents an attractive alternative to current serotyping methods and may allow for improved acquisition of GBS serotype data.
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spelling pubmed-51335372017-01-27 Real-time PCR-based serotyping of Streptococcus agalactiae Breeding, Kathleen M. Ragipani, Bhavana Lee, Kun-Uk David Malik, Martin Randis, Tara M. Ratner, Adam J. Sci Rep Article Group B Streptococcus (GBS) is an encapsulated, gram-positive pathogen that is an important cause of neonatal invasive infections, including sepsis and meningitis. There are ten known GBS serotypes based on distinct capsule compositions (Ia, Ib, II-IX), and current candidate capsular polysaccharide conjugate vaccines target only a subset of these. Serotyping of GBS isolates is important for understanding local epidemiology and for monitoring for serotype replacement or capsular switching. However, serotyping generally requires either latex agglutination, multiplex PCR with analysis of band sizes, or analysis of whole genome sequences–all techniques that are either expensive or not widely available. Here we report the development of a robust real-time PCR assay for determining GBS serotypes. Using both a diverse reference set of strains encompassing all ten serotypes and a collection of clinical isolates, we demonstrate concordance between real-time PCR serotyping and latex agglutination. We propose that real-time PCR serotyping represents an attractive alternative to current serotyping methods and may allow for improved acquisition of GBS serotype data. Nature Publishing Group 2016-12-02 /pmc/articles/PMC5133537/ /pubmed/27910939 http://dx.doi.org/10.1038/srep38523 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Breeding, Kathleen M.
Ragipani, Bhavana
Lee, Kun-Uk David
Malik, Martin
Randis, Tara M.
Ratner, Adam J.
Real-time PCR-based serotyping of Streptococcus agalactiae
title Real-time PCR-based serotyping of Streptococcus agalactiae
title_full Real-time PCR-based serotyping of Streptococcus agalactiae
title_fullStr Real-time PCR-based serotyping of Streptococcus agalactiae
title_full_unstemmed Real-time PCR-based serotyping of Streptococcus agalactiae
title_short Real-time PCR-based serotyping of Streptococcus agalactiae
title_sort real-time pcr-based serotyping of streptococcus agalactiae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133537/
https://www.ncbi.nlm.nih.gov/pubmed/27910939
http://dx.doi.org/10.1038/srep38523
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