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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-5133537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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