Cargando…

Revisitingmolecular serotyping of Streptococcus pneumoniae

BACKGROUND: Ninety-two Streptococcus pneumoniae serotypes have been described so far, but the pneumococcal conjugate vaccine introduced in the Brazilian basic vaccination schedule in 2010 covers only the ten most prevalent in the country. Pneumococcal serotype-shifting after massive immunization is...

Descripción completa

Detalles Bibliográficos
Autores principales: Camargo, Dhian RA, Pais, Fabiano S, Volpini, Ângela C, Oliveira, Marluce AA, Coimbra, Roney S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460616/
https://www.ncbi.nlm.nih.gov/pubmed/26041622
http://dx.doi.org/10.1186/1471-2164-16-S5-S1
_version_ 1782375398399541248
author Camargo, Dhian RA
Pais, Fabiano S
Volpini, Ângela C
Oliveira, Marluce AA
Coimbra, Roney S
author_facet Camargo, Dhian RA
Pais, Fabiano S
Volpini, Ângela C
Oliveira, Marluce AA
Coimbra, Roney S
author_sort Camargo, Dhian RA
collection PubMed
description BACKGROUND: Ninety-two Streptococcus pneumoniae serotypes have been described so far, but the pneumococcal conjugate vaccine introduced in the Brazilian basic vaccination schedule in 2010 covers only the ten most prevalent in the country. Pneumococcal serotype-shifting after massive immunization is a major concern and monitoring this phenomenon requires efficient and accessible serotyping methods. Pneumococcal serotyping based on antisera produced in animals is laborious and restricted to a few reference laboratories. Alternatively, molecular serotyping methods assess polymorphisms in the cps gene cluster, which encodes key enzymes for capsular polysaccharides synthesis in pneumococci. In one such approach, cps-RFLP, the PCR amplified cps loci are digested with an endonuclease, generating serotype-specific fingerprints on agarose gel electrophoresis. METHODS: In this work, in silico and in vitro approaches were combined to demonstrate that XhoII is the most discriminating endonuclease for cps-RFLP, and to build a database of serotype-specific fingerprints that accommodates the genetic diversity within the cps locus of 92 known pneumococci serotypes. RESULTS: The expected specificity of cps-RFLP using XhoII was 76% for serotyping and 100% for serogrouping. The database of cps-RFLP fingerprints was integrated to Molecular Serotyping Tool (MST), a previously published web-based software for molecular serotyping. In addition, 43 isolates representing 29 serotypes prevalent in the state of Minas Gerais, Brazil, from 2007 to 2013, were examined in vitro; 11 serotypes (nine serogroups) matched the respective in silico patterns calculated for reference strains. The remaining experimental patterns, despite their resemblance to their expected in silico patterns, did not reach the threshold of similarity score to be considered a match and were then added to the database. CONCLUSION: The cps-RFLP method with XhoII outperformed the antisera-based and other molecular serotyping methods in regard of the expected specificity. In order to accommodate the genetic variability of the pneumococci cps loci, the database of cps-RFLP patterns will be progressively expanded to include new variant in vitro patterns. The cps-RFLP method with endonuclease XhoII coupled with MST for computer-assisted interpretation of results may represent a relevant contribution to the real time detection of changes in regional pneumococci population diversity in response to mass immunization programs.
format Online
Article
Text
id pubmed-4460616
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-44606162015-06-29 Revisitingmolecular serotyping of Streptococcus pneumoniae Camargo, Dhian RA Pais, Fabiano S Volpini, Ângela C Oliveira, Marluce AA Coimbra, Roney S BMC Genomics Research BACKGROUND: Ninety-two Streptococcus pneumoniae serotypes have been described so far, but the pneumococcal conjugate vaccine introduced in the Brazilian basic vaccination schedule in 2010 covers only the ten most prevalent in the country. Pneumococcal serotype-shifting after massive immunization is a major concern and monitoring this phenomenon requires efficient and accessible serotyping methods. Pneumococcal serotyping based on antisera produced in animals is laborious and restricted to a few reference laboratories. Alternatively, molecular serotyping methods assess polymorphisms in the cps gene cluster, which encodes key enzymes for capsular polysaccharides synthesis in pneumococci. In one such approach, cps-RFLP, the PCR amplified cps loci are digested with an endonuclease, generating serotype-specific fingerprints on agarose gel electrophoresis. METHODS: In this work, in silico and in vitro approaches were combined to demonstrate that XhoII is the most discriminating endonuclease for cps-RFLP, and to build a database of serotype-specific fingerprints that accommodates the genetic diversity within the cps locus of 92 known pneumococci serotypes. RESULTS: The expected specificity of cps-RFLP using XhoII was 76% for serotyping and 100% for serogrouping. The database of cps-RFLP fingerprints was integrated to Molecular Serotyping Tool (MST), a previously published web-based software for molecular serotyping. In addition, 43 isolates representing 29 serotypes prevalent in the state of Minas Gerais, Brazil, from 2007 to 2013, were examined in vitro; 11 serotypes (nine serogroups) matched the respective in silico patterns calculated for reference strains. The remaining experimental patterns, despite their resemblance to their expected in silico patterns, did not reach the threshold of similarity score to be considered a match and were then added to the database. CONCLUSION: The cps-RFLP method with XhoII outperformed the antisera-based and other molecular serotyping methods in regard of the expected specificity. In order to accommodate the genetic variability of the pneumococci cps loci, the database of cps-RFLP patterns will be progressively expanded to include new variant in vitro patterns. The cps-RFLP method with endonuclease XhoII coupled with MST for computer-assisted interpretation of results may represent a relevant contribution to the real time detection of changes in regional pneumococci population diversity in response to mass immunization programs. BioMed Central 2015-05-26 /pmc/articles/PMC4460616/ /pubmed/26041622 http://dx.doi.org/10.1186/1471-2164-16-S5-S1 Text en Copyright © 2015 Camargo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Camargo, Dhian RA
Pais, Fabiano S
Volpini, Ângela C
Oliveira, Marluce AA
Coimbra, Roney S
Revisitingmolecular serotyping of Streptococcus pneumoniae
title Revisitingmolecular serotyping of Streptococcus pneumoniae
title_full Revisitingmolecular serotyping of Streptococcus pneumoniae
title_fullStr Revisitingmolecular serotyping of Streptococcus pneumoniae
title_full_unstemmed Revisitingmolecular serotyping of Streptococcus pneumoniae
title_short Revisitingmolecular serotyping of Streptococcus pneumoniae
title_sort revisitingmolecular serotyping of streptococcus pneumoniae
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460616/
https://www.ncbi.nlm.nih.gov/pubmed/26041622
http://dx.doi.org/10.1186/1471-2164-16-S5-S1
work_keys_str_mv AT camargodhianra revisitingmolecularserotypingofstreptococcuspneumoniae
AT paisfabianos revisitingmolecularserotypingofstreptococcuspneumoniae
AT volpiniangelac revisitingmolecularserotypingofstreptococcuspneumoniae
AT oliveiramarluceaa revisitingmolecularserotypingofstreptococcuspneumoniae
AT coimbraroneys revisitingmolecularserotypingofstreptococcuspneumoniae