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Development of a TaqMan Array Card for Pneumococcal Serotyping on Isolates and Nasopharyngeal Samples

Streptococcus pneumoniae is both a commensal and a major pathogen that causes invasive disease in people of all ages. The introduction of serotype-specific pneumococcal vaccines has reduced the burden of disease but has also led to replacement with new strains; thus, serotyping remains important for...

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Autores principales: Pholwat, Suporn, Sakai, Fuminori, Turner, Paul, Vidal, Jorge E., Houpt, Eric R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922116/
https://www.ncbi.nlm.nih.gov/pubmed/27170020
http://dx.doi.org/10.1128/JCM.00613-16
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author Pholwat, Suporn
Sakai, Fuminori
Turner, Paul
Vidal, Jorge E.
Houpt, Eric R.
author_facet Pholwat, Suporn
Sakai, Fuminori
Turner, Paul
Vidal, Jorge E.
Houpt, Eric R.
author_sort Pholwat, Suporn
collection PubMed
description Streptococcus pneumoniae is both a commensal and a major pathogen that causes invasive disease in people of all ages. The introduction of serotype-specific pneumococcal vaccines has reduced the burden of disease but has also led to replacement with new strains; thus, serotyping remains important for vaccine-related disease surveillance. Conventional serotyping methods are laborious and expensive. We developed an easy-to-perform genotypic TaqMan array card (TAC) to identify S. pneumoniae strains, including lytA-based sequences, and 53 sequence-specific PCRs to identify 74 serotypes/serogroups covering all current vaccine types as well as prevalent nonvaccine types. The TAC method was evaluated on 146 clinical S. pneumoniae isolates and 13 nonpneumococcal species that naturally inhabit the upper respiratory tract and yielded 97% (142/146) sensitivity and 100% (13/13) specificity versus results of standard Quellung serotyping. The calculated limit of detection was 20 to 200 fg (∼8 to 84 genome equivalents) per reaction. On 23 blinded nasopharyngeal specimens that were pneumococcus culture positive, the TAC pan-pneumococcus lytA assay was positive in 21 (91% sensitivity versus culture). On TAC lytA-positive specimens, a serotype result was obtained on 86%, and the result was 95% accurate versus the subsequent culture's Quellung result. TAC also detected mixed serotypes in two specimens where Quellung detected only the predominant serotype. This TAC method yields fast and comprehensive serotyping compared to the standard method and may be useful on direct specimens.
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spelling pubmed-49221162016-07-12 Development of a TaqMan Array Card for Pneumococcal Serotyping on Isolates and Nasopharyngeal Samples Pholwat, Suporn Sakai, Fuminori Turner, Paul Vidal, Jorge E. Houpt, Eric R. J Clin Microbiol Bacteriology Streptococcus pneumoniae is both a commensal and a major pathogen that causes invasive disease in people of all ages. The introduction of serotype-specific pneumococcal vaccines has reduced the burden of disease but has also led to replacement with new strains; thus, serotyping remains important for vaccine-related disease surveillance. Conventional serotyping methods are laborious and expensive. We developed an easy-to-perform genotypic TaqMan array card (TAC) to identify S. pneumoniae strains, including lytA-based sequences, and 53 sequence-specific PCRs to identify 74 serotypes/serogroups covering all current vaccine types as well as prevalent nonvaccine types. The TAC method was evaluated on 146 clinical S. pneumoniae isolates and 13 nonpneumococcal species that naturally inhabit the upper respiratory tract and yielded 97% (142/146) sensitivity and 100% (13/13) specificity versus results of standard Quellung serotyping. The calculated limit of detection was 20 to 200 fg (∼8 to 84 genome equivalents) per reaction. On 23 blinded nasopharyngeal specimens that were pneumococcus culture positive, the TAC pan-pneumococcus lytA assay was positive in 21 (91% sensitivity versus culture). On TAC lytA-positive specimens, a serotype result was obtained on 86%, and the result was 95% accurate versus the subsequent culture's Quellung result. TAC also detected mixed serotypes in two specimens where Quellung detected only the predominant serotype. This TAC method yields fast and comprehensive serotyping compared to the standard method and may be useful on direct specimens. American Society for Microbiology 2016-06-24 2016-07 /pmc/articles/PMC4922116/ /pubmed/27170020 http://dx.doi.org/10.1128/JCM.00613-16 Text en Copyright © 2016 Pholwat et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Bacteriology
Pholwat, Suporn
Sakai, Fuminori
Turner, Paul
Vidal, Jorge E.
Houpt, Eric R.
Development of a TaqMan Array Card for Pneumococcal Serotyping on Isolates and Nasopharyngeal Samples
title Development of a TaqMan Array Card for Pneumococcal Serotyping on Isolates and Nasopharyngeal Samples
title_full Development of a TaqMan Array Card for Pneumococcal Serotyping on Isolates and Nasopharyngeal Samples
title_fullStr Development of a TaqMan Array Card for Pneumococcal Serotyping on Isolates and Nasopharyngeal Samples
title_full_unstemmed Development of a TaqMan Array Card for Pneumococcal Serotyping on Isolates and Nasopharyngeal Samples
title_short Development of a TaqMan Array Card for Pneumococcal Serotyping on Isolates and Nasopharyngeal Samples
title_sort development of a taqman array card for pneumococcal serotyping on isolates and nasopharyngeal samples
topic Bacteriology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922116/
https://www.ncbi.nlm.nih.gov/pubmed/27170020
http://dx.doi.org/10.1128/JCM.00613-16
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