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Development of a melting-curve based multiplex real-time PCR assay for simultaneous detection of Streptococcus agalactiae and genes encoding resistance to macrolides and lincosamides

BACKGROUND: Streptococcus agalactiae or Group B Streptococcus (GBS) remains the leading cause of infections in newborns worldwilde. Prenatal GBS screening of pregnant women for vaginal-rectal colonization is recommended in many countries to manage appropriate intrapartum antimicrobial prophylaxis fo...

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Autores principales: Otaguiri, Eliane Saori, Morguette, Ana Elisa Belotto, Morey, Alexandre Tadachi, Tavares, Eliandro Reis, Kerbauy, Gilselena, de Almeida Torres, Rosângela S. L., Chaves Júnior, Mauricio, Tognim, Maria Cristina Bronharo, Góes, Viviane Monteiro, Krieger, Marco Aurélio, Perugini, Marcia Regina Eches, Yamauchi, Lucy Megumi, Yamada-Ogatta, Sueli Fumie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934892/
https://www.ncbi.nlm.nih.gov/pubmed/29724169
http://dx.doi.org/10.1186/s12884-018-1774-5
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author Otaguiri, Eliane Saori
Morguette, Ana Elisa Belotto
Morey, Alexandre Tadachi
Tavares, Eliandro Reis
Kerbauy, Gilselena
de Almeida Torres, Rosângela S. L.
Chaves Júnior, Mauricio
Tognim, Maria Cristina Bronharo
Góes, Viviane Monteiro
Krieger, Marco Aurélio
Perugini, Marcia Regina Eches
Yamauchi, Lucy Megumi
Yamada-Ogatta, Sueli Fumie
author_facet Otaguiri, Eliane Saori
Morguette, Ana Elisa Belotto
Morey, Alexandre Tadachi
Tavares, Eliandro Reis
Kerbauy, Gilselena
de Almeida Torres, Rosângela S. L.
Chaves Júnior, Mauricio
Tognim, Maria Cristina Bronharo
Góes, Viviane Monteiro
Krieger, Marco Aurélio
Perugini, Marcia Regina Eches
Yamauchi, Lucy Megumi
Yamada-Ogatta, Sueli Fumie
author_sort Otaguiri, Eliane Saori
collection PubMed
description BACKGROUND: Streptococcus agalactiae or Group B Streptococcus (GBS) remains the leading cause of infections in newborns worldwilde. Prenatal GBS screening of pregnant women for vaginal-rectal colonization is recommended in many countries to manage appropriate intrapartum antimicrobial prophylaxis for those identified as carriers. In this study, a novel melting-curve based multiplex real-time PCR assay for the simultaneous detection of GBS and macrolide and lincosamide resistance markers was developed. The usefulness of the assay was evaluated for rapid and accurate prenatal GBS screening. METHODS: One hundred two pregnant women who were at 35–37 weeks of gestation were enrolled in this study. The analytical performance of the multiplex real-time PCR was first tested using a panel of reference and clinical bacterial and fungal strains. To test the clinical performance, vaginal-rectal swabs were obtained from pregnant women who were seen at the teaching hospital for regular prenatal care. The results of real-time were compared with those obtained from microbiological analyses. RESULTS: The real-time PCR assay showed 100% specificity and a limit of detection of 10(4) colony forming units equivalent per reaction. The prevalence of GBS colonization among the population studied was 15.7% (16/102) based on a positive culture and the real-time PCR results. Agreement between the two assays was found for 11 (68.75%) GBS colonized women. Using the culture-based results as a reference, the multiplex real-time PCR had a sensitivity of 91.7% (11/12, CI 59.7–99.6%), a specificity of 95.5% (86/90, CI 89.8–98.7%), a positive predictive value of 73.3% (11/15, CI 44.8–91.1%) and a negative predictive value of 98.9% (86/87, CI 92.9–99.9%). CONCLUSION: The multiplex real-time PCR is a rapid, affordable and sensitive assay for direct detection of GBS in vaginal-rectal swabs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12884-018-1774-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-59348922018-05-11 Development of a melting-curve based multiplex real-time PCR assay for simultaneous detection of Streptococcus agalactiae and genes encoding resistance to macrolides and lincosamides Otaguiri, Eliane Saori Morguette, Ana Elisa Belotto Morey, Alexandre Tadachi Tavares, Eliandro Reis Kerbauy, Gilselena de Almeida Torres, Rosângela S. L. Chaves Júnior, Mauricio Tognim, Maria Cristina Bronharo Góes, Viviane Monteiro Krieger, Marco Aurélio Perugini, Marcia Regina Eches Yamauchi, Lucy Megumi Yamada-Ogatta, Sueli Fumie BMC Pregnancy Childbirth Research Article BACKGROUND: Streptococcus agalactiae or Group B Streptococcus (GBS) remains the leading cause of infections in newborns worldwilde. Prenatal GBS screening of pregnant women for vaginal-rectal colonization is recommended in many countries to manage appropriate intrapartum antimicrobial prophylaxis for those identified as carriers. In this study, a novel melting-curve based multiplex real-time PCR assay for the simultaneous detection of GBS and macrolide and lincosamide resistance markers was developed. The usefulness of the assay was evaluated for rapid and accurate prenatal GBS screening. METHODS: One hundred two pregnant women who were at 35–37 weeks of gestation were enrolled in this study. The analytical performance of the multiplex real-time PCR was first tested using a panel of reference and clinical bacterial and fungal strains. To test the clinical performance, vaginal-rectal swabs were obtained from pregnant women who were seen at the teaching hospital for regular prenatal care. The results of real-time were compared with those obtained from microbiological analyses. RESULTS: The real-time PCR assay showed 100% specificity and a limit of detection of 10(4) colony forming units equivalent per reaction. The prevalence of GBS colonization among the population studied was 15.7% (16/102) based on a positive culture and the real-time PCR results. Agreement between the two assays was found for 11 (68.75%) GBS colonized women. Using the culture-based results as a reference, the multiplex real-time PCR had a sensitivity of 91.7% (11/12, CI 59.7–99.6%), a specificity of 95.5% (86/90, CI 89.8–98.7%), a positive predictive value of 73.3% (11/15, CI 44.8–91.1%) and a negative predictive value of 98.9% (86/87, CI 92.9–99.9%). CONCLUSION: The multiplex real-time PCR is a rapid, affordable and sensitive assay for direct detection of GBS in vaginal-rectal swabs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12884-018-1774-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-03 /pmc/articles/PMC5934892/ /pubmed/29724169 http://dx.doi.org/10.1186/s12884-018-1774-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Article
Otaguiri, Eliane Saori
Morguette, Ana Elisa Belotto
Morey, Alexandre Tadachi
Tavares, Eliandro Reis
Kerbauy, Gilselena
de Almeida Torres, Rosângela S. L.
Chaves Júnior, Mauricio
Tognim, Maria Cristina Bronharo
Góes, Viviane Monteiro
Krieger, Marco Aurélio
Perugini, Marcia Regina Eches
Yamauchi, Lucy Megumi
Yamada-Ogatta, Sueli Fumie
Development of a melting-curve based multiplex real-time PCR assay for simultaneous detection of Streptococcus agalactiae and genes encoding resistance to macrolides and lincosamides
title Development of a melting-curve based multiplex real-time PCR assay for simultaneous detection of Streptococcus agalactiae and genes encoding resistance to macrolides and lincosamides
title_full Development of a melting-curve based multiplex real-time PCR assay for simultaneous detection of Streptococcus agalactiae and genes encoding resistance to macrolides and lincosamides
title_fullStr Development of a melting-curve based multiplex real-time PCR assay for simultaneous detection of Streptococcus agalactiae and genes encoding resistance to macrolides and lincosamides
title_full_unstemmed Development of a melting-curve based multiplex real-time PCR assay for simultaneous detection of Streptococcus agalactiae and genes encoding resistance to macrolides and lincosamides
title_short Development of a melting-curve based multiplex real-time PCR assay for simultaneous detection of Streptococcus agalactiae and genes encoding resistance to macrolides and lincosamides
title_sort development of a melting-curve based multiplex real-time pcr assay for simultaneous detection of streptococcus agalactiae and genes encoding resistance to macrolides and lincosamides
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934892/
https://www.ncbi.nlm.nih.gov/pubmed/29724169
http://dx.doi.org/10.1186/s12884-018-1774-5
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