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The development of a 16S rRNA gene based PCR for the identification of Streptococcus pneumoniae and comparison with four other species specific PCR assays
BACKGROUND: Streptococcus pneumoniae is one of the most frequently encountered pathogens in humans but its differentiation from closely related but less pathogenic streptococci remains a challenge. METHODS: This report describes a newly-developed PCR assay (Spne-PCR), amplifying a 217 bp product of...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874796/ https://www.ncbi.nlm.nih.gov/pubmed/20426878 http://dx.doi.org/10.1186/1471-2334-10-104 |
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author | El Aila, Nabil Abdullah Emler, Stefan Kaijalainen, Tarja De Baere, Thierry Saerens, Bart Alkan, Elife Deschaght, Pieter Verhelst, Rita Vaneechoutte, Mario |
author_facet | El Aila, Nabil Abdullah Emler, Stefan Kaijalainen, Tarja De Baere, Thierry Saerens, Bart Alkan, Elife Deschaght, Pieter Verhelst, Rita Vaneechoutte, Mario |
author_sort | El Aila, Nabil Abdullah |
collection | PubMed |
description | BACKGROUND: Streptococcus pneumoniae is one of the most frequently encountered pathogens in humans but its differentiation from closely related but less pathogenic streptococci remains a challenge. METHODS: This report describes a newly-developed PCR assay (Spne-PCR), amplifying a 217 bp product of the 16S rRNA gene of S. pneumoniae, and its performance compared to other genotypic and phenotypic tests. RESULTS: The new PCR assay designed in this study, proved to be specific at 57°C for S. pneumoniae, not amplifying S. pseudopneumoniae or any other streptococcal strain or any strains from other upper airway pathogenic species. PCR assays (psaA, LytA, ply, spn9802-PCR) were previously described for the specific amplification of S. pneumoniae, but psaA-PCR was the only one found not to cross-react with S. pseudopneumoniae. CONCLUSION: Spne-PCR, developed for this study, and psaA-PCR were the only two assays which did not mis-identify S. pseudopneumoniae as S. pneumoniae. Four other PCR assays and the AccuProbe assay were unable to distinguish between these species. |
format | Text |
id | pubmed-2874796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28747962010-05-24 The development of a 16S rRNA gene based PCR for the identification of Streptococcus pneumoniae and comparison with four other species specific PCR assays El Aila, Nabil Abdullah Emler, Stefan Kaijalainen, Tarja De Baere, Thierry Saerens, Bart Alkan, Elife Deschaght, Pieter Verhelst, Rita Vaneechoutte, Mario BMC Infect Dis Research Article BACKGROUND: Streptococcus pneumoniae is one of the most frequently encountered pathogens in humans but its differentiation from closely related but less pathogenic streptococci remains a challenge. METHODS: This report describes a newly-developed PCR assay (Spne-PCR), amplifying a 217 bp product of the 16S rRNA gene of S. pneumoniae, and its performance compared to other genotypic and phenotypic tests. RESULTS: The new PCR assay designed in this study, proved to be specific at 57°C for S. pneumoniae, not amplifying S. pseudopneumoniae or any other streptococcal strain or any strains from other upper airway pathogenic species. PCR assays (psaA, LytA, ply, spn9802-PCR) were previously described for the specific amplification of S. pneumoniae, but psaA-PCR was the only one found not to cross-react with S. pseudopneumoniae. CONCLUSION: Spne-PCR, developed for this study, and psaA-PCR were the only two assays which did not mis-identify S. pseudopneumoniae as S. pneumoniae. Four other PCR assays and the AccuProbe assay were unable to distinguish between these species. BioMed Central 2010-04-29 /pmc/articles/PMC2874796/ /pubmed/20426878 http://dx.doi.org/10.1186/1471-2334-10-104 Text en Copyright ©2010 El Aila et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article El Aila, Nabil Abdullah Emler, Stefan Kaijalainen, Tarja De Baere, Thierry Saerens, Bart Alkan, Elife Deschaght, Pieter Verhelst, Rita Vaneechoutte, Mario The development of a 16S rRNA gene based PCR for the identification of Streptococcus pneumoniae and comparison with four other species specific PCR assays |
title | The development of a 16S rRNA gene based PCR for the identification of Streptococcus pneumoniae and comparison with four other species specific PCR assays |
title_full | The development of a 16S rRNA gene based PCR for the identification of Streptococcus pneumoniae and comparison with four other species specific PCR assays |
title_fullStr | The development of a 16S rRNA gene based PCR for the identification of Streptococcus pneumoniae and comparison with four other species specific PCR assays |
title_full_unstemmed | The development of a 16S rRNA gene based PCR for the identification of Streptococcus pneumoniae and comparison with four other species specific PCR assays |
title_short | The development of a 16S rRNA gene based PCR for the identification of Streptococcus pneumoniae and comparison with four other species specific PCR assays |
title_sort | development of a 16s rrna gene based pcr for the identification of streptococcus pneumoniae and comparison with four other species specific pcr assays |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874796/ https://www.ncbi.nlm.nih.gov/pubmed/20426878 http://dx.doi.org/10.1186/1471-2334-10-104 |
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