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SaQuant: a real-time PCR assay for quantitative assessment of Staphylococcus aureus

BACKGROUND: Molecular assays are important tools for pathogen detection but need to be periodically re-evaluated with the discovery of additional genetic diversity that may cause assays to exclude target taxa or include non-target taxa. A single well-developed assay can find broad application across...

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Autores principales: Wood, Colin, Sahl, Jason, Maltinsky, Sara, Coyne, Briana, Russakoff, Benjamin, Yagüe, David Panisello, Bowers, Jolene, Pearson, Talima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188689/
https://www.ncbi.nlm.nih.gov/pubmed/34103012
http://dx.doi.org/10.1186/s12866-021-02247-6
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author Wood, Colin
Sahl, Jason
Maltinsky, Sara
Coyne, Briana
Russakoff, Benjamin
Yagüe, David Panisello
Bowers, Jolene
Pearson, Talima
author_facet Wood, Colin
Sahl, Jason
Maltinsky, Sara
Coyne, Briana
Russakoff, Benjamin
Yagüe, David Panisello
Bowers, Jolene
Pearson, Talima
author_sort Wood, Colin
collection PubMed
description BACKGROUND: Molecular assays are important tools for pathogen detection but need to be periodically re-evaluated with the discovery of additional genetic diversity that may cause assays to exclude target taxa or include non-target taxa. A single well-developed assay can find broad application across research, clinical, and industrial settings. Pathogen prevalence within a population is estimated using such assays and accurate results are critical for formulating effective public health policies and guiding future research. A variety of assays for the detection of Staphylococcus aureus are currently available. The utility of commercial assays for research is limited, given proprietary signatures and lack of transparent validation. RESULTS: In silico testing of existing peer-reviewed assays show that most suffer from a lack of sensitivity and specificity. We found no assays that were specifically designed and validated for quantitative use. Here we present a qPCR assay, SaQuant, for the detection and quantification of S. aureus as might be collected on sampling swabs. Sensitivity and specificity of the assay was 95.6 and 99.9 %, respectively, with a limit of detection of between 3 and 5 genome equivalents and a limit of quantification of 8.27 genome equivalents. The presence of DNA from non-target species likely to be found in a swab sample, did not impact qualitative or quantitative abilities of the assay. CONCLUSIONS: This assay has the potential to serve as a valuable tool for the accurate detection and quantification of S. aureus collected from human body sites in order to better understand the dynamics of prevalence and transmission in community settings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02247-6.
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spelling pubmed-81886892021-06-10 SaQuant: a real-time PCR assay for quantitative assessment of Staphylococcus aureus Wood, Colin Sahl, Jason Maltinsky, Sara Coyne, Briana Russakoff, Benjamin Yagüe, David Panisello Bowers, Jolene Pearson, Talima BMC Microbiol Research BACKGROUND: Molecular assays are important tools for pathogen detection but need to be periodically re-evaluated with the discovery of additional genetic diversity that may cause assays to exclude target taxa or include non-target taxa. A single well-developed assay can find broad application across research, clinical, and industrial settings. Pathogen prevalence within a population is estimated using such assays and accurate results are critical for formulating effective public health policies and guiding future research. A variety of assays for the detection of Staphylococcus aureus are currently available. The utility of commercial assays for research is limited, given proprietary signatures and lack of transparent validation. RESULTS: In silico testing of existing peer-reviewed assays show that most suffer from a lack of sensitivity and specificity. We found no assays that were specifically designed and validated for quantitative use. Here we present a qPCR assay, SaQuant, for the detection and quantification of S. aureus as might be collected on sampling swabs. Sensitivity and specificity of the assay was 95.6 and 99.9 %, respectively, with a limit of detection of between 3 and 5 genome equivalents and a limit of quantification of 8.27 genome equivalents. The presence of DNA from non-target species likely to be found in a swab sample, did not impact qualitative or quantitative abilities of the assay. CONCLUSIONS: This assay has the potential to serve as a valuable tool for the accurate detection and quantification of S. aureus collected from human body sites in order to better understand the dynamics of prevalence and transmission in community settings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02247-6. BioMed Central 2021-06-08 /pmc/articles/PMC8188689/ /pubmed/34103012 http://dx.doi.org/10.1186/s12866-021-02247-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wood, Colin
Sahl, Jason
Maltinsky, Sara
Coyne, Briana
Russakoff, Benjamin
Yagüe, David Panisello
Bowers, Jolene
Pearson, Talima
SaQuant: a real-time PCR assay for quantitative assessment of Staphylococcus aureus
title SaQuant: a real-time PCR assay for quantitative assessment of Staphylococcus aureus
title_full SaQuant: a real-time PCR assay for quantitative assessment of Staphylococcus aureus
title_fullStr SaQuant: a real-time PCR assay for quantitative assessment of Staphylococcus aureus
title_full_unstemmed SaQuant: a real-time PCR assay for quantitative assessment of Staphylococcus aureus
title_short SaQuant: a real-time PCR assay for quantitative assessment of Staphylococcus aureus
title_sort saquant: a real-time pcr assay for quantitative assessment of staphylococcus aureus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188689/
https://www.ncbi.nlm.nih.gov/pubmed/34103012
http://dx.doi.org/10.1186/s12866-021-02247-6
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