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A Multiplex Assay for Detection of Staphylococcal and Streptococcal Exotoxins
Staphylococcal and streptococcal exotoxins, also known as superantigens, mediate a range of diseases including toxic shock syndrome, and they exacerbate skin, pulmonary and systemic infections caused by these organisms. When present in food sources they can cause enteric effects commonly known as fo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4549143/ https://www.ncbi.nlm.nih.gov/pubmed/26305471 http://dx.doi.org/10.1371/journal.pone.0135986 |
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author | Sharma, Preeti Wang, Ningyan Chervin, Adam S. Quinn, Cheryl L. Stone, Jennifer D. Kranz, David M. |
author_facet | Sharma, Preeti Wang, Ningyan Chervin, Adam S. Quinn, Cheryl L. Stone, Jennifer D. Kranz, David M. |
author_sort | Sharma, Preeti |
collection | PubMed |
description | Staphylococcal and streptococcal exotoxins, also known as superantigens, mediate a range of diseases including toxic shock syndrome, and they exacerbate skin, pulmonary and systemic infections caused by these organisms. When present in food sources they can cause enteric effects commonly known as food poisoning. A rapid, sensitive assay for the toxins would enable testing of clinical samples and improve surveillance of food sources. Here we developed a bead-based, two-color flow cytometry assay using single protein domains of the beta chain of T cell receptors engineered for high-affinity for staphylococcal (SEA, SEB and TSST-1) and streptococcal (SpeA and SpeC) toxins. Site-directed biotinylated forms of these high-affinity agents were used together with commercial, polyclonal, anti-toxin reagents to enable specific and sensitive detection with SD(50) values of 400 pg/ml (SEA), 3 pg/ml (SEB), 25 pg/ml (TSST-1), 6 ng/ml (SpeA), and 100 pg/ml (SpeC). These sensitivities were in the range of 4- to 80-fold higher than achieved with standard ELISAs using the same reagents. A multiplex format of the assay showed reduced sensitivity due to higher noise associated with the use of multiple polyclonal agents, but the sensitivities were still well within the range necessary for detection in food sources or for rapid detection of toxins in culture supernatants. For example, the assay specifically detected toxins in supernatants derived from cultures of Staphylococcus aureus. Thus, these reagents can be used for simultaneous detection of the toxins in food sources or culture supernatants of potential pathogenic strains of Staphylococcus aureus and Streptococcus pyogenes. |
format | Online Article Text |
id | pubmed-4549143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45491432015-09-01 A Multiplex Assay for Detection of Staphylococcal and Streptococcal Exotoxins Sharma, Preeti Wang, Ningyan Chervin, Adam S. Quinn, Cheryl L. Stone, Jennifer D. Kranz, David M. PLoS One Research Article Staphylococcal and streptococcal exotoxins, also known as superantigens, mediate a range of diseases including toxic shock syndrome, and they exacerbate skin, pulmonary and systemic infections caused by these organisms. When present in food sources they can cause enteric effects commonly known as food poisoning. A rapid, sensitive assay for the toxins would enable testing of clinical samples and improve surveillance of food sources. Here we developed a bead-based, two-color flow cytometry assay using single protein domains of the beta chain of T cell receptors engineered for high-affinity for staphylococcal (SEA, SEB and TSST-1) and streptococcal (SpeA and SpeC) toxins. Site-directed biotinylated forms of these high-affinity agents were used together with commercial, polyclonal, anti-toxin reagents to enable specific and sensitive detection with SD(50) values of 400 pg/ml (SEA), 3 pg/ml (SEB), 25 pg/ml (TSST-1), 6 ng/ml (SpeA), and 100 pg/ml (SpeC). These sensitivities were in the range of 4- to 80-fold higher than achieved with standard ELISAs using the same reagents. A multiplex format of the assay showed reduced sensitivity due to higher noise associated with the use of multiple polyclonal agents, but the sensitivities were still well within the range necessary for detection in food sources or for rapid detection of toxins in culture supernatants. For example, the assay specifically detected toxins in supernatants derived from cultures of Staphylococcus aureus. Thus, these reagents can be used for simultaneous detection of the toxins in food sources or culture supernatants of potential pathogenic strains of Staphylococcus aureus and Streptococcus pyogenes. Public Library of Science 2015-08-25 /pmc/articles/PMC4549143/ /pubmed/26305471 http://dx.doi.org/10.1371/journal.pone.0135986 Text en © 2015 Sharma et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Sharma, Preeti Wang, Ningyan Chervin, Adam S. Quinn, Cheryl L. Stone, Jennifer D. Kranz, David M. A Multiplex Assay for Detection of Staphylococcal and Streptococcal Exotoxins |
title | A Multiplex Assay for Detection of Staphylococcal and Streptococcal Exotoxins |
title_full | A Multiplex Assay for Detection of Staphylococcal and Streptococcal Exotoxins |
title_fullStr | A Multiplex Assay for Detection of Staphylococcal and Streptococcal Exotoxins |
title_full_unstemmed | A Multiplex Assay for Detection of Staphylococcal and Streptococcal Exotoxins |
title_short | A Multiplex Assay for Detection of Staphylococcal and Streptococcal Exotoxins |
title_sort | multiplex assay for detection of staphylococcal and streptococcal exotoxins |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4549143/ https://www.ncbi.nlm.nih.gov/pubmed/26305471 http://dx.doi.org/10.1371/journal.pone.0135986 |
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