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Detection of Gastrointestinal Pathogens from Stool Samples on Hemoccult Cards by Multiplex PCR
Purpose. Up to 30% of international travelers are affected by travelers' diarrhea (TD). Reliable data on the etiology of TD is lacking. Sufficient laboratory capacity at travel destinations is often unavailable and transporting conventional stool samples to the home country is inconvenient. We...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376410/ https://www.ncbi.nlm.nih.gov/pubmed/28408937 http://dx.doi.org/10.1155/2017/3472537 |
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author | Alberer, Martin Schlenker, Nicklas Bauer, Malkin Helfrich, Kerstin Mengele, Carolin Löscher, Thomas Nothdurft, Hans Dieter Bretzel, Gisela Beissner, Marcus |
author_facet | Alberer, Martin Schlenker, Nicklas Bauer, Malkin Helfrich, Kerstin Mengele, Carolin Löscher, Thomas Nothdurft, Hans Dieter Bretzel, Gisela Beissner, Marcus |
author_sort | Alberer, Martin |
collection | PubMed |
description | Purpose. Up to 30% of international travelers are affected by travelers' diarrhea (TD). Reliable data on the etiology of TD is lacking. Sufficient laboratory capacity at travel destinations is often unavailable and transporting conventional stool samples to the home country is inconvenient. We evaluated the use of Hemoccult cards for stool sampling combined with a multiplex PCR for the detection of model viral, bacterial, and protozoal TD pathogens. Methods. Following the creation of serial dilutions for each model pathogen, last positive dilution steps (LPDs) and thereof calculated last positive sample concentrations (LPCs) were compared between conventional stool samples and card samples. Furthermore, card samples were tested after a prolonged time interval simulating storage during a travel duration of up to 6 weeks. Results. The LPDs/LPCs were comparable to testing of conventional stool samples. After storage on Hemoccult cards, the recovery rate was 97.6% for C. jejuni, 100% for E. histolytica, 97.6% for norovirus GI, and 100% for GII. Detection of expected pathogens was possible at weekly intervals up to 42 days. Conclusion. Stool samples on Hemoccult cards stored at room temperature can be used in combination with a multiplex PCR as a reliable tool for testing of TD pathogens. |
format | Online Article Text |
id | pubmed-5376410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-53764102017-04-13 Detection of Gastrointestinal Pathogens from Stool Samples on Hemoccult Cards by Multiplex PCR Alberer, Martin Schlenker, Nicklas Bauer, Malkin Helfrich, Kerstin Mengele, Carolin Löscher, Thomas Nothdurft, Hans Dieter Bretzel, Gisela Beissner, Marcus Can J Infect Dis Med Microbiol Research Article Purpose. Up to 30% of international travelers are affected by travelers' diarrhea (TD). Reliable data on the etiology of TD is lacking. Sufficient laboratory capacity at travel destinations is often unavailable and transporting conventional stool samples to the home country is inconvenient. We evaluated the use of Hemoccult cards for stool sampling combined with a multiplex PCR for the detection of model viral, bacterial, and protozoal TD pathogens. Methods. Following the creation of serial dilutions for each model pathogen, last positive dilution steps (LPDs) and thereof calculated last positive sample concentrations (LPCs) were compared between conventional stool samples and card samples. Furthermore, card samples were tested after a prolonged time interval simulating storage during a travel duration of up to 6 weeks. Results. The LPDs/LPCs were comparable to testing of conventional stool samples. After storage on Hemoccult cards, the recovery rate was 97.6% for C. jejuni, 100% for E. histolytica, 97.6% for norovirus GI, and 100% for GII. Detection of expected pathogens was possible at weekly intervals up to 42 days. Conclusion. Stool samples on Hemoccult cards stored at room temperature can be used in combination with a multiplex PCR as a reliable tool for testing of TD pathogens. Hindawi 2017 2017-03-16 /pmc/articles/PMC5376410/ /pubmed/28408937 http://dx.doi.org/10.1155/2017/3472537 Text en Copyright © 2017 Martin Alberer et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Alberer, Martin Schlenker, Nicklas Bauer, Malkin Helfrich, Kerstin Mengele, Carolin Löscher, Thomas Nothdurft, Hans Dieter Bretzel, Gisela Beissner, Marcus Detection of Gastrointestinal Pathogens from Stool Samples on Hemoccult Cards by Multiplex PCR |
title | Detection of Gastrointestinal Pathogens from Stool Samples on Hemoccult Cards by Multiplex PCR |
title_full | Detection of Gastrointestinal Pathogens from Stool Samples on Hemoccult Cards by Multiplex PCR |
title_fullStr | Detection of Gastrointestinal Pathogens from Stool Samples on Hemoccult Cards by Multiplex PCR |
title_full_unstemmed | Detection of Gastrointestinal Pathogens from Stool Samples on Hemoccult Cards by Multiplex PCR |
title_short | Detection of Gastrointestinal Pathogens from Stool Samples on Hemoccult Cards by Multiplex PCR |
title_sort | detection of gastrointestinal pathogens from stool samples on hemoccult cards by multiplex pcr |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376410/ https://www.ncbi.nlm.nih.gov/pubmed/28408937 http://dx.doi.org/10.1155/2017/3472537 |
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