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Real-time PCR TaqMan assay for rapid screening of bloodstream infection
BACKGROUND: Sepsis is one of the main causes of mortality and morbidity. The rapid detection of pathogens in blood of septic patients is essential for adequate antimicrobial therapy and better prognosis. This study aimed to accelerate the detection and discrimination of Gram-positive (GP) and Gram-n...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898783/ https://www.ncbi.nlm.nih.gov/pubmed/24393579 http://dx.doi.org/10.1186/1476-0711-13-3 |
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author | Wang, Hye-young Kim, Sunghyun Kim, Hyunjung Kim, Jungho Kim, Yeun Park, Soon-Deok Jin, Hyunwoo Choi, Yeonim Uh, Young Lee, Hyeyoung |
author_facet | Wang, Hye-young Kim, Sunghyun Kim, Hyunjung Kim, Jungho Kim, Yeun Park, Soon-Deok Jin, Hyunwoo Choi, Yeonim Uh, Young Lee, Hyeyoung |
author_sort | Wang, Hye-young |
collection | PubMed |
description | BACKGROUND: Sepsis is one of the main causes of mortality and morbidity. The rapid detection of pathogens in blood of septic patients is essential for adequate antimicrobial therapy and better prognosis. This study aimed to accelerate the detection and discrimination of Gram-positive (GP) and Gram-negative (GN) bacteria and Candida species in blood culture samples by molecular methods. METHODS: The Real-GP®, -GN®, and -CAN® real-time PCR kit (M&D, Wonju, Republic of Korea) assays use the TaqMan probes for detecting pan-GP, pan-GN, and pan-Candida species, respectively. The diagnostic performances of the real-time PCR kits were evaluated with 115 clinical isolates, 256 positive and 200 negative blood culture bottle samples, and the data were compared to results obtained from conventional blood culture. RESULTS: Eighty-seven reference strains and 115 clinical isolates were correctly identified with specific probes corresponding to GP-bacteria, GN-bacteria and Candida, respectively. The overall sensitivity and specificity of the real-time PCR kit with blood culture samples were 99.6% and 89.5%, respectively. CONCLUSIONS: The Real-GP®, -GN®, and -CAN® real-time PCR kits could be useful tools for the rapid and accurate screening of bloodstream infections (BSIs). |
format | Online Article Text |
id | pubmed-3898783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38987832014-01-23 Real-time PCR TaqMan assay for rapid screening of bloodstream infection Wang, Hye-young Kim, Sunghyun Kim, Hyunjung Kim, Jungho Kim, Yeun Park, Soon-Deok Jin, Hyunwoo Choi, Yeonim Uh, Young Lee, Hyeyoung Ann Clin Microbiol Antimicrob Research BACKGROUND: Sepsis is one of the main causes of mortality and morbidity. The rapid detection of pathogens in blood of septic patients is essential for adequate antimicrobial therapy and better prognosis. This study aimed to accelerate the detection and discrimination of Gram-positive (GP) and Gram-negative (GN) bacteria and Candida species in blood culture samples by molecular methods. METHODS: The Real-GP®, -GN®, and -CAN® real-time PCR kit (M&D, Wonju, Republic of Korea) assays use the TaqMan probes for detecting pan-GP, pan-GN, and pan-Candida species, respectively. The diagnostic performances of the real-time PCR kits were evaluated with 115 clinical isolates, 256 positive and 200 negative blood culture bottle samples, and the data were compared to results obtained from conventional blood culture. RESULTS: Eighty-seven reference strains and 115 clinical isolates were correctly identified with specific probes corresponding to GP-bacteria, GN-bacteria and Candida, respectively. The overall sensitivity and specificity of the real-time PCR kit with blood culture samples were 99.6% and 89.5%, respectively. CONCLUSIONS: The Real-GP®, -GN®, and -CAN® real-time PCR kits could be useful tools for the rapid and accurate screening of bloodstream infections (BSIs). BioMed Central 2014-01-07 /pmc/articles/PMC3898783/ /pubmed/24393579 http://dx.doi.org/10.1186/1476-0711-13-3 Text en Copyright © 2014 Wang 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. 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 Wang, Hye-young Kim, Sunghyun Kim, Hyunjung Kim, Jungho Kim, Yeun Park, Soon-Deok Jin, Hyunwoo Choi, Yeonim Uh, Young Lee, Hyeyoung Real-time PCR TaqMan assay for rapid screening of bloodstream infection |
title | Real-time PCR TaqMan assay for rapid screening of bloodstream infection |
title_full | Real-time PCR TaqMan assay for rapid screening of bloodstream infection |
title_fullStr | Real-time PCR TaqMan assay for rapid screening of bloodstream infection |
title_full_unstemmed | Real-time PCR TaqMan assay for rapid screening of bloodstream infection |
title_short | Real-time PCR TaqMan assay for rapid screening of bloodstream infection |
title_sort | real-time pcr taqman assay for rapid screening of bloodstream infection |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898783/ https://www.ncbi.nlm.nih.gov/pubmed/24393579 http://dx.doi.org/10.1186/1476-0711-13-3 |
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