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Rapid and sensitive identification of pleural and peritoneal infections by droplet digital PCR
Pleural and peritoneal infections cause substantial morbidity and mortality. Traditional diagnostic methods rely on the cultivation of clinical samples, which usually takes days to obtain report and holds a low detection sensitivity. In this study, we evaluated a 5-fluorescent-channel droplet digita...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648221/ https://www.ncbi.nlm.nih.gov/pubmed/33159654 http://dx.doi.org/10.1007/s12223-020-00834-0 |
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author | Zhou, Fangmei Sun, Shoudong Sun, Xiling Chen, Ye Yang, Xuejing |
author_facet | Zhou, Fangmei Sun, Shoudong Sun, Xiling Chen, Ye Yang, Xuejing |
author_sort | Zhou, Fangmei |
collection | PubMed |
description | Pleural and peritoneal infections cause substantial morbidity and mortality. Traditional diagnostic methods rely on the cultivation of clinical samples, which usually takes days to obtain report and holds a low detection sensitivity. In this study, we evaluated a 5-fluorescent-channel droplet digital PCR (ddPCR) system and 5 assay panels for culture-independent rapid pathogen detections directly from pleural and peritoneal fluid samples. Traditional culture of the same sample was used as reference. A total of 40 pleural fluid samples and 19 peritoneal fluid samples were tested in this study. Twenty-five positives including 4 polymicrobial infections by culture and 26 positives including 11 polymicrobial infections by ddPCR were detected for pleural fluid samples; 14 positives including 2 polymicrobial infections by culture and 15 positives including 3 polymicrobial infections by ddPCR were detected for peritoneal fluid samples. Klebsiella pneumoniae was the most common bacterium detected both in pleural and in peritoneal fluid samples. The sensitivity of the ddPCR assay for pleural and peritoneal fluid samples was 96% (95% confidence interval (CI) = 79.65 to 99.90%) and 92.86% (95% CI = 66.13 to 99.82%), respectively. The turnaround time of the ddPCR assay was approximately 3 h comparing with 38.30 ± 22.44 h for culture-based identifications. Our results demonstrated that the ddPCR assay is a rapid and sensitive method for identifying pathogens responsible for pleural and peritoneal infections and would be a promising approach for early diagnosis and optimizing treatment of infections. |
format | Online Article Text |
id | pubmed-7648221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-76482212020-11-09 Rapid and sensitive identification of pleural and peritoneal infections by droplet digital PCR Zhou, Fangmei Sun, Shoudong Sun, Xiling Chen, Ye Yang, Xuejing Folia Microbiol (Praha) Original Article Pleural and peritoneal infections cause substantial morbidity and mortality. Traditional diagnostic methods rely on the cultivation of clinical samples, which usually takes days to obtain report and holds a low detection sensitivity. In this study, we evaluated a 5-fluorescent-channel droplet digital PCR (ddPCR) system and 5 assay panels for culture-independent rapid pathogen detections directly from pleural and peritoneal fluid samples. Traditional culture of the same sample was used as reference. A total of 40 pleural fluid samples and 19 peritoneal fluid samples were tested in this study. Twenty-five positives including 4 polymicrobial infections by culture and 26 positives including 11 polymicrobial infections by ddPCR were detected for pleural fluid samples; 14 positives including 2 polymicrobial infections by culture and 15 positives including 3 polymicrobial infections by ddPCR were detected for peritoneal fluid samples. Klebsiella pneumoniae was the most common bacterium detected both in pleural and in peritoneal fluid samples. The sensitivity of the ddPCR assay for pleural and peritoneal fluid samples was 96% (95% confidence interval (CI) = 79.65 to 99.90%) and 92.86% (95% CI = 66.13 to 99.82%), respectively. The turnaround time of the ddPCR assay was approximately 3 h comparing with 38.30 ± 22.44 h for culture-based identifications. Our results demonstrated that the ddPCR assay is a rapid and sensitive method for identifying pathogens responsible for pleural and peritoneal infections and would be a promising approach for early diagnosis and optimizing treatment of infections. Springer Netherlands 2020-11-07 2021 /pmc/articles/PMC7648221/ /pubmed/33159654 http://dx.doi.org/10.1007/s12223-020-00834-0 Text en © Institute of Microbiology, Academy of Sciences of the Czech Republic, v.v.i. 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Zhou, Fangmei Sun, Shoudong Sun, Xiling Chen, Ye Yang, Xuejing Rapid and sensitive identification of pleural and peritoneal infections by droplet digital PCR |
title | Rapid and sensitive identification of pleural and peritoneal infections by droplet digital PCR |
title_full | Rapid and sensitive identification of pleural and peritoneal infections by droplet digital PCR |
title_fullStr | Rapid and sensitive identification of pleural and peritoneal infections by droplet digital PCR |
title_full_unstemmed | Rapid and sensitive identification of pleural and peritoneal infections by droplet digital PCR |
title_short | Rapid and sensitive identification of pleural and peritoneal infections by droplet digital PCR |
title_sort | rapid and sensitive identification of pleural and peritoneal infections by droplet digital pcr |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648221/ https://www.ncbi.nlm.nih.gov/pubmed/33159654 http://dx.doi.org/10.1007/s12223-020-00834-0 |
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