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The application research of xTAG GPP multiplex PCR in the diagnosis of persistent and chronic diarrhea in children
BACKGROUND: Persistent and chronic diarrhea is difficult to treat, and infection is still the main cause. In this study, we investigate the application value of xTAG gastrointestinal pathogen panel (xTAG GPP) multiplex PCR in the early diagnosis of persistent and chronic diarrhea in children and to...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318512/ https://www.ncbi.nlm.nih.gov/pubmed/32590971 http://dx.doi.org/10.1186/s12887-020-02206-6 |
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author | Wang, Chunli Zhou, Xiaoying Zhu, Mengshu Yin, Hanjun Tang, Jiamei Huang, Yan Zheng, Bixia Jin, Yu Liu, Zhifeng |
author_facet | Wang, Chunli Zhou, Xiaoying Zhu, Mengshu Yin, Hanjun Tang, Jiamei Huang, Yan Zheng, Bixia Jin, Yu Liu, Zhifeng |
author_sort | Wang, Chunli |
collection | PubMed |
description | BACKGROUND: Persistent and chronic diarrhea is difficult to treat, and infection is still the main cause. In this study, we investigate the application value of xTAG gastrointestinal pathogen panel (xTAG GPP) multiplex PCR in the early diagnosis of persistent and chronic diarrhea in children and to understand the epidemiology of intestinal diarrhea pathogens. METHODS: One hundred ninety-nine specimens were collected from Nanjing Children’s Hospital Affiliated to Nanjing Medical University (Nanjing, China). We compared the xTAG GPP multiplex PCR assay with traditional methods (culture, rapid enzyme immunoassay chromatography, and microscopic examination) and performed a statistical analysis. RESULTS: The positive rate of the xTAG GPP multiplex PCR assay of diarrhea specimens from 199 patients was 72.86% (145/199). The virus detection rate was 48.7%, and rotavirus A was the most common organism detected (34.67%), concentrated in winter, and was common in children. The second most common organism detected was norovirus GI/GII (20.6%). The positive rate of this bacteria was 40.2%, and Campylobacter (22.11%, 44/199) was most frequently detected. C. difficile toxins A/B and Salmonella was detected in 44 and 17 samples, respectively. Infections with Shigella occurred 4 times, and E. coli O157 was only detected once. Three samples were parasitic (1.51%), two samples were positive for Entamoeba histolytica, and one was positive for Cryptosporidium. Adenovirus 40/41, STEC, ETEC, Giardia, Yersinia enterocolitica and Vibrio cholerae were not detected. In total, 86 (43.2%) infected specimens with a single pathogen were detected. There were 59 coinfections (29.65% of the samples) of viruses and/or bacteria and/or parasites. Coinfections involved 49 double infections (24.62%), 9 triple infections (4.52%) and 1 quadruple infections (0.5%). Norovirus GI/GII was found to have the highest involvement, with 32 coinfections (16.08%). CONCLUSION: The xTAG GPP multiplex PCR assay is simple, sensitive, and specific and can be used as a quick way to diagnose persistent and chronic diarrhea in children. |
format | Online Article Text |
id | pubmed-7318512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73185122020-06-29 The application research of xTAG GPP multiplex PCR in the diagnosis of persistent and chronic diarrhea in children Wang, Chunli Zhou, Xiaoying Zhu, Mengshu Yin, Hanjun Tang, Jiamei Huang, Yan Zheng, Bixia Jin, Yu Liu, Zhifeng BMC Pediatr Research Article BACKGROUND: Persistent and chronic diarrhea is difficult to treat, and infection is still the main cause. In this study, we investigate the application value of xTAG gastrointestinal pathogen panel (xTAG GPP) multiplex PCR in the early diagnosis of persistent and chronic diarrhea in children and to understand the epidemiology of intestinal diarrhea pathogens. METHODS: One hundred ninety-nine specimens were collected from Nanjing Children’s Hospital Affiliated to Nanjing Medical University (Nanjing, China). We compared the xTAG GPP multiplex PCR assay with traditional methods (culture, rapid enzyme immunoassay chromatography, and microscopic examination) and performed a statistical analysis. RESULTS: The positive rate of the xTAG GPP multiplex PCR assay of diarrhea specimens from 199 patients was 72.86% (145/199). The virus detection rate was 48.7%, and rotavirus A was the most common organism detected (34.67%), concentrated in winter, and was common in children. The second most common organism detected was norovirus GI/GII (20.6%). The positive rate of this bacteria was 40.2%, and Campylobacter (22.11%, 44/199) was most frequently detected. C. difficile toxins A/B and Salmonella was detected in 44 and 17 samples, respectively. Infections with Shigella occurred 4 times, and E. coli O157 was only detected once. Three samples were parasitic (1.51%), two samples were positive for Entamoeba histolytica, and one was positive for Cryptosporidium. Adenovirus 40/41, STEC, ETEC, Giardia, Yersinia enterocolitica and Vibrio cholerae were not detected. In total, 86 (43.2%) infected specimens with a single pathogen were detected. There were 59 coinfections (29.65% of the samples) of viruses and/or bacteria and/or parasites. Coinfections involved 49 double infections (24.62%), 9 triple infections (4.52%) and 1 quadruple infections (0.5%). Norovirus GI/GII was found to have the highest involvement, with 32 coinfections (16.08%). CONCLUSION: The xTAG GPP multiplex PCR assay is simple, sensitive, and specific and can be used as a quick way to diagnose persistent and chronic diarrhea in children. BioMed Central 2020-06-26 /pmc/articles/PMC7318512/ /pubmed/32590971 http://dx.doi.org/10.1186/s12887-020-02206-6 Text en © The Author(s) 2020 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/. 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 in a credit line to the data. |
spellingShingle | Research Article Wang, Chunli Zhou, Xiaoying Zhu, Mengshu Yin, Hanjun Tang, Jiamei Huang, Yan Zheng, Bixia Jin, Yu Liu, Zhifeng The application research of xTAG GPP multiplex PCR in the diagnosis of persistent and chronic diarrhea in children |
title | The application research of xTAG GPP multiplex PCR in the diagnosis of persistent and chronic diarrhea in children |
title_full | The application research of xTAG GPP multiplex PCR in the diagnosis of persistent and chronic diarrhea in children |
title_fullStr | The application research of xTAG GPP multiplex PCR in the diagnosis of persistent and chronic diarrhea in children |
title_full_unstemmed | The application research of xTAG GPP multiplex PCR in the diagnosis of persistent and chronic diarrhea in children |
title_short | The application research of xTAG GPP multiplex PCR in the diagnosis of persistent and chronic diarrhea in children |
title_sort | application research of xtag gpp multiplex pcr in the diagnosis of persistent and chronic diarrhea in children |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318512/ https://www.ncbi.nlm.nih.gov/pubmed/32590971 http://dx.doi.org/10.1186/s12887-020-02206-6 |
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