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Evaluation of a commercial latex agglutination test for detecting rotavirus A and human adenovirus in children's stool specimens
OBJECTIVES: Rotavirus A and human adenovirus are the two most common causes of infantile diarrhea; thus, it is of great importance to find out a rapid and accurate diagnostic method. This study aimed to evaluate the diagnostic significance of latex agglutination test for detection of rotavirus A and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246382/ https://www.ncbi.nlm.nih.gov/pubmed/31930752 http://dx.doi.org/10.1002/jcla.23208 |
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author | Xiang, Wenqing Peng, Zhaoyang Xu, Jialu Shen, Hongqiang Li, Wei |
author_facet | Xiang, Wenqing Peng, Zhaoyang Xu, Jialu Shen, Hongqiang Li, Wei |
author_sort | Xiang, Wenqing |
collection | PubMed |
description | OBJECTIVES: Rotavirus A and human adenovirus are the two most common causes of infantile diarrhea; thus, it is of great importance to find out a rapid and accurate diagnostic method. This study aimed to evaluate the diagnostic significance of latex agglutination test for detection of rotavirus A and human adenovirus. METHODS: A prospective study was conducted on 214 diarrhea children from September 2018 to March 2019 in our hospital. Fresh stool samples were collected for detection of rotavirus A and human adenovirus by latex agglutination test and quantitative reverse transcription polymerase chain reaction (RT‐qPCR). Then, the consistency of results detected by these two methods was analyzed. RESULTS: With performing the latex agglutination test, it was revealed that positive rates for detecting rotavirus A virus and human adenovirus were 23.83% (51/214) and 25.24% (54/214), respectively. Meanwhile, results of RT‐qPCR showed that positive rates for detecting rotavirus A virus and human adenovirus were 58 (27.10%) and 59 (27.57%), respectively. Using RT‐qPCR as the gold standard, the sensitivity and specificity of the latex agglutination test for detecting rotavirus A were 81.03% and 97.44%, and the corresponding values for detecting human adenovirus were 76.27% and 94.19%, respectively. CONCLUSION: This latex agglutination test showed a satisfactory consistency with RT‐qPCR for detecting rotavirus A and human adenovirus. The mentioned commercial assay may be highly appropriate for rapid screening of rotavirus A and human adenovirus. |
format | Online Article Text |
id | pubmed-7246382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72463822020-06-01 Evaluation of a commercial latex agglutination test for detecting rotavirus A and human adenovirus in children's stool specimens Xiang, Wenqing Peng, Zhaoyang Xu, Jialu Shen, Hongqiang Li, Wei J Clin Lab Anal Brief Reports OBJECTIVES: Rotavirus A and human adenovirus are the two most common causes of infantile diarrhea; thus, it is of great importance to find out a rapid and accurate diagnostic method. This study aimed to evaluate the diagnostic significance of latex agglutination test for detection of rotavirus A and human adenovirus. METHODS: A prospective study was conducted on 214 diarrhea children from September 2018 to March 2019 in our hospital. Fresh stool samples were collected for detection of rotavirus A and human adenovirus by latex agglutination test and quantitative reverse transcription polymerase chain reaction (RT‐qPCR). Then, the consistency of results detected by these two methods was analyzed. RESULTS: With performing the latex agglutination test, it was revealed that positive rates for detecting rotavirus A virus and human adenovirus were 23.83% (51/214) and 25.24% (54/214), respectively. Meanwhile, results of RT‐qPCR showed that positive rates for detecting rotavirus A virus and human adenovirus were 58 (27.10%) and 59 (27.57%), respectively. Using RT‐qPCR as the gold standard, the sensitivity and specificity of the latex agglutination test for detecting rotavirus A were 81.03% and 97.44%, and the corresponding values for detecting human adenovirus were 76.27% and 94.19%, respectively. CONCLUSION: This latex agglutination test showed a satisfactory consistency with RT‐qPCR for detecting rotavirus A and human adenovirus. The mentioned commercial assay may be highly appropriate for rapid screening of rotavirus A and human adenovirus. John Wiley and Sons Inc. 2020-01-13 /pmc/articles/PMC7246382/ /pubmed/31930752 http://dx.doi.org/10.1002/jcla.23208 Text en © 2020 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals, Inc This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Brief Reports Xiang, Wenqing Peng, Zhaoyang Xu, Jialu Shen, Hongqiang Li, Wei Evaluation of a commercial latex agglutination test for detecting rotavirus A and human adenovirus in children's stool specimens |
title | Evaluation of a commercial latex agglutination test for detecting rotavirus A and human adenovirus in children's stool specimens |
title_full | Evaluation of a commercial latex agglutination test for detecting rotavirus A and human adenovirus in children's stool specimens |
title_fullStr | Evaluation of a commercial latex agglutination test for detecting rotavirus A and human adenovirus in children's stool specimens |
title_full_unstemmed | Evaluation of a commercial latex agglutination test for detecting rotavirus A and human adenovirus in children's stool specimens |
title_short | Evaluation of a commercial latex agglutination test for detecting rotavirus A and human adenovirus in children's stool specimens |
title_sort | evaluation of a commercial latex agglutination test for detecting rotavirus a and human adenovirus in children's stool specimens |
topic | Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246382/ https://www.ncbi.nlm.nih.gov/pubmed/31930752 http://dx.doi.org/10.1002/jcla.23208 |
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