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Evaluation of a real-time PCR assay for diagnosis of schistosomiasis japonica in the domestic goat

BACKGROUND: Schistosomiasis japonica is an infectious disease caused by Schistosoma japonicum that seriously endangers human health. Domestic animals have important roles in disease transmission and goats are considered a primary reservoir host and source of infection. The prevalence and intensity o...

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Autores principales: Guo, Qinghong, Chen, Cheng, Zhou, Keke, Li, Yugang, Tong, Laibao, Yue, Yongcheng, Zhou, Kerou, Liu, Jinming, Fu, Zhiqiang, Lin, Jiaojiao, Zhao, Jiaxi, Sun, Pengxiang, Hong, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590668/
https://www.ncbi.nlm.nih.gov/pubmed/33109260
http://dx.doi.org/10.1186/s13071-020-04420-8
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author Guo, Qinghong
Chen, Cheng
Zhou, Keke
Li, Yugang
Tong, Laibao
Yue, Yongcheng
Zhou, Kerou
Liu, Jinming
Fu, Zhiqiang
Lin, Jiaojiao
Zhao, Jiaxi
Sun, Pengxiang
Hong, Yang
author_facet Guo, Qinghong
Chen, Cheng
Zhou, Keke
Li, Yugang
Tong, Laibao
Yue, Yongcheng
Zhou, Kerou
Liu, Jinming
Fu, Zhiqiang
Lin, Jiaojiao
Zhao, Jiaxi
Sun, Pengxiang
Hong, Yang
author_sort Guo, Qinghong
collection PubMed
description BACKGROUND: Schistosomiasis japonica is an infectious disease caused by Schistosoma japonicum that seriously endangers human health. Domestic animals have important roles in disease transmission and goats are considered a primary reservoir host and source of infection. The prevalence and intensity of schistosomiasis infections have significantly decreased in China, and a more sensitive, specific detection method is urgently needed. The aim of this study was to develop a real-time PCR assay for accurate detection of S. japonicum infection in goats. METHODS: A real-time PCR method for detecting schistosomiasis japonica in goats was developed by amplification of a specific S. japonicum DNA fragment, and validated using a total of 94 negative and 159 positive plasma and serum samples collected in our previous study of S. japonicum infection. Both plasma and serum samples were evaluated by real-time PCR and enzyme-linked immunosorbent assay (ELISA). In addition, 120 goat plasma samples from an S. japonicum-endemic area (Wangjiang) and 33 from a non-endemic region (Weihai) were collected and evaluated using our method. RESULTS: The sensitivity and specificity of the real-time PCR for detecting infected samples were 98.74% (157/159, 95% CI: 95.53–99.85%) and 100% (94/94, 95% CI: 96.15–100%), respectively. For the ELISA, sensitivity and specificity were 98.11% (156/159, 95% CI: 94.59–99.61%) and 90.43% (85/94, 95% CI: 82.60–95.53%), respectively. Further, we found positivity rates for S. japonicum infection in Wangjiang and Weihai of 8.33% (10/120, 95% CI: 4.07–14.79%) and 0% (0/33, 95% CI: 0–10.58%), respectively. CONCLUSIONS: The results of this study indicate that our real-time PCR method exhibits higher sensitivity and specificity than ELISA and is a useful method for detection of S. japonicum infection in goats. [Image: see text]
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spelling pubmed-75906682020-10-27 Evaluation of a real-time PCR assay for diagnosis of schistosomiasis japonica in the domestic goat Guo, Qinghong Chen, Cheng Zhou, Keke Li, Yugang Tong, Laibao Yue, Yongcheng Zhou, Kerou Liu, Jinming Fu, Zhiqiang Lin, Jiaojiao Zhao, Jiaxi Sun, Pengxiang Hong, Yang Parasit Vectors Research BACKGROUND: Schistosomiasis japonica is an infectious disease caused by Schistosoma japonicum that seriously endangers human health. Domestic animals have important roles in disease transmission and goats are considered a primary reservoir host and source of infection. The prevalence and intensity of schistosomiasis infections have significantly decreased in China, and a more sensitive, specific detection method is urgently needed. The aim of this study was to develop a real-time PCR assay for accurate detection of S. japonicum infection in goats. METHODS: A real-time PCR method for detecting schistosomiasis japonica in goats was developed by amplification of a specific S. japonicum DNA fragment, and validated using a total of 94 negative and 159 positive plasma and serum samples collected in our previous study of S. japonicum infection. Both plasma and serum samples were evaluated by real-time PCR and enzyme-linked immunosorbent assay (ELISA). In addition, 120 goat plasma samples from an S. japonicum-endemic area (Wangjiang) and 33 from a non-endemic region (Weihai) were collected and evaluated using our method. RESULTS: The sensitivity and specificity of the real-time PCR for detecting infected samples were 98.74% (157/159, 95% CI: 95.53–99.85%) and 100% (94/94, 95% CI: 96.15–100%), respectively. For the ELISA, sensitivity and specificity were 98.11% (156/159, 95% CI: 94.59–99.61%) and 90.43% (85/94, 95% CI: 82.60–95.53%), respectively. Further, we found positivity rates for S. japonicum infection in Wangjiang and Weihai of 8.33% (10/120, 95% CI: 4.07–14.79%) and 0% (0/33, 95% CI: 0–10.58%), respectively. CONCLUSIONS: The results of this study indicate that our real-time PCR method exhibits higher sensitivity and specificity than ELISA and is a useful method for detection of S. japonicum infection in goats. [Image: see text] BioMed Central 2020-10-27 /pmc/articles/PMC7590668/ /pubmed/33109260 http://dx.doi.org/10.1186/s13071-020-04420-8 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
Guo, Qinghong
Chen, Cheng
Zhou, Keke
Li, Yugang
Tong, Laibao
Yue, Yongcheng
Zhou, Kerou
Liu, Jinming
Fu, Zhiqiang
Lin, Jiaojiao
Zhao, Jiaxi
Sun, Pengxiang
Hong, Yang
Evaluation of a real-time PCR assay for diagnosis of schistosomiasis japonica in the domestic goat
title Evaluation of a real-time PCR assay for diagnosis of schistosomiasis japonica in the domestic goat
title_full Evaluation of a real-time PCR assay for diagnosis of schistosomiasis japonica in the domestic goat
title_fullStr Evaluation of a real-time PCR assay for diagnosis of schistosomiasis japonica in the domestic goat
title_full_unstemmed Evaluation of a real-time PCR assay for diagnosis of schistosomiasis japonica in the domestic goat
title_short Evaluation of a real-time PCR assay for diagnosis of schistosomiasis japonica in the domestic goat
title_sort evaluation of a real-time pcr assay for diagnosis of schistosomiasis japonica in the domestic goat
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590668/
https://www.ncbi.nlm.nih.gov/pubmed/33109260
http://dx.doi.org/10.1186/s13071-020-04420-8
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