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Evaluation of recombinant multi-epitope proteins for diagnosis of goat schistosomiasis by enzyme-linked immunosorbent assay

BACKGROUND: Schistosomiasis is a huge threat to human and animal health. Apart from bovines, goats play an important role in the transmission of schistosomiasis in some endemic areas of China. An accessible, quality-assured goat schistosomiasis diagnostic technique is needed. Recently, our laborator...

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Autores principales: Lv, Chao, Hong, Yang, Fu, Zhiqiang, Lu, Ke, Cao, Xiaodan, Wang, Tao, Zhu, Chuangang, Li, Hao, Xu, Rui, Jia, Bingguang, Han, Qian, Dou, Xuefeng, Shen, Yuanxi, Zhang, Zuhang, Zai, Jinli, Feng, Jintao, Lin, Jiaojiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4784438/
https://www.ncbi.nlm.nih.gov/pubmed/26955957
http://dx.doi.org/10.1186/s13071-016-1418-4
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author Lv, Chao
Hong, Yang
Fu, Zhiqiang
Lu, Ke
Cao, Xiaodan
Wang, Tao
Zhu, Chuangang
Li, Hao
Xu, Rui
Jia, Bingguang
Han, Qian
Dou, Xuefeng
Shen, Yuanxi
Zhang, Zuhang
Zai, Jinli
Feng, Jintao
Lin, Jiaojiao
author_facet Lv, Chao
Hong, Yang
Fu, Zhiqiang
Lu, Ke
Cao, Xiaodan
Wang, Tao
Zhu, Chuangang
Li, Hao
Xu, Rui
Jia, Bingguang
Han, Qian
Dou, Xuefeng
Shen, Yuanxi
Zhang, Zuhang
Zai, Jinli
Feng, Jintao
Lin, Jiaojiao
author_sort Lv, Chao
collection PubMed
description BACKGROUND: Schistosomiasis is a huge threat to human and animal health. Apart from bovines, goats play an important role in the transmission of schistosomiasis in some endemic areas of China. An accessible, quality-assured goat schistosomiasis diagnostic technique is needed. Recently, our laboratory identified two recombinant diagnostic antigens, SjPGM and SjRAD23 via an immuno-proteomic method. The application of these two recombinant antigens to develop a higher sensitivity and specificity technique for the sheep schistosomiasis diagnosis is urgently needed. METHODS: Epitopes of SjPGM and SjRAD23 were predicted and three polypeptides, two from SjRAD23 and one from SjPGM, were selected. Recombinant plasmids containing two to three DNA sequences encoding predicted polypeptides or large hydrophilic region of Sj23 (LHD-Sj23) were constructed and expressed. Eight recombinant schistosome antigens including four multi-epitope proteins and four recombinant single-molecule antigens as well as SEA, were assessed by ELISA in 91 sera from schistosome-infected goats, 44 sera from non-infected goats, 37 sera from Orientobilharzia-infected goats, and 12 from Haemonchus contortus-infected goats. RESULTS: ELISA tests showed that three multi-epitope proteins had higher sensitivity than the four single-molecule antigens (rSjRAD23, rSjPGM, rBSjRAD23-1, rBSj23) and the multi-epitope protein rBSjPGM-BSjRAD23-1-BSj23 had the highest sensitivity (97.8 %, 89/91) and maintained good specificity (100 %, 44/44) as well as low cross-reactivity with haemonchosis (8.33 %, 3/12) and orientobilharziasis (13.51 %, 5/37) in the diagnosis of goat schistosomiasis. In contrast, when SEA was applied as a diagnosis antigen, it had 100 % (91/91) sensitivity, 75 % (33/44) specificity, 25 and 83.78 % cross-reactivity with haemonchosis (3/12) and orientobilharziasis (31/37), respectively. CONCLUSIONS: The application of recombinant multi-epitope proteins may increase the sensitivity of diagnosis technique and retain high specificity of single-molecule antigens for schistosomiasis, and the recombinant antigen rBSjPGM-BSjRAD23-1-BSj23 has the potential to be used as a diagnosis antigen for goat schistosomiasis.
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spelling pubmed-47844382016-03-10 Evaluation of recombinant multi-epitope proteins for diagnosis of goat schistosomiasis by enzyme-linked immunosorbent assay Lv, Chao Hong, Yang Fu, Zhiqiang Lu, Ke Cao, Xiaodan Wang, Tao Zhu, Chuangang Li, Hao Xu, Rui Jia, Bingguang Han, Qian Dou, Xuefeng Shen, Yuanxi Zhang, Zuhang Zai, Jinli Feng, Jintao Lin, Jiaojiao Parasit Vectors Research BACKGROUND: Schistosomiasis is a huge threat to human and animal health. Apart from bovines, goats play an important role in the transmission of schistosomiasis in some endemic areas of China. An accessible, quality-assured goat schistosomiasis diagnostic technique is needed. Recently, our laboratory identified two recombinant diagnostic antigens, SjPGM and SjRAD23 via an immuno-proteomic method. The application of these two recombinant antigens to develop a higher sensitivity and specificity technique for the sheep schistosomiasis diagnosis is urgently needed. METHODS: Epitopes of SjPGM and SjRAD23 were predicted and three polypeptides, two from SjRAD23 and one from SjPGM, were selected. Recombinant plasmids containing two to three DNA sequences encoding predicted polypeptides or large hydrophilic region of Sj23 (LHD-Sj23) were constructed and expressed. Eight recombinant schistosome antigens including four multi-epitope proteins and four recombinant single-molecule antigens as well as SEA, were assessed by ELISA in 91 sera from schistosome-infected goats, 44 sera from non-infected goats, 37 sera from Orientobilharzia-infected goats, and 12 from Haemonchus contortus-infected goats. RESULTS: ELISA tests showed that three multi-epitope proteins had higher sensitivity than the four single-molecule antigens (rSjRAD23, rSjPGM, rBSjRAD23-1, rBSj23) and the multi-epitope protein rBSjPGM-BSjRAD23-1-BSj23 had the highest sensitivity (97.8 %, 89/91) and maintained good specificity (100 %, 44/44) as well as low cross-reactivity with haemonchosis (8.33 %, 3/12) and orientobilharziasis (13.51 %, 5/37) in the diagnosis of goat schistosomiasis. In contrast, when SEA was applied as a diagnosis antigen, it had 100 % (91/91) sensitivity, 75 % (33/44) specificity, 25 and 83.78 % cross-reactivity with haemonchosis (3/12) and orientobilharziasis (31/37), respectively. CONCLUSIONS: The application of recombinant multi-epitope proteins may increase the sensitivity of diagnosis technique and retain high specificity of single-molecule antigens for schistosomiasis, and the recombinant antigen rBSjPGM-BSjRAD23-1-BSj23 has the potential to be used as a diagnosis antigen for goat schistosomiasis. BioMed Central 2016-03-09 /pmc/articles/PMC4784438/ /pubmed/26955957 http://dx.doi.org/10.1186/s13071-016-1418-4 Text en © Lv et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Lv, Chao
Hong, Yang
Fu, Zhiqiang
Lu, Ke
Cao, Xiaodan
Wang, Tao
Zhu, Chuangang
Li, Hao
Xu, Rui
Jia, Bingguang
Han, Qian
Dou, Xuefeng
Shen, Yuanxi
Zhang, Zuhang
Zai, Jinli
Feng, Jintao
Lin, Jiaojiao
Evaluation of recombinant multi-epitope proteins for diagnosis of goat schistosomiasis by enzyme-linked immunosorbent assay
title Evaluation of recombinant multi-epitope proteins for diagnosis of goat schistosomiasis by enzyme-linked immunosorbent assay
title_full Evaluation of recombinant multi-epitope proteins for diagnosis of goat schistosomiasis by enzyme-linked immunosorbent assay
title_fullStr Evaluation of recombinant multi-epitope proteins for diagnosis of goat schistosomiasis by enzyme-linked immunosorbent assay
title_full_unstemmed Evaluation of recombinant multi-epitope proteins for diagnosis of goat schistosomiasis by enzyme-linked immunosorbent assay
title_short Evaluation of recombinant multi-epitope proteins for diagnosis of goat schistosomiasis by enzyme-linked immunosorbent assay
title_sort evaluation of recombinant multi-epitope proteins for diagnosis of goat schistosomiasis by enzyme-linked immunosorbent assay
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4784438/
https://www.ncbi.nlm.nih.gov/pubmed/26955957
http://dx.doi.org/10.1186/s13071-016-1418-4
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