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Highly sensitive serological methods for detecting tomato yellow leaf curl virus in tomato plants and whiteflies

BACKGROUND: Tomato yellow leaf curl virus (TYLCV) is a member of the genus Begomovirus in the family Geminiviridae, which causes severe losses in tomato production in tropic and subtropic regions. METHODS: The purified TYLCV virions were used as the immunogen to produce monoclonal antibodies (MAbs)...

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Autores principales: Xie, Yan, Jiao, Xiaoyang, Zhou, Xueping, Liu, Huan, Ni, Yuequn, Wu, Jianxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684515/
https://www.ncbi.nlm.nih.gov/pubmed/23647724
http://dx.doi.org/10.1186/1743-422X-10-142
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author Xie, Yan
Jiao, Xiaoyang
Zhou, Xueping
Liu, Huan
Ni, Yuequn
Wu, Jianxiang
author_facet Xie, Yan
Jiao, Xiaoyang
Zhou, Xueping
Liu, Huan
Ni, Yuequn
Wu, Jianxiang
author_sort Xie, Yan
collection PubMed
description BACKGROUND: Tomato yellow leaf curl virus (TYLCV) is a member of the genus Begomovirus in the family Geminiviridae, which causes severe losses in tomato production in tropic and subtropic regions. METHODS: The purified TYLCV virions were used as the immunogen to produce monoclonal antibodies (MAbs) using the hybridoma technology. MAb-based dot enzyme-linked immunosorbent assay (dot-ELISA) and direct tissue blot immunoassay (DTBIA) were developed for sensitive, simple, and rapid detection of TYLCV in field tomato and whitefly (Bemisia tabaci) samples collected from TYLCV prevalent provinces in China. RESULTS: Using the hybridoma technology, six murine MAbs (1C4, 8D10, 6E3, 2F2, 3F4 and 4G3) against TYLCV were prepared. Using the MAb 1C4, dot-ELISA and DTBIA were then established for detecting TYLCV in field tomato and whitefly samples collected from TYLCV prevalent provinces in China. The dot-ELISA could detect TYLCV in infected tissue crude extract diluted at 1:5,120 (w/v, g mL(-1)), and in viruliferous whitefly homogenate diluted at 1:128 (individual whitefly/μL), respectively. Field tomato samples (n=487) and whitefly samples (n=110) from TYLCV prevalent districts in China were screened for the presence of TYLCV using the two developed methods, and the results were further confirmed by PCR and nucleotide sequencing. The survey revealed that TYLCV is widespread on tomato plants in Zhejiang, Shandong and Henan provinces in China. CONCLUSIONS: The developed dot-ELISA is very suitable for the routine detection of TYLCV in field tomato and whitefly samples, and the DTBIA is more suitable for the routine detection of TYLCV in large-scale tomato plant samples collected from TYLCV prevalent areas.
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spelling pubmed-36845152013-06-18 Highly sensitive serological methods for detecting tomato yellow leaf curl virus in tomato plants and whiteflies Xie, Yan Jiao, Xiaoyang Zhou, Xueping Liu, Huan Ni, Yuequn Wu, Jianxiang Virol J Research BACKGROUND: Tomato yellow leaf curl virus (TYLCV) is a member of the genus Begomovirus in the family Geminiviridae, which causes severe losses in tomato production in tropic and subtropic regions. METHODS: The purified TYLCV virions were used as the immunogen to produce monoclonal antibodies (MAbs) using the hybridoma technology. MAb-based dot enzyme-linked immunosorbent assay (dot-ELISA) and direct tissue blot immunoassay (DTBIA) were developed for sensitive, simple, and rapid detection of TYLCV in field tomato and whitefly (Bemisia tabaci) samples collected from TYLCV prevalent provinces in China. RESULTS: Using the hybridoma technology, six murine MAbs (1C4, 8D10, 6E3, 2F2, 3F4 and 4G3) against TYLCV were prepared. Using the MAb 1C4, dot-ELISA and DTBIA were then established for detecting TYLCV in field tomato and whitefly samples collected from TYLCV prevalent provinces in China. The dot-ELISA could detect TYLCV in infected tissue crude extract diluted at 1:5,120 (w/v, g mL(-1)), and in viruliferous whitefly homogenate diluted at 1:128 (individual whitefly/μL), respectively. Field tomato samples (n=487) and whitefly samples (n=110) from TYLCV prevalent districts in China were screened for the presence of TYLCV using the two developed methods, and the results were further confirmed by PCR and nucleotide sequencing. The survey revealed that TYLCV is widespread on tomato plants in Zhejiang, Shandong and Henan provinces in China. CONCLUSIONS: The developed dot-ELISA is very suitable for the routine detection of TYLCV in field tomato and whitefly samples, and the DTBIA is more suitable for the routine detection of TYLCV in large-scale tomato plant samples collected from TYLCV prevalent areas. BioMed Central 2013-05-06 /pmc/articles/PMC3684515/ /pubmed/23647724 http://dx.doi.org/10.1186/1743-422X-10-142 Text en Copyright © 2013 Xie et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Xie, Yan
Jiao, Xiaoyang
Zhou, Xueping
Liu, Huan
Ni, Yuequn
Wu, Jianxiang
Highly sensitive serological methods for detecting tomato yellow leaf curl virus in tomato plants and whiteflies
title Highly sensitive serological methods for detecting tomato yellow leaf curl virus in tomato plants and whiteflies
title_full Highly sensitive serological methods for detecting tomato yellow leaf curl virus in tomato plants and whiteflies
title_fullStr Highly sensitive serological methods for detecting tomato yellow leaf curl virus in tomato plants and whiteflies
title_full_unstemmed Highly sensitive serological methods for detecting tomato yellow leaf curl virus in tomato plants and whiteflies
title_short Highly sensitive serological methods for detecting tomato yellow leaf curl virus in tomato plants and whiteflies
title_sort highly sensitive serological methods for detecting tomato yellow leaf curl virus in tomato plants and whiteflies
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684515/
https://www.ncbi.nlm.nih.gov/pubmed/23647724
http://dx.doi.org/10.1186/1743-422X-10-142
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