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Development of polyclonal antisera against movement proteins from three poleroviruses infecting cucurbits

Authors
  • Zhang, Shao-Kang1, 1
  • Zhao, Tian-Yu1, 1
  • Shi, Xing1, 1
  • Liu, Yu-Zi1, 1
  • Wang, Ying1, 1
  • Zhang, Zong-Ying1, 1
  • Li, Da-Wei1, 1
  • Yu, Jia-Lin1, 1
  • Shang, Qiao-Xia2
  • Han, Cheng-Gui1, 1
  • 1 China Agricultural University, Beijing, 100193, People’s Republic of China , Beijing (China)
  • 2 Beijing University of Agriculture, Beijing, 102206, People’s Republic of China , Beijing (China)
Type
Published Article
Journal
Phytopathology Research
Publisher
BioMed Central
Publication Date
Sep 02, 2020
Volume
2
Issue
1
Identifiers
DOI: 10.1186/s42483-020-00065-8
Source
Springer Nature
Keywords
License
Green

Abstract

Cucurbit aphid-borne yellows virus (CABYV), melon aphid-borne yellows virus (MABYV) and suakwa aphid-borne yellows virus (SABYV) are three poleroviruses that infect cucurbit crops. Developing specific antisera against such viruses is crucial for their detection and functional understanding of related genes. However, no studies have yet reported viral detection using antisera against movement proteins (MP) in these three viruses. In this study, we generated plasmids expressing three viral MP genes, and transformed them into the Escherichia coli strain, Rosetta, to recombinantly express and purify fusion proteins. Then, polyclonal antisera were derived by immunizing New Zealand white rabbits, after which western blotting was used to determine the titer, sensitivity and specificity of the antisera. The antisera titers against MPCABYV, MPMABYV and MPSABYV were 1:512000, 1:256000 and 1:256000, respectively. The optimized working concentrations for the three antisera ranged between 1:10000 and 1:64000. Additionally, antisera against MPCABYV and MPMABYV only reacted with their corresponding MP proteins. Antiserum against MPSABYV not only had the strongest reaction with its MP, but also reacted weakly with MPCABYV and MPMABYV. All three antisera exerted no serological reactions with other poleroviruses. Furthermore, our data showed that all antisera specifically detected MPs in both Nicotiana benthamiana and cucumber leaves. Thus, we have established a system that sensitively detects three poleroviruses infecting cucurbits, using antisera against MPs. We provide a foundation for future research on the serological detection of these viruses, and interaction mechanisms between viruses and host plants.

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