State Key Laboratory of Rice Biology, Institute of Biotechnology, Zhejiang University, Hangzhou 310058, China.
Ocean College, Zhejiang University, Hangzhou 310058, China.
J Zhejiang Univ Sci B. 2017;18(12):1075-1082. doi: 10.1631/jzus.B1600561.
Potato virus S (PVS) often causes significant losses in potato production in potato-growing countries. In this study, the ordinary strain of PVS (PVS) was purified from PVS-infected potato plants and used as the immunogen to produce hybridomas secreting monoclonal antibodies (MAbs). Five highly specific and sensitive murine MAbs (1A3, 16C10, 18A9, 20B12, and 22H4) against PVS were prepared using conventional hybridoma technology. Using these MAbs, tissue print-enzyme-linked immunosorbent assay (ELISA), dot-ELISA, and double-antibody sandwich (DAS)-ELISA were developed for sensitive and specific detection of PVS infection in potato plants. The results of sensitivity assays revealed that PVS could be reliably detected in PVS-infected leaf crude extracts diluted at 1:10 240 and 1:163 840 (w/v, g/ml) in phosphate buffer saline (PBS) by dot-ELISA and DAS-ELISA, respectively. Twenty-two samples collected from potato fields in Yunnan Province, China were tested for PVS infection using the serological assays we had developed, and 14 of them were found to be positive. This indicates that PVS is now prevalent in potato fields in Yunnan Province.
马铃薯 S 病毒(PVS)常导致马铃薯种植国家的马铃薯生产遭受重大损失。本研究从 PVS 感染的马铃薯植株中纯化普通株系的 PVS(PVS)作为免疫原,产生分泌单克隆抗体(MAb)的杂交瘤细胞。使用常规杂交瘤技术制备了针对 PVS 的 5 种高度特异性和灵敏的鼠源单克隆抗体(1A3、16C10、18A9、20B12 和 22H4)。利用这些单抗,建立了组织印斑酶联免疫吸附试验(ELISA)、斑点 ELISA 和双抗体夹心 ELISA 用于灵敏和特异检测马铃薯植株中的 PVS 感染。敏感性检测结果表明,通过斑点 ELISA 和 DAS-ELISA,PVS 可在 PBS 稀释的 1:10 240 和 1:163 840(w/v,g/ml)的 PVS 感染叶片粗提物中可靠检测到。使用我们开发的血清学检测方法,对来自中国云南省马铃薯田的 22 个样本进行 PVS 感染检测,其中 14 个样本呈阳性。这表明 PVS 目前在云南省的马铃薯田普遍存在。