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首页> 外文期刊>Virology Journal >Development and use of three monoclonal antibodies for the detection of rice black-streaked dwarf virus in field plants and planthopper vectors
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Development and use of three monoclonal antibodies for the detection of rice black-streaked dwarf virus in field plants and planthopper vectors

机译:三种单克隆抗体在田间植物和飞虱载体中检测水稻黑纹矮化病毒的开发和应用

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Background Rice black-streaked dwarf virus (RBSDV) causes great losses in rice, maize and wheat production in Asian countries. The use of serological methods for RBSDV detection depends on the availability of antibodies. In this study, three highly sensitive and specific murine monoclonal antibodies (MAbs) against RBSDV antigens were produced using crude extracts from tumors of RBSDV-infected maize as the immunogen, and two serological assays, antigen-coated-plate enzyme-linked immunosorbent assay (ACP-ELISA) and dot enzyme-linked immunosorbent assay (dot-ELISA) were developed for RBSDV detection. Results All three MAbs reacted strongly and specifically with the crude extracts from RBSDV-infected plant and planthopper tissues. The detection endpoints of three MAbs (12E10, 18F10 and 5G5) in ACP-ELISA were respectively 1:40,960, 1:40,960, 1:81,920 (w/v, g?mL-1) with the crude extract of infected maize, 1:10,240, 1:20,480, 1:20,480 (w/v, g?mL-1) with the crude extract of infected rice, 1:5,120, 1:10,240, 1:10,240 (w/v, g?mL-1) with the crude extract of infected wheat, 1:9,600, 1:9,600, 19,200 (individual planthopper/μL) with the crude extract of infected planthopper. The newly developed ACP-ELISA could detect the virus in the infected maize, wheat, rice tissue crude extracts diluted at 1:81,920, 1:20,480, 1:10,240 (w/v, g?mL-1), respectively, and in individual viruliferous planthopper extract diluted at 1:19200 (individual planthopper/μL). The dot-ELISA was proved to detect the virus in the infected maize, wheat and rice tissue crude extracts diluted at 1:320 (w/v, g?mL-1), and in individual viruliferous planthopper extract diluted at 1:1,600 (individual planthopper/μL), respectively. Field plants (915) and planthopper samples (594) from five provinces of China were screened for the presence of RBSDV using the two developed serological assays. The results indicated that 338 of the 915 plant samples and 19 of the 594 planthopper samples were infected by RBSDV. Conclusions The newly developed ACP-ELISA and dot-ELISA were highly sensitive and specific to detect RBSDV in field plant and planthopper samples. The field survey demonstrated that RBSDV is widespread in rice, maize and wheat crops in Jiangsu, Zhejiang, Shandong provinces of China.
机译:背景技术水稻黑纹矮化病毒(RBSDV)在亚洲国家造成水稻,玉米和小麦生产的重大损失。使用血清学方法检测RBSDV取决于抗体的可用性。在这项研究中,使用RBSDV感染的玉米肿瘤的粗提取物作为免疫原,制备了三种针对RBSDV抗原的高度敏感和特异性的鼠单克隆抗体(MAb),并进行了两种血清学检测,抗原包被的酶联免疫吸附测定(开发了用于RBSDV检测的ACP-ELISA和点酶联免疫吸附测定(dot-ELISA)。结果所有三种单克隆抗体均与RBSDV感染的植物和飞虱组织中的粗提物强烈且特异地反应。 ACP-ELISA中三种MAb(12E10、18F10和5G5)的检测终点分别为1:40,960、1:40,960、1:81,920(w / v,g?mL -1 ),受感染玉米的粗提液,1:10,240,1:20,480,1:20,480(w / v,g?mL -1 )与受感染的大米的粗提液,1:5,120,1:10,240 ,1:10,240(w / v,g?mL -1 )与被感染小麦的粗提物,1:9,600、1:9,600、19,200(个别飞虱/μL)与被感染的小麦的粗提物受感染的飞虱。新开发的ACP-ELISA可在受感染的玉米,小麦,水稻组织粗提物中按1:81,920、1:20,480、1:10,240(w / v,g?mL -1 ),并在1:16200(单个飞虱/μL)中稀释的单个有毒飞虱提取物中。事实证明,通过点酶联免疫吸附法可以在受感染的玉米,小麦和水稻组织粗提物中以1:320(w / v,g?mL -1 )稀释,并在单个有毒飞虱中检测到该病毒。提取物分别以1:1,600(单个飞虱/μL)稀释。使用两种开发的血清学检测方法,筛选了中国五个省份的田间植物(915)和飞虱样品(594)是否存在RBSDV。结果表明,在915份植物样品中有338份和594份稻飞虱样品中的19份被RBDSV感染。结论新开发的ACP-ELISA和dot-ELISA对田间植物和飞虱样品中RBSDV的检测具有很高的灵敏度和特异性。实地调查表明,RBDSV在中国江苏,浙江和山东省的水稻,玉米和小麦作物中普遍存在。

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