几种新疆加工型辣椒种子病毒的检测和鉴定
本研究采用双抗体夹心酶联免疫吸附法(DAS-ELISA)对新疆巴音郭楞蒙古自治州和静地区9个品种的加工型辣椒种子样品进行9种主要病毒的检测。针对检测呈阳性的病毒,进一步通过反转录聚合酶链式反应(RT-PCR),对其基因克隆和序列分析验证。结果表明,检测的辣椒种子中携带CMV、BBWV和PMMo V,以CMV的检出率最高,为55.6%,其次是BBWV,检出率为22.2%,PMMo V的检出率最低,为11.1%。CMV不仅是种子携带的优势毒源,且与BBWV和PMMo V复合侵染。种子传毒试验表明其种子传毒率为4.7%~17.4%。研究发现,辣椒种植地域、辣椒品种(种类)影响种子携带病毒种类、带毒率...
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          | Published in | 西南农业学报 Vol. 27; no. 6; pp. 2385 - 2392 | 
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| Main Author | |
| Format | Journal Article | 
| Language | Chinese | 
| Published | 
            新疆自治区高校农林有害生物监测与安全防控重点实验室,新疆乌鲁木齐830052%新疆巴音郭楞蒙古自治州农业科学研究所,新疆库尔勒,841000%新疆库尔勒市农业技术推广中心,新疆库尔勒,841000
    
        2014
     新疆农业大学农学院,新疆乌鲁木齐830052  | 
| Subjects | |
| Online Access | Get full text | 
| ISSN | 1001-4829 | 
| DOI | 10.16213/j.cnki.scjas.2014.06.025 | 
Cover
| Summary: | 本研究采用双抗体夹心酶联免疫吸附法(DAS-ELISA)对新疆巴音郭楞蒙古自治州和静地区9个品种的加工型辣椒种子样品进行9种主要病毒的检测。针对检测呈阳性的病毒,进一步通过反转录聚合酶链式反应(RT-PCR),对其基因克隆和序列分析验证。结果表明,检测的辣椒种子中携带CMV、BBWV和PMMo V,以CMV的检出率最高,为55.6%,其次是BBWV,检出率为22.2%,PMMo V的检出率最低,为11.1%。CMV不仅是种子携带的优势毒源,且与BBWV和PMMo V复合侵染。种子传毒试验表明其种子传毒率为4.7%~17.4%。研究发现,辣椒种植地域、辣椒品种(种类)影响种子携带病毒种类、带毒率和种传率。本研究结果是新疆加工型辣椒种子病毒首次报道。 | 
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| Bibliography: | 51-1213/S ZHANG Qiang,LUO Ming,LI Ke-mei,ZHANG Chun-zhu,CHU Jin-ping,MA Jian-jiang( 1. Agricultural College of Xinjiang Agricultural University,Xinjiang Urumqi 830052 ,China;2. Key Laboratory of Xinjiang Autonomous Region Universities Forestry Harmful Biological Monitoring and Safety Prevention, Xinjiang Urumqi 830052, China;3. Institute of Agricultural Sciences of Bayinguoleng Mongol Autonomous Prefecture in Xinjiang, Xinjiang Korla 841000, China;4. Agricultural Technology Promotion Center of Korla in Xinjiang, Xinjiang Korla 841000, China) In this study,9 main viruses which came from 9 varieties of processing pepper seed samples were collected at Hejing in Bayinguoleng Mongolia Autonomous Region of Xinjiang were detected by double antibody sandwich enzyme-linked immunosorbent assay( DASELISA). In the light of the virus' test which showed positive,using reverse transcription polymerase chain reaction( RT-PCR),their gene cloning and sequence were analyzed and verified. The results showed that among the detected  | 
| ISSN: | 1001-4829 | 
| DOI: | 10.16213/j.cnki.scjas.2014.06.025 |