植物保护
植物保護
식물보호
PLANT PROTECTION
2014年
5期
117-120
,共4页
周朋%余乃通%章绍延%王健华%胡加谊%王祥%梁洁%刘志昕
週朋%餘迺通%章紹延%王健華%鬍加誼%王祥%樑潔%劉誌昕
주붕%여내통%장소연%왕건화%호가의%왕상%량길%류지흔
香蕉束顶病毒%DAS-ELISA%病毒检测
香蕉束頂病毒%DAS-ELISA%病毒檢測
향초속정병독%DAS-ELISA%병독검측
Banana bunchy top virus%DAS-ELISA%virus detection
为了解海南海口香蕉分化芽携带香蕉束顶病毒(Banana bunchy top virus ,BBTV)的情况,本研究建立了双抗夹心酶联免疫反应(DAS-ELISA)检测法,对来自海南地区组培厂的香蕉分化芽进行检测。检测结果表明,6个品种1852个香蕉分化芽平均带毒率为2.1%,其中‘皇帝蕉’为1.98%,‘粤科1号’为2.07%,‘广粉蕉’为1.98%,‘大蕉’为6.25%,‘218’为1.89%,‘巴西蕉’为2.25%。为了进一步验证 ELISA 结果的可靠性,随机选取12个阳性样品提取总 DNA 进行 PCR 鉴定。鉴定结果显示,12个样品中11个检测出有 BBTV,表明 DAS-ELISA 方法的准确率较高,与分子检测结果基本一致,可以胜任日常香蕉组培苗 BBTV 的检测。
為瞭解海南海口香蕉分化芽攜帶香蕉束頂病毒(Banana bunchy top virus ,BBTV)的情況,本研究建立瞭雙抗夾心酶聯免疫反應(DAS-ELISA)檢測法,對來自海南地區組培廠的香蕉分化芽進行檢測。檢測結果錶明,6箇品種1852箇香蕉分化芽平均帶毒率為2.1%,其中‘皇帝蕉’為1.98%,‘粵科1號’為2.07%,‘廣粉蕉’為1.98%,‘大蕉’為6.25%,‘218’為1.89%,‘巴西蕉’為2.25%。為瞭進一步驗證 ELISA 結果的可靠性,隨機選取12箇暘性樣品提取總 DNA 進行 PCR 鑒定。鑒定結果顯示,12箇樣品中11箇檢測齣有 BBTV,錶明 DAS-ELISA 方法的準確率較高,與分子檢測結果基本一緻,可以勝任日常香蕉組培苗 BBTV 的檢測。
위료해해남해구향초분화아휴대향초속정병독(Banana bunchy top virus ,BBTV)적정황,본연구건립료쌍항협심매련면역반응(DAS-ELISA)검측법,대래자해남지구조배엄적향초분화아진행검측。검측결과표명,6개품충1852개향초분화아평균대독솔위2.1%,기중‘황제초’위1.98%,‘월과1호’위2.07%,‘엄분초’위1.98%,‘대초’위6.25%,‘218’위1.89%,‘파서초’위2.25%。위료진일보험증 ELISA 결과적가고성,수궤선취12개양성양품제취총 DNA 진행 PCR 감정。감정결과현시,12개양품중11개검측출유 BBTV,표명 DAS-ELISA 방법적준학솔교고,여분자검측결과기본일치,가이성임일상향초조배묘 BBTV 적검측。
In order to understand the situation of Banana bunchy top virus (BBTV)infection in banana differentiated shoots in Hainan,1 852 shoot samples from 6 banana varieties were detected by DAS-ELISAmethod.The results showed that the average BBTV-carrying rate was 2.1%,while 1.98% of ‘Huangdi’banana,2.07% of ‘Yueke No.1’banana, 1.98% of ‘Guangfen’banana,6.25% of Musa sapientum ,1.89% of ‘218’banana,and 2.25% of ‘Brazil’banana, respectively.To further confirm the accuracy of DAS-ELISA result,12 BBTV-carrying samples were selected for molec-ular detection by PCR.The results showed that 11 of them were BBTV positive,indicating DAS-ELISA method with the high accuracy can be used for BBTV detection in banana differentiated shoots.