韦金菊, 魏春燕, 宋修鹏, 覃振强, 谭宏伟, 张荣华, 庞天, 王伦旺, 刘璐, 李杨瑞. 2018: 广西北海蔗区甘蔗白条病发生情况调查. 南方农业学报, 49(2): 264-270. DOI: 10.3969/j.issn.2095-1191.2018.02.10
引用本文: 韦金菊, 魏春燕, 宋修鹏, 覃振强, 谭宏伟, 张荣华, 庞天, 王伦旺, 刘璐, 李杨瑞. 2018: 广西北海蔗区甘蔗白条病发生情况调查. 南方农业学报, 49(2): 264-270. DOI: 10.3969/j.issn.2095-1191.2018.02.10
WEI Jin-ju, WEI Chun-yan, SONG Xiu-peng, QIN Zhen-qiang, TAN Hong-wei, ZHANG Rong-hua, PANG Tian, WANG Lun-wang, LIU Lu, LI Yang-rui. 2018: Sugarcane leaf scald disease in sugarcane planting areas of Beihai,Guangxi. Journal of Southern Agriculture, 49(2): 264-270. DOI: 10.3969/j.issn.2095-1191.2018.02.10
Citation: WEI Jin-ju, WEI Chun-yan, SONG Xiu-peng, QIN Zhen-qiang, TAN Hong-wei, ZHANG Rong-hua, PANG Tian, WANG Lun-wang, LIU Lu, LI Yang-rui. 2018: Sugarcane leaf scald disease in sugarcane planting areas of Beihai,Guangxi. Journal of Southern Agriculture, 49(2): 264-270. DOI: 10.3969/j.issn.2095-1191.2018.02.10

广西北海蔗区甘蔗白条病发生情况调查

Sugarcane leaf scald disease in sugarcane planting areas of Beihai,Guangxi

  • 摘要: 目的对广西北海蔗区疑似发生甘蔗白条病的样本进行PCR检测鉴定,明确甘蔗白条病在广西北海的发生情况,为甘蔗白条病的防控提供科学依据.方法2016年11月,在广西北海合浦县、银海区和铁山港区采集疑似甘蔗白条病样本372份,涉及19个甘蔗品种/系,采用甘蔗白条病病原白条黄单胞菌Xanthomonas albilineans(Ashby) Dowson特异引物XAF1和XAR1对采集样本的DNA进行PCR检测.对部分有阳性条带的PCR产物进行切胶回收,并送样测序,然后在NCBI上进行BLAST比对分析.结果所采集的372份样本中,有78份样本扩增出目的条带,阳性检出率为20.97%;19个甘蔗品种中,有13个品种检测出阳性条带,检出率为68.42%,其中白叶病检出率较高的是柳城07-95、桂糖46号、桂糖42号和柳城07-536,检出率分别为75.00%、68.75%、48.15%和33.33%.部分阳性条带经克隆后测序,在NCBI上进行BLAST比对分析,发现其与广西白条病分离物KY315212.1的同源性为99%,表明它们均属于甘蔗白条病基因片段序列.结论甘蔗白条病已在广西北海蔗区发生危害,今后需加强检疫工作,防止从疫区调运感病蔗种,以控制病害进一步扩散蔓延.

     

    Abstract: ObjectiveSugarcane with suspected leaf scald disease in Beihai sugarcane fields in Guangxi were identi-fied by PCR test to determine whether the disease occurs in Beihai,Guangxi,and to provide scientific basis for the con-trol of sugarcane leaf scald.MethodIn November,2016,372 sugarcane samples with suspected leaf scald disease in Hepu County,Yinhai District and Tieshangang District of Beihai,Guangxi were collected,which belonged to 19 varie-ties/lines. PCR test was conducted on DNA of the samples collected using specific primers XAF1 and XAR1 of Xan-thomonas albilineans(Ashby)Dowson(pathogeny of sugarcane leaf scald).PCR products with positive bands were reco-vered and sequenced,than BLAST comparison of the results were conducted in NCBI.ResultIn the 372 samples,there were 78 samples amplified target bands with positive detection rate being 20.97%.Out of 19 sugarcane varieties,13 ones had target band with positive detection rate being 68.42%.The sugarcane varieties with high positive detection rate of sugar-cane leaf scaldwere Liucheng 07-95(75.00%),Guitang 46(68.75%),Guitang 42(48.15%),Liucheng 07-536(33.33%). Partial positive bands were cloned and sequenced,then BLAST comparison of their sequences were conducted in NCBI. The results showed that they had 99% homology with the Guangxi leaf scald disease isolate KY315212.1,which con-firmed that they belonged to leaf scald disease gene fragment sequences.ConclusionSugarcane leaf scald disease occurs in Beihai,Guangxi.Therefore,quarantine must be strengthened and diseased sugarcane cannot be transported from in-fected area to prevent the further spread of the disease.

     

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