首页 | 本学科首页   官方微博 | 高级检索  
     检索      

兜兰炭疽病病原鉴定及其室内防治药剂筛选
引用本文:徐波,宋凤鸣,冯淑杰,张荣,刘海涛,曾宋君.兜兰炭疽病病原鉴定及其室内防治药剂筛选[J].南方农业学报,2018,49(2):271-279.
作者姓名:徐波  宋凤鸣  冯淑杰  张荣  刘海涛  曾宋君
作者单位:华南农业大学 林学与风景园林学院,广州,510642华南农业大学 园艺学院,广州,510642中国科学院 华南植物园广东省应用植物学重点实验室,广州,510650
基金项目:广东省应用植物学重点实验室开放项目广东省科技计划项目中国科学院战略生物资源服务网络计划植物种质资源创新项目国家重点研发计划项目
摘    要:目的]对兜兰炭疽病病原菌进行鉴定,并进行室内防治药剂筛选,为兜兰炭疽病的大田防控提供参考依据.方法]采集具有典型症状的兜兰炭疽病标本,以组织分离法进行病原物分离培养,通过形态学观察和rDNA-ITS序列分析对兜兰炭疽病病原菌进行鉴定;通过室内温度、光照控制和培养基中不同pH、碳源、氮源的差异试验确定病原菌菌丝生长、产孢量和孢子萌发条件等生物学特性;选用12种杀菌剂进行兜兰炭疽病病原菌室内药效试验,并对筛选出效果理想的药剂进行室内毒力测定.结果]通过形态学观察和rDNA-ITS序列分析,确定分离获得的兜兰炭疽病病原菌的无性态为半知菌类黑盘孢目刺盘孢属胶孢炭疽菌(Colletotrichum gloeosporioides).胶孢炭疽菌菌丝生长和分生孢子萌发温度为9~36℃,最适温度27℃;产孢温度12~36℃,最适温度30℃.胶孢炭疽菌菌丝在55℃下处理20 min死亡,孢子在50℃下处理30 min或55℃下处理20 min死亡.菌丝生长和产孢的pH为2~13,最适为pH 8;分生孢子萌发的pH为2~12,最适为pH 7.连续光照有利于胶孢炭疽菌菌丝生长、产孢及分生孢子萌发.培养基中不同碳源和氮源对菌丝生长、产孢及分生孢子萌发具有显著影响(P<0.05).500 mg/L的恶霉灵、硫磺·甲硫灵、福·福锌和咪鲜胺锰盐4种杀菌剂对胶孢炭疽菌菌丝抑制率和产孢抑制率均达100.00%,其中咪鲜胺锰盐的毒力最强、反应灵敏度最高,半最大效应浓度(EC50)为0.09 mg/L.结论]引起兜兰炭疽病的病原菌为胶孢炭疽菌(C. gloeosporioides).咪鲜胺锰盐、硫磺·甲硫灵、恶霉灵和福·福锌4种杀菌剂可在室内有效防治兜兰炭疽病,其中以500 mg/L咪鲜胺锰盐的防治效果最佳.

关 键 词:兜兰    炭疽病    病原鉴定    生物学特性    杀菌剂筛选

Identification for anthracnose pathogen of Paphiopedilum and selection of its indoor chemical control chemicals
XU Bo,SONG Feng-ming,FENG Shu-jie,ZHANG Rong,LIU Hai-tao,ZENG Song-jun.Identification for anthracnose pathogen of Paphiopedilum and selection of its indoor chemical control chemicals[J].Journal of Southern Agriculture,2018,49(2):271-279.
Authors:XU Bo  SONG Feng-ming  FENG Shu-jie  ZHANG Rong  LIU Hai-tao  ZENG Song-jun
Abstract:Objective]Anthracnose pathogen of Paphiopedilum was identified and indoor control chemicals were se-lected to provide theoretical basis for prevention and control of Paphiopedilum anthracnose.Method]The samples of Paphiopedilum with typical anthracnose symptoms were collected.The pathogen was isolated and cultured through tissue isolation.Anthracnose pathogen of Paphiopedilum was identified by morphological observation and rDNA-ITS sequence analysis.The biological characteristics such as pathogen mycelial growth,spore production and spore germination were determined by experiment including indoor temperature,illumination and culture media with different pH values,carbon and nitrogen sources.Sensitivity to 12 fungicides of anthracnose pathogen of Paphiopedilum was tested and then fungi-cides with fine effects were selected to conduct indoor toxicity test.Result]Through morphological observation and rD-NA-ITS sequence analysis,the anamorph of isolated anthracnose pathogen of Paphiopedilum was Colletotrichum gloeo-sporioides,belonging to Colletotrichum,Melanconiales,fungi imperfecti.The temperature for mycelial growth and co-nidial germination was 9℃to 36℃,and the optimal temperature was 27℃.Sporulation temperature was 12-36℃,and the optimum temperature was 30℃.Lethal temperature for C.gloeosporioides mycelia was 55℃maintaining for 20 min, and lethal temperature of conidia was 50℃maintaining for 30 min or 55℃maintaining for 20 min.pH range for both my-celial growth and sporulation was 2-13 and the optimum pH for the both was 8.pH range for conidial germination was 2-12 and the optimum one was 7.Continuous illumination was good for mycelial growth,sporulation and conidial germina-tion.The carbon and nitrogen sources in media had significant difference on mycelial growth,sporulation and conidial germination(P<0.05).Under the concentration 500 mg/L,hymexazol,sulfur·Jialiulin,Fufuxin and prochloraz-manga-nese chloride complex could effectively control mycelial growth and sporulation of anthracnose pathogen,the success rates were both 100.00%.Among the four fungicides,prochloraz had the strongest toxicity and reaction sensitivity,and its concentration for 50% of maximum effect(EC50)was 0.09 mg/L.Conclusion]The anthracnose pathogen of Paphiope-dilum is Colletotrichum gloeosporioides. Hymexazol,sulfur·Jialiulin,Fufuxin and prochloraz can effectively control Paphiopedilum anthracnose,and prochloraz-manganese chloride complex with concentration of 500 mg/L has the best control effects.
Keywords:
本文献已被 CNKI 等数据库收录!
点击此处可从《南方农业学报》浏览原始摘要信息
点击此处可从《南方农业学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号