摘要
本研究以罗伯茨绿僵菌为研究对象,针对5′-3′核糖核酸外切酶基因(MrXrn1,MAA_09154,5′-3′exoribonuclease 1),利用农杆菌介导的同源重组方法进行基因敲除。对获得的MrXrn1基因敲除株(ΔMrXrn1)与野生型进行表型分析结果发现,与野生型相比,ΔMrXrn1的营养生长无明显变化,而产孢能力显著下降,其中产孢量降低了75.75%;以大蜡螟为试虫的体壁侵染毒力分析显示ΔMrXrn1的毒力显著减少,也即半致死时间(LT50:9.16 d)显著长于野生型的(5.96 d),但注射接种情况下不同菌株的毒力无差异;进一步的研究表明ΔMrXrn1的附着孢形成率降低了43.58%。这些结果说明MrXrn1基因对绿僵菌的产孢及毒力起着重要的调控作用。本研究为进一步有效提高真菌杀虫剂的生防效果提供了基础。
In the present study,functional analysis for the gene of MrXrn1(5′-3′exoribonuclease,MAA_09154)was performed by using gene deletion(based on homologous recombination)and phenotypic analysis in Metarhizium robertsii.Our results showed that the conidial yields ofΔMrXrn1 were significantly decreased by 75.75%,compared to the wild-type(WT).More importantly,the results of bioassay showed reduced virulence for theΔMrXrn1 mutants against Galleria mellonella through cuticle infection,the LT50 ofΔMrXrn1 against G.mellonella was markedly longer than that of the WT.However,different fungal strains exhibited similar virulence in the direction injection bioassays.Furthermore,the results of appressorium formation assays showed that the induced appressorium formation rates were markedly decreased by 43.58%for the deletion mutants,compared with the WT.These results indicated that MrXrn1 is involved in the regulation of sporulation and virulence in M.robertsii.Our research provided a basis for improving the biocontrol effect of fungal insecticides.
作者
汪章勋
徐秀珍
冯健雨
周权
黄勃
WANG Zhangxun;XU Xiuzhen;FENG Jianyu;ZHOU Quan;HUANG Bo(Key Laboratory of Biology and Sustainable Management of Plant Diseases and Pests of Anhui Higher Education Institutes/College of Plant Protection,Anhui Agricultural University,Hefei 230036,China;Anhui Provincial Key Laboratory of Microbial Pest Control,Anhui Agricultural University,Hefei 230036,China)
出处
《中国生物防治学报》
CSCD
北大核心
2020年第5期721-728,共8页
Chinese Journal of Biological Control
基金
国家自然科学基金(31572060,31772226,31972332)
安徽省高校自然科学研究重点项目(KJ2019A0192)
安徽省高校优秀青年人才支持计划重点项目(gxyqZD2020007)
国家重点研发计划(2017YFD0200400)。