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Application of Soil-borne Actinomycetes for Biological Control against Fusarium Wilt of Chickpea (Cicer arietinum) caused by Fusarium solani fsp pisi

机译:土传放线菌在防治黄瓜枯萎病引起的鹰嘴豆枯萎病中的应用

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摘要

Black root rot, caused by Fusarium solani f.sp.pisi, is a devastating soil-borne disease in chickpea in Iran with no effective control measures. With the aim of finding applicable biocontrol agents to alleviate the malady, isolates of Actinomycetes isolated from soil and their antagonistic effect against F.solani f.sp.pisi were evaluated both invitro and invivo. More than 100 Actinomycetes isolates were screened for their antifungal activities against the pathogen. The most active isolates were evaluated in greenhouse for their biocontrol performance. Based on the results of dual cultures in screening evaluations, the size of inhibition zone of fungal growth, and the most effective antagonist isolates (S3, S12 and S40) were selected for further studies. Identity of active isolates was determined, in this regard, 16S rDNA of isolates were amplified using universal bacterial primers FD1 and RP2. The PCR products were purified and sequenced. Sequence analysis of 16S rDNA was then performed using NCBI BLAST method. Comparison of the near full length 16S rRNA sequence of isolates to GenBank sequences demonstrated that isolates S3 and S12 were most similar to Streptomyces antibioticus, while isolate S40 was most similar to Streptomyces peruviensis. Biocontrol studies of these isolates in control of the disease in greenhouse significantly decreased the disease severity. Actinomycetes isolate S12 demonstrated the greatest effect in reducing disease than the other two. Results of this research are at preliminary stage for developing biocontrol agents. These data can be utilized as a platform for future studies with the aim of commercializing these biocontrol products and hoping to step towards sustainable agriculture.
机译:由茄枯萎病菌引起的黑根腐烂病是伊朗鹰嘴豆的一种毁灭性土壤传播疾病,没有有效的控制措施。为了找到减轻生病的适用生物防治剂,从土壤中分离了放线菌的分离株以及它们对F.solani f.sp.pisi的拮抗作用。筛选了100多个放线菌分离株对病原体的抗真菌活性。在温室中评估了活性最高的分离株的生物防治性能。根据筛选评估中双重培养的结果,选择真菌生长抑制区的大小以及最有效的拮抗物(S3,S12和S40)进行进一步研究。确定了活性分离物的身份,在这方面,使用通用细菌引物FD1和RP2扩增了分离物的16S rDNA。纯化PCR产物并测序。然后使用NCBI BLAST方法进行16S rDNA的序列分析。分离株的近全长16S rRNA序列与GenBank序列的比较表明,分离株S3和S12与抗生素链霉菌最相似,而分离株S40与秘鲁链霉菌最相似。这些分离株在温室中控制病害的生物防治研究显着降低了病害的严重程度。放线菌分离物S12在减少疾病方面显示出比其他两种方法最大的效果。这项研究的结果处于开发生物防治剂的初步阶段。这些数据可以用作未来研究的平台,目的是将这些生物防治产品商业化并希望迈向可持续农业。

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