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首页> 外文期刊>Biological Control: Theory and Application in Pest Management >Quantification of Pseudomonas protegens FD6 and Bacillus subtilis NCD-2 in soil and the wheat rhizosphere and suppression of root pathogenic Rhizoctonia solani AG-8
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Quantification of Pseudomonas protegens FD6 and Bacillus subtilis NCD-2 in soil and the wheat rhizosphere and suppression of root pathogenic Rhizoctonia solani AG-8

机译:土壤中假单胞菌氏菌和枯草芽孢杆菌的定量和枯草芽孢杆菌和小麦根际和根部致病性Rhizoctonia solani Ag-8的抑制作用

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摘要

Bacillus subtilis strain NCD-2 and Pseudomonas protegens strain FD6 produce a range of antimicrobial metabolites known to be effective against soil-borne plant pathogens. Quantitative qPCR assays were designed from sequence characterized amplified fragment length polymorphisms (AFLP) diagnostic for each inoculant genotype. The qPCR minimum detection thresholds (MDT) for NCD-2 and FD6 ranged between 5.2 x 10(3) (log 3.71) and 1.5 x 10(6) (log 6.18) genome (cell) equivalents g(-1) of soil or wheat mot tissue and were independent of soil type. Wheat rhizosphere populations of strains FD6 and NCD-2 significantly declined during the first 14 days postinoculation and then remained stable for the next 14 days. Colonization of wheat mots, rhizosphere soil and bulk (nonrhizosphere) soil by FD6 was significantly greater than that of NCD-2. Strains FD6 and NCD-2 significantly decreased in vitro growth of wheat mot pathogenic Rhizoctonia solani AG-8, Pythium irregulare and Gaeumannomyces graminis var. tritici, fungal antibiosis by FD6 greater than NCD-2. Wheat rhizosphere colonization by NCD-2 and FD6 significantly decreased abundance of R. solani AG-8 in the rhizosphere by 3- and 13-fold respectively, pathogen suppression increasing (21%-29%) foliar biomass of wheat seedlings to levels not significantly different to the non-diseased control. The qPCR assays developed in this study were used to monitor soil and rhizosphere populations of P. protegens FD6 and B. subtilis NCD-2 and their suppressive efficacies against R. solani AG-8 in wheat. These assays can be applied to monitor the dynamics of these inoculants in suppressing Rhizoctonia root rot and other crop diseases.
机译:枯草芽孢杆菌菌株NCD-2和假单胞菌蛋白菌株FD6产生一系列已知对土壤传播的植物病原体有效的抗菌代谢产物。根据每个接种基因型的序列特征扩增片段长度多态性(AFLP)诊断设计定量qPCR分析。NCD-2和FD6的qPCR最小检测阈值(MDT)介于土壤或小麦mot组织的5.2 x 10(3)(对数3.71)和1.5 x 10(6)(对数6.18)基因组(细胞)当量g(-1)之间,且与土壤类型无关。菌株FD6和NCD-2的小麦根际种群在伤害后的前14天内显著下降,然后在接下来的14天内保持稳定。FD6对小麦mots、根际土壤和散装(非根际)土壤的定殖作用显著大于NCD-2。菌株FD6和NCD-2显著降低了小麦mot致病性立枯病丝核菌AG-8、不规则腐霉和小麦Gaeumannyces graminis var.tritici的体外生长,FD6对真菌的抗菌作用大于NCD-2。NCD-2和FD6在小麦根际定殖后,根际R.solani AG-8的丰度分别显著降低了3倍和13倍,病原抑制使小麦幼苗的叶生物量(21%-29%)增加到与未发病对照无显著差异的水平。本研究中开发的qPCR分析用于监测P.protegens FD6和B.subtilis NCD-2的土壤和根际种群,以及它们对小麦中R.solani AG-8的抑制效果。这些检测可用于监测这些菌剂抑制丝核菌根腐病和其他作物病害的动态。

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