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通过菌株特异性PCR标记从目标杂草苘麻和土壤中检测生防菌炭疽菌(183088)。

Detection of the biocontrol agent Colletotrichum coccodes (183088) from the target weed velvetleaf and from soil by strain-specific PCR markers.

作者信息

Dauch A L, Watson A K, Jabaji-Hare S H

机构信息

Department of Plant Science, Macdonald Campus of McGill University, 21, 111 Lakeshore Road, Raymond Building, Ste-Anne de Bellevue, Québec, H9X 3V9, Canada.

出版信息

J Microbiol Methods. 2003 Oct;55(1):51-64. doi: 10.1016/s0167-7012(03)00116-7.

Abstract

Diagnostic molecular markers, generated from random amplified polymorphic DNA (RAPD) and used in polymerase chain reaction (PCR), were developed to selectively recognize and detect the presence of a single strain of the biocontrol fungus Colletotrichum coccodes (183088) on the target weed species Abutilon theophrasti and from soil samples. Several isolates of C. coccodes, 15 species of Colletotrichum, a variety of heterogeneous organisms and various plant species were first screened by RAPD-PCR, and a strain specific marker was identified for C. coccodes (183088). No significant sequence similarity was found between this marker and any other sequences in the databases. The marker was converted into a sequence-characterised amplified region (SCAR), and specific primer sets (N5F/N5R, N5Fi/N5Ri) were designed for use in PCR detection assays. The primer sets N5F/N5R and N5Fi/N5Ri each amplified a single product of 617 and 380 bp, respectively, with DNA isolated from strain 183088. The specificity of the primers was confirmed by the absence of amplified products with DNA from other C. coccodes isolates, other species representing 15 phylogenetic groups of the genus Colletotrichum and 11 other organisms. The SCAR primers (N5F/N5R) were successfully used to detect strain 183088 from infected velvetleaf plants but not from seeded greenhouse soil substrate or from soil samples originating from deliberate-released field experiments. The sensitivity of the assay was substantially increased 1000-fold when nested primers (N5Fi/N5Ri) were used in a second PCR run. N5Fi/N5Ri selectively detected strain 183088 from seeded greenhouse soils as well as from deliberate-released field soil samples without any cross-amplification with other soil microorganisms. This rapid PCR assay allows an accurate detection of C. coccodes strain 183088 among a background of soil microorganisms and will be useful for monitoring the biocontrol when released into natural field soils.

摘要

利用随机扩增多态性DNA(RAPD)技术并应用于聚合酶链反应(PCR),开发了诊断分子标记,用于选择性识别和检测目标杂草物种苘麻以及土壤样本中生物防治真菌可可毛色二孢(183088)单一菌株的存在。首先通过RAPD-PCR对几种可可毛色二孢分离株、15种炭疽菌属物种、多种异源生物和各种植物物种进行筛选,确定了可可毛色二孢(183088)的菌株特异性标记。该标记与数据库中的任何其他序列均无显著序列相似性。将该标记转化为序列特征性扩增区域(SCAR),并设计了特异性引物对(N5F/N5R、N5Fi/N5Ri)用于PCR检测分析。引物对N5F/N5R和N5Fi/N5Ri分别从菌株183088分离的DNA中扩增出一条617 bp和380 bp的单一产物。通过使用来自其他可可毛色二孢分离株、代表炭疽菌属15个系统发育组的其他物种以及11种其他生物的DNA未扩增出产物,证实了引物的特异性。SCAR引物(N5F/N5R)成功用于从受感染的苘麻植物中检测菌株183088,但不能从播种的温室土壤基质或来自故意释放田间试验的土壤样本中检测到。当在第二次PCR反应中使用巢式引物(N5Fi/N5Ri)时,检测灵敏度大幅提高了1000倍。N5Fi/N5Ri能够从播种的温室土壤以及故意释放的田间土壤样本中选择性检测菌株183088,且不会与其他土壤微生物发生交叉扩增。这种快速PCR检测方法能够在土壤微生物背景中准确检测可可毛色二孢菌株183088,对于监测其释放到自然田间土壤中的生物防治效果将非常有用。

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