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高分辨率熔解分析作为一种强大的工具,可用于区分和基因分型假单胞菌 savastanoi 致病变种和菌株。

High-resolution melting analysis as a powerful tool to discriminate and genotype Pseudomonas savastanoi pathovars and strains.

机构信息

Laboratorio di Patologia Vegetale e Molecolare, Dipartimento di Biotecnologie Agrarie, Università degli Studi di Firenze, Sesto Fiorentino, Firenze, Italy.

出版信息

PLoS One. 2012;7(1):e30199. doi: 10.1371/journal.pone.0030199. Epub 2012 Jan 25.

Abstract

Pseudomonas savastanoi is a serious pathogen of Olive, Oleander, Ash, and several other Oleaceae. Its epiphytic or endophytic presence in asymptomatic plants is crucial for the spread of Olive and Oleander knot disease, as already ascertained for P. savastanoi pv. savastanoi (Psv) on Olive and for pv. nerii (Psn) on Oleander, while no information is available for pv. fraxini (Psf) on Ash. Nothing is known yet about the distribution on the different host plants and the real host range of these pathovars in nature, although cross-infections were observed following artificial inoculations. A multiplex Real-Time PCR assay was recently developed to simultaneously and quantitatively discriminate in vitro and in planta these P. savastanoi pathovars, for routine culture confirmation and for epidemiological and diagnostical studies. Here an innovative High-Resolution Melting Analysis (HRMA)-based assay was set up to unequivocally discriminate Psv, Psn and Psf, according to several single nucleotide polymorphisms found in their Type Three Secretion System clusters. The genetic distances among 56 P. savastanoi strains belonging to these pathovars were also evaluated, confirming and refining data previously obtained by fAFLP. To our knowledge, this is the first time that HRMA is applied to a bacterial plant pathogen, and one of the few multiplex HRMA-based assays developed so far. This protocol provides a rapid, sensitive, specific tool to differentiate and detect Psv, Psn and Psf strains, also in vivo and against other related bacteria, with lower costs than conventional multiplex Real-Time PCR. Its application is particularly suitable for sanitary certification programs for P. savastanoi, aimed at avoiding the spreading of this phytopathogen through asymptomatic plants.

摘要

丁香假单胞菌是橄榄、夹竹桃、悬铃木和其他几种木犀科植物的严重病原体。它在无症状植物中的附生或内生存在对于传播橄榄和夹竹桃结瘤病至关重要,这已经在橄榄上的丁香假单胞菌 pv. savastanoi(Psv)和夹竹桃上的 pv. nerii(Psn)中得到证实,而悬铃木上的 pv. fraxini(Psf)则没有相关信息。目前还不清楚这些致病变种在不同宿主植物上的分布情况,以及它们在自然界中的真实宿主范围,尽管在人工接种后观察到了交叉感染。最近开发了一种多重实时 PCR 检测方法,用于在体外和体内同时定量区分这些丁香假单胞菌致病变种,用于常规培养确认以及流行病学和诊断研究。在这里,根据其 III 型分泌系统簇中发现的几个单核苷酸多态性,建立了一种创新的高分辨率熔解分析(HRMA)检测方法,用于明确区分 Psv、Psn 和 Psf。还评估了属于这些致病变种的 56 株丁香假单胞菌菌株之间的遗传距离,证实并细化了之前通过 fAFLP 获得的数据。据我们所知,这是 HRMA 首次应用于细菌植物病原体,也是迄今为止开发的少数几种多重 HRMA 检测方法之一。该方案提供了一种快速、敏感、特异的工具,可区分和检测 Psv、Psn 和 Psf 菌株,也可在体内和对抗其他相关细菌,成本低于常规多重实时 PCR。其应用特别适合于丁香假单胞菌的卫生认证计划,旨在避免通过无症状植物传播这种植物病原体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d32c/3266268/531e70242f19/pone.0030199.g002.jpg

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