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基于 pilA 基因序列开发的多重 PCR 检测方法用于检测不同类型的柑橘酸腐病菌。

Development of a multiplex PCR assay based on the pilA gene sequences to detect different types of Acidovorax citrulli.

机构信息

State Key Laboratory for Biology of Plant Diseases and Insect Pests, Chinese Academy of Agricultural Sciences, Institute of Plant Protection, Beijing, China; College of Plant Protection, China Agricultural University, Beijing, China.

Department of Plant Pathology, University of Georgia, Athens, GA, USA.

出版信息

J Microbiol Methods. 2019 Mar;158:93-98. doi: 10.1016/j.mimet.2019.02.003. Epub 2019 Feb 8.

Abstract

Bacterial fruit blotch (BFB) of cucurbits, caused by Acidovorax citrulli, is a major threat to commercial watermelon and melon production worldwide. At present, there are at least two genetically distinct sub-populations (group I and II) of A. citrulli that differ in host preference among cucurbit species and copper sensitivity. In this study, we analyzed the pilA gene sequences of 103 A. citrulli strains from China and other countries. Based on these data, we classified all tested A. citrulli strains into three types. The pilA-based type 1 strains in this study coincided with the previously established group I strains; while the type 2 strains coincided with group II strains. Ten strains that did not cluster with group I or II strains were classified into a new type, designated type 3. Based on differences in pilA sequences, we designed a multiplex PCR assay to distinguish the three A. citrulli pilus types. This multiplex PCR assay has proven to be viable for strain typing of 139 A. citrulli strains and for the detection of this pathogen in artificially inoculated seeds and leaves and naturally infected leaves and fruits. This assay proved to be rapid, accurate, reliable and applicable for early distinction of A. citrulli types associated with BFB epidemics. It may also inform the judicious and environmentally sound use of bactericides, especially copper-based compounds.

摘要

细菌果斑病(BFB)是由酸噬果胶杆菌(Acidovorax citrulli)引起的一种主要病害,对全球商业西瓜和甜瓜生产构成严重威胁。目前,酸噬果胶杆菌至少存在两个在宿主偏好和铜敏感性方面存在差异的遗传上明显不同的亚群(I 组和 II 组)。在本研究中,我们分析了来自中国和其他国家的 103 株酸噬果胶杆菌的 pilA 基因序列。基于这些数据,我们将所有测试的酸噬果胶杆菌菌株分为三种类型。本研究基于 pilA 的 I 型菌株与先前建立的 I 组菌株一致;而 II 型菌株与 II 组菌株一致。10 株与 I 组或 II 组菌株不聚类的菌株被归类为新的 III 型。基于 pilA 序列的差异,我们设计了一种多重 PCR 检测方法来区分三种酸噬果胶杆菌菌毛类型。该多重 PCR 检测方法已被证明可用于 139 株酸噬果胶杆菌菌株的分型,以及人工接种种子和叶片、自然感染叶片和果实中该病原体的检测。该检测方法快速、准确、可靠,适用于早期区分与 BFB 流行相关的酸噬果胶杆菌类型。它还可以为合理和环保地使用杀菌剂,特别是铜基化合物提供信息。

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