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基于III型效应子的多重PCR检测十字花科作物中引起黑腐病的pv.

The type-III effectors-based multiplex PCR for detection of pv. causing black rot disease in crucifer crops.

作者信息

Singh Dinesh, Kesharwani Amit Kumar, Avasthi Anupama Sharma

机构信息

Division of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012 India.

Amity Institute of Biotechnology, Amity University, Noida, Uttar Pradesh 201303 India.

出版信息

3 Biotech. 2023 Aug;13(8):272. doi: 10.1007/s13205-023-03691-z. Epub 2023 Jul 11.

DOI:10.1007/s13205-023-03691-z
PMID:37449249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10335992/
Abstract

UNLABELLED

The black rot disease in crucifer crops is caused by pv. (Xcc) which drastically reduces the productivity of crops. Three Xcc races, such as races 1, 4, and 6, have been identified from India that possess nine avr genes, or type-III effectors (T3Es). Here, we used three T3Es- and to identify Xcc from bacterial DNA, bacterial suspensions, Xcc-infected seeds, and the sap of the infected leaves using multiplex PCR. The T3Es were amplified using gene-specific primers with gDNA of Xcc. Then, the multiplex PCR was optimized and amplified T3Es using the sap of black rot-infected cauliflower leaves. Further, this method amplified T3Es from artificially infected seeds (1-100%) of cauliflower and from Xcc colonies (0.1-100%) grown on nutrient agar medium. The primer specificity of T3E genes elucidates that these are specifically detected in all Indian Xcc strains and races, while no bands were observed with other unrelated bacteria, such as pv. , , , , and . Further, this PCR possesses high sensitivity and amplifies T3E genes using up to 0.01 ng Xcc DNA. The high specificity and sensitivity of T3Es-based multiplex PCR make it a potential method and can be used to amplify Xcc from various templates, such as purified DNA, Xcc-infected seeds and leaves, crude extracts, etc., without the need to extract plant or bacterial DNA.

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1007/s13205-023-03691-z.

摘要

未标记

十字花科作物的黑腐病由野油菜黄单胞菌致病变种(Xcc)引起,该病会大幅降低作物产量。已从印度鉴定出三种Xcc小种,即小种1、4和6,它们拥有9个无毒基因或III型效应因子(T3Es)。在此,我们使用三种T3Es,通过多重PCR从细菌DNA、细菌悬液、Xcc感染的种子以及感染叶片的汁液中鉴定Xcc。使用Xcc的基因组DNA和基因特异性引物扩增T3Es。然后,对多重PCR进行优化,并使用黑腐病感染的花椰菜叶片的汁液扩增T3Es。此外,该方法还能从人工感染的花椰菜种子(1 - 100%)和在营养琼脂培养基上生长的Xcc菌落(0.1 - 100%)中扩增T3Es。T3E基因的引物特异性表明,这些基因能在所有印度Xcc菌株和小种中被特异性检测到,而在其他不相关细菌中未观察到条带,如油菜黄单胞菌致病变种、丁香假单胞菌、荧光假单胞菌、嗜麦芽窄食单胞菌和成团泛菌。此外,该PCR具有高灵敏度,使用低至0.01 ng的Xcc DNA就能扩增T3E基因。基于T3Es的多重PCR的高特异性和灵敏度使其成为一种有潜力的方法,可用于从各种模板(如纯化的DNA、Xcc感染的种子和叶片、粗提物等)中扩增Xcc,而无需提取植物或细菌DNA。

补充信息

在线版本包含可在10.1007/s13205 - 023 - 03691 - z获取的补充材料。