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韩国首次报告携带抗性基因的感染抗性突破菌株。

First report of a resistance-breaking strain of infecting carrying the resistance gene in South Korea.

作者信息

Yoon Ju-Yeon, Her Nam-Han, Cho In Sook, Chung Bong Nam, Choi Seung-Kook

机构信息

National Institute of Horticultural & Herbal Science, 100 Nongsaengmyeong ro, Iseomyeon, Wanju, Korea (the Republic of), 55365;

Department of Plant Pathology, Anseong-si, Gyeonggi-do, Korea (the Republic of);

出版信息

Plant Dis. 2021 Feb 16. doi: 10.1094/PDIS-09-20-1952-PDN.

Abstract

(TSWV) was first reported in 2004 from paprika in South Korea (Kim et al., 2004), where it is currently widespread. TSWV infections were reported in chili pepper, tomato, weeds, and ornamental plant species in South Korea (Choi et al., 2014; Choi and Choi, 2015; Yoon et al., 2016; Yoon et al., 2018; Yoon et al., 2019). One of the best strategies for TSWV management is planting resistant cultivars containing the Tsw gene. In 2019 virus-like symptoms were observed in chili pepper (Capsicum annuum) plants bearing the Tsw gene in Anseong-si, South Korea. The infected chili peppers showed mosaic and wilting followed by necrosis on leaves and fruits in the field. To identify the causal virus, symptomatic leaf samples were analyzed using ImmunoStrip kits (Agdia, USA); we detected three pepper-infecting viruses: Pepper mild mottle virus, Cucumber mosaic virus, and TSWV. TSWV was only detected from 40 naturally infected chili pepper plants exhibiting virus-like symptoms. To further confirm the presence of TSWV (named TSWV-P1), we amplified reverse-transcription polymerase chain reaction (RT-PCR) products for L, M, and S RNA segments using tospovirus-specific and TSWV-specific primers (Batuman et al., 2014). Expected fragments of 445, 868, and 777 bp in length were amplified and sequenced. The complete genome sequences of TSWV-P1 from a symptomatic chili pepper plant were also determined using TSWV-specific primers (Choi et al., 2014; Lian et al., 2013). The complete genome sequences of TSWV-P1 were deposited to GenBank (LC549179, LC549180, and LC549181). The sequences of each fragment were identical to a consensus sequence, showing 99.1%, 98.5%, and 98.6% identity with TSWV-L, M, and S RNA (KP008132, AY744492, and KP008134), respectively. These results clearly showed only a single TSWV infection among the naturally infected chili pepper plants, without reassortment between TSWV and another tospovirus. To confirm whether TSWV-P1 is a resistance-breaking (RB) strain, Nicotiana rustica was mechanically inoculated with sap from leaves of the infected pepper samples to propagate TSWV-P1. A non-RB TSWV isolate (TSWV-Kor-lisianthus) from lisianthus was used as a control (Yoon et al., 2017). Two resistant (with Tsw) and two susceptible chili pepper cultivars (20 plants per cultivar) were mechanically inoculated with sap from leaves of the TSWV-infected N. rustica. The incidence rates of disease caused by TSWV-P1 were 90-100% for resistant and 95-100% for susceptible cultivars. In contrast, TSWV-Kor-lisianthus caused symptoms only in the susceptible pepper cultivars (90-100% incidence). TSWV infection in representative plants was confirmed using the TSWV- ImmunoStrip kit and RT-PCR. The NSs gene of TSWV-P1 consists of 1,404 nucleotides (468 amino acids); sequence analysis of the TSWV-P1 NSs gene showed high nucleotide (99.7%) and amino acid identities (99.8%) with the NSs sequences of two TSWV isolates (FR693035, CBX24121). Protein sequence analysis of TSWV-P1 NSs revealed that no amino acid mutation was associated with those of a representative TSWV RB strain, as previously described (Almási et al., 2017), suggesting that TSWV-P1 is a RB strain. Because this TSWV-P1 can overcome resistance conferred by the Tsw gene in commercially grown chili pepper cultivars, it represents a potential threat to pepper production in South Korea.

摘要

番茄斑萎病毒(TSWV)于2004年首次在韩国的甜椒中被报道(Kim等人,2004年),目前在韩国广泛传播。韩国曾报道在辣椒、番茄、杂草和观赏植物品种中发现TSWV感染(Choi等人,2014年;Choi和Choi,2015年;Yoon等人,2016年;Yoon等人,2018年;Yoon等人,2019年)。TSWV管理的最佳策略之一是种植含有Tsw基因的抗性品种。2019年,在韩国安城市携带Tsw基因的辣椒(Capsicum annuum)植株上观察到病毒样症状。田间受感染的辣椒出现花叶和萎蔫,随后叶片和果实坏死。为了鉴定致病病毒,使用免疫试纸条试剂盒(美国Agdia公司)对有症状的叶片样本进行分析;我们检测到三种感染辣椒的病毒:辣椒轻斑驳病毒、黄瓜花叶病毒和TSWV。仅在40株表现出病毒样症状的自然感染辣椒植株中检测到TSWV。为了进一步确认TSWV(命名为TSWV-P1)的存在,我们使用番茄斑萎病毒特异性引物和TSWV特异性引物(Batuman等人,2014年)扩增了L、M和S RNA片段的逆转录聚合酶链反应(RT-PCR)产物。扩增出预期长度分别为445、868和777 bp的片段并进行测序。还使用TSWV特异性引物确定了来自有症状辣椒植株的TSWV-P1的完整基因组序列(Choi等人,2014年;Lian等人,2013年)。TSWV-P1的完整基因组序列已存入GenBank(LC549179、LC549180和LC549181)。每个片段的序列与一个共有序列相同,与TSWV-L、M和S RNA(KP008132、AY744492和KP008134)的同一性分别为99.1%、98.5%和98.6%。这些结果清楚地表明,在自然感染的辣椒植株中仅存在单一的TSWV感染,TSWV与另一种番茄斑萎病毒之间没有重配。为了确认TSWV-P1是否是一个打破抗性(RB)的菌株,用感染辣椒样本叶片的汁液对黄花烟草进行机械接种以繁殖TSWV-P1。来自洋桔梗的一个非RB TSWV分离株(TSWV-Kor-lisianthus)用作对照(Yoon等人,2017年)。用来自感染TSWV的黄花烟草叶片的汁液对两个抗性(含Tsw)和两个感病辣椒品种(每个品种20株)进行机械接种。TSWV-P1引起的发病率在抗性品种中为90 - 100%,在感病品种中为95 - 100%。相比之下,TSWV-Kor-lisianthus仅在感病辣椒品种中引起症状(发病率为90 - 100%)。使用TSWV免疫试纸条试剂盒和RT-PCR确认了代表性植株中的TSWV感染。TSWV-P1的NSs基因由1404个核苷酸(468个氨基酸)组成;TSWV-P1 NSs基因的序列分析显示,与两个TSWV分离株(FR693035、CBX24121)的NSs序列具有高核苷酸同一性(99.7%)和氨基酸同一性(99.8%)。TSWV-P1 NSs的蛋白质序列分析表明,没有氨基酸突变与先前描述的代表性TSWV RB菌株相关(Almási等人,2017年),这表明TSWV-P1是一个RB菌株。由于这种TSWV-P1能够克服商业种植的辣椒品种中Tsw基因赋予的抗性,它对韩国的辣椒生产构成了潜在威胁。

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