First report of paprika as a natural host plant for tomato chlorosis virus in Korea.

IF 4.4 2区 农林科学 Q1 PLANT SCIENCES
Hae-Ryun Kwak, Dong-Wan Kang, Hee-Seong Byun, Bongchoon Lee, Inyoung Han
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引用次数: 0

Abstract

Paprika (Capsicum annuum var. grossum (L.) Sendtn.), also called bell pepper or sweet pepper, is a valuable greenhouse crop that is mostly consumed as fresh fruit in Korea. In 2022, it was cultivated on 726 ha in Korea and 82,042 tons were produced (KOSIS, 2023). In April 2023, interveinal chlorosis and yellowing were observed on the lower and middle leaves of greenhouse paprika in Jinju and Haman, South Korea, and many whiteflies (Bemisia tabaci) were present. The disease incidence was 30-40% on five farms (approximately 4.5 ha) in the two areas. The typical symptoms and presence of whiteflies in greenhouses indicated potential infection by the whitefly-transmitted crinivirus, tomato chlorosis virus (ToCV). Six samples collected from symptomatic plants were examined by leaf dip using transmission electron microscopy (TEM) and revealed filamentous virus particles about 800 nm long. To confirm the TEM results, six symptomatic paprika leaf samples were subject to RT-PCR using the specific primers ToCV-M-4F and ToCV-M-4R to detect ToCV (Choi, 2023). All tested samples were positive for ToCV. To confirm the presence of other viruses and obtain the complete genome sequences, one of the six ToCV-positive samples (ToCV-PAP-JJ6) was subject to high-throughput sequencing (HTS). Total RNA was extracted from symptomatic leaves using the RNeasy Plant Mini Kit (QIAGEN, Germany) and a transcriptome library was generated using the TruSeq Stranded Total RNA LT Sample Prep Kit (Illumina, San Diego, CA, USA) according to standard protocols. HTS was performed on an Illumina NovaSeq 6000 system (Macrogen, Korea). De novo transcriptome assembly of the 85,668,854 reads with Trinity software (r20140717) yielded 817,303 contigs of 201 to 38,987 nucleotides (nt). BLASTn and BLASTx analysis of the contigs against the NCBI viral reference database showed that three large contigs were virus sequences, two of which were homologous to ToCV-RNA1 and -RNA2 and one to bell pepper alphaendornavirus (BPEV). The ToCV-RNA1 (genome 8,594 nt, 11,212 mapped reads, mean read coverage 196.2 times) and ToCV-RNA2 (genome 8,242 nt, 40,122 mapped reads, mean read coverage 734.9 times) contigs showed 100% coverage and 99% base pair matching (8,583/8,594 and 8,233/8,242, respectively) with known genome sequences of ToCV-RNA1 (MG813908) and ToCV-RNA2 (KP114534) isolated from tomato in Korea (Lee et al. 2018). The sequences were deposited in GenBank as isolates ToCV-PAP-JJ6 RNA1 (OR865222) and ToCV-PAP-JJ6 RNA2 (OR865223). The BPEV contig (genome 14,728 nt, 2,928,519 mapped reads, mean read coverage 15,012.4 times) was detected at very high read depth and RT-PCR for BPEV confirmed that all six samples were coinfected with ToCV. BPEV was recently reported in paprika and red pepper in Korea (Jo et al., 2022). The BPEV-infected pepper cultivars have been reported not to produce any symptoms (Escalante & Valverde 2019). ToCV was first reported in tomato greenhouses in Korea in 2013 and is a problematic virus in tomato crops, along with tomato yellow leaf curl virus (Jo et al. 2023; Lee et al. 2018). Due to the continuous presence of ToCV, whiteflies, and natural weed hosts (Kil et al. 2015) in tomato greenhouses, ToCV has spread to other crops, including paprika. To the best of our knowledge, this is the first report of ToCV infecting paprika in Korea. A nationwide study is needed to prevent the spread of ToCV, a new threat to paprika farms.

在韩国首次报告辣椒是番茄萎黄病病毒的天然宿主植物。
辣椒(Capsicum annuum var.2022 年,韩国的种植面积为 726 公顷,产量为 82 042 吨(KOSIS,2023 年)。2023 年 4 月,在韩国晋州和咸安,温室红辣椒的中下部叶片出现叶脉间枯萎和黄化现象,并有许多粉虱(Bemisia tabaci)。这两个地区的五个农场(约 4.5 公顷)的发病率为 30-40%。温室中的典型症状和粉虱的存在表明可能感染了由粉虱传播的番茄萎黄病病毒(ToCV)。利用透射电子显微镜(TEM)对从有症状植株上采集的六个样本进行了叶片浸渍检查,发现了长约 800 nm 的丝状病毒颗粒。为了证实透射电子显微镜的结果,使用特异引物 ToCV-M-4F 和 ToCV-M-4R 对六个有症状的辣椒叶片样本进行了 RT-PCR 检测(Choi,2023 年)。所有检测样本对 ToCV 均呈阳性。为了确认是否存在其他病毒并获得完整的基因组序列,对六个 ToCV 阳性样本中的一个(ToCV-PAP-JJ6)进行了高通量测序(HTS)。使用 RNeasy Plant Mini Kit(QIAGEN,德国)从有症状的叶片中提取总 RNA,并按照标准协议使用 TruSeq Stranded Total RNA LT Sample Prep Kit(Illumina,San Diego, CA, USA)生成转录组文库。HTS 在 Illumina NovaSeq 6000 系统(Macrogen,韩国)上进行。使用 Trinity 软件(r20140717)对 85,668,854 个读数进行从头转录组组装,得到 817,303 个 201 至 38,987 个核苷酸(nt)的等位组。对照 NCBI 病毒参考数据库对等位基因进行的 BLASTn 和 BLASTx 分析表明,有三个大的等位基因是病毒序列,其中两个与 ToCV-RNA1 和 -RNA2 同源,一个与甜椒α-内多角体病毒(BPEV)同源。ToCV-RNA1 (基因组 8,594 nt,11,212 个映射读数,平均读数覆盖率 196.2 倍)和 ToCV-RNA2 (基因组 8,242 nt,40,122 个映射读数,平均读数覆盖率 734.9倍)等位基因与已知的从韩国番茄中分离出来的ToCV-RNA1(MG813908)和ToCV-RNA2(KP114534)的基因组序列(Lee等人,2018年)显示出100%的覆盖率和99%的碱基对匹配率(分别为8,583/8,594和8,233/8,242)。这些序列作为分离物 ToCV-PAP-JJ6 RNA1 (OR865222) 和 ToCV-PAP-JJ6 RNA2 (OR865223) 保存在 GenBank 中。BPEV contig(基因组 14,728 nt,2,928,519 个映射读数,平均读数覆盖率 15,012.4 倍)以极高的读数深度被检测到,BPEV 的 RT-PCR 检测证实所有六个样本都同时感染了 ToCV。最近在韩国的辣椒和红辣椒中发现了 BPEV(Jo 等人,2022 年)。据报道,受 BPEV 感染的辣椒品种不会产生任何症状(Escalante & Valverde,2019 年)。ToCV 于 2013 年首次在韩国的番茄温室中被报道,与番茄黄叶卷曲病毒一起成为番茄作物中的问题病毒(Jo 等,2023 年;Lee 等,2018 年)。由于番茄温室中持续存在 ToCV、粉虱和天然杂草宿主(Kil 等,2015 年),ToCV 已扩散到其他作物,包括辣椒。据我们所知,这是韩国首次报道 ToCV 感染辣椒。需要在全国范围内开展研究,以防止 ToCV 的传播,这是对辣椒农场的一个新威胁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Plant disease
Plant disease 农林科学-植物科学
CiteScore
5.10
自引率
13.30%
发文量
1993
审稿时长
2 months
期刊介绍: Plant Disease is the leading international journal for rapid reporting of research on new, emerging, and established plant diseases. The journal publishes papers that describe basic and applied research focusing on practical aspects of disease diagnosis, development, and management.
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