Cho In Sook, Kim Tae-Bok, Yoon Ju-Yeon, Chung Bong Nam, Hammond John, Lim Hyoun-Sub
Rural Development Administration, National Institute of Horticultural & Herbal Sciences, 30,Subong-ro, Gwonseon-gu, Suwon-si, Gyeonggi-do, Suwon, Korea (the Republic of), 441-440.
Korea (the Republic of);
Plant Dis. 2021 Feb 2. doi: 10.1094/PDIS-11-20-2375-PDN.
In December 2018, virus-like symptoms (yellowing, vein clearing) were observed on 2% of muskmelon (Cucumis melo L.) plants in plastic houses on a farm in Gyeongsang province, Korea Total RNA from two symptomatic and two asymptomatic plants was extracted using RNeasy Plant Mini Kit (Qiagen, Germany) for high throughput sequencing (HTS). After pre-processing and Ribo-Zero rRNA removal, a cDNA library was prepared (Illumina TruSeq Stranded Total RNA kit) and sequenced (Illumina NovaSeq 6000 system: Macrogen Inc. Korea). De novo assembly of 88,222,684 HTS reads with Trinity software (r20140717) yielded 146,269 contigs of 201-28,442 bp, which were screened against the NCBI viral genome database by BLASTn. Contigs from cucumber mosaic virus (CMV), melon necrotic spot virus (MNSV), tobacco mosaic virus (TMV) and watermelon mosaic virus (WMV) were identified, all previously reported in Korea. Two contigs (8,539 and 8,040 bp) with 99.9% sequence identity to distinct cucurbit chlorotic yellows virus (CCYV) isolates (JN641883, RNA1, Taiwan; MH819191, RNA2, China) were also identified. The ten sequences most closely related to each RNA of the Korean isolate (≥99% coverage, ≥99.6% nt identity) were from Japan, China, Taiwan, or Israel. CCYV presence was confirmed by reverse transcription-PCR (RT-PCR) using newly designed specific primers, RdRp-F/RdRp-R (5'-ACCGAACACTTGGCTATCCAA-3'/5'-CTTAATGCCGCGTATGAACTCA-3') span style="font-family:'Times New Roman'; letter-spacing:-0.5pt">and HSP-F/HSP-R (5'-TGAACGACACTGAGTTCATTCCTA-3'/5'-CGCCAAGATCGTACATGAGGAA-3'), against RNA dependent RNA polymerase (RdRp; RNA1) and the heat shock protein 70 homolog (HSP70h; RNA2). Symptomatic samples yielded products of expected sizes (RdRp,450 bp; HSP70h, 510 bp) while asymptomatic samples did not. The amplicons were cloned, and two clones of each were sequenced (BIONEER, Korea; GenBank acc. nos. LC592226 and LC592227) showing 100% and 99.2% nt identity with RdRp and HSP70h genes of Chinese CCYV isolate SD (MH819190 and MH819191, respectively) and other Asian isolates. Primers specific for CMV, WMV, beet pseudo-yellows virus (BPYV) (Okuda et al., 2007), TMV (Kim et al., 2018), MNSV (F/R, 5'-ATCTCGCATTTGGCATTACTC-3'/5'-ATTTGTAGAGATGCCAACGTA-3'), cucurbit yellow stunting disorder virus (CYSDV; Zeng et al., 2011) and cucurbit aphid-borne yellows virus (CABYV; F/R, 5'-CGGTCTATTGTCTGCAGTACCA-3'/5'- GTAGAGGATCTTGAATTGGTCCTCA-3') were also used. None of these viruses were detected in the symptomatic samples, but both asymptomatic plants were positive for CMV and WMV, and one also for MNSV. In June and September 2020, muskmelon and oriental melon (Cucumis melo L. var. makuwa) plants with yellowing disease (incidence 80-90%) and whiteflies were observed in all investigated plastic houses of one muskmelon and one oriental melon farm in Gyeonggi and Jeolla provinces. Symptomatic samples (14 muskmelon; 6 oriental melon) were collected and RT-PCR tested as above; 19/20 samples were positive for CCYV, but none for the other viruses. The oriental melon sequence (LC592895, LC592230) showed 99.7% and 100% nt identity with the RdRp and HSP70h genes of Chinese isolate SD, respectively. CCYV was first reported in Japan (Okuda et al., 2010), Taiwan, and China (Huang et al., 2010; Gu et al., 2011); to our knowledge, this is the first report of CCYV infecting muskmelon and oriental melon in Korea. Whitefly-transmitted CCYV could present a serious threat of yield losses to cucurbit crops in Korea, requiring control of vector populations to prevent spread of CCYV.
2018年12月,在韩国庆尚南道一个农场的塑料大棚中,2%的甜瓜(Cucumis melo L.)植株出现了类似病毒的症状(发黄、叶脉失绿)。使用RNeasy Plant Mini试剂盒(德国Qiagen公司)从两株有症状和两株无症状的植株中提取总RNA,用于高通量测序(HTS)。经过预处理和去除Ribo-Zero核糖体RNA后,制备了cDNA文库(Illumina TruSeq Stranded Total RNA试剂盒)并进行测序(Illumina NovaSeq 6000系统:韩国Macrogen公司)。使用Trinity软件(r20140717)对88,222,684条高通量测序读数进行从头组装,得到了146,269个重叠群,长度为201 - 28,442 bp,通过BLASTn在NCBI病毒基因组数据库中进行筛选。鉴定出了黄瓜花叶病毒(CMV)、甜瓜坏死斑点病毒(MNSV)、烟草花叶病毒(TMV)和西瓜花叶病毒(WMV)的重叠群,这些病毒此前在韩国均有报道。还鉴定出了两个与不同的葫芦褪绿黄化病毒(CCYV)分离株(台湾的JN641883,RNA1;中国的MH819191,RNA2)具有99.9%序列同一性的重叠群(8,539和8,040 bp)。与韩国分离株的每个RNA最密切相关的十个序列(覆盖率≥99%,核苷酸同一性≥99.6%)来自日本、中国、台湾或以色列。使用新设计的特异性引物RdRp-F/RdRp-R(5'-ACCGAACACTTGGCTATCCAA-3'/5'-CTTAATGCCGCGTATGAACTCA-3')和HSP-F/HSP-R(5'-TGAACGACACTGAGTTCATTCCTA-3'/5'-CGCCAAGATCGTACATGAGGAA-3')通过逆转录PCR(RT-PCR)确认了CCYV的存在,这两对引物分别针对RNA依赖的RNA聚合酶(RdRp;RNA1)和热休克蛋白70同源物(HSP70h;RNA2)。有症状的样本产生了预期大小的产物(RdRp为450 bp;HSP70h为510 bp),而无症状的样本没有。扩增产物被克隆,每个克隆的两个克隆进行了测序(韩国BIONEER公司;GenBank登录号LC592226和LC592227),显示与中国CCYV分离株SD的RdRp和HSP70h基因具有100%和99.2%的核苷酸同一性,以及与其他亚洲分离株的情况。还使用了针对CMV、WMV、甜菜假黄化病毒(BPYV)(Okuda等人,2007)、TMV(Kim等人,2018)、MNSV(F/R,5'-ATCTCGCATTTGGCATTACTC-3'/5'-ATTTGTAGAGATGCCAACGTA-3')、葫芦黄化矮化病毒(CYSDV;Zeng等人,2011)和葫芦蚜传黄化病毒(CABYV;F/R,5'-CGGTCTATTGTCTGCAGTACCA-3'/5'- GTAGAGGATCTTGAATTGGTCCTCA-3')的特异性引物。在有症状的样本中未检测到这些病毒,但两株无症状植株对CMV和WMV呈阳性,其中一株对MNSV也呈阳性。2020年6月和9月,在京畿道和全罗道的一个甜瓜农场和一个东方甜瓜农场的所有调查塑料大棚中,观察到有发黄病(发病率80 - 90%)的甜瓜和东方甜瓜(Cucumis melo L. var. makuwa)植株以及粉虱。采集了有症状的样本(14个甜瓜样本;6个东方甜瓜样本)并如上进行RT-PCR检测;20个样本中有19个对CCYV呈阳性,但对其他病毒均为阴性。东方甜瓜序列(LC592895,LC592230)分别与中国分离株SD的RdRp和HSP70h基因具有99.7%和100%的核苷酸同一性。CCYV首次在日本(Okuda等人,2010)、台湾和中国(Huang等人,2010;Gu等人,2011)被报道;据我们所知,这是CCYV在韩国感染甜瓜和东方甜瓜的首次报道。粉虱传播的CCYV可能对韩国的葫芦科作物产量造成严重损失,需要控制媒介种群以防止CCYV传播。