Kumar Manish, Torrance Ty, McAvoy Theodore, Bag Sudeep
University of Georgia - Tifton Campus, 117299, Plant Pathology, Tifton, Georgia, United States;
University of Georgia College of Agricultural and Environmental Sciences, 96665, Extension Service , 1468 Carpenter Road South, Tifton, Georgia, United States, 31793;
Plant Dis. 2024 Jan 22. doi: 10.1094/PDIS-12-23-2628-PDN.
Tomatillo (Physalis philadelphica L.) is an annual plant native to Mexico and Guatemala, and cultivated in other tropical and subtropical regions. In October 2023, tomatillo plants with interveinal yellowing of leaves, marginal chlorosis, leaf thickening, and leaf rolling symptoms (Figure 1) were observed at Colquitt and Tift County, Georgia, US. The disease incidence ranged from 80-100 % which reduced fruit quality and marketability. Twenty tomatillo leaves exhibiting severe symptoms were collected, and, sub-sampled of the leaves were pooled into microcentrifuge tubes. Further, MagMAX 96 viral RNA isolation kit (Thermo Fisher Scientific, US), was used for the extraction of (n=4) total nucleic acid (TNA) (Kavalappara et al. 2021). Symptomatic leaves were tested for the presence of insect-transmitted viruses such as begomovirus (tomato yellow leaf curl virus, TYLCV), potyvirus (turnip mosaic virus, TuMV), crinivirus (tomato infectious chlorosis virus, TICV; tomato chlorosis virus, ToCV), and tospovirus (orthotospovirus tomatomaculae, TSWV). Polymerase chain reaction (PCR) was performed for detecting TYLCV, using gene-specific primers (Kumar et al., 2023). However, for ToCV, TuMV and TICV detection, cDNA was prepared using 100 ng of TNA as a template, followed by the PCR ( Liu et al., 2012). Moreover, the detection of TSWV was conducted using immuno-strips (Adgia, US) following the manufacturer's instructions. ToCV was detected from all the tested samples, while TuMV, TICV, TYLCV and TSWV were not detected in any symptomatic tissues. In addition, RT-PCR was performed using gene-specific primers targeting the RNA-dependent RNA polymerase (RdRP) gene and the heat-shock protein 70 (Hsp70) gene of ToCV. The PCR amplicon of 439 bp encoding Hsp70 and 643 bp corresponding to RdRP was gel-purified and Sanger sequenced (Azenta Life Sciences, US). BLASTn analysis shows RdRP gene from ToCV-tomatillo (OR905600) has 100 % identity with ToCV of RNA1 segment (RdRP, GenBank accession no. AY903447, Florida, US), while Hsp70 gene (OR900219) has 100 % identity with ToCV of RNA2 segment (Hsp70, GenBank accession no. LC778246, Cairo, Egypt). In addition, the symptomatic tomatillo leaves were studied for transmission assay using tomato, employing non-viruliferous whiteflies (Bemisia tabaci) with 48 h of acquisition access period. Further, two weeks post-infection, the presence of ToCV was detected from the test plants while other whitefly-transmitted viruses remins undetected. In 2023, ToCV is widespread in tomato-growing counties, infecting commercially grown tomato cultivars with intermediate resistance against TYLCV-IL (Israel strain). However, tomatillo plants infected with TuMV in California (Liu et al., 2012), TSWV in Georgia, (Díaz-Pérez and Pappu 2000) and TYLCV in Mexico (Gámez-Jiménez et al. 2009) were reported. This study suggests that tomatillo could be a permissive host for ToCV while restrictive to other prevalent viruses in the region. A recent investigation speculates a potential synergistic interaction between ToCV and TYLCV-IL, exacerbating the breakdown of host resistance in tomato (Fiallo-Olivé et al. 2019, Kumar et al. 2023). To the best of our knowledge, this is the first report for the natural incidence of ToCV on tomatillo within the US. The findings will contribute to developing more effective management strategies against emerging viral threats.
灯笼果(酸浆属)是一种一年生植物,原产于墨西哥和危地马拉,在其他热带和亚热带地区也有种植。2023年10月,在美国佐治亚州的科尔奎特县和蒂夫特县观察到叶片出现脉间黄化、边缘黄化、叶片增厚和叶片卷曲症状的灯笼果植株(图1)。发病率在80%-100%之间,这降低了果实品质和市场适销性。采集了20片表现出严重症状的灯笼果叶片,并将叶片的子样本汇集到微量离心管中。此外,使用MagMAX 96病毒RNA分离试剂盒(美国赛默飞世尔科技公司)提取(n = 4)总核酸(TNA)(卡瓦拉帕拉等人,2021年)。对有症状的叶片检测是否存在昆虫传播的病毒,如双生病毒(番茄黄化曲叶病毒,TYLCV)、马铃薯Y病毒(芜菁花叶病毒,TuMV)、毛形病毒(番茄感染性褪绿病毒,TICV;番茄褪绿病毒,ToCV)和番茄斑萎病毒(番茄正番茄斑萎病毒,TSWV)。使用基因特异性引物进行聚合酶链反应(PCR)检测TYLCV(库马尔等人,2023年)。然而,对于ToCV、TuMV和TICV的检测,以100 ng TNA为模板制备cDNA,然后进行PCR(刘等人,2012年)。此外,按照制造商的说明使用免疫试纸条(美国Adgia公司)检测TSWV。在所有测试样本中均检测到ToCV,而在任何有症状的组织中均未检测到TuMV、TICV、TYLCV和TSWV。此外,使用针对ToCV的RNA依赖性RNA聚合酶(RdRP)基因和热休克蛋白70(Hsp70)基因的基因特异性引物进行逆转录PCR(RT-PCR)。对编码Hsp70的439 bp和对应于RdRP的643 bp的PCR扩增子进行凝胶纯化并进行桑格测序(美国Azenta生命科学公司)。BLASTn分析表明,来自ToCV-灯笼果的RdRP基因(OR905600)与RNA1片段的ToCV(RdRP,GenBank登录号AY903447,美国佛罗里达州)具有100%的同一性,而Hsp70基因(OR900219)与RNA2片段的ToCV(Hsp70,GenBank登录号LC778246,埃及开罗)具有100%的同一性。此外,使用番茄对有症状的灯笼果叶片进行传播试验研究,采用无病毒烟粉虱(烟粉虱),获取期为48小时。此外,在感染后两周,在试验植株中检测到ToCV的存在,而其他粉虱传播的病毒仍未检测到。2023年,ToCV在美国番茄种植县广泛传播,感染了对TYLCV-IL(以色列株系)具有中等抗性的商业种植番茄品种。然而,曾有报道称加利福尼亚州的灯笼果植株感染TuMV(刘等人,2012年)、佐治亚州的灯笼果植株感染TSWV(迪亚兹-佩雷斯和帕普2000年)以及墨西哥的灯笼果植株感染TYLCV(加梅斯-希门尼斯等人,2009年)。本研究表明,灯笼果可能是ToCV的适宜寄主,而对该地区其他流行病毒具有抗性。最近的一项调查推测ToCV与TYLCV-IL之间可能存在协同相互作用,加剧了番茄中寄主抗性的丧失(菲亚洛-奥利韦等人,2019年;库马尔等人,2023年)。据我们所知,这是美国境内关于ToCV在灯笼果上自然发生情况的首次报道。这些发现将有助于制定更有效的应对新出现病毒威胁的管理策略。