Khoo Ying Wei, Khaw Yam Sim, Tan Hui Teng, Li Shi-Fang, Chong Khim Phin
Chinese Academy of Agricultural Sciences, 12661, Institute of Plant Protection, No. 2 West Yuanmingyuan Rd.,, Haidian District, Beijing, China, 100193.
Universiti Malaysia Sabah, 60606, Faculty Of Science And Natural Resources, Jalan UMS, Kota Kinabalu, Sabah, Malaysia, 88400;
Plant Dis. 2022 May 17. doi: 10.1094/PDIS-03-22-0699-PDN.
'Thai Gold' yellow pitahaya (family Cactaceae, ) is a new crop being planted commercially in Malaysia. In May 2021, reddish-brown necrotic lesions were observed on the stems of approximately 60% of 'yellow pitahaya' plants in the field (~8 ha) located in the district Keningau of Sabah, Malaysia (5°20'53.1"N 116°06'23.0"E). As the disease progressed, the smaller lesions merged into larger irregularly shaped areas that formed dark brown in color. Stems with reddish-brown spot symptoms from ten plants were collected from the field and brought to the laboratory in sterilized paper bags. The symptom margin was excised into small blocks (5 x 5 x 5 mm). The blocks were surface sterilized based on Khoo et al. (2022), and placed on potato dextrose agar (PDA). The pathogens were isolated (three isolates were obtained) and cultured on potato dextrose agar (PDA) at 25°C for 5 days in the dark. The isolates developed floccose, white colony that darkened with age in PDA. Conidia ( = 30) were single celled, black, smooth, globose to subglobose, 13.9 to 18.7 μm in diameter, and borne singly on a hyaline vesicle at the tip of each conidiophore. Genomic DNA was extracted from fresh mycelia based on Khoo et al. (2021) and Khoo et al. (2022). Amplification of the internal transcribed spacer (ITS) region of rDNA, () region and () genes were performed using ITS1/ITS4 (White et al. 1990), EF1-728F/EF2 (O'Donnell et al. 1998; Carbone and Kohn, 1999) and T10/Bt2b (Glass and Donaldson, 1995; O'Donnell and Cigelnik, 1997) primer sets, respectively. The products were sent to Apical Scientific Sdn. Bhd. for purification and sequencing. BLASTn analysis of the newly generated ITS (OK448496, OM832586, OM832589) were 100% identical to isolate 1SS (MN339998) (507/507 bp), tef1-a (OM223859, OM826971, OM826972) were 100% identical to isolate F (MT708197) (497/497 bp) and tub2 (OL697400, OM826973, OM826974) were 100% identical to isolate SN180517 (MN719407) (434/434 bp). The isolates established a supported clade to the related type sequences, according to phylogenetic analysis using maximum likelihood based on the concatenated ITS, and sequences. Morphological and molecular characterization matched the description of (Kee et al. 2019). Koch's postulates were performed by spray inoculation (10 spores/ml) of isolate Keningau on the stem of three 'Thai Gold' yellow pitahaya plants in growth stage 4 (BBCH code: 419) (Kishore, 2016), while water was sprayed on three mock controls. The experiment was repeated using isolate Keningau02 and Keningau03 as inoculants. The inoculated stems on yellow pitahaya plants were covered with plastics for 48 h, and the plants were maintained in a greenhouse at room temperature 25 to 28°C with a relative humidity of 80 to 90%. All the inoculated stems developed symptoms 5 days post-inoculation, whereas no symptoms occurred on mock controls, thus fulfilling the Koch's postulates. No pathogen was isolated from the mock controls. The experiments were repeated two more times for each isolate. The reisolated fungi were identical to morphologically and molecularly. Previously, has been reported to cause stem brown spot disease on in the Philippines (Taguiam et al. 2020). To our knowledge, this is the first report of causing stem brown spot on 'Thai Gold' in Malaysia. Our findings serve as a warning for the authorities and farmers that the disease threat has appeared for the Malaysian yellow pitahaya production.
“泰国黄金”黄火龙果(仙人掌科)是马来西亚正在商业化种植的一种新作物。2021年5月,在马来西亚沙巴州根地咬区(北纬5°20'53.1",东经116°06'23.0")一块约8公顷的田地里,约60%的“黄火龙果”植株的茎上出现了红棕色坏死斑。随着病情发展,较小的病斑融合成更大的不规则形状区域,颜色变为深棕色。从田间采集了十株有红棕色斑点症状的茎,用无菌纸袋带到实验室。将症状边缘切成小方块(5×5×5毫米)。根据Khoo等人(2022年)的方法对这些方块进行表面消毒,然后置于马铃薯葡萄糖琼脂(PDA)上。分离出病原体(获得了三个分离株),并在马铃薯葡萄糖琼脂(PDA)上于25°C黑暗条件下培养5天。这些分离株在PDA上形成絮状、白色菌落,随着时间推移颜色变深。分生孢子(n = 30)单细胞,黑色,表面光滑,球形至近球形,直径13.9至18.7微米,单个着生于每个分生孢子梗顶端的透明泡囊上。根据Khoo等人(2021年)和Khoo等人(2022年)的方法从新鲜菌丝体中提取基因组DNA。分别使用ITS1/ITS4(White等人,1990年)、EF1-728F/EF2(O'Donnell等人,1998年;Carbone和Kohn,1999年)以及T10/Bt2b(Glass和Donaldson,1995年;O'Donnell和Cigelnik,1997年)引物对rDNA的内部转录间隔区(ITS)区域、tef1-α区域和tub2基因进行扩增。产物送至Apical Scientific私人有限公司进行纯化和测序。对新生成的ITS(OK448496、OM832586、OM832589)进行BLASTn分析,结果显示与尖孢镰刀菌分离株1SS(MN339998)(507/507碱基对)100%相同,tef1-α(OM223859、OM826971、OM826972)与尖孢镰刀菌分离株F(MT708197)(497/497碱基对)100%相同,tub2(OL697400、OM826973、OM826974)与尖孢镰刀菌分离株SN180517(MN719407)(434/434碱基对)100%相同。根据基于串联的ITS、tef1-α和tub2序列的最大似然法进行系统发育分析,这些分离株与相关尖孢镰刀菌类型序列形成一个支持的分支。形态学和分子特征与尖孢镰刀菌(Kee等人,2019年)的描述相符。通过将根地咬分离株以10个孢子/毫升的浓度喷雾接种到三株处于生长阶段4(BBCH编码:419)(Kishore,2016年)的“泰国黄金”黄火龙果植株的茎上进行柯赫氏法则验证,同时对三个 mock对照植株喷水。使用根地咬02和根地咬03分离株作为接种物重复该实验。接种后,用塑料覆盖黄火龙果植株的接种茎48小时,并将植株置于室温25至28°C、相对湿度80至90%的温室中。接种后5天,所有接种茎均出现症状,而mock对照植株未出现症状,从而满足柯赫氏法则。mock对照植株未分离到病原体。每个分离株又重复进行了两次实验。重新分离的真菌在形态学和分子学上与尖孢镰刀菌相同。此前,据报道尖孢镰刀菌在菲律宾导致了番木瓜的茎褐斑病(Taguiam等人,2020年)。据我们所知,这是马来西亚首次报道尖孢镰刀菌导致“泰国黄金”黄火龙果茎褐斑病。我们的研究结果向当局和农民发出警告,马来西亚黄火龙果生产已出现病害威胁。