Gao Jing, Zhang Yuanyuan, Liu Xiangping, Liu Yan, Kang Liru, Jun Zhang, Lian Yong, Yang Zhigang, Wang Yong
Inner Mongolia Academy of Agricultural and Animal Husbandry Sciences, 232813, Hohhot, Inner Mongolia, China;
Chinese Academy of Agricultural Sciences Grassland Research Institute, 243815, Hohhot, Inner Mongolia, China;
Plant Dis. 2022 Mar 20. doi: 10.1094/PDIS-10-21-2210-PDN.
Chinese cabbage [Brassica rapa L. subsp. pekinensis (Lour.) Hanelt] has been grown commercially for many decades in Huade County, Inner Mongolia. In 2018 and 2019, an unusual stem and leaf wilt disease with an average disease incidence of approximately 3% was observed. Diseased plants with spindle-shaped stem lesions were collected and small pieces (0.3 × 0.3 cm) of the diseased tissues were cut from the margins of stem lesions, surface sterilized with 75% alcohol for 3 to 5 s, 0.1% NaClO for 2 to 3 min, and washed three times with sterilized water. The treated tissues were placed on 1.5% (w/v) water agar plates and incubated at 25°C for 3 days. The mycelia were cut and transferred onto potato dextrose agar (PDA) for culture purification. Three isolates with similar morphology were obtained and named as BC-2, BC3-2 and BG2. To confirm their pathogenicity, Chinese cabbage (cv. Chunqiuhuang) seed was planted into plugs. After 30 days, the fibrous roots were wounded with a fruit knife and root-dipped in the conidium suspension (1 × 106 conidia/ml) for 20 min. Inoculated seedlings were transplanted in pots (30 × 25 cm) with sterilized nursery soil, with one seeding per pot. The roots of control plants were also wounded and dipped in sterilized water. Five seedlings were inoculated with each isolate and the experiment was repeated three times. Treated seedlings were maintained in a greenhouse at 25 to 28°C under a 12-h photoperiod. Chlorosis and wilting were observed approximately 4 weeks after inoculation, and the outer layer of leaves of the inoculated seedlings developed discoloration and wilted symptoms after 50 days. The symptoms induced by all three isolates were the same as the symptoms observed in the field, whereas no symptoms developed on the control plants. To confirm the Koch's postulates, the fungus was successfully re-isolated from the infected leaves and had similar growth and morphology as the original isolates. The three isolates were cultured for both morphology and molecular identification. The 14-day-old colonies on PDA were buff or salmon pink with few aerial hyphae, and slimy surfaces. Aerial hyphae were sparse with simple or branched conidiophores. Conidia were ellipsoidal, hyaline, surface smooth, septate or aseptate, and (4.0 to 9.7 μm × 2.0 to 3.9 μm). Such characteristics are typical of Plectosphaerella spp. (Palm et al. 1995). For molecular identification, the internal transcribed spacer (ITS) region of rDNA was amplified using the primer pair ITS1/ITS4 (White et al. 1990), and the products were directly sequenced. BLAST analysis showed that the sequences of Isolates BC-2 (511 bp out of 515 bp), BC3-2 (512 bp out of 516 bp) and BG2 (503 bp out of 505 bp) showed 99% identity to an isolate of P. cucumerina (acc. no. KT826571.1) from Bottle gourd [Lagenaria siceraria (Molina) Standl.] (Yan et al. 2016). The sequences of Isolates BC-2, BC3-2 and BG2 were deposited in GenBank (acc. nos. MW320463, MW320462 and MW320464). Although P. cucumerina was reported causing root rot of cabbage (B. oleracea) in Gansu, China (Li et al. 2017), to our knowledge, this is the first report of P. cucumerina causing Chinese cabbage wilt in Inner Mongolia, China. The presence of the disease could cause significant economic losses in Chinese cabbage production. For this reason, strategies for the management and control of this disease should be implemented.
大白菜[Brassica rapa L. subsp. pekinensis (Lour.) Hanelt]在内蒙古化德县已经商业化种植了几十年。2018年和2019年,观察到一种不寻常的茎叶枯萎病,平均发病率约为3%。收集具有纺锤形茎部病斑的患病植株,并从茎部病斑边缘切取小块(0.3×0.3厘米)患病组织,用75%酒精表面消毒3至5秒,0.1%次氯酸钠消毒2至3分钟,并用无菌水冲洗三次。将处理后的组织放置在1.5%(w/v)水琼脂平板上,在25°C下培养3天。切取菌丝体并转移到马铃薯葡萄糖琼脂(PDA)上进行培养纯化。获得了三个形态相似的分离株,命名为BC-2、BC3-2和BG2。为了确认它们的致病性,将大白菜(品种春秋黄)种子种植在育苗钵中。30天后,用水果刀划伤须根并将根浸入分生孢子悬浮液(1×106个分生孢子/毫升)中20分钟。接种后的幼苗移植到装有消毒育苗土的花盆(30×25厘米)中,每盆一株。对照植株的根也进行划伤并浸入消毒水中。每个分离株接种五株幼苗,实验重复三次。处理后的幼苗在温室中保持在25至28°C,光照周期为12小时。接种后约4周观察到黄化和枯萎,接种后50天接种幼苗的外层叶片出现变色和枯萎症状。所有三个分离株诱导的症状与田间观察到的症状相同,而对照植株未出现症状。为了证实柯赫氏法则,该真菌成功地从感染叶片中重新分离出来,其生长和形态与原始分离株相似。对这三个分离株进行培养以进行形态学和分子鉴定。PDA上14天龄的菌落为浅黄色或鲑鱼粉红色,气生菌丝很少,表面有黏液。气生菌丝稀疏,分生孢子梗简单或有分支。分生孢子椭圆形,透明,表面光滑,有隔膜或无隔膜,大小为(4.0至9.7微米×2.0至3.9微米)。这些特征是盘多毛孢属(Plectosphaerella spp.)的典型特征(Palm等人,1995年)。为了进行分子鉴定,使用引物对ITS1/ITS4(White等人,1990年)扩增rDNA的内部转录间隔区(ITS)区域,并对产物进行直接测序。BLAST分析表明,分离株BC-2(515 bp中的511 bp)、BC3-2(516 bp中的512 bp)和BG2(505 bp中的503 bp)的序列与来自葫芦[Lagenaria siceraria (Molina) Standl.]的黄瓜盘多毛孢(P. cucumerina)分离株(登录号KT826571.)的序列有99%的同一性(Yan等人,2016年)。分离株BC-2、BC3-2和BG2的序列已存入GenBank(登录号MW320463、MW320462和MW320464)。虽然在中国甘肃报道了黄瓜盘多毛孢引起甘蓝(B. oleracea)根腐病(Li等人,2017年),但据我们所知,这是中国内蒙古首次报道黄瓜盘多毛孢引起大白菜枯萎病。该病的存在可能会给大白菜生产造成重大经济损失。因此,应实施该病的管理和控制策略。