Li Jiaxi, Gu Ran, Zhang An, Han Kexin, Yang Na, Liu Yan, Zhang Yaowei
Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (Northeast Region), Ministry of Agriculture and Rural Affairs, Harbin, China.
Northeast Agricultural University, 12430, College of Horticulture and Landscape Architecture, Harbin, China;
Plant Dis. 2022 Apr 29. doi: 10.1094/PDIS-12-21-2825-PDN.
Chinese cabbage ( L. ssp. ) is one of the main biennial vegetables in China and its flowers can be produced in the second year. In May 2021, approximately 50% of the flower stalks of Chinese cabbage wilted in a field in Laizhou, China. Water-soaked lesions were first observed on the lateral shoots of flower stalks, leading to wilting at a later stage. Small diseased tissues were excised from the margin of lesions, surface disinfected in 75% alcohol, rinsed in distilled water twice, and transferred onto potato dextrose agar (PDA) medium for incubation at 28 ℃. Five fungal isolates were obtained using single spore isolation method. The fungal colonies were initially white and became gray or black within 5 days. The columella was globose to subglobose and 82.86±5.25 μm (n=5) in diameter; sporangiophores were smooth-walled, simple or branched; the globose sporangia were 86.06±15.37 μm (n=5) in diameter and black; the sporangiospores were subglobose and abundant and 5.23±0.98 μm (n=5) in diameter; and the rhizoids were dark brown and 5.69±1.82 μm (n=5) wide. A cetyl tri-methyl ammonium bromide method was used to extract DNA from 3-day-old hyphae (Ausubel et al. 1987). PCR was performed for ITS (White et al. 1990), the RNA polymerase II large subunit () gene (Voigt et al. 2000) and the actin () gene (Stiller et al. 1997). The DNA sequences of the five isolates were identical, therefore, the sequence of Isolate RO21 was submitted to GenBank. According to BLAST search, the ITS (MZ452687), (OK431470), and (OK431471) sequences showed 99.66% similarity to Strain CBS 112.07 (NR103595), 100% to Strain CBS 127.08 (KJ566325) and 100% to Strain CBS 102660 (KJ551423), respectively. A neighbor-joining phylogenetic tree was reconstructed based on the ITS of Isolate RO21 and 14 other species sequences obtained from GenBank. Isolate RO21 was found to be most closely related to and far from other species. Based on morphological and phylogenetic characteristics, Isolate RO21 was identified as (Dolatabadi et al. 2014, Kwon et al. 2015, Palemón-Alberto et al. 2020). Sporangiospores were harvested from 5-day-old PDA cultures, suspended in sterilized distilled water, adjusted to 10 spores/ml and amended with 0.1% Tween-80. Chinese cabbage inbred line "A54-1" was inoculated near the middle of the flower stalk by applying 20 μl of spore suspension (10 spores/ml) to each of three sites wounded using a sterilized knife or to the unwounded site. Sterilized distilled water was used as the control. Forty flower stalks (20 for the inoculation treatment and the rest for the control) selected from ten plants were used for pathogenicity test. All plants were incubated in a growth chamber at 28/22 °C (day/night), with 80 to 90% of relative humidity. Wilting symptoms similar to those in the field were observed in the wounded flower stalks after 5 days and in the non-wounded flower stalks after 15 days. All control flower stalks remained asymptomatic. The fungus was re-isolated from the artificially infected flower stalks and identified as by morphological characteristics and sequencing to fulfill the Koch's postulates. To our knowledge, this is the first report that causes flower stalk wilting on Chinese cabbage in China. The results can provide the basis for future studies on the occurrence, prevention and management of this disease.
大白菜(L. ssp.)是中国主要的二年生蔬菜之一,其花在第二年形成。2021年5月,中国莱州一块地里约50%的大白菜花茎萎蔫。最初在花茎侧枝上观察到水渍状病斑,随后导致萎蔫。从病斑边缘切取小块病组织,用75%酒精进行表面消毒,在蒸馏水中冲洗两次,然后转移到马铃薯葡萄糖琼脂(PDA)培养基上,于28℃培养。采用单孢分离法获得了5株真菌分离物。真菌菌落最初为白色,5天内变为灰色或黑色。孢囊梗球形至近球形,直径82.86±5.25μm(n = 5);孢囊梗壁光滑,单生或分枝;球形孢子囊直径86.06±15.37μm(n = 5),黑色;孢子囊孢子近球形,数量众多,直径5.23±0.98μm(n = 5);假根深褐色,宽5.69±1.82μm(n = 5)。采用十六烷基三甲基溴化铵法从3日龄菌丝中提取DNA(奥苏贝尔等人,1987年)。对ITS(怀特等人,1990年)、RNA聚合酶II大亚基()基因(沃伊特等人,2000年)和肌动蛋白()基因(斯蒂勒等人,1997年)进行PCR扩增。5株分离物的DNA序列相同,因此,将分离物RO21的序列提交到GenBank。根据BLAST搜索,ITS(MZ452687)、(OK431470)和(OK431471)序列与菌株CBS 112.07(NR103595)的相似性分别为99.66%、与菌株CBS 127.08(KJ566325)的相似性为100%、与菌株CBS 102660(KJ551423)的相似性为100%。基于分离物RO21的ITS和从GenBank获得的其他14种疫霉属物种序列重建了邻接法系统发育树。发现分离物RO21与紧密相关,与其他物种距离较远。根据形态学和系统发育特征,分离物RO21被鉴定为(多拉塔巴迪等人,2014年;权等人,2015年;帕莱蒙 - 阿尔贝托等人,2020年)。从5日龄PDA培养物中收获孢子囊孢子,悬浮于灭菌蒸馏水中,调整至10个孢子/毫升,并添加0.1%吐温 - 80。用灭菌刀在大白菜自交系“A54 - 1”花茎中部附近的三个伤口部位或未受伤部位分别接种20μl孢子悬浮液(10个孢子/毫升)。用灭菌蒸馏水作为对照。从10株植物中选取40个花茎(20个用于接种处理,其余用于对照)进行致病性测试。所有植株在生长室中于28/22℃(昼/夜)、相对湿度80%至90%的条件下培养。接种后5天,受伤花茎出现与田间相似的萎蔫症状,未受伤花茎在15天后出现症状。所有对照花茎均无症状。从人工感染的花茎中重新分离出该真菌,并通过形态学特征和测序鉴定为,以满足柯赫氏法则。据我们所知,这是在中国首次报道引起大白菜花茎萎蔫。这些结果可为今后该病害的发生、预防和管理研究提供依据。