Sha Shuaishuai, Hao Haiting, Wang Lan, Wang Zhe, Yan Cheng Cai, Feng Hongzu
Tarim University, 12483, College of Plant Science, Tarim University, Alar City, Xinjiang Uygur Autonomous Region, Aral, Xinjiang, China, 843300;
Tarim University, College of Plant Science, Tarim University, Alar, Xinjiang, China, Aral, China, 843300.
Plant Dis. 2022 Jun 24. doi: 10.1094/PDIS-02-22-0387-PDN.
Apple (Malus pumila Mill.) is an important fruit crop in Xinjiang, China. In September 2021, apple tree canker was observed in a 21-year-old commercial apple orchard cv. Fuji in Xinjiang (38°17'51.43"N, 77°9'50.81"E) , northwest of China. Of the 200 plants surveyed, 25% were symptomatic. The diseased trees showed branch dieback and cankers. The cankers observed on the wood were sunken, shriveled, and discolored. After the bark was peeled off, the diseased wood was dark brown, and the necrosis was obvious on the cross-section of the diseased branch. To identify the causal agent, five symptomatic trees were collected and analyzed in the laboratory. Apple wood samples (0.5×0.5 cm) were surface-disinfected with 1% v/v sodium hypochlorite and 75% v/v ethanol, rinsed with sterile distilled water, transferred onto potato dextrose agar (PDA), and incubated in the dark at 25 °C for 5 days. Conidia were induced on sterilized pine needles covered with 2% w/v water agar under near-UV light. The colonies of five isolates were white to gray with sparse aerial mycelium that gradually became dark olive green in the later stage. Conidia were initially hyaline but becoming brown at maturity, 1-septate, oval, rounded at both ends, and with dimensions of 24.9-32.1 × 15.1-21.5 µm (n =50) and the aspect ratio of 1.6. Based on the cultural and morphological features of Phillips (2002), the isolates were identified initially as Diplodia mutila (Fr. : Fr.) Mont. To confirm species identification, genomic DNA was extracted from the representative isolate SC-8A. The primer ITS1/ITS4, EF1-728F/EF1-986R and BT2a/BT2b were used to amplify the rDNA sequences of, respectively, the internal transcribed spacer (ITS), translation elongation factor 1-alpha (EF1-α) gene, and a portion of beta-tubulin (tub2) gene. The nucleotide sequences indicated ≥99% identity to D. mutila (CBS 112553) for three DNA regions. Consensus sequences were deposited in GenBank. as accession numbers OM618108, OM676657 and OM676658 for ITS, EF1-α and tub2, respectively. To fulfill Koch's postulates, pathogenicity tests were performed using isolate SC-8A on one year old branches of cv. Fuji (n=5). Wounds were created in the middle of the branches using a sterilized hole punch (5mm diameter) and were immediately inoculated with mycelial plugs of the same diameter. For the control treatment, sterile agar plugs were used (n=5) in the branches. The inoculated and control branches were wrapped with sterile parafilm. On the 10th day after inoculation, canker lesions appeared on the inoculated branches, but no lesions were observed in the negative control. D. mutila was re-isolated from 100% of the inoculated shoots and was not re-isolated from any of the negative controls, the Koch's postulates were met. Previously, D. mutila has been reported in Canada (Úrbez-Torres et al., 2016), Argentina (Lódolo et al., 2022) and Chile (Díaz et al., 2022) causing Botryosphaeria canker and dieback in apples. To our knowledge, this is the first report of D. mutila causing Botryosphaeria canker and dieback in apple trees in China.
苹果(Malus pumila Mill.)是中国新疆一种重要的水果作物。2021年9月,在中国西北部新疆一个种植21年的富士商业苹果园中发现了苹果树溃疡病(38°17'51.43"N,77°9'50.81"E)。在调查的200株植株中,25%出现症状。患病树木表现出枝条枯死和溃疡。在木材上观察到的溃疡凹陷、皱缩且变色。树皮剥落后,患病木材呈深褐色,患病枝条横截面上坏死明显。为鉴定病原菌,采集了5株有症状的树木并在实验室进行分析。苹果木样本(0.5×0.5厘米)用1% v/v次氯酸钠和75% v/v乙醇进行表面消毒,用无菌蒸馏水冲洗,转移到马铃薯葡萄糖琼脂(PDA)上,在25℃黑暗条件下培养5天。在近紫外光下,在覆盖有2% w/v水琼脂的灭菌松针上诱导产生分生孢子。5个分离株的菌落白色至灰色,气生菌丝稀疏,后期逐渐变为深橄榄绿色。分生孢子最初无色透明,但成熟时变为褐色,具1个隔膜,椭圆形,两端圆形,大小为24.9 - 32.1×15.1 - 21.5微米(n = 50),长宽比为1.6。根据菲利普斯(2002年)的培养和形态特征,这些分离株最初被鉴定为毁灭葡萄座腔菌(Diplodia mutila (Fr. : Fr.) Mont.)。为确认物种鉴定,从代表性分离株SC - 8A中提取基因组DNA。分别使用引物ITS1/ITS4、EF1 - 728F/EF1 - 986R和BT2a/BT2b扩增核糖体DNA序列的内部转录间隔区(ITS)、翻译延伸因子1 - α(EF1 - α)基因和部分β - 微管蛋白(tub2)基因。三个DNA区域的核苷酸序列与毁灭葡萄座腔菌(CBS 112553)的同一性≥99%。一致序列分别作为登录号OM618108、OM676657和OM676658保存在GenBank中,对应ITS、EF1 - α和tub2。为完成柯赫氏法则验证,使用分离株SC - 8A对富士品种一年生枝条进行致病性测试(n = 5)。使用灭菌打孔器(直径5毫米)在枝条中部造成伤口,并立即接种相同直径的菌丝块。作为对照处理,在枝条中使用无菌琼脂块(n = 5)。对接种和对照枝条用无菌 parafilm包裹。接种后第10天,接种枝条上出现溃疡病斑,但阴性对照中未观察到病斑。从100%的接种枝条中重新分离出毁灭葡萄座腔菌,而阴性对照中均未重新分离到该菌,满足了柯赫氏法则。此前,在加拿大(Úrbez - Torres等人,2016年)、阿根廷(Lódolo等人,2022年)和智利(Díaz等人,2022年)已报道毁灭葡萄座腔菌在苹果上引起葡萄座腔菌溃疡病和枝条枯死。据我们所知,这是毁灭葡萄座腔菌在中国苹果树中引起葡萄座腔菌溃疡病和枝条枯死的首次报道。