El Komy Mahmoud H, Gao Xuewen, Almasrahi Ali, Ibrahim Yasser E, Sharafaddin Anwar H, Saleh Amgad A, Hamad Younis K
King Saud University College of Food and Agriculture Sciences, 108787, Plant Protection, Riyadh, Riyadh, Saudi Arabia;
Nanjing, China;
Plant Dis. 2023 Apr 20. doi: 10.1094/PDIS-02-23-0333-PDN.
Onion (Allium cepa L.) is a globally important crop worldwide including Saudi Arabia. In November 2020, 2-month-old onion plants (cv. Redwing) in commercial fields within the Sajir area of Riyadh region (∼ 1.4 ha), showed symptoms of yellowing, wilting, stunting, bulb discoloration, rot in the basal parts of bulb and decrease in roots. In the advanced stages, the affected plants collapsed and died. The incidence of symptomatic plants ranged from 30 to 65% in the surveyed fields. To isolate the pathogen, symptomatic onion plants (n =20) were sampled. Diseased tissues from roots and bulbs were cut into small pieces (4 × 4 mm), sanitized with 1% sodium hypochlorite solution for 2 min, submerged in 70% alcohol for 20 s, then rinsed with sterile water, before plating on potato dextrose agar (PDA) medium. The plates were incubated at 25°C for 6 days. Subcultures of the mycelia grown out of the diseased tissues produced purplish pink fungal colonies on PDA. On carnation leaf agar, cultures were characteristic of Fusarium oxysporum as described by Leslie and Summerell (2006), with the presence of unicellular microconidia (3.8 to 7.8 × 1.7 to 2.5 μm, n= 50) without septa in false heads or short monophialides and slightly curved macroconidia (16.3 to 28 × 4.2 to 6.1 μm, n= 50) with two to four septa. Older mycelia developed many chlamydospores that were single or in short chains. To further confirm the pathogen identification, DNA was extracted from single-spore cultures of three representative isolates using the DNeasy Plant Mini kit (QIAGEN, Hilden, Germany). Three different fungal nuclear regions of internal transcribed spacer (ITS), elongation factor 1-α, (TEF1-α) and the second largest subunit of DNA-directed RNA polymerase II (RPB2) DNA were amplified by PCR and sequenced with the following primers: ITS4 and ITS5 (White et al. 1990); EF-1 and EF-2 (O'Donnell et al. 2008); and fRPB2-5F and fRPB2-7cR (Liu et al. 1999), respectively. Phylogenetic analysis based on the alignment of the ITS, TEF1-α, and RPB2 sequences using MEGA7 placed these isolates in the F. oxysporum clade. The ITS, TEF1-α, and RPB2 sequences of an isolate FOC-OR9 were submitted to GenBank (OL721757, OL764494, and OL764495 respectively). To confirm the forma specialis cepae, a fragment of the F. oxysporum f. sp. cepae gene Secreted In Xylem 3 (SIX3) was amplified by PCR (Kalman et al. 2020). The SIX3 amplicon (∼ 277-bp) was sent for sequencing, and the sequence was submitted to GenBank (OL828265). BLASTn analysis of the sequences showed 100% identity with F. oxysporum f. sp. cepae (KP746408). To fulfill Koch's postulates, pathogenicity tests were performed with healthy onion bulbs cv. "Redwing" of 100-150 g each. Prior to inoculation of onion bulbs, the dry bulb scales, one of the fleshy inner scales, as well as the roots were removed. Bulbs were then surface sterilized (as described above) and injected with 20 µl of a conidial suspension (106 spores/ ml) into the basal plate of each bulb and approximately 1 cm deep into the tissue. Six bulbs were inoculated for each isolate, placed in a mesh bag, and incubated at 28 °C in the dark. Six bulbs injected with sterile water and six non-inoculated bulbs served as controls. At the 4th week post inoculation, necrotic rot symptoms and brown discoloration were observed on the basal plates of these inoculated bulbs (similar symptoms to those observed in the field), while control treatments showed no symptoms. The pathogen was re-isolated from the basal plates onto PDA and identified morphologically and molecularly as F. oxysporum f. sp. cepae, thus fulfilling Koch's postulates. The test was repeated twice. This pathogen was previously reported causing onion basal rot in United Kingdom (Taylor, et al., 2013). To our knowledge, this is the first report of basal rot in onion caused by F. oxysporum f. sp. cepae in Saudi Arabia. It is recommended that preventive management should be considered as this disease may cause significant economic losses for onion growers in Saudi Arabia. Also, Fusarium mycotoxin contamination of onion bulb could pose a public health risk.
洋葱(Allium cepa L.)是一种在全球包括沙特阿拉伯在内都具有重要意义的作物。2020年11月,利雅得地区萨吉尔区(约1.4公顷)商业田中的2月龄洋葱植株(品种为Redwing)出现了黄化、萎蔫、生长受阻、鳞茎变色、鳞茎基部腐烂以及根系减少的症状。在发病后期,受影响的植株倒伏并死亡。在调查的田块中,有症状植株的发病率在30%至65%之间。为了分离病原体,对有症状的洋葱植株(n = 20)进行了采样。将根和鳞茎的患病组织切成小块(4×4毫米),用1%次氯酸钠溶液消毒2分钟,浸入70%酒精中20秒,然后用无菌水冲洗,再接种到马铃薯葡萄糖琼脂(PDA)培养基上。平板在25°C下培养6天。从患病组织长出的菌丝体进行继代培养,在PDA上产生了紫红色的真菌菌落。在康乃馨叶琼脂上,培养物具有莱斯利和萨默雷尔(2006年)描述的尖孢镰刀菌的特征,存在单细胞小分生孢子(3.8至7.8×1.7至2.5微米,n = 50),在假头或短单瓶梗中无隔膜,以及稍弯曲的大分生孢子(16.3至28×4.2至6.1微米,n = 50),有两到四个隔膜。较老的菌丝体产生许多单个或短链状的厚垣孢子。为了进一步确认病原体的鉴定,使用DNeasy植物微量提取试剂盒(QIAGEN,德国希尔德)从三个代表性分离株的单孢子培养物中提取DNA。通过PCR扩增内部转录间隔区(ITS)、延伸因子1-α(TEF1-α)和DNA指导的RNA聚合酶II第二大亚基(RPB2)DNA的三个不同真菌核区域,并用以下引物进行测序:ITS4和ITS5(怀特等人,1990年);EF-1和EF-2(奥唐奈等人,2008年);以及fRPB2-5F和fRPB2-7cR(刘等人,1999年)。基于使用MEGA7对ITS、TEF1-α和RPB2序列进行比对的系统发育分析将这些分离株置于尖孢镰刀菌分支中。分离株FOC-OR9的ITS、TEF1-α和RPB2序列已提交至GenBank(分别为OL721757、OL764494和OL764495)。为了确认洋葱专化型,通过PCR扩增尖孢镰刀菌洋葱专化型基因分泌到木质部3(SIX3)的一个片段(卡尔曼等人,2020年)。将SIX3扩增子(约277碱基对)送去测序,并将序列提交至GenBank(OL828265)。对这些序列的BLASTn分析显示与尖孢镰刀菌洋葱专化型(KP746408)有100%的同一性。为了满足科赫法则,对每个重100 - 150克的健康洋葱鳞茎品种“Redwing”进行了致病性测试。在接种洋葱鳞茎之前,去除干燥的鳞茎鳞片、一层肉质内鳞片以及根系。然后对鳞茎进行表面消毒(如上所述),并向每个鳞茎的基部平板注射20微升分生孢子悬浮液(10⁶个孢子/毫升),并深入组织约1厘米。每个分离株接种6个鳞茎,放入网袋中,在28°C黑暗条件下培养。注射无菌水的6个鳞茎和未接种的6个鳞茎作为对照。接种后第4周,在这些接种鳞茎的基部平板上观察到坏死腐烂症状和褐色变色(与在田间观察到的症状相似),而对照处理没有症状。从基部平板将病原体重新分离到PDA上,并在形态和分子水平上鉴定为尖孢镰刀菌洋葱专化型,从而满足了科赫法则。该测试重复了两次。此前在英国曾报道过这种病原体导致洋葱基部腐烂(泰勒等人,2013年)。据我们所知,这是沙特阿拉伯首次关于尖孢镰刀菌洋葱专化型引起洋葱基部腐烂的报道。建议考虑采取预防性管理措施,因为这种疾病可能给沙特阿拉伯的洋葱种植者造成重大经济损失。此外,洋葱鳞茎的镰刀菌霉菌毒素污染可能会带来公共卫生风险。