Rahman Muhammad Ziaur, Ahmad Khairulmazmi, Siddiqui Yasmeen, Saad Norsazilawati, Hun Tan Geok, Mohd Hata Erneeza, Rashed Osamah, Hossain Md Imam, Kutawa Abdulaziz Bashir
Universiti Putra Malaysia, 37449, Faculty of Agriculture, Department of Plant protection, , Serdang, Selangor, Malaysia.
Bangladesh Agricultural Research Institute (BARI), Plant Pathology Division, Gazipur-1701, Dhaka, Bangladesh;
Plant Dis. 2021 May 27. doi: 10.1094/PDIS-04-21-0780-PDN.
Fusarium wilt disease incited by Fusarium oxysporum f. sp. niveum (FON) is the utmost devastating soil-inhabiting fungal pathogen limiting watermelon (Citrullus lanatus) production in Malaysia and globally. The field disease survey of fusarium wilt was carried out during December 2019 and November 2020, in three major production areas (3 farmer fields per location) in Peninsular Malaysia namely, Mersing, Serdang and Kuantan and disease incidence of 30 and 45%, was recorded for each year, respectively. Infected watermelon plants showed symptoms such as vascular discoloration, brown necrotic lesions to the soil line or the crown, one-sided wilt of a plant, or a runner or the whole plant. Infected root and stem tissues, 1-2 cm pieces were surface sterilized with 0.6% NaOCl for 1 minute followed by double washing with sterile water. The disinfected tissues were air-dried and transferred onto semi-selective Komada's medium (Komada 1975) and incubated for 5 days. The fungal colonies produced were placed on potato dextrose agar (PDA) to attain a pure culture and incubated at 25±2℃ for 15 days. The pure fungal colony was flat, round and light purple in color. Macroconidia were straight to slightly curved, 18.56-42.22 µm in length, 2.69-4.08 µm width, predominantly 3 septate and formed in sporodochia. Microconidia measured 6.16-10.86 µm in length and 2.49-3.83 µm in width, kidney-shaped, aseptate and were formed on short monophialides in false-heads. Chlamydospores were single or in pairs with smooth or rough walls, found both terminally or intercalary. To confirm their pathogenicity, two-week-old watermelon seedlings (cv. NEW BEAUTY) were dipped into spore suspension (1 ˟ 106 spores/ml) of representative isolates of JO20 (Mersing), UPM4 (Serdang) and KU41 (Kuantan) for 30 second and then moved into 10 cm diameter plastic pots containing 300 g sterilized soil mix. Disease symptoms were assessed weekly for one month. Control seedlings were immersed in sterile distilled water before transplanting. The inoculated seedlings showed typical Fusarium wilt symptoms like yellowing, stunted growth, and wilting, which is similar to the farmer field infected plants. However, the seedlings inoculated by sterile distilled water remained asymptomatic. The pathogen was successfully re-isolated from the infected seedlings onto Komada's medium, fulfilling the Koch's postulate. For the PCR amplification, primers EF-1 and EF-2 were used to amplify the tef1-α region. A Blastn analysis of the tef1-α sequences of the isolates JO20 (accession nos. MW315902), UPM4 (MW839560) and KU41 (MW839562) showed 100% similarity; with e-value of zero, to the reference sequences of F. oxysporum isolate FJAT-31690 (MN507110) and F. oxysporum f. sp. niveum isolate FON2 790-2 (MN057702). In Fusarium MLST database, isolates JO20, UPM4 and KU41 revealed 100% identity with the reference isolate of NRRL 22518 (accession no. FJ985265). Though isolate FJ985265 belongs to the f. sp. melonis, earlier findings had revealed Fusarium oxysporum f. sp. are naturally polyphyletic and making clusters with diverse groups of the Fusarium oxysporum species complex (O'Donnell et al. 2015). The isolates JO20, UPM4 and KU41 were identified as F. oxysporum f. sp. niveum based on the aligned sequences of tef1-α and molecular phylogenetic exploration by the maximum likelihood method. To the best of our knowledge, this is the first report of F. oxysporum f. sp. niveum as a causative pathogen of Fusarium wilt disease of watermelon in Malaysia. Malaysia enables to export watermelon all-year-round in different countries like Singapore, Hong-Kong, The United Arab Emirates (UAE), and Netherlands. The outburst of this destructive soil-borne fungal pathogen could cause hindrance to watermelon cultivation in Malaysia. Thus, growers need to choice multiple management tactics such as resistant varieties, cultural practices (soil amendments and solarization), grafting, cover crops and fungicide application to control this new pathogen.
尖孢镰刀菌西瓜专化型(FON)引起的枯萎病是最具毁灭性的土壤栖息真菌病原体,限制了马来西亚乃至全球的西瓜(西瓜属)产量。2019年12月至2020年11月,在马来西亚半岛的三个主要产区(每个地点3个农田),即丰盛港、雪兰莪和关丹,对枯萎病进行了田间病害调查,每年记录的发病率分别为30%和45%。受感染的西瓜植株表现出诸如维管束变色、土壤线或茎基部出现褐色坏死斑、植株一侧枯萎、或瓜蔓或整株枯萎等症状。将受感染的根和茎组织切成1-2厘米的小段,用0.6%的次氯酸钠进行表面消毒1分钟,然后用无菌水冲洗两次。消毒后的组织风干后转移到半选择性的小田培养基(小田,1975)上,培养5天。将产生的真菌菌落接种到马铃薯葡萄糖琼脂(PDA)上以获得纯培养物,并在25±2℃下培养15天。纯真菌菌落扁平、圆形,颜色浅紫。大型分生孢子直或略弯曲,长18.56-42.22 µm,宽2.69-4.08 µm,主要为3隔膜,形成于分生孢子盘。小型分生孢子长6.16-10.86 µm,宽2.49-3.83 µm,肾形,无隔膜,形成于假头状的短单瓶梗上。厚垣孢子单个或成对,壁光滑或粗糙,顶生或间生。为了确认其致病性,将两周大的西瓜幼苗(品种:新美人)浸入JO20(丰盛港)、UPM4(雪兰莪)和KU41(关丹)代表性分离株的孢子悬浮液(1×106孢子/ml)中30秒,然后移入直径10厘米的塑料盆中,盆中装有300克消毒土壤混合物。每周评估一次病害症状,持续一个月。对照幼苗在移栽前浸入无菌蒸馏水中。接种的幼苗表现出典型的枯萎病症状,如发黄、生长受阻和枯萎,这与农田中受感染的植株相似。然而,用无菌蒸馏水接种的幼苗没有症状。病原体成功地从受感染的幼苗中重新分离到小田培养基上,符合科赫法则。对于PCR扩增,使用引物EF-1和EF-2扩增tef1-α区域。对分离株JO20(登录号MW315902)、UPM4(MW839560)和KU41(MW839562)的tef1-α序列进行Blastn分析,结果显示与尖孢镰刀菌分离株FJAT-31690(MN507110)和尖孢镰刀菌西瓜专化型分离株FON2 790-2(MN057702)的参考序列100%相似,e值为零。在镰刀菌多位点序列分型数据库中,分离株JO20、UPM4和KU41与参考分离株NRRL 22518(登录号FJ985265)显示100%的同一性。尽管分离株FJ985265属于甜瓜专化型,但早期研究结果表明尖孢镰刀菌专化型在自然条件下是多系的,并与尖孢镰刀菌物种复合体的不同类群聚类(奥唐奈等人,2015年)。根据tef1-α的比对序列和最大似然法的分子系统发育探索,分离株JO20、UPM4和KU41被鉴定为尖孢镰刀菌西瓜专化型。据我们所知,这是马来西亚首次报道尖孢镰刀菌西瓜专化型是西瓜枯萎病的致病病原体。马来西亚能够全年向不同国家出口西瓜,如新加坡、中国香港、阿拉伯联合酋长国(阿联酋)和荷兰。这种具有破坏性的土传真菌病原体的爆发可能会阻碍马来西亚的西瓜种植。因此,种植者需要选择多种管理策略,如抗性品种、栽培措施(土壤改良和太阳能消毒)、嫁接、覆盖作物和施用杀菌剂来控制这种新病原体。