Ismagulova Altynai, Spanbayev Aidar, Tulegenova Zhanar, Eken Cafer
L N Gumilyov Eurasian National University, 112657, Nur-Sultan, Akmola, Kazakhstan;
L.N. Gumilyov Eurasian National University, General Biology and Genomics, 2 Satbayev Str., Astana, Kazakhstan, 010000;
Plant Dis. 2020 Aug 17. doi: 10.1094/PDIS-03-20-0525-PDN.
Strawberry (Fragaria × ananassa Duch.) is an important soft fruit crop in Kazakhstan and is cultivated on more than 1.000 ha each year. Gray mold caused by the fungus Botrytis cinerea is one of the most important fruit rot diseases of cultivated strawberry worldwide. In July 2017, strawberry fruit with gray mold symptoms (approximately 40% incidence) were observed in strawberry fields of Semey province in Kazakhstan. Fruit had light brown lesions that enlarged quickly and were covered with a gray, fuzzy mass of spores and mycelium followed by a soft rot. To isolate the causal agent, sporulating lesions from symptomatic fruit were cut into 3- 5 mm diameter pieces, surface disinfested for 1 min in 2% NaOCI, and plated onto potato dextrose agar (PDA) and incubated at 25°C for 4 to 5 days. Fungal colonies that were consistently isolated were transferred to PDA using single spore isolation. Fungal colonies were colorless at first and became gray to brown when the conidiophores and conidia developed. Conidia measured 4.99 to 9.36 × 3.70 to 6.36 μm, and were colorless to pale-brown, one-celled, ellipsoidal, globose and borne on tree-like conidiophores. The fungus was tentatively identified as Botrytis cinerea (Ellis 1971). In total, 56 isolates of Botrytis cinerea were obtained. The internal transcribed spacer (ITS) region of the ribosomal RNA was amplified using primers ITS1/ITS4 (White et al. 1990) and sequenced (GenBank Accession No. MT150132). The sequence was compared to the GenBank database through nucleotide BLAST search and the isolate (KAB-14) showed 99.62% homology to B. cinerea (MH992149.1). On the basis of morphological data and nucleotide homology, the isolate was determined to be B. cinerea. One isolate (KAB-14) of B. cinerea and strawberry fruit cv. Sabrina were used for assessing pathogenicity. Pathogenicity tests were confirmed by inoculation of 20 healthy strawberry fruit with single PDA 7-mm-diameter plugs containing actively growing mycelium and incubated at 25 °C in airtight plastic bags. Strawberry fruit had been disinfested by spraying fruit with 2% NaOCl and then rinsed two times with sterile distilled water. Noncolonized PDA plugs were used for 20 control fruit. After 2 days of incubation, typical gray mold symptoms were observed on inoculated fruit except controls. The pathogenicity test was repeated twice with identical results. Koch's postulates were fulfilled by the reisolation of B. cinerea from symptomatic fruit. After reisolation on PDA, morphological characteristics were similar to the original isolate. To the best of our knowledge, this is the first report of B. cinerea causing preharvest fruit rot of strawberry in Kazakhstan. This disease could have a high economic impact as strawberry production increases in Kazakhstan.
草莓(Fragaria × ananassa Duch.)是哈萨克斯坦一种重要的软果作物,每年种植面积超过1000公顷。由灰葡萄孢菌(Botrytis cinerea)引起的灰霉病是全球栽培草莓最重要的果实腐烂病害之一。2017年7月,在哈萨克斯坦塞米省的草莓田中观察到有灰霉病症状的草莓果实(发病率约40%)。果实上有浅褐色病斑,病斑迅速扩大,覆盖着一层灰色的、毛茸茸的孢子和菌丝体,随后发生软腐。为了分离病原菌,将有症状果实上产生孢子的病斑切成直径3 - 5毫米的小块,在2%次氯酸钠中表面消毒1分钟,然后接种到马铃薯葡萄糖琼脂(PDA)上,于25°C培养4至5天。通过单孢分离将持续分离得到的真菌菌落转移到PDA上。真菌菌落最初无色,当分生孢子梗和分生孢子形成时变为灰色至褐色。分生孢子大小为4.99至9.36×3.70至6.36μm,无色至浅褐色,单细胞,椭圆形、球形,着生于树状分生孢子梗上。该真菌初步鉴定为灰葡萄孢菌(Ellis 1971)。共获得56株灰葡萄孢菌分离物。使用引物ITS1/ITS4(White等人,1990)扩增核糖体RNA的内部转录间隔区(ITS)区域并进行测序(GenBank登录号MT150132)。通过核苷酸BLAST搜索将该序列与GenBank数据库进行比较,分离物(KAB - 14)与灰葡萄孢菌(MH992149.1)的同源性为99.62%。根据形态学数据和核苷酸同源性,确定该分离物为灰葡萄孢菌。选取一株灰葡萄孢菌分离物(KAB - 14)和草莓品种Sabrina用于致病性评估。通过用含有活跃生长菌丝体的直径7毫米的单个PDA菌块接种20个健康草莓果实,并在25°C下置于密封塑料袋中培养来进行致病性测试。草莓果实已通过用2%次氯酸钠喷洒进行消毒,然后用无菌蒸馏水冲洗两次。20个对照果实使用未接种的PDA菌块。培养2天后,除对照外,接种果实上观察到典型的灰霉病症状。致病性测试重复两次,结果相同。从有症状果实中再次分离出灰葡萄孢菌,从而满足了柯赫氏法则。在PDA上再次分离后,形态特征与原始分离物相似。据我们所知,这是哈萨克斯坦首次报道灰葡萄孢菌引起草莓采前果实腐烂。随着哈萨克斯坦草莓产量的增加,这种病害可能会产生很高的经济影响。