First Report of Fusarium kyushuense Causing Leaf Spot on Sweet Persimmon in China.

IF 4.4 2区 农林科学 Q1 PLANT SCIENCES Plant disease Pub Date : 2024-08-15 DOI:10.1094/PDIS-04-24-0925-PDN
Shangbo Jiang, Jin Zhang, Di Yang, Chan Juan Du, Yunfeng Ye, Lian Fu Pan, Gang Fu
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Abstract

Sweet persimmon (Diospyros kaki L.) is a fruit of significant nutritional and commercial value in Asia. In summer 2023, leaf spots were observed affecting 20 to 30% of sweet persimmon trees in a commercial orchard located in Gongcheng City, Guangxi, China. Initially, the infected leaves exhibited sparse light brown spots on their upper surface, which subsequently evolved into brown circular to irregular lesions encircled by a yellow halo. Eventually, these lesions became densely distributed across the leaves leading to insufficient nutrient accumulation in the fruit. To isolate the pathogen, diseased leaves were cut into small pieces (5×5 mm), disinfected with 75% ethanol for 15 seconds, followed by 1% NaClO for 1minute, rinsed three times with sterile water, and then transferred onto potato dextrose agar (PDA) plates. The plates were then incubated in darkness for 3 days at 25°C. Pure cultures were obtained using the hyphal-tip method and single-spore isolation. On PDA, the colonies initially appeared fluffy and white after 24 hours, turning yellowish or red after 3 days. Macroconidia (average length of 26.1 μm in length × 4.3 μm in width, n = 50) exhibited dorsiventral curvature and were hyaline, with 3 to 5 septa. Microconidia (average length of 9.45 μm in length × 3.4 μm in width, n = 50) were hyaline, aseptate, and oval. Two representative isolates, Gxfky1 and Gxfky2, were selected for further molecular analyses. Their internal transcribed spacer (ITS) region rDNA gene were amplified via PCR and sanger sequenced (GenBank Accession Nos. PP506475, PP506593) using the primer pair ITS1/ITS4 (White et al. 1990), showing more than 99% sequence identity with Fusarium kyushuense type-material strain NRRL3509 (NR_152943) according to BLASTn analysis in NCBI. To further confirm the identity of the isolates, four gene sequences were amplified: RPB1 (PP532864, PP532865), RPB2 (PP532866, PP532867), TEF1 (PP580505, PP580506), and TUB2 (PP532862, PP532863), using the F5/G2R, 5f2/11ar, EF1/EF2, and T1/T2 primer sets, respectively (O'Donnell et al., 1997; O'Donnell et al., 2010). A multi-locus maximum likelihood phylogenetic analysis revealed that Gxfky1 and Gxfky2 clustered with strains F. kyushuense with 100% bootstrap support. Pathogenicity tests using Gxfky1 and Gxfky2 were conducted on leaves of two-year-old sweet persimmon plants using non-wound inoculation. Specifically, 5-mm mycelial plugs and sterile agar plugs were placed on six leaves and secured with cling film, with six plugs each for the inoculation treatment and negative control, respectively. They were then incubated in a greenhouse at room temperature (25 ± 2°C) with a relative humidity of 70 to 80%. After 5 days, the same symptoms on naturally infected plants were observed on leaves inoculated with mycelium, while no symptoms were observed on the controls. The same fungus were reisolated from the inoculated leaves and identified based on morphology and the TEF1 gene sequence, thus fulfilling Koch's postulates. Fusarium kyushuense has previously been reported to cause diseases in various plant species, including maize (Cao et al., 2021), rice (Wang et al., 2024), and tobacco (Wang et al., 2013). To our knowledge, this is the first report of F. kyushuense causing leaf spot on sweet persimmon in China, which expands the known host range of this pathogen.

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中国首次报告由九州镰刀菌引起的甜柿叶斑病。
甜柿(Diospyros kaki L.)是亚洲一种具有重要营养和商业价值的水果。2023 年夏季,在中国广西恭城的一个商品果园中,20% 至 30% 的甜柿树受到叶斑病的影响。最初,受感染的叶片上表面出现稀疏的淡褐色斑点,随后演变成褐色圆形至不规则形病斑,周围有黄色晕圈。最后,这些病斑在叶片上密集分布,导致果实营养积累不足。为了分离病原体,将病叶切成小块(5×5 毫米),用 75% 的乙醇消毒 15 秒,然后用 1% 的 NaClO 消毒 1 分钟,再用无菌水冲洗三次,然后转移到马铃薯葡萄糖琼脂(PDA)平板上。然后在 25°C 黑暗条件下培养 3 天。用吸头法和单孢子分离法获得纯培养物。在 PDA 上,菌落最初在 24 小时后呈白色绒毛状,3 天后变为淡黄色或红色。大锥体(平均长度为长 26.1 微米×宽 4.3 微米,n = 50)呈现背腹弯曲,呈透明状,有 3 至 5 个隔膜。微孢子囊(平均长度为长 9.45 μm × 宽 3.4 μm,n = 50)呈透明、无隔膜和椭圆形。选取了两个具有代表性的分离物 Gxfky1 和 Gxfky2 进行进一步的分子分析。它们的内部转录间隔(ITS)区域 rDNA 基因经 PCR 扩增,并使用引物对 ITS1/ITS4(White 等,1990 年)进行了桑格测序(GenBank 登录号:PP506475、PP506593),根据 NCBI 的 BLASTn 分析,它们与 Fusarium kyushuense 型材料菌株 NRRL3509(NR_152943)的序列同一性超过 99%。为进一步确认分离物的身份,扩增了四个基因序列:分别使用 F5/G2R、5f2/11ar、EF1/EF2 和 T1/T2 引物组(O'Donnell 等,1997 年;O'Donnell 等,2010 年)扩增了 RPB1(PP532864、PP532865)、RPB2(PP532866、PP532867)、TEF1(PP580505、PP580506)和 TUB2(PP532862、PP532863)。多焦点最大似然系统进化分析表明,Gxfky1 和 Gxfky2 与 F. kyushuense 株系聚类,引导支持率为 100%。使用 Gxfky1 和 Gxfky2 对两年生甜柿植株的叶片进行了无伤口接种的致病性试验。具体来说,在六片叶子上放置 5 毫米的菌丝塞和无菌琼脂塞,并用保鲜膜固定,接种处理和阴性对照各放置六个菌丝塞。然后将其置于室温(25 ± 2°C)、相对湿度为 70% 至 80% 的温室中培养。5 天后,在接种菌丝体的叶片上观察到与自然感染植株相同的症状,而对照组则未观察到任何症状。根据形态学和 TEF1 基因序列,从接种的叶片上重新分离出了相同的真菌并进行了鉴定,从而验证了科赫假说。据报道,久树镰刀菌可引起多种植物病害,包括玉米(Cao 等人,2021 年)、水稻(Wang 等人,2024 年)和烟草(Wang 等人,2013 年)。据我们所知,这是中国首次报道 F. kyushuense 在甜柿上引起叶斑病,从而扩大了该病原体的已知寄主范围。
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来源期刊
Plant disease
Plant disease 农林科学-植物科学
CiteScore
5.10
自引率
13.30%
发文量
1993
审稿时长
2 months
期刊介绍: Plant Disease is the leading international journal for rapid reporting of research on new, emerging, and established plant diseases. The journal publishes papers that describe basic and applied research focusing on practical aspects of disease diagnosis, development, and management.
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