尖孢镰刀菌引起巴基斯坦苦瓜叶斑病的首次报道。

First report of Fusarium equiseti causing leaf spots of Bitter gourd (Momordica charantia) in Pakistan.

作者信息

Rehman Ateeq Ur, Rauf Abdul, Ali Amjad, Shakeel Muhammad Taimoor, Naqvi Syed Atif Hasan, Shahid Muhammad, Umar Ummad Ud Din

机构信息

Bahauddin Zakariya University Faculty of Agriculture Science and Technology, 511772, Plant Pathology, Multan, Punjab, Pakistan;

Sivas University of Applied Sciences and Technology, 566933, Department of Plant Protection, Sivas, Sivas, Turkey;

出版信息

Plant Dis. 2022 Oct 24. doi: 10.1094/PDIS-04-22-0786-PDN.

Abstract

Bitter gourd (Momordica charantia L.) is an important vegetable crop of the Cucurbitaceae family widely cultivated in Pakistan and around the world. In October 2020, a nutrition management trial of Bitter gourd cv. Seminis-200) was conducted on an area of 10,860 sq. ft. (99×110 feet) at the Agricultural Research farm of Bahauddin Zakariya University, Multan (30.2601° N, 71.5158° E), Pakistan. Symptoms of large, brown necrotic leaf spots were observed on the leaves of bitter gourd vines. The disease started from the yellowing of leaves within the reticulate venation and turned brown. Irregular brown leaf spots coalesced to form large necrotic areas followed by foliar chlorosis then wilting that occurred very late. There were no crown rot symptoms although there was slight discoloration of roots and when cut longitudinally, browning of tissues was observed. The disease was assessed visually with 37% incidence which resulted in poor quality and yield in terms of reduced size and yellowing of fruit. Infected vines along with the roots were collected for the isolation of pathogen. A total of 34 leaves and 22 root samples were collected from the field for isolation. The leaf, collar and root portions were cut into 0.5 to 1 cm in length and surface disinfected with 1% sodium hypochlorite (NaOCl) for 2-3 minutes followed by washing twice with autoclaved distilled water and after drying, placed on potato dextrose agar (PDA) medium, and incubated at 25±2 °C for one week. The fungal colonies of fluffy white growth with light orange pigment were isolated. For morphological characterization, a total of 4 pure cultures were isolated from leaves, collar region and root by single spore technique on carnation leaf agar (CLA) medium after 15 days of incubation at 25±2℃. Curved and thick-walled macroconidia with elongated or pointed apical characteristic foot-shaped basal cells were produced in sporodochia. Macroconidia with 5-7 septa measured 22.50-41.80 μm × 2.90-4.20 μm (n = 60). Thick, brown with roughened walls and subglobose ellipsoidal chlamydospores were observed in clumps or chains with the dimension of 5.8 to 10.8 μm (n = 20). On morphological characteristics, the fungus was identified as Fusarium equiseti (Corda) Sacc. according to Leslie and Summerell (2006). Two single spore isolates were used for molecular identification by amplifying ribosomal DNA of the internal transcribed spacer (ITS) region with ITS1/ITS4 primers (White et al. 1990) and for β-tubulin gene region, primers T1/Bt-2b (O'Donnell and Cigelnik, 1997) were used. The obtained sequences were deposited in GenBank with accession numbers MW880179 and MW880198 from the ITS region and BLAST search in GenBank showed 100 and 98.11% alignment with previously published sequences of F. equiseti with accessions OM992323.1and MT558569.1 respectively. Accession number OM867571from the β-tubulin region showed 100% sequence similarity with F. equiseti with accession MN653163.1. For pathogenicity, macroconidia from 2-week-old cultures on CLA medium were harvested to prepare spore suspension (1 × 106 conidia/ml). Koch's postulates were confirmed on nine bitter gourd plants (cv. Seminis-200) by applying spore suspension of fungal inoculum at 3-4 leaf stage separately on leaves by automizer, on collar region after making incision spore suspension was applied and in the root zone, 20ml spore suspension was added whereas distilled water was used as a control with three replications. Plants were kept under controlled conditions in the greenhouse with 65% to 75% humidity and the temperature was maintained at 32±2 °C for one week. After 7-8 days, inoculated plants began to exhibit symptoms of brown, necrotic leaf spots on the leaves of bitter gourd vines followed by yellowing of leaves that eventually turned brown. Roots showed slight discoloration and browning of vascular bundles and finally, the plants wilted after four weeks. while control plants remained symptomless. The symptoms resembled those noticed in the field. The fungus was re-isolated from leaves, collar region and roots, followed by morphological identification, and finally confirmed as F. equiseti. To the best of our knowledge, this is the first report of a leaf spot caused by F. equiseti in a bitter gourd from Pakistan. If the disease is not managed properly, it may cause a drastic effect on yield under favorable environmental conditions. The pathogen may also damage other cucurbitaceous crops cultivated in the area.

摘要

苦瓜(Momordica charantia L.)是葫芦科的一种重要蔬菜作物,在巴基斯坦及世界各地广泛种植。2020年10月,在巴基斯坦木尔坦巴哈丁·扎卡里亚大学农业研究农场(北纬30.2601°,东经71.5158°)一块10860平方英尺(99×110英尺)的土地上,对苦瓜品种Seminis - 200进行了营养管理试验。在苦瓜藤蔓的叶片上观察到大型褐色坏死叶斑症状。病害从网状叶脉内的叶片发黄开始,随后变为褐色。不规则的褐色叶斑合并形成大的坏死区域,接着是叶片黄化,然后是很晚才出现的萎蔫。虽然根部有轻微变色,纵向切开时观察到组织褐变,但没有冠腐症状。通过目测评估,该病发病率为37%,导致果实尺寸减小和发黄,品质和产量不佳。采集感染的藤蔓及其根部用于分离病原菌。从田间共采集了34片叶子和22个根样本用于分离。将叶片、茎基部和根部切成0.5至1厘米长,用1%次氯酸钠(NaOCl)表面消毒2 - 3分钟,然后用高压灭菌蒸馏水冲洗两次,干燥后置于马铃薯葡萄糖琼脂(PDA)培养基上,在25±2℃下培养一周。分离出了生长蓬松白色、带有浅橙色色素的真菌菌落。为进行形态学鉴定,在25±2℃下培养15天后,通过单孢技术在香石竹叶琼脂(CLA)培养基上从叶片、茎基部区域和根部共分离出4个纯培养物。在分生孢子盘上产生了弯曲且壁厚的大分生孢子,顶端细长或尖锐,基部细胞呈足形。具有5 - 7个隔膜的大分生孢子大小为22.50 - 41.80μm×2.90 - 4.20μm(n = 60)。观察到厚壁、褐色且壁粗糙的近球形至椭圆形厚垣孢子成簇或成链状,尺寸为5.8至10.8μm(n = 20)。根据莱斯利和萨默雷尔(2006年)的描述,从形态特征上,该真菌被鉴定为木贼镰刀菌(Fusarium equiseti (Corda) Sacc.)。使用两个单孢分离物通过用ITS1/ITS4引物(怀特等人,1990年)扩增内部转录间隔区(ITS)区域的核糖体DNA以及用引物T1/Bt - 2b(奥唐奈和齐格尔尼克,1997年)扩增β - 微管蛋白基因区域进行分子鉴定。获得的序列保存在GenBank中,ITS区域的登录号为MW880179和MW880198,在GenBank中进行BLAST搜索显示,分别与已发表的木贼镰刀菌序列OM992323.1和MT558569.1的比对率为100%和98.11%。β - 微管蛋白区域的登录号OM867571与登录号MN653163.1的木贼镰刀菌序列显示100%的序列相似性。为进行致病性测定,从CLA培养基上培养2周的培养物中收获大分生孢子以制备孢子悬浮液(1×10⁶个孢子/毫升)。通过在9株苦瓜植株(品种Seminis - 200)上进行柯赫氏法则验证,在3 - 4叶期分别用喷雾器将真菌接种物的孢子悬浮液施用于叶片上,在茎基部区域切开后施用孢子悬浮液,并在根区加入20毫升孢子悬浮液,而用蒸馏水作为对照,进行三次重复。将植株置于温室中的可控条件下,湿度保持在65%至75%,温度维持在32±2℃一周。7 - 8天后,接种的植株开始在苦瓜藤蔓的叶片上出现褐色坏死叶斑症状,随后叶片发黄,最终变为褐色。根部显示轻微变色和维管束褐变,最后,四周后植株萎蔫。而对照植株无症状。这些症状与在田间观察到的症状相似。从叶片、茎基部区域和根部重新分离出该真菌,随后进行形态学鉴定,最终确认为木贼镰刀菌。据我们所知,这是巴基斯坦苦瓜上由木贼镰刀菌引起叶斑病的首次报道。如果该病管理不当,在有利的环境条件下可能会对产量造成严重影响。该病原菌也可能损害该地区种植的其他葫芦科作物。

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