Mahadevakumar S, Janardhana G R
Mycology and Phytopathology Laboratory, Department of Studies in Botany, University of Mysore, Manasagangotri, Mysore 570 006, Karnataka, India.
Plant Dis. 2014 May;98(5):686. doi: 10.1094/PDIS-02-13-0171-PDN.
Cowpea (Vigna unguiculata (L.) Walp) is an important legume crop cultivated in arid and semi-arid regions in underdeveloped and developing countries. India is a leading cowpea producer. In addition to India, Nigeria and Niger are the predominant producers of cowpea in the world. Brazil, Haiti, Myanmar, Sri Lanka, and the United States are also significant producers of cowpea. This is a drought-tolerant annual crop that thrives in warm weather (3), and is more well-adapted to the drier regions of the tropics than any other legume. Cowpea fields (190 ha) surveyed in Mysore district (Karnataka State) from 2010 to 2012 were found affected by a new leaf spot disease. Over 60% of surveyed fields were affected by this disease, with individual fields ranging from 30 to 75% disease incidence. Individual fields experienced an estimated 10 to 15% yield loss. Initially, leaf spot symptoms appeared as small, dark, necrotic lesions that increased to a diameter of 0.5 to 1.0 cm. These spots later enlarged to form brown, circular, elliptical, and irregular spots with halo margins. Symptoms persisted throughout the cropping season. Under severe infection, defoliation occurred. Black, sessile, discoid conidiomata were observed in lesions and exuded a pink spore mass that later turned brown. The fungus was isolated from affected leaf tissues that were surface sterilized with 2% NaOCl solution, washed thrice with sterile water, blotter dried, and inoculated onto potato dextrose agar (PDA). White mycelia produced black globular acervuli with conidia on PDA after 7 days of incubation at 28 ± 2°C with a 12-h alternate light and dark period. Conidia had 5-celled (21.37 to 24.89 × 6.3 to 6.9 μm) segmentation with darker median cells and hyaline end cells. The apical cell typically had three appendages (sometimes 2 to 4) measuring 22.0 to 27.3 μm long and the basal appendage was 3.47 to 6.2 μm long. Based on these morphological features, the fungal pathogen was identified as Pestalotiopsis species. The isolated fungus was tested for pathogenecity on 30-day-old healthy cowpea plants grown under greenhouse conditions. A conidial suspension was prepared from 7-day-old culture by flooding with 2 to 4 ml of sterile distilled water. Spores were collected with a sterile micropipette and spore concentration was adjusted to 3 × 10 conidia/ml and applied as foliar spray onto 15 plants each in three replicates. Non-inoculated control plants were sprayed with sterile water. The plants were kept under high humidity (80%) for 5 days and at ambient temperature (28 ± 2°C). After 10 to 12 days post-inoculation, leaf spot symptoms appeared on inoculated plants, and the fungal pathogen was re-isolated and no such symptoms were found on control plants. The pathogen was confirmed by micro-morphological features. The ITS region of the ribosomal RNA gene was amplified using primers ITS1 and ITS4 (2). The amplified PCR product was purified and sequenced. nBLAST search comparison of sequences revealed 99% homology to Pestalotiopsis photiniae (AY682946.1). A representative sequence was deposited in GenBank (KC568288.1). Pestalotiopsis is an important pathogen on many crop plants and has been recorded on a wide variety of hosts, primarily on leaves, fruits, and in the rhizosphere. In recent times, cowpea is susceptible to a wide range of fungal pathogens causing severe yield loss at all stages of growth and development (1). Leaf spot caused by Pestalotiopsis species are becoming a major constraint for cowpea production in India. No previous reports are available on Pestalotiopsis species causing leaf spot of cowpea in India. References: (1) S. Mahadevakumar and G. R. Janardhana. New Dis. Rep. 25:17, 2012. (2) T. J. White et al. PCR Protocols: A Guide to Methods and Applications, page 315. Academic Press, San Diego, 1990. (3) A. A. Zohri et al. Korean Mycol. 20:252, 1992.
豇豆(Vigna unguiculata (L.) Walp)是一种重要的豆类作物,在欠发达国家和发展中国家的干旱和半干旱地区种植。印度是主要的豇豆生产国。除印度外,尼日利亚和尼日尔是世界上主要的豇豆生产国。巴西、海地、缅甸、斯里兰卡和美国也是重要的豇豆生产国。这是一种耐旱的一年生作物,在温暖的天气中生长旺盛(3),比任何其他豆类更能适应热带较干燥的地区。2010年至2012年在迈索尔区(卡纳塔克邦)调查的190公顷豇豆田被发现受到一种新的叶斑病影响。超过60%的调查田块受到这种病害影响,单个田块的发病率在30%至75%之间。单个田块估计减产10%至15%。最初,叶斑症状表现为小的、深色的坏死斑,直径增加到0.5至1.0厘米。这些斑点后来扩大形成褐色、圆形、椭圆形和不规则斑点,边缘有晕圈。症状在整个种植季节持续存在。在严重感染下,会发生落叶。在病斑中观察到黑色、无柄、盘状的分生孢子盘,散发出粉红色的孢子团,后来变成褐色。从受影响的叶片组织中分离真菌,这些组织用2%次氯酸钠溶液进行表面消毒,用无菌水冲洗三次,吸干水分,然后接种到马铃薯葡萄糖琼脂(PDA)上。在28±2°C、12小时明暗交替的条件下培养7天后,白色菌丝体在PDA上产生带有分生孢子的黑色球状分生孢子盘。分生孢子有5个细胞(21.37至24.89×6.3至6.9μm),中间细胞较深,末端细胞透明。顶端细胞通常有三个附属物(有时2至4个),长22.0至27.3μm,基部附属物长3.47至6.2μm。基于这些形态特征,真菌病原体被鉴定为拟盘多毛孢属物种。对在温室条件下生长的30日龄健康豇豆植株测试分离出的真菌的致病性。用2至4毫升无菌蒸馏水淹没7日龄培养物制备分生孢子悬浮液。用无菌微量移液器收集孢子,将孢子浓度调整到3×10分生孢子/毫升,并作为叶面喷雾分别施用于15株植物,共三个重复。未接种的对照植株用无菌水喷雾。植株在高湿度(80%)下保持5天,在环境温度(28±2°C)下。接种后10至12天,接种植株上出现叶斑症状,真菌病原体被重新分离,对照植株上未发现此类症状。通过微观形态特征确认了病原体。使用引物ITS1和ITS4扩增核糖体RNA基因的ITS区域(2)。对扩增的PCR产物进行纯化和测序。序列的nBLAST搜索比较显示与光叶拟盘多毛孢(AY682946.1)有99%的同源性。一个代表性序列保存在GenBank(KC568288.1)中。拟盘多毛孢是许多作物上的重要病原体,已在多种寄主上有记录,主要在叶片、果实和根际。近年来,豇豆易受多种真菌病原体影响,在生长发育的各个阶段造成严重减产(1)。由拟盘多毛孢属物种引起的叶斑病正成为印度豇豆生产的主要限制因素。此前没有关于印度拟盘多毛孢属物种引起豇豆叶斑病的报道。参考文献:(1)S. Mahadevakumar和G. R. Janardhana。New Dis. Rep. 25:17,2012。(2)T. J. White等人。PCR Protocols: A Guide to Methods and Applications,第315页。Academic Press,圣地亚哥,1990。(3)A. A. Zohri等人。Korean Mycol. 20:252,1992。