Mahadevakumar S, Yadav Vandana, Tejaswini G S, Sandeep S N, Janardhana G R
Mycology and Phytopathology Laboratory, Department of Studies in Botany, Manasagangotri, University of Mysore, Mysore-570 006, Karnataka, India.
Department of Studies in Microbiology, Manasagangotri, University of Mysore, Mysore-570 006, Karnataka, India.
Plant Dis. 2014 Sep;98(9):1281. doi: 10.1094/PDIS-04-14-0388-PDN.
Lemon (Citrus lemon (L.) Burm. f.) is an important fruit crop cultivated worldwide, and is grown practically in every state in India (3). During a survey conducted in 2013, a few small trees in a lemon orchard near Mysore city (Karnataka) (12°19.629' N, 76°31.892' E) were found affected by dieback disease. Approximately 10 to 20% of trees were affected as young shoots and branches showed progressive death from the apical region downward. Different samples were collected and diagnosed via morphological methods. The fungus was consistently isolated from the infected branches when they were surface sanitized with 1.5% NaOCl and plated on potato dextrose agar (PDA). Plates were incubated at 26 ± 2°C for 7 days at 12/12 h alternating light and dark period. Fungal colonies were whitish with pale brown stripes having an uneven margin and pycnidia were fully embedded in the culture plate. No sexual state was observed. Pycnidia were globose, dark, 158 to 320 μm in diameter, and scattered throughout the mycelial growth. Both alpha and beta conidia were present within pycnidia. Alpha conidia were single celled (5.3 to 8.7 × 2.28 to 3.96 μm) (n = 50), bigittulate, hyaline, with one end blunt and other truncated. Beta conidia (24.8 to 29.49 × 0.9 to 1.4 μm) (n = 50) were single celled, filiform, with one end rounded and the other acute and curved. Based on the morphological and cultural features, the fungal pathogen was identified as Phomopsis citri H.S. Fawc. Pathogenicity test was conducted on nine healthy 2-year-old lemon plants via foliar application of a conidial suspension (3 × 10); plants were covered with polythene bags for 6 days and maintained in the greenhouse. Sterile distilled water inoculated plants (in triplicate) served as controls and were symptomless. Development of dieback symptoms was observed after 25 days post inoculation and the fungal pathogen was re-isolated from the inoculated lemon trees. The internal transcribed spacer region (ITS) of the isolated fungal genomic DNA was amplified using universal-primer pair ITS1/ITS4 and sequenced to confirm the species-level diagnosis (4). The sequence data of the 558-bp amplicon was deposited in GenBank (Accession No. KJ477016.1) and nBLAST search showed 99% homology with Diaporthe citri (teleomorph) strain 199.39 (KC343051.1). P. citri is known for its association with melanose disease of citrus in India, the United States, and abroad. P. citri also causes stem end rot of citrus, which leads to yield loss and reduction in fruit quality (1,2). Dieback disease is of serious concern for lemon growers as it affects the overall productivity level of the tree. To the best of our knowledge, this is the first report of P. citri causing dieback of lemon in India. References: (1) I. H. Fischer et al. Sci. Agric. (Piracicaba). 66:210, 2009. (2) S. N. Mondal et al. Plant Dis. 91:387, 2007. (3) S. P. Raychaudhuri. Proc. Int. Soc. Citriculture 1:461, 1981. (4) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, CA, 1990.
柠檬(Citrus lemon (L.) Burm. f.)是一种在全球范围内广泛种植的重要水果作物,在印度的每个邦几乎都有种植(3)。在2013年进行的一项调查中,迈索尔市(卡纳塔克邦)附近(北纬12°19.629',东经76°31.892')的一个柠檬果园里,发现几棵小树受到了枝枯病的影响。大约10%至20%的树木受到影响,因为嫩梢和树枝从顶端区域向下逐渐死亡。采集了不同样本并通过形态学方法进行诊断。当用1.5%次氯酸钠对受感染的枝条进行表面消毒并接种在马铃薯葡萄糖琼脂(PDA)上时,始终能从这些枝条上分离出真菌。平板在26±2°C下培养7天,光照和黑暗周期为12/12小时交替。真菌菌落呈白色,带有浅棕色条纹,边缘不整齐,分生孢子器完全嵌入培养平板中。未观察到有性态。分生孢子器呈球形,深色,直径158至320μm,散布在整个菌丝生长中。分生孢子器内同时存在α和β分生孢子。α分生孢子为单细胞(5.3至8.7×2.28至3.96μm)(n = 50),双凸透镜状,透明,一端钝圆,另一端截形。β分生孢子(24.8至29.49×0.9至1.4μm)(n = 50)为单细胞,丝状,一端圆形,另一端尖锐且弯曲。根据形态和培养特征,该真菌病原体被鉴定为柑橘拟茎点霉(Phomopsis citri H.S. Fawc.)。通过叶面喷施分生孢子悬浮液(3×10)对9株健康的2年生柠檬植株进行了致病性测试;植株用聚乙烯袋覆盖6天,并保持在温室中。接种无菌蒸馏水的植株(一式三份)作为对照,无症状。接种后25天观察到枝枯症状的发展,并且从接种的柠檬树上重新分离出了真菌病原体。使用通用引物对ITS1/ITS4扩增分离的真菌基因组DNA的内部转录间隔区(ITS)并进行测序,以确认种水平的诊断(4)。558bp扩增子的序列数据保存在GenBank中(登录号KJ477016.1),nBLAST搜索显示与柑橘间座壳菌(Diaporthe citri)(有性型)菌株199.39(KC343051.1)的同源性为99%。柑橘拟茎点霉在印度、美国及其他国家与柑橘的黑腐病有关。柑橘拟茎点霉还会导致柑橘的蒂腐病,从而导致产量损失和果实品质下降(1,2)。枝枯病是柠檬种植者严重关注的问题,因为它会影响树木的整体生产力水平。据我们所知,这是柑橘拟茎点霉在印度导致柠檬枝枯病的首次报道。参考文献:(1)I. H. Fischer等人,《科学农业(皮拉西卡巴)》,66:210,2009年。(2)S. N. Mondal等人,《植物病害》,91:387,2007年。(3)S. P. Raychaudhuri,《国际柑橘学会会议论文集》,1:461,1981年。(4)T. J. White等人,见《PCR实验指南:方法与应用》第315页,学术出版社,加利福尼亚州圣地亚哥,1990年。