Hamid M I, Hussain M, Ghazanfar M U, Raza M, Liu X Z
Department of Plant Pathology, University College of Agriculture, University of Sargodha, 40100, Pakistan, and State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China.
Department of Plant Pathology, University College of Agriculture, University of Sargodha, 40100, Pakistan.
Plant Dis. 2014 Sep;98(9):1271. doi: 10.1094/PDIS-01-14-0051-PDN.
During a field survey of greenhouses and fresh markets in 2013, fruits of tomato, oranges, and apples exhibited rot symptoms with white mycelial growth and salmon-color sporulation in the vicinity of Sargodha city (32°5'1″ N, 72°40'16″ E), Pakistan. Diseased fruit samples were collected in plastic bags and taken to laboratory on ice for further diagnosis. Diseased fruits were observed under a stereo microscope and single spores were removed using an inoculating needle. Isolation from single spores showed pink to white colonies on potato dextrose agar (PDA) containing hyaline, 2-celled, ellipsoid to pyriform conidia (17 to 24 × 7 to 11 μm) with slanting and truncate basal mark and produced in clusters. Conidiophores were branched (105 to 254 × 2 to 4 μm) and hyphae were hyaline (3 to 5 μm in diameter). These characteristics of the fungus were similar to Trichothecium roseum (Pers.) as reported by Inácio et al. (1). Genomic DNA was extracted by using CTAB buffer from a single pure colony of one isolate of the fungus and PCR analysis was performed for ITS region and part of the 5' end of the beta tubulin (TUB) gene (2,3). Single fragments of 550 bp and 1.5 kb length from ITS and TUB gene were amplified and sequenced (GenBank Accession Nos. KF975702 and KJ607590, respectively). Sequence analysis showed 99% similarity with T. roseum isolates from different regions of the world. Phylogenetic analysis (MEGA version 5.2 with WAG model) showed the close relatedness to the isolates of T. roseum from Pakistan and isolates from other parts of the world that revealed the low genetic variability of ITS region. TUB gene sequence analysis indicated 100% homology with isolates of T. roseum and to the other species in Hypocreales. Pathogenicity tests were performed on tomato cvs. Nova Mech and Rio Grande, orange cv. Kinnow, and on apple cv. Golden Delicious by inoculating five fruits from each cultivar. Spore suspensions (10 conidia/ml of sterilized distilled water) were inoculated into all wounded fruits (9 wounds/fruit) of each cultivar and incubated at 25°C for the development of symptoms. Five wounded fruits of each cultivar were inoculated with sterilized distilled water as a control treatment. The fruits were kept in plastic boxes and incubated in humid chambers for 5 days. The symptoms on apples were observed as brown rot with pinkish spores on rotted tissue. The cross section of apple fruits also showed the brown rotted tissues internally. The fungus developed mycelium and spores on the surface and caused severe rotting inside the tomato and citrus fruits. T. roseum was re-isolated by picking a single spore from rotted tissues of fruits under a stereo microscope, and culturing on PDA. The re-isolated fungus was confirmed morphologically and by molecular techniques. Tomato and apple has been reported as a host for T. roseum (1,4,5) but oranges have not. To our knowledge, this is the first record of T. roseum infecting tomato, oranges, and apples in Pakistan. References: (1) C. A. Inácio et al. Plant Dis. 95:1318. 2011. (2) K. O'Donnell, and E. Cigelnik. Mol. Phylogenet. Evol. 7:103, 1997. (3) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, CA, 1990. (4) Y. H. Yun et al. Afr. J. Microbiol. Res. 7:1128, 2013. (5) M. Žabka et al. Mycopathologia. 162:65, 2006.
2013年在巴基斯坦萨戈达市(北纬32°5'1″,东经72°40'16″)附近的温室和生鲜市场进行实地调查期间,番茄、橙子和苹果果实出现了腐烂症状,在病斑附近有白色菌丝生长和鲑鱼色的孢子形成。患病果实样本用塑料袋收集,并在冰上运往实验室进行进一步诊断。在体视显微镜下观察患病果实,并用接种针挑出单个孢子。从单个孢子分离培养后,在含有透明、2细胞、椭圆形至梨形分生孢子(17至24×7至11μm)且基部有倾斜和截断痕迹并成簇产生的马铃薯葡萄糖琼脂(PDA)上形成粉红色至白色菌落。分生孢子梗呈分枝状(105至254×2至4μm),菌丝透明(直径3至5μm)。该真菌的这些特征与伊纳西奥等人(1)报道的粉红单端孢霉(Pers.)相似。使用CTAB缓冲液从该真菌一个分离株的单个纯菌落中提取基因组DNA,并对ITS区域和β微管蛋白(TUB)基因5'端的部分进行PCR分析(2,3)。从ITS和TUB基因分别扩增出长度为550bp和1.5kb的单片段并进行测序(GenBank登录号分别为KF975702和KJ607590)。序列分析显示与来自世界不同地区的粉红单端孢霉分离株有99%的相似性。系统发育分析(使用WAG模型的MEGA 5.2版本)表明与来自巴基斯坦的粉红单端孢霉分离株以及来自世界其他地区的分离株亲缘关系密切,这表明ITS区域的遗传变异性较低。TUB基因序列分析表明与粉红单端孢霉分离株以及肉座菌目的其他物种有100%的同源性。对番茄品种新星机械和里奥格兰德、橙子品种金诺以及苹果品种金冠进行致病性测试,每个品种接种5个果实。将孢子悬浮液(10个分生孢子/毫升无菌蒸馏水)接种到每个品种的所有受伤果实(每个果实9个伤口)中,并在25°C下培养以观察症状发展。每个品种的5个受伤果实接种无菌蒸馏水作为对照处理。果实保存在塑料盒中,在湿度箱中培养5天。苹果上的症状表现为褐色腐烂,腐烂组织上有粉红色孢子。苹果果实的横切面内部也显示出褐色腐烂组织。该真菌在番茄和柑橘类果实表面形成菌丝和孢子,并导致内部严重腐烂。通过在体视显微镜下从果实腐烂组织中挑取单个孢子,并在PDA上培养,重新分离出粉红单端孢霉。通过形态学和分子技术对重新分离的真菌进行了确认。番茄和苹果已被报道为粉红单端孢霉的寄主(1,4,5),但橙子尚未见报道。据我们所知,这是粉红单端孢霉在巴基斯坦感染番茄、橙子和苹果的首次记录。参考文献:(1)C.A.伊纳西奥等人,《植物病害》95:1318,2011年。(2)K.奥唐奈和E.齐格尔尼克,《分子系统发育与进化》7:103,1997年。(3)T.J.怀特等人,载于《PCR协议:方法与应用指南》第315页,学术出版社,加利福尼亚州圣地亚哥,1990年。(4)Y.H.尹等人,《非洲微生物学研究杂志》7:1128,2013年。(5)M.扎布卡等人,《真菌病理学》162:65,2006年。