Chebil S, Fersi R, Yakoub A, Chenenaoui S, Chattaoui M, Melki I, Zemni H, Rhouma A, Durante G, Zacchi E, Mliki A
Laboratory of Plant Molecular Physiology, Biotechnology Center of Borj-cédria (CBBC), Hammam-lif, Tunisia.
Laboratory of Improvement and Protection of Genetic Resources of Olive, Olive Tree Institute, Avenue H. Karray, 1002 Tunis Belvedere, Tunis, Tunisia.
Plant Dis. 2014 Mar;98(3):420. doi: 10.1094/PDIS-05-13-0530-PDN.
In 2011, common symptoms of grapevine dieback were frequently observed in 2- to 5-year-old table grape (Vitis vinifera L.) cvs. in four vineyards located in northern Tunisia. The symptoms included dead spur and cordons, shoot dieback, and sunken necrotic bark lesions, which progressed into the trunk resulting in the death of large sections of the vine. Longitudinal and transversal sections of cordons and spurs from symptomatic vines revealed brown wedge-shaped cankers of hard consistency. Twelve symptomatic samples from spur and cordons were collected, surface disinfected by dipping into 5% (v/v) sodium hypochlorite for 2 min, and small pieces from the edge of necrotic and healthy tissue were removed and plated onto potato dextrose agar (PDA) at 25°C in the dark. Based on colony and conidia morphological characteristics, isolates were divided in three species, named Diplodia seriata, Botryosphaeria dothidea, and Neofusicoccum luteum. D. seriata colonies were gray-brown with dense aerial mycelium producing brown cylindric to ellipsoid conidia rounded at both ends and averaged 22.4 × 11.7 μm (n = 50). B. dothidea colonies were initially white with abundant aerial mycelium, gradually becoming dark green olivaceous. Conidia were fusiform to fusiform elliptical with a subobtuse apex and averaged 24.8 × 4.7 μm (n = 50). N. luteum colonies were initially pale to colorless, gradually darkening with age and becoming gray to dark gray producing a yellow pigment that diffuses into the agar. Conidia were hyaline, thin-walled, aseptate, fusiform to fusiform elliptical, and averaged 19.8 × 5.5 μm (n = 50). Identity of the different taxa was confirmed by sequence analyses of the internal transcribed spacer (ITS1-5.8S-ITS2) region of the rDNA and part of the elongation factor 1-alpha (EF1-α) gene. BLAST analysis of sequences indicated that six isolates were identified as D. seriata (GenBank: AY259094, AY343353), one isolate as B. dothidea (AY236949, AY786319) and one isolate as N. luteum (AY259091, AY573217). Sequences were deposited in GenBank under accessions from KC178817 to KC178824 and from KF546829 to KF546836 for ITS region and EF1-α gene, respectively. A pathogenicity test was conducted on detached green shoots cv. Italia for the eight Botryosphaeriaceae isolates. Shoots were inoculated by placing a colonized agar plug (5 mm diameter) from the margin of a 7-day-old colony on fresh wound sites made with a sterilized scalpel. Each wound was covered with moisturized cotton and sealed with Parafilm. Control shoots were inoculated using non-colonized PDA plugs. After 6 weeks, discoloration of xylem and phloem and necrosis with average length of 38.8, 17.6, and 11.2 mm were observed from inoculated shoots with D. seriata, N. luteum, and B. dothidea, respectively, and all three fungi were re-isolated from necrotic tissue, satisfying Koch's postulates. Control shoots showed no symptoms of the disease and no fungus was re-isolated. In Tunisia, Botryosphaeria-related dieback was reported only on citrus tree caused by B. ribis (2), on Pinus spp. caused by D. pinea (4), on Quercus spp. caused by D. corticola (3), and on olive tree (Olea europea) caused by D. seriata (1). To our knowledge, this is the first report of D. seriata, B. dothidea, and N. luteum associated with grapevine dieback in Tunisia. References: (1) M. Chattaoui et al. Plant Dis. 96:905, 2012. (2) H. S. Fawcett. Calif. Citrogr. 16:208, 1931. (3) B. T. Linaldeddu et al. J. Plant Pathol. 91:234. 2009. (4) B. T. Linaldeddu et al. Phytopathol. Mediterr. 47:258, 2008.
2011年,在突尼斯北部四个葡萄园的2至5年生鲜食葡萄(欧亚种葡萄)品种中,经常观察到葡萄藤枯死的常见症状。症状包括枯死的短枝和主蔓、新梢枯死以及树皮坏死凹陷病斑,这些病斑蔓延至树干,导致葡萄藤大片死亡。对有症状葡萄藤的主蔓和短枝进行纵切和横切,发现有坚硬质地的褐色楔形溃疡。从短枝和主蔓上采集了12个有症状的样本,将其浸入5%(v/v)次氯酸钠中表面消毒2分钟,然后从坏死组织和健康组织边缘取下小块组织,接种到马铃薯葡萄糖琼脂(PDA)培养基上,于25°C黑暗条件下培养。根据菌落和分生孢子的形态特征,分离菌株分为三个种,分别命名为葡萄座腔菌、葡萄球座菌和黄新壳梭孢。葡萄座腔菌菌落为灰褐色,气生菌丝浓密,产生两端圆形的褐色圆柱形至椭圆形分生孢子,平均大小为22.4×11.7μm(n = 50)。葡萄球座菌菌落最初为白色,气生菌丝丰富,逐渐变为深绿色橄榄色。分生孢子为梭形至梭形椭圆形,顶端近钝形,平均大小为24.8×4.7μm(n = 50)。黄新壳梭孢菌落最初为浅色至无色,随时间逐渐变暗,变为灰色至深灰色,产生黄色色素并扩散到琼脂中。分生孢子透明,薄壁,无隔膜,梭形至梭形椭圆形,平均大小为19.8×5.5μm(n = 50)。通过对核糖体DNA的内部转录间隔区(ITS1-5.8S-ITS2)区域和部分延伸因子1-α(EF1-α)基因进行序列分析,确认了不同分类单元的身份。序列的BLAST分析表明,六个分离菌株被鉴定为葡萄座腔菌(GenBank:AY259094,AY343353),一个分离菌株为葡萄球座菌(AY236949,AY786319),一个分离菌株为黄新壳梭孢(AY259091,AY573217)。ITS区域和EF1-α基因的序列分别以登录号KC178817至KC178824和KF546829至KF546836存入GenBank。对八个葡萄座腔菌科分离菌株在离体的“意大利”品种绿色新梢上进行了致病性测试。用无菌手术刀在新梢上造成新鲜伤口,将7日龄菌落边缘的带菌琼脂块(直径5mm)放置在伤口处进行接种。每个伤口用湿棉花覆盖,并用Parafilm密封。对照新梢接种未带菌的PDA琼脂块。6周后,接种葡萄座腔菌、黄新壳梭孢和葡萄球座菌的新梢分别观察到木质部和韧皮部变色以及坏死,平均长度分别为38.8、17.6和11.2mm,并且从坏死组织中重新分离出了所有三种真菌,满足科赫法则。对照新梢未表现出该病症状,也未重新分离出真菌。在突尼斯,仅报道过由葡萄座腔菌引起的柑橘树葡萄座腔菌相关枯死病(2)、由松色二孢引起的松树葡萄座腔菌相关枯死病(4)、由皮层葡萄座腔菌引起的栎树葡萄座腔菌相关枯死病(3)以及由葡萄座腔菌引起的橄榄树(油橄榄)葡萄座腔菌相关枯死病(1)。据我们所知,这是突尼斯首次报道葡萄座腔菌、葡萄球座菌和黄新壳梭孢与葡萄藤枯死有关。参考文献:(1)M. Chattaoui等人,《植物病害》96:905,2012年。(2)H. S. Fawcett,《加利福尼亚柑橘》16:208,1931年。(3)B. T. Linaldeddu等人,《植物病理学杂志》91:234,2009年。(4)B. T. Linaldeddu等人,《地中海植物病理学》47:258,2008年。