Perez B A, Farinon O M, Berretta M F
INTA, IMYZA, Nicolas Repetto y De Los Reseros, Hurlingham 1686, Buenos Aires, Argentina.
Plant Dis. 2011 Jun;95(6):774. doi: 10.1094/PDIS-01-11-0074.
In October 2007, blighted shoots were observed on highbush blueberry (Vaccinium corymbosum L. cv. O'Neal) plants in La Plata, Buenos Aires Province, Argentina. Isolations from surface-disinfested shoots onto carrot agar and Spezieller Nahrstoffarmer Agar (SNA) consistently yielded white colonies that produced black sclerotia, mainly near the edge of the culture plates, after 7 days. Sclerotia were transferred to SNA tubes and kept at 5°C for several months. The germination of sclerotia produced numerous 6 mm long initials, stipitate pale brown cup-shaped apothecia (10 × 6 mm) with eight-spored asci (137 × 7 μm) at 18°C and continuous light conditions. Asci with uniseriate ascospores were cylindrical and narrow at the base. Ascospores (11 to 12 × 4 μm) were hyaline, unicellular, smooth, and ellipsoid. This isolated fungus was morphologically identified as Sclerotinia sclerotiorum (Lib.) de Bary (2,3). The isolate was deposited in the IMYZA Microbial Collection as INTA-IMC 87. Mycelium was cultured in 100 ml of Czapek's-Dox medium, supplemented with sucrose, peptone, yeast extract, sodium nitrate, and vitamins (1), for 3 days and fungal DNA was obtained using a DNA extraction kit. ITS1 and ITS2 of ribosomal genes were amplified by PCR using universal primers (4) and the PCR product was sequenced. A BLAST algorithm search revealed 100% identity of the sequence with 12 GenBank entries for S. sclerotiorum. The nucleotide sequence was deposited in the GenBank with Accession No. JF277567. Pathogenicity testing was achieved by placing detached leaves of cvs. Emerald, Misty, and Start on water agar (WA) plates, inoculating with 9-mm mycelial blocks, and incubating at 20°C with 12 h of light. Young shoots of highbush blueberry, Misty and O'Neal, were inoculated by the cut shoot method with micropipette tips filled with mycelium and kept under greenhouse conditions at 24°C and 14 h of light. On control plants, WA blocks or WA-filled micropipette tips were used. Leaf blight was observed after 5 to 6 days and sclerotia appeared after 7 days on inoculated tissues. Shoot blight was recorded on inoculated plants after 5 days. The fungus was reisolated from inoculated tissues, with no symptoms showing on controls. To our knowledge, this is the first report of Sclerotinia rot caused by S. sclerotiorum in blueberry in Argentina. References: (1) J.F. Leslie and B. A. Summerell. The Fusarium Laboratory Manual. Blackwell Publishing, Hoboken, NJ, 2006. (2). J. E. M. Mourde and P. Holliday. No. 513 in: CMI Descriptions of Pathogenic Fungi and Bacteria. Kew, Surrey, UK, 1976. (3) S. Umemoto et al. Gen. Plant Pathol. 73:290, 2007. (4) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, 1990.
2007年10月,在阿根廷布宜诺斯艾利斯省拉普拉塔的高丛蓝莓(Vaccinium corymbosum L. cv. O'Neal)植株上观察到了枯萎枝条。将表面消毒后的枝条接种到胡萝卜琼脂和特殊营养贫瘠琼脂(SNA)上,7天后始终长出白色菌落,这些菌落在培养皿边缘附近产生黑色菌核。将菌核转移到SNA试管中,并在5°C下保存数月。在18°C和连续光照条件下,菌核萌发产生许多6毫米长的初始体,具柄的浅褐色杯状子囊盘(10×6毫米),有含8个孢子的子囊(137×7微米)。具有单列子囊孢子的子囊呈圆柱形,基部狭窄。子囊孢子(11至12×4微米)透明、单细胞、光滑且呈椭圆形。这种分离出的真菌在形态上被鉴定为核盘菌(Sclerotinia sclerotiorum (Lib.) de Bary)(2,3)。该分离株保藏于IMYZA微生物保藏中心,编号为INTA - IMC 87。将菌丝体在100毫升添加了蔗糖、蛋白胨、酵母提取物、硝酸钠和维生素的察氏培养基(1)中培养3天,然后使用DNA提取试剂盒获得真菌DNA。使用通用引物通过PCR扩增核糖体基因的ITS1和ITS2,并对PCR产物进行测序。BLAST算法搜索显示该序列与GenBank中12个核盘菌条目具有100%的同一性。核苷酸序列已存入GenBank,登录号为JF277567。通过将品种Emerald、Misty和Start的离体叶片放置在水琼脂(WA)平板上,接种9毫米的菌丝块,并在20°C、12小时光照条件下培养来进行致病性测试。用装满菌丝体的微量移液器吸头通过切枝法接种高丛蓝莓品种Misty和O'Neal的嫩枝,并在温室条件下24°C、14小时光照下培养。对于对照植株,使用WA块或装有WA的微量移液器吸头。接种组织在5至6天后观察到叶枯病,7天后出现菌核。接种植株在5天后记录到枝枯病。从接种组织中重新分离出该真菌,对照植株未出现症状。据我们所知,这是阿根廷蓝莓中由核盘菌引起的菌核病的首次报道。参考文献:(1)J.F. Leslie和B.A. Summerell。《镰刀菌实验室手册》。Blackwell Publishing,新泽西州霍博肯,2006年。(2)J.E.M. Mourde和P. Holliday。载于《英联邦真菌研究所病原真菌和细菌描述》第513号。英国萨里郡邱园,1976年。(3)S. Umemoto等人。《植物病理学报》73:290,2007年。(4)T.J. White等人。载于《PCR实验方案:方法与应用指南》第315页。学术出版社,圣地亚哥,1990年。