Serrato-Diaz L M, Latoni-Brailowsky E I, Rivera-Vargas L I, Goenaga R, Crous P W, French-Monar R D
Department of Plant Pathology and Microbiology, Texas A&M AgriLife Extension Service, Amarillo.
Department of Crops and Agro-Environmental Sciences, University of Puerto Rico, Mayaguez Campus.
Plant Dis. 2013 Aug;97(8):1117. doi: 10.1094/PDIS-01-13-0008-PDN.
Fruit rot of rambutan is a pre- and post-harvest disease problem of rambutan orchards. In 2011, fruit rot was observed at USDA-ARS orchards in Mayaguez, Puerto Rico. Infected fruit were collected and 1 mm tissue sections were surface disinfested with 70% ethanol followed by 0.5% sodium hypochlorite. Infected fruit were rinsed with sterile, deionized, double-distilled water and transferred to acidified potato dextrose agar (APDA). Plates were incubated at 25 ± 1°C for 6 days. Three isolates of Calonectria hongkongensis (Cah), CBS134083, CBS134084, and CBS134085, were identified morphologically using taxonomic keys (2,3). In APDA, colonies of Cah produced raw sienna to rust-colored aerial mycelial growth. Conidiophores of Cah had a penicillate arrangement of primary to quaternary branches of 2 to 6 phialides. Conidia (n = 50) were cylindrical, hyaline, 1-septate, rounded at both ends, and 44 to 52 μm × 3.5 to 4.5 μm. Conidiophores produced terminal and lateral stipe extensions with terminal sphaeropedunculate vesicles that were 8 to 12 μm wide. Subglobose to ovoid perithecia, 300 to 500 μm × 200 to 350 μm and orange to red-brown, were produced in groups of 3. Asci were clavate and contained 8 ascospores aggregated at the top of the ascus. Ascospores (n = 50) were hyaline, guttulate, fusoid with rounded ends, straight to curved, 1-septate with constriction at the septum, and 28 to 36 μm × 4 to 7 μm. For molecular identification, the ITS rDNA, fragments of β-tubulin (BT), histone H3 (HIS3), and elongation factor (EF1-α) genes were amplified by PCR, sequenced, and compared using BLASTn with Calonectria spp. submitted to the NCBI GenBank. The sequences of Cah submitted to GenBank include accessions KC342208, KC342206, and KC342207 for ITS; KC342217, KC342215, and KC342216 for BT; KC342211, KC342209, and KC342210 for HIS3; and KC342214, KC342212, and KC342213 for EF1α. The sequences were >99% or identical with the ex-type specimen of Cah CBS 114828 for all genes used. Pathogenicity tests were conducted on 5 healthy superficially sterilized fruits per isolate. Both scalpel-wounded and unwounded fruit tissues were inoculated with 5-mm mycelial disks from 8-day-old pure cultures grown in APDA. Untreated controls were inoculated with APDA disks only. Fruits were kept in a humid chamber for 8 days at 25°C under 12 h of fluorescent light. The test was repeated once. Three days after inoculation (DAI), white mycelial growth was observed on the fruit. Five DAI, the fruit changed color from red to brown and yellowish mycelia colonized 50 to 62% of the fruit surface. Eight DAI, all the fruit turned brown, the mycelium growth covered the entire fruit, and conidiophores were produced on spinterns (hairlike appendages). Fruit rot of spinterns, exocarp (skin), endocarp (aril), and light brown discoloration were observed inside the fruit. Untreated controls showed no symptoms of fruit rot and no fungi were reisolated from tissue. Cah was reisolated from diseased tissue, fulfilling Koch's postulates. Calonectria spp. (or their Cylindrocladium asexual states) have been associated with lychee decline syndrome in North Vietnam (1). Both fruits belong to the Sapindaceae family. To our knowledge, this is the first report of Cah causing fruit rot of rambutan. References: (1) L. M. Coates et al. Diseases of Longan, Lychee and Rambutan. Pages 307-325 in: Diseases of Tropical Fruit Crops. R. C. Ploetz, ed. CABI Publishing, Cambridge, MA, 2003. (2) P. W. Crous. Taxonomy and Pathology of Cylindrocladium (Calonectria) and Allied Genera. APS Press, St Paul, MN, 2002. (3) P. W. Crous, et al. Stud. Mycol. 50:415, 2004.
红毛丹果实腐烂是红毛丹果园采前和采后的病害问题。2011年,在美国农业部农业研究局位于波多黎各马亚圭斯的果园中观察到果实腐烂现象。采集受感染的果实,将1毫米厚的组织切片先用70%乙醇进行表面消毒,再用0.5%次氯酸钠处理。受感染的果实用无菌去离子双蒸水冲洗后,转移至酸化马铃薯葡萄糖琼脂(APDA)培养基上。平板在25±1°C下培养6天。使用分类学检索表从形态学上鉴定出3株香港红丝壳菌(Cah),分别为CBS134083、CBS134084和CBS134085。在APDA培养基上,Cah的菌落产生生赭色至铁锈色的气生菌丝生长。Cah的分生孢子梗具有2至6个瓶梗,从一级到四级分支呈帚状排列。分生孢子(n = 50)呈圆柱形,透明,具1个隔膜,两端圆形,大小为44至52μm×3.5至4.5μm。分生孢子梗产生顶端和侧面的柄状延伸物,顶端有球形柄状囊泡,宽8至12μm。3个一组产生近球形至卵形的子囊壳,大小为300至500μm×200至350μm,颜色为橙色至红棕色。子囊呈棒状,每个子囊包含8个聚集在子囊顶部的子囊孢子。子囊孢子(n = 50)透明,具油滴,两端圆形呈梭形,直或弯曲,具1个隔膜且在隔膜处缢缩,大小为28至36μm×4至7μm。为进行分子鉴定,通过PCR扩增ITS rDNA、β-微管蛋白(BT)、组蛋白H3(HIS3)和延伸因子(EF1-α)基因的片段,进行测序,并使用BLASTn与提交到NCBI基因库的红丝壳菌属物种进行比较。提交到基因库的Cah序列包括ITS的登录号KC342208、KC342206和KC342207;BT的KC342217、KC342215和KC342216;HIS3的KC342211、KC342209和KC342210;以及EF1α的KC342214、KC342212和KC342213。所使用的所有基因序列与Cah CBS 114828的模式标本序列相似度>99%或完全相同。对每个分离株在5个健康表面消毒的果实上进行致病性测试。用在APDA培养基上生长8天的纯培养物的5毫米菌丝圆盘接种手术刀划伤和未划伤的果实组织。未处理的对照仅接种APDA圆盘。果实置于湿度箱中,在25°C、12小时荧光灯下放置8天。该试验重复一次。接种后3天(DAI),在果实上观察到白色菌丝生长。接种后5天,果实颜色从红色变为棕色,淡黄色菌丝定殖在50%至62%的果实表面。接种后8天,所有果实变为棕色,菌丝生长覆盖整个果实,并在刺状物(毛发状附属物)上产生分生孢子梗。在果实内部观察到刺状物、外果皮(表皮)、内果皮(假种皮)的果实腐烂以及浅棕色变色。未处理的对照未表现出果实腐烂症状,且未从组织中重新分离到真菌。从患病组织中重新分离到Cah,满足科赫法则。红丝壳菌属物种(或其柱枝双孢霉无性态)与越南北部的荔枝衰退综合征有关。这两种果实都属于无患子科。据我们所知,这是关于Cah引起红毛丹果实腐烂的首次报道。参考文献:(1)L.M.科茨等人。《龙眼、荔枝和红毛丹的病害》。载于《热带水果作物病害》,R.C.普洛茨编。CABI出版社,马萨诸塞州剑桥,2003年,第307 - 325页。(2)P.W.克劳斯。《柱枝双孢霉(红丝壳菌)及相关属的分类学与病理学》。美国植物病理学会出版社,明尼苏达州圣保罗,2002年。(3)P.W.克劳斯等人。《真菌学研究》50:415,2004年。