Mirabolfathy M, Groenewald J Z, Crous P W
Iranian Plant Protection Research Institute, No. 1 Yaman (Tabnak) Ave., Chamran Highway, Tehran, Iran.
CBS-KNAW, Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, the Netherlands.
Plant Dis. 2010 Feb;94(2):278. doi: 10.1094/PDIS-94-2-0278A.
In the autumn of 2008, a severe disease of Anthurium andraeanum with wilting and root and crown rot symptoms was observed in a greenhouse in the Varamin area of Tehran. A species of Calonectria was isolated consistently from symptomatic tissues on 2% potato dextrose agar (PDA). The fungus produced perithecia and a Cylindrocladium anamorph when incubated on carnation leaf agar under near-ultraviolet light at 25°C. Perithechia were reddish brown, subglobose to ovoid, and 300 to 400 μm in diameter. Asci were clavate, hyaline, 90 to 140 × 12 to 19 μm, and tapering to a long thin stalk. Ascospores were fusoid, straight to slightly curved, 1- (-3) septate, and (30-) 37 to 50 (-65) × (4-) 5 to 6.5 (-7) μm (mean = 45 × 6 μm; n = 30). Penicillate conidiophores gave rise to stipe extensions that terminated in sphaeropedunculate vesicles (6-) 7 to 10 (-12) μm in diameter. Conidia were hyaline, cylindrical, rounded at both ends, straight, (45-) 70 to 82 (-90) × (4-) 5 to 6.5(-7) μm (mean = 62 × 6 μm; n = 30), and (1-) 3-septate. On the basis of morphology, the fungus was identified as Calonectria ilicicola Boedijin & Reitsma. Koch's postulates were fulfilled by spray inoculating 1-month-old seedlings with a conidial and mycelial suspension (10 particles per ml) of the fungus obtained from 14-day-old single-spore colonies grown on PDA at 25°C. Following inoculation, all plants were maintained in plastic bags in a glasshouse at 25 ± 1°C. After 15 to 25 days, symptoms resembling those seen in the diseased glasshouse were detected on inoculated plants. C. ilicicola was reisolated from the artificially infected tissues. No symptoms were detected on the control plants. Nucleotide sequences of the internal transcribed spacer (ITS) regions of the nrDNA operon and the partial histone H3 gene were determined for derived strain CPC 16334 as described previously (1,3). The ITS sequence (GenBank Accession No. GU057378) matched 100% (644/644 bp) with the sequence of C. ilicicola strain CBS 463.76 (GenBank AF493963) and the histone H3 sequence (GenBank GU057379) matched 99% (456/458 bp; due to two versus three AC repeats in the sequence) with that of C. ilicicola strain CBS 112217 (GenBank AY725686). To our knowledge, this is the first report of Calonectria and Cylindrocladium genera and the disease caused by C. ilicicola from Iran. References: (1) R. Cheewangkoon et al. Persoonia 23:55, 2009. (2) P. W. Crous and M. J. Wingfield. Mycotaxon 51:341, 1994. (3) P. W. Crous et al. Stud. Mycol. 50:415, 2004.
2008年秋,在德黑兰瓦拉明地区的一个温室中,观察到红掌出现严重病害,症状为萎蔫以及根和冠腐。在2%马铃薯葡萄糖琼脂(PDA)培养基上,从有症状的组织中持续分离出一种痂圆孢属真菌。该真菌在25°C近紫外光下于康乃馨叶琼脂上培养时产生子囊壳和柱枝双孢霉无性型。子囊壳呈红棕色,近球形至卵形,直径300至400μm。子囊呈棒状,透明,90至140×12至19μm,逐渐变细形成细长的柄。子囊孢子呈梭形,直或稍弯曲,有1 - (-3)个隔膜,(30 - )37至50(-65)×(4 - )5至6.5(-7)μm(平均 = 45×6μm;n = 30)。帚状分生孢子梗产生的梗延伸部分末端为球形柄状囊泡(直径6 - )7至10(-12)μm。分生孢子透明,圆柱形,两端圆形,直,(45 - )70至82(-90)×(4 - )5至6.5(-7)μm(平均 = 62×6μm;n = 30),有(1 - )3个隔膜。根据形态学,该真菌被鉴定为冬青痂圆孢(Calonectria ilicicola Boedijin & Reitsma)。通过用从在25°C下于PDA上生长14天的单孢菌落获得的真菌分生孢子和菌丝体悬浮液(每毫升10个颗粒)喷雾接种1月龄幼苗,满足了柯赫氏法则。接种后,所有植株置于温室的塑料袋中,温度为25±1°C。接种15至25天后,在接种植株上检测到与患病温室中所见症状相似的症状。从人工感染的组织中再次分离出冬青痂圆孢。对照植株未检测到症状。如先前所述(1,3),对衍生菌株CPC 16334的nrDNA操纵子的内部转录间隔区(ITS)区域和部分组蛋白H3基因的核苷酸序列进行了测定。ITS序列(GenBank登录号GU057378)与冬青痂圆孢菌株CBS 463.76(GenBank AF493963)的序列100%匹配(644/644 bp),组蛋白H3序列(GenBank GU057379)与冬青痂圆孢菌株CBS 112217(GenBank AY725686)的序列99%匹配(456/458 bp;由于序列中有两个与三个AC重复)。据我们所知,这是来自伊朗的痂圆孢属和柱枝双孢霉属以及由冬青痂圆孢引起的病害的首次报道。参考文献:(1) R. Cheewangkoon等人,《Persoonia》23:55,2009年。(2) P. W. Crous和M. J. Wingfield,《Mycotaxon》51:341,1994年。(3) P. W. Crous等人,《Stud. Mycol.》50:415,2004年。