Zhao Y Z, Liu Z H
Laboratory of Fungi, College Plant Protection, Shenyang Agricultural University, Shenyang 110866, China.
Plant Dis. 2012 Oct;96(10):1580. doi: 10.1094/PDIS-04-12-0416-PDN.
Cherry (Cerasus pseudocerasus) has become an economically important fruit in China in recent years. In June 2010, fruit spots were discovered on fruit grown in Dalian City, Liaoning Province, China and 30% of local-orchard trees were infected with the disease, reducing yield and fruit quality. Disease incidence increased up to 75% in 2011. At the initial stage of the infection, some small, light brown spots appeared on the fruit that gradually became round or irregular and dark brown, and a black-brown concentric ring formed in the advanced stage of the infection. As disease progressed, the lesions expanded, causing the fruit surface to become pitted, withered, and dead. The pathogen was isolated from infected fruit of four orchards by a tissue isolation method (1) and cultured on potato dextrose agar (PDA) at 25°C in the dark for one week. Colonies on PDA were initially white and became grayish brown over time. Conidiophores were single or fasciculate, straight or knee curved, gray-brown with regular septa, branched or unbranched, and 12.5 to 90.0 × 2.0 to 5.0 μm. Conidia were oval, obclavate, or obpyriform, brown or dark brown, surface smooth or spinulose with short columnar beaks, and 20.0 to 42.0 × 7.5 to 14.5 μm with three to eight transverse septa and zero to three longitudinal or oblique septa. The sporulation pattern appeared in bush branches. According to the morphology, the pathogen was identified as Alternaria alternata (Fr:Fr.) Keissler (2,3). The internal transcribed spacer (ITS) region of rDNA was amplified using the primers ITS1/ITS4 and the ITS sequence was 99% identical to A. alternata (GenBank Accession No. FJ228163). Pathogenicity tests were performed on detached, asymptomatic fruit. Six fruit were inoculated by placing a PDA plug containing mycelia on the upper surface of the fruit. Another six fruit received sterile PDA plugs. Fruit were cultured in petri dishes with a 12-h photoperiod at 25°C and 90% relative humidity. Black spot symptoms were observed on inoculated fruit but not control fruit after 5 days. The pathogen was reisolated from inoculated fruit and confirmed to be A. alternata. The pathogenicity test was repeated once. A. alternata has a broad host range, but to our knowledge, this is the first report of A. alternata infecting cherries in China. References: (1) Z. D. Fang. Research Methods of Plant Disease, 124, 1998. (2) E. G. Simmons. Alternaria themes and variations. Mycotaxon 37: 79, 1990. (3) T. Y. Zhang et al. Fungi Notes-Genera Alternaria in China, 16:32, 2003.
近年来,樱桃(中国樱桃)在中国已成为一种具有重要经济价值的水果。2010年6月,在中国辽宁省大连市种植的樱桃果实上发现了果斑,当地果园中30%的樱桃树感染了这种病害,导致产量和果实品质下降。2011年,发病率增至75%。在感染初期,果实上出现一些小的浅褐色斑点,这些斑点逐渐变成圆形或不规则形,颜色变为深褐色,在感染后期形成黑褐色同心环。随着病害发展,病斑扩大,导致果实表面出现凹陷、枯萎和坏死。通过组织分离法(1)从四个果园的感染果实中分离出病原菌,并在25℃黑暗条件下于马铃薯葡萄糖琼脂(PDA)培养基上培养一周。PDA培养基上的菌落最初为白色,随着时间推移变为灰褐色。分生孢子梗单生或簇生,直立或膝状弯曲,灰褐色,具规则隔膜,有分枝或无分枝,大小为12.5至90.0×2.0至5.0μm。分生孢子椭圆形、倒棍棒形或倒梨形,褐色或深褐色,表面光滑或具短柱状喙的小刺,大小为20.0至42.0×7.5至14.5μm,具三至八个横隔膜和零至三个纵隔膜或斜隔膜。产孢模式出现在丛生枝条上。根据形态学特征,病原菌被鉴定为链格孢(Alternaria alternata (Fr:Fr.) Keissler)(2,3)。使用引物ITS1/ITS4扩增rDNA的内部转录间隔区(ITS)区域,其ITS序列与链格孢(GenBank登录号:FJ228163)的序列一致性为99%。对离体无症状果实进行致病性测试。通过在果实上表面放置一个含有菌丝体的PDA菌块对接种六个果实。另外六个果实接种无菌PDA菌块。将果实置于培养皿中,在25℃、光周期12小时、相对湿度90%的条件下培养。5天后,接种果实上观察到黑斑症状,而对照果实未出现症状。从接种果实中重新分离出病原菌,并确认为链格孢。致病性测试重复进行一次。链格孢具有广泛的寄主范围,但据我们所知,这是链格孢在中国感染樱桃的首次报道。参考文献:(1)方中达。植物病害研究方法,124,1998。(2)E.G.西蒙斯。链格孢的主题与变异。真菌分类学报37:79,1990。(3)张天宇等。中国真菌志 - 链格孢属,16:32,2003。