Yang G H, Conner R L, Chen Y Y
Phytopathology Lab of Yunnan Province, Yunnan Agricultural University, 650201, China.
Agriculture and Agri-Food Canada, Morden Research Station, Unit 100-101, Route 100, Morden, MB, Canada R6M 1Y5.
Plant Dis. 2007 Nov;91(11):1516. doi: 10.1094/PDIS-91-11-1516A.
During July, 2003, damping-off of Swiss chard (Beta vulgaris subsp. cicla L.) was observed in a seedling (approximately 1 month after germination) field (approximately 2 ha) in Yuanmou County in the Cuxiong District of Yunnan, China. More than 80% of the seedlings showed symptoms of the disease. Symptoms on newly emerged plants consisted of wilting, a brown necrosis of the lower taproot, and eventual death of seedlings. Among the 15 isolates of Rhizoctonia spp. isolated from Swiss chard with damping-off symptoms, 12 isolates of Rhizoctonia solani with dark brown sclerotia on potato dextrose agar (PDA) anastomosed with tester isolates of each subgroup AG-4 HG I, AG-4 HG II, and AG-4 HG III, giving a C2 hyphal fusion (1) reaction at a high frequency. The other three binucleate Rhizoctonia spp. (BNR) isolates whose mycelia were white with floccose aerial hyphae on PDA anastomosed freely with two BNR AG-A tester isolates producing a C2 hyphal reaction. The 5.8S rDNA-ITS of a single isolate of R. solani and a single isolate of BNR was sequenced. The sequence of the AG-4 isolate (GenBank Accession No. EF679777) exhibited 99 to 100% homology with isolates of R. solani AG-4, subgroup 4HG I (GenBank Accession No. AY154307). The sequence from the AG-A isolate (GenBank Accession No. EF679778) exhibited 98% homology with BNR AG-A (GenBank Accession Nos. AB000040 and AF354092). Swiss chard (cv. Baijin) seedlings (approximately 5 cm high) were planted in potting soil at a density of one seedling per vinyl pot (8 cm diameter, 9 cm high). Two isolates each of R. solani and BNR were used in pathogenicity testing. Each seedling was inoculated in the root zone with approximately 7 g of artificially infested soil. Control plants were inoculated with autoclaved soil. The experiments were conducted three times, each time with three replicates, in a greenhouse with a photoperiod of 16 h of light and 8 of h dark at 30 and 16°C, respectively. After 7 days, disease severity was measured based on a scale in which 0 = no symptom; 1 = small lesions on seedlings, no blight; 2 = leaves blight, no stem blight; 3 = stem blight; and 4 = plant dead. The two AG-4 and two of AG-A isolates were pathogenic on the Swiss chard seedlings and caused damping-off symptoms with a disease index 1.7 to 4.0, and there were no significant differences (P = 0.05) among them. We reisolated and confirmed the presence of R. solani and BNR AG-A from diseased plants. AG-3 isolates were reported to cause the damping-off of Swiss chard in the United States (2). To our knowledge, this is the first report of damping-off of Swiss chard caused by Rhizoctonia solani AG-4 HG I and BNR AG-A. References: (1) D. E. Carling. Page 37 in: Grouping in Rhizoctonia solani by Hyphal Anastomosis Reaction. Kluwer Academic Publishers, Dordecht, the Netherlands, 1996. (2) S. T. Koike and K. V. Subbarao. Plant Dis. 83:695, 1999.
2003年7月,在中国云南省楚雄地区元谋县一块约2公顷的幼苗田(发芽后约1个月)中,观察到瑞士甜菜(Beta vulgaris subsp. cicla L.)发生猝倒病。超过80%的幼苗表现出该病症状。新出土植株的症状包括萎蔫、主根下部褐色坏死,最终幼苗死亡。从表现出猝倒症状的瑞士甜菜中分离出的15个丝核菌属菌株中,有12个在马铃薯葡萄糖琼脂(PDA)上带有深褐色菌核的立枯丝核菌菌株与AG-4 HG I、AG-4 HG II和AG-4 HG III各亚组的测试菌株形成菌丝融合,在高频下产生C2菌丝融合反应(1)。另外三个双核丝核菌属(BNR)菌株,其菌丝在PDA上为白色且有絮状气生菌丝,与两个产生C2菌丝反应的BNR AG-A测试菌株自由融合。对一个立枯丝核菌菌株和一个BNR菌株的5.8S rDNA-ITS进行了测序。AG-4分离株的序列(GenBank登录号EF679777)与立枯丝核菌AG-4亚组4HG I的分离株(GenBank登录号AY154307)具有99%至100%的同源性。AG-A分离株的序列(GenBank登录号EF679778)与BNR AG-A(GenBank登录号AB000040和AF354092)具有98%的同源性。将瑞士甜菜(品种“白金”)幼苗(约5厘米高)以每盆(直径8厘米,高9厘米)一株的密度种植在盆栽土壤中。在致病性测试中使用了立枯丝核菌和BNR各两个分离株。每株幼苗在根区接种约7克人工感染的土壤。对照植株接种经高压灭菌的土壤。实验进行了三次,每次三个重复,在温室中进行,光照周期为16小时光照和8小时黑暗,温度分别为30°C和16°C。7天后,根据以下分级标准测量病情严重程度:0 = 无症状;1 = 幼苗上有小病变,无枯萎;2 = 叶片枯萎,无茎枯萎;3 = 茎枯萎;4 = 植株死亡。两个AG-4和两个AG-A分离株对瑞士甜菜幼苗具有致病性,并导致猝倒症状,病情指数为1.7至4.0,它们之间无显著差异(P = 0.05)。我们从患病植株中重新分离并确认了立枯丝核菌和BNR AG-A的存在。据报道,AG-3分离株在美国会导致瑞士甜菜猝倒(2)。据我们所知,这是首次关于立枯丝核菌AG-4 HG I和BNR AG-A引起瑞士甜菜猝倒的报道。参考文献:(1)D. E. Carling。见:《通过菌丝融合反应对立枯丝核菌进行分组》。Kluwer学术出版社,荷兰多德雷赫特,1996年,第37页。(2)S. T. Koike和K. V. Subbarao。《植物病害》83:695,1999年。