Li Y, Shen J, Pan B H, Guo M X, Wang Q X, Ouyang C B, Yan D D, Cao A C
Department of Pesticides, Key Laboratory of Pesticide Chemistry and Application, State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Plant Dis. 2014 Aug;98(8):1153. doi: 10.1094/PDIS-09-13-1005-PDN.
Marigold (Tagetes erecta) is an important commercial crop and 200 ha are planted every year in the Beijing district of China. A leaf spot disease of T. erecta was observed during 2012 and 2013 in the Beijing district. The disease was widespread, with 60 to 75% of the fields affected. Leaves of the affected plants had small, brown, necrotic spots on most of the foliage. Yield losses of flowers of up to 20 to 30% were reported. The spots gradually enlarged, becoming irregular in shape, or remained circular, and with concentric rings or zones. In the later stages of infection, the spots coalesced, and the leaves withered, dried, and fell from the plants (4). A fungus was consistently isolated on potato dextrose agar (PDA) from the infected leaves of T. erecta. After 6 days of incubation at 26°C and a 12-h photoperiod, the fungus produced colonies that were flat, with a rough upper surface (2). The conidiophores were short. Conidia varied from 18 × 6 to 47 × 15 μm and were medium to dark brown or olive-brown in color, short beaked, borne in long chains, oval and bean shaped, with 1 to 5 transverse septa and 0 to 2 longitudinal septa. The rDNA of the internal transcribed spacer regions 1 and 2 and the 5.8S gene in seven isolates were amplified using primers ITS1 (5'-TCCGTAGGTGAACCTGCGG-3') and ITS4 (5'-TCCTCCGCTTATTGATATGC-3'). The nucleotide sequence was the same as isolate No. 7, which was deposited in GenBank (Accession No. KF307207). A BLAST search showed 97% identity with the strain Alternaria alternata GNU-F10 (KC752593). Seven isolates were also confirmed as A. alternata by PCR identification performed by specific primers (C_for/C_rev) of A. alternata (1). Seven isolates were grown on PDA for 2 weeks and the conidia harvested. A 5-μl drop of spore suspension (1 × 10 spores/ml) was placed on each leaflet of 140 detached, surface-sterilized T. erecta leaves. Twenty leaves were inoculated with sterile distilled water as a control. The leaves were incubated in a growth chamber at 80 to 90% relative humidity, 50 to 60 klx/m light intensity, and a 12-h photoperiod. After 6 days, leaf spots similar to the original developed at inoculation sites for all isolates and A. alternata was consistently re-isolated. The control leaves remained symptomless. The pathogenicity test was performed three times. Leaf spot of T. erecta caused by Alternaria spp. is well known in Asian countries such as Japan (3). To our knowledge, this is the first report of A. alternata on T. erecta in the Beijing district of China. References: (1) T. Gat. Plant Dis. 96:1513, 2012. (2) E. Mirkova. J. Phytopathol. 151:323, 2003. (3) K. Tomioka. J. Gen. Plant Pathol. 66:294, 2000. (4) T. Y. Zhang. Page 284 in: Flora Fungorum Sinicorum, Volume 16: Alternaria. Science Press, Beijing, 2003.
万寿菊(孔雀草)是一种重要的经济作物,中国北京地区每年种植面积达200公顷。2012年至2013年期间,在北京地区观察到万寿菊发生叶斑病。该病传播广泛,60%至75%的田地受到影响。患病植株的叶片在大部分叶面上有小的褐色坏死斑点。据报道,花朵产量损失高达20%至30%。斑点逐渐扩大,形状变得不规则,或保持圆形,并带有同心环或带。在感染后期,斑点融合,叶片枯萎、干枯并从植株上掉落。从感染的万寿菊叶片上,在马铃薯葡萄糖琼脂(PDA)上始终能分离到一种真菌。在26°C、12小时光周期下培养6天后,该真菌产生的菌落扁平,上表面粗糙。分生孢子梗短。分生孢子大小从18×6微米到47×15微米不等,颜色为中褐色至深褐色或橄榄褐色,有短喙,成链状着生,椭圆形和豆形,有1至5个横隔膜和0至2个纵隔膜。使用引物ITS1(5'-TCCGTAGGTGAACCTGCGG-3')和ITS4(5'-TCCTCCGCTTATTGATATGC-3')扩增了7个分离株的内部转录间隔区1和2以及5.8S基因的rDNA。核苷酸序列与保藏于GenBank(登录号KF307207)的7号分离株相同。BLAST搜索显示与链格孢菌株GNU-F10(KC752593)有97%的同一性。通过链格孢的特异性引物(C_for/C_rev)进行的PCR鉴定也确认7个分离株为链格孢。7个分离株在PDA上培养2周后收获分生孢子。将5微升孢子悬浮液(1×10孢子/毫升)滴在140片离体、表面消毒的万寿菊叶片的每片小叶上。20片叶子接种无菌蒸馏水作为对照。叶片在生长室中培养,相对湿度为80%至90%,光照强度为50至60千勒克斯/米,光周期为12小时。6天后,所有分离株在接种部位都出现了与最初相似的叶斑,并且始终能再次分离到链格孢。对照叶片无症状。致病性试验进行了3次。链格孢属引起的万寿菊叶斑病在日本等亚洲国家很常见。据我们所知,这是中国北京地区关于链格孢侵染万寿菊的首次报道。参考文献:(1)T. Gat.《植物病害》96:1513,2012。(2)E. Mirkova.《植物病理学杂志》151:323,2003。(3)K. Tomioka.《植物病理学报》66:294,2000。(4)T. Y. Zhang.《中国真菌志 第16卷:链格孢属》第284页。科学出版社,北京,2003。