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First Report of Green Mould on Leaf of Phaseolus vulgaris Caused by Cladosporium tenuissimum in Liaoning, China.
Gao, Xiaomei; Yang, Xiaohe; Li, Yang; Yu, Miao; Ao, Jing; Liu, Xiaohui; Sun, Yulu; Song, Liqun; Chen, Fei; Guo, Lingling.
Affiliation
  • Gao X; Microbial Research Institute of Liaoning Province, No. 820 Longshan Street, Shuangta District, Chaoyang , Chaoyang, Liaoning, China, 122000; gaoxiaomei8115@163.com.
  • Yang X; Jiamusi Branch of Heilongjiang Academy of Agricultural Sciences, Jiamusi, Heilongjiang, China; yangxiaohe_2000@163.com.
  • Li Y; Microbial Research Institute of Liaoning Province, Chaoyang, Liaoning, China; liyang_0223@163.com.
  • Yu M; Microbial Research Institute of Liaoning Province, Chaoyang, Liaoning, China; 52638019@qq.com.
  • Ao J; Microbial Research Institute of Liaoning Province, Chaoyang, Liaoning, China; aojing07@163.com.
  • Liu X; Microbial Research Institute of Liaoning Province, Chaoyang, Liaoning, China; xiaohuiliu94083@aliyun.com.
  • Sun Y; Microbial Research Institute of Liaoning Province, Chaoyang, Liaoning, China; 117121314@qq.com.
  • Song L; Microbial Research Institute of Liaoning Province, Chaoyang, Liaoning, China; 15840122615@163.com.
  • Chen F; Microbial Research Institute of Liaoning Province, Chaoyang, Liaoning, China; chenfei3033@vip.sina.com.
  • Guo L; Microbial Research Institute of Liaoning Province, Chaoyang, Liaoning, China; lnwsw2013@163.com.
Plant Dis ; 2024 Feb 29.
Article in En | MEDLINE | ID: mdl-38422439
ABSTRACT
Phaseolus vulgaris Linn. is a widely cultivated vegetable throughout the world. From spring 2019 to 2022, green mould symptoms were observed on leaves of P. vulgaris in the greenhouse in Liaoning, China, with disease incidence of 8-75% (plants) and 6-23% (leaves). Symptoms appeared as chlorotic lesions covered with dark green mould. The infections started at the apex or margin of the leaves and then spread inward with a characteristic "V" shape. Lesions exhibited curly morphology. 15 leaf samples with typical symptoms were collected from 5 different greenhouses. A total of 75 (5 replicates of each sample) leaf tissues (0.5 cm × 0.5 cm) were selected from the boundary between diseased and healthy parts. These samples were surface sterilized in 0.5% NaClO formin, rinsed 3 times in sterile distilled water and subsequently incubated at 28℃ on potato dextrose agar (PDA) supplemented with streptomycin (50 µg/ml). Numerous morphologically uniform colonies had been purified, with no other fungi observed. Afterwards, the strains were subcultured on malt extract agar (MEA). Colonies on MEA reached 70 to 80 mm diam after 14 days, smoke-grey to pale olivaceous-grey, woolly, sometimes radially wrinkled. The mycelia were pale olivaceous-grey, with hyphae measuring 1-5 µm wide (n = 20). The conidiophores were solitary or in groups of 2 to 5, and measured 50-280(-350) × 2.5-4 µm (n = 20), with 2-7 septa. The conidiogenous cells exhibited a cylindrical-oblong morphology and measured 10-44 × 5 µm (n = 20), with 0-2 septa, and the loci frequently thickened. The conidia were catenate in densely branched chains, ellipsoid to obovoid, smooth, and measured 2.5-5 × 2-3 µm (n = 50), with 0-4 septa. The morphological characteristics were similar to Cladosporium tenuissimum (Zhang 2003). The representative isolate KZ-19 was selected for molecular identification. The rDNA-ITS, translation elongation factor 1-α and actin genes were amplified, sequenced, and the resulting sequence data were submitted to GenBank (ITS OQ931048; EF-1α OQ954495; ACT OQ954496). The BLAST results exhibited a 99 to 100% similarity with the sequences of C. tenuissimum type strain CBS 125995(ITS HM148197; EF-1α HM148442; ACT HM148687). Furthermore, a multi-locus phylogenetic tree was constructed using the PhyloSuite (v 1. 2. 2) software, which revealed that the strains were most closely related to C. tenuissimum (Zhang et al. 2020). Based on both morphological and molecular characteristics, KZ-19 was finally identified as C. tenuissimum (Bensch 2012). Pathogenicity testing was performed on healthy 1-month-old P. vulgaris plants by inoculating the spore suspension (1×106 conidia/ml) of KZ-19 onto leaf surfaces, while control plants were simulated inoculated with sterile water, and five pots were used for each treatment. The test was performed under field conditions of 16-28°C (temperature) and 24-56% (relative humidity). Chlorotic lesions became evident within 2 days of inoculation, followed by the appearance of green mold on leaves after 7 days. No symptoms were observed in the control group. To fulfill Koch's postulates, the pathogen was re-isolated from three inoculated leaves. The morphological identification of re-isolated pathogens was similar to that of originally isolated pathogens. No infection was observed in non-inoculated control. To the best of our knowledge, this is the first report of C. tenuissimum causing green mould on P. vulgaris. As a ubiquitous saprobic hyphomycete, C. tenuissimum has been implicated in leaf mold in Punica granatum and Trifolium repens, larch bud blight, and strawberry blossom blight in previous years (He et al. 1987; Zhang et al. 2003; Zheng et al. 2010; Nam et al. 2015), presenting a potential threat to numerous crops. Therefore, an investigation of its distribution and pathogenic potential is essential in addition to the development of effective disease management strategies.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Plant Dis Year: 2024 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Plant Dis Year: 2024 Document type: Article Country of publication: United States