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|a 10.1094/PDIS-08-23-1503-PDN
|2 doi
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|a pubmed24n1253.xml
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|a eng
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|a Lin, Junbin
|e verfasserin
|4 aut
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| 245 |
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|a First Report of Lecanicillium aphanocladii Causing Rot of Sparassis crispa in China
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|c 2024
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|a Text
|b txt
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|a ƒaComputermedien
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|a ƒa Online-Ressource
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|a Date Revised 08.01.2024
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|a published: Print-Electronic
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|a Citation Status Publisher
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|a Sparassis crispa, also known as cauliflower mushroom, is a new popularly edible mushroom in China, also a medicinal mushroom, which possesses various biological activities, such as immunopotentiation, anti-diabetes, anti-cancer, and anti-inflammatory effects. (Han et al., 2018). In recent years, the artificial cultivation of S. crispa has gained considerable public attention in China. In 2023, approximately 20% of S. crispa (about 0.05 ha of the planting area) showed obvious rot with white molds symptoms in mushroom hothouse, located in Shuangliu county, Sichuan province, China (GPS, 104°7'51"N, 30°25'2"E). Infected fruiting bodies were covered by white mycelia that later turned red or fuchsia. In the final stages of infection, the S. crispa fruiting bodies turned dark red or brown before rotting. The pathogen was isolated from the margin of the lesions by plating onto potato dextrose agar (PDA), and incubated at 25℃ in the dark for a week. Five pure culture fungal isolates were obtained. Collected isolates with similar morphology were described as Lecanicillium spp. (Zare et al., 2001). The colonies were raised, covered with white, the reverse side were violet brown, produced diffusing reddish-purple pigment. Conidiogenous cells produced singly, in pairs, verticillate or in dense irregular clusters on prostrate hyphae, at first flask-shaped, tapering into threadlike neck, with a size of 3.0-6.2×0.8-2.2 μm. Conidia were solitary, oval to subglobose, and 2.3-4.0×1.1-2.1 μm in size, similar to L. aphanocladii (Higo et al., 2021). For pathogenicity testing, ten fruiting bodies of S. crispa (planted in the bottles) were selected. Fungal cake of the isolate Bx-Ljb of L. aphanocladii were applied to the fruiting body of S. crispa, whereas pieces of sterile PDA medium were used as controls. All the bottles were incubated at 19±1℃, 85-100% relative humidity, and 18 h of light in the mushroom hothouse. A week later, the inoculated fruiting bodies developed brown spots and gradually expanding, with symptoms similar to the original diseased fruiting bodies. The controls remained healthy. The same fungus was reisolated from the infected fruiting bodies and subsequently identified by morphological characteristics and DNA sequence analysis. The pathogenicity test was repeated three times with similar results. For molecular identification, the DNA of the isolates was extracted using a Fungi Genomic DNA Extraction kit (Solarbio, Beijing). The SSU, LSU, and TEF1-α genes were amplified with the primer as previously described (Zhou et al., 2018). The generated sequences were deposited in GenBank with accession numbers OR206377, OR206378, and OR204702, respectively. BLASTn analyses showed >99.2% identity with previously deposited sequences of L. aphanocladii. Based on the maximum likelihood method, phylogenetic analysis revealed 99% bootstrap support values with L. aphanocladii. The fungus was identified as L. aphanocladii based on morphological and multilocus phylogenetic analyses. To our knowledge, there are two reports of L. aphanocladii on fruiting bodies of Tremella fuciformis and Morchella sextelata in China, and this is the first report of this fungus causing rot of S. crispa in China. It may be a reminder that the risk of L. aphanocladii in mushroom production in China is gradually increasing. These results will contribute to developing managemental strategies for this disease in S. crispa
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|a Journal Article
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4 |
|a Lecanicillium aphanocladii
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| 650 |
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4 |
|a Rot
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| 650 |
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4 |
|a Sparassis crispa
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| 650 |
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4 |
|a edible fungi
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| 700 |
1 |
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|a Gan, Ying
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Tong, Zong-Jun
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Yan, Junjie
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Han, Xing
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Duan, Xinlian
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Gan, Bingcheng
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Chen, Jie
|e verfasserin
|4 aut
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| 773 |
0 |
8 |
|i Enthalten in
|t Plant disease
|d 1997
|g (2024) vom: 08. Jan.
|w (DE-627)NLM098181742
|x 0191-2917
|7 nnns
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|g year:2024
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|u http://dx.doi.org/10.1094/PDIS-08-23-1503-PDN
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