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  1. Article ; Online: First Report of Fusarium equiseti Causing Bulb Rot on Lily (Lilium ‘White Planet’) in China

    Yang, Panpan / Hao, Zehui / Qu, Yuxiao / Liang, Rui / Xu, Leifeng / Zhang, Kezhong / Ming, Jun

    Plant Disease. 2023 Sept. 01, v. 107, no. 9 p.2847-

    2023  

    Abstract: Lily (Lilium spp.) is one of the main ornamental plants grown in the world. In addition, bulbs of lily have been extensively used as edible and medicinal herbs in northern and eastern Asia, especially in China (China Pharmacopoeia Committee 2020; Tang et ...

    Abstract Lily (Lilium spp.) is one of the main ornamental plants grown in the world. In addition, bulbs of lily have been extensively used as edible and medicinal herbs in northern and eastern Asia, especially in China (China Pharmacopoeia Committee 2020; Tang et al. 2021; Yu et al. 2015). In August of 2021, a disease of stem and leaf rot was observed on the lily cultivar White planet with approximately 25% disease incidence in the greenhouse and fields at the Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences (Beijing, China). The bulbs of symptomatic plants were brown and rotten, with sunken lesions. Symptomatic plants showed short and discolored leaves, which eventually lead to stem wilt and death of the whole plant. Infected bulbs were surface sterilized in 75% ethanol for 30 s and then in 2% sodium hypochlorite for 5 min and rinsed three times with sterile distilled water. A 0.5 × 0.5-cm tissue piece was then placed on potato dextrose agar (PDA) medium and incubated at 25 ± 1°C. After 5 days, the isolate was purified by single-spore isolation technique. The single-spored fungal colony was characterized by fluffy white aerial mycelia and produced orange pigments with age. After 7 days on Spezieller Nährstoffarmer agar (SNA), conidia were produced from simple lateral phialides. Macroconidia had pronounced typical dorsiventral curvature, significantly enlarged in the middle, a tapered whip-like pointed apical cell, a characteristic foot-shaped basal cell, and 3 to 6 septa, measuring 18.71 to 43.01 × 2.89 to 5.56 μm with an average size of 26.98 × 3.90 μm (n = 30). Microconidia were not observed. Typical thick verrucose chlamydospores with rough walls were profuse in chains or clumps and ellipsoidal to subglobose in shape. These morphological characteristics were consistent with Fusarium spp. (Leslie and Summerell 2006). For molecular identification, the internal transcribed spacer (ITS), translation elongation factor subunit 1-alpha (TEF1-α), and RNA polymerase subunit 2 (RPB2) genes were amplified using the primers ITS1/ITS4, EF1/EF2, and 5F2/7cR, respectively, and sequenced (Jiang et al. 2018; O’Donnell et al. 2007; White et al. 1990). Sequences were submitted to GenBank under accession numbers OM078499 (ITS), OM638086 (TEF1-α), and OM638085 (RPB2). BLAST analysis showed that ITS, TEF1-α, and RPB2 sequences shared 100, 99.8, and 99.2% identity to Fusarium equiseti (OM956073, KY081599, and MW364892) in GenBank, respectively. In addition, ITS, TEF1-α, and RPB2 sequences shared 100, 99.53, and 100% identity with F. lacertarum (LC7927, F. incarnatum-equiseti species complex) in the Fusarium-ID database. Based on the morphological characteristics and molecular sequences, the isolates were identified as F. equiseti. A pathogenicity test was performed on potted lily (‘White planet’) under greenhouse conditions (25 ± 1°C with a 16-h light and 8-h dark cycle). Three healthy lily bulbs were selected, and one bulb was planted in each pot filled with sterilized soil. Each pot was inoculated with 5 ml of conidia suspension (1 × 10⁷ conidia/ml) in the soil around bulbs, with an equal amount of sterilized water as a control. This test had three replicates. After 15 days of inoculation, typical symptoms of bulb rot, like those observed in the greenhouse and fields, developed on the inoculated plants but not on the controls. The same fungus was consistently reisolated from the diseased plants. To our knowledge, this is the first report of F. equiseti causing bulb rot on Lilium spp. in China. Our result will help in future monitoring and control of lily wilt disease.
    Keywords DNA-directed RNA polymerase ; Fusarium equiseti ; Lilium ; agar ; bulbs ; chlamydospores ; conidia ; cultivars ; culture media ; databases ; death ; disease incidence ; ethanol ; fungi ; greenhouses ; internal transcribed spacers ; isolation techniques ; leaves ; mycelium ; pathogenicity ; peptide elongation factors ; sodium hypochlorite ; soil ; soil sterilization ; vascular wilt ; China ; herbaceous/flowering plants ; ornamentals ; pathogen detection
    Language English
    Dates of publication 2023-0901
    Publishing place The American Phytopathological Society
    Document type Article ; Online
    ZDB-ID 754182-x
    ISSN 0191-2917
    ISSN 0191-2917
    DOI 10.1094/PDIS-01-23-0199-PDN
    Database NAL-Catalogue (AGRICOLA)

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  2. Article: First report of Fusarium equiseti causing bulb rot on lily (Lilium 'White planet' ) in China.

    Yang, Panpan / Hao, Zehui / Qu, Yuxiao / Liang, Rui / Xu, Leifeng / Zhang, Kezhong / Ming, Jun

    Plant disease

    2023  

    Abstract: Lily (Lilium spp.) is one of the main ornamental plants grown in the world. In addition, bulbs of lily have been extensively used as edible and medicinal herbs in northern and eastern Asia, especially in China (Yu et al. 2015; China Pharmacopoeia ... ...

    Abstract Lily (Lilium spp.) is one of the main ornamental plants grown in the world. In addition, bulbs of lily have been extensively used as edible and medicinal herbs in northern and eastern Asia, especially in China (Yu et al. 2015; China Pharmacopoeia Committee 2020; Tang et al. 2021). In August of 2021, a disease of stem and leaf rot was observed on lily cultivar 'White planet' with approximately 25% disease incidence in the greenhouse and fields at the Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences (Beijing, China). The bulbs of symptomatic plants were brown and rotten, with sunken lesions. Symptomatic plants showed short, discolored leaves, and eventually lead to stem wilt and death of the whole plants. Infected bulbs were surface sterilized in 75% ethanol for 30 s, then in 2% sodium hypochlorite for 5 min, and rinsed three times with sterile distilled water. A 0.5×0.5 cm2 tissue piece was then placed on potato dextrose agar (PDA) medium and incubated at 25±1℃. After 5 days, the isolate was purified by single spore isolation technique. The singled-spored fungal colony was characterized by fluffy white aerial mycelia, and produced orange pigments with age. After seven days on Spezieller Nahrstoffarmer agar (SNA), conidia produced from simple lateral phialides. Macroconidia have pronounced dorsiventral curvature typical, significantly enlarged in the middle, a tapered whip-liked pointed apical cell and characteristic foot-shaped basal cell, 3 to 6 septate, measuring 18.71 to 43.01×2.89 to 5.56 μm with an average size of 26.98×3.90 μm (n=30). Microconidia were not observed. Typical verrucose thick chlamydospore with rough walls were profuse in chains or clumps, ellipsoidal to subglobose. These morphological characteristics were consistent with Fusarium spp. (Leslie et al. 2006). For molecular identification, the internal transcribed spacer (ITS), translation elongation factor subunit 1-alpha (TEF1-α) and RNA polymeraseⅡsubunit 2 (RPB2) genes were amplified using primers ITS1/ITS4, EF1/EF2 and 5F2/7cR respectively and sequenced (White et al. 1990; Jiang et al. 2018; O'Donnell et al. 2007). Sequences were submitted to GenBank under accession numbers OM078499 (ITS), Accession OM638086 (TEF1-α) and OM638085 (RPB2). BLAST analysis showed that ITS, TEF1-α and RPB2 sequences shared 100%, 99.8%, 99.2% identity to F. equiseti (OM956073, KY081599, MW364892) in GenBank, respectively. In addition, ITS, TEF1-α and RPB2 sequences shared 100%, 99.53%, 100% identity with Fusarium lacertarum (LC7927, Fusarium incarnatum-equiseti species complex) in the Fusarium-ID database. Based on the morphological characteristics and molecular sequences, the isolates were identified as Fusarium equiseti. A pathogenicity test was performed on potted lily ('White planet') under greenhouse conditions (25±1℃ with a 16 h light and 8 h dark cycle). Three healthy lily bulbs were selected and one bulb was planted in each pot filled with sterilized soil. Each pot was inoculated with 5 mL of conidia suspension (1×107 conidia/mL) in te soil around bulbs with a stem length of 3 cm, with an equal amount of sterilized water as a control. This test had three replicates. After 15 days of inoculation, typical symptoms of bulb rotten, like those observed in the greenhouse and fields, developed on the inoculated plants but not on the controls. The same fungus was consistently reisolated from the diseased plants. To our knowledge, this is the first report that F. equiseti caused bulb rot on Lilium in China. Our result should help with future monitoring and control of lily wilt disease.
    Language English
    Publishing date 2023-05-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 754182-x
    ISSN 0191-2917
    ISSN 0191-2917
    DOI 10.1094/PDIS-01-23-0199-PDN
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: First Report of

    Wang, JiaWen / Hao, Zehui / Bi, Mengmeng / Liu, Xin / Yang, Panpan / Ming, Jun / Xu, Leifeng

    Plant disease

    2024  

    Abstract: Lilium davidii var. willmottiae, known as Lanzhou lily, is widely cultivated in China for its edible bulbs. In July 2023, symptoms of bulb rot were observed on Lanzhou lilies harvested from Lanzhou, Gansu Province, during storage at the Institute of ... ...

    Abstract Lilium davidii var. willmottiae, known as Lanzhou lily, is widely cultivated in China for its edible bulbs. In July 2023, symptoms of bulb rot were observed on Lanzhou lilies harvested from Lanzhou, Gansu Province, during storage at the Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences (Beijing, China), at an incidence of nearly 70%. The surface of the lily scales had dark water-stained spots, after the development of which the color gradually darkened, the bulbs became soft, accompanied by a pungent smell. Finally, the whole bulb became ruined and rotten, and there were thick mycelium layers on the bulbs. The infected bulbs were washed with clean water, sterilized with 75% ethanol for 30 s and 2% sodium hypochlorite for 5 min, and then rinsed three times with sterile distilled water. The 5 mm×5 mm tissue pieces from the junction of the diseased part and the healthy part were clipped, placed on potato dextrose agar (PDA) medium and subsequently incubated at 25 °C. Pure cultures were obtained by transferring hyphal tips to new PDA plates. A total of 10 fungal isolates were obtained, all of which exhibited typical Fusarium characteristics. The colonies were white to pink with white to cream-colored aerial mycelia. After 10 to 15 days of incubation, the macroconidia (n = 50) were hyaline, relatively slender with a curve, three to five septate, and 8.73 to 33.24 × 2.16 to 4.19 μm in length. The microconidia (n = 50) were hyaline and pyriform, without septa, and measured 4.04 to 8.48 × 1.24 to 2.65 μm. These morphological characteristics were similar to those described for Fusarium proliferatum (Leslie and Summerell 2006). For molecular identification, a cetyltrimethylammonium bromide (CTAB) protocol was used to extract total genomic DNA (O'Donnell et al., 1998), after which the internal transcribed spacer (ITS), translation elongation factor subunit 1-alpha (TEF1-α) and RNA polymerase Ⅱ subunit 2 (RPB2) genes were amplified using the universal primers ITS1/ITS4, EF1/EF2 and RPB2-5f2/fRPB2-7cr, respectively, and subsequently sequenced (White et al., 1990; O'Donnell et al., 1998; Liu et al., 1999; Reeb et al., 2004; O'Donnell et al., 2007; Jiang et al., 2018). The sequences of a representative isolate (CAAS01) were analyzed and submitted to GenBank under accession numbers OR554007 (ITS), OR594233 (TEF1-α) and OR603932 (RPB2). A BLAST analysis revealed that the sequences of the ITS, TEF1-α, and RPB2 genes shared 100%, 100%, and 100% identity, respectively, with those of Fusarium proliferatum (MT466521.1, MK952792.1, and LT841266.1) in GenBank. In addition, the ITS, TEF1-α and RPB2 sequences shared 100%, 100%, and 100% identity with those of Fusarium annulatum (LC13675, the Fusarium fujikuroi species complex; previously known as the Gibberella fujikuroi species complex) in the Fusarium-ID database. Fusarium proliferatum, whose common synonyms are Gibberella fujikuroi mating population D and Gibberella fujikuroi var. intermedia, is the anamorphic form of the Gibberella fujikuroi complex that belongs to the Nectriaceae family. A phylogenetic tree was constructed based on the combined TEF1-α and RPB2 sequences of CAAS01 and other Fusarium isolates, revealing that CAAS01 was grouped with Fusarium proliferatum. Based on sequence alignment and phylogenetic analysis, the isolate was identified as Fusarium proliferatum. To determine the pathogenicity of the isolated fungi, healthy bulbs were punctured with disposable sterilized needles and soaked in equal amounts of sterile water and conidial suspension (1×107 conidia/mL) for 30 min respectively. The pathogenicity experiment was repeated three times. After 7 days of inoculation at 25 °C and 80% relative humidity, the surface of the inoculated bulbs produced water-stained spots and mycelium layers consistent with the symptoms exhibited by Lilium davidii var. willmottiae bulbs during storage, while the uninoculated lily bulbs remained symptomless. Fusarium proliferatum was reisolated from the infected bulbs and identified based on morphological and molecular characteristics, fulfilling Koch's postulates. To our knowledge, this is the first report of bulb rot on Lilium davidii var. willmottiae caused by Fusarium proliferatum in China. This study will contribute to the development of management strategies for this postharvest disease in Lilium davidii var. willmottiae.
    Language English
    Publishing date 2024-01-19
    Publishing country United States
    Document type Journal Article
    ZDB-ID 754182-x
    ISSN 0191-2917
    ISSN 0191-2917
    DOI 10.1094/PDIS-10-23-2215-PDN
    Database MEDical Literature Analysis and Retrieval System OnLINE

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