scholarly journals First Report of Leaf Sheath Rot of Areca Nut (Areca catechu) Caused by Athelia rolfsii from Tripura, India

Plant Disease ◽  
2020 ◽  
Vol 104 (11) ◽  
pp. 3070
Author(s):  
Deeba Kamil ◽  
Amar Bahadur ◽  
Prasenjit Debnath ◽  
Anjali Kumari ◽  
Shiv Pratap Choudhary ◽  
...  
Plant Disease ◽  
2021 ◽  
Author(s):  
Yue Sun ◽  
Rui Wang ◽  
Kaibin Qiao ◽  
Hongyu Pan ◽  
Fengting Wang ◽  
...  

Bush lily (Clivia miniata) is an important indoor flower. It is the city flower of Changchun City and has important ornamental and medicinal value in China where it is culitvated on an area of 125 hectare. During the summer of 2018, symptoms of a leaf sheath rot disease were observed on bush lily in 103 greenhouses in Changchun city, Jilin Province. The disease incidence ranged from 25 to 60% in 11 surveyed greenhouses. At the early stage, the diseased plants displayed symptoms as initial leaf sheath lesions. Progressively, the whole leaves wilted, and even the plant ultimately died. Once a leaf exhibits leaf sheath lesions, the whole plant’s ornamental value significantly drops. To identify the pathogen, symptomatic leaves were cut into pieces, surface sterilized, placed on potato dextrose agar (PDA) and incubated for 7 days at 25°C in the dark (Cao et al. 2013; the e-Xtra description for details). Fusarium single-spore isolates were obtained from characteristic colonies (Leslie et al. 2006). Two single-spore isolates were selected for further study. The isolates were identified as Fusarium spp. based on microscopic morphology on PDA. Fusarium-like colonies were white to slightly yellow with abundant cottony mycelia. Single or two-celled (single septum) microconidia were reniform or oval, 8.0 to 9.6×4.0 to 6.0m in size. The elongated conidiophores bearing microconidia in monophialides were observed (Summerbell et al. 2002). Macroconidia were abundant, sickle shaped, 18.8 to 34.8×6.4 to 6.8m, with one to three septa (Taylor et al. 2019). For molecular identification, five regions of ITS, EF1-α, RPB1, RPB2 and β-tubulin genes were amplified and sequenced. Sequences of five different regions exhibited at least 97.98% similiarity with the corresponding DNA sequences in F. solani species complex (FSSC) (the e-Xtra description for details). The phylogenetic analysis based on the EF1-α, RPB1, RPB2 and β-tubulin region sequences revealed that the isolated strain in this study was clustered with only F. solani species in the phylogenetic tree for each region. Based on morphological and molecular analysis, the isolated fungal strains were identified as F. solani. Pathogenicity was confirmed by injecting a conidial suspension (106 spores/mL) of the isolated strains in to surface surface-disinfested leaf sheath of 2-year-old potted healthy plants. As a negative control, four plants were injected with sterilized water. All plants were kept in a greenhouse with controlled conditions: 26°C, 50% to 75% relative humidity. The similar rot symptoms were observed on the leaf sheathes in the inoculated plants 30 days after inoculation whereas the control plants remained asymptomatic. The fungi reisolated from the experimental plants were confirmed to be F. solani by morphology and sequences analysis, thus completing Koch’s postulates. To the best of our knowledge, this is the first report of F. solani causing leaf sheath rot of bush lily in China, where this pathogen has been reported to cause rot diseases of other economically important ornamental plants such as Phalaenopsis, Dendrobium according to the U.S. National Fungus Collections (Farr et al. 2020). In recent years, other Fusarium species have been reported to cause rot diseases on bush lily, including F. proliferatum and F. oxysporum (Farr et al. 2020). This study will also provide critical information on the causal agent for growers to implement disease management strategies.


Plants ◽  
2021 ◽  
Vol 10 (9) ◽  
pp. 1844
Author(s):  
Ya-Min Ma ◽  
Jun-Zi Zhu ◽  
Xiao-Gang Li ◽  
Lai-Liang Wang ◽  
Jie Zhong

Zizania latifolia is a perennial plant native to East Asia. The swollen culm of Z. latifolia is a popular vegetable and traditional herbal medicine consumed in China and some other Asian countries. From 2019 to 2021, a sheath rot disease was found in Zhejiang Province of China. Symptoms mainly occurred in the leaf sheath showing as brown necrotic lesions surrounded by yellow halos. The pathogen fungal isolates were isolated from the affected sheaths. Ten representative isolates were selected for morphological and molecular identification by phylogenetic analyses of the translation elongation factor 1-α (TEF1) and the RNA polymerase II subunit beta (RPB2) gene regions. Based on the combined datasets, the fungal isolates were identified as Fusarium andiyazi. Koch’s postulates were confirmed by pathogenicity test, re-isolation and re-identification of the fungal isolates. To the best of our knowledge, this is the first report of sheath rot caused by F. andiyazi in Z. latifolia in China.


Author(s):  
Shih-Ya Chiu ◽  
Yi-Ru Lai ◽  
Wen-Shi Tsai ◽  
Chien-Jui Huang

Author(s):  
Jefferson Bertin Vélez-Olmedo ◽  
Sergio Vélez-Zambrano ◽  
Bianca Samay Angelino Bonfim ◽  
Edisson Cuenca Cuenca ◽  
Susana García ◽  
...  

Author(s):  
Shivannegowda Mahadevakumar ◽  
Yelandur Somaraju Deepika ◽  
Kandikere Ramaiah Sridhar ◽  
Kestur Nagaraj Amruthesh ◽  
Nanjaiah Lakshmidevi

Plant Disease ◽  
2009 ◽  
Vol 93 (6) ◽  
pp. 673-673 ◽  
Author(s):  
C. J. Li ◽  
Z. F. Wang ◽  
N. Chen ◽  
Z. B. Nan

Orchardgrass or cocksfoot (Dactylis glomerata L.) has been widely cultivated as a forage crop in many provinces of China (1). It is also a native perennial forage grass, which grows at the edge of forests, shrubs, and mountainous grasslands in Xinjiang and Sichuan (2). In September of 2007, signs of choke disease on orchardgrass were observed in a native grassland under birch woodland near Altai City, Xinjiang, China. Stromata, which formed on culms of diseased grass, enclosing the inflorescence and leaf sheath, were 4.5 to 5.5 mm long, smooth or wrinkled, white and later becoming yellowish or yellow, tuberculate, dry, and covered with perithecia. Inflorescences surrounded by fungal stromata were choked and failed to mature, thus restricting seed production. Pure cultures were obtained by directly scraping stromata from the surface and incubating it on antibiotic potato dextrose agar (PDA). The colonies were cottony, white on the upper surface, and white to yellow on the reverse. The growth rate was 13 to 21 mm per week at 25°C on PDA. Conidia were hyaline, lunate to reniform, and measured 4.1 ± 0.5 × 2.2 ± 0.5 μm. They accumulated in small globose heads at the tips of conidiogenous cells and were produced singly on conidiophores of 13 to 33 μm long and 2.7 to 4.1 μm wide at the base. Internal transcribed spacer (ITS) sequence by BLAST search had 99% similarity with an Epichloë typhina isolate of orchardgrass in Spain (GenBank Accession No. AM262420.1). Cultural characteristics, microscopic examination, and phylogenetic analysis showed that this choke disease on D. glomerata was caused by the fungus E. typhina (Pers.) Tul. & C. Tul. as described by White (4). To our knowledge, this is the first report of E. typhina causing choke disease on orchardgrass in China. The pathogen has been identified in France, England, Germany, Sweden, Switzerland, and the United States (3,4) with the same symptoms as those reported here. In 1997, choke disease was found in 70% of the fields in the Willamette Valley of Oregon, with disease incidences ranging from 0.05 to 28%. It was predicted to increase and spread under the prevailing climatic conditions (3). This new disease report is to provide observational and diagnostic information to help with recognition and prevention of disease spread in orchardgrass cultivation regions of China. References: (1) X. R. Chao et al. Shandong Agric. Sci. 1:7, 2005. (2) S. X. Jia, ed. China Forage Plant Flora. China Agriculture Press, Beijing, 1987. (3) W. F. Pfender and S. C. Alderman. Plant Dis. 83:754, 1999. (4) J. W. White. Mycologia 85:444, 1993.


Plant Disease ◽  
2019 ◽  
Vol 103 (1) ◽  
pp. 150-150 ◽  
Author(s):  
H. Wang ◽  
L. Xu ◽  
Z. Zhang ◽  
J. Lin ◽  
X. Huang

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