First report ofPythium sylvaticum causing potato tuber rot

2005 ◽  
Vol 82 (2) ◽  
pp. 173-177 ◽  
Author(s):  
R. D. Peters ◽  
H. W. Bud Platt ◽  
C. A. Lévesque
Plant Disease ◽  
2020 ◽  
Vol 104 (2) ◽  
pp. 596
Author(s):  
Yanzhi Mao ◽  
Gengbin Yang ◽  
Dewei Kong ◽  
Lele Liu ◽  
Yanfeng Hu

1956 ◽  
Vol 2 ◽  
pp. 5-7
Author(s):  
I. TANAKA ◽  
K. MIYAMOTO ◽  
H. FUJII ◽  
H. AIKAWA

Plant Disease ◽  
2012 ◽  
Vol 96 (7) ◽  
pp. 1067-1067 ◽  
Author(s):  
V. Gupta ◽  
D. John ◽  
V. K. Razdan ◽  
S. K. Gupta

Bunium persicum (Kala zeera, also black cumin) is an economically important culinary crop that is cultivated for its seed pods and its tuberlike roots. In India, high-altitude regions of Himachal Pradesh, including the Padder valley and the Gurez area of Jammu and Kashmir, are areas of kalazeera production (3). In 2008 to 2009, tuber rot disease of kala zeera was observed during the late spring season in the Padder valley. Symptomatic plants were distributed in localized areas in the field and the symptoms included drying of foliage and rotting of tubers. White mycelia were found on the tubers at the late stages of disease development. Incidence of infection in the surveyed area was 80 to 90%. Yield losses were 50 to 60%. To isolate the causal pathogen, we cultured tissues from symptomatic tubers. Small bits of the infected tissue were surface disinfested in 0.1% mercuric chloride, followed by rinsing three times in sterile distilled water. The surface disinfested tissues were plated on potato dextrose agar (PDA) and incubated at 27°C for 4 days. Pure cultures of the mycelium from the diseased tissues were transferred to a second set of PDA for species identification. The fungus produced three types of spores: small, one-celled, oval microconidia; large, slightly curved, septate macroconidia; and rounded, thick-walled chlamydospores. Microconidia were mostly non-septate and 8.91 to 15.73 × 2.3 to 3.5 μm, whereas macroconidia were three- to five-septate and were 35.55 to 54.74 × 3.91 to 6.5 μm. On the basis of morphological characteristics (1), the fungus was identified and deposited as a member of the Fusarium solani species complex in the Indian Type Culture Collection, New Delhi (ID No. 8422.11). To confirm pathogenicity, healthy tubers were submerged for 20 min in a conidial suspension of the isolated fungus (1 × 105 cfu/ml), which was prepared in potato dextrose broth, incubated for 10 days at 27°C, and centrifuged at 140 rpm. Noninoculated controls were submerged in distilled water. Inoculated and control tubers were then planted in separate pots filled with sterilized soil and kept in a shade house. Symptoms appeared on inoculated tubers 9 to 10 days after planting. Signs of the pathogen in the form of mycelia were present. The tubers rotted and died 12 to 15 days after inoculation. Control tubers did not display any symptoms. F. solani species complex was reisolated from inoculated tubers, fulfilling Koch's postulates. F. solani has been reported to cause corm rot on gladiolus and saffron (2). To our knowledge, this is the first report of the F. solani species complex as pathogenic to tubers of kalazeera in India. References: (1) C. Booth. The Genus Fusarium. 47, 1971. (2) L. Z. Chen et al. J. Shanghai Agric. College 12:240, 1994. (3) K. S. Panwar et al. Agriculture Situation in India. 48:151, 1993.


Plant Disease ◽  
2021 ◽  
Author(s):  
Jin Cheon Park ◽  
Yeonghoon Lee ◽  
Eom-Ji Hwang ◽  
Da Eun Kwon ◽  
won park ◽  
...  

Apios americana Medik, commonly known as American groundnut, is a leguminous perennial vine crop native to North America and is cultivated in Japan and Korea (Chu et al. 2019). Its tubers are edible and believed to be very nutritious, especially for women just after childbirth. The tubers also contain secondary metabolites, saponin and genistein, which is good for human health (Ichige et al. 2013). However, the storage of tubers at inappropriate temperatures and humidity levels can cause severe fungal infection, and adversely affect tuber quality. During March and April 2020, a white to pale-orange fungal mycelia were observed on stored American groundnut tubers, with 10 to 15% of seed tubers rotten. Infected tubers were collected, and fungal isolates were isolated on potato dextrose agar (PDA) using the single spore isolation method (Leslie and Summerell 2006). A pure culture (isolate JC20003) was obtained and stored at the Bioenergy Crop Research Institute, NICS, Muan, Republic of Korea. The fungus was cultured on PDA and V8 liquid media for 7 days at 25℃ to observe its morphological characteristics. The length and width of macroconidia ranged from 20.6 to 52.9 μm and 2.9 to 5.1 μm, respectively (n = 30). The microconidia were 8.5 to 14.9 μm and 2.3 to 4.2 μm in length and width, respectively (n = 30). Macroconidia were broadly falcate, strongly septate, 2 to 6 septations with dorsiventral curvature; chlamydospores were formed in chains; and microconidia were fusiform with 0 to 1 septation observed. Genomic DNA of the isolate was extracted using Solgent DNA extraction kit (Solgent, Daejeon, Korea), followed by PCR analysis using the internal transcribed spacer (ITS5/ITS4) and elongation factor (EF-1/EF2) genes (White et al. 1990; O’Donnel 2000). PCR products were sequenced and analyzed to confirm species identity (Yang et al. 2018). These sequences were deposited in GenBank (accession numbers MT703859/ITS and MT731939/EF). BLASTn search analysis showed 100% sequence similarity with Fusarium acuminatum (isolates N-51-1/ITS and WXWH24/EF). Based on morphological and molecular data analysis, the fungus was identified as F. acuminatum (Leslie and Summerell 2006; Marin et al. 2012). Pathogenicity tests were conducted on five tubers inoculated with 5 mm mycelial plugs with three replicates, while a non-mycelial plug served as the control. After 5 days of incubation in plastic containers at 25 °C with high humidity, typical symptoms developed. No symptoms were observed on the control tubers; F. acuminatum was re-isolated from artificially inoculated tubers to complete Koch’s postulates. This is the first report on post-harvest tuber rot caused by F. acuminatum in Apios americana.


Plant Disease ◽  
1997 ◽  
Vol 81 (6) ◽  
pp. 694-694 ◽  
Author(s):  
M. C. Serra ◽  
H. L. Weidemann

During the last 2 years, potato (Solanum tuberosum L.) tubers displaying superficial necrotic arcs and rings were found in central Portugal. These symptoms increased during storage, and diminished tuber quality of ware (fresh-market) potatoes; however, no internal necrosis, which is typical for infections caused by tobacco rattle virus or potato mop top virus, was observed. The symptoms led to the preliminary diagnosis of potato tuber ringspot disease (PTNRD), caused by a tuber necrosis (TN)-inducing isolate of the tobacco veinal necrosis strain group of potato virus Y (PVYN) that was named PVYNTN. The occurrence of PVYNTN has been reported by a number of European countries. Suspect PTNRD tubers of the cv. Monalisa were obtained from several Portuguese potato growers and were tested with polyclonal antibodies (pabs) that reacted generally with PVY, and with monoclonal antibodies (mabs) raised against PVYN. Serogical tests were carried out in a double antibody sandwich (DAS) enzyme-linked immunosorbent assay (ELISA) with pabs and in a triple antibody sandwich (TAS) ELISA when mabs were used. As a result, the tubers were found to be infected with a virus isolate belonging to the PVYN strain group. Since PVYNTN cannot be distinguished serologically from other members of the PVYN strain group due to the similarities of their coat proteins (1), reverse transcription-polymerase chain reaction combined with immunocapture was applied for diagnostic purposes. The olignucleotide primers used were located in the 5′ non-coding region at nucleotide 103 and in the adjacent P1 protein gene coding region at position 919. This primer pair can be used to distinguish PVYNTN from other members of the PVYN strain group (2). Tests were carried out with plant sap from tubers and from plants grown from eye-cuttings and also from tobacco plants that were inoculated with plant sap of these potato tubers and plants. Control samples included sap from un-infected tobacco plants and from tobacco plants infected with a PVYN isolate and with the PVYNTN type strain “Hungary”. The expected amplification product of 835 bp appeared in the agarose gel with samples originally obtained from the tubers and with the PVYNTN control but not with the PVYNTN control, indicating that the tuber symptoms in potato cv. Monalisa were caused by infections with PVYNTN. This is the first report of the occurrence of PVYNTN in Portugal. References: (1) T. Dalmay and E. Balazs. Nucleic Acids Res. 18: 6721, 1990. (2) H. L. Weidemann and E. Maiss. Z. Pflanzenkr. Pflanzenschutz 103:337, 1996.


Nematology ◽  
2015 ◽  
Vol 17 (2) ◽  
pp. 193-202 ◽  
Author(s):  
Peter Mwaura ◽  
Björn Niere ◽  
Stefan Vidal

Glasshouse experiments were conducted to evaluate the effect of initial population densities () of Ditylenchus destructor and D. dipsaci on potato tuber damage and nematode reproduction. Ditylenchus destructor did not influence tuber numbers but influenced tuber weight at high levels. Ditylenchus dipsaci influenced tuber numbers and weights at a level of 14.29 (g growing medium)−1. Tolerance limit estimates according to the Seinhorst model were very low indicating both nematode species have a major impact on potato tuber weight. External and internal tuber rot caused by both species increased with levels. Ditylenchus destructor caused more tuber rot than D. dipsaci at all levels. Reproduction rates of D. destructor were higher at all levels studied compared to D. dipsaci. The equilibrium density of 1.3 and 0.6 for D. destructor and D. dipsaci, respectively, was observed at level of 14.29 (g growing medium)−1.


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