Management measures to reduce sweet potato foot rot caused by Diaporthe destruens in seed potatoes during storage

2021 ◽  
Vol 87 (4) ◽  
pp. 239-250
Author(s):  
K. NISHIOKA ◽  
Y. NISHI ◽  
N. OMATSU ◽  
O. SUEKAWA ◽  
S. KODAMA ◽  
...  
Author(s):  
Ai Maeda ◽  
Ayaka Minoshima ◽  
Shinji Kawano ◽  
Misa Nakamura ◽  
Tetsuya Takushi ◽  
...  

2019 ◽  
pp. 79-82
Author(s):  
R.B. Pereira ◽  
G.B. Amaro ◽  
G.C. Lucas ◽  
L.S. Mendes ◽  
J.B. Pinheiro

Plant Disease ◽  
2021 ◽  
Author(s):  
LiFei Huang ◽  
Xin-Xin Zhang ◽  
Yi-Ling Yang ◽  
Hong-Da Zou ◽  
boping Fang ◽  
...  

Foot rot of sweet potato caused by Diaporthe destruens severely affects yield and quality worldwide. Research on this pathogen is limited due to non-availability of genome resources. Here, we report a high-quality genome sequence of D. destruens isolate CRI 305-2,which was originally isolated from infected stem of sweet potato in Taizhou City, Zhejiang Province, China. The genome comprised a total length of 56,108,228 bp, consisted of 47 scaffolds with an overall G+C content of 48.7% and an N50 of 2,479,481 bp. This resource that can be used as a reference for evolution mechanisms and comparative genomic research.


Agriculture ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1046
Author(s):  
Jackeline Rossetti Mateus ◽  
Isabella Dal’Rio ◽  
Diogo Jurelevicius ◽  
Fabio Faria da Mota ◽  
Joana Montezano Marques ◽  
...  

Sweet potato (Ipomoea batatas) tuberous roots are used for human consumption, animal feed, and many industrial products. However, the crop is susceptible to various pests and diseases, including foot rot disease caused by the phytopathogenic fungus Plenodomus destruens. Biological control of plant pathogens by Bacillus species is widely disseminated in agrosystems, but specific biological control agents against the foot rot disease-causing fungus are not yet available. Our previous studies showed that two Bacillus strains isolated from sweet potato roots—B. safensis T052-76 and B. velezensis T149-19—were able to inhibit P. destruens in vitro, but data from in vivo experiments using simultaneously the fungus and the bacteria were missing. In this study, both strains were shown to protect the plant from the disease and to mitigate the symptoms of foot rot disease in pot experiments. Total fungal community quantification using real-time PCR showed a significant decrease in the number of copies of the ITS gene when the bacteria were inoculated, compared to the control (with the fungus only). To determine the genes encoding antimicrobial substances likely to inhibit the fungus, their genomes were sequenced and annotated. Genes coding for mycosubtilin, bacillaene, macrolactin, bacillibactin, bacilysin, plantazolicin, plipastatin, dificidine, fengycin and surfactin were found in B. velezensis T149-19, while those coding for bacylisin, lichenysin, bacillibactin, fengycin and surfactin were found in B. safensis T052-76. Altogether, the data presented here contribute to advancing the knowledge for the use of these Bacillus strains as biocontrol products in sweet potato.


2016 ◽  
Vol 82 (4) ◽  
pp. 181-185 ◽  
Author(s):  
Yunpeng Gai ◽  
Haijie Ma ◽  
Xinglong Chen ◽  
Jianyu Zheng ◽  
Haohao Chen ◽  
...  

Plant Disease ◽  
2020 ◽  
Vol 104 (1) ◽  
pp. 284-284
Author(s):  
T. R. P. Almeida ◽  
I. L. Coelho ◽  
L. S. B. Vasconcelos ◽  
M. A. Pontes ◽  
W. A. S. Vieira ◽  
...  
Keyword(s):  
Foot Rot ◽  

2021 ◽  
Vol 12 ◽  
Author(s):  
Kazuki Fujiwara ◽  
Yuki O. Kobayashi ◽  
Manami Usui ◽  
Kazuya Nishioka ◽  
Misa Nakamura ◽  
...  

Foot rot disease caused by Diaporthe destruens (formerly Plenodomus destruens) has become a major concern for the production of sweet potato [Ipomoea batatas (L.) Lam.] in Japan. A related fungus Diaporthe batatas, which causes dry rot disease of sweet potato, is native and is widespread in fields in Japan. The similar characteristics of these two pathogens pose a challenge for conventional disease diagnosis. Currently, there are no effective molecular measures for identifying and distinguishing D. destruens and D. batatas. Here, we demonstrate a real-time PCR assay that distinguishes and quantifies D. batatas and D. destruens from co-infected sweet potato. The assay was performed with various simulated DNA combinations of D. batatas and D. destruens ranging from 1:1 to 1:100000. The assay was also used with the ratios of D. batatas: D. destruens: sweet potato DNA ranging from 1:1:1 to 1:1:100000. These assays produced a specific amplification product for each of the pathogens, and quantified the fungal biomass over the entire range tested without detecting false positives. The assay was validated by using infected sweet potato collected from various fields; it showed sufficient sensitivity and specificity to quantify and distinguish D. batatas and D. destruens from these field samples. Thus, our real-time PCR assay would be a useful tool for diagnosis of D. batatas and D. destruens and is expected to provide the foundation for the design of integrated disease management strategies for foot rot disease in sweet potato.


Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
D Rosas-Ramírez ◽  
R Pereda-Miranda
Keyword(s):  

2020 ◽  
Vol 2 (2) ◽  
Author(s):  
Musdar Musdar ◽  
Lukmanul Hakim ◽  
Juliani Juliani ◽  
Jailani Jailani

White sweet potato starch (Ipomea batatas L.) and avocado seed starch (Parsea americana Mill) derived from local plants have the potential to be developed as agricultural products. Starch is a hydrocolloid compound as a potential local resource to be utilized. Glycerol function as an anti-freezing which is hygroscopic. This study aims to determine the ratio of white sweet potato starch with avocado seed starch and the concentration of glycerol for making edible film. This study was an experiment using a completely randimized factorial design with 2 (two) main factor consisting of a comparison of white sweet potato starch and avocado seed with 3 levels: P1 = 35%:65%., P2=50%:50%., P3=65%:35% and glycerol concentration with 3 levels: G1=1%., G2=2%., G3=3%. The best result reasearch were content of 23.03% (tratment P1G1), solubility of 55.57% (treatment P3G2)., swelling test of 9.83% (treatment P2g3)., elongation of 8.18% (treatment P3G2)


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