scholarly journals Phytotoxicity of the new metabolites produced by Phoma betae, the cause of phoma root rot and leaf spot in sugar beet (Beta vulgaris L.).

1985 ◽  
Vol 51 (2) ◽  
pp. 219-222 ◽  
Author(s):  
Ryutaro SAKAI ◽  
Yosuke MINO ◽  
Akitami ICHIHARA ◽  
Sadao SAKAMURA
2019 ◽  
Vol 72 ◽  
pp. 21-26
Author(s):  
Nitesh Chand ◽  
E. Eirian Jones ◽  
Seona Casonato

Phoma betae is an economically important pathogen of red beet causing preemergence seedling damping, leaf spot and root rot. However, the pathogenicity of P. betae is unknown in New Zealand despite the economic importance of this pathogen. Twenty-five isolates were collected from a survey of red beet seed farms in Canterbury, New Zealand during 2016/2017 and three of these PB101 (from seeds), PB103 (from roots) and PB106 (from leaves) were used for pathogenicity testing of two red-beet cultivars. Isolate PB106 was further used to investigate its effects on spinach and fodder beet as well as red beet under greenhouse conditions. All three P. betae isolates were pathogenic on both red-beet cultivars tested, causing leaf-spot symptoms. Isolates PB101 and PB106 produced significantly larger leaf-spot lesions (P<0.001) compared with PB103. Phoma betae isolate PB106 was pathogenic to both red-beet cultivars, spinach and fodder beet but fodder beet was less susceptible than the other species tested. Regardless of cultivar, <i>P. betae </i>is an important pathogen of beets and is capable of causing leaf spots.


Euphytica ◽  
2010 ◽  
Vol 173 (3) ◽  
pp. 409-418 ◽  
Author(s):  
Kazunori Taguchi ◽  
Kazuyuki Okazaki ◽  
Hiroyuki Takahashi ◽  
Tomohiko Kubo ◽  
Tetsuo Mikami

2011 ◽  
Vol 1 (4) ◽  
pp. 283-291 ◽  
Author(s):  
Kazunori Taguchi ◽  
Tomohiko Kubo ◽  
Hiroyuki Takahashi ◽  
Hideyuki Abe

2021 ◽  
Author(s):  
Rebecca Spanner ◽  
Jonathan Neubauer ◽  
Thies M. Heick ◽  
Michael Grusak ◽  
Olivia Hamilton ◽  
...  

Cercospora leaf spot (CLS) is a globally important disease of sugar beet (Beta vulgaris L.) caused by the fungus Cercospora beticola. Long-distance movement of C. beticola has been indirectly evidenced in recent population genetic studies, suggesting potential dispersal via seed. Commercial sugar beet “seed” consists of the reproductive fruit (true seed surrounded by maternal pericarp tissue) coated in artificial pellet material. In this study, we confirmed the presence of viable C. beticola in sugar beet fruit for 10 of 37 tested seed lots. All isolates harbored the G143A mutation associated with quinone outside inhibitor resistance and 32 of 38 isolates had reduced demethylation inhibitor sensitivity (EC50 > 1 µg/ml). Planting of commercial sugar beet seed demonstrated the ability of seed-borne inoculum to initiate CLS in sugar beet. Cercospora beticola DNA was detected in DNA isolated from xylem sap, suggesting the vascular system is used to systemically colonize the host. We established nuclear ribosomal internal transcribed spacer region amplicon sequencing using the MinION platform to detect fungi in sugar beet fruit. Fungi from 19 different genera were identified from 11 different sugar beet seed lots, but Fusarium, Alternaria, and Cercospora were consistently the three most dominant taxa, comprising an average of 93% relative read abundance over 11 seed lots. We also present evidence that C. beticola resides in the pericarp of sugar beet fruit, rather than the true seed. The presence of seed-borne inoculum should be considered when implementing integrated disease management strategies for CLS of sugar beet in the future.


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