scholarly journals Standardization of Screening Technique for Eucalyptus Canker Disease and Evaluation of Eucalyptus Clones against Cryptosporiopsis eucalypti

Author(s):  
M.K. Prasanna Kumar ◽  
Boby Vattekkattu Unnikrishnan ◽  
Kalavati Teli ◽  
M.C. Hemavathi ◽  
Gurumurthy Demlapura Shankaranarayana
Mycologist ◽  
2004 ◽  
Vol 18 (1) ◽  
pp. 39-45 ◽  
Author(s):  
CLAUDINE D.S. SEIXAS ◽  
ROBERT W. BARRETO ◽  
ACELINO C. ALFENAS ◽  
FRANCISCO A. FERREIRA

2017 ◽  
Vol 137 (9) ◽  
pp. 272-277
Author(s):  
Takahito Tsukada ◽  
Yuki Hasegawa ◽  
Hidekazu Uchida
Keyword(s):  

2020 ◽  
Vol 53 (1) ◽  
Author(s):  
Asma Asma ◽  
Iqbal Hussain ◽  
Muhammad Yasin Ashraf ◽  
Muhammad Arslan Ashraf ◽  
Rizwan Rasheed ◽  
...  

Crop Science ◽  
1987 ◽  
Vol 27 (3) ◽  
pp. 598-600 ◽  
Author(s):  
G. K. Rufener ◽  
R. B. Hammond ◽  
R. L. Cooper ◽  
S. K. St. Martin

Mycologia ◽  
2000 ◽  
Vol 92 (6) ◽  
pp. 1085-1090 ◽  
Author(s):  
Karen Wikler ◽  
Thomas R. Gordon ◽  
Sharon L. Clark ◽  
Michael J. Wingfield ◽  
Henriette Britz

1993 ◽  
Vol 7 (10) ◽  
pp. 745-748 ◽  
Author(s):  
K. G. Hanson ◽  
Jitendra D. Desai ◽  
Anjana J. Desai

BMC Genomics ◽  
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Xiaojie Liu ◽  
Xiaoshuang Li ◽  
Xuejing Wen ◽  
Yan Zhang ◽  
Yu Ding ◽  
...  

Abstract Background Valsa canker is a serious disease in the stem of Malus sieversii, caused by Valsa mali. However, little is known about the global response mechanism in M. sieversii to V. mali infection. Results Phytohormone jasmonic acid (JA) and salicylic acid (SA) profiles and transcriptome analysis were used to elaborate on the dynamic response mechanism. We determined that the JA was initially produced to respond to the necrotrophic pathogen V. mali infection at the early response stage, then get synergistically transduced with SA to respond at the late response stage. Furthermore, we adopted Pacific Biosciences (PacBio) full-length sequencing to identify differentially expressed transcripts (DETs) during the canker response stage. We obtained 52,538 full-length transcripts, of which 8139 were DETs. Total 1336 lncRNAs, 23,737 alternative polyadenylation (APA) sites and 3780 putative transcription factors (TFs) were identified. Additionally, functional annotation analysis of DETs indicated that the wild apple response to the infection of V. mali involves plant-pathogen interaction, plant hormone signal transduction, flavonoid biosynthesis, and phenylpropanoid biosynthesis. The co-expression network of the differentially expressed TFs revealed 264 candidate TF transcripts. Among these candidates, the WRKY family was the most abundant. The MsWRKY7 and MsWRKY33 were highly correlated at the early response stage, and MsWRKY6, MsWRKY7, MsWRKY19, MsWRKY33, MsWRKY40, MsWRKY45, MsWRKY51, MsWRKY61, MsWRKY75 were highly correlated at the late stage. Conclusions The full-length transcriptomic analysis revealed a series of immune responsive events in M. sieversii in response to V. mali infection. The phytohormone signal pathway regulatory played an important role in the response stage. Additionally, the enriched disease resistance pathways and differentially expressed TFs dynamics collectively contributed to the immune response. This study provides valuable insights into a dynamic response in M. sieversii upon the necrotrophic pathogen V. mali infection, facilitates understanding of response mechanisms to canker disease for apple, and provides supports in the identification of potential resistance genes in M. sieversii.


2021 ◽  
Vol 9 (6) ◽  
pp. 1176
Author(s):  
Simone Cristina Picchi ◽  
Laís Moreira Granato ◽  
Maria Júlia Festa Franzini ◽  
Maxuel Oliveira Andrade ◽  
Marco Aurélio Takita ◽  
...  

Xanthomonas citri subsp. citri (X. citri) is a plant pathogenic bacterium causing citrus canker disease. The xanA gene encodes a phosphoglucomutase/phosphomannomutase protein that is a key enzyme required for the synthesis of lipopolysaccharides and exopolysaccharides in Xanthomonads. In this work, firstly we isolated a xanA transposon mutant (xanA::Tn5) and analyzed its phenotypes as biofilm formation, xanthan gum production, and pathogenesis on the sweet orange host. Moreover, to confirm the xanA role in the impaired phenotypes we further produced a non-polar deletion mutant (ΔxanA) and performed the complementation of both xanA mutants. In addition, we analyzed the percentages of the xanthan gum monosaccharides produced by X. citri wild-type and xanA mutant. The mutant strain had higher ratios of mannose, galactose, and xylose and lower ratios of rhamnose, glucuronic acid, and glucose than the wild-type strain. Such changes in the saccharide composition led to the reduction of xanthan yield in the xanA deficient strain, affecting also other important features in X. citri, such as biofilm formation and sliding motility. Moreover, we showed that xanA::Tn5 caused no symptoms on host leaves after spraying, a method that mimetics the natural infection condition. These results suggest that xanA plays an important role in the epiphytical stage on the leaves that is essential for the successful interaction with the host, including adaptive advantage for bacterial X. citri survival and host invasion, which culminates in pathogenicity.


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