An automatic phytopathometry system for chlorosis and necrosis severity evaluation of asian soybean rust infection

Author(s):  
Diego Alves da Silva ◽  
Cristiane Lemes Hamawaki ◽  
Breno Cezar Marinho Juliatti ◽  
Lucas dos Santos Nascimento ◽  
Osvaldo Toshiyuki Hamawaki ◽  
...  
2007 ◽  
Vol 20 (8) ◽  
pp. 887-899 ◽  
Author(s):  
Martijn van de Mortel ◽  
Justin C. Recknor ◽  
Michelle A. Graham ◽  
Dan Nettleton ◽  
Jaime D. Dittman ◽  
...  

Asian soybean rust (ASR), caused by Phakopsora pachyrhizi, is now established in all major soybean-producing countries. Currently, there is little information about the molecular basis of ASR–soybean interactions, which will be needed to assist future efforts to develop effective resistance. Toward this end, abundance changes of soybean mRNAs were measured over a 7-day ASR infection time course in mock-inoculated and infected leaves of a soybean accession (PI230970) carrying the Rpp2 resistance gene and a susceptible genotype (Embrapa-48). The expression profiles of differentially expressed genes (ASR-infected compared with the mock-inoculated control) revealed a biphasic response to ASR in each genotype. Within the first 12 h after inoculation (hai), which corresponds to fungal germination and penetration of the epidermal cells, differential gene expression changes were evident in both genotypes. mRNA expression of these genes mostly returned to levels found in mock-inoculated plants by 24 hai. In the susceptible genotype, gene expression remained unaffected by rust infection until 96 hai, a time period when rapid fungal growth began. In contrast, gene expression in the resistant genotype diverged from the mock-inoculated control earlier, at 72 h, demonstrating that Rpp2-mediated defenses were initiated prior to this time. These data suggest that ASR initially induces a non-specific response that is transient or is suppressed when early steps in colonization are completed in both soybean genotypes. The race-specific resistance phenotype of Rpp2 is manifested in massive gene expression changes after the initial response prior to the onset of rapid fungal growth that occurs in the susceptible genotype.


2018 ◽  
Vol 18 (4) ◽  
pp. 390-398 ◽  
Author(s):  
João Vitor Maldonado dos Santos ◽  
Naoki Yamanaka ◽  
Francismar Corrêa Marcelino-Guimarães ◽  
José Francisco Ferraz de Toledo ◽  
Carlos Alberto Arrabal Arias ◽  
...  

Author(s):  
Ralph von Qualen ◽  
Xiao-Bing Yang

Author(s):  
Ralph von Qualen ◽  
Xiao-Bing Yang

2021 ◽  
Vol 42 (11) ◽  
pp. 4177-4198
Author(s):  
Renato Herrig Furlanetto ◽  
Marcos Rafael Nanni ◽  
Monica Sayuri Mizuno ◽  
Luís Guilherme Teixeira Crusiol ◽  
Camila Rocco da Silva

2011 ◽  
Vol 5 (1) ◽  
pp. 118-122 ◽  
Author(s):  
H. Roger Boerma ◽  
Maria J. Monteros ◽  
Bo-Keun Ha ◽  
E. Dale Wood ◽  
Daniel V. Phillips ◽  
...  

2013 ◽  
Vol 40 (10) ◽  
pp. 1029 ◽  
Author(s):  
Aguida M. A. P. Morales ◽  
Jamie A. O'Rourke ◽  
Martijn van de Mortel ◽  
Katherine T. Scheider ◽  
Timothy J. Bancroft ◽  
...  

Rpp4 (Resistance to Phakopsora pachyrhizi 4) confers resistance to Phakopsora pachyrhizi Sydow, the causal agent of Asian soybean rust (ASR). By combining expression profiling and virus induced gene silencing (VIGS), we are developing a genetic framework for Rpp4-mediated resistance. We measured gene expression in mock-inoculated and P. pachyrhizi-infected leaves of resistant soybean accession PI459025B (Rpp4) and the susceptible cultivar (Williams 82) across a 12-day time course. Unexpectedly, two biphasic responses were identified. In the incompatible reaction, genes induced at 12 h after infection (hai) were not differentially expressed at 24 hai, but were induced at 72 hai. In contrast, genes repressed at 12 hai were not differentially expressed from 24 to 144 hai, but were repressed 216 hai and later. To differentiate between basal and resistance-gene (R-gene) mediated defence responses, we compared gene expression in Rpp4-silenced and empty vector-treated PI459025B plants 14 days after infection (dai) with P. pachyrhizi. This identified genes, including transcription factors, whose differential expression is dependent upon Rpp4. To identify differentially expressed genes conserved across multiple P. pachyrhizi resistance pathways, Rpp4 expression datasets were compared with microarray data previously generated for Rpp2 and Rpp3-mediated defence responses. Fourteen transcription factors common to all resistant and susceptible responses were identified, as well as fourteen transcription factors unique to R-gene-mediated resistance responses. These genes are targets for future P. pachyrhizi resistance research.


2016 ◽  
Vol 34 (6) ◽  
pp. 661-665 ◽  
Author(s):  
Cintia G Kawashima ◽  
Gustavo Augusto Guimarães ◽  
Sônia Regina Nogueira ◽  
Dan MacLean ◽  
Doug R Cook ◽  
...  

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