Understanding the Bacterial Blight Pathogen-Combining Pathotyping and Molecular Marker Studies

2010 ◽  
Vol 1 (2) ◽  
pp. 58-68 ◽  
Author(s):  
M. Lalitha Shanti ◽  
C. Mohan Kumar Varm ◽  
P. Premalatha ◽  
G. Lalitha Devi ◽  
Usha Zehr ◽  
...  
Plant Disease ◽  
2014 ◽  
Vol 98 (4) ◽  
pp. 448-455 ◽  
Author(s):  
Defu Wang ◽  
Yajun Wang ◽  
Maoqiang Fu ◽  
Shuyuan Mu ◽  
Bing Han ◽  
...  

Powdery mildew, one of devastating diseases of wheat worldwide, is caused by Erysiphe graminis f. sp. tritici, a fungal species with constant population changes, which often poses challenges in disease management with host resistance. Transgenic approaches that utilize broad-spectrum resistance may limit changes of pathogen populations and contribute to effective control of the disease. The harpin protein Hpa1, produced by the rice bacterial blight pathogen, can induce resistance to bacterial blight and blast in rice. The fragment comprising residues 10 through 42 of Hpa1, Hpa110-42, is reportedly three- to eightfold more effective than the full-length protein. This study evaluated the transgenic expression of the Hpa110-42 gene for resistance to powdery mildew in wheat caused by E. graminis f. sp. tritici. Nine Hpa110-42 transgenic wheat lines were generated. The genomic integration of Hpa110-42 was confirmed, and expression of the transgene was detected at different levels in the individual transgenic lines. Following inoculation with the E. graminis f. sp. tritici isolate Egt15 in the greenhouse, five transgenic lines had significantly higher levels of resistance to powdery mildew compared with nontransformed plants. Thus, transgenic expression of Hpa110-42 conferred resistance to one isolate of E. graminis f. sp. tritici in wheat in the greenhouse.


2010 ◽  
Vol 158 (4) ◽  
pp. 288-295 ◽  
Author(s):  
Sascha D. Braun ◽  
Janine Hofmann ◽  
Annette Wensing ◽  
Helge Weingart ◽  
Matthias S. Ullrich ◽  
...  

Cancer ◽  
2008 ◽  
Vol 112 (8) ◽  
pp. 1862-1868 ◽  
Author(s):  
Andrew J. Vickers ◽  
Kwang Jang ◽  
Daniel Sargent ◽  
Hans Lilja ◽  
Michael W. Kattan

1990 ◽  
Vol 40 (3) ◽  
pp. 329-338
Author(s):  
Tsugufumi OGAWA ◽  
Tsuyoshi YAMAMOTO ◽  
Gurdev S. KHUSH ◽  
Twng-Wah MEW

2020 ◽  
Vol 11 ◽  
Author(s):  
Xuyan Mo ◽  
Liyuan Zhang ◽  
Yan Liu ◽  
Xuan Wang ◽  
Jiaqi Bai ◽  
...  

Plant Disease ◽  
2019 ◽  
Vol 103 (3) ◽  
pp. 422-429 ◽  
Author(s):  
Xiao-Qiang Wang ◽  
Tom W. Allen ◽  
Hui Wang ◽  
Daniel G. Peterson ◽  
Robert L. Nichols ◽  
...  

Bacterial blight, historically a seed-borne disease of cotton (Gossypium hirsutum) is caused by Xanthomonas citri pv. malvacearum, resulted in significant economic losses prior to development of resistant varieties and implementation of acid-delinting of planting seed. Periodic outbreaks have been associated with seed since the early twentieth century; of note, the disease has experienced a resurgence since 2011. Effective management of bacterial blight is dependent on accurate diagnosis and detection of the pathogen. Currently, detection of X. citri pv. malvacearum is performed by time-consuming microbiological methods. In this study, a novel and sensitive TaqMan-based qPCR protocol was developed to test for X. citri pv. malvacearum in cotton plant tissue. The primers developed are specific to five races of X. citri pv. malvacearum, but not to other Xanthomonas species or cotton-associated nonpathogenic bacteria. The efficiency of this assay was evaluated on artificially inoculated cotton leaves and seed, on naturally infected cotton leaves, and on bolls and seed originating from bacterial blight symptomatic bolls. The protocol’s efficiency from artificially inoculated plant tissue was 102 copies g−1 and 37 copies from 1 g seed for leaves and seed, respectively. In addition, X. citri pv. malvacearum was detected from 94% of the seed samples originating from blight symptomatic bolls. The qPCR protocol provides a rapid and accurate method for diagnosis and detection of bacterial blight and offers a tool for monitoring X. citri pv. malvacearum and potentially reducing its spread in seed.


2003 ◽  
Vol 117A (3) ◽  
pp. 282-288 ◽  
Author(s):  
A. Slavotinek ◽  
L. Poyser ◽  
A. Wallace ◽  
F. Martin ◽  
L. Gaunt ◽  
...  

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