Identification of a Gene inArabidopsis thalianaControlling Resistance to Clubroot (Plasmodiophora brassicae)and Characterization of the Resistance Response

1996 ◽  
Vol 9 (2) ◽  
pp. 091 ◽  
Author(s):  
Harald Fuchs
2018 ◽  
Vol 108 (12) ◽  
pp. 1486-1492 ◽  
Author(s):  
Jing Zheng ◽  
Xuliang Wang ◽  
Qian Li ◽  
Shu Yuan ◽  
Shiqing Wei ◽  
...  

Clubroot disease is an important disease on cruciferous crops caused by Plasmodiophora brassicae infections. The pathotypes have been classified based on the reactions of differential hosts. However, molecular markers of particular pathotypes for P. brassicae are limited. In this study, we found five genetic markers in association with different pathotypes. Different gene expression patterns among different pathotypes (P4, P7, P9, and P11) were assayed according to the transcriptome data. The assay indicated that molecular markers PBRA_007750 and PBRA_009348 could be used to distinguish P11 from P4, P7, and P9; PBRA_009348 and Novel342 could distinguish P9 from P4, P7, and P11; and PBRA_008439 and Novel342 could represent a kind of P4. Polymerase chain reaction cycles ranging from 25 to 30 were able to identify the predominant pathotype in general. Therefore, these molecular markers would be a valuable tool to identify and discriminate pathotypes in P. brassicae population.


2004 ◽  
Vol 31 (2) ◽  
pp. 149 ◽  
Author(s):  
Claudia Stange ◽  
José Tomás Matus ◽  
Alvaro Elorza ◽  
Patricio Arce-Johnson

Nicotiana tabacum cv. Xanthi nn plants are susceptible to infection by most tobamoviruses (TMV). However, such plants display a partial hypersensitive resistance response (HR-like response) to TMV-Cg. The genetic mechanism of the HR-like response has yet not been determined, but it may involve a gene with a function similar to that of a resistance gene, responsible for HR in resistant plants. We have cloned a gene homologous to the resistance N gene, named NH, from Nicotiana Xanthi nn plants. The coding region of NH is 5.028 base pairs (bp) long and has 82.6% nucleotide identity with the N gene. In contrast to the N gene, the NH gene lacks intron 4 and does not have sites for alternative splicing of intron 3. Analysis of its sequence revealed that NH belongs to the TIR / NSB / LRR gene class. We were able to detect stable levels of NH-transcript in Nicotiana Xanthi nn plants from 0 to 18 h post-inoculation (hpi) with TMV-Cg. Transcript levels increased slightly at 24 hpi and dropped below basal values at 48 hpi. The NH transcript was also detected in a range of resistant Nicotiana plants (N. tabacum Xanthi NN, N. glutinosa, N. glauca and N. rustica) suggesting that NH is a homologue of the N gene, rather than an allele. We have cloned and characterised the NH gene (GenBank acc. no. bankit598573 AY535010) from nn susceptible plants and postulate that this gene might be involved in the HR-like response seen in these plants.


PLoS ONE ◽  
2013 ◽  
Vol 8 (1) ◽  
pp. e54745 ◽  
Author(s):  
Katsunori Hatakeyama ◽  
Keita Suwabe ◽  
Rubens Norio Tomita ◽  
Takeyuki Kato ◽  
Tsukasa Nunome ◽  
...  

Plant Disease ◽  
2021 ◽  
Author(s):  
Mingcan Lv ◽  
Yifan Liu ◽  
Yue Wu ◽  
Jing Zhang ◽  
Xuyao Liu ◽  
...  

Clubroot, caused by Plasmodiophora brassicae, is a soil-borne disease that occurs in cruciferous crops worldwide. P. brassicae usually exists as a mixture of several pathotypes, which has hampered the research on resistance mechanisms of cruciferous crops against P. brassicae. In this study, clubroot galls were collected from a field in Shenyang, China, as a pathogen source to develop an efficient protocol for a single-spore isolation system of P. brassicae by optimizing the seedling age for inoculation, host inoculation method, and plant culture method. The operational steps of the single-spore isolation method were optimized as follows: the use of two-day-old seedlings for inoculation, substituting a cryobox (100 × 2.0 mL vials) for culture dishes, the addition of nutrient solution culture, and microscopic observations of single spores. The rate of infection success was substantially improved, and single-spore isolates of four pathotypes: 4, 8, 9, and 11, were acquired in this system. Subsequently, the optimized system was used to isolate and characterize the pathotypes of single-spore isolates of P. brassicae collected from five fields in regions in China. Approximately 4 to 9 pathotypes were isolated from each region. Among these, pathotype 4 was the most prevalent. This study provides a source of valuable information that can eventually be used for the genetic analysis of host–P. brassicae interaction.


2009 ◽  
Vol 128 (6) ◽  
pp. 665-670 ◽  
Author(s):  
E. Barilli ◽  
J. C. Sillero ◽  
A. Moral ◽  
D. Rubiales
Keyword(s):  

2018 ◽  
Vol 47 (5) ◽  
pp. 531-541 ◽  
Author(s):  
Yu Ning ◽  
Yong Wang ◽  
Zhiyuan Fang ◽  
Mu Zhuang ◽  
Yangyong Zhang ◽  
...  

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