scholarly journals A Gene-for-Gene Relationship Underlying the Species-Specific Parasitism of Avena/Triticum Isolates of Magnaporthe grisea on Wheat Cultivars

2002 ◽  
Vol 92 (11) ◽  
pp. 1182-1188 ◽  
Author(s):  
N. Takabayashi ◽  
Y. Tosa ◽  
H. S. Oh ◽  
S. Mayama

To elucidate genetic mechanisms of the species-specific parasitism of Magnaporthe grisea, a Triticum isolate (pathogenic on wheat) was crossed with an Avena isolate (pathogenic on oat), and resulting F1 progeny were subjected to segregation analyses on wheat cvs. Norin 4 and Chinese Spring. We found two fungal loci, Pwt3 and Pwt4, which are involved in the specific parasitism on wheat. Pwt3 operated on both cultivars while Pwt4 operated only on ‘Norin 4’. Using the cultivar specificity of Pwt4, its corresponding resistance gene was successfully identified in ‘Norin 4’ and designated as Rmg1 (Rwt4). The presence of the corresponding resistance gene indicated that Pwt4 is an avirulence locus. Pwt3 was assumed to be an avirulence locus because of its temperature sensitivity. We suggest that gene-for-gene interactions underlie the species-specific parasitism of M. grisea.

Genome ◽  
1994 ◽  
Vol 37 (5) ◽  
pp. 758-762 ◽  
Author(s):  
Y. Tosa

Genetic mechanisms of the incompatibility between Erysiphe graminis f.sp. secalis and wheat cultivars were analyzed using F1 hybrids between E. graminis f.sp. secalis, Sk-1, and f.sp. tritici, Tk-1. The avirulence of Sk-1 on Triticum aestivum 'Norin 4', 'Chinese Spring', and 'Kokeshi-komugi' was controlled by a single gene. The resistance of the three cultivars to Sk-1 was also controlled by a single gene, Pm15, a gene for resistance to E. graminis f.sp. agropyri. Implications of these results were discussed in terms of host–parasite coevolution.Key words: powdery mildew, Erysiphe graminis, resistance, wheat.


2003 ◽  
Vol 93 (1) ◽  
pp. 42-45 ◽  
Author(s):  
J. Murakami ◽  
R. Tomita ◽  
T. Kataoka ◽  
H. Nakayashiki ◽  
Y. Tosa ◽  
...  

Host species specificity of Magnaporthe grisea toward foxtail millet was analyzed using F1 cultures derived from a cross between a Triticum isolate (pathogenic on wheat) and a Setaria isolate (pathogenic on foxtail millet). On foxtail millet cvs. Beni-awa and Oke-awa, avirulent and virulent cultures segregated in a 1:1 ratio, suggesting that a single locus is involved in the specificity. This locus was designated as Pfm1. On cv. Ki-awa, two loci were involved and one of them was Pfm1. The other locus was designated as Pfm2. Interestingly, Pfm1 was not involved in the pathogenic specificity on cv. Kariwano-zairai. These results suggest that there is no “master gene” that determines the pathogenic specificity on all foxtail millet cultivars and that the species specificity of M. grisea toward foxtail millet is governed by cultivar-dependent genetic mechanisms that are similar to gene-for-gene interactions controlling race-cultivar specificity.


2002 ◽  
Vol 80 (10) ◽  
pp. 1088-1095 ◽  
Author(s):  
H S Oh ◽  
Y Tosa ◽  
N Takabayashi ◽  
S Nakagawa ◽  
R Tomita ◽  
...  

An isolate of Magnaporthe grisea was collected from a blast lesion on oat in Brazil. Sequence analysis of the rDNA-ITS-2 region and DNA fingerprinting with repetitive elements revealed that the Avena isolate belongs to the "crop isolate group" and is similar to Triticum isolates. At high temperature (28°C), the Avena isolate caused severe disease symptoms on primary leaves of oat and wheat. When the temperature was decreased to 20°C, wheat leaves expressed resistance to the Avena isolate. Cytologically, this temperature-dependent resistance was associated with an increase in the incidences of papilla formation and a hypersensitive reaction. Pathogenicity tests with various plant species at 20°C revealed that the Avena isolate is exclusively parasitic on oat. To elucidate genetic mechanisms of this species-specific parasitism, the Avena isolate was crossed with a Triticum isolate and resulting F1 progenies were subjected to pathogenicity tests on oat seedlings. In the F1 population, avirulent and virulent cultures segregated in a 1:1 ratio, suggesting that the specific parasitism on oat is controlled by a single gene. This locus was designated as Pat1.Key words: Magnaporthe grisea, species-specific parasitism, oat, temperature sensitive.


Genome ◽  
2006 ◽  
Vol 49 (8) ◽  
pp. 873-881 ◽  
Author(s):  
Q H Chen ◽  
Y C Wang ◽  
X B Zheng

We analyzed host-species specificity of Magnaporthe grisea on rice using 110 F1 progeny derived from a cross between the Oryza isolate CH87 (pathogenic to rice) and the Digitaria isolate 6023 (pathogenic to crabgrass). To elucidate the genetic mechanisms controlling species specificity in M. grisea, we performed a genetic analysis of species-specific avirulence on this rice population. Avirulent and virulent progeny segregated in a 1:1 ratio on the 2 rice cultivars 'Lijiangxintuanheigu' (LTH) and 'Shin2', suggesting that a single locus, designated PRE1, was involved in the specificity. In a combination between 'Kusabue' and 'Tsuyuake', the segregation of the 4 possible phenotypes of F1 progeny was significantly different from the expected 3:1:3:1 and instead fit a ratio of 2:0:1:1. This indicated that 2 loci, PRE1 and AVR2, were involved in specific parasitism on rice. These results suggest that the species specificity of M. grisea on rice is governed by species-dependent genetic mechanisms that are similar to the gene-for-gene interactions controlling cultivar specificity. Pathogenicity tests with various plant species revealed that the Digitaria isolate 6023 was exclusively parasitic on crabgrass. Genetic linkage analysis showed that PRE1 was mapped on chromosome 3 with respect to RAPD and SSR markers. RAPD marker S361 was linked to the avirulence gene at a distance of ~6.4 cM. Two SSR markers, m677–678 and m77–78, were linked to the PRE1 gene on M. grisea chromosome 3 at distances of 5.9 and 7.1 cM, respectively. Our results will facilitate positional cloning and functional studies of this gene.Key words: genetic analysis, graminaceous plants, Magnaporthe grisea, species-specific avirulence gene.


Genetics ◽  
1984 ◽  
Vol 106 (2) ◽  
pp. 309-324
Author(s):  
Anne Crossway ◽  
Jan Dvořák

ABSTRACT Metaphase I (MI) pairing of wheat homologous chromosomes is usually reduced in hybrids between cultivars relative to the parental inbred lines. Previous work suggested that this phenomenon is caused by polymorphism in nucleotide sequences (nonstructural chromosome variation) among wheat cultivars. The present work investigated the distribution of this variation along three selected chromosome arms between cultivars Chinese Spring and Cheyenne. Chinese Spring ditelosomics 3Aq, 6Ap and 6Bp were crossed with disomic substitutions of Cheyenne chromosomes 3A, 6A and 6B in Chinese Spring, respectively. The resulting F1 plants, called substituted monotelodisomics, were crossed with the respective Chinese Spring monosomics, producing potentially "recombinant" substituted monosomics. When these "recombinant" chromosomes were combined with the parental Chinese Spring telosomes, marked reductions in mean telosome-pairing frequency were found compared with the corresponding Chinese Spring monotelodisomics. The mean pairing frequencies of the "recombinant" chromosomes showed a continuous distribution between those of the substituted and Chinese Spring monotelodisomics. The results suggest that the nonstructural variation that reduces MI pairing between chromosomes of different wheat cultivars is not localized in a specific site but distributed along each chromosome arm. Little variation was found among monotelodisomics for either the number of ring bivalents per cell or the number of univalents other than those constituting the heteromorphic pair. This implies that the reductions in MI pairing between the Cheyenne and Chinese Spring chromosomes are caused by something residing within these specific chromosomes that does not affect the pairing of the remaining Chinese Spring chromosomes in the same cell. Furthermore, the absence of parental types among the "recombinant"-substituted monotelodisomics suggests that the sequences involved in the variation studied here are capable of converting heterohomologous chromosomes to something intermediate in nature in the span of only a single generation.


2003 ◽  
Vol 107 (6) ◽  
pp. 1139-1147 ◽  
Author(s):  
R. Berruyer ◽  
H. Adreit ◽  
J. Milazzo ◽  
S. Gaillard ◽  
A. Berger ◽  
...  

2021 ◽  
Author(s):  
Shizhen Wang ◽  
Jiaoyu Wang ◽  
Zhen Zhang ◽  
Zhongna Hao ◽  
Xueming Zhu ◽  
...  

Triticum pathotype (MoT) of Magnaporthe oryzae (syn. Pyricularia oryzae) causes wheat blast, which has recently spread to Asia. To assess the potential risk of wheat blast in rice-wheat growing regions, we investigated the pathogenicity of 14 isolates of P. oryzae on 32 wheat cultivars, among which MoO isolates were completely avirulent on the wheat cultivars at 22℃, but caused various infection degrees at 25℃. These reactions at 25℃ were isolate- and cultivar- dependent like race-cultivar specificity which was also recognized at the heading stage and caused typical blast symptoms on spikes. Microscopic analyses indicated that a compatible MoO isolates produced appressoria and infection hyphae on wheat as on rice. By comparing transcriptomes in wheat-MoO interactions, a bulk of pathogen-related genes was up-/down- regulated in compatible and incompatible patterns, but that changes of gene transcription were more significant in compatible pattern. These results indicate that the temperature could influence the infection ratio of wheat with MoO, and some MoO strains could be potential pathogens that increase the risk for the outbreak of wheat blast in wheat-rice growing regions with global warming. In addition, certain wheat cultivars exhibited resistance and are assumed to carry promoting resistant genes to the MoO strains.


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