Chemical Regulation of Mating Type in Phytophthora parasitica

Mycologia ◽  
1986 ◽  
Vol 78 (1) ◽  
pp. 134 ◽  
Author(s):  
W. H. Ko ◽  
C. J. Lee ◽  
H. J. Su

Mycologia ◽  
1986 ◽  
Vol 78 (1) ◽  
pp. 134-136 ◽  
Author(s):  
W. H. Ko ◽  
C. J. Lee ◽  
H. J. Su


Plant Disease ◽  
2019 ◽  
Vol 103 (10) ◽  
pp. 2599-2605 ◽  
Author(s):  
Qiang Zhang ◽  
Ruirui Feng ◽  
Qing Zheng ◽  
Jinyang Li ◽  
Zhirou Liu ◽  
...  

Tobacco black shank, caused by Phytophthora parasitica, is one of the most notorious tobacco diseases and causes huge economic losses worldwide. Understanding the genetic variation of P. parasitica populations is essential to the development of disease control measures. In this research, 210 simple sequence repeat (SSR) markers for P. parasitica were identified, 10 of which were polymorphic among nine reference strains. We further performed population genetic analysis of 245 P. parasitica isolates randomly collected from tobacco fields in Chongqing for mating type, molecular variation at 14 SSR loci (four of which were identified previously), and sensitivity to the fungicide metalaxyl. The results showed that the A2 mating type was dominant and no A1 mating type isolate was discovered. SSR genotyping distinguished 245 P. parasitica isolates into 46 genotypes, four of which were dominant in the population. Low genotypic diversity and excess heterozygosity were common in nearly all of the populations from Chongqing. Population analysis showed that no differentiation existed among different populations. All isolates tested were highly sensitive to metalaxyl. Taken together, our results showed that the P. parasitica populations from tobacco fields in Chongqing belonged to a clonal lineage and were highly sensitive to metalaxyl.



2005 ◽  
Vol 51 (11) ◽  
pp. 934-940 ◽  
Author(s):  
Yu-Huan Gu ◽  
Wen-Hsiung Ko

When protoplasts carrying metalaxyl-resistant (Mr) nuclei from the A1 isolate of Phytophthora parasitica were fused with protoplasts carrying chloroneb-resistant (Cnr) nuclei from the A2 isolate of the same species, fusion products carrying Mr nuclei were either the A2 or A1A2 type, while those carrying Cnr nuclei were the A1, A2, or A1A2 type. Fusion products carrying Mr and Cnr nuclei also behaved as the A1, A2, or A1A2 type. The result refutes the hypothesis that mating types in Phytophthora are controlled by nuclear genes. When nuclei from the A1 isolate of P. parasitica were fused with protoplasts from the A2 isolate of the same species and vice versa, all of the nuclear hybrids expressed the mating type characteristics of the protoplast parent. The same was true when the nuclei from the A1 isolate of P. parasitica were fused with the protoplasts from the A0 isolate of Phytophthora capsici and vice versa. These results confirm the observation that mating type genes are not located in the nuclei and suggest the presence of mating type genes in the cytoplasms of the recipient protoplasts. When mitochondria from the A1 isolate of P. parasitica were fused with protoplasts from the A2 isolate of the same species, the mating type of three out of five regenerated protoplasts was changed to the A1 type. The result demonstrated the decisive effect of mitochondrial donor sexuality on mating type characteristics of mitochondrial hybrids and suggested the presence of mating type genes in mitochondria. All of the mitochondrial hybrids resulting from the transfer of mitochondria from the A0 isolate of P. capsici into protoplasts from the A1 isolate of P. parasitica were all of the A0 type. The result supports the hypothesis of the presence of mating type genes in mitochondria in Phytophthora.Key words: mating type, mitochondrial gene, Phytophthora parasitica, Phytophthora capsici.



Microbiology ◽  
1981 ◽  
Vol 125 (2) ◽  
pp. 451-454
Author(s):  
W. H. KO


2013 ◽  
Vol 65 (1) ◽  
pp. 69-78 ◽  
Author(s):  
Philipp B. Gannibal ◽  
Igor A. Kazartsev
Keyword(s):  


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