Fitness Studies Between Field Isolates of Magnaporthe oryzae Resistant and Sensitive to Scytalone Dehydratase Inhibitors of Melanin Biosynthesis (Mbi-Ds) and Decline of Frequency of Resistant Isolates at a Rice Field

2015 ◽  
Vol 122 (5-6) ◽  
pp. 224-228 ◽  
Author(s):  
Norio Kimura ◽  
Hiroaki Fujimoto
2020 ◽  
Vol 11 ◽  
Author(s):  
Qun Wang ◽  
Jinbin Li ◽  
Lin Lu ◽  
Chengxing He ◽  
Chengyun Li

Plant Disease ◽  
2020 ◽  
Vol 104 (3) ◽  
pp. 717-723
Author(s):  
Zhen Zhang ◽  
Yulin Jia ◽  
Yanli Wang ◽  
Guochang Sun

Magnaporthe oryzae is the causal agent for the devastating disease rice blast. The avirulence (AVR) genes in M. oryzae are required to initiate robust disease resistance mediated by the corresponding resistance (R) genes in rice. Therefore, monitoring pathogen AVR genes is important to predict the stability of R gene-mediated blast resistance. In the present study, we analyzed the DNA sequence dynamics of five AVR genes, namely, AVR-Pita1, AVR-Pik, AVR-Pizt, AVR-Pia, and AVR-Pii, in field isolates of M. oryzae in order to understand the effectiveness of the R genes, Pi-ta, Pi-k, Pi-zt, Pia, and Pii in the Southern U.S. rice growing region. Genomic DNA of 258 blast isolates collected from commercial fields of the Southern UNITED STATES during 1975–2009 were subjected to PCR amplification with AVR gene-specific PCR markers. PCR products were obtained from 232 isolates. The absence of PCR products in the remaining 26 isolates suggests that these isolates do not contain the tested AVR genes. Amplified PCR products were subsequently gel purified and sequenced. Based on the presence or absence of the five AVR genes, 232 field isolates were classified into 10 haplotype groups. The results revealed that 174 isolates of M. oryzae carried AVR-Pita1, 225 isolates carried AVR-Pizt, 44 isolates carried AVR-Pik, 3 isolates carried AVR-Pia, and one isolate carried AVR-Pii. AVR-Pita1 was highly variable, and 40 AVR-Pita1 haplotypes were identified in avirulent isolates. AVR-Pik had four nucleotide sequence site changes resulting in amino acid substitutions, whereas three other AVR genes, AVR-Pizt, AVR-Pia, and AVR-Pii, were relatively stable. Two AVR genes, AVR-Pik and AVR-Pizt, were found to exist in relatively larger proportions of the tested field isolates, which suggested that their corresponding R genes Pi-k and Pi-zt can be deployed in preventing blast disease in the Southern UNITED STATES in addition to Pi-ta. This study demonstrates that continued AVR gene monitoring in the pathogen population is critical for ensuring the effectiveness of deployed blast R genes in commercial rice fields.


Crop Science ◽  
2015 ◽  
Vol 55 (6) ◽  
pp. 2620-2627 ◽  
Author(s):  
Junjie Xing ◽  
Melissa H Jia ◽  
James C. Correll ◽  
Longping Yuan ◽  
Huangfeng Deng ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Masayuki Nakamura ◽  
Yuta Okamura ◽  
Hisashi Iwai

AbstractThe CRISPR-Cas9 system has a potential for wide application in organisms that particularly present low homologous integration rates. In this study, we developed three different methods using this system to replace a gene through homology-directed repair in the plant pathogenic fungus Colletotrichum sansevieriae, which has a low recombination frequency. The gene encoding scytalone dehydratase was used as the target so that mutants can be readily distinguished owning to a lack of melanin biosynthesis. First, we performed a plasmid-based method using plasmids containing a Cas9 expression cassette and/or a single-guide RNA (sgRNA) under the control of the endogenous U6 snRNA promoter, and 67 out of 69 (97.1%) transformants exhibited a melanin-deficient phenotype with high efficiency. Second, we performed a transformation using a Cas9 protein/sgRNA complex and obtained 23 out of 28 (82.1%) transformants. Lastly, we developed a hybrid system combining a Cas9 protein and donor DNA-sgRNA expression plasmid, which yielded 75 out of 84 (89.2%) transformants. This system was also applicable to four other genes at different loci of the fungus. This is the first study to establish a CRISPR/Cas9 gene replacement system in Colletotrichum spp. and it presents a potential application for a broad range of use in other species of the genus.


Genomics Data ◽  
2015 ◽  
Vol 5 ◽  
pp. 284-291 ◽  
Author(s):  
Malali Gowda ◽  
Meghana D. Shirke ◽  
H.B. Mahesh ◽  
Pinal Chandarana ◽  
Anantharamanan Rajamani ◽  
...  

2010 ◽  
Vol 47 (12) ◽  
pp. 973-980 ◽  
Author(s):  
Yuntao Dai ◽  
Yulin Jia ◽  
James Correll ◽  
Xueyan Wang ◽  
Yanli Wang

2021 ◽  
Vol 12 (07) ◽  
pp. 713-725
Author(s):  
Kailing Chen ◽  
Jinqi Feng ◽  
Shen Chen ◽  
Jing Su ◽  
Jianyuan Yang ◽  
...  

1998 ◽  
Vol 23 (1) ◽  
pp. 58-61 ◽  
Author(s):  
Takayuki MOTOYAMA ◽  
Kinya IMANISHI ◽  
Taro KINBARA ◽  
Yoshio KURAHASHI ◽  
Isamu YAMAGUCHI

BMC Genomics ◽  
2013 ◽  
Vol 14 (1) ◽  
pp. 887 ◽  
Author(s):  
Chenxi Chen ◽  
Bi Lian ◽  
Jinnan Hu ◽  
Huanchen Zhai ◽  
Xingxing Wang ◽  
...  

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