scholarly journals Disease Occurrence in Transgenic Rice Plant Transformed with Silbene Synthase Gene and Evaluation of Possible Horizontal Gene Transfer to Plant Pathogens

2014 ◽  
Vol 20 (3) ◽  
pp. 189-195
Author(s):  
Sang-Mi Yu ◽  
Ui-Seon Jeong ◽  
Ha Kyung Lee ◽  
So Hyeon Baek ◽  
Soon Jong Kwon ◽  
...  
2010 ◽  
Vol 20 (1) ◽  
pp. 187-192 ◽  
Author(s):  
Sung Eun Kim ◽  
Jae Sun Moon ◽  
Jung Kyu Kim ◽  
Won Sik Choi ◽  
Sang Han Lee ◽  
...  

2020 ◽  
Vol 8 (2) ◽  
pp. 131-140
Author(s):  
So Young Kim ◽  
Hyemin Lim ◽  
Min Kang ◽  
Kyong Mi Jun ◽  
Seung Uk Ji ◽  
...  

Microbiology ◽  
2009 ◽  
Vol 155 (10) ◽  
pp. 3187-3199 ◽  
Author(s):  
Marianna Naum ◽  
Eric W. Brown ◽  
Roberta J. Mason-Gamer

This study uses sequences from four genes, which are involved in the formation of the type III secretion apparatus, to determine the role of horizontal gene transfer in the evolution of virulence genes for the enterobacterial plant pathogens. Sequences of Erwinia, Brenneria, Pectobacterium, Dickeya and Pantoea were compared (a) with one another, (b) with sequences of enterobacterial animal pathogens, and (c) with sequences of plant pathogenic γ and β proteobacteria, to evaluate probable paths of lateral exchange leading to the current distribution of virulence determinants among these micro-organisms. Phylogenies were reconstructed based on hrcC, hrcR, hrcJ and hrcV gene sequences using parsimony and maximum-likelihood algorithms. Virulence gene phylogenies were also compared with several housekeeping gene loci in order to evaluate patterns of lateral versus vertical acquisition. The resulting phylogenies suggest that multiple horizontal gene transfer events have occurred both within and among the enterobacterial plant pathogens and plant pathogenic γ and β proteobacteria. hrcJ sequences are the most similar, exhibiting anywhere from 2 to 50 % variation at the nucleotide level, with the highest degree of variation present between plant and animal pathogen sequences. hrcV sequences are conserved among plant and animal pathogens at the N terminus. The C-terminal domain is conserved only among the enterobacterial plant pathogens, as are the hrcC and hrcR sequences. Additionally, hrcJ and hrcV sequence phylogenies suggest that at least some type III secretion system virulence genes from enterobacterial plant pathogens are related more closely to those of the genus Pseudomonas, a conclusion neither supported nor refuted by hrcC or hrcR.


2002 ◽  
Vol 47 (12) ◽  
pp. 998-1002 ◽  
Author(s):  
Rongtian Li ◽  
Zhongming Zhang ◽  
Qifa Zhang

2020 ◽  
Vol 11 ◽  
Author(s):  
Dong Liang ◽  
Christian Benjamin Andersen ◽  
Ramesh R. Vetukuri ◽  
Daolong Dou ◽  
Laura J. Grenville-Briggs

Crop protection strategies that are effective but that reduce our reliance on chemical pesticides are urgently needed to meet the UN sustainable development goals for global food security. Mycoparasitic oomycetes such as Pythium oligandrum and Pythium periplocum, have potential for the biological control of plant diseases that threaten crops and have attracted much attention due to their abilities to antagonize plant pathogens and modulate plant immunity. Studies of the molecular and genetic determinants of mycoparasitism in these species have been less well developed than those of their fungal counterparts. Carbohydrate-active enzymes (CAZymes) from P. oligandrum and P. periplocum are predicted to be important components of mycoparasitism, being involved in the degradation of the cell wall of their oomycete and fungal prey species. To explore the evolution of CAZymes of these species we performed an in silico identification and comparison of the full CAZyme complement (CAZyome) of the two mycoparasitic Pythium species (P. oligandrum and P. periplocum), with seven other Pythium species, and four Phytophthora species. Twenty CAZy gene families involved in the degradation of cellulose, hemicellulose, glucan, and chitin were expanded in, or unique to, mycoparasitic Pythium species and several of these genes were expressed during mycoparasitic interactions with either oomycete or fungal prey, as revealed by RNA sequencing and quantitative qRT-PCR. Genes from three of the cellulose and chitin degrading CAZy families (namely AA9, GH5_14, and GH19) were expanded via tandem duplication and predominantly located in gene sparse regions of the genome, suggesting these enzymes are putative pathogenicity factors able to undergo rapid evolution. In addition, five of the CAZy gene families were likely to have been obtained from other microbes by horizontal gene transfer events. The mycoparasitic species are able to utilize complex carbohydrates present in fungal cell walls, namely chitin and N-acetylglucosamine for growth, in contrast to their phytopathogenic counterparts. Nonetheless, a preference for the utilization of simple sugars for growth appears to be a common trait within the oomycete lineage.


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