Tools to kill: Genome of one of the most destructive plant pathogenic fungi Macrophomina phaseolina

被引:173
作者
Islam, Md Shahidul [1 ]
Haque, Md Samiul [1 ]
Islam, Mohammad Moinul [1 ]
Emdad, Emdadul Mannan [1 ]
Halim, Abdul [1 ]
Hossen, Quazi Md Mosaddeque [1 ]
Hossain, Md Zakir [1 ]
Ahmed, Borhan [1 ]
Rahim, Sifatur [1 ]
Rahman, Md Sharifur [1 ]
Alam, Md Monjurul [1 ]
Hou, Shaobin [2 ]
Wan, Xuehua [2 ]
Saito, Jennifer A. [3 ]
Alam, Maqsudul [1 ,2 ]
机构
[1] Bangladesh Jute Res Inst, Basic & Appl Res Jute Project, Dhaka 1207, Bangladesh
[2] Univ Hawaii, Honolulu, HI 96822 USA
[3] Univ Sains Malaysia, Ctr Chem Biol, George Town 11800, Malaysia
关键词
Genome sequencing; Phytopathogens; Charcoal rot; Phenotypic microarray; MAGNAPORTHE-GRISEA; CHARCOAL ROT; PEPTIDE SYNTHETASE; 1ST REPORT; APPRESSORIUM FORMATION; GENE; INFECTION; ALIGNMENT; ANNOTATION; PROTEINS;
D O I
10.1186/1471-2164-13-493
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Macrophomina phaseolina is one of the most destructive necrotrophic fungal pathogens that infect more than 500 plant species throughout the world. It can grow rapidly in infected plants and subsequently produces a large amount of sclerotia that plugs the vessels, resulting in wilting of the plant. Results: We sequenced and assembled similar to 49 Mb into 15 super-scaffolds covering 92.83% of the M. phaseolina genome. We predict 14,249 open reading frames (ORFs) of which 9,934 are validated by the transcriptome. This phytopathogen has an abundance of secreted oxidases, peroxidases, and hydrolytic enzymes for degrading cell wall polysaccharides and lignocelluloses to penetrate into the host tissue. To overcome the host plant defense response, M. phaseolina encodes a significant number of P450s, MFS type membrane transporters, glycosidases, transposases, and secondary metabolites in comparison to all sequenced ascomycete species. A strikingly distinct set of carbohydrate esterases (CE) are present in M. phaseolina, with the CE9 and CE10 families remarkably higher than any other fungi. The phenotypic microarray data indicates that M. phaseolina can adapt to a wide range of osmotic and pH environments. As a broad host range pathogen, M. phaseolina possesses a large number of pathogen-host interaction genes including those for adhesion, signal transduction, cell wall breakdown, purine biosynthesis, and potent mycotoxin patulin. Conclusions: The M. phaseolina genome provides a framework of the infection process at the cytological and molecular level which uses a diverse arsenal of enzymatic and toxin tools to destroy the host plants. Further understanding of the M. phaseolina genome-based plant-pathogen interactions will be instrumental in designing rational strategies for disease control, essential to ensuring global agricultural crop production and security.
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