The use of T-DNA tagging to isolate mutants of Colletotrichum gloeosporioides and Colletotrichum acutatum with reduced virulence against Hevea brasiliensis
文献类型: 外文期刊
作者: Lin, C. -H. 1 ; Cai, Z. -Y. 1 ; Shi, T. 2 ; Dai, Y. -K. 2 ; Li, C. -P. 3 ; Huang, G. -X. 3 ;
作者机构: 1.Chinese Acad Trop Agr Sci, Environm & Plant Protect Inst, Danzhou, Peoples R China
2.Minist Agr China, Key Lab Integrated Pest Management Trop Grops, Danzhou, Peoples R China
3.Hainan Engn Res Ctr Biol Control Trop Crops Dis &, Danzhou 571737, Hainan, Peoples R China
期刊名称:FOREST PATHOLOGY ( 影响因子:1.363; 五年影响因子:1.595 )
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收录情况: SCI
摘要: Agrobacterium tumefaciens-mediated transformation (ATMT) is being increasingly recognized as an effective insertional mutagenesis tool in studies of filamentous fungi for gene discovery and functional analysis. We developed and optimized ATMT for 2 Colletotrichum species, Colletotrichum gloeosporioides and Colletotrichum acutatum, the causative agents of Colletotrichum leaf disease in rubber trees in Southern China. A.tumefaciens strain AGL-1 carrying an ILV1 gene and a green fluorescent protein gene were used to transform the conidia of these 2 Colletotrichum species. The transformation efficiency was correlated with the co-cultivation duration and bacterial cell concentrations, which reached 300-400 transformants per 1x10(6) conidia after optimization. Southern blot analysis indicated that about 60.0% of the C.gloeosporioides transformants and 46.2% of the C.acutatum transformants had a single copy of T-DNA in their genomes. Fungal genomic DNA segments flanking the T-DNA were identified in the transformants through thermal asymmetrical interlaced polymerase chain reaction followed by sequencing. The flanking sequences from 4 C.acutatum and 7 C.gloeosporioides transformants showed moderate or weak homology to the NCBI database entries. Some sequences matching those reported virulence-related genes. The results suggest that the T-DNA inserted mutants banks constructed are useful for the discovery of new or important genes and to elucidate their function in the 2 Colletotrichum species.
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