URP-based DNA Fingerprinting of Bipolaris sorokiniana Isolates Causing Spot Blotch of Wheat

被引:33
|
作者
Aggarwal, Rashmi [1 ]
Singh, Veer B. [1 ]
Shukla, Renu [1 ]
Gurjar, Malkhan Singh [1 ]
Gupta, Sangeeta [1 ]
Sharma, Tilak R. [1 ]
机构
[1] Indian Agr Res Inst, Div Plant Pathol, Fungal Mol Biol Lab, New Delhi 110012, India
关键词
Bipolaris sorokiniana; wheat; spot blotch; molecular variability; URP-PCR; AMPLIFIED POLYMORPHIC DNA; COMMON ROOT-ROT; PCR; DIFFERENTIATION; PATHOGEN; STRAINS; FUNGI;
D O I
10.1111/j.1439-0434.2009.01603.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Spot blotch, caused by the pathogen Bipolaris sorokiniana is an important disease of wheat and is responsible for large economic losses world wide. In this study, molecular variability in B. sorokiniana isolates collected from different regions of India was investigated using URP-PCR technique. All the 40 isolates used in the study were pathogenic when tested on susceptible host, Agra local, although they varied in pathogenicity. Isolate BS-49 was least virulent showing 4.5 infection index while BS-75 was the most virulent with 63.4 infection index. The universal rice primers (URPs') are primers which have been derived from DNA repeat sequences in the rice genome. Out of the 12 URP markers used in the study, 10 markers were effective in producing polymorphic fingerprint patterns from DNA of B. sorokiniana isolates. The analysis of entire fingerprint profile using unweighted pair group method with arithmetic averages (UPGMA) differentiated B. sorokiniana isolates obtained from different geographic regions. One isolate BS-53 from northern hill zone was different from rest of the isolates showing less than 50% similarity. Broadly, three major clusters were obtained using UPGMA method. One cluster consisted of isolates from North western plain zone; second cluster having isolates from North eastern plain zone and third cluster consisted of isolates from Peninsular zone showing more than 75% genetic similarity among them. One of the markers, URP-2F (5'GTGTGCGATCAGTTGCTGGG3') amplified three monomorphic bands of 0.60, 0.80 and 0.90 kb size which could be used as specific markers for identification of B. sorokiniana. Further, based on URP-PCR analysis, the grouping of the isolates according to the geographic origin was possible. This analysis also provided important information on the degree of genetic variability and relationship between the isolates of B. sorokiniana.
引用
收藏
页码:210 / 216
页数:7
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