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Genetic diversity of Agrobacterium vitis as determined by DNA fingerprints of the 5′‐end of the 23S rRNA gene and Random Amplified Polymorphic DNA
Author(s) -
Momol E.A.,
Burr T.J.,
Reid C.L.,
Momol M.T.,
Hseu S.H.,
Otten L.
Publication year - 1998
Publication title -
journal of applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.889
H-Index - 156
eISSN - 1365-2672
pISSN - 1364-5072
DOI - 10.1111/j.1365-2672.1998.00581.x
Subject(s) - library science , biology , plant biology , botany , computer science
Sixty‐nine strains of Agrobacterium vitis , the causal agent of grape crown gall, originating from different geographical regions of the USA and Europe, were characterized by fingerprint analysis of the 5′‐end of the 23S rRNA gene and by Random Amplified Polymorphic DNA (RAPD) markers. For 5′‐end 23S fingerprinting, amplicons were digested with Taq I, Rsa I, Ava I, Cfo I and Alu I. For RAPD analysis, three 10‐mer primers were used to generate PCR products. There was a high degree of correlation between strain groupings generated by the two methods. However, more diversity was identified when groupings were based on RAPDs. For example, 28 of 29 strains having nopaline type Ti plasmids generated identical 5′‐end 23S patterns but formed two distinct RAPD groups that separated strains originating from the USA and Hungary. Similarly by RAPDs, one cluster of strains carrying vitopine‐type Ti plasmids could be separated into those originating in the USA and Europe. The composition of strain groups generated by 5′‐end 23S and RAPDs were highly correlated with a previous fingerprint analysis of the intergenic spacer region (located between the 16S and 23S rRNA genes) and with RFLP analysis for characterizing Ti plasmids. These findings show that among Ag. vitis strains there is a high level of correlation between two regions of the rRNA operon, total genomic DNA (as determined by RAPDs) and the type of Ti plasmid they carry.