Am. Griffen et al., RIBOSOMAL, MITOCHONDRIAL AND AMPLIFIED DNA POLYMORPHISMS IN VERTICILLIUM-ALBO-ATRUM PATHOGENIC TO HOPS, LUCERNE AND OTHER PLANTS, Mycological research, 101, 1997, pp. 1085-1091
Forty-seven isolates of Verticillium albo-alrum, 35 from hop (Humulus
lupulus), seven from Lucerne (alfalfa, Medicago sativa) and five from
four other hosts, were analysed for DNA polymorphisms. Restriction fra
gment length polymorphisms (RFLPs) were detected in ribosomal RNA gene
s (rDNA) using Southern hybridization. Polymorphisms in mitochondrial
DNA (mtDNA) were detected in ethidium bromide stained gels after diges
tion of total genomic DNA with restriction enzymes which recognize fou
r bases containing only G and C Amplified polymorphic DNA (APD) was an
alysed using primers based on rDNA sequences from the intergenic space
r (IGS) and 25S regions. These data were used to construct phenograms
using either squared Euclidean dissimilarity coefficients (SEDC) and d
uster analysis, or unweighted pair grouping with arithmetic averaging
(UPGMA). rDNA RFLPs revealed one group with 44 isolates, a second grou
p with two atypical hop isolates, and a third group containing a singl
e avirulent lucerne isolate. mtDNA RFLPs separated rDNA group one into
two subgroups, one group containing 38 isolates from different hosts
and the other containing all six virulent lucerne isolates. APD analys
is divided the isolates into 16 phenotypes, IZ of which contained most
of the hop isolates, but there was no correlation with origin, hop cu
ltivar, pathogenicity or year of isolation. One APD phenotype containe
d all six virulent lucerne isolates. indicating the genetic differenti
ation between hop and lucerne isolates. Two further APD phenotypes coi
ncided with the second atypical group containing two hop isolates and
a distinct avirulent lucerne isolate, respectively. The three methods
revealed that three isolates differed markedly from those of the main
group.