Cytological and genetical studies on Puccinia striiformis westend
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Date
1978Author
Wright, Robert Geoffrey
Metadata
Abstract
Cytological and genetical studies were carried out on the possible
mechanism(s) involved in the production of new physiologic races of the
yellow rust pathogen, Puccinia striiformis.
The size and structure of dividing and non-dividing nuclei in hyphae and
basidiospores was ascertained using light and electron microscopy. The
parallel observations of the dividing somatic nucleus by the two techniques
permitted a relatively complete sequence of events to be established for
mitosis. Chromosome studies revealed that P. striiformis has a basic chromosome
number of three, although some nuclei from basidiospores were seen to possess
four chromosomes. Preparations in which hyphae were possibly fusing were
observed using the light and electron microscope. The results of the
cytological work are discussed with reference to the physical basis of genetic
variation in the yellow rust fungus.
Genetical studies included tests on the progeny of a mixture of two races,
following the inoculation of susceptible and differentially resistant varieties.
A new race, designated 105E137> was identified following the mixed inoculation
of races 104E137 and 33E32. Induced mutation experiments established that the
rate of mutation in the pathogen for specific virulence factors was less than
one in 2 x 10 . The results of the study are discussed and genetic models are
presented to explain how race 105E137 may have evolved.
In a series of experiments on quantitative variation in P^_ striiformis
differences between isolates in spore production and colony growth rate were
established. An isolate of race *fOE8 was the most prolific genotype in
experimental studies on a range of host varieties. Isolates tended to rank
similarly on the test varieties although there was some evidence of isolate-host
interactions. Detailed studies on the various stages of infection revealed
that the prolificacy of the race 40E8 isolate could be detected at all
stages of pathogen development.