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The Eleventh Regional Wheat Workshop For Eastern ... - Cimmyt

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Assessment ofpathogenic variability in stripe rust - Wellings et al.<br />

distinctive forma specialis, although the geographic distribution outside the USA remains<br />

unclear.<br />

A potentially new form of P. striiformis was described in Australia by WeI lings et al. (2000).<br />

<strong>The</strong> pathogen was closely associated with weedy Hordeum species, showed broad avirulence<br />

on the wheat differential testers and appeared to contrast at one isozyme locus with Pst. <strong>The</strong><br />

pathogen, temporarily referred to as barley grass stripe rust (BGYR), was observed to cause<br />

disease on certain barley cultivars naturally infected in the field.<br />

2. Pathotype variation within P. striijormis f. sp. tritici<br />

Pathotype variability has traditionally been studied using defined sets of host genotypes<br />

inoculated with pathogen isolates in controlled environments. Such studies have almost<br />

entirely focussed on greenhouse testing of seedling plants and, when most effective, have<br />

attempted to relate the results to resistance genes deployed in commercial agriculture. <strong>The</strong><br />

various sets of differential genotypes employed in the study of Pst were reviewed by<br />

McIntosh et al., (1995). <strong>The</strong> set of Johnson et al. (1972), as modified by Wellings and<br />

McIntosh (1990), have been used for continuing studies of pathotype variability in the cereal<br />

rust laboratory at PBI Cobbitty since the first introduction of Pst to Australia in 1979. During<br />

this period, pathotype evolution arising from progressive single step mutation has resulted in<br />

the detection of over twenty variants. <strong>The</strong> results are summarized in Figures 1 and 2. While<br />

the majority of new pathotypes have represented a progressive increase in virulence, several<br />

reversions to avirulence have also been detected. With the exception of pathotype 64 El A-,<br />

all new pathotypes have only varied by one gene for virulence compared to a previously<br />

detected pathotype. On the basis of these observations, it can be concluded that there has<br />

been no evidence of further exotic introduction ofPst into Australia.<br />

Similar studies of Pst have been conducted by various groups around the world. <strong>The</strong> most<br />

notable contribution was that of the late R.W. Stubbs at the Research Institute for Plant<br />

Protection (IPO), Wageningen, <strong>The</strong> Netherlands. Although Stubbs work was focussed on<br />

Europe, he was able to accept Pst isolates from around the world under an agreement with<br />

CIMMYT, and so was able to gain some insight into global variability. Investigations of<br />

recent stripe rust epidemics in Central Asia discovered that <strong>The</strong> Institute of Genetics,<br />

Tashkent, Uzbekistan, has conducted similar Pst surveys for the former Soviet Union over<br />

many years, although the data has remained essentially unavailable to the Western scientific<br />

community.<br />

As a result of the recurring epidemics noted in the above regions, and in the absence of a<br />

consistent monitoring program for pathotype change in Pst over large areas of the world's<br />

wheat growing areas, an alternative method employing near isogenic lines in trap nurseries is<br />

being evaluated. This has become a joint project between CIMMYT, ICARDA and PBI<br />

Cobbitty, with some funding provided by the Australian Center for International Agricultural<br />

Research. <strong>The</strong> method provides advantages in being less reliant on specialist facilities and<br />

expertise, and can potentially sample pathogen populations over the period that the nursery<br />

remains viable in the field.<br />

<strong>The</strong> nurseries distributed as four cohorts have resulted in the collection of 58 data sets.<br />

Several of these collections represent multiple observations across several years at a single<br />

site. Low disease responses on the recurrent parent Avocet S has indicated poor and uneven<br />

infection or the presence of highly avirulent pathotypes at several sites. In these situations<br />

137

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