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ICARDA annual report 2004

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<strong>ICARDA</strong> Annual Report <strong>2004</strong><br />

32<br />

stored for further Amplified<br />

Fragment Length Polymorphism<br />

(AFLP) analysis. DNA fingerprints<br />

were produced by up to 60 primer<br />

combinations, resulting in more<br />

than 100 polymorphic DNA fragments<br />

or markers. This allowed<br />

each isolate to be characterized<br />

with a high degree of confidence.<br />

Only two pathotypes were<br />

found in 2002. These differed<br />

slightly in their ability to infect the<br />

range of host varieties used in the<br />

tests. Both pathotypes were also<br />

found in 2003, in addition to a third<br />

which occurred at a low frequency.<br />

One of the pathotypes displayed<br />

a number of virulence traits commonly<br />

found in Mediterranean isolates;<br />

the other two shared a previously-undescribed<br />

virulence phenotype.<br />

There was no obvious<br />

aggregation of specific pathotypes<br />

on specific wheat varieties, suggesting<br />

that most wheat varieties in<br />

Eritrea lack yellow-rust resistance.<br />

However, the resistance of Eritrean<br />

wheat varieties has not yet been<br />

formally tested. The results indicate<br />

that resistance breeding programs<br />

could greatly improve the control<br />

of yellow rust in wheat in Eritrea.<br />

Understanding the evolution<br />

of the barley scald<br />

pathogen<br />

Scald, caused by the fungus<br />

Rhynchosporium secalis, is an economically<br />

important disease of barley.<br />

Cultivated barley is, genetically,<br />

extremely vulnerable to scald and<br />

breeding for scald resistance is difficult<br />

because the fungus evolves<br />

quickly. In addition, the climatic<br />

conditions and cultural practices<br />

found in many barley-growing<br />

areas encourage scald development.<br />

Knowledge of R. secalis’s evolutionary<br />

potential is vital to the<br />

development of sustainable resistance<br />

breeding strategies. An under-<br />

standing of its genetic structure has<br />

provided useful insights into the<br />

evolutionary processes that affect<br />

R. secalis population genetics.<br />

However, specific hypotheses<br />

about the pathogen’s evolution<br />

have not been tested in controlled<br />

and repeatable field experiments.<br />

In collaboration with the<br />

Phytopathology Group at ETH-<br />

Zurich, <strong>ICARDA</strong> is using an innovative,<br />

replicated, mark–release– recapture<br />

field experiment to quantify the<br />

relative impacts of sexual reproduction,<br />

asexual propagation, immigration,<br />

and selection on the genetic<br />

structure of an experimental random<br />

population of R. secalis in Syria.<br />

More than 1500 scald isolates collected<br />

from field plots were assayed<br />

for eight individual microsatellite<br />

loci (Fig. 10). Researchers found<br />

eight isolates that differed markedly<br />

in their ability to infect, compete<br />

and reproduce on individual barley<br />

genotypes and barley mixtures.<br />

Significant differences were<br />

observed in the frequencies with<br />

which the inoculants were found,<br />

over time, on the different hosts<br />

tested. In addition, a considerable<br />

number of new R. secalis genotypes<br />

were found, based on their multilocus<br />

haplotype.<br />

These results showed that use of<br />

the mark–release–recapture strate-<br />

Fig. 10. Chromatogram of a representative Genescan gel illustrating microsatellite<br />

DNA fragment analysis of R. secalis.<br />

Culturing scald in order to<br />

understand pathotypic and<br />

genotypic relationships.

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