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Meeting the Challenge of Yellow Rust in Cereal Crops - ICARDA

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<strong>the</strong> greenhouse. APR genes are <strong>in</strong>vestigated at <strong>the</strong> adult plant stage under field<br />

conditions. The first differential system for physiological races <strong>of</strong> wheat yellow<br />

rust was established <strong>in</strong> 1930 (Allison and Isenbeck, 1930). The present system<br />

for identification <strong>of</strong> races, which is utilized <strong>in</strong> many parts <strong>of</strong> <strong>the</strong> world, was<br />

proposed by Johnson and Taylor (1972). This system was modified by Well<strong>in</strong>gs<br />

and McIntosh (1990).<br />

Until now, many resistance genes have been recognized, among <strong>the</strong>m <strong>the</strong><br />

genes Yr11, Yr12, Yr13, Yr14, Yr16 and Yr18. They are APR genes. The first<br />

study on virulence factors <strong>of</strong> wheat yellow rust was conducted <strong>in</strong> a trap<br />

nursery by Zadoks (1961). The seedl<strong>in</strong>g-resistance genes are naturally<br />

expressed at all growth stages, and thus can be surveyed <strong>in</strong> field condition (<strong>in</strong><br />

trap nurseries). Besides seedl<strong>in</strong>g-resistance genes, APR genes can be expressed<br />

as well. In order to monitor annual changes <strong>in</strong> races and virulence factors <strong>of</strong><br />

wheat yellow rust, national experiments have been carried out s<strong>in</strong>ce 1993 <strong>in</strong><br />

Iran. In some <strong>of</strong> <strong>the</strong>se studies, virulence factors <strong>of</strong> pathogen have been<br />

dist<strong>in</strong>guished, and effective resistance genes have also been recognized. For<br />

example, results <strong>of</strong> Nazari and associates showed that Ardabil races have<br />

virulence for genes Yr9, Yr7, Yr8, Yr2, Yr6, YrSU, Yr19, Yr8, Yr17, Yr25, Yr23,<br />

Yr22 and Yr10. In <strong>the</strong>ir study <strong>the</strong>y also concluded that genes YrSP, Yr1, Yr3,<br />

Yr49, Yr5, Yr16, Yr24, Yr13, Yr14, Yr15 and YrCV were effective genes (Nazari<br />

et al., 2000).<br />

Virulence on Yr1 and Yr17 has spread rapidly <strong>in</strong> central Asia. Virulence on<br />

Yr1 was first observed <strong>in</strong> Tajikistan <strong>in</strong> 1999 and by 2004 it was found across<br />

central and West Asia. Virulence on Yr10 and Yr17 was observed <strong>in</strong> Yemen <strong>in</strong><br />

1999, virulence on Yr18, 27 and 24 were recorded <strong>in</strong> 2002, and by 2005 <strong>the</strong>se<br />

virulence types were recovered at many locations <strong>in</strong> CWANA (Yahyaoui,<br />

2006).<br />

Comprehensive <strong>in</strong>formation on pathogen virulence and variation, and<br />

epidemiological <strong>in</strong>formation on pathogen movements, provides a basis for <strong>the</strong><br />

development <strong>of</strong> early warn<strong>in</strong>g systems (Yahyaoui et al., 2001).<br />

The objective <strong>of</strong> this study was to determ<strong>in</strong>e effective and <strong>in</strong>effective<br />

resistance genes to wheat yellow rust <strong>in</strong> <strong>the</strong> period 2006–2009.<br />

Material and methods<br />

In this <strong>in</strong>vestigation 192 different genotypes were used. The entries <strong>in</strong>cluded<br />

differential cultivars with seedl<strong>in</strong>g-resistance genes, cultivars with APR and<br />

durable resistance genes, near-isogenic l<strong>in</strong>es and promis<strong>in</strong>g l<strong>in</strong>es. The entries<br />

were sown <strong>in</strong> Ardabil agricultural research station under natural <strong>in</strong>fection<br />

conditions. Each entry was planted <strong>in</strong> two 1-m long rows 30 cm apart. Plots<br />

were spaced at 65 cm. One susceptible cultivar (Bollani) was used after each 10<br />

entries. The disease severity was estimated based on a modified Cobb scale

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