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Meeting the Challenge of Yellow Rust in Cereal Crops - ICARDA

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The wheat stripe rust pathogen oversummers on volunteer wheat and<br />

possibly certa<strong>in</strong> species <strong>of</strong> Aegilops, Agropyron, Bromus and Elymus <strong>in</strong> Europe<br />

(Stubbs, 1985). Stripe rust uredospores can be w<strong>in</strong>d-borne <strong>in</strong> a viable state for<br />

at least 800 km (Zadoks, 1961). O’Brien et al. (1980) reported <strong>the</strong> <strong>in</strong>troduction <strong>of</strong><br />

wheat stripe rust to Australia, which was probably aided by man. In 1980, <strong>the</strong><br />

pathotype first found <strong>in</strong> Australia appeared <strong>in</strong> New Zealand, presumably<br />

hav<strong>in</strong>g been air-borne from Australia, a distance <strong>of</strong> approximately 2000 km<br />

(Beresford, 1982). In Iran, yellow rust epidemics were recorded dur<strong>in</strong>g <strong>the</strong><br />

1993/94 and 1994/95 seasons (Torabi et al., 1995), with crop losses estimated at<br />

1.5 and 1 million tonne, respectively. In Yemen and Ethiopia, early yellow rust<br />

epidemics have been recorded s<strong>in</strong>ce 1988 (Mamluk, EL-Naimi and Hakim,<br />

1996). Torabi et al. (2001) noted that <strong>the</strong> majority <strong>of</strong> Iranian yellow rust<br />

pathotypes had virulence on plant with genes Yr2, Yr6, Yr7, Yr9, Yr22, Yr23<br />

and YrA. Surveys <strong>of</strong> Pst pathotypes and <strong>the</strong> genetic variation with<strong>in</strong> <strong>the</strong><br />

pathotypes are important and valuable <strong>in</strong>formation for <strong>the</strong> breed<strong>in</strong>g<br />

programme. This study reports on <strong>the</strong> prevail<strong>in</strong>g pathotypes <strong>of</strong> <strong>the</strong> wheat<br />

yellow rust pathogen <strong>in</strong> Iran.<br />

53<br />

Materials and methods<br />

For this study, 15 isolates <strong>of</strong> stripe rust agent were collected from different<br />

parts <strong>of</strong> Iran, <strong>in</strong>clud<strong>in</strong>g Gazve<strong>in</strong>, Mogan, Dezful, Islam Abad, Hamadan, Sari,<br />

Maneh, Mashhad, Borojerd, Darab, Gachsaran and Ahvaz, Yazd, with one<br />

isolate from Kyrgyzstan. Spores <strong>of</strong> each isolate, after <strong>in</strong>creas<strong>in</strong>g, were<br />

<strong>in</strong>oculated on an <strong>in</strong>ternational standard differential set <strong>of</strong> yellow rust l<strong>in</strong>es <strong>in</strong><br />

<strong>the</strong> greenhouse. A set <strong>of</strong> <strong>the</strong> World (8 genotypes) and European (8 genotypes)<br />

wheat yellow rust differentials, as proposed by Johnson et al. (1972), was used<br />

<strong>in</strong> <strong>the</strong> study, <strong>in</strong> addition to 10 supplementary varieties that <strong>in</strong>cluded<br />

Federation*4/Kavkas (Yr9), Anza (YrA), Avocet R (YrA), Kalyansona (Yr2),<br />

Triticum spelta var. album (Yr5), TP981 (Yr25), Meer<strong>in</strong>g 24 (Yr24), Bolani<br />

(susceptible check), Avocet S and TP 1295.<br />

For <strong>in</strong>oculation, uredospores were mixed with talcum powder (1:4). After<br />

each <strong>in</strong>oculation, spray equipment was thoroughly washed <strong>in</strong> water and dried<br />

<strong>in</strong> an oven at 60°C to avoid contam<strong>in</strong>ation when successively <strong>in</strong>oculat<strong>in</strong>g with<br />

different pathotypes. Inoculation conditions consisted <strong>of</strong> a tray with a base tray<br />

conta<strong>in</strong><strong>in</strong>g 2 cm <strong>of</strong> tap water. After <strong>in</strong>oculation, <strong>the</strong> seedl<strong>in</strong>gs were placed <strong>in</strong><br />

<strong>the</strong> trays and covered with plastic hoods. Trays were placed <strong>in</strong> an <strong>in</strong>cubation<br />

room at 10°C where <strong>the</strong> differential temperatures between <strong>the</strong> water and room<br />

temperature resulted <strong>in</strong> dew formation. Seedl<strong>in</strong>gs were held for 24 h at 10°C<br />

and 100% RH <strong>in</strong> <strong>the</strong> dark. Follow<strong>in</strong>g <strong>in</strong>cubation, plants were moved to a<br />

greenhouse. The temperature was ma<strong>in</strong>ta<strong>in</strong>ed at 18 to 19°C for yellow rust.<br />

Infection types were recorded 16–19 days after <strong>in</strong>oculation, depend<strong>in</strong>g upon<br />

<strong>the</strong> disease and temperature. The objective was to record reactions when <strong>the</strong>

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