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Meeting the Challenge of Yellow Rust in Cereal Crops - ICARDA

Meeting the Challenge of Yellow Rust in Cereal Crops - ICARDA

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225<br />

Development <strong>of</strong> a detached leaf assay for stripe [yellow]<br />

rust resistance screen<strong>in</strong>g<br />

A. Loladze, 1 K. Garland Campbell, 2 X.M. Chen 2 and K. Kidwell 1<br />

1. Department <strong>of</strong> Crop and Soil Sciences, Wash<strong>in</strong>gton State University, Pullman,<br />

WA, USA; 2. Wheat Genetics, Quality, Physiology and Disease Research Unit,<br />

USDA-ARS, WSU, Pullman, WA, USA<br />

Stripe [yellow] rust caused by Pucc<strong>in</strong>ia striiformis Westend. f.sp. tritici Eriks. is a<br />

major disease <strong>of</strong> wheat (Triticum aestivum L. em Thell.) worldwide, caus<strong>in</strong>g<br />

significant yield and quality losses. Screen<strong>in</strong>g wheat germplasm for resistance<br />

to stripe rust is conducted us<strong>in</strong>g greenhouse and field-based trials <strong>in</strong> <strong>the</strong><br />

seedl<strong>in</strong>g and adult stages <strong>of</strong> plant development, respectively. Because <strong>of</strong> <strong>the</strong>ir<br />

efficiency, detached leaf assays have been developed for screen<strong>in</strong>g cereal crops<br />

for resistance to several foliar pathogens; however, <strong>the</strong> long latent period <strong>of</strong><br />

stripe rust complicates detached leaf assay development for resistance to this<br />

pathogen. The objective <strong>of</strong> this study was to develop an effective, efficient<br />

detached leaf assay for screen<strong>in</strong>g wheat germplasm for resistance to stripe rust.<br />

Detached seedl<strong>in</strong>g leaves <strong>of</strong> seven wheat differential cultivars were placed<br />

on <strong>the</strong> artificial media, which consisted <strong>of</strong> 0.5% water-agar with <strong>the</strong> addition <strong>of</strong><br />

10 mg/L k<strong>in</strong>et<strong>in</strong>, a plant senescence retardant, and <strong>the</strong> pH <strong>of</strong> <strong>the</strong> media was<br />

adjusted to 7. Leaf segments were <strong>in</strong>oculated with three races <strong>of</strong> stripe rust<br />

us<strong>in</strong>g a f<strong>in</strong>e pa<strong>in</strong>tbrush and placed <strong>in</strong> a dark growth chamber for 24 h at 10°C.<br />

After <strong>the</strong> 24-h <strong>in</strong>cubation period, <strong>the</strong> photoperiod conditions were set to 16/8<br />

hours (day/night) at a temperature <strong>of</strong> 15–17/11–13°C (day/night).<br />

Simultaneously, <strong>the</strong> same plant material was grown for 10–14 days and<br />

<strong>in</strong>oculated <strong>in</strong> <strong>the</strong> greenhouse with a mixture <strong>of</strong> stripe rust spores and talcum<br />

powder (1:20). The reactions <strong>of</strong> <strong>the</strong> wheat genotypes to stripe rust races were<br />

recorded as <strong>in</strong>fection types on a 0 (no <strong>in</strong>fection) to 9 (completely susceptible)<br />

scale. Infection types from <strong>the</strong> detached leaf assay matched those <strong>of</strong> <strong>the</strong> whole<br />

seedl<strong>in</strong>g assay for all cultivars. The detached leaf assay provides a new method<br />

for screen<strong>in</strong>g for stripe rust resistance that requires less space and time than<br />

seedl<strong>in</strong>g evaluation methods and elim<strong>in</strong>ates <strong>the</strong> need for greenhouse space<br />

and dew chamber access.

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