Department of Molecular Biology and Biotechnology, AECS, P. O. Box 6091, Damascus, Syria(Received on July 27, 2010; Accepted on November 3, 2010)New sources of barley (Hordeum vulgare L.) resistant tospot blotch, caused by Cochliobolus sativus, are neededto provide effective resistance because of the rapidchange pathotype patterns of C. sativus in fields. Thepurposes of our study were to develop a method toscreen barley for resistance to spot blotch disease andthen use this methodology to screen barley genotypesfor resistance to the major virulent pathotype Pt4 inbarley populations in Syria. A transparent tape method,in which a conidial suspension of C. sativus was droppedonto transparent tape and placed, treated-side down, onthe second leaf surface of barley plants. Disease symp-toms of fungus were easily detected on the leaves coveredby the transparent tape after 48h of inoculation. Thetransparent tape method was repeatable and the diseasescores obtained were correlated ( r = 0.91, P = 0.001) withthose obtained by the seedling assay. This method maybe beneficial in various plant pathology breeding prog-rams. Keywords : Cochliobolus sativus, Hordeum vulgare L.,resistance test, spot blotchCochliobolus sativus (Ito & Kurib.) Drechsl. ex Dast.[anamorph: Bipolaris sorokiniana (Sacc. in Sorok.) Shoem.],the cause of spot blotch (SB), is a common foliar pathogenof barley (Hordeum vulgare), a disease responsible forheavy crop losses (Wilcoxon et al., 1990; Kumar et al.,2002). Although fungicides can be effective in reducing SBseverity (Kiesling, 1985), the most effective and environ-mentally sound means of control is the use of resistantcultivars. However, development of stable forms resistantto foliar diseases depends upon identification of resistanceseffective against the prevalent isolates in barley growingareas (Gupta et al., 2001). A fast, accurate, and precise screening method that can beused to identify sources of tolerant, partially resistant, andpathotype specific resistant barley germplasm would aid inthe development of cultivars for optimal control of C.sativus. Resistance in barley to SB is often evaluated at theseedling and adult plant stages by determining the visibledisease symptoms as a percentage of infected leaf area(Fetch and Steffenson, 1999; Ghazvini and Tekauz, 2008).This method is time-consuming and several environmentalinteractions make it impossible to obtain error-free esti-mates (Gilchrist et al., 1995). Recently, a detached seedlingfirst leaf technique (Arabi and Jawhar, 2007) has been usedfor evaluating barley resistance to SB. However, this methodbased on testing detached leaves in vitro far away from themother plant, and the assessment should be done duringshort time using artificial media, antibiotics and Petri dishes.In classifying the disease reactions of barley lines forbreeding purposes or for studies on host parasite genetics, itis important to have a reliable screening technique forreducing the inconvenience of field tests. The objectives ofour research were to develop a C. sativus screening methodfor barley and then screen barley genotypes for resistance tothe major virulent pathotype Pt4 in barley populations inSyria. Inoculum preparation. The major Syrian pathotype C.sativus (Pt4) used in the study was the most virulent of 117isolates collected in 1998 and 2004 from naturally infectedbarley in different regions of Syria, as described by Arabiand Jawhar (2003). The fungal mycelia were transferredfrom a stock culture into Petri dishes containing potatodextrose agar (PDA, DIFCO, Detroit, MI, USA) with 13mg/l kanamycin sulphate and incubated for 10 days at 21 ±1°C in the dark. Then, conidia were collected with 10 mLof sterile distilled water. The conidial suspension wasadjusted to 2 × 10