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Annual Progress Report on Malting Barley Research March, 2007

Annual Progress Report on Malting Barley Research March, 2007

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CI9214, PI552963 (Heartland), and NDB112. All other resistance sources were<br />

susceptible to at least <strong>on</strong>e isolate collected in 2005.<br />

What were the most significant accomplishments?<br />

The most significant accomplishment in this work was the identificati<strong>on</strong> of which<br />

resistant sources are overcome and which <strong>on</strong>es c<strong>on</strong>tain potentially durable net<br />

blotch resistance that could be used in combating net blotch in this regi<strong>on</strong> as well as<br />

the identificati<strong>on</strong> of virulence changes within the pathogen populati<strong>on</strong> from year to<br />

year.<br />

Objective:<br />

Net blotch caused by the fungus Pyrenophora teres Drechs. f. teres Smedeg.<br />

(anamorph: Drechslera teres) is <strong>on</strong>e of the most ec<strong>on</strong>omically important diseases in<br />

barley growing regi<strong>on</strong>s of the United States and the world. This disease is a<br />

perennial problem especially in cool, wet barley growing regi<strong>on</strong>s although it has<br />

been seen in dry regi<strong>on</strong>s as well (Mathre 1982). The majority of barley cultivars<br />

grown in the United States are moderately to highly susceptible to net blotch of<br />

barley. Therefore, it is critical that we have an understanding of the pathogen<br />

populati<strong>on</strong> to properly develop barley cultivars with durable resistance to net blotch.<br />

The objective of this project was to evaluate the North Dakota field populati<strong>on</strong> at two<br />

locati<strong>on</strong> with two significantly different envir<strong>on</strong>ments. This study focused <strong>on</strong> the<br />

level of variability present in the P. teres populati<strong>on</strong> as it relates to identified host<br />

resistance in a differential barley set.<br />

Methodologies:<br />

Host differential set<br />

A host differential set of 20 barley lines (Table 1) was chosen based <strong>on</strong><br />

published differential reacti<strong>on</strong> of these lines. (Jalli 2004, Wu et al. 2003, Cromey<br />

and Parks 2003, Gupta and Loughman 2001, J<strong>on</strong>ss<strong>on</strong> et al. 1997, Steffens<strong>on</strong> and<br />

Webster 1992, Tekauz 1990, Kahn 1982, Kahn and Boyd 1969). This was d<strong>on</strong>e by<br />

evaluating the most thorough publicati<strong>on</strong>s <strong>on</strong> differential sets. All lines used in this<br />

differential set have been shown to have different resistance patterns when<br />

inoculated with isolates from around the world indicating that each line harbors at<br />

least <strong>on</strong>e different resistance gene. NDB112 and Heartland (Table 1) have also<br />

been added to this set based <strong>on</strong> their use as resistance sources in the North Dakota<br />

and Minnesota barley breeding program, respectively.<br />

Field collecti<strong>on</strong> and pathotype analysis <strong>on</strong> the barley differential set<br />

Field plots of the near universal susceptible cultivar Hector were planted <strong>on</strong><br />

barley stubble to ensure the best disease possible. Hector plots were established<br />

at Fargo and Langd<strong>on</strong>, ND in both 2004 and 2005. Diseased leaves were collected<br />

throughout the growing seas<strong>on</strong>. Leaves were plated <strong>on</strong> sterile water agar and<br />

single spore isolates were picked from net blotch lesi<strong>on</strong>s. Isolates were grown and<br />

93

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