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Home Publications Tree Improvement and Genetics Southern Forest Tree Improvement Conference 34th Southern Forest Tree Improvement Conference (2017) Development of an In Vitro Assay for Resistance to Phytophthora cinnamomi in Chestnut

Development of an In Vitro Assay for Resistance to Phytophthora cinnamomi in Chestnut

While the story of the devastation of American chestnut (Castanea dentata) by chestnut blight is familiar to those who work with this tree, less well-known is the fact the another disease—Phytophthora root rot, caused by the oomycete pathogen Phytophthora cinnamomi—had already extirpated American chestnut from the Piedmont and Coastal Plain regions of the southeastern U.S. decades before the arrival of the chestnut blight fungus, Cryphonectria parasitica. The lack of resistance to P. cinnamomi may pose a major barrier to introducing the products of The American Chestnut Foundation’s (TACF) breeding program to the southern portion of the American chestnut’s original range. The integration of genes for P. cinnamomi resistance from Chinese chestnut into TACF’s hybrid chestnuts is now proceeding, but it will take additional years of breeding and selection. Combining somatic embryogenesis-based propagation of chestnut hybrids with a reliable in vitro assay for resistance to P. cinnamomi would help to more quickly evaluate chestnut cultivars thought to carry these resistance genes—which in turn should accelerate the production of elite chestnut cultivars with resistance to both C. parasitica and P. cinnamomi for planting throughout the eastern U.S. We tested different in vitro screening approaches to rapidly identify P. cinnamomi-resistant chestnut cultivars using embryogenic cultures, shoots, and whole plantlets of wildtype American chestnut, transgenic American chestnut carrying putative P. cinnamomi resistance genes, and Chinese chestnut. Inoculation of cultures of embryogenic callus grown in 48-well plates with two isolates of P. cinnamomi failed to distinguish between American chestnut and Chinese chestnut because embryogenic callus of both species failed to turn to the blue-black color described in previous reports for chestnut callus derived from cambium tissue; instead, callus of both species turned brown after 3-4 weeks. However, American chestnut shoots derived by axillary multiplication that were stuck into 6% water-agar gel and inoculated with P. cinnamomi developed obvious symptoms, including wilting and blue-black lesions on the stems, but the ultimate cause of death could not be determined because the shoots had no roots. Whole plantlets (i.e. rooted shoots) of American chestnut and Chinese chestnut grown in 2% low melting point agarose gel showed differential responses to P. cinnamomi inoculation. American chestnut plantlets rapidly wilted and stems blackened while Chinese chestnut plantlets remained symptom-free for at least 6 weeks; however, stem lesions eventually did appear on these plantlets. Some transgenic American chestnut plantlets expressing candidate P. cinnamomi-resistance genes showed evidence of limited resistance, but these still succumbed to root rot more rapidly than Chinese chestnut plantlets.


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Author(s): Scott A. Merkle, Heather J. Gladfelter, Steven N. Jeffers

Publication: Tree Improvement and Genetics - Southern Forest Tree Improvement Conference - 2017

Section: Posters