November
1999
, Volume
12
, Number
11
Pages
969
-
975
Authors
Regina S.
Redman
,
1
,
2
Judith C.
Ranson
,
1
and
Rusty J.
Rodriguez
1
,
2
Affiliations
1Western Fisheries Research Center, Biological Resources Division, USGS, 6505 N.E. 65th St., Seattle, WA 98115, U.S.A.; 2Department of Botany, University of Washington, Seattle 98195-5325, U.S.A.
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RelatedArticle
Accepted 4 August 1999.
Abstract
Hygromycin-resistant transformants of the cucurbit pathogen Colletotrichum magna (teleomorph: Glomerella magna) were generated by restriction enzyme-mediated integration (REMI) transformation. A rapid pathogenicity assay involving watermelon (Citrullus lanatus) seedlings was developed and 14,400 REMI transformants were screened and assessed for their ability to cause disease, colonize plant tissues, and confer disease resistance against wild-type C. magna. A total of 176 nonpathogenic REMI mutants capable of colonizing cucurbit plants were isolated and assigned to three groups based on their ability to confer disease resistance: phenotype A, 80 to 100% disease protection; phenotype B, 10 to 65% disease protection; and phenotype C, 0 to 4% disease protection. Molecular and genetic analyses of one REMI mutant (R1) indicated that the nonpathogenic phenotype A resulted from a single-site integration. R1 showed a 1:1 segregation of hygromycin resistance and nonpathogenicity and all hygro-mycin-resistant progeny were nonpathogenic. The integrated vector and 5.5 kb of flanking fungal genomic DNA were isolated from R1 and designated pGMR1. To verify that pGMR1 contained pathogenicity gene sequences, a wild-type isolate of C. magna was transformed with pGMR1 to induce gene disruptions by homologous integration. Approximately 47% of the pGMR1 transformants expressed phenotype A, indicating homologous integration and gene disruption.
JnArticleKeywords
Additional keywords:
plant pathogen,
plasmid rescue.
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ArticleCopyright
The American Phytopathological Society, 1999