Crops Pathology and Genetics Research Site Logo
ARS Home About Us Helptop nav spacerContact Us En Espanoltop nav spacer
Printable VersionPrintable Version     E-mail this pageE-mail this page
Agricultural Research Service United States Department of Agriculture
Search
  Advanced Search
 
Programs and Projects
Subjects of Investigation
 

Research Project: SUSTAINABLE VINEYARD PRODUCTION SYSTEMS

Location: Crops Pathology and Genetics Research

Title: Transgene expression in the basidiomycete root pathogen Armillaria mellea.

Authors
item Baumgartner, Kendra
item Bailey, Andy - UNIV OF BRISTOL, U.K.
item Foster, Gary - UNIV OF BRISTOL, U.K.
item Kilaru, Sreedhar - UNIV OF BRISTOL, U.K.

Submitted to: Phytopathology
Publication Type: Abstract Only
Publication Acceptance Date: March 13, 2008
Publication Date: July 1, 2008
Citation: Baumgartner, K., Bailey, A., Foster, G., Kilaru, S. 2008. Transgene expression in the basidiomycete root pathogen Armillaria mellea.. Phytopathology. 98:S19.

Technical Abstract: Toward development of a genetic transformation system for Armillaria mellea, we used particle bombardment to identify promoters for driving transgene expression. The plasmid tested was pYES-hph-004iGFP, on which the green fluorescence protein gene, gfp, is linked to the Agaricus bisporus gpdII promoter and the Phanerochaete chrysosporium mnp1 terminator. Malt extract agar was inoculated with A. mellea (incubated at 25C, 24 d). YMGT agar (0.4% yeast extract, 1% malt extract, 1% agar, 0.01% tryptophan, 0.04% Dglucose) was inoculated with Coprinopsis cinerea (incubated at 37C, 5 d; positive control). Gene gun cartridges were prepared the day of use (6.25 mg 0.6-'m gold, 0.05M spermidine, 0.05 mg/ml PVP, 100 'g DNA per 25 in. tubing). Cartridges prepared with plasmid DNA or no DNA (negative control) were applied at 150 and 200 psi to each of 21 A. mellea and C. cinerea colonies (Helios Gene Gun; Bio-Rad, Hercules, CA). Petri plates without lids were positioned 4 cm from the cartridge, with no screen between the barrel and agar surface. Each culture received two shots per cartridge. After 2 d, cultures were examined under fluorescent light on a compound microscope (Leica MZFL111; 100X, 450-490 nm excitation filters, 510 nm dichroic filter, 515 nm emission filter). The presence of a green dot among A. mellea hyphae bombarded with pYES-hph-004iGFP-coated particles verified that a single cell was penetrated by a particle, and that A. mellea is capable of translating gfp under control of the Agaricus bisporus gpdII promoter. This is the first instance of transgene expression in Armillaria. Expression was visible for at least one week, but subcultures did not express gfp after one month; expression was transient. Nonetheless, this is an achievement because plasmids for both Agrobacterium-mediated and protoplast/PEG mediated transformation that have been shown to give the highest transformation success among other Basidiomycetes with the Agaricus bisporus gpdII promoter.

   

 
Project Team
Baumgartner, Kendra
Steenwerth, Kerri
McElrone, Andrew
Kluepfel, Daniel
Sudarshana, Mysore
 
Publications
   Publications
 
Related National Programs
  Plant Diseases (303)
  Crop Production (305)
 
 
Last Modified: 05/21/2013
ARS Home | USDA.gov | Site Map | Policies and Links 
FOIA | Accessibility Statement | Privacy Policy | Nondiscrimination Statement | Information Quality | USA.gov | White House