Vegetable and Forage Crops Research Laboratory 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
Alfalfa
Beans
BioFuel
Weeds
Peas
Potatoes
 

Research Project: POTATO VARIETY IMPROVEMENT THROUGH GENE TRANSFER AND VIROLOGICAL STUDIES

Location: Vegetable and Forage Crops Research Laboratory

Title: Tomato susceptibility to root-knot nematodes requires an intact jasmonic Acid signaling pathway

Authors
item Bhattarai, Kishor - UC RIVERSIDE
item Xie, Qi-Guang - UC RIVERSIDE
item Mantelin, S - UC RIVERSIDE
item Bishnoi, Usha - UC RIVERSIDE
item Girke, Thomas - UC RIVERSIDE
item Navarre, Duroy
item Kaloshian, Isgouhi - UC RIVERSIDE

Submitted to: Molecular Plant-Microbe Interactions
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: May 15, 2008
Publication Date: September 1, 2008
Citation: Bhattarai, K.K., Xie, Q., Mantelin, S., Bishnoi, U., Girke, T., Navarre, D.A., Kaloshian, I. 2008. Tomato susceptibility to root-knot nematodes requires an intact jasmonic Acid signaling pathway. Molecular Plant-Microbe Interactions. 21(9):1205-14.

Interpretive Summary: Root-Knot nematodes are major pests of solanaceous crops, including Tomato and Potato. This study identifies mechanisms involved in host-resistance to root-knot nematodes. Results suggested that jasmonate-dependent signaling does not play a role in Mi-1 mediated nematode defense, but does play a role in basal defense against root-knot nematodes. Microarray analysis identified 1497 genes differentially regulated 24 hours after root-knot infection in resistant plants and 750 genes differentially regulated in susceptible plants.

Technical Abstract: Response of tomato (Solanum lycopersicum) to root-knot nematode (RKN; Meloidogyne spp.) infection was monitored using TOM1 cDNA microarray with resistant (`Motelle¿; Mi-1) and susceptible (`Moneymaker¿; mi) tomato at 24 h after RKN infection. The array analysis identified 1497 genes and 750 genes differentially regulated (P < 0.05) in the incompatible and compatible interactions, respectively. Thirty seven percent of the differentially regulated genes were specific to the incompatible interactions. In the incompatible interactions, 880 genes were 2-fold up-regulated and 332 were 1.5-fold down-regulated. In the compatible interactions, 677 were 2-fold up-regulated and 62 were 1.5-fold down-regulated. Both jasmonic acid (JA) biosynthetic genes and JA-regulated genes were up-regulated in both compatible and incompatible interactions. Of the limited number of known salicylic acid (SA)-regulated genes present on the array, majority was regulated in both interactions. To test a role for JA and SA signaling pathways in both Mi-1 resistance and basal defense to RKN, the jai1 mutant and NahG transgenic line were used in the presence or absence of the RKN resistance gene Mi-1. RKN did not reproduce on Mi-1 jai1 plants and reproduced less on jai1 mutant compared to the wild-type parent `CM¿. Similarly, RKN did not reproduce on Mi-1 NahG plants and reproduced at similar levels on NahG and wild-type parent `Moneymaker¿. No detectable increases in SA levels were detected after RKN infection of jai1 roots. Our results suggest that JA-dependent signaling does not play a role in Mi-1-mediated defense but plays a role in basal defense against RKN in tomato.

   

 
Project Team
Brown, Charles - Chuck
Crosslin, James - Jim
Navarre, Duroy - Roy
Alva, Ashok
 
Publications
   Publications
 
Related National Programs
  Plant Genetic Resources, Genomics and Genetic Improvement (301)
  Plant Biological and Molecular Processes (302)
 
 
Last Modified: 10/23/2008
ARS Home | USDA.gov | Site Map | Policies and Links 
FOIA | Accessibility Statement | Privacy Policy | Nondiscrimination Statement | Information Quality | USA.gov | White House