Grant Information

CONTROL CITRUS HLB BY BLOCKING THE FUNCTIONS OF TWO CRITICAL EFFECTORS ENCODED BY 'CANDIDATUS LIBERIBACTER ASIATICUS'

Sponsoring Institution Agricultural Research Service/USDA
Status ACTIVE
Funding Source USDA INHOUSE
Reporting Frequency Annual
Project Director DUAN Y
Accession Number 425020
Project Number 6034-22000-039-42R
Dates 2013-05-01 - 2016-04-30
Recipient Organization AGRICULTURAL RESEARCH SERVICE
219 SOUTH ROCK ROAD
FT PIERCE,FL 34945
Keywords asiaticus
autotransporter
candidatus
citrus
huanglongbing
liberibacter
Research Effort Applied (30%)
Basic (60%)
Developmental (10%)
Classification Parameters
Knowledge AreaSubject of InvestigationField of SciencePercent
212 - Pathogens and Nematodes Affecting Plants 910 - Grapefruit 1040 - Molecular biology 25%
212 - Pathogens and Nematodes Affecting Plants 920 - Orange 1060 - Biology (whole systems) 25%
212 - Pathogens and Nematodes Affecting Plants 1114 - Peach 1040 - Molecular biology 10%
212 - Pathogens and Nematodes Affecting Plants 1122 - Strawberry 1060 - Biology (whole systems) 10%
212 - Pathogens and Nematodes Affecting Plants 1429 - Cucurbits, other (includes pumpkin, squash, gourd) 1040 - Molecular biology 10%
212 - Pathogens and Nematodes Affecting Plants 1460 - Tomato 1060 - Biology (whole systems) 10%
212 - Pathogens and Nematodes Affecting Plants 2110 - Ornamental trees and shrubs 1040 - Molecular biology 10%
Goals / Objectives
As an intracellular plant pathogen, 'Candidatus Liberibacter asiaticus' (Las) lacks type III and IV secretion systems and their related effectors. However, we have recently demonstrated that Las encodes two novel autotransporters that target host mitochondria. We hypothesize that these autotransporters modulate the host's energy biosynthesis and/or defense response for their own survival and multiplication. By blocking the functions of these two important effectors using inhibitory molecules, we expect to disable Las bacterial growth in planta.
Methods (unparsed)

We will characterize the molecular interactions between the effectors and the host mitochondrial proteins. Then we will screen for molecules that inhibit the effector functions. These will be tested initially in the greenhouse and then under field conditions. Successful candidates will be developed to control HLB.

Methods
We will characterize the molecular interactions between the effectors and the host mitochondrial proteins. Then we will screen for molecules that inhibit the effector functions. These will be tested initially in the greenhouse and then under field conditions. Successful candidates will be developed to control HLB.