Grant Information

IMPROVED SENSITIVE DETECTION OF THE HLB PATHOGEN BY NEW GENE PRIMERS FOR REAL TIME AND DROPLET DIGITAL PCR ANALYSES

Sponsoring Institution Agricultural Research Service/USDA
Status ACTIVE
Funding Source USDA INHOUSE
Reporting Frequency Annual
Project Director YOKOMI R K
Accession Number 431214
Project Number 2034-22000-013-06T
Dates 2017-01-01 - 2020-02-25
Recipient Organization AGRICULTURAL RESEARCH SERVICE

PARLIER,CA 93648
Keywords (hlb)
clas
ddpcr
huanglongbing
qpcr
Research Effort Applied (40%)
Basic (50%)
Developmental (10%)
Classification Parameters
Knowledge AreaSubject of InvestigationField of SciencePercent
212 - Pathogens and Nematodes Affecting Plants 920 - Orange 1160 - Pathology 75%
212 - Pathogens and Nematodes Affecting Plants 930 - Lemon 1170 - Epidemiology 25%
Goals / Objectives
The research objective is to improve reliable diagnosis of "Candidatus Liberibacter asiaticus", presumptive causal agent of huanglongbing (HLB)in the U.S.
Methods (unparsed)

The approach includes deep sequencing using MiSeq Illumina to improve full length sequence data of 'Ca. Liberibacter asiaticus'; and bioinformatic analysis, employing primer design software, Taqman probes, real time quantitative PCR, droplet digital PCR, high throughput robotic DNA extraction and purification of nucleic acid.

Methods
The approach includes deep sequencing using MiSeq Illumina to improve full length sequence data of 'Ca. Liberibacter asiaticus'; and bioinformatic analysis, employing primer design software, Taqman probes, real time quantitative PCR, droplet digital PCR, high throughput robotic DNA extraction and purification of nucleic acid.