Tick and Biting Fly 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: MINING THE GENOME OF RHIPICEPHALUS MICROPLUS TO DEVELOP NOVEL CONTROL TECHNOLOGY AND VACCINES

Location: Tick and Biting Fly Research

Title: Optimization of RNA interference (RNAi) targeting acetylcholinesterase in the Southern cattle tick (Rhipicephalus microplus)

Authors
item Tuckow, Alexander
item Temeyer, Kevin

Submitted to: Meeting Abstract
Publication Type: Abstract Only
Publication Acceptance Date: November 15, 2011
Publication Date: N/A

Technical Abstract: Acetylcholinesterase (AChE) is the primary target for organophosphate (OP) acaricides. OP resistant strains of the Southern cattle tick Rhipicephalus microplus have been identified and represent a major threat to the control of this important disease vector. R. microplus ticks possess at least three AChE genes with different enzyme kinetics as well as additional noncatalytic functions. Alterations in the expression of the AChE genes in the synganglia of OP resistant strains have been reported and represent one mechanism for OP resistance. In order to elucidate the molecular basis for altered expression of the AChE genes in OP resistant strains, a dual luciferase reporter construct is being utilized to investigate the transcriptional and/or posttranscriptional regulation of these genes. In addition, the reporter facilitates quantitative analysis of the efficacy of RNA interference (RNAi) molecules designed to target different regions of the AChE genes. Upon establishing the most potent RNAi molecules, gene silencing experiments will be performed in vivo in R. microplus ticks. Preliminary evidence from our laboratory suggests that microinjection of dsRNA constructs targeting the three AChE genes simultaneously results in greater mortality of R. microplus ticks than targeting the AChE genes invidivually. Understanding the complex regulation of the AChE family of genes represents an important step in abating OP resistance and maintaining control of R. microplus. USDA is an equal opportunity provider and employer

   

 
Project Team
Guerrero, Felix
Temeyer, Kevin
Miller, Robert
Li, Andrew
Perez De Leon, Adalberto - Beto
Olafson, Pia
Goolsby, John
Thomas, Donald
Osbrink, Weste
Showler, Allan
 
Publications
   Publications
 
Related National Programs
  Animal Health (103)
  Veterinary, Medical and Urban Entomology (104)
 
Related Projects
   INVESTIGATION OF ELECTROPORATION AS A MEANS OF TRANSFORMATION OF THE HORN FLY WITH GREEN FLUORESCENT PROTEIN
   SEQUENCING OF BAC ENDS FROM A RHIPICEPHALUS MICROPLUS BAC LIBRARY
   DEVELOPMENT OF A MALE-ONLY STRAIN OF THE NEW WORLD SCREWWORM, COCHLIOMYIA HOMINIVORAX (DIPTERA, CALLIPHORIDAE)
   SYSTEMS BIOLOGY INVESTIGATIONS OF ARTHROPOD-BORNE DISEASES TO CONTROL VECTORS OF PATHOGENS
   USE OF SYNERGIZED ACARICIDE FORMULATIONS FOR THE CONTROL OF RESISTANT POPULATIONS OF RHIPICEPHALUS MICROPLUS IN THE MEXICAN TROPICS
   INVESTIGATIONS OF NOVEL TARGET-SPECIFIC LIGANDS FOR ACETYLCHOLINESTERASES OF ARTHROPOD PESTS
   FUNCTIONAL CHARACTERIZATION AND TARGET VALIDATION OF TICK (BOOPHILUS MICROPLUS) G PROTEIN-COUPLED RECEPTORS
   CATTLE TICK GENOME SEQUENCING AND TRANSCRIPTOME ANALYSIS
   PRODUCTION AND EFFICACY TESTING OF BM86-TEXAS ANTI-TICK VACCINE FOR THE CATTLE FEVER TICK ERADICATION PROGRAM
   EVALUATION OF CANDIDATE ANTI-TICK VACCINE ANTIGENS
   EVALUATION OF IMMUNE RESPONSE OF WHITE-TAILED DEER FOLLOWING VACCINATION WITH ANTI-CATTLE TICK VACCINE CANDIDATE ANTIGENS
   EXPERIMENTAL BM86-BASED VACCINE FOR THE CATTLE FEVER TICK ERADICATION PROGRAM
   Evaluation of Immune Response of Canines Following Vaccination with Anti-Tick Vaccine Candidate Antigens
 
 
Last Modified: 05/23/2013
ARS Home | USDA.gov | Site Map | Policies and Links 
FOIA | Accessibility Statement | Privacy Policy | Nondiscrimination Statement | Information Quality | USA.gov | White House