Arthropod-Borne Animal Diseases 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: INTEGRATED APPROACHES FOR PROTECTION OF ANIMALS FROM VECTOR-BORNE PATHOGENS

Location: Arthropod-Borne Animal Diseases Research

Title: The affect of Pseudomonas aeruginosa ingestion on antimicrobial peptide (AMP) and lysozyme expression in the common housefly (Musca domestica L.)

Authors
item Joyner, Chester -
item Mills, Mary -
item Evett, Christopher -
item Nayduch, Dana

Submitted to: Meeting Abstract
Publication Type: Abstract Only
Publication Acceptance Date: July 30, 2011
Publication Date: July 30, 2011
Repository URL: http://esa.confex.com/esa/2011/webprogram/Paper58605.html
Citation: Joyner, C., Mills, M.K., Evett, C., Nayduch, D. 2011. The affect of Pseudomonas aeruginosa ingestion on antimicrobial peptide (AMP) and lysozyme expression in the common housefly (Musca domestica L.). Meeting Abstract. 58605.

Technical Abstract: The common house fly (Musca domestica L.) lives and thrives in one of the most septic niches on Earth, making bacterial exposure imminent. House flies often ingest bacteria and have both physical and chemical defenses utilized to protect themselves from harmful microbes. For example, defense molecules such as antimicrobial peptides (AMPs) and lysozyme are manufactured by tissues both locally (gut epithelium) and systemically (fat body). These molecules serve to neutralize or lyse bacteria, yet some species are still able to persist through the digestive tract, making the fly a potential biological vector. We found that Pseudomonas aeruginosa was able to survive passage through the fly alimentary canal and exit the digestive tract by 10 h post-ingestion. This study aimed to elucidate the systemic and local AMP and lysozyme responses in house flies after P. aeruginosaingestion. We analyzed the temporal expression of three AMPs (cecropin, defensin and diptericin) and lysozyme 1, 2, 6, 8, and 10 h after ingesting a known amount of P.aeruginosa. Tissue-specific expression was measured on both the mRNA and protein level using qRT-PCR and Western analysis. It is suspected that P. aeruginosa is able to pass through the fly alimentary canal either due to AMP and lysozyme resistance, or by bacteria altering the expression of AMPs and/or lysozyme in order to enhance their survival. By understanding the spatial and temporal molecular interactions between house fly defenses and P. aeruginosa, we can better understand the potential flies have for vectoring these bacteria.

   

 
Project Team
Cohnstaedt, Lee
McVey, D Scott - Scott
Nayduch, Dana
Ruder, Mark
Pfannenstiel, Robert - Bob
Drolet, Barbara
Wilson, William
 
Publications
   Publications
 
Related National Programs
  Animal Health (103)
  Veterinary, Medical and Urban Entomology (104)
  Crop Protection & Quarantine (304)
 
Related Projects
   EVALUATION OF NEW MOLECULAR TARGETS TO CONTROL ARBOVIRUS TRANSMISSION
   ANIMAL HEALTH AND PLANT HEALTH RESEARCH
   ESTABLISH A GENERAL FRAMEWORK FOR COOPERATION AND COORDINATION BETWEEN THE CENTER FOR GRAIN AND ANIMAL HEALTH RESEARCH AND KANSAS ST. UNIV.
   POPULATION GENETICS OF NORTH AMERICAN RIFT VALLEY FEVER DISEASE VECTORS
   MOLECULAR CHARACTERIZATION OF FACTORS AFFECTING COMPETENCE OF INSECTS FOR VIRUS INFECTION AND TRANSMISSION
   EVALUATION OF NEW MOLECULAR TARGETS TO CONTROL ARBOVIRUS TRANSMISSION
   NETWORK BASED MODELING OF ARTHROPODS, HUMANS, AND ANIMALS TO BETTER UNDERSTAND VECTOR-BORNE DISEASE TRANSMISSION
   VECTOR COMPETENCE OF NORTH AMERICAN RIFT VALLEY FEVER DISEASE VECTORS
   CULICOIDES CONTROL PROJECT
   CULICOIDES SONORENSIS TRANSCRIPTOME PROJECT
 
 
Last Modified: 06/18/2013
ARS Home | USDA.gov | Site Map | Policies and Links 
FOIA | Accessibility Statement | Privacy Policy | Nondiscrimination Statement | Information Quality | USA.gov | White House