Source: UNIVERSITY OF TENNESSEE submitted to
DEVELOPMENT OF A SEROLOGICAL ASSAY FOR ELAEOPHORA SCHNEIDERI
Sponsoring Institution
Cooperating Schools of Veterinary Medicine
Project Status
COMPLETE
Funding Source
Reporting Frequency
Annual
Accession No.
1004439
Grant No.
(N/A)
Cumulative Award Amt.
(N/A)
Proposal No.
(N/A)
Multistate No.
(N/A)
Project Start Date
Sep 4, 2014
Project End Date
Jun 30, 2015
Grant Year
(N/A)
Program Code
[(N/A)]- (N/A)
Project Director
Gerhold, RI, .
Recipient Organization
UNIVERSITY OF TENNESSEE
2621 MORGAN CIR
KNOXVILLE,TN 37996-4540
Performing Department
Biomedical & Diagnostic Sciences
Non Technical Summary
Elaeophora schneideriis a nematode wormthat infests several mammalian hosts in North America. It is transmitted by horse flies, and infection in normal hostsseldom produces clinical symptoms. In other hosts, such as moose, sheep, elk, and goats, infection with E. schneideri leads tonecrosis of the muzzle, ears, and optic nerves; lack of coordination; facial or lower limb dermatitis; horn deformities; blindness; and even death.Using sera from known Elaeophora-infected and uninfected moose, we will develop a live-animal ELISA to accurately test for E. schneideri. The sera initially tested will be banked, and subsequently collected sera from moose and other sympatric ungulates (cervids and bovids) will be tested later. Both a PCR test and an ELISA will be pursued. Test sensitivity and specificity will be determined, as well as infection prevalence for various regions and species.The goal is to make the test readily available at a low cost.Montana Fish, Wildlife & Parks, $10,000
Animal Health Component
100%
Research Effort Categories
Basic
(N/A)
Applied
100%
Developmental
(N/A)
Classification

Knowledge Area (KA)Subject of Investigation (SOI)Field of Science (FOS)Percent
31339101110100%
Goals / Objectives
Investigate the role of parasites in the population decline and health of moose.Develop a more sensitive and specific live-animal test to detect E. schneideri.
Project Methods
Using sera from known Elaeophora-infected and uninfected moose, we will develop a live-animal ELISA test. The sera initially tested will be banked, and subsequently collected sera from moose and other sympatric ungulates (cervids and bovids) will be tested later. Both a PCR test and an ELISA will be pursued. Test sensitivity and specificity will be determined, as well as infection prevalence for various regions and species.