OIE Reference Laboratory Reports Activities in 2011 Name of disease (or topic) for which you are a designated OIE Reference Laboratory: Address of laboratory: Equine rhinopneumonitis Gluck Equine Research Center University of Kentucky Lexington, KY 40546 UNITED STATES OF AMERICA Tel.: (+1-859) 218-1094 Fax: (+1-859) 257-8542 e-mail address: ptimoney@uky.edu website: Name (including Title and Position) of Head of Laboratory (Responsible Official): http://www.ca.uky.edu/gluck/servpoe/as[ Dr Mats Troedsson Name(including Title and Position) of OIE Reference Expert: Dr Peter Timoney Name (including Title and Position) of writer of this report (if different from above): Dr Peter Timoney Annual reports of OIE Reference Centres, 2011 1 Equine rhinopneumonitis Part I: Summary of general activities related to the disease 1. 2. Test(s) in use/or available for the specified disease/topic at your laboratory Test For Specificity Total rPCR Nucleic acid detection Type – EHV-1 Type – EHV-4 551 Type 47 VN Antibody Rk-13/ EEC cell culture Virus Isolation FAT Antigen detection 200 49 Type 555 Production and distribution of diagnostic reagents The following non-OIE approved diagnostic reagents for equine herpesvirus 1 & 4 (EHV-1 & 4) infections are available for distribution: cell lines (RK-13 continuous rabbit kidney cells, ATCC37; equine endothelial diploid cell line) for virus isolation and quantitation, virus strains and PCR kits for EHV-1 &4 virus detection. Estimated quantities of reagents used in-house/distributed nationally: RK-13 cell line: 105 x 150 cm2 flasks Equine endothelial cell line: 85 x75 cm2 flasks Part II: Activities specifically related to the mandate of OIE Reference Laboratories 3. International harmonisation and standardisation of methods for diagnostic testing or the production and testing of vaccines a) Establishment and maintenance of a network with other OIE Reference Laboratories designated for the same pathogen or disease and organisation of regular inter-laboratory proficiency testing to ensure comparability of results None undertaken or participated in during 2011. b) Organisation of inter-laboratory proficiency testing with laboratories other than OIE Reference Laboratories for the same pathogens and diseases to ensure equivalence of results None undertaken or participated in during 2011. 4. Preparation and supply of international reference standards for diagnostic tests or vaccines Currently, there are no OIE formally approved reference materials for EHV-1 or EHV-4 available from this laboratory. No requests have been received for reference virus strains, monospecific antisera against either EHV-1 or 4, or test materials for evaluation of proficiency in agent detection or antibody determination in 2011. 5. 2 Research and development of new procedures for diagnosis and control Annual reports of OIE Reference Centres, 2011 Equine rhinopneumonitis Three research studies currently in progress at the Gluck Center relate 1) to evaluation of the antiviral activity of herpesvirus DNA polymerase inhibitors against neuropathgenic and non-neuropathogenic strains of EHV-1, 2) to investigation of the molecular characteristics of neuropathogenic strains of EHV-1, and 3) to assessment of the sensitivity and specificity of a new allelic discrimination rPCR assay for identification of EHV-1 and determination of virus genotype in clinical materials. 6. Collection, analysis and dissemination of epizootiological data relevant to international disease control Studies are in progress aimed at a) determining the genetic diversity among strains of EHV-1 linked to equine neurologic disease, and b) investigating the possible association of EHV-1with EHV-2, and/or EHV-5, in causing respiratory disease in weanling/yearling horses. 7. Maintenance of a system of quality assurance, biosafety and biosecurity relevant to the pathogen and the disease concerned Since its initial designation as an OIE Reference Center for equine rhinopneumonitis in 2009, the Laboratory has functioned/operated under stringent standards in all aspects of specimen handling, performance of tests for agent detection or antibody determination, maintenance of a comprehensive record keeping system and reporting of test results. It is currently engaged in improvement of various diagnostic tests and their validation as well as development of a modified live vaccine virus for the prevention and control of equine rhinopneumonitis, especially equine herpesvirus myeloencephalopathy. Performance of all test procedures is carried out in strict conformity with the methodologies detailed in the OIE Standards Manual. A comprehensive set of Standard Operating Procedures is in place; these provide detailed information on all aspects of the functioning of the reference laboratory consistent with the recommendations set out in the OIE Quality Standard and Guidelines for Veterinary Laboratories: Infectious Diseases (2nd edition, 2008). 8. Provision of consultant expertise to OIE or to OIE Member Countries Consultation and collaboration on establishing the genotypic characteristics of strains of EHV-1 with proven ability to cause neurologic disease. There was no participation in any OIE meetings or international missions in 2011. 9. Provision of scientific and technical training to personnel from other OIE Member Countries None in 2011. 10. Provision of diagnostic testing facilities to other OIE Member Countries No diagnostic services were provided to other Member Countries. 11. Organisation of international scientific meetings on behalf of OIE or other international bodies No international meetings on equine herpesvirus 1 & 4 related diseases were organized in 2011. 12. Participation in international scientific collaborative studies No international collaborative studies are currently in progress. 13. Publication and dissemination of information relevant to the work of OIE (including list of scientific publications, internet publishing activities, presentations at international conferences) None. _______________ Annual reports of OIE Reference Centres, 2011 3