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United States Department of Agriculture

Agricultural Research Service

Title: Classification of Marek's Disease Viruses According to Pathotype-Philosophy and Methodology

Authors
item WITTER, RICHARD
item Calnek, B - CORNELL UNIVERSITY
item Buscaglia, C - LA PLATA UNIV ARGENTINA
item Gimeno, Isabel
item Schat, K - CORNELL UNIVERSITY

Submitted to: Avian Pathology
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: January 10, 2005
Publication Date: April 30, 2005
Citation: Witter, R.L., Calnek, B.W., Buscaglia, C., Gimeno, I.M., Schat, K.A. 2005. Classification of Marek's disease viruses according to pathotype--philosophy and methodology. Avian Pathology. 34:75-90.

Interpretive Summary: Marek's disease (MD), a virus-induced cancer-like disease of chickens, is considered as a major disease problem in commercial poultry. Vaccination has dramatically reduced the incidence of the disease, but efforts to develop a standard method for determining the disease causing ability of individual virus strains have met with limited success in the past. The objective of this research was to evaluate methods for classifying Marek's disease viruses according to their ability to cause disease and to recommend improved procedures. We have determined that previous methods are not suitable for international use. However, we describe a new, improved procedure based on commercially available chickens and standard reference virus strains which could be widely used. This important information will help scientists in academia and industry understand the prospects for classifying Marek's disease viruses and eventually lead to better control of the disease.

Technical Abstract: The concept of pathotype in Marek's disease (MD) probably dates from the recognition of a more virulent form of the disease in the late 1950s (Benton & Cover, 1957). Distinctions between MD virus (MDV) strains were further expanded with the description of the vv pathotype in the early 1980s and of the vv+ pathotype in the 1990s. Pathotype designations reflect important biological properties that correlate with the break-through of vaccinal immunity in the field. However, pathotyping methods applied by various laboratories have not been uniform, preventing critical comparison of results. Better uniformity of pathotyping procedures is desirable. The Avian Disease and Oncology Laboratory (ADOL) method is based on induction of lymphoproliferative lesions in vaccinated chickens. This method has been used to pathotype more than 45 isolates and is the basis for the current pathotype classification of MDV strains. Its limitations include requirements for a specific type of chickens (15x7 ab+), large numbers of animals, and a statistical method to compare lesion responses to those of JM/102W and Md5 control strains. Because of these limitations, it has not been and is not likely to be used in other laboratories. Comparability in pathotyping can be improved by the comparison of field isolates to standard prototype strains such as JM/102W, Md5 and 648A (American Type Culture Collection) or their equivalents. Data may be generated by different in vivo procedures that measure tumor induction, neurological disease (both neoplastic and non-neoplastic lesions), or solely non-neoplastic criteria (such as lymphoid organ weights or virus replication). Methods based on neoplastic criteria, especially when generated in MD-immunized chickens, will likely correlate most closely with that of the ADOL method and be most relevant to evolution of MD virus in the field. Based on data from several trials, a modification of the ADOL method that utilizes fewer chickens and can be conducted with commercial SPF strains is proposed. The modified method is based on 'best fit' comparisons to prototype strains, and is expected to provide results generally comparable to the original method. A variety of other alternative criteria (see above) are also evaluated both for primary pathotyping and as adjuncts to other pathotyping methods. Advantages and disadvantages of alternative methods are presented.

Last Modified: 7/25/2014
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