, tissues from four captive white-tailed deer were observed to have histologic lesions of systemic lymphocytic vasculitis. These lesions suggested malignant catarrhal fever, although epizootic hemorrhagic disease and bluetongue were included in the differential diagnosis. Initial diagnostic efforts, including virus isolation and reverse transcription-PCR for epizootic hemorrhagic disease virus and bluetongue virus, failed to identify an etiologic agent. However, consensus primer PCR targeted to the herpesvirus DNA polymerase gene detected viral genomic DNA in each of these four cases. Nucleotide sequence analysis of the amplified product demonstrated that the detected virus was identical over the compared region to the recently described malignant catarrhal fever virus of white-tailed deer (H. Li, N. Dyer, J. Keller, and T. B. Crawford, J. Clin. Microbiol. 38:1313-1318, 2000). Additional nucleotide sequencing of both the DNA polymerase gene and DNA packaging gene followed by phylogenetic analysis solidified this newly recognized herpesvirus as a member of the Gammaherpesvirinae and suggests that this virus, along with ovine herpesvirus 2, alcelaphine herpesvirus 1, alcelaphine herpesvirus 2 and caprine herpesvirus 2, may be part of a separate clade within this subfamily.Malignant catarrhal fever (MCF) affects a broad range of domestic and exotic ruminants (12,20), including at least 13 species of deer (22). The distribution of MCF is worldwide, and the clinical course is typically severe and frequently fatal (20), although inapparent infections do occur in susceptible hosts (13) and cattle have been reported to be chronically infected with and to recover from MCF (18). MCF is usually sporadic, with limited morbidity in a population, although severe epizootics with high morbidity and mortality have been reported (3,10,27). Two gammaherpesviruses, alcelaphine herpesvirus 1 (AHV1) and ovine herpesvirus 2 (OHV2) (previously referred to as sheep-associated MCF virus), are considered to be the principal etiologic agents of MCF. Both AHV1 and OHV2 are apathogenic in their natural hosts, i.e., wildebeest and sheep, respectively. Transmission to susceptible ruminants can usually be associated with close contact between carrier sheep or wildebeest calves. However, spread by contact between infected cattle, and presumably other susceptible ruminants as well, does not readily occur (5,20). While the reason for the lack of transmission between susceptible animals has not been proven, it is likely that the clinically susceptible hosts do not shed sufficient levels of cell-free, infectious virus to infect herdmates.Recently, a third gammaherpesvirus was detected from the tissues of white-tailed deer with lesions that were characteristic of MCF (14). A combination of molecular and virological testing demonstrated that the affected deer were negative for OHV2 and AHV1 as well as a number of other potential etiologic agents. Genetically, this newly identified herpesvirus was found to be closely related to the other viruses known ...