ABSTRACT. Japanese domestic cats were surveyed for circulating antibodies to the p10 and p24 proteins of the Borna disease virus (BDV) by Western blotting. Twenty-four of 52 cats (46.2%) with ataxia and other neurologic symptoms of unknown cause were positive for antibodies to BDV p10 and/or p24. In contrast, cats without neurological symptoms gave a significantly lower prevalence of anti-BDV antibodies to p10 and/or p24 (36 of 152 cats, 23.7%). Thirty specific pathogen-free (SPF) cats tested as controls were uniformly negative to BDV p10 and p24 antigens. These results suggest that BDV may play a role in ataxia in cats. Additionally, our results suggest that it is necessary to use both p10 and p24 as antigens to detect circulating antibodies to BDV in cats. KEY WORDS: anti-BDV antibody, ataxia, Borna disease virus, feline.J. Vet. Med. Sci. 63(12): 1279-1285, 2001 Borna disease (BD) is a progressive encephalomyelitis of horses and sheep caused by infection with the neurotropic Borna disease virus (BDV) that is an enveloped, non-segmented, negative-stranded (NNS) RNA virus [6,8,19,39]. BDV is the prototype genus of the new family of Bornaviridae. Epidemiological studies have documented that diverse species of warm-blooded animals including cats possess circulating antibodies to BDV. In cats, a spontaneous non-suppurative meningoencephalomyelitis with clinical signs of ataxia and behavioral abnormalities, referred to as staggering disease (SD), is thought to be a counterpart of Borna-encephalitis, because the prevalence of BDV-specific antibodies seen in these cats is higher than that seen in randomly selected domestic cats, not having neurological disorders [18,20,22,23,28,30,31,34]. Moreover, a feline BDV has been isolated from the central nervous system of cats with SD [24]. Cats also developed neurological signs and encephalitis when experimentally infected with this feline BDV isolate [21]. These findings support the hypothesis that BDV may correlate with SD in cats.Molecular biological studies on BDV have shown that the BDV antigenome consists of at least 6 open reading frames (ORFs), ORF I to ORF V and ORFx1 [5,9,10]. ORF I encodes the viral nucleoprotein N (p38/40) of 38/40 kDa [25,33,40]. ORF II encodes the phosphoprotein P (p24) of approximately 24 kDa [40,41], and ORF V encodes for a 190-kDa protein that may be the putative viral polymerase L [43]. Studies on the replication of other NNS-RNA viruses have shown that the minimal replicative and infectious unit for these viruses is the ribonucleoprotein containing the genomic RNA that is tightly associated with the N, P and L proteins, whereas the precise nature of the minimal replicative unit of BDV is unclear. Unlike other NNS-RNA viruses, BDV replicates in the nucleus [6,8]. We and others have studied the BDV protein p10 of approximately 10 kDa that is encoded by ORFx1, and translated from mRNA representing the second transcription unit of the BDV genome [27,44]. The p10 are found in brain cells of naturally and experimentally infected animals as well a...