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Journal of Clinical Microbiology, February 2001, p. 419-429, Vol. 39, No. 2
0095-1137/01/$04.00+0   DOI: 10.1128/JCM.39.2.419-429.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Immunological and PCR Analyses for Borna Disease Virus in Psychiatric Patients and Blood Donors in Japan

Koji Fukuda,1,2,dagger Kazuo Takahashi,1,* Yasuhide Iwata,2 Norio Mori,2 Kenji Gonda,1 Tsuguhiro Ogawa,2 Kouichi Osonoe,3 Minako Sato,4 Shin-ichi Ogata,5 Taisuke Horimoto,6 Takashi Sawada,7 Masato Tashiro,8 Kazunari Yamaguchi,9 Shin-ichi Niwa,10 and Shiro Shigeta1

Department of Microbiology1 and Department of Neuropsychiatry,10 School of Medicine, Fukushima Medical University, Fukushima-shi, Fukushima 960-1295, Department of Psychiatry and Neurology, Hamamatsu University School of Medicine, Hamamatsu-shi, Shizuoka 431-3192,2 Department of Psychiatry, Takeda General Hospital,3 Yamamori Hospital,4 and Hibarigaoka Hospital,5 Fukushima, Osaka Prefecture University, Osaka,6 Diagnostic Division, Eisai, Tsukuba Research Laboratories, Tsukuba,7 National Institute of Infectious Diseases, Tokyo,8 and Blood Transfusion Service and Internal Medicine, Kumamoto,9 Japan

Received 10 April 2000/Returned for modification 24 August 2000/Accepted 9 November 2000

The involvement of Borna disease virus (BDV) in psychiatric diseases in humans remains controversial. T-cell memory response and seroprevalence of BDV in patients with psychiatric disorders and blood donors in Japan were evaluated collectively by Western blot (WB) analysis with inhibition test, electrochemiluminescence immunoassay, immunofluorescence assay, and T-cell proliferative response as well as detection of BDV p24 RNA in peripheral blood mononuclear cells (PBMCs). Positive proliferative responses to both BDV p40 and p24 proteins were detected in 9% of patients with mood disorders (4 of 45), 4% of schizophrenic patients (2 of 45), and 2% of blood donors (1 of 45). By WB analysis, the antibody to BDV p40 was detected only in 2% of patients with mood disorders (1 of 45). The BDV p24 antibody was detected in 2% of patients with mood disorders (1 of 45) and 9% of schizophrenic patients. (4 of 45) No plasma reacted with both BDV proteins. The finding of a lower seroprevalence than previously reported suggests the presence of false-positive cases in the previous report. BDV RNA was detected only in 2% of patients with mood disorders (1 of 45). In these three serological assays, T-cell responses, and PCR analysis, there was no significant difference in the prevalence among the three groups. However, we found three psychiatric patients who were positive for both BDV antibodies and T-cell proliferative responses and one patient who was positive for BDV RNA in PBMCs. These findings suggest the usefulness of the proliferative T-cell response and that certain individuals are infected with BDV or a BDV-related virus.


* Corresponding author. Mailing address: Department of Microbiology, School of Medicine, Fukushima Medical University, 1 Hikarigaoka, Fukushima-shi, Fukushima 960-1295, Japan. Phone: 81-24-548-2111, ext. 2162. Fax: 81-24-548-5072. E-mail: k-tak{at}cc.fmu.ac.jp.

dagger Present address: Department of Psychiatry and Neurology, Hamamatsu University School of Medicine, Hamamatsu-shi, Shizuoka 431-3192, Japan.


Journal of Clinical Microbiology, February 2001, p. 419-429, Vol. 39, No. 2
0095-1137/01/$04.00+0   DOI: 10.1128/JCM.39.2.419-429.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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