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Antibodies against viral nucleo-, phospho-, and X protein contribute to serological diagnosis of fatal Borna disease virus 1 infections.

Authors :
Neumann B
Angstwurm K
Linker RA
Knoll G
Eidenschink L
Rubbenstroth D
Schlottau K
Beer M
Schreiner P
Soutschek E
Böhmer MM
Lampl BMJ
Pregler M
Scheiter A
Evert K
Zoubaa S
Riemenschneider MJ
Asbach B
Gessner A
Niller HH
Schmidt B
Bauswein M
Source :
Cell reports. Medicine [Cell Rep Med] 2022 Jan 18; Vol. 3 (1), pp. 100499. Date of Electronic Publication: 2022 Jan 18 (Print Publication: 2022).
Publication Year :
2022

Abstract

Borna disease virus 1 (BoDV-1) causes rare but often fatal encephalitis in humans. Late diagnosis prohibits an experimental therapeutic approach. Here, we report a recent case of fatal BoDV-1 infection diagnosed on day 12 after hospitalization by detection of BoDV-1 RNA in the cerebrospinal fluid. In a retrospective analysis, we detect BoDV-1 RNA 1 day after hospital admission when the cell count in the cerebrospinal fluid is still normal. We develop a new ELISA using recombinant BoDV-1 nucleoprotein, phosphoprotein, and accessory protein X to detect seroconversion on day 12. Antibody responses are also shown in seven previously confirmed cases. The individual BoDV-1 antibody profiles show variability, but the usage of three different BoDV-1 antigens results in a more sensitive diagnostic tool. Our findings demonstrate that early detection of BoDV-1 RNA in cerebrospinal fluid and the presence of antibodies against at least two different viral antigens contribute to BoDV-1 diagnosis. Physicians in endemic regions should consider BoDV-1 infection in cases of unclear encephalopathy and initiate appropriate diagnostics at an early stage.<br />Competing Interests: P.S. is an employee of Mikrogen GmbH. E.S. is CEO and a shareholder of Mikrogen GmbH. The other authors declare no competing interests.<br /> (© 2022 The Authors.)

Details

Language :
English
ISSN :
2666-3791
Volume :
3
Issue :
1
Database :
MEDLINE
Journal :
Cell reports. Medicine
Publication Type :
Academic Journal
Accession number :
35106511
Full Text :
https://doi.org/10.1016/j.xcrm.2021.100499