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Abstract

It has been previously shown that antibodies contained in human plasma directed towards the Coxsackievirus B4 (CVB4)E2 capsid protein VP4 can enhance the CVBE2-induced production of IFN-alpha by peripheral blood mononuclear cells (PBMC). The aim of this study was to produce a VP4 fusion protein to investigate the role of the internal capsid protein VP4 and anti-VP4 antibodies in the plasma-dependent enhancement of CVB4E2 infection of PBMC. A fusion protein MBPVP4 containing the VP4 insert of CVB4E2 and a control fusion protein MBP-beta-gal-alpha, were produced in Escherichia coli K12 TB1. The CVB4E2 infection of PBMC was quantified by using a real time PCR method amplifying CVB4E2-negative strand RNA. IFN-alpha concentrations in culture supernatants were assayed by DELFIA. MBPVP4 but not MBP-beta-gal-alpha, preincubated with plasma inhibited the plasma-dependent enhancement of CVB4E2-induced production of IFN-alpha by PBMC. Human plasma samples, antibodies contained in plasma eluted from MBPVP4-coated plates, but not from MBP-beta-gal-alpha-coated plates, incubated with CVB4E2 enhanced the infection of PBMC and the production of IFN-alpha by infected cells. Together our results show that VP4 and anfi-VP4 antibodies play a role in the plasma-dependent enhancement of CVB4E2 infection of PBMC. (c) 2007 Elsevier B.V. All rights reserved.

Keywords

fusion protein; VP4; plasma; peripheral blood mononuclear cells; coxsackievirus B4

Published in

Virus Research
2007, volume: 125, number: 2, pages: 183-190
Publisher: ELSEVIER SCIENCE BV

SLU Authors

  • Alm, Gunnar

    • Department of Molecular Biosciences, Swedish University of Agricultural Sciences

UKÄ Subject classification

Veterinary Science
Animal and Dairy Science

Publication identifier

  • DOI: https://doi.org/10.1016/j.virusres.2007.01.001

Permanent link to this page (URI)

https://res.slu.se/id/publ/16360