Role of the capsid protein VP4 in the plasma-dependent enhancement of the Coxsackievirus B4E2-infection of human peripheral blood cells

Virus Res. 2007 May;125(2):183-90. doi: 10.1016/j.virusres.2007.01.001. Epub 2007 Feb 8.

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 CVB4E2-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 anti-VP4 antibodies play a role in the plasma-dependent enhancement of CVB4E2 infection of PBMC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Capsid Proteins / physiology*
  • Carrier Proteins / biosynthesis
  • Enterovirus B, Human / physiology*
  • Humans
  • Interferon-alpha / biosynthesis
  • Leukocytes, Mononuclear / virology*
  • Maltose-Binding Proteins
  • Plasma / physiology*

Substances

  • Capsid Proteins
  • Carrier Proteins
  • Interferon-alpha
  • Maltose-Binding Proteins