Journal of Clinical Virology
Volume 35, Issue 2 , Pages 154-159, February 2006

Evaluation of a Crimean-Congo hemorrhagic fever virus recombinant antigen expressed by Semliki Forest suicide virus for IgM and IgG antibody detection in human and animal sera collected in Iran

  • S. Garcia

      Affiliations

    • Unité de génétique moléculaire des Bunyaviridés, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France
    • Laboratoire de virologie, CRSSA Emile Pardé, Grenoble, France
  • ,
  • S. Chinikar

      Affiliations

    • Arboviruses and Hemorrhagic Fever National Laboratory, Institut Pasteur, Tehran, Iran
  • ,
  • D. Coudrier

      Affiliations

    • Unité de génétique moléculaire des Bunyaviridés, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France
  • ,
  • A. Billecocq

      Affiliations

    • Unité de génétique moléculaire des Bunyaviridés, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France
  • ,
  • B. Hooshmand

      Affiliations

    • Center for Disease Control, Ministry of Health, Iran
  • ,
  • J.M. Crance

      Affiliations

    • Laboratoire de virologie, CRSSA Emile Pardé, Grenoble, France
  • ,
  • D. Garin

      Affiliations

    • Laboratoire de virologie, CRSSA Emile Pardé, Grenoble, France
  • ,
  • M. Bouloy

      Affiliations

    • Unité de génétique moléculaire des Bunyaviridés, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France
    • Corresponding Author InformationCorresponding author. Tel.: +33 140 613157; fax: +33 140 613151.

Received 22 July 2004; received in revised form 1 October 2004; accepted 1 February 2005. published online 08 August 2005.

Abstract 

Crimean-Congo hemorrhagic fever virus (CCHFV) is transmitted to humans by ticks or by direct contact with infected blood. It causes severe, often fatal, hemorrhagic diseases in humans but infection in animals is asymptomatic. CCHFV can spread from person to person and has caused many nosocomial outbreaks. Because the virus is very pathogenic for humans it must be manipulated in a biosafety level 4 (BSL4) laboratory, rendering the production of antigen for serological diagnosis difficult. To replace the native antigen, we produced a recombinant nucleoprotein expressed in mammalian cells via the recombinant Semliki Forest alphavirus replicon and developed an indirect immunofluorescence assay (IFA) as well as an enzyme-linked immunosorbent assay (ELISA) by immunocapture to detect IgM and IgG in human and animal serum. Using these methods, we analyzed clinical samples from human patients and sera from domestic animals collected in Iran and we show that this novel antigen provides a novel, sensitive and specific tool for CCHF diagnosis.

Keywords: Diagnosis, ELISA, IgM and IgG, Indirect immunofluorescence

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PII: S1386-6532(05)00173-3

doi:10.1016/j.jcv.2005.02.016

Journal of Clinical Virology
Volume 35, Issue 2 , Pages 154-159, February 2006