Characterization of the glycoproteins of Crimean-Congo hemorrhagic fever virus

J Virol. 2002 Jul;76(14):7263-75. doi: 10.1128/jvi.76.14.7263-7275.2002.

Abstract

Crimean-Congo hemorrhagic fever (CCHF) virus is the cause of an important tick-borne disease of humans throughout regions of Africa, Europe, and Asia. Like other members of the genus Nairovirus, family Bunyaviridae, the CCHF virus M genome RNA segment encodes the virus glycoproteins. Sequence analysis of the CCHF virus (Matin strain) M RNA segment revealed one major open reading frame that potentially encodes a precursor polyprotein 1,689 amino acids (aa) in length. Comparison of the deduced amino acid sequences of the M-encoded polyproteins of Nigerian, Pakistani, and Chinese CCHF virus strains revealed two distinct protein regions. The carboxyl-terminal 1,441 aa are relatively highly conserved (up to 8.4% identity difference), whereas the amino-terminal 243 to 248 aa are highly variable (up to 56.4% identity difference) and have mucin-like features, including a high serine, threonine, and proline content (up to 47.3%) and a potential for extensive O-glycosylation. Analysis of released virus revealed two major structural glycoproteins, G2 (37 kDa) and G1 (75 kDa). Virus protein analysis by various techniques, including pulse-chase analysis and/or reactivity with CCHF virus-specific polyclonal and antipeptide antibodies, demonstrated that the 140-kDa (which contains the mucin-like region) and 85-kDa nonstructural proteins are the precursors of the mature G2 and G1 proteins, respectively. The amino termini of the CCHF virus (Matin strain) G2 and G1 proteins were established by microsequencing to be equivalent to aa 525 and 1046, respectively, of the encoded polyprotein precursor. The tetrapeptides RRLL and RKPL are immediately upstream of the cleavage site for mature G2 and G1, respectively. These are completely conserved among the predicted polyprotein sequences of all the CCHF virus strains and closely resemble the tetrapeptides that represent the major cleavage recognition sites present in the glycoprotein precursors of arenaviruses, such as Lassa fever virus (RRLL) and Pichinde virus (RKLL). These results strongly suggest that CCHF viruses (and other members of the genus Nairovirus) likely utilize the subtilase SKI-1/S1P-like cellular proteases for the major glycoprotein precursor cleavage events, as has recently been demonstrated for the arenaviruses.

MeSH terms

  • Animals
  • Cell Line
  • Chlorocebus aethiops
  • Glycoproteins / chemistry*
  • Glycoproteins / metabolism*
  • Hemorrhagic Fever Virus, Crimean-Congo / genetics
  • Hemorrhagic Fever Virus, Crimean-Congo / metabolism*
  • Hemorrhagic Fever, Crimean / virology
  • Humans
  • Molecular Sequence Data
  • Polyproteins / metabolism
  • Protein Precursors / chemistry
  • Protein Precursors / metabolism
  • RNA, Viral / genetics
  • RNA, Viral / metabolism
  • Sequence Analysis, DNA
  • Vero Cells
  • Viral Proteins / chemistry*
  • Viral Proteins / metabolism*

Substances

  • Glycoproteins
  • Polyproteins
  • Protein Precursors
  • RNA, Viral
  • Viral Proteins

Associated data

  • GENBANK/AF467768