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Comparative Study
. 2002 Apr 25;296(1):177-89.
doi: 10.1006/viro.2002.1412.

The group-specific murine coronavirus genes are not essential, but their deletion, by reverse genetics, is attenuating in the natural host

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Comparative Study

The group-specific murine coronavirus genes are not essential, but their deletion, by reverse genetics, is attenuating in the natural host

Cornelis A M de Haan et al. Virology. .

Abstract

In addition to a characteristic set of essential genes coronaviruses contain several so-called group-specific genes. These genes differ distinctly among the three coronavirus groups and are specific for each group. While the essential genes encode replication and structural functions, hardly anything is known about the products and functions of the group-specific genes. As a first step to elucidate their significance, we deleted the group-specific genes from the group 2 mouse hepatitis virus (MHV) genome via a novel targeted recombination system based on host switching (L. Kuo, G. J.Godeke, M. J. Raamsman, P. S. Masters, and P. J. M. Rottier, 2000, J. Virol. 74, 1393-1406). Thus, we obtained recombinant viruses from which the two clusters of group-specific genes were deleted either separately or in combination in a controlled genetic background. As all recombinant deletion mutant viruses appeared to be viable, we conclude that the MHV group-specific genes are nonessential, accessory genes. Importantly, all deletion mutant viruses were attenuated when inoculated into their natural host, the mouse. Therefore, deletion of the coronavirus group-specific genes seems to provide an attractive approach to generate attenuated live coronavirus vaccines.

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References

    1. Almazan F., Gonzalez J.M., Penzes Z., Izeta A., Calvo E., Plana-Duran J., Enjuanes L. Engineering the largest RNA virus genome as an infectious bacterial artificial chromosome. Proc. Natl. Acad. Sci. USA. 2000;97:5516–5521. - PMC - PubMed
    1. Bredenbeek P.J., Noten A.F., Horzinek M.C., Spaan W.J. Identification and stability of a 30-kDa nonstructural protein encoded by mRNA 2 of mouse hepatitis virus in infected cells. Virology. 1990;175:303–306. - PMC - PubMed
    1. Bredenbeek P.J., Pachuk C.J., Noten A.F., Charite J., Luytjes W., Weiss S.R., Spaan W.J. The primary structure and expression of the second open reading frame of the polymerase gene of the coronavirus MHV-A59; a highly conserved polymerase is expressed by an efficient ribosomal frameshifting mechanism. Nucleic Acids Res. 1990;18:1825–1832. - PMC - PubMed
    1. Brian D.A., Hogue B.G., Kienzle T.E. The coronavirus hemagglutinin esterase glycoprotein. In: Siddell S.G., editor. The Coronaviridae. Plenum Press; New York: 1995. pp. 165–179.
    1. Brown T.D.K., Brierly I. The coronavirus nonstructural proteins. The coronavirus hemagglutinin esterase glycoprotein. In: Siddell S.G., editor. The Coronaviridae. Plenum Press; New York: 1995. pp. 191–217.

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