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Journal of Virology, October 1998, p. 7830-7839, Vol. 72, No. 10
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Serp2, an Inhibitor of the
Interleukin-1
-Converting Enzyme, Is Critical in the Pathobiology
of Myxoma Virus
Frederique
Messud-Petit,1
Jacqueline
Gelfi,1
Maxence
Delverdier,2
Marie-France
Amardeilh,2
Robert
Py,1
Gerd
Sutter,3 and
Stephane
Bertagnoli1,*
Laboratoire Associe de Microbiologie
Moleculaire1 and
Laboratoire d'Anatomie
Pathologique,2 Institut National de la Recherche
Agronomique and Ecole Nationale Vétérinaire, Toulouse,
France, and
GSF-Institute of Molecular Virology,
Oberscheissheim, Germany3
Received 9 March 1998/Accepted 2 July 1998
Recently, myxoma virus was shown to encode an additional member of
the serpin superfamily. The viral gene, called serp2, was cloned, and the Serp2 protein was shown to specifically bind to interleukin-1
(IL-1
)-converting enzyme (ICE), thus inhibiting the
cleavage of pro-IL-1
by the protease (F. Petit, S. Bertagnoli, J. Gelfi, F. Fassy, C. Boucraut-Baralon, and A. Milon, J. Virol. 70:5860-5866, 1996). Here, we address the role of Serp2 in the development of myxomatosis, a lethal infectious disease of the European
rabbit. A Serp2 mutant myxoma virus was constructed by disruption of
the single-copy serp2 gene and insertion of the Escherichia coli gpt gene serving as the selectable marker.
A revertant virus was obtained by replacing the E. coli gpt
gene by the intact serp2 open reading frame. The
Serp2
mutant virus replicated with wild-type kinetics
both in rabbit fibroblasts and a rabbit CD4+ T-cell line
(RL5). Moderate reduction of cell surface levels of major
histocompatibility complex I was observed after infection with
wild-type or Serp2
mutant myxoma virus, and both produced
white pocks on the chorioallantoic membrane of the chick embryo. After
the infection of European rabbits, the Serp2
mutant virus
proved to be highly attenuated compared to wild-type myxoma virus, as
demonstrated by the clinical course of myxomatosis and the survival
rates of infected animals. Pathohistological examinations revealed that
infection with wild-type myxoma virus resulted in a blockade of the
inflammatory response at the vascular level. In contrast, rapid
inflammatory reactions occurred upon infection with the
Serp2
mutant virus. Furthermore, lymphocytes in lymph
nodes derived from animals inoculated with Serp2 mutant virus were
shown to rapidly undergo apoptosis. We postulate that the virulence of myxoma virus in the European rabbit can be partially attributed to an
impairment of host inflammatory processes and to the prevention of
apoptosis in lymphocytes. The weakening of host defense is directly
linked to serp2 gene function and is likely to involve the
inhibition of IL-1
-converting-enzyme-dependent pathways.
*
Corresponding author. Mailing address: Laboratoire
Associe de Microbiologie Moleculaire, INRA-ENVT, Ecole Nationale
Vétérinaire, 23 Chemin des Capelles, F-31076 Toulouse cedex
3, France. Phone: (33) 561-19-38-78. Fax: (33) 561-19-39-74. E-mail:
s.bertagnoli{at}envt.fr.
Journal of Virology, October 1998, p. 7830-7839, Vol. 72, No. 10
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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