Natural resistance to infection with mouse cytomegalovirus (MCMV) is controlled by a dominant locus, Cmv1. Cmv1 is linked to the Ly49 family of natural killer receptors on distal chromosome 6. While some studies localized Cmv1 as distal to the Ly49 gene cluster, genetic and functional analysis identified Ly49h as a pivotal factor in resistance to MCMV. The role of these two independent genomic domains in MCMV resistance was evaluated by functional complementation using transgenesis of bacterial artificial chromosomes (BAC) in genetically susceptible mice. Phenotypic and genetic characterization of the transgenic animals traced the resistance gene to a single region spanning the Ly49h gene. The appearance of the Ly49H protein in NK cells of transgenic mice coincided with the emergence of MCMV resistance, and there was a threshold Ly49H protein level associated with full recovery. Finally, transgenic expression of Ly49H in the context of either of the two independent susceptibility alleles, Cmv1sBALB or Cmv1sFVB, conferred resistance to MCMV infection. These results demonstrate that Ly49h is necessary and sufficient to confer MCMV resistance, and formally demonstrate allelism between Cmv1 and Ly49h. This panel of transgenic animals provides a unique resource to study possible pleiotropic effect of Cmv1.
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17 February 2003
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February 10 2003
Transgenic Expression of the Activating Natural Killer Receptor Ly49H Confers Resistance to Cytomegalovirus in Genetically Susceptible Mice
Seung-Hwan Lee,
Seung-Hwan Lee
1Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada
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Ahmed Zafer,
Ahmed Zafer
2Centre for Molecular Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario K1H 8L6, Canada
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Yves de Repentigny,
Yves de Repentigny
2Centre for Molecular Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario K1H 8L6, Canada
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Rashmi Kothary,
Rashmi Kothary
2Centre for Molecular Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario K1H 8L6, Canada
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Michel L. Tremblay,
Michel L. Tremblay
3Department of Biochemistry, McGill University, Montreal, Quebec H3G 1Y6, Canada
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Philippe Gros,
Philippe Gros
3Department of Biochemistry, McGill University, Montreal, Quebec H3G 1Y6, Canada
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Pascale Duplay,
Pascale Duplay
4Institut National de la Recherche Scientifique-Institut Armand-Frappier, Universite du Quebec, Laval, Quebec H7V 1B7, Canada
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John R. Webb,
John R. Webb
1Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada
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Silvia M. Vidal
Silvia M. Vidal
1Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada
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Seung-Hwan Lee
1Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada
Ahmed Zafer
2Centre for Molecular Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario K1H 8L6, Canada
Yves de Repentigny
2Centre for Molecular Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario K1H 8L6, Canada
Rashmi Kothary
2Centre for Molecular Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario K1H 8L6, Canada
Michel L. Tremblay
3Department of Biochemistry, McGill University, Montreal, Quebec H3G 1Y6, Canada
Philippe Gros
3Department of Biochemistry, McGill University, Montreal, Quebec H3G 1Y6, Canada
Pascale Duplay
4Institut National de la Recherche Scientifique-Institut Armand-Frappier, Universite du Quebec, Laval, Quebec H7V 1B7, Canada
John R. Webb
1Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada
Silvia M. Vidal
1Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada
Address correspondence to Silvia M. Vidal, Faculty of Medicine, University of Ottawa, Room 4207, 451 Smyth Rd., Ottawa, Ontario K1H 8M5, Canada. Phone: 613-562-5800 (8592); Fax: 613-562-5452; E-mail: [email protected]
*
Abbreviations used in this paper: BAC, bacterial artificial chromosome; GST, glutathione S transferase; MCMV, mouse CMV; NKC, NK cell gene complex; PAMP, pathogen associated molecular pattern; STS, sequence tagged site; TCF-1, T cell factor 1.
Received:
October 30 2002
Revision Received:
November 25 2002
Accepted:
January 13 2003
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2003
J Exp Med (2003) 197 (4): 515–526.
Article history
Received:
October 30 2002
Revision Received:
November 25 2002
Accepted:
January 13 2003
Citation
Seung-Hwan Lee, Ahmed Zafer, Yves de Repentigny, Rashmi Kothary, Michel L. Tremblay, Philippe Gros, Pascale Duplay, John R. Webb, Silvia M. Vidal; Transgenic Expression of the Activating Natural Killer Receptor Ly49H Confers Resistance to Cytomegalovirus in Genetically Susceptible Mice . J Exp Med 17 February 2003; 197 (4): 515–526. doi: https://doi.org/10.1084/jem.20021713
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