Mx1 but Not MxA Confers Resistance against Tick-Borne Dhori Virus in Mice

Robert Thimme, Michael Frese, Georg Kochs, Otto Haller

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

The interferon-induced nuclear Mx1 protein is responsible for innate resistance of mice to influenza virus it has been unclear why mice are equipped with a powerful and specific defense mechanism against influenza viruses for which they are not natural hosts. Here, we show that Dhori virus, an influenza-like virus transmitted by ticks and known to infect small mammals, is sensitive to the Mx1 resistance mechanism. Influenza virus-susceptible BALB/c and C57BL/6 mice (lacking a functional Mx1 gene) developed severe disease symptoms and died within a few days after intraperitoneal infection with a lethal dose of Dhori virus. In contrast, Mx1-congenic, influenza virus-resistant BALB.A2G-Mx1 and B6.A2G-Mx1 mice remained healthy and survived. The Mx1 resistance phenotype was expressed in cultured peritoneal macrophages and interferon-treated embryonic cells obtained from these mice. Moreover, stable lines of transfected mouse 3T3 cells constitutively expressing Mx1 protein were protected from Dhori virus infection. The MxA protein of human cells shows a high degree of sequence similarity to Mx1 but, unlike Mx1, inhibits a broad range of RNA viruses. Transgenic mice that permanently express the human MxA protein in various organs became resistant to infection with Thogoto virus but remained fully susceptible to Dhori virus. These in vivo results show that DHO virus is unique in being resistant to human MxA but susceptible to mouse Mx1 protein. They further indicate that the Mx1 system functions as a potent defense mechanism against tick-borne influenza-like viruses in mice.

Original languageEnglish
Article number71404
Pages (from-to)296-301
Number of pages6
JournalVirology
Volume211
Issue number1
DOIs
Publication statusPublished - 1 Aug 1995
Externally publishedYes

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Thogotovirus
Ticks
Orthomyxoviridae
Interferons
3T3 Cells
RNA Viruses
Peritoneal Macrophages
Virus Diseases
Nuclear Proteins
Infection
Inbred C57BL Mouse
Transgenic Mice
Mammals
Viruses
Phenotype

Cite this

Thimme, Robert ; Frese, Michael ; Kochs, Georg ; Haller, Otto. / Mx1 but Not MxA Confers Resistance against Tick-Borne Dhori Virus in Mice. In: Virology. 1995 ; Vol. 211, No. 1. pp. 296-301.
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abstract = "The interferon-induced nuclear Mx1 protein is responsible for innate resistance of mice to influenza virus it has been unclear why mice are equipped with a powerful and specific defense mechanism against influenza viruses for which they are not natural hosts. Here, we show that Dhori virus, an influenza-like virus transmitted by ticks and known to infect small mammals, is sensitive to the Mx1 resistance mechanism. Influenza virus-susceptible BALB/c and C57BL/6 mice (lacking a functional Mx1 gene) developed severe disease symptoms and died within a few days after intraperitoneal infection with a lethal dose of Dhori virus. In contrast, Mx1-congenic, influenza virus-resistant BALB.A2G-Mx1 and B6.A2G-Mx1 mice remained healthy and survived. The Mx1 resistance phenotype was expressed in cultured peritoneal macrophages and interferon-treated embryonic cells obtained from these mice. Moreover, stable lines of transfected mouse 3T3 cells constitutively expressing Mx1 protein were protected from Dhori virus infection. The MxA protein of human cells shows a high degree of sequence similarity to Mx1 but, unlike Mx1, inhibits a broad range of RNA viruses. Transgenic mice that permanently express the human MxA protein in various organs became resistant to infection with Thogoto virus but remained fully susceptible to Dhori virus. These in vivo results show that DHO virus is unique in being resistant to human MxA but susceptible to mouse Mx1 protein. They further indicate that the Mx1 system functions as a potent defense mechanism against tick-borne influenza-like viruses in mice.",
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Mx1 but Not MxA Confers Resistance against Tick-Borne Dhori Virus in Mice. / Thimme, Robert; Frese, Michael; Kochs, Georg; Haller, Otto.

In: Virology, Vol. 211, No. 1, 71404, 01.08.1995, p. 296-301.

Research output: Contribution to journalArticle

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