Toll-like receptors 9 and 3 as essential components of innate immune defense against mouse cytomegalovirus infection

K Tabeta, P Georgel, E Janssen, X Du… - Proceedings of the …, 2004 - National Acad Sciences
K Tabeta, P Georgel, E Janssen, X Du, K Hoebe, K Crozat, S Mudd, L Shamel, S Sovath…
Proceedings of the National Academy of Sciences, 2004National Acad Sciences
Several subsets of dendritic cells have been shown to produce type I IFN in response to viral
infections, thereby assisting the natural killer cell-dependent response that eliminates the
pathogen. Type I IFN production can be induced both by unmethylated CpG-
oligodeoxynucleotide and by double-stranded RNA. Here, we describe a codominant CpG-
ODN unresponsive phenotype that results from an N-ethyl-N-nitrosourea-induced missense
mutation in the Tlr9 gene (Tlr9CpG1). Mice homozygous for the Tlr9CpG1 allele are highly …
Several subsets of dendritic cells have been shown to produce type I IFN in response to viral infections, thereby assisting the natural killer cell-dependent response that eliminates the pathogen. Type I IFN production can be induced both by unmethylated CpG-oligodeoxynucleotide and by double-stranded RNA. Here, we describe a codominant CpG-ODN unresponsive phenotype that results from an N-ethyl-N-nitrosourea-induced missense mutation in the Tlr9 gene (Tlr9CpG1). Mice homozygous for the Tlr9CpG1 allele are highly susceptible to mouse cytomegalovirus infection and show impaired infection-induced secretion of IFN-α/β and natural killer cell activation. We also demonstrate that both the Toll-like receptor (TLR) 9 → MyD88 and TLR3 → Trif signaling pathways are activated in vivo on viral inoculation, and that each pathway contributes to innate defense against systemic viral infection. Whereas both pathways lead to type I IFN production, neither pathway offers full protection against mouse cytomegalovirus infection in the absence of the other. The Tlr9CpG1 mutation alters a leucine-rich repeat motif and lies within a receptor domain that is conserved within the evolutionary cluster encompassing TLRs 7, 8, and 9. In other TLRs, including three mouse-specific TLRs described in this paper, the affected region is not represented. The phenotypic effect of the Tlr9CpG1 allele thus points to a critical role for TLR9 in viral sensing and identifies a vulnerable amino acid within the ectodomain of three TLR proteins, essential for a ligand response.
National Acad Sciences