A NK complex-linked locus restricts the spread of herpes simplex virus type 1 in the brains of C57BL/6 mice

L.F. Kastrukoff, A.S. Lau, F. Takei, F.R. Carbone, Tony Scalzo

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15 Citations (Scopus)


© 2015 Australasian Society for Immunology Inc. All rights reserved. The most frequent cause of sporadic viral encephalitis in western countries is Herpes simplex virus (HSV). Despite treatment, mortality rates reach 20-30% while survivors often suffer from significant morbidity. In mice, resistance to lethal Herpes simplex encephalitis (HSE) is multifactorial and influenced by mouse and virus strain as well as route of infection. The ability to restrict viral spread in the brain is one factor contributing to resistance. After infection of the oral mucosa with HSV type 1 (HSV-1), virus spreads throughout the brains of susceptible strains but is restricted in resistant C57BL/6 mice. To further investigate restriction of viral spread in the brain, mendelian analysis was combined with studies of congenic, intra-natural killer complex (intra-NKC) recombinant and antibody-depleted mice. Results from mendelian analysis support the restriction of viral spread as a dominant trait and consistent with a single gene effect. In congenic mice, the locus maps to the NKC on chromosome 6 and is provisionally termed Herpes Resistance Locus 2 (Hrl2). In intra-NKC recombinants, the locus is further mapped to the segment Cd69 through D6Wum34; a different location from previously identified loci (Hrl and Rhs1) also associated with HSV-1 infection. Studies with antibody-depleted mice indicate the effect of this locus is mediated by NK1.1 + expressing cells. This model increases our knowledge of lethal HSE, which may lead to new treatment options.
Original languageEnglish
Pages (from-to)877-884
JournalImmunology and Cell Biology
Issue number10
Publication statusPublished - 2015


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