Alzheimer's disease-associated β-amyloid does not protect against herpes simplex virus 1 infection in the mouse brain

Alzheimer's disease (AD) is a devastating fatal neurodegenerative disease. An alternative to the amyloid cascade hypothesis is that a viral infection is key to the etiology of late-onset AD, with beta-amyloid (A beta) peptides playing a protective role. In the current study, young 5XFAD mice that overexpress mutant human amyloid precursor protein with the Swedish, Florida, and London familial AD mutations were infected with one of two strains of herpes simplex virus 1 (HSV-1), 17syn+ and McKrae, at three different doses. Contrary to previous work, 5XFAD genotype failed to protect mice against HSV-1 infection. The region- and cell-specific tropisms of HSV-1 were not affected by the 5XFAD genotype, indicating that host-pathogen interactions were not altered. Seven- to ten-month-old 5XFAD animals in which extracellular A beta aggregates were abundant showed slightly better survival rate relative to their wild-type (WT) littermates, although the difference was not statistically significant. In these 5XFAD mice, HSV-1 replication centers were partially excluded from the brain areas with high densities of A beta aggregates. A beta aggregates were free of HSV-1 viral particles, and the limited viral invasion to areas with a high density of A beta aggregates was attributed to phagocytic activity of reactive microglia. In the oldest mice (12-15 months old), the survival rate did not differ between 5XFAD and WT littermates. While the current study questions the antiviral role of A beta, it neither supports nor refutes the viral etiology hypothesis of late-onset AD.

Automated summary

The study found that the 5XFAD genotype did not protect mice against HSV-1 infection, and the tropisms of HSV-1 were not affected by the genotype. 5XFAD mice with abundant A β aggregates showed slightly better survival rates. Additionally, HSV-1 viral particles were excluded from brain areas with high densities of A β aggregates, partially due to the phagocytic activity of reactive microglia.