No conflicts of interest were declared.
Herpes simplex virus type 1 DNA is located within Alzheimer's disease amyloid plaques†
Version of Record online: 18 SEP 2008
Copyright © 2008 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
The Journal of Pathology
Volume 217, Issue 1, pages 131–138, January 2009
How to Cite
Wozniak, M., Mee, A. and Itzhaki, R. (2009), Herpes simplex virus type 1 DNA is located within Alzheimer's disease amyloid plaques. J. Pathol., 217: 131–138. doi: 10.1002/path.2449
- Issue online: 5 DEC 2008
- Version of Record online: 18 SEP 2008
- Accepted manuscript online: 18 SEP 2008 12:00AM EST
- Manuscript Accepted: 5 SEP 2008
- Manuscript Revised: 6 AUG 2008
- Manuscript Received: 24 JUN 2008
- Alzheimer's disease;
- herpes simplex encephalitis;
- herpes simplex virus type 1;
- amyloid plaques;
- apolipoprotein E;
- in situ polymerase chain reaction;
- thioflavin S staining;
The brains of Alzheimer's disease sufferers are characterized by amyloid plaques and neurofibrillary tangles. However, the cause(s) of these features and those of the disease are unknown, in sporadic cases. We previously showed that herpes simplex virus type 1 is a strong risk factor for Alzheimer's disease when in the brains of possessors of the type 4 allele of the apolipoprotein E gene (APOE-ε4), and that β-amyloid, the main component of plaques, accumulates in herpes simplex virus type 1-infected cell cultures and mouse brain. The present study aimed to elucidate the relationship of the virus to plaques by determining their proximity in human brain sections. We used in situ polymerase chain reaction to detect herpes simplex virus type 1 DNA, and immunohistochemistry or thioflavin S staining to detect amyloid plaques. We discovered a striking localization of herpes simplex virus type 1 DNA within plaques: in Alzheimer's disease brains, 90% of the plaques contained the viral DNA and 72% of the DNA was associated with plaques; in aged normal brains, which contain amyloid plaques at a lower frequency, 80% of plaques contained herpes simplex virus type 1 DNA but only 24% of the viral DNA was plaque-associated (p < 0.001). We suggest that this is because in aged normal individuals, there is a lesser production and/or greater removal of β-amyloid (Aβ), so that less of the viral DNA is seen to be associated with Aβ in the brain. Our present data, together with our finding of Aβ accumulation in herpes simplex virus type 1-infected cells and mouse brain, suggest that this virus is a major cause of amyloid plaques and hence probably a significant aetiological factor in Alzheimer's disease. They point to the usage of antiviral agents to treat the disease and possibly of vaccination to prevent it. Copyright © 2008 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.