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Dissecting Host-virus Interaction in Lytic Replication of a Model Herpesvirus
Published on: October 7, 2011
Comparative pathology of infections with baboon and African green monkey alpha-herpesviruses in mice
J W Ritchey1, K A Ealey, M E Payton
1Department of Veterinary Pathobiology, College of Veterinary Medicine, Oklahoma State University, Stillwater, OK, 74078, USA.
Abstract:
The comparative pathology of Herpesvirus papio 2 (HVP2) of baboons and SA8 virus of African green monkeys relative to that of herpes simplex virus (HSV1) of man was investigated in young adult mice inoculated intramuscularly and observed for 21 days. The 50% infectious dose (ID(50)) for HVP2 was approximately 10(2.0) plaque-forming units (PFU), while the ID(50) for HSV1 and SA8 was 10(2.5) and 10(3.8), respectively. There were marked differences in the ability of these three viruses to invade the central nervous system (CNS) and cause clinical neurological disease. HSV1 produced neurological signs in a few animals given 10(6)PFU, but SA8 did not. In contrast, HVP2 readily invaded the CNS and produced fatal disease with doses as low as 10(2)PFU. Two isolates of HVP2 tested had a 50% CNS disease dose (CNSD(50)) of 10(2.5) and 10(3.0)PFU and an LD(50) of 10(3.8) and 10(4.3)PFU, respectively. Histopathological examination of tissue from HVP2-infected mice revealed severe lesions of inflammation and necrosis in the central, peripheral and autonomic nervous systems, as well as of other tissues including skin, adrenal glands and the gastrointestinal tract. Viral antigens were detected immunohistochemically in lesions. This study showed that while both HVP2 and SA8 could infect mice, there were marked differences in the ability of these two closely related viruses to cause clinical disease and CNS lesions. This murine model may prove useful in the investigation of viral or host determinants responsible for the varying neurovirulence of these simian alpha-herpesviruses.
Insights
Herpesvirus papio 2 (HVP2) readily invades the central nervous system (CNS) in mice, causing fatal disease and severe lesions. This contrasts with SA8 and herpes simplex virus (HSV1), highlighting HVP2
Area of Science:
- Comparative pathology
- Virology
- Neuroscience
Background:
- Herpesvirus papio 2 (HVP2) and SA8 virus are simian alpha-herpesviruses.
- Herpes simplex virus type 1 (HSV1) is a human pathogen.
- Understanding the neurovirulence of these viruses is crucial.
Purpose of the Study:
- To compare the pathogenicity and neurovirulence of HVP2, SA8, and HSV1 in a murine model.
- To investigate the ability of these viruses to invade the central nervous system (CNS).
- To establish a murine model for studying simian alpha-herpesvirus neurovirulence.
Main Methods:
- Young adult mice were inoculated intramuscularly with HVP2, SA8, or HSV1.
- Infectious doses (ID50), CNS disease doses (CNSD50), and lethal doses (LD50) were determined.
- Histopathological examination and immunohistochemistry were used to assess tissue damage and viral antigen presence.
Main Results:
- HVP2 demonstrated higher infectivity and readily invaded the CNS, causing fatal disease.
- HSV1 caused mild neurological signs in some mice, while SA8 did not induce neurological disease.
- HVP2 infection resulted in severe inflammation and necrosis in the nervous system and other organs.
Conclusions:
- HVP2 exhibits significant neurovirulence in mice, unlike SA8 and HSV1.
- Marked differences exist in the neuroinvasive and disease-causing capabilities of HVP2 and SA8.
- The developed murine model is valuable for investigating viral and host factors influencing simian alpha-herpesvirus neurovirulence.

