Defective entry of herpes simplex virus types 1 and 2 into porcine cells and lack of infection in infant pigs indicate species tropism

• Published in: Journal of general virology Vol. 76; no. 9; pp. 2375 - 2379
• Main Authors: Subramanian, G, LeBlac, R.A, Wardley, R.C, Fuller, A.O
• Format: Journal Article
• Language: English
• Published: England Soc General Microbiol 01-09-1995
• Subjects: Animals; Animals, Newborn; Antibodies, Viral - analysis; Cell Line; cell lines; Cytopathogenic Effect, Viral; DNA, Viral - analysis; embryo (animal); experimental infection; experimental infections; herpes simplex virus; herpes simplex virus 1; herpes simplex virus 2; Herpesvirus 1, Human - pathogenicity; Herpesvirus 1, Human - physiology; Herpesvirus 2, Human - pathogenicity; Herpesvirus 2, Human - physiology; Humans; Lung - cytology; Lung - virology; lungs; Male; Membrane Fusion; neonates; pathogenicity; Receptors, Virus - metabolism; species differences; Swine; symptoms; testes; Testis - cytology; Testis - virology
• ISSN: 0022-1317; 1465-2099
• DOI: 10.1099/0022-1317-76-9-2375

We have determined if a defect at entry of the human pathogen herpes simplex virus type 1 (HSV-1) into cultured porcine cells extends to HSV-2 and if the poor susceptibility of porcine cells for these viruses is indicative of in vivo species tropism. HSV-1 replicates poorly in swine testis (ST) and other porcine cells which lack a functional non-heparan sulphate receptor(s) required for virus entry. By several criteria, ST cells resist infection by either HSV-1 or HSV-2. Infection can be restored if normal entry is bypassed by PEG-mediated virion-cell membrane fusion. Neither HSV serotype infects, replicates or produces clinical symptoms in infant pigs. No virus was isolated from any of multiple sites and seroconversion did not occur. The in vitro defect in porcine cells blocking HSV entry correlates with, and is likely to be at least partly responsible for, in vivo resistance of pigs to infection.