A growth and latency compromised herpes simplex virus type 2 mutant (ICP10Delta PK) has prophylactic and therapeutic protective activity in guinea pigs

A growth compromised herpes simplex virus type 2 (HSV-2) mutant which is de leted in the PK domain of the large subunit of ribonucleotide reductase (IC P10 Delta PK) protects from fatal HSV-2 challenge in the mouse model (Aurel ian L, Kokuba H, Smith CC. Vaccine potential of a Herpes Simplex Virus type 2 mutant deleted in the PK domain of the large subunit of ribonucleotide r eductase (ICP10). Vaccine 1999;17:1951-1963). Here we report the results of our studies with ICP10 Delta PK in the guinea pig model of recurrent HSV-2 disease. ICP10 Delta PK was also compromised for growth and disease causat ion in this model. It was not isolated from latently infected ganglia by ex plant co-cultivation. The proportions of latently infected ganglia were sig nificantly lower for ICP10 Delta PK than HSV-2 [3/25 (12%) and 7/10 (70%), respectively]. Similar results were obtained for the levels of viral DNA (8 x 10(3) and 2 x 10(5) molecules/ganglion for ICP10 Delta PK and HSV-2, res pectively]. ICP10 Delta PK immunization caused a significant (P less than o r equal to 0.001) decrease in the proportion of animals with primary [1/14 (6%) and 16/16 (100%) for ICP10 Delta PK and PBS, respectively) and recurre nt [1/14 (6%) and 11/14(79%) for ICP10 Delta PK and PBS, respectively) HSV- 2 skin lesions. It also protected from genital HSV-2 disease [1/10 and 10/1 0 for ICP10 Delta PK and PBS, respectively] and decreased the severity of t he lesions in both models. Quantitative PCR (Q-PCR) with primers that disti nguish. between HSV-2 and ICP10 Delta PK indicated that immunization reduce d the proportion of ganglia positive for HSV-2 DNA [8/25 (32%) and 7/10 (70 %) for ICP10 Delta PK and PBS, respectively) and its levels [3 x 10(3) and 2 x 10(5) molecules/ganglion for ICP10 Delta PK and PBS, respectively]. The proportion of HSV-2 infected animals with recurrent disease was also signi ficantly (P less than or equal to 0.001) decreased by immunization with ICP 10 Delta PK [1/15 (7%) and 11/14 (79%) with recurrent disease for ICP10 Del ta PK and PBS, respectively], suggesting that ICP10 Delta PK has prophylact ic and therapeutic activity in the guinea pig. (C) 2001 Elsevier Science Lt d. All rights reserved.