Differences in the Likelihood of Acyclovir Resistance-Associated Mutations in the Thymidine Kinase Genes of Herpes Simplex Virus 1 and Varicella-Zoster Virus

Acyclovir (ACV) resistance-associated mutations in two recombinant herpes simplex virus 1 (HSV-1) clones were compared. Recombinant HSV-1 lacking its thymidine kinase (TK) and expressing varicella-zoster virus (VZV) TK ectopically had no mutations in the VZV TK gene. Acyclovir (ACV) resistance-assoc...

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Published inAntimicrobial agents and chemotherapy Vol. 63; no. 5
Main Authors Fujii, Hikaru, Harada, Shizuko, Yoshikawa, Tomoki, Yamada, Souichi, Omura, Natsumi, Shibamura, Miho, Inagaki, Takuya, Kato, Hirofumi, Fukushi, Shuetsu, Saijo, Masayuki
Format Journal Article
LanguageEnglish
Published United States American Society for Microbiology 01.05.2019
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Summary:Acyclovir (ACV) resistance-associated mutations in two recombinant herpes simplex virus 1 (HSV-1) clones were compared. Recombinant HSV-1 lacking its thymidine kinase (TK) and expressing varicella-zoster virus (VZV) TK ectopically had no mutations in the VZV TK gene. Acyclovir (ACV) resistance-associated mutations in two recombinant herpes simplex virus 1 (HSV-1) clones were compared. Recombinant HSV-1 lacking its thymidine kinase (TK) and expressing varicella-zoster virus (VZV) TK ectopically had no mutations in the VZV TK gene. In contrast, recombinant HSV-1 expressing HSV-1 TK ectopically harbored mutations in the HSV-1 TK gene. These results suggest that the relatively low frequency of ACV-resistant VZV is a consequence of the characteristics of the TK gene.
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Citation Fujii H, Harada S, Yoshikawa T, Yamada S, Omura N, Shibamura M, Inagaki T, Kato H, Fukushi S, Saijo M. 2019. Differences in the likelihood of acyclovir resistance-associated mutations in the thymidine kinase genes of herpes simplex virus 1 and varicella-zoster virus. Antimicrob Agents Chemother 63:e00017-19. https://doi.org/10.1128/AAC.00017-19.
H.F. and S.H. contributed equally to this study.
ISSN:0066-4804
1098-6596
1098-6596
DOI:10.1128/AAC.00017-19