RRC ID 72098
著者 Wang S, Hou F, Yao YF, Pan D.
タイトル Efficient establishment of reactivatable latency by an acyclovir-resistant herpes simplex virus 1 thymidine kinase substitution mutant with reduced neuronal replication.
ジャーナル Virology
Abstract Herpes simplex virus 1 causes recurrent diseases by reactivating from latency, which requires the viral thymidine kinase (TK) gene. An acyclovir-resistant mutation in TK, V204G, was previously repeatedly identified in a patient with recurrent herpetic keratitis. We found that compared with its parental strain KOS, a laboratory-derived V204G mutant virus was impaired in replication in cultured neurons despite little defect in non-neuronal cells. After corneal inoculation of mice, V204G exhibited defects in ocular replication that were modest over the first three days but severe afterward. Acute replication of V204G in trigeminal ganglia was significantly impaired. However, V204G established latency with viral loads as high as KOS and reactivated with high frequency albeit reduced kinetics. Acyclovir treatment that drastically decreased ocular and ganglionic replication of KOS had little effect on V204G. Thus, despite reduced neuronal replication due to impaired TK activity, this clinically relevant drug-resistant mutant can efficiently establish reactivatable latency.
巻・号 556
ページ 140-148
公開日 2021-4-1
DOI 10.1016/j.virol.2021.01.016
PII S0042-6822(21)00032-5
PMID 33631413
MeSH Animals Cell Line, Tumor Chlorocebus aethiops Epithelial Cells Herpesvirus 1, Human* / genetics Herpesvirus 1, Human* / pathogenicity Humans Keratitis, Herpetic / virology* Mice Neurons / virology* Vero Cells Virus Activation Virus Replication
IF 2.819
リソース情報
ヒト・動物細胞 HCE-T(RCB2280)