Acyclovir Sensitivity and Neurovirulence of Herpes Simplex Virus Type 1 with Amino Acid Substitutions in the Viral Thymidine Kinase Gene, Which Were Detected in the Patients with Intractable Herpes Simplex Encephalitis Previously Reported

Jpn J Infect Dis. 2018 Sep 21;71(5):343-349. doi: 10.7883/yoken.JJID.2018.176. Epub 2018 May 31.

Abstract

Several cases of herpes simplex encephalitis (HSE) caused by acyclovir (ACV)-resistant herpes simplex virus type 1 (HSV-1) have been reported. Amino acid substitutions of R41H, Q125H, and A156V in the viral thymidine kinase (vTK) gene have been reported to confer ACV resistance. Recombinant HSV-1 clones, containing each amino acid substitution in the vTK gene, were generated using the bacterial artificial chromosome system. A recombinant HSV-1 with the Q125H substitution showed ACV resistance while the R41H or A156V substitutions were ACV-sensitive. Furthermore, the Q125H recombinant HSV-1 was less virulent than the repaired virus, but it maintained neurovirulence in mice at relatively high levels. Substitution of Q125H, which was detected in the neonatal HSE patient, conferred ACV resistance, but the substitutions of R41H and A156V, which were detected in immunocompetent adult HSE patients, did not. This suggests that HSE caused by ACV-resistant HSV-1 might be a very rare event to occur during the course of ACV treatment in immunocompetent patients. Showing resistance to ACV treatment does not always indicate emergence of ACV-resistant HSV-1 in HSE patients.

Keywords: acyclovir; herpes simplex encephalitis; herpes simplex virus type 1; resistance; thymidine kinase.

MeSH terms

  • Acyclovir / pharmacology*
  • Adult
  • Aged
  • Amino Acid Substitution*
  • Animals
  • Antiviral Agents / pharmacology*
  • Cell Line
  • Chromosomes, Artificial, Bacterial
  • Disease Models, Animal
  • Drug Resistance, Viral
  • Encephalitis, Herpes Simplex / pathology
  • Encephalitis, Herpes Simplex / virology*
  • Female
  • Herpesvirus 1, Human / drug effects*
  • Herpesvirus 1, Human / genetics
  • Herpesvirus 1, Human / isolation & purification
  • Herpesvirus 1, Human / pathogenicity*
  • Humans
  • Infant, Newborn
  • Male
  • Mice, Inbred ICR
  • Microbial Sensitivity Tests
  • Middle Aged
  • Mutant Proteins / genetics
  • Reverse Genetics
  • Thymidine Kinase / genetics*
  • Virulence
  • Virulence Factors / genetics

Substances

  • Antiviral Agents
  • Mutant Proteins
  • Virulence Factors
  • Thymidine Kinase
  • Acyclovir