Activation of checkpoint kinase 2 is critical for herpes simplex virus type 1 replication in corneal epithelium.

ABSTRACT:

Background/aims

Herpes simplex virus (HSV) type I keratitis remains a leading cause of corneal morbidity, despite the availability of effective antiviral drugs. Improved understanding of virus-host interactions at the level of the host DNA damage response (DDR), a known factor in the development of HSV-1 keratitis, may shed light on potential new therapeutic targets. This report examines the role of checkpoint kinase 2 (Chk2), a DDR mediator protein, in corneal epithelial HSV-1 infection.

Methods

A small-molecule inhibitor of Chk2 (Chk2 inhibitor II) was applied to HSV-1-infected cultured human corneal epithelial cells (hTCEpi and HCE) as well as to explanted and organotypically cultured human and rabbit corneas. Infection levels were assessed by plaque assay and real-time P

SUBMITTER: Alekseev O 

PROVIDER: S-EPMC4380435 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature