Herpes simplex virus spreads rapidly in human foreskin, partly driven by chemokine-induced redistribution of Nectin-1 on keratinocytes

PLoS Pathog. 2024 Jun 10;20(6):e1012267. doi: 10.1371/journal.ppat.1012267. eCollection 2024 Jun.

Abstract

HSV infects keratinocytes in the epidermis of skin via nectin-1. We established a human foreskin explant infection model to investigate HSV entry and spread. HSV1 entry could only be achieved by the topical application of virus via high density microarray projections (HD-MAPs) to the epidermis, which penetrated beyond one third of its thickness, simulating in vivo microtrauma. Rapid lateral spread of HSV1 to a mean of 13 keratinocytes wide occurred after 24 hours and free virus particles were observed between keratinocytes, consistent with an intercellular route of spread. Nectin-1 staining was markedly decreased in foci of infection in the epidermis and in the human keratinocyte HaCaT cell line. Nectin-1 was redistributed, at the protein level, in adjacent uninfected cells surrounding infection, inducible by CCL3, IL-8 (or CXCL8), and possibly CXCL10 and IL-6, thus facilitating spread. These findings provide the first insights into HSV1 entry and spread in human inner foreskin in situ.

MeSH terms

  • Cell Adhesion Molecules / metabolism
  • Chemokines* / metabolism
  • Foreskin* / cytology
  • Foreskin* / virology
  • Herpes Simplex* / metabolism
  • Herpes Simplex* / virology
  • Herpesvirus 1, Human* / physiology
  • Humans
  • Keratinocytes* / metabolism
  • Keratinocytes* / virology
  • Male
  • Nectins* / metabolism
  • Virus Internalization

Substances

  • Nectins
  • NECTIN1 protein, human
  • Chemokines
  • Cell Adhesion Molecules

Grants and funding

A.L.C. received project grant 1163748 and investigator grant 1177942 from the National Health and Medical Research Council of Australia, URL: https://www.nhmrc.gov.au. H.R. received a Research Training Stipend from The University of Sydney. The Westmead Scientific Platforms was supported by the Westmead Research Hub, the Westmead Institute for Medical Research, the Cancer Institute New South Wales, the National Health and Medical Research Council and the Ian Potter Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.