Major Virion Tegument Protein VP22 Targets Nuclear Matrix and Chromatin upon Entry into Cells during Productive Herpes Simplex Virus 1 Infection

Author:

Chi Isabella12,Blaho John A.3

Affiliation:

1. Department of Microbiology, Mount Sinai School of Medicine, New York, NY 10029, USA

2. Medical Diagnostic Laboratories LLC, Hamilton, NJ 08690, USA

3. Innovation and Applied Research Division, City University of New York, New York, NY 10031, USA

Abstract

HSV-1 major tegument protein VP22 is present in multiple subcellular locations in the late stages of productive viral infection. We initially performed a detailed time course experiment and observed that VP22 was detected in nuclear and nuclear matrix fractions as early as 4 hpi. The goal was to determine the fate of virion-derived incoming VP22, and we report the following: (i) VP22 was detected in nuclear matrix fractions 1 hpi. (ii) In the presence of cycloheximide (CHX), VP22 was present in the nuclear matrix 1–6 hpi, demonstrating the stability of the protein. (iii) The nuclear matrix targeting of VP22 occurred in infected Vero, HEp-2, and human mammary epithelial (HME) cells and following synchronized infection. Based on these results, we conclude that (iv) VP22 targets the nuclear matrix and chromatin upon entry into cells during productive HSV-1 infection.

Publisher

MDPI AG

Reference65 articles.

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5. Characterization of the herpes simplex virion-associated factor responsible for the induction of alpha genes;Batterson;J. Virol.,1983

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