Assessment of the subcellular localization of the herpes simplex virus structural protein VP22 in the absence of other viral gene products

• Published in: Virus research Vol. 81; no. 1; pp. 57 - 68
• Main Authors: Blouin, Amanda, Blaho, John A
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 04.12.2001
• Subjects: Animals; Cell Nucleus - metabolism; Cercopithecus aethiops; Fixing conditions; Fluorescent Antibody Technique, Indirect - methods; Herpes simplex virus 1; Herpes simplex virus type 1; Herpesvirus 1, Human - metabolism; Nuclear versus cytoplasmic localization; Plasmids - genetics; Subcellular Fractions - metabolism; Tissue Fixation - methods; Transfection; Vero Cells; Viral Proteins - metabolism; Viral Structural Proteins - genetics; Viral Structural Proteins - metabolism; VP22; VP22 protein; VP22; Fixing conditions; Herpes simplex virus type 1; Nuclear versus cytoplasmic localization
• ISSN: 0168-1702; 1872-7492
• DOI: 10.1016/S0168-1702(01)00355-0

We previously demonstrated that the herpes simplex virus type 1 (HSV-1) structural protein VP22 exists in the cytoplasm early in infection and migrates to and accumulates in the nucleus late in infection (J. Virol. 73(8) (1999) 6769). The goal of this study is to document the behavior of VP22 in cells in the absence of other viral polypeptides. We characterized the effects of various indirect immunofluorescence sample preparation conditions on the localization of VP22 in cells and have determined the following. (i) Fixing with formaldehyde and permeabilizing with acetone maintains the structure of microtubules in cells, in as much as we observed classic microtubule organizing centers. (ii) Acetone or methanol alone did not completely fix the cells. (iii) Triton X-100 decreased tubulin immunofluorescence signals in our system. (iv) VP22 predominated in the nucleus of cells that were fixed with formaldehyde. Based on our results, we conclude the following. (v) Due to the partial fixation by acetone or methanol alone, microtubules form diffuse irregular shapes. (vi) VP22 is detected in the cytoplasm of cells fixed with acetone or methanol only due to its seepage from the nucleus. Taken together, these findings indicate that (vii) the nuclear localization of VP22 does not require additional viral factors.