TY - JOUR
T1 - High-resolution immuno-scanning electron microscopy using a non-coating method
T2 - Study of herpes simplex virus glycoproteins on the surface of virus particles and infected cells
AU - Padilla, Jorge A.
AU - Uno, Fumio
AU - Yamada, Masao
AU - Namba, Hikaru
AU - Nii, Shiro
PY - 1997
Y1 - 1997
N2 - The expression of two glycoproteins, i.e. glycoprotein C (gC) and glycoprotein D (gD), of herpes simplex virus type 1 (HSV-1) on the surface of extracellular particles of this virus was examined by immuno-scanning electron microscopy. Scanning electron microscopy specimens of infected cells immuno-labelled against the glycoproteins with colloidal gold particles were prepared by a conventional coating and a non-coating method. Surface ultrastructure of infected cells and gold particles were observed more clearly with specimens prepared by the non-coating method. The appearance of virus particles in association with glycoprotein expression on these particles and on the surface of infected cells was then studied. Progeny virus particles began to appear 6 h after infection, increased in number as the infection proceeded, and covered most of the cell surface by 16 h. Six to 24 h after the infection, the labelling density for each glycoprotein on virus particles remained constant. The labelling density for gD was always higher than that for gC. The patch-like distribution of gold-labelling against gD was often detected on infected cell monolayers at the exponential and late stage of one cycle of virus growth. The labelling density for gD on virus particles was the highest on these produced in Vero and L-929 cells, moderate in MRC-5, BHK-21 and FL cells, and the lowest in HEp-2 cells.
AB - The expression of two glycoproteins, i.e. glycoprotein C (gC) and glycoprotein D (gD), of herpes simplex virus type 1 (HSV-1) on the surface of extracellular particles of this virus was examined by immuno-scanning electron microscopy. Scanning electron microscopy specimens of infected cells immuno-labelled against the glycoproteins with colloidal gold particles were prepared by a conventional coating and a non-coating method. Surface ultrastructure of infected cells and gold particles were observed more clearly with specimens prepared by the non-coating method. The appearance of virus particles in association with glycoprotein expression on these particles and on the surface of infected cells was then studied. Progeny virus particles began to appear 6 h after infection, increased in number as the infection proceeded, and covered most of the cell surface by 16 h. Six to 24 h after the infection, the labelling density for each glycoprotein on virus particles remained constant. The labelling density for gD was always higher than that for gC. The patch-like distribution of gold-labelling against gD was often detected on infected cell monolayers at the exponential and late stage of one cycle of virus growth. The labelling density for gD on virus particles was the highest on these produced in Vero and L-929 cells, moderate in MRC-5, BHK-21 and FL cells, and the lowest in HEp-2 cells.
KW - Glycoprotein C
KW - Glycoprotein D
KW - Herpes simplex virus
KW - Immuno-gold-labelling
KW - Non-coating method
KW - Ultrahigh-resolution SEM
UR - http://www.scopus.com/inward/record.url?scp=0031005599&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0031005599&partnerID=8YFLogxK
U2 - 10.1093/oxfordjournals.jmicro.a023505
DO - 10.1093/oxfordjournals.jmicro.a023505
M3 - Article
C2 - 9180032
AN - SCOPUS:0031005599
SN - 2050-5698
VL - 46
SP - 171
EP - 180
JO - Microscopy (Oxford, England)
JF - Microscopy (Oxford, England)
IS - 2
ER -