J Gen Virol Try Microbiology Online
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 72 (1991), 1985-1989; DOI 10.1099/0022-1317-72-8-1985
© 1991 Society for General Microbiology

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Darlington, J.
Right arrow Articles by Emery, V. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Darlington, J.
Right arrow Articles by Emery, V. C.
Agricola
Right arrow Articles by Darlington, J.
Right arrow Articles by Emery, V. C.

Use of the Polymerase Chain Reaction to Analyse Sequence Variation Within a Major Neutralizing Epitope of Glycoprotein B (gp58) in Clinical Isolates of Human Cytomegalovirus

Jonathan Darlington, Michael Super, Kamalesh Patel, Jane E. Grundy, Paul D. Griffiths and Vincent C. Emery

Division of Communicable Diseases, Royal Free Hospital School of Medicine, Rowland Hill Street, Hampstead, London NW3 2QG, U.K.

The heterogeneity of low passage human cytomegalovirus (HCMV) strains was determined by HindIII typing of 28 clinical isolates from transplant patients. These data have shown that, in general, each patient's strain has a unique restriction profile, usually comprising combinations of HindIII sites present in one or more of the tissue culture-adapted strains AD169, Towne and Davis. To map sequence changes in a more refined manner we performed detailed analyses of 33 low passage clinical isolates, including those aforementioned, analysing a sequence within glycoprotein B containing a major neutralizing epitope. A 149 bp sequence containing the epitope (amino acids 608 to 625) was amplified using the polymerase chain reaction, the products were cloned and their DNA sequence was determined. Comparison of the DNA and deduced amino acid sequences with those of HCMV strain AD169 revealed that there was a high degree of conservation of the epitope between the 33 clinical isolates. However 10 of the isolates possessed silent mutations and three isolates contained mutations producing amino acid changes within the neutralizing epitope. The possible functional significance of these changes is discussed.

Received 28 August 1990; accepted 8 May 1991.


This article has been cited by other articles:


Home page
J. Virol.Home page
R. Holtappels, C. O. Simon, M. W. Munks, D. Thomas, P. Deegen, B. Kuhnapfel, T. Daubner, S. F. Emde, J. Podlech, N. K. A. Grzimek, et al.
Subdominant CD8 T-Cell Epitopes Account for Protection against Cytomegalovirus Independent of Immunodomination
J. Virol., June 15, 2008; 82(12): 5781 - 5796.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
J. Nugent, I. Birch-Machin, K. C. Smith, J. A. Mumford, Z. Swann, J. R. Newton, R. J. Bowden, G. P. Allen, and N. Davis-Poynter
Analysis of Equid Herpesvirus 1 Strain Variation Reveals a Point Mutation of the DNA Polymerase Strongly Associated with Neuropathogenic versus Nonneuropathogenic Disease Outbreaks.
J. Virol., April 1, 2006; 80(8): 4047 - 4060.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
M. Franti, J.-T. Aubin, G. De Saint-Maur, H. Kosuge, K. Yamanishi, A. Gautheret-Dejean, A. Garbarg-Chenon, J.-M. Huraux, and H. Agut
Immune Reactivity of Human Sera to the Glycoprotein B of Human Herpesvirus 7
J. Clin. Microbiol., January 1, 2002; 40(1): 44 - 51.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
A. M. Kearns, B. Draper, W. Wipat, A. J. L. Turner, J. Wheeler, R. Freeman, J. Harwood, F. K. Gould, J. H. Dark, L. Schaade, et al.
LightCycler-Based Quantitative PCR for Detection of Cytomegalovirus in Blood, Urine, and Respiratory Samples
J. Clin. Microbiol., June 1, 2001; 39(6): 2364 - 2365.
[Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
V. C. Emery and P. D. Griffiths
Prediction of cytomegalovirus load and resistance patterns after antiviral chemotherapy
PNAS, June 14, 2000; (2000) 140123497.
[Abstract] [Full Text]


Home page
J. Clin. Microbiol.Home page
R. N. Jones, M. L. Neale, B. Beattie, D. Westmoreland, and J. D. Fox
Development and Application of a PCR-Based Method Including an Internal Control for Diagnosis of Congenital Cytomegalovirus Infection
J. Clin. Microbiol., January 1, 2000; 38(1): 1 - 6.
[Abstract] [Full Text]


Home page
J. Gen. Virol.Home page
A. Speckner, D. Glykofrydes, M. Ohlin, and M. Mach
Antigenic domain 1 of human cytomegalovirus glycoprotein B induces a multitude of different antibodies which, when combined, results in incomplete virus neutralization
J. Gen. Virol., August 1, 1999; 80(8): 2183 - 2191.
[Abstract] [Full Text]


Home page
J. Exp. Med.Home page
V. C. Emery, A. V. Cope, E. F. Bowen, D. Gor, and P. D. Griffiths
The Dynamics of Human Cytomegalovirus Replication In Vivo
J. Exp. Med., July 19, 1999; 190(2): 177 - 182.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
B. Zweygberg Wirgart, M. Brytting, A. Linde, B. Wahren, and L. Grillner
Sequence Variation within Three Important Cytomegalovirus Gene Regions in Isolates from Four Different Patient Populations
J. Clin. Microbiol., December 1, 1998; 36(12): 3662 - 3669.
[Abstract] [Full Text]


Home page
Proc. Natl. Acad. Sci. USAHome page
V. C. Emery and P. D. Griffiths
Prediction of cytomegalovirus load and resistance patterns after antiviral chemotherapy
PNAS, July 5, 2000; 97(14): 8039 - 8044.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1991 by the Society for General Microbiology.