Detection and quantitation of human immunodeficiency virus type-1 particles by confocal microscopy

被引:7
作者
Bhattacharya, B
Weiss, RA
Davis, C
Holmes, H
Hockley, D
Fassati, A
机构
[1] Royal Free & UCL, Sch Med, Windeyer Inst Med Sci, Dept Immunol & Mol Pathol, London W1T 4JF, England
[2] Natl Inst Biol Stand & Controls, Blanche Lane, Div Retrovirol, Potters Bar EN6 3QG, Herts, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
HIV-1; virions quantitation; visualization; confocal microscopy;
D O I
10.1016/j.jviromet.2004.03.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A method is described to visualise directly human immunodeficiency virus type-1 (HIV-1) particles. HIV-1 containing samples were adsorbed onto a plastic surface and doubly labeled with antibodies specific for viral proteins and sensitive nucleic acids dyes. Laser scanning confocal microscopy detected co-localization of viral proteins and nucleic acids, thus allowing specific identification of HIV. Using this technique, we have quantified eight different HIV-1 sub-types and three HIV-1 groups in tissue culture supernatants from infected peripheral blood mononuclear cells (PBMCs). Confocal counts correlated well with electron microscopy (EM) counts and HIV-1 RNA loads as determined by quantitative PCR. Confocal microscopy may prove to be a simple alternative to electron microscopy for virus identification and quantitation. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 21
页数:9
相关论文
共 27 条
[1]   Use of the confocal microscope to determine polyomavirus recombinant capsid-like particle entry into mouse 3T6 cells [J].
An, K ;
Lovgren, TR ;
Tilley, MB ;
Consigli, RA .
JOURNAL OF VIROLOGICAL METHODS, 2000, 84 (02) :153-159
[2]  
[Anonymous], 1997, METHOD ENZYMOL
[3]  
[Anonymous], WHOBS031961
[4]   Development of multiplexed nucleic acid testing for human immunodeficiency virus type 1 and hepatitis C virus [J].
Cleland, A ;
Davis, C ;
Adams, N ;
Lycett, C ;
Jarvis, LM ;
Holmes, H ;
Simmonds, P .
VOX SANGUINIS, 2001, 81 (02) :93-101
[5]   Diverse HIV-1 genetic subtypes in UK [J].
Clewley, JP ;
Arnold, C ;
Barlow, KL ;
Grant, PR ;
Parry, JV .
LANCET, 1996, 347 (9013) :1487-1487
[6]   Evaluation of performance of the Gen-Probe human immunodeficiency virus type 1 viral load assay using primary subtype A, C, and D isolates from Kenya [J].
Emery, S ;
Bodrug, S ;
Richardson, BA ;
Giachetti, C ;
Bott, MA ;
Panteleeff, D ;
Jagodzinski, LL ;
Michael, NL ;
Nduati, R ;
Bwayo, J ;
Kreiss, JK ;
Overbaugh, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (07) :2688-2695
[7]   Quantitative assay for group M (subtype A-H) and group OHIV-1 RNA detection in plasma [J].
Ernest, I ;
Alexandre, I ;
Zammatteo, N ;
Herman, M ;
Houbion, A ;
De Lenner, F ;
Fransen, K ;
van der Groen, G ;
Remacle, J .
JOURNAL OF VIROLOGICAL METHODS, 2001, 93 (1-2) :1-14
[8]   Characterization of intracellular reverse transcription complexes of human immunodeficiency virus type 1 [J].
Fassati, A ;
Goff, SP .
JOURNAL OF VIROLOGY, 2001, 75 (08) :3626-3635
[9]   CHARACTERIZATION OF MONOCLONAL-ANTIBODIES AGAINST THE HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) GAG PRODUCTS AND THEIR USE IN MONITORING HIV ISOLATE VARIATION [J].
FERNS, RB ;
TEDDER, RS ;
WEISS, RA .
JOURNAL OF GENERAL VIROLOGY, 1987, 68 :1543-1551
[10]   Comparison of levels of human immunodeficiency virus type 1 RNA in plasma as measured by the NucliSens nucleic acid sequence-based amplification and quantiplex branched-DNA assays [J].
Ginocchio, CC ;
Tetali, S ;
Washburn, D ;
Zhang, F ;
Kaplan, MH .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (04) :1210-1212