A role for arrays in clinical virology: fact or fiction?

被引:29
作者
Clewley, JP [1 ]
机构
[1] Cent Publ Hlth Lab, Sexually Transmitted & Blood Borne Virus Lab, London NW9 5HT, England
关键词
virology; DNA probes; microarrays; DNA chips;
D O I
10.1016/j.jcv.2003.08.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Microarrays of DNA probes have at least three roles in clinical virology. These are: firstly, in diagnosis, to recognise the causative agent of an illness; secondly, for molecular typing for (i) patient management, (ii) epidemiological reasons (e.g. investigating routes of transmission), (iii) purposes related to vaccine use; and thirdly, in research, to investigate the interactions between the virus and the host cell. Microarrays intended for syndromic diagnostic purposes require genome specific probes to capture the unknown target viral sequences and thereby reveal the presence of that virus in a test sample. Microarrays intended for typing and patient management, e.g. monitoring antiviral drug resistant mutations require a set of probes representing the important sequence variants of one or more viral genes. Microarrays intended for research into virus-host interactions require probes representative of each individual gene or mRNA of either the virus or the host genome. Diagnostic microarrays are dependent for their utility and versatility on generic, multiplex or random polymerase chain reactions that will amplify any of several (unknown) viral target sequences from a patient sample. In this review, the existing and potential applications of microarrays in virology, and the problems that need to be overcome for future success, are discussed. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:2 / 12
页数:11
相关论文
共 109 条
[1]   Comparison of sequence analysis and the INNO-LiPA HBV DR line probe assay for detection of lamivudine-resistant hepatitis B virus strains in patients under various clinical conditions [J].
Aberle, SW ;
Kletzmayr, J ;
Watschinger, B ;
Schmied, B ;
Vetter, N ;
Puchhammer-Stöckl, E .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (05) :1972-1974
[2]   Sequence diversity of Jeryl Lynn strain of mumps virus: Quantitative mutant analysis for vaccine quality control [J].
Amexis, G ;
Rubin, S ;
Chizhikov, V ;
Pelloquin, F ;
Carbone, K ;
Chumakov, K .
VIROLOGY, 2002, 300 (02) :171-179
[3]   A METHOD FOR THE RAPID SEQUENCE-INDEPENDENT AMPLIFICATION OF MICRODISSECTED CHROMOSOMAL MATERIAL [J].
BOHLANDER, SK ;
ESPINOSA, R ;
LEBEAU, MM ;
ROWLEY, JD ;
DIAZ, MO .
GENOMICS, 1992, 13 (04) :1322-1324
[4]   Detection of potato viruses using microarray technology: towards a generic method for plant viral disease diagnosis [J].
Boonham, N ;
Walsh, K ;
Smith, P ;
Madagan, K ;
Graham, I ;
Barker, I .
JOURNAL OF VIROLOGICAL METHODS, 2003, 108 (02) :181-187
[5]   A METHOD FOR TYPING POLYMORPHISM AT THE HLA-A LOCUS USING PCR AMPLIFICATION AND IMMOBILIZED OLIGONUCLEOTIDE PROBES [J].
BUGAWAN, TL ;
APPLE, R ;
ERLICH, HA .
TISSUE ANTIGENS, 1994, 44 (03) :137-147
[6]   A PCR primer system for detecting oncoretroviruses based on conserved DNA sequence motifs of animal retroviruses and its application to human leukaemias and lymphomas [J].
Burmeister, T ;
Schwartz, S ;
Thiel, E .
JOURNAL OF GENERAL VIROLOGY, 2001, 82 :2205-2213
[7]  
Bystrická D, 2003, ACTA VIROL, V47, P41
[8]  
Calvario A, 2002, J CLIN VIROL, V25, pS71, DOI 10.1016/S1386-6532(02)00036-7
[9]  
Casas I, 1999, J MED VIROL, V57, P145, DOI 10.1002/(SICI)1096-9071(199902)57:2&lt
[10]  
145::AID-JMV10&gt