Multiplex PCR: Optimization and application in diagnostic virology

被引:639
作者
Elnifro, EM
Ashshi, AM
Cooper, RJ
Klapper, PE
机构
[1] Univ Manchester, Sch Med, Manchester, Lancs, England
[2] Cent Manchester Healthcare Trust, Manchester, Lancs, England
关键词
D O I
10.1128/CMR.13.4.559-570.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
PCR has revolutionized the field of infectious disease diagnosis. To overcome the inherent disadvantage of cost and to improve the diagnostic capacity of the test, multiplex PCR a variant of the test in which more than one target sequence is amplified using more than one pair of primers, has been developed. Multiplex PCRs to detect viral bacterial and/or other infectious agents in one reaction tube have been described Early studies highlighted the obstacles that can jeopardize the production of sensitive and specific multiplex assays, brit more recent studies have provided systematic protocols and technical improvements for simple test design. The most useful of these are the empirical choice of oligonucleotide primers and the use of hot start-based PCR methodology. These advances along with others to enhance sensitivity and specificity and to facilitate automation have resulted in the appearance of numerous publications regarding the application of multiplex PCR in the diagnosis of infectious agents, especially those which target viral nucleic acids. This article reviews the principles, optimization, and application of multiplex PCR for the detection of viruses of clinical and epidemiological importance.
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页码:559 / +
页数:13
相关论文
共 145 条
  • [71] Detection of Chlamydia trachomatis, Neisseria gonorrhoeae, Ureaplasma urealyticum, and Mycoplasma genitalium in first-void urine specimens by multiplex polymerase chain reaction
    Mahony, JB
    Jang, D
    Chong, S
    Luinstra, K
    Sellors, J
    Tyndall, M
    Chernesky, M
    [J]. MOLECULAR DIAGNOSIS, 1997, 2 (03): : 161 - 168
  • [72] MULTIPLEX PCR FOR DETECTION OF CHLAMYDIA-TRACHOMATIS AND NEISSERIA-GONORRHOEAE IN GENITOURINARY SPECIMENS
    MAHONY, JB
    LUINSTRA, KE
    TYNDALL, M
    SELLORS, JW
    KREPEL, J
    CHERNESKY, M
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (11) : 3049 - 3053
  • [73] Markoulatos P, 1999, J CLIN LAB ANAL, V13, P99, DOI 10.1002/(SICI)1098-2825(1999)13:3<99::AID-JCLA2>3.0.CO
  • [74] 2-E
  • [75] MULTIPLEX POLYMERASE CHAIN-REACTION FOR HUMAN HERPESVIRUS-6, HUMAN CYTOMEGALOVIRUS, AND HUMAN BETA-GLOBIN DNA
    MCELHINNEY, LM
    COOPER, RJ
    MORRIS, DJ
    [J]. JOURNAL OF VIROLOGICAL METHODS, 1995, 53 (2-3) : 223 - 233
  • [76] Amplification of the six major human herpesviruses from cerebrospinal fluid by a single PCR
    Minjolle, S
    Michelet, C
    Jusselin, I
    Joannes, M
    Cartier, F
    Colimon, R
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (04) : 950 - 953
  • [77] SIMULTANEOUS DETECTION OF 3 COMMON SEXUALLY-TRANSMITTED AGENTS BY POLYMERASE CHAIN-REACTION
    MITRANIROSENBAUM, S
    TSVIELI, R
    LAVIE, O
    BOLDES, R
    ANTEBY, E
    SHIMONOVITCH, S
    LAZAROVITCH, T
    FRIEDMANN, A
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1994, 171 (03) : 784 - 790
  • [78] Mitsuhashi M, 1996, J CLIN LAB ANAL, V10, P285, DOI 10.1002/(SICI)1098-2825(1996)10:5<285::AID-JCLA9>3.0.CO
  • [79] 2-7
  • [80] Comparison of clinical diagnosis and standard laboratory and molecular methods for the diagnosis of genital ulcer disease in lesotho: Association with human immunodeficiency virus infection
    Morse, SA
    Trees, DL
    Htun, Y
    Radebe, F
    Orle, KA
    Dangor, Y
    BeckSague, CM
    Schmid, S
    Fehler, G
    Weiss, JB
    Ballard, RC
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1997, 175 (03) : 583 - 589