5′ nuclease PCR assay to detect Yersinia pestis

被引:75
作者
Higgins, JA
Ezzell, J
Hinnebusch, BJ
Shipley, M
Henchal, EA
Ibrahim, MS
机构
[1] USA, Med Res Inst Infect Dis, Diagnost Syst Div, Ft Detrick, MD 21702 USA
[2] NIAID, Rocky Mt Labs, Microbial Struct & Funct Lab, Hamilton, MT 59840 USA
关键词
D O I
10.1128/JCM.36.8.2284-2288.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The 5' nuclease PCR assay uses a fluorescently labeled oligonucleotide probe (TaqMan) to rapidly detect and quantitate DNA templates in clinical samples. We developed a 5' nuclease PCR assay targeting the plasminogen activator gene (pla) of Yersinia pestis. The assay is species specific, with a detection threshold of 2.1 x 10(5) copies of the pla target or 1.6 pg of total cell DNA. The assay detected Y. pestis in experimentally infected Xenopsylla cheopis fleas and in experimentally infected monkey blood and oropharyngeal swabs. The TaqMan assay is simple to perform and rapid and shows promise as a future field-adaptable technique.
引用
收藏
页码:2284 / 2288
页数:5
相关论文
共 22 条
  • [1] USE OF A FLUOROGENIC PROBE IN A PCR-BASED ASSAY FOR THE DETECTION OF LISTERIA-MONOCYTOGENES
    BASSLER, HA
    FLOOD, SJA
    LIVAK, KJ
    MARMARO, J
    KNORR, R
    BATT, CA
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1995, 61 (10) : 3724 - 3728
  • [2] RAPID AND SPECIFIC IDENTIFICATION OF YERSINIA-PESTIS BY USING A NESTED POLYMERASE CHAIN-REACTION PROCEDURE
    CAMPBELL, J
    LOWE, J
    WALZ, S
    EZZELL, J
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (03) : 758 - 759
  • [3] DETECTION OF YERSINIA-PESTIS FRACTION-1 ANTIGEN WITH A FIBER OPTIC BIOSENSOR
    CAO, LK
    ANDERSON, GP
    LIGLER, FS
    EZZELL, J
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (02) : 336 - 341
  • [4] The evaluation of a fluorogenic polymerase chain reaction assay for the detection of Salmonella species in food commodities
    Chen, S
    Yee, A
    Griffiths, M
    Larkin, C
    Yamashiro, CT
    Behari, R
    PaszkoKolva, C
    Rahn, K
    DeGrandis, SA
    [J]. INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1997, 35 (03) : 239 - 250
  • [5] Davis KJ, 1996, ARCH PATHOL LAB MED, V120, P156
  • [6] A novel method for real time quantitative RT PCR
    Gibson, UEM
    Heid, CA
    Williams, PM
    [J]. GENOME RESEARCH, 1996, 6 (10): : 995 - 1001
  • [7] Role of the Yersinia pestis hemin storage (hms) locus in the transmission of plague by fleas
    Hinnebusch, BJ
    Perry, RD
    Schwan, TG
    [J]. SCIENCE, 1996, 273 (5273) : 367 - 370
  • [8] NEW METHOD FOR PLAGUE SURVEILLANCE USING POLYMERASE CHAIN-REACTION TO DETECT YERSINIA-PESTIS IN FLEAS
    HINNEBUSCH, J
    SCHWAN, TG
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (06) : 1511 - 1514
  • [9] DETECTION OF SPECIFIC POLYMERASE CHAIN-REACTION PRODUCT BY UTILIZING THE 5'-]3' EXONUCLEASE ACTIVITY OF THERMUS-AQUATICUS DNA-POLYMERASE
    HOLLAND, PM
    ABRAMSON, RD
    WATSON, R
    GELFAND, DH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) : 7276 - 7280
  • [10] Detection of Rift Valley fever virus in mosquitoes by RT-PCR
    Ibrahim, MS
    Turell, MJ
    Knauert, FK
    Lofts, RS
    [J]. MOLECULAR AND CELLULAR PROBES, 1997, 11 (01) : 49 - 53