Detection of Bacillus anthracis spores in soil by PCR

被引:14
|
作者
Sjostedt, A [1 ]
Eriksson, U [1 ]
Ramisse, V [1 ]
Garrigue, H [1 ]
机构
[1] CTR ETUD BOUCHET,LAB BIOCHEM IMMUNOCHEM,VERT LE PETIT,FRANCE
关键词
Bacillus anthracis; spores; soil; polymerase chain reaction; detection;
D O I
10.1016/S0168-6496(97)00023-8
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A polymerase chain reaction (PCR)-based protocol was developed for rapid detection of Bacillus anthracis spores in various types of soil. Eleven soil samples representing miscellaneous vegetation types were mixed with anthrax spores and incubated overnight. In no case could the spores of the mixtures be detected directly by PCR. The PCR was based on primers derived from the capsule-encoding cap genes of the pXO2 plasmid. Therefore, the focus of the study became to develop a suitable method for preparation of DNA that would allow rapid detection of the anthrax spews. Various published techniques were investigated, but none enabled detection Of the spores from a majority of the samples. A successful Protocol was eventually developed based on a combination of a published preparative technique and a form of nested PCR. First, amplification by PCR was performed with a degenerate primer and then samples were diluted and subjected to a second round of amplification using the B. anthracis-specific cap primers. The protocol is rapid and resulted in DNA of sufficient purity from. all of the 11 investigated soil samples to permit detection of B. anthracis spores.
引用
收藏
页码:159 / 168
页数:10
相关论文
共 50 条
  • [11] A disclosure gel for visual detection of live Bacillus anthracis spores
    Robinson, C., V
    Bishop, A. H.
    JOURNAL OF APPLIED MICROBIOLOGY, 2019, 126 (06) : 1700 - 1707
  • [12] PCR assay to detect Bacillus anthracis spores in heat-treated specimens
    Fasanella, A
    Losito, S
    Adone, R
    Ciuchini, F
    Trotta, T
    Altamura, SA
    Chiocco, D
    Ippolito, G
    JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (02) : 896 - 899
  • [13] Development of internal controls for PCR detection of Bacillus anthracis
    Brightwell, C
    Pearce, M
    Leslie, D
    MOLECULAR AND CELLULAR PROBES, 1998, 12 (06) : 367 - 377
  • [14] Environmental sampling for spores of Bacillus anthracis
    Teshale, EH
    Painter, J
    Burr, GA
    Mead, P
    Wright, SV
    Cseh, LF
    Zabrocki, R
    Collins, R
    Kelley, KA
    Hadler, JL
    Swerdlow, DL
    EMERGING INFECTIOUS DISEASES, 2002, 8 (10) : 1083 - 1087
  • [15] The immune response to Bacillus anthracis spores
    Swiecki, M
    Steichen, C
    Tumbough, CL
    Kearney, JF
    FASEB JOURNAL, 2003, 17 (07): : C173 - C174
  • [16] Unsupported conclusions on the Bacillus anthracis spores
    Mereish, Kay A.
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2007, 73 (15) : 5074 - 5074
  • [17] Evaluation of a micro-fabricated pyrolyzer for the detection of Bacillus anthracis spores
    Havey, CD
    Basile, F
    Mowry, C
    Voorhees, KJ
    JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 2004, 72 (01) : 55 - 61
  • [18] Species-specific peptide ligands for the detection of Bacillus anthracis spores
    Williams, DD
    Benedek, O
    Turnbough, CL
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (10) : 6288 - 6293
  • [19] Rapid Detection of Bacillus anthracis Spores Using Immunomagnetic Separation and Amperometry
    Waller, David F.
    Hew, Brian E.
    Holdaway, Charlie
    Jen, Michael
    Peckham, Gabriel D.
    BIOSENSORS-BASEL, 2016, 6 (04):
  • [20] Environmental Persistence of Bacillus anthracis and Bacillus subtilis Spores
    Wood, Joseph P.
    Meyer, Kathryn M.
    Kelly, Thomas J.
    Choi, Young W.
    Rogers, James V.
    Riggs, Karen B.
    Willenberg, Zachary J.
    PLOS ONE, 2015, 10 (09):