Identification and characterization of IS2404 and IS2606:: Two distinct repeated sequences for detection of Mycobacterium ulcerans by PCR

被引:135
作者
Stinear, T
Ross, BC
Davies, JK
Marino, L
Robins-Browne, RM
Oppedisano, F
Sievers, A
Johnson, PDR
机构
[1] Monash Univ, Dept Microbiol, Clayton, Vic 3168, Australia
[2] CSL Ltd, Res & Dev, Melbourne, Vic, Australia
[3] Royal Childrens Hosp, Dept Microbiol & Infect Dis, Melbourne, Vic, Australia
[4] Victorian Infect Dis Reference Lab, Melbourne, Vic, Australia
[5] Monash Med Ctr, Dept Infect Dis & Clin Epidemiol, Clayton, Vic, Australia
关键词
D O I
10.1128/JCM.37.4.1018-1023.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Molecular analysis of Mycobacterium ulcerans has revealed two new insertion sequences (ISs), IS2404 and IS2606, IS2404 was identified by complete sequencing of a previously described repetitive DNA segment from M. ulcerans, This element is 1,274 bp long, contains 12-bp inverted repeats and a single open reading frame (ORF) potentially encoding a protein of 327 amino acids (aa), and apparently generates 7-bp direct repeats upon transposition. Amino acid similarity was found between the putative transposase and those encoded by ISs in other bacterial sequences from Aeromonas salmonicida (AsIs1), Escherichia coli (N repeat element), Vibrio cholerae (VcIS1), and Porphyromonas gingivalis (PGIS2). The second IS, IS2606, was discovered by sequence analysis of a HaeIII fragment of M. ulcerans genomic DNA containing a repetitive sequence. This element is 1,404 bp long, with 12-bp, inverted repeats and a single ORF potentially encoding a protein of 445 aa, Database searches revealed a high degree of amino acid identity (70%) with the putative transposase of IS1554 from M. tuberculosis, Significant amino acid identity (40%) was also observed with transposases from several other microorganisms, including Rhizobium meliloti (ISRm3), Burkholderia cepacia (IS1356), Corynebacterium diphtheriae, and Yersinia pestis. PCR screening of DNA from 35 other species of mycobacteria with primers fur IS2404 confirm that this element is found only in M. ulcerans, However, by PCR, IS2606 was also found in Mycobacterium lentiflavum, another slow-growing member of the genus Mycobacterium that is apparently genetically distinct from M. ulcerans. Testing the sensitivity of PCR based on IS2404 and IS2606 primers demonstrated the ability to detect 0.1 and 1 M. ulcerans genome equivalents, respectively, The ability to detect small numbers of cells by using two gene targets will be particularly useful fur analyzing environmental samples, where there may be law concentrations of M. ulcerans among large numbers of other environmental mycobacteria.
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页码:1018 / 1023
页数:6
相关论文
共 36 条
  • [1] BAIRNSDALE ULCER
    ALSOP, DG
    [J]. AUSTRALIAN AND NEW ZEALAND JOURNAL OF SURGERY, 1972, 41 (04): : 317 - &
  • [2] Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
    Altschul, SF
    Madden, TL
    Schaffer, AA
    Zhang, JH
    Zhang, Z
    Miller, W
    Lipman, DJ
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (17) : 3389 - 3402
  • [3] Ausubel FM, 1995, CURRENT PROTOCOLS MO
  • [4] EPIDEMIOLOGY OF MYCOBACTERIUM-ULCERANS INFECTION
    BARKER, DJP
    [J]. TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1973, 67 (01) : 43 - 50
  • [5] BODDINGHAUS B, 1990, J CLIN MICROBIOL, V28, P1751
  • [6] A RAPID PROCEDURE FOR COLONY SCREENING USING NYLON FILTERS
    BULUWELA, L
    FORSTER, A
    BOEHM, T
    RABBITTS, TH
    [J]. NUCLEIC ACIDS RESEARCH, 1989, 17 (01) : 452 - 452
  • [7] Caetano-Anolles G., 1994, PROMEGA NOTES, V45, P13
  • [8] Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence
    Cole, ST
    Brosch, R
    Parkhill, J
    Garnier, T
    Churcher, C
    Harris, D
    Gordon, SV
    Eiglmeier, K
    Gas, S
    Barry, CE
    Tekaia, F
    Badcock, K
    Basham, D
    Brown, D
    Chillingworth, T
    Connor, R
    Davies, R
    Devlin, K
    Feltwell, T
    Gentles, S
    Hamlin, N
    Holroyd, S
    Hornby, T
    Jagels, K
    Krogh, A
    McLean, J
    Moule, S
    Murphy, L
    Oliver, K
    Osborne, J
    Quail, MA
    Rajandream, MA
    Rogers, J
    Rutter, S
    Seeger, K
    Skelton, J
    Squares, R
    Squares, S
    Sulston, JE
    Taylor, K
    Whitehead, S
    Barrell, BG
    [J]. NATURE, 1998, 393 (6685) : 537 - +
  • [9] PROGRESSIVE SEQUENCE ALIGNMENT AS A PREREQUISITE TO CORRECT PHYLOGENETIC TREES
    FENG, DF
    DOOLITTLE, RF
    [J]. JOURNAL OF MOLECULAR EVOLUTION, 1987, 25 (04) : 351 - 360
  • [10] THE PILE GENE OF NEISSERIA-GONORRHOEAE MS11 IS TRANSCRIBED FROM A SIGMA(70) PROMOTER DURING GROWTH IN-VITRO
    FYFE, JAM
    CARRICK, CS
    DAVIES, JK
    [J]. JOURNAL OF BACTERIOLOGY, 1995, 177 (13) : 3781 - 3787