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Comparative Study
. 1999 Apr;37(4):1018-23.
doi: 10.1128/JCM.37.4.1018-1023.1999.

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

Affiliations
Comparative Study

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

T Stinear et al. J Clin Microbiol. 1999 Apr.

Abstract

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 (H 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 45 other species of mycobacteria with primers for 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 for analyzing environmental samples, where there may be low concentrations of M. ulcerans among large numbers of other environmental mycobacteria.

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Figures

FIG. 1
FIG. 1
Southern blot hybridization analysis of selected M. ulcerans strains probed with IS2404 (A) and IS2606 (B). Lane 1, strain 5142; lane 2, strain 13822/70; lanes 3 to 5, Chant strain. Genomic DNA was digested with PvuII (lanes 1 to 3), NcoI (lane 4), and EcoRI (lane 5); lane M, λ HindIII molecular size marker (Boehringer Mannheim).
FIG. 2
FIG. 2
Phylogenetic relationships among transposase amino acid sequences from IS2404, IS2606, and selected IS elements as determined by maximum-parsimony analysis.
FIG. 3
FIG. 3
PCR analysis of selected mycobacteria designed to detect IS2404 (A), IS2606 (B), and 16S rDNA (C), as described in Materials and Methods and in Table 2. Lanes 1, M. ulcerans; lanes 2, M. marinum; lanes 3, Mycobacterium haemophilum; lanes 4, M. tuberculosis; lanes 5, M. lentiflavum; lanes 6, no-template negative control; lane M, φx174 HaeIII molecular size marker (Promega).
FIG. 4
FIG. 4
Sensitivity of PCR in detection of M. ulcerans genomes by amplification of IS2404 (lanes 1 to 4) and IS2606 (lanes 5 to 8), as determined by silver-stained polyacrylamide gel electrophoresis. Lanes 1 and 5, 10 genomes; lanes 2 and 6, 1 genome; lanes 3 and 7, 0.1 genome; lanes 4 and 8, 0 genomes; lane M, 100-bp ladder size 1arker (Gibco).

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