Polymerase chain reaction for
insertion sequence 6110
20 OXA-48-like] VIMF GTGAGTATCCGACAGTC [bla.sub.VIM-1] 18 VIMR GAGCAAGTCTAGACCG [bla.sub.VIM-1] 18 KPCF TGTCACTGTATCGCCGTC [bla.sub.KPC-1] 21 KPCR CTCAGTGCTCTACAGAAAACC [bla.sub.KPC-1] 21 SPMF CTGCTTGGATTCATGGGCGC [bla.sub.SPM-1] 22 SPMR CCTTTTCCGCGACCTTGATC [bla.sub.SPM-1] 22 Extended-spectrum [beta]-lactamases CTXM1F CGCTTTGCGATGTGCAG [bla.sub.CTX-M-1] 17 CTXM1R ACCGCGATATCGTTGGT [bla.sub.CTX-M-1] 17 SHVC AGAAGGGTTATTCT [bla.sub.SHV] 17 TATTTGTCGC SHVD TCTTTCCGATGCC [bla.sub.SHV] 23 GCCGCCAGTCA DEB ATGAGTAAACTTGGTCTGAC [bla.sub.TEM] 24 3061TEM AGGAAGCAAAGCTGAAAG [bla.sub.TEM] 25 GAATCAAATTTGG
Insertion sequence ISEcp1F GCAGGTCTTTTTCTGCTCC [ISE.sub.cpl] 26 transposase ISEcp1R TTTCCGCAGCACCGTTTGC [ISE.sub.cpl] 26 transposase Table 2.
mallei fliP gene and
insertion sequence in GenBank accession NC_006348).
tuberculosis isolates, the use of
insertion sequence IS6110 is the most widely used method.
microti has been identified with the
insertion sequence IS6110 which is considered as specific to the members of the MTB complex (Haddad et al., 2004).
This indicated that the
insertion sequence can inhibit the interaction between tobacco 14-3-3s and SPSA in yeast.
Conventional genotyping of the ACE I/D polymorphism involves PCR, using primers that flank the
insertion sequence, and exploits the different migration velocities of I- and D-allele-specific PCR products during electrophoresis in gel matrices (32).
Other authors have shown that exoU has a different G+C content and is adjacent to a probable
insertion sequence and therefore may be acquired by horizontal transfer.
The genome sequences to be examined were aligned with the phage- and
insertion sequence (IS)-masked chromosome sequence of the STEC O157:H7 strain Sakai (22) using MUMmer (34) to identify conserved regions (cutoff thresholds [greater than or equal to] 98% sequence identity and [greater than or equal to] 1,000-bp alignment length) in each strain and the SNP sites located therein.
We extracted DNA from grown colonies after heat inactivation by ultrasonic cell lysis and analyzed the DNA by PCRs targeting
insertion sequence (IS) 1245, IS900, and IS901.
The main difference between the 2 prophages was an
insertion sequence element, a common source of prophage variation (Figure 2).
IS,
insertion sequence; KR, ketoreductase B domain of mycolactone polyketide synthase genes; ND, not detected.