Partridge Sally R, Brown Heidi J, Hall Ruth M
CSIRO Molecular Science, North Ryde, New South Wales 2113, Australia.
Antimicrob Agents Chemother. 2002 May;46(5):1288-94. doi: 10.1128/AAC.46.5.1288-1294.2002.
Two putative transposons, Tn2521 and Tn1405, carrying determinants for the PSE-4 beta-lactamase and for resistance to streptomycin, spectinomycin, and sulfonamides were previously isolated from the chromosome of Pseudomonas aeruginosa Dalgleish. Detailed mapping and determination of the complete sequence of Tn2521 revealed that it is a class 1 integron, here renamed In33, with a backbone structure identical to that of In4 from Tn1696. In33 contains two gene cassettes, blaP1 and aadA1, replacing the aacC1-orfE-aadA2-cmlA1 cassette array in In4. Although In33 does not include any transposition genes, movement of In33 (Tn2521) targeted to a single location in the IncP-1 plasmid R18-18 has been reported previously (M. I. Sinclair and B. W. Holloway, J. Bacteriol. 151:569-579, 1982). A 5-bp duplication of the target, which lies within the res site recognized by the ParA resolvase of R18-18, was present, indicating that the mechanism of movement was transposition. Together, these data indicate that class 1 integrons that are defective in self-transposition can move under appropriate circumstances. The Tn1405 isolate studied was found to represent only the cassette array of In33, which had replaced the cassette array in the recipient plasmid R388, probably by homologous recombination.
先前从铜绿假单胞菌Dalgleish的染色体中分离出两个推定的转座子Tn2521和Tn1405,它们携带PSE-4β-内酰胺酶以及对链霉素、壮观霉素和磺胺类药物的抗性决定簇。对Tn2521的详细图谱绘制和完整序列测定表明,它是1类整合子,在此重新命名为In33,其主干结构与来自Tn1696的In4相同。In33包含两个基因盒blaP1和aadA1,取代了In4中的aacC1-orfE-aadA2-cmlA1基因盒阵列。虽然In33不包括任何转座基因,但先前已有报道In33(Tn2521)移动到IncP-1质粒R18-18中的单个位点(M. I. Sinclair和B. W. Holloway,《细菌学杂志》151:569 - 579,1982年)。在R18-18的ParA解离酶识别的res位点内存在目标的5 bp重复,这表明移动机制是转座。这些数据共同表明,自身转座有缺陷的1类整合子在适当情况下可以移动。所研究的Tn1405分离株被发现仅代表In33的基因盒阵列,它可能通过同源重组取代了受体质粒R388中的基因盒阵列。