Naas T, Mikami Y, Imai T, Poirel L, Nordmann P
Service de Bactériologie-Virologie, Hôpital de Bicêtre, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine Paris-Sud, 94275 Le Kremlin-Bicêtre, France.
J Bacteriol. 2001 Jan;183(1):235-49. doi: 10.1128/JB.183.1.235-249.2001.
Further characterization of the genetic environment of the gene encoding the Escherichia coli extended-spectrum beta-lactamase, bla(VEB-1), revealed the presence of a plasmid-located class 1 integron, In53, which carried eight functional resistance gene cassettes in addition to bla(VEB-1). While the aadB and the arr-2 gene cassettes were identical to those previously described, the remaining cassettes were novel: (i) a novel nonenzymatic chloramphenicol resistance gene of the cmlA family, (ii) a qac allele encoding a member of the small multidrug resistance family of proteins, (iii) a cassette, aacA1b/orfG, which encodes a novel 6'-N-acetyltransferase, and (iv) a fused gene cassette, oxa10/aadA1, which is made of two cassettes previously described as single cassettes. In addition, oxa10 and aadA1 genes were expressed from their own promoter sequence present upstream of the oxa10 cassette. arr-2 coded for a protein that shared 54% amino acid identity with the rifampin ADP-ribosylating transferase encoded by the arr-1 gene from Mycobacterium smegmatis DSM43756. While in M. smegmatis, the main inactivated compound was 23-ribosyl-rifampin, the inactivated antibiotic recovered from E. coli culture was 23-O-ADP-ribosyl-rifampin. The integrase gene of In53 was interrupted by an IS26 insertion sequence, which was also present in the 3' conserved segment. Thus, In53 is a truncated integron located on a composite transposon, named Tn2000, bounded by two IS26 elements in opposite orientations. Target site duplication at both ends of the transposon indicated that the integron likely was inserted into the plasmid through a transpositional process. This is the first description of an integron located on a composite transposon.
对编码大肠杆菌超广谱β-内酰胺酶bla(VEB-1)的基因的遗传环境进行进一步表征,发现存在一个位于质粒上的1类整合子In53,除bla(VEB-1)外,它还携带8个功能性耐药基因盒。虽然aadB和arr-2基因盒与先前描述的相同,但其余的基因盒是新的:(i) cmlA家族的一个新型非酶促氯霉素耐药基因;(ii) 一个编码小多药耐药蛋白家族成员的qac等位基因;(iii) 一个编码新型6'-N-乙酰转移酶的基因盒aacA1b/orfG;(iv) 一个融合基因盒oxa10/aadA1,它由两个先前被描述为单个基因盒的基因盒组成。此外,oxa10和aadA1基因从位于oxa10基因盒上游的自身启动子序列表达。arr-2编码一种蛋白质,该蛋白质与耻垢分枝杆菌DSM43756的arr-1基因编码的利福平ADP-核糖基化转移酶具有54%的氨基酸同一性。在耻垢分枝杆菌中,主要的失活化合物是23-核糖基-利福平,而从大肠杆菌培养物中回收的失活抗生素是23-O-ADP-核糖基-利福平。In53的整合酶基因被一个IS26插入序列中断,该序列也存在于3'保守区段中。因此,In53是一个位于复合转座子上的截短整合子,该复合转座子名为Tn2000,由两个方向相反的IS26元件界定。转座子两端的靶位点重复表明该整合子可能是通过转座过程插入到质粒中的。这是对位于复合转座子上的整合子的首次描述。