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Complete sequences of two novel blaNDM-1-harbouring plasmids from two Acinetobacter towneri isolates in China associated with the acquisition of Tn125

机译:来自中国两个乡土不动杆菌分离株的两个新颖blaNDM-1携带质粒的完整序列与Tn125的获得有关

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摘要

Two novel New Delhi metallo-β-lactamase-1 (NDM-1)-positive plasmids containing a complete composite transposon, Tn125, from two respective Acinetobacter towneri isolates were characterized. Plasmid pNDM-GJ01 (30,293 bp) isolated from A. towneri G165 did not show homology to any known plasmid structure, except for the transposon Tn125 containing bla NDM-1. A novel repB gene and two XRE-type transcriptional regulators were found in pNDM-GJ01. Plasmid pNDM-GJ02 (62,011 bp) isolated from A. towneri G295 showed the highest homology to pBJAB0715 (41% coverage, 99% nucleotide identity). In addition to the bla NDM-1-harbouring transposon Tn125, pNDM-GJ02 also had an IS26-composite transposon, which contains ISCR1 and two class 1 integrons carrying different cassette arrays. Both clinical isolates were highly resistant to β-lactams and susceptible to tigecycline and colistin. Ten other resistance genes were detected in G295, and one other resistance gene was detected in G165. No transconjugant was obtained from any of the donors by broth and filter mating. The emergence of these two novel plasmids carrying NDM-1 in Acinetobacter spp., pNDM-GJ01 and pNDM-GJ02, suggests Tn125 mobile integration.
机译:鉴定了两个新德里新金属-β-内酰胺酶-1(NDM-1)阳性质粒,其中含有来自两个相应不动杆菌的完整分离子Tn125。从A.towneri G165中分离出的质粒pNDM-GJ01(30,293bp)与任何已知的质粒结构没有同源性,只是含有bla NDM-1的转座子Tn125。在pNDM-GJ01中发现了一个新的repB基因和两个XRE型转录调节因子。从A.towneri G295分离的质粒pNDM-GJ02(62,011bp)显示出与pBJAB0715的最高同源性(41%覆盖,99%核苷酸同一性)。除了bla NDM-1携带型转座子Tn125,pNDM-GJ02还具有IS26复合型转座子,其中包含ISCR1和两个携带不同盒序列的1类整合素。两种临床分离株均对β-内酰胺类具有高度耐药性,并易受替加环素和粘菌素的影响。在G295中检测到其他十个抗性基因,在G165中检测到另一个抗性基因。通过肉汤和过滤器交配没有从任何供体获得转偶联剂。这两个在不动杆菌属中携带NDM-1的新质粒pNDM-GJ01和pNDM-GJ02的出现表明Tn125可移动整合。

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