两株新型产ndm -1的非典型肠聚集性大肠杆菌分离株的分子特征

IF 1.8 4区 生物学 Q3 GENETICS & HEREDITY Plasmid Pub Date : 2021-05-01 DOI:10.1016/j.plasmid.2021.102568
Pengcheng Du , Pei Zhang , Juan Wang , Ruichao Li , Séamus Fanning , Li Bai
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引用次数: 2

摘要

为研究349型非典型肠聚集性大肠杆菌(aEAEC)产ndm -1的情况,对分离株13ZX28和13ZX36进行了药敏试验、偶联和全基因组测序。尽管质粒谱不同,但在染色体中只检测到一个单核苷酸突变。这两株菌株对介导碳青霉烯抗性的blaNDM-1均呈阳性。从13ZX28中分离出新的质粒p13ZX28-272 (~272-kb)编码blaNDM-1。有趣的是,其序列与来自13ZX36的两个质粒p13ZX36-200 (~200-kb)和p13ZX36-70 (~70-kb)相同。前一个片段的形成可能通过位于后两个质粒上的4948bp大片段进行同源重组。此外,p13ZX28-272质粒在接合后通过IS26重排可分解为约98-kb的子质粒。质粒的可塑性是公认的,这需要进一步的研究来评估潜在的公共健康风险,并了解抗生素选择压力如何驱动这一过程。
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Molecular characterization of two novel NDM-1-producing atypical enteroaggregative Escherichia coli isolates from patients

To investigate NDM-1-producing atypical Enteroaggregative Escherichia coli (aEAEC) of sequence type 349 from hospitalized patients, the isolates 13ZX28 and 13ZX36 were subjected to antimicrobial susceptibility testing, conjugation and whole genome sequencing. Only one single nucleotide mutation was detected in chromosomes despite different plasmid profiles. Both isolates were positive for blaNDM-1 mediating resistance to carbapenem. A novel plasmid p13ZX28–272 (~272-kb) from 13ZX28 encodes blaNDM-1. Interestingly, its sequence was identical to the two plasmids p13ZX36–200 (~200-kb) and p13ZX36–70 (~70-kb) from 13ZX36. Formation of the former episome possibly involved homologous recombination through a 4948-bp large fragment located on each of the two latter plasmids. Furthermore, plasmid p13ZX28–272 could be resolved into a ~ 98-kb daughter plasmid by IS26 rearrangement following conjugation. The plasticity of the plasmids is recognized, which warrants further investigation to evaluate the underlying public health risk and understand how antibiotic selection pressure drives this process.

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来源期刊
Plasmid
Plasmid 生物-遗传学
CiteScore
4.70
自引率
3.80%
发文量
21
审稿时长
53 days
期刊介绍: Plasmid publishes original research on genetic elements in all kingdoms of life with emphasis on maintenance, transmission and evolution of extrachromosomal elements. Objects of interest include plasmids, bacteriophages, mobile genetic elements, organelle DNA, and genomic and pathogenicity islands.
期刊最新文献
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