从北极环境中分离出的新型雪旺氏菌中出现了 mcr-4.3 基因。

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES
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引用次数: 0

摘要

移动可乐定耐药性(mcr)基因是导致人类感染产生最后一线抗菌素耐药性的关键因素。雪旺菌历来被认为是一种具有金属还原能力的自然环境细菌,最近在临床环境中也被观察到。然而,人们对非临床菌株和临床菌株之间的遗传差异了解有限。在本研究中,我们对 6 株北极菌株进行了全基因组测序,并对已发表的 393 株雪旺菌菌株进行了系统发育关系图解,将雪旺菌属分为 4 个系(L1 至 L4)。超过86.4%的临床菌株组(CG)菌株属于L1和L4,携带mcr-4基因和完整的金属还原途径基因簇。值得注意的是,L3中的一株新型北极雪旺菌与CG菌株具有相似的遗传特征,都携带mcr-4基因和完整的金属还原途径基因簇。这引起了人们对环境向临床传播能力的关注,从而导致潜在的感染,并强调了监测新出现的人类感染菌株的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emergence of mcr-4.3 genes in a novel Shewanella specie isolated from the Arctic environment

Mobile colistin resistance (mcr) genes are pivotal contributors to last-line of antimicrobial resistance in human infections. Shewanella, historically recognized as a natural environmental bacterium with metal reduction capabilities, recently has been observed in clinical settings. However, limited knowledge has been explored on genetic differences between strains from non-clinical and clinical strains. In this study, we conducted the whole genome sequencing on six Arctic strains, illustrated the phylogenetic relationships on published 393 Shewanella strains that categorized the genus into four lineages (L1 to L4). Over 86.4% of clinical strain group (CG) strains belonged to L1 and L4, carrying mcr-4 genes and a complete metal-reduction pathways gene cluster. Remarkably, a novel Arctic Shewanella strain in L3, exhibits similar genetic characteristics with CG strains that carried both mcr-4 genes and a complete metal reduction pathway gene cluster. It raised concerns about the transmission ability from environment to clinic setting causing in the potential infections, and emphasized the need for monitoring the emerging strains with human infections.

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来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
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