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评估 435 个携带 KPC 基因的质粒的遗传多样性和相似性。

Assessing genetic diversity and similarity of 435 KPC-carrying plasmids.

机构信息

Institute for Infectious Diseases and Infection Control, Jena University Hospital, Jena, Germany.

BioCenter, Department of Molecular Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.

出版信息

Sci Rep. 2019 Aug 2;9(1):11223. doi: 10.1038/s41598-019-47758-5.

Abstract

The global spread and diversification of multidrug-resistant Gram-negative (MRGN) bacteria poses major challenges to healthcare. In particular, carbapenem-resistant Klebsiella pneumoniae strains have been frequently identified in infections and hospital-wide outbreaks. The most frequently underlying resistance gene (bla) has been spreading over the last decade in the health care setting. bla seems to have rapidly diversified and has been found in various species and on different plasmid types. To review the progress and dynamics of this diversification, all currently available KPC plasmids in the NCBI database were analysed in this work. Plasmids were grouped into 257 different representative KPC plasmids, of which 79.4% could be clearly assigned to incompatibility (Inc) group or groups. In almost half of all representative plasmids, the KPC gene is located on Tn4401 variants, emphasizing the importance of this transposon type for the transmission of KPC genes to other plasmids. The transposons also seem to be responsible for the occurrence of altered or uncommon fused plasmid types probably due to incomplete transposition. Moreover, many KPC plasmids contain genes that encode proteins promoting recombinant processes and mutagenesis; in consequence accelerating the diversification of KPC genes and other colocalized resistance genes.

摘要

全球耐多药革兰氏阴性(MRGN)细菌的传播和多样化对医疗保健构成了重大挑战。特别是,耐碳青霉烯类肺炎克雷伯菌菌株在感染和医院范围内的暴发中经常被发现。在过去十年中,最常见的潜在耐药基因(bla)在医疗保健环境中传播。bla 似乎已经迅速多样化,并在不同的物种和不同的质粒类型上发现。为了回顾这种多样化的进展和动态,本研究分析了 NCBI 数据库中所有现有的 KPC 质粒。将质粒分为 257 个不同的代表性 KPC 质粒,其中 79.4%可以明确归属于不相容性(Inc)组或组。在几乎所有代表性质粒的一半中,KPC 基因位于 Tn4401 变体上,这强调了这种转座子类型对于将 KPC 基因传递给其他质粒的重要性。转座子似乎也负责发生改变或不常见的融合质粒类型,可能是由于不完全转座。此外,许多 KPC 质粒包含编码促进重组过程和突变的蛋白质的基因;因此,加速了 KPC 基因和其他共存耐药基因的多样化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f42/6677891/272ce97c3557/41598_2019_47758_Fig1_HTML.jpg

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