Suppr超能文献

多个质粒转移起始区可能有助于将抗生素耐药性传播给人类病原体。

Multiple plasmid origin-of-transfer regions might aid the spread of antimicrobial resistance to human pathogens.

机构信息

Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.

出版信息

Microbiologyopen. 2020 Dec;9(12):e1129. doi: 10.1002/mbo3.1129. Epub 2020 Oct 27.

Abstract

Antimicrobial resistance poses a great danger to humanity, in part due to the widespread horizontal gene transfer of plasmids via conjugation. Modeling of plasmid transfer is essential to uncovering the fundamentals of resistance transfer and for the development of predictive measures to limit the spread of resistance. However, a major limitation in the current understanding of plasmids is the incomplete characterization of the conjugative DNA transfer mechanisms, which conceals the actual potential for plasmid transfer in nature. Here, we consider that the plasmid-borne origin-of-transfer substrates encode specific DNA structural properties that can facilitate finding these regions in large datasets and develop a DNA structure-based alignment procedure for typing the transfer substrates that outperforms sequence-based approaches. Thousands of putative DNA transfer substrates are identified, showing that plasmid mobility can be twofold higher and span almost twofold more host species than is currently known. Over half of all putative mobile plasmids contain the means for mobilization by conjugation systems belonging to different mobility groups, which can hypothetically link previously confined host ranges across ecological habitats into a robust plasmid transfer network. This hypothetical network is found to facilitate the transfer of antimicrobial resistance from environmental genetic reservoirs to human pathogens, which might be an important driver of the observed rapid resistance development in humans and thus an important point of focus for future prevention measures.

摘要

抗微生物药物耐药性对人类构成巨大威胁,部分原因是质粒通过接合广泛横向转移基因。质粒转移建模对于揭示耐药性转移的基本原理以及开发预测性措施限制耐药性传播至关重要。然而,目前对抗生素耐药质粒理解的一个主要局限性是对可转移的 DNA 转移机制的不完全表征,这掩盖了自然界中质粒转移的实际潜力。在这里,我们认为质粒携带的转移起始底物编码特定的 DNA 结构特性,这些特性可以帮助在大型数据集找到这些区域,并开发一种基于 DNA 结构的转移底物分型方法,其性能优于基于序列的方法。鉴定出数千个假定的 DNA 转移底物,表明质粒的迁移能力比目前已知的高出两倍,并且跨越的宿主物种范围几乎扩大了两倍。超过一半的假定可移动质粒包含通过属于不同移动性群的接合系统进行动员的手段,这可以假设性地将先前局限于生态生境的宿主范围连接到一个强大的质粒转移网络中。该假设网络被发现有助于将抗微生物药物耐药性从环境遗传库转移到人类病原体,这可能是人类观察到的快速耐药性发展的一个重要驱动因素,因此是未来预防措施的一个重要重点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b10/7755788/c970b5965efb/MBO3-9-e1129-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验