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基于生态位适应的质粒共存提高了多药耐药质粒的维持。

Piggybacking on Niche Adaptation Improves the Maintenance of Multidrug-Resistance Plasmids.

机构信息

Department of Pharmacy, Faculty of Health Sciences, UiT The Arctic University of Norway, Tromsø, Norway.

Department of Microbiology and Infection Control, University Hospital of North Norway, Tromsø, Norway.

出版信息

Mol Biol Evol. 2021 Jul 29;38(8):3188-3201. doi: 10.1093/molbev/msab091.

Abstract

The persistence of plasmids in bacterial populations represents a puzzling evolutionary problem with serious clinical implications due to their role in the ongoing antibiotic resistance crisis. Recently, major advancements have been made toward resolving this "plasmid paradox" but mainly in a nonclinical context. Here, we propose an additional explanation for the maintenance of multidrug-resistance plasmids in clinical Escherichia coli strains. After coevolving two multidrug-resistance plasmids encoding resistance to last resort carbapenems with an extraintestinal pathogenic E. coli strain, we observed that chromosomal media adaptive mutations in the global regulatory systems CCR (carbon catabolite repression) and ArcAB (aerobic respiration control) pleiotropically improved the maintenance of both plasmids. Mechanistically, a net downregulation of plasmid gene expression reduced the fitness cost. Our results suggest that global chromosomal transcriptional rewiring during bacterial niche adaptation may facilitate plasmid maintenance.

摘要

在细菌种群中,质粒的持续存在是一个令人费解的进化问题,具有严重的临床意义,因为它们在持续的抗生素耐药性危机中发挥了作用。最近,人们在解决这一“质粒悖论”方面取得了重大进展,但主要是在非临床环境中。在这里,我们提出了另一种解释,用于解释临床大肠杆菌菌株中多药耐药质粒的维持。在与一种肠外致病性大肠杆菌菌株共同进化了两种编码对最后手段碳青霉烯类抗生素耐药的多药耐药质粒后,我们观察到,在全球调控系统 CCR(碳源分解物阻遏)和 ArcAB(需氧呼吸控制)中的染色体介质适应性突变,多效性地改善了两种质粒的维持。从机制上讲,质粒基因表达的净下调降低了适应性代价。我们的研究结果表明,在细菌小生境适应过程中,全球染色体转录重布线可能有助于质粒的维持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08ff/8321521/03910c6e4fa3/msab091f1.jpg

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