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临床相关的代谢基因调控区域突变有助于大肠杆菌对环丙沙星的早期适应。

Clinically relevant mutations in regulatory regions of metabolic genes facilitate early adaptation to ciprofloxacin in Escherichia coli.

机构信息

Kusuma School of Biological Sciences, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.

Department of Zoology, Raiganj Surendranath Mahavidyalaya, Sudarshanpur, Raiganj, Uttar Dinajpur, West Bengal733134, India.

出版信息

Nucleic Acids Res. 2024 Sep 23;52(17):10385-10399. doi: 10.1093/nar/gkae719.

DOI:10.1093/nar/gkae719
PMID:39180403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11417348/
Abstract

The genomic landscape associated with early adaptation to ciprofloxacin is poorly understood. Although the interplay between core metabolism and antimicrobial resistance is being increasingly recognized, mutations in metabolic genes and their biological role remain elusive. Here, we exposed Escherichia coli to increasing gradients of ciprofloxacin with intermittent transfer-bottlenecking and identified mutations in three non-canonical targets linked to metabolism including a deletion (tRNA-ArgΔ414-bp) and point mutations in the regulatory regions of argI (ARG box) and narU. Our findings suggest that these mutations modulate arginine and carbohydrate metabolism, facilitate anaerobiosis and increased ATP production during ciprofloxacin stress. Furthermore, mutations in the regulatory regions of argI and narU were detected in over 70% of sequences from clinical E. coli isolates and were overrepresented among ciprofloxacin-resistant isolates. In sum, we have identified clinically relevant mutations in the regulatory regions of metabolic genes as a central theme that drives physiological changes necessary for adaptation to ciprofloxacin stress.

摘要

早期适应环丙沙星的基因组景观尚不清楚。尽管核心代谢与抗微生物药物耐药性之间的相互作用正日益受到关注,但代谢基因的突变及其生物学作用仍难以捉摸。在这里,我们用间歇性瓶颈转移法使大肠杆菌暴露于不断增加的环丙沙星梯度中,并鉴定出与代谢相关的三个非典型靶标中的突变,包括 tRNA-ArgΔ414-bp 的缺失和 argI(ARG 盒)和 narU 的调控区的点突变。我们的研究结果表明,这些突变调节精氨酸和碳水化合物代谢,促进耐环丙沙星应激的厌氧和增加 ATP 生成。此外,在临床分离的大肠杆菌中超过 70%的序列中检测到 argI 和 narU 调控区的突变,在耐环丙沙星的分离株中更为突出。总之,我们已经确定了与代谢基因调控区相关的临床相关突变,这是驱动适应环丙沙星应激所需的生理变化的一个核心主题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/a37d856121f4/gkae719fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/e26fde35a07d/gkae719figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/c10cf33d2410/gkae719fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/9d634a1d8ac3/gkae719fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/7c78658cbc8d/gkae719fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/712da1fdf0fe/gkae719fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/a37d856121f4/gkae719fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/e26fde35a07d/gkae719figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/c10cf33d2410/gkae719fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/9d634a1d8ac3/gkae719fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/7c78658cbc8d/gkae719fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/712da1fdf0fe/gkae719fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/11417348/a37d856121f4/gkae719fig5.jpg

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