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抗菌肽LL37对非生长状态的细胞具有强大作用,尽管其作用速率较慢。

Antimicrobial peptide LL37 is potent against non-growing cells despite a slower action rate.

作者信息

Mohammadi Salimeh, Saucedo Derek, Taheri-Araghi Sattar

机构信息

Department of Physics and Astronomy, California State University, Northridge, California, USA.

出版信息

mSphere. 2025 Jan 28;10(1):e0021124. doi: 10.1128/msphere.00211-24. Epub 2024 Dec 23.

Abstract

UNLABELLED

Antimicrobial peptides (AMPs) have long been considered as potential agents against non-growing, dormant cells due to their membrane-targeted action, which is largely independent of the cell's growth state. However, the relationship between the action of AMPs and the physiological state of their target cells has been unclear, with recent reports offering conflicting views on the efficacy of AMPs against bacteria in a stationary phase. In this study, we employ single-cell approaches combined with population-level experiments to examine the action of human LL37 peptides against cells in different growth phases. Time-lapse, single-cell data from our experiments reveal that LL37 peptides act faster on large, dividing cells than on small, newborn cells. We extend this investigation to non-growing cells in a stationary phase, where we observe that the action of LL37 peptides is slower on non-growing cells compared to exponentially growing cells. This slower action rate is, however, not mirrored in the minimum bactericidal concentration (MBC) measurements. Notably, we find that the MBC for non-growing cells is lower than for exponentially growing cells, indicating that, given sufficient time, LL37 peptides exhibit strong potency against non-growing cells. We propose that the enhanced potency of LL37 peptides against non-growing cells, despite their slower action, can be attributed to continuous absorption of AMPs on the cell membrane over time.

IMPORTANCE

Antibiotic treatments can fail because of the regrowth of a bacterial subpopulation that resumes proliferation once the treatment ceases. This resurgence is primarily driven by non-growing, dormant bacterial cells that withstand the action of antibiotics without developing resistance. In this study, we explore the potency of the human antimicrobial peptide LL37 against non-growing cells. Our findings reveal that despite a slower initial action, LL37 peptides, given sufficient time, demonstrate strong efficacy against non-growing cells. These insights suggest a potential role of antimicrobial peptides in combating persistent bacterial infections by targeting the non-growing cells.

摘要

未标注

抗菌肽(AMPs)长期以来被认为是针对非生长、休眠细胞的潜在药物,因为它们的膜靶向作用在很大程度上不依赖于细胞的生长状态。然而,AMPs的作用与其靶细胞生理状态之间的关系一直不明确,最近的报告对于AMPs对处于稳定期细菌的功效给出了相互矛盾的观点。在本研究中,我们采用单细胞方法结合群体水平实验,来研究人LL37肽对不同生长阶段细胞的作用。我们实验的延时单细胞数据显示,LL37肽对大型、正在分裂的细胞的作用比对小型、新生细胞的作用更快。我们将这项研究扩展到处于稳定期的非生长细胞,发现在此状态下,LL37肽对非生长细胞的作用比对指数生长期细胞的作用更慢。然而,这种较慢的作用速率在最低杀菌浓度(MBC)测量中并未体现。值得注意的是,我们发现非生长细胞的MBC低于指数生长期细胞,这表明在给予足够时间的情况下,LL37肽对非生长细胞具有强大的效力。我们提出,尽管LL37肽对非生长细胞的作用较慢,但其对非生长细胞增强的效力可归因于随着时间推移AMPs在细胞膜上的持续吸附。

重要性

抗生素治疗可能会失败,因为一旦治疗停止,细菌亚群会重新增殖。这种复发主要由非生长、休眠的细菌细胞驱动,这些细胞能耐受抗生素的作用而不产生耐药性。在本研究中,我们探索了人抗菌肽LL37对非生长细胞的效力。我们的研究结果表明,尽管初始作用较慢,但在给予足够时间的情况下,LL37肽对非生长细胞显示出强大的功效。这些见解表明抗菌肽在通过靶向非生长细胞对抗持续性细菌感染方面具有潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a114/11774018/317bf19ee272/msphere.00211-24.f001.jpg

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