通过单细胞追踪揭示细菌与哺乳动物细胞之间的相互作用

IF 4.4 1区 生物学 Q1 BIOLOGY BMC Biology Pub Date : 2024-11-11 DOI:10.1186/s12915-024-02056-z
Narendra K Dewangan, Sayed Golam Mohiuddin, Shayne Sensenbach, Prashant Karki, Mehmet A Orman
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引用次数: 0

摘要

背景:细菌病原体与宿主细胞之间的相互作用具有多种复杂性,从而导致各种不同的结果。尽管开展了大量研究,但我们对细菌在复杂环境中的运动如何影响其耐受抗生素和粘附到哺乳动物细胞表面的能力的了解仍然有限。我们面临的挑战在于如何揭示这些相互作用的复杂性,并开发定量显微镜方法来预测细菌种群的行为:为了应对这一挑战,我们将工作重点放在了铜绿假单胞菌和大肠杆菌上,铜绿假单胞菌是一种以在囊性纤维化患者肺部产生厚膜而闻名的致病细菌,大肠杆菌则被用作开发和展示单细胞追踪方法的概念验证。我们的研究结果表明,铜绿假单胞菌在哺乳动物细胞表面表现出多种复杂的相互作用,如粘附、旋转运动和游动,而大肠埃希菌的相互作用行为较少。我们的分析表明,与大肠杆菌相比,铜绿假单胞菌表现出较低的均方位移(MSD)值和较强的哺乳动物细胞粘附性,而大肠杆菌则表现出较高的MSD斜率和较少的粘附频率。铜绿假单胞菌膜蛋白的基因突变导致了位移模式的改变和粘附力的降低,ΔfliD突变体显示出更高斯的位移分布,对哺乳动物细胞的粘附力明显降低。粘附和耐受机制是多样而复杂的,可能涉及不同的途径;然而,我们的研究结果突显了靶向fliD基因(编码一种关键的鞭毛蛋白)的治疗潜力,因为删除该基因不仅会降低粘附性,还会降低抗生素耐受性:总之,我们的研究结果强调了单细胞追踪在短时间内准确评估细菌行为的重要性,并突出了其在指导有效干预策略方面的巨大潜力。
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Uncovering bacterial-mammalian cell interactions via single-cell tracking.

Background: The interactions between bacterial pathogens and host cells are characterized by a multitude of complexities, leading to a wide range of heterogeneous outcomes. Despite extensive research, we still have a limited understanding of how bacterial motility in complex environments impacts their ability to tolerate antibiotics and adhere to mammalian cell surfaces. The challenge lies in unraveling the complexity of these interactions and developing quantitative microscopy approaches to predict the behavior of bacterial populations.

Results: To address this challenge, we directed our efforts towards Pseudomonas aeruginosa, a pathogenic bacterium known for producing thick films in the lungs of cystic fibrosis patients, and Escherichia coli, used as a proof of concept to develop and demonstrate our single-cell tracking approaches. Our results revealed that P. aeruginosa exhibits diverse and complex interactions on mammalian cell surfaces, such as adhesion, rotational motion, and swimming, unlike the less interactive behavior of Escherichia coli. Our analysis indicated that P. aeruginosa demonstrated lower mean-squared displacement (MSD) values and greater adherence to mammalian cells compared to E. coli, which showed higher MSD slopes and less frequent adherence. Genetic mutations in membrane proteins of P. aeruginosa resulted in altered displacement patterns and reduced adhesion, with the ΔfliD mutant displaying a more Gaussian displacement distribution and significantly less adherence to mammalian cells. Adhesion and tolerance mechanisms are diverse and complex, potentially involving distinct pathways; however, our findings highlight the therapeutic potential of targeting the fliD gene (encoding a critical flagellum protein), as its deletion not only reduced adherence but also antibiotic tolerance.

Conclusions: Overall, our findings underscore the importance of single cell tracking in accurately assessing bacterial behavior over short time periods and highlight its significant potential in guiding effective intervention strategies.

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来源期刊
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
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