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肠道细菌感染的体外和离体建模。

In vitro and ex vivo modeling of enteric bacterial infections.

机构信息

Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.

Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Gut Microbes. 2023 Jan-Dec;15(1):2158034. doi: 10.1080/19490976.2022.2158034.

Abstract

Enteric bacterial infections contribute substantially to global disease burden and mortality, particularly in the developing world. 2D monolayer cultures have provided critical insights into the fundamental virulence mechanisms of a multitude of pathogens, including serovars Typhimurium and Typhi, spp., and , which have led to the identification of novel targets for antimicrobial therapy and vaccines. In recent years, the arsenal of experimental systems to study intestinal infections has been expanded by a multitude of more complex models, which have allowed to evaluate the effects of additional physiological and biological parameters on infectivity. Organoids recapitulate the cellular complexity of the human intestinal epithelium while 3D bioengineered scaffolds and microphysiological devices allow to emulate oxygen gradients, flow and peristalsis, as well as the formation and maintenance of stable and physiologically relevant microbial diversity. Additionally, advancements in cultures and intravital imaging have opened new possibilities to study the effects of enteric pathogens on fluid secretion, barrier integrity and immune cell surveillance in the intact intestine. This review aims to present a balanced and updated overview of current intestinal and methods for modeling of enteric bacterial infections. We conclude that the different paradigms are complements rather than replacements and their combined use promises to further our understanding of host-microbe interactions and their impacts on intestinal health.

摘要

肠细菌感染是全球疾病负担和死亡率的主要原因,特别是在发展中国家。二维单层培养为研究多种病原体(包括鼠伤寒血清型和伤寒血清型、志贺氏菌和霍乱弧菌)的基本毒力机制提供了重要的见解,这些机制导致了新型抗菌治疗和疫苗的靶点的鉴定。近年来,研究肠道感染的实验系统库通过多种更复杂的模型得到了扩展,这些模型允许评估其他生理和生物学参数对传染性的影响。类器官重现了人类肠道上皮的细胞复杂性,而三维生物工程支架和微生理设备允许模拟氧气梯度、流动和蠕动,以及稳定和生理相关微生物多样性的形成和维持。此外,在培养和体内成像方面的进展为研究肠病原体对完整肠道中液体分泌、屏障完整性和免疫细胞监视的影响开辟了新的可能性。本综述旨在对当前用于模拟肠细菌感染的肠道感染和模型方法进行平衡和更新的概述。我们得出的结论是,不同的范例是互补的,而不是替代的,它们的联合使用有望进一步加深我们对宿主-微生物相互作用及其对肠道健康影响的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3795/9809952/06627358fabc/KGMI_A_2158034_F0001_OC.jpg

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