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解析感染瓶颈处的细胞-病原体相互作用

Untangling Cellular Host-Pathogen Encounters at Infection Bottlenecks.

机构信息

Department of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Infect Immun. 2023 Apr 18;91(4):e0043822. doi: 10.1128/iai.00438-22. Epub 2023 Mar 20.

Abstract

Bacterial pathogens can invade the tissue and establish a protected intracellular niche at the site of invasion that can spread locally (e.g., microcolonies) or to systemic sites (e.g., granulomas). Invasion of the tissue and establishment of intracellular infection are rare events that are difficult to study in the setting but have critical clinical consequences, such as long-term carriage, reinfections, and emergence of antibiotic resistance. Here, I discuss Salmonella interactions with its host macrophage during early stages of infection and their critical role in determining infection outcome. The dynamics of host-pathogen interactions entail highly heterogenous host immunity, bacterial virulence, and metabolic cross talk, requiring analysis at single-cell resolution. I discuss models and single-cell approaches that provide a global understanding of the establishment of a protected intracellular niche within the tissue and the host-pathogen landscape at infection bottlenecks during early stages of infection. Studying cellular host-pathogen interactions can improve our knowledge of the trajectory of infection between the initial inoculation with a dose of pathogens and the appearance of symptoms of disease.

摘要

细菌病原体可以入侵组织,并在入侵部位建立一个受保护的细胞内小生境,可以在局部(例如微菌落)或全身部位(例如肉芽肿)传播。组织的入侵和细胞内感染的建立是罕见的事件,在这种情况下很难进行研究,但具有关键的临床后果,例如长期携带、再感染和抗生素耐药性的出现。在这里,我讨论了沙门氏菌在感染早期与宿主巨噬细胞的相互作用及其在决定感染结果中的关键作用。宿主-病原体相互作用的动态涉及高度异质的宿主免疫、细菌毒力和代谢交叉对话,需要在单细胞分辨率下进行分析。我讨论了模型和单细胞方法,这些方法提供了对组织内受保护的细胞内小生境的建立以及在感染早期感染瓶颈处的宿主-病原体景观的全面了解。研究细胞宿主-病原体相互作用可以提高我们对从最初接种一定剂量的病原体到出现疾病症状之间的感染轨迹的认识。

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Untangling Cellular Host-Pathogen Encounters at Infection Bottlenecks.解析感染瓶颈处的细胞-病原体相互作用
Infect Immun. 2023 Apr 18;91(4):e0043822. doi: 10.1128/iai.00438-22. Epub 2023 Mar 20.

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