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配对的单细胞宿主分析与多重标记的细菌突变体揭示了细胞内的毒力-免疫网络。

Paired single-cell host profiling with multiplex-tagged bacterial mutants reveals intracellular virulence-immune networks.

机构信息

Department of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 7610001, Israel.

出版信息

Proc Natl Acad Sci U S A. 2023 Jul 11;120(28):e2218812120. doi: 10.1073/pnas.2218812120. Epub 2023 Jul 3.

Abstract

Encounters between host cells and intracellular bacterial pathogens lead to complex phenotypes that determine the outcome of infection. Single-cell RNA sequencing (scRNA-seq) is increasingly used to study the host factors underlying diverse cellular phenotypes but has limited capacity to analyze the role of bacterial factors. Here, we developed scPAIR-seq, a single-cell approach to analyze infection with a pooled library of multiplex-tagged, barcoded bacterial mutants. Infected host cells and barcodes of intracellular bacterial mutants are both captured by scRNA-seq to functionally analyze mutant-dependent changes in host transcriptomes. We applied scPAIR-seq to macrophages infected with a library of Typhimurium secretion system effector mutants. We analyzed redundancy between effectors and mutant-specific unique fingerprints and mapped the global virulence network of each individual effector by its impact on host immune pathways. ScPAIR-seq is a powerful tool to untangle bacterial virulence strategies and their complex interplay with host defense strategies that drive infection outcome.

摘要

宿主细胞与细胞内细菌病原体的相互作用导致了决定感染结局的复杂表型。单细胞 RNA 测序(scRNA-seq)越来越多地被用于研究决定多种细胞表型的宿主因子,但它分析细菌因子作用的能力有限。在这里,我们开发了 scPAIR-seq,这是一种单细胞分析方法,用于分析带有多重标记、条形码细菌突变体的混合文库的感染。通过 scRNA-seq 同时捕获感染的宿主细胞和细胞内细菌突变体的条形码,以功能分析宿主转录组中突变体依赖性的变化。我们将 scPAIR-seq 应用于感染沙门氏菌分泌系统效应器突变体的巨噬细胞。我们分析了效应物之间的冗余性以及突变体特异性的独特指纹,并通过其对宿主免疫途径的影响来绘制每个效应物的全局毒力网络。scPAIR-seq 是一种强大的工具,可以理清细菌毒力策略及其与宿主防御策略的复杂相互作用,从而驱动感染结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3940/10334762/67f940e50717/pnas.2218812120fig01.jpg

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