毒力
生物
效应器
突变体
表型
多路复用
转录组
分泌物
微生物学
寄主(生物学)
细胞内
免疫系统
计算生物学
遗传学
基因
细胞生物学
基因表达
生物化学
作者
Ori Heyman,Dror Yehezkel,Camilla Ciolli Mattioli,Neta Blumberger,Gili Rosenberg,Aryeh Solomon,Dotan Hoffman,Noa Bossel Ben-Moshe,Roi Avraham
标识
DOI:10.1073/pnas.2218812120
摘要
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 Salmonella 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.
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