TY - JOUR
T1 - Paired single-cell host profiling with multiplex-tagged bacterial mutants reveals intracellular virulence-immune networks
AU - Heyman, Ori
AU - Yehezkel, Dror
AU - Ciolli Mattioli, Camilla
AU - Blumberger, Neta
AU - Rosenberg, Gili
AU - Solomon, Aryeh
AU - Hoffman, Dotan
AU - Bossel Ben-Moshe, Noa
AU - Avraham, Roi
N1 - Publisher Copyright: Copyright © 2023 the Author(s).
PY - 2023/7/11
Y1 - 2023/7/11
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85164001083&partnerID=8YFLogxK
U2 - 10.1073/pnas.2218812120
DO - 10.1073/pnas.2218812120
M3 - مقالة
C2 - 37399397
SN - 0027-8424
VL - 120
JO - Proceedings of the National Academy of Sciences
JF - Proceedings of the National Academy of Sciences
IS - 28
M1 - e2218812120
ER -