Deciphering viral infections at single-cell resolution: From immune dynamics to host-pathogen interactions.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Deciphering viral infections at single-cell resolution: From immune dynamics to host-pathogen interactions.
Συγγραφείς: Zhou W; Department of Gastroenterology, University-Town Hospital of Chongqing Medical University, Chongqing, China., Xu P; Department of Clinical Laboratory, University-Town Hospital of Chongqing Medical University, Chongqing, China. Electronic address: panxu@hospital.cqmu.edu.cn.
Πηγή: Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases [Infect Genet Evol] 2026 Sep; Vol. 143, pp. 105969. Date of Electronic Publication: 2026 Jun 17.
Τύπος έκδοσης: Journal Article; Review
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: Elsevier Science Country of Publication: Netherlands NLM ID: 101084138 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1567-7257 (Electronic) Linking ISSN: 15671348 NLM ISO Abbreviation: Infect Genet Evol Subsets: MEDLINE
Imprint Name(s): Original Publication: Amsterdam ; New York : Elsevier Science, c2001-
Ιατρικοί όροι (MeSH): Host-Pathogen Interactions*/immunology , Host-Pathogen Interactions*/genetics , Virus Diseases*/immunology , Virus Diseases*/virology , Virus Diseases*/genetics , Single-Cell Analysis*/methods, Humans ; Animals ; Single-Cell Gene Expression Analysis
Περίληψη: Single-cell RNA sequencing (scRNA-seq) has emerged as a transformative technology in infectious disease research, enabling high-resolution characterization of cellular heterogeneity, immune dynamics, and host-pathogen interactions at the single-cell level. In the context of viral infections-including SARS-CoV-2, hepatitis B virus (HBV), human immunodeficiency virus (HIV), influenza virus, and respiratory syncytial virus (RSV)-scRNA-seq has provided critical insights into immune-cell heterogeneity, immune landscape remodeling, and the emergence of previously unrecognized cellular states. Beyond immune profiling, scRNA-seq enables direct detection of viral transcripts within infected cells. This allows discrimination between productively infected and bystander cells and reveals virus-induced transcriptional reprogramming within target tissues. Additionally, single-cell approaches facilitate the analysis of adaptive immune repertoires through integrated integrated T-cell receptor (TCR) and B-cell receptor (BCR) sequencing sequencing and uncover intra-host viral diversity and evolutionary dynamics at unprecedented resolution. This review summarizes recent advances in the application of scRNA-seq in viral infection research, with a focus on immune regulation, host-pathogen co-transcriptomics, inflammatory signaling pathways, biomarker discovery, and translational implications. Comparative single-cell studies across acute and chronic viral infections have further revealed both shared antiviral programs and virus-specific immune adaptations.We further discuss current technical limitations and emerging computational strategies, as well as future integration with spatial transcriptomics and multi-omics platforms. Collectively, these developments highlight the potential of single-cell technologies to advance mechanistic understanding and guide precision diagnostics and therapeutic strategies in viral diseases.
(Copyright © 2026 The Authors. Published by Elsevier B.V. All rights reserved.)
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Contributed Indexing: Keywords: Comparative virology; Host–pathogen interactions; Immune heterogeneity; Single-cell RNA sequencing; Viral infections
Entry Date(s): Date Created: 20260617 Date Completed: 20260725 Latest Revision: 20260725
Update Code: 20260726
DOI: 10.1016/j.meegid.2026.105969
PMID: 42309184
Βάση Δεδομένων: MEDLINE
Περιγραφή
ISSN:1567-7257
DOI:10.1016/j.meegid.2026.105969