Collective interactions, human mobility and viral evolution shaped the SARS-CoV-2 transmission in Mainland China

Publication date: Dec 17, 2025

Collective interaction of individuals in various settings is crucial for exposure to infections, encompassing complex viral interplay and amplifying infectious risk through phenomena such as social reinforcement, clustering and superspreading events, during the COVID-19 pandemic. However, standard epidemic models often inadequately capture such heterogeneity, overlooking the higher-order social structural. Spatiotemporal variation in transmission, an essential feature of the pandemic, remains poorly quantified at various scales, particularly in integrating high-resolution data streams and complex network approaches. We introduced a higher-order simplicial model that unifies human mobility data, genetic diversity and antigenic drift to systematically investigate the role of social reinforcement, spatiotemporal variation and genetic mutations in SARS-CoV-2 transmission. We found a median of 5.3%-14.4% of infections across provinces were attributed to social reinforcement, while cluster heterogeneity contributed to a median of 17%-71% increase in susceptibility. Multiple viral interactions elevated transmissibility by 68%-70% across the periods of dominant variants. The reconstructed transmission networks underscore distinct spatiotemporal variation, with dynamic critical locations, varying mobility patterns, and evolving geographic cluster structures, by assessing complex networks. The influence of human mobility was found to be positive on transmission, effective distance was negatively associated with infection risks, while greater genetic diversity and antigenic drift were linked to higher susceptibility and transmissibility. Our proposed data-driven higher-order framework could help us to understand epidemics better by accounting the role of collective interactions, population mobility, and genetic mutation in transmission, which could inform the targeted interventions to mitigate SARS-CoV-2 and other respiratory pathogens.

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Concepts Keywords
China Al
Neurosciences Collective
Restaurants Covid
Virus Doi
Dynamics
Fig
Higher
Https
Infection
Interactions
Mobility
Org
Reinforcement
Social
Transmission

Semantics

Type Source Name
disease MESH infections
disease MESH COVID-19 pandemic
drug DRUGBANK Tropicamide
drug DRUGBANK Etodolac
disease MESH Park
disease MESH strains
disease MESH plan
disease MESH IFs
disease MESH imported infections
drug DRUGBANK Huperzine B
disease MESH included
pathway REACTOME Immune System
disease MESH infectious diseases
disease MESH secondary infection
disease MESH pneumonia
disease MESH Dis
disease MESH emergency
disease MESH influenza
disease MESH pneumococcal pneumonia
disease MESH mpox
pathway KEGG Quorum sensing
drug DRUGBANK Medical air
drug DRUGBANK L-Citrulline
disease MESH burn

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