Short-range airborne transmission is an important driver of the respiratory disease spread.
Short-range airborne transmission is an important driver of the respiratory disease spread. However, the early postemission recovery of viable pathogen-laden droplets (VPLDs), relevant to close-contact exposure and transmission, remains poorly understood. Using an impactor-based platform, we assessed how solute composition, pathogen load, and indoor relative humidity (RH) influence postequilibration VPLD counts within a physiologically relevant aerodynamic range. Clinically relevant titers of Phi6 (1 × 105 and 5 × 105 plaque-forming units/mL), a SARS-CoV-2 surrogate, were suspended in proxy solutions reflecting airway solute content in healthy (1.5% w/v) and disease-relevant (3–6% w/v) conditions. Droplets equilibrated under indoor winter-like (15 ± 5% RH) or summer-like (50 ± 5% RH) environments. At low viral titer, recovered counts of VPLD (1.73 to 20.28 μm) were significantly higher under low-solute/low-RH than under high-solute/intermediate-RH conditions. Conversely, the solute content and RH did not significantly alter recovered counts of VPLD within the largest fraction (18.65 to ≥20.28 μm). At high viral titer, solute and RH conditions did not alter recovered counts of VPLD within smaller fractions (1.73 to 13.62 μm); however, within the largest fraction, recovered counts increased significantly under high-solute/intermediate-RH conditions. These findings suggest that droplet microphysics, host physiology, and seasonal humidity variations indoors influence the postemission recovery of VPLD.
No takes yet. Share an insight, caveat, or question.
Thirugnanasampanthar et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: