Dissecting Phenotype from Genotype with Clinical Isolates of SARS-CoV-2 First Wave Variants
2023
Mariah K. Taylor | Evan P. Williams | Yi Xue | Piroon Jenjaroenpun | Thidathip Wongsurawat | Amanda P. Smith | Amber M. Smith | Jyothi Parvathareddy | Ying Kong | Peter Vogel | Xueyuan Cao | Walter Reichard | Briana Spruill-Harrell | Amali E. Samarasinghe | Intawat Nookaew | Elizabeth A. Fitzpatrick | Micholas Dean Smith | Michelle Aranha | Jeremy C. Smith | Colleen B. Jonsson
The emergence and availability of closely related clinical isolates of SARS-CoV-2 offers a unique opportunity to identify novel nonsynonymous mutations that may impact phenotype. Global sequencing efforts show that SARS-CoV-2 variants have emerged and then been replaced since the beginning of the pandemic, yet we have limited information regarding the breadth of variant-specific host responses. Using primary cell cultures and the K18-hACE2 mouse, we investigated the replication, innate immune response, and pathology of closely related, clinical variants circulating during the first wave of the pandemic. Mathematical modeling of the lung viral replication of four clinical isolates showed a dichotomy between two B.1. isolates with significantly faster and slower infected cell clearance rates, respectively. While isolates induced several common immune host responses to infection, one B.1 isolate was unique in the promotion of eosinophil-associated proteins IL-5 and CCL11. Moreover, its mortality rate was significantly slower. Lung microscopic histopathology suggested further phenotypic divergence among the five isolates showing three distinct sets of phenotypes: (i) consolidation, alveolar hemorrhage, and inflammation, (ii) interstitial inflammation/septal thickening and peribronchiolar/perivascular lymphoid cells, and (iii) consolidation, alveolar involvement, and endothelial hypertrophy/margination. Together these findings show divergence in the phenotypic outcomes of these clinical isolates and reveal the potential importance of nonsynonymous mutations in nsp2 and ORF8.
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