tetano
Editor, Senior Moderator
J Med Virol
. 2023 Jun;95(6):e28847.
doi: 10.1002/jmv.28847. Comparative spatial transcriptomic profiling of severe acute respiratory syndrome coronavirus 2 Delta and Omicron variants infections in the lungs of cynomolgus macaques
Taehwan Oh[SUP] 1 [/SUP], Green Kim[SUP] 1 [/SUP], Seung Ho Baek[SUP] 1 [/SUP], YoungMin Woo[SUP] 1 2 [/SUP], Bon-Sang Koo[SUP] 1 [/SUP], Eun-Ha Hwang[SUP] 1 [/SUP], Kyuyoung Shim[SUP] 1 2 [/SUP], You Jung An[SUP] 1 [/SUP], Yujin Kim[SUP] 1 [/SUP], Jae-Hak Park[SUP] 3 [/SUP], Jung Joo Hong[SUP] 1 2 [/SUP]
Affiliations
Recently emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variants are generally less pathogenic than previous strains. However, elucidating the molecular basis for pulmonary immune response alterations is challenging owing to the virus's heterogeneous distribution within complex tissue structure. Here, we revealed the spatial transcriptomic profiles of pulmonary microstructures at the SARS-CoV-2 infection site in the nine cynomolgus macaques upon inoculation with the Delta and Omicron variants. Delta- and Omicron-infected lungs had upregulation of genes involved in inflammation, cytokine response, complement, cell damage, proliferation, and differentiation pathways. Depending on the tissue microstructures (alveoli, bronchioles, and blood vessels), there were differences in the types of significantly upregulated genes in each pathway. Notably, a limited number of genes involved in cytokine and cell damage response were differentially expressed between bronchioles of the Delta- and Omicron-infection groups. These results indicated that despite a significant antigenic shift in SARS-CoV-2, the host immune response mechanisms induced by the variants were relatively consistent, with limited transcriptional alterations observed only in large airways. This study may aid in understanding the pathogenesis of SARS-CoV-2 and developing a clinical strategy for addressing immune dysregulation by identifying potential transcriptional biomarkers within pulmonary microstructures during infection with emerging variants.
Keywords: SARS-CoV-2 variants; host immune response; nonhuman primates; pulmonary structure; spatial transcriptomics.
. 2023 Jun;95(6):e28847.
doi: 10.1002/jmv.28847. Comparative spatial transcriptomic profiling of severe acute respiratory syndrome coronavirus 2 Delta and Omicron variants infections in the lungs of cynomolgus macaques
Taehwan Oh[SUP] 1 [/SUP], Green Kim[SUP] 1 [/SUP], Seung Ho Baek[SUP] 1 [/SUP], YoungMin Woo[SUP] 1 2 [/SUP], Bon-Sang Koo[SUP] 1 [/SUP], Eun-Ha Hwang[SUP] 1 [/SUP], Kyuyoung Shim[SUP] 1 2 [/SUP], You Jung An[SUP] 1 [/SUP], Yujin Kim[SUP] 1 [/SUP], Jae-Hak Park[SUP] 3 [/SUP], Jung Joo Hong[SUP] 1 2 [/SUP]
Affiliations
- PMID: 37272485
- DOI: 10.1002/jmv.28847
Recently emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variants are generally less pathogenic than previous strains. However, elucidating the molecular basis for pulmonary immune response alterations is challenging owing to the virus's heterogeneous distribution within complex tissue structure. Here, we revealed the spatial transcriptomic profiles of pulmonary microstructures at the SARS-CoV-2 infection site in the nine cynomolgus macaques upon inoculation with the Delta and Omicron variants. Delta- and Omicron-infected lungs had upregulation of genes involved in inflammation, cytokine response, complement, cell damage, proliferation, and differentiation pathways. Depending on the tissue microstructures (alveoli, bronchioles, and blood vessels), there were differences in the types of significantly upregulated genes in each pathway. Notably, a limited number of genes involved in cytokine and cell damage response were differentially expressed between bronchioles of the Delta- and Omicron-infection groups. These results indicated that despite a significant antigenic shift in SARS-CoV-2, the host immune response mechanisms induced by the variants were relatively consistent, with limited transcriptional alterations observed only in large airways. This study may aid in understanding the pathogenesis of SARS-CoV-2 and developing a clinical strategy for addressing immune dysregulation by identifying potential transcriptional biomarkers within pulmonary microstructures during infection with emerging variants.
Keywords: SARS-CoV-2 variants; host immune response; nonhuman primates; pulmonary structure; spatial transcriptomics.