tetano
Editor, Senior Moderator
Viruses
. 2021 Sep 5;13(9):1773.
doi: 10.3390/v13091773.
SARS-CoV-2 Delta Variant Pathogenesis and Host Response in Syrian Hamsters
Sreelekshmy Mohandas[SUP] 1 [/SUP], Pragya Dhruv Yadav[SUP] 1 [/SUP], Anita Shete[SUP] 1 [/SUP], Dimpal Nyayanit[SUP] 1 [/SUP], Gajanan Sapkal[SUP] 1 [/SUP], Kavita Lole[SUP] 1 [/SUP], Nivedita Gupta[SUP] 2 [/SUP]
Affiliations
Abstract
B.1.617 is becoming a dominant Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2) lineage worldwide with many sublineages, of which B.1.617.2 is designated as a variant of concern. The pathogenicity of B.1.617.2 (Delta) and B.1.617.3 lineage of SARS-CoV-2 was evaluated and compared with that of B.1, an early virus isolate with D614G mutation in a Syrian hamster model. Viral load, antibody response, and lung disease were studied. There was no significant difference in the virus shedding pattern among these variants. High levels of SARS-CoV-2 sub genomic RNA were detected in the respiratory tract of hamsters infected with the Delta variant for 14 days, which warrants further transmission studies. The Delta variant induced lung disease of moderate severity in about 40% of infected animals, which supports the attributed disease severity of the variant. Cross neutralizing antibodies were detected in animals infected with B.1, Delta, and B.1.617.3 variant, but neutralizing capacity was significantly lower with B.1.351 (Beta variant).
Keywords: B.1.617.2; B.1.617.3; Delta variant; SARS-CoV-2; Syrian hamster; pathogenicity.
. 2021 Sep 5;13(9):1773.
doi: 10.3390/v13091773.
SARS-CoV-2 Delta Variant Pathogenesis and Host Response in Syrian Hamsters
Sreelekshmy Mohandas[SUP] 1 [/SUP], Pragya Dhruv Yadav[SUP] 1 [/SUP], Anita Shete[SUP] 1 [/SUP], Dimpal Nyayanit[SUP] 1 [/SUP], Gajanan Sapkal[SUP] 1 [/SUP], Kavita Lole[SUP] 1 [/SUP], Nivedita Gupta[SUP] 2 [/SUP]
Affiliations
- PMID: 34578354
- DOI: 10.3390/v13091773
Abstract
B.1.617 is becoming a dominant Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2) lineage worldwide with many sublineages, of which B.1.617.2 is designated as a variant of concern. The pathogenicity of B.1.617.2 (Delta) and B.1.617.3 lineage of SARS-CoV-2 was evaluated and compared with that of B.1, an early virus isolate with D614G mutation in a Syrian hamster model. Viral load, antibody response, and lung disease were studied. There was no significant difference in the virus shedding pattern among these variants. High levels of SARS-CoV-2 sub genomic RNA were detected in the respiratory tract of hamsters infected with the Delta variant for 14 days, which warrants further transmission studies. The Delta variant induced lung disease of moderate severity in about 40% of infected animals, which supports the attributed disease severity of the variant. Cross neutralizing antibodies were detected in animals infected with B.1, Delta, and B.1.617.3 variant, but neutralizing capacity was significantly lower with B.1.351 (Beta variant).
Keywords: B.1.617.2; B.1.617.3; Delta variant; SARS-CoV-2; Syrian hamster; pathogenicity.