The Hyundai Ioniq 6 looks... interesting 🧐
Hyundai has officially lifted the lid on its long-awaited Ioniq 6 electric sedan – and the Tesla Model 3 could finally have a genuine competitor on its hands.
Hyundai, however, has said that the car’s shape embodies the concepts of “Sensuous Sportiness” and “Optimistic Futurism”, which may as well be marketing jargon for"the Ioniq 6 is the automotive lovechild of aSeen from the rear, the sedan definitely fits the Porsche-Beetle mold, with a width-spanning line of tail lights adding a perceptible sense of modernity to an otherwise classic design.
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Differential Pathogenesis of SARS-CoV-2 Variants of Concern in Human ACE2-Expressing MiceSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused the current pandemic, resulting in millions of deaths worldwide. Increasingly contagious variants of concern (VoC) have fueled recurring global infection waves. A major question is the relative severity of the disease caused by previous and currently circulating variants of SARS-CoV-2. In this study, we evaluated the pathogenesis of SARS-CoV-2 variants in human ACE-2-expressing (K18-hACE2) mice. Eight-week-old K18-hACE2 mice were inoculated intranasally with a representative virus from the original B.1 lineage or from the emerging B.1.1.7 (alpha), B.1.351 (beta), B.1.617.2 (delta), or B.1.1.529 (omicron) lineages. We also infected a group of mice with the mouse-adapted SARS-CoV-2 (MA10). Our results demonstrate that B.1.1.7, B.1.351 and B.1.617.2 viruses are significantly more lethal than the B.1 strain in K18-hACE2 mice. Infection with the B.1.1.7, B.1.351, and B.1.617.2 variants resulted in significantly higher virus titers in the lungs and brain of mice compared with the B.1 virus. Interestingly, mice infected with the B.1.1.529 variant exhibited less severe clinical signs and a high survival rate. We found that B.1.1.529 replication was significantly lower in the lungs and brain of infected mice in comparison with other VoC. The transcription levels of cytokines and chemokines in the lungs of B.1- and B.1.1.529-infected mice were significantly less when compared with those challenged with other VoC. Together, our data provide insights into the pathogenesis of previous and circulating SARS-CoV-2 VoC in mice.
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