“…With the continuous discovery of SARS-CoV-2 variants, including but not limited to B.1.1.7 (Alpha), B.1.351 (Beta), P.1 (Gamma), B.1.617.1 (Kappa) B.1.617.2 (Delta), B.1.526 (Iota), B.1.351, A.23.1, and most recently, the highly convoluted B.1.1.529 (Omicron) (Callaway, 2021) [ 85 , 86 , 87 , 88 ], SARS-CoV-2 treatment and vaccination are both constantly challenged. Although specific mutations in the spike protein, including the B.1.1.7 and B.1.351 variants, are generally effectively neutralized by existing vaccines [ 85 ], the response of vaccines to other variants, including the P.1 andB.1.617.2 display significantly reduced neutralization of SARS-CoV-2, with other variants such as the B.1.1.529 posing as novel challenges toward herd immunity. The B.1.617.2 variant, initially identified in India [ 89 ], possesses mutations granting enhanced transmissibility and producing more severe symptoms characteristic of higher viral loads within the respiratory tract, in addition to a unique symptom of gangrene secondary to severe blood clots.…”