“…In addition, the co-circulation of several mutant strains increases the risk of co-infection, which may modify the viral pathogeny and eventually promote potential inter-strain recombination [ 1 , 2 ], mainly occurring in ORF1a and in the S gene [ 3 ], especially in the 174–2692 nt region of ORF1ab, 21,801–22,281 nt and 24,174–24,648 nt in the S gene in Sarbecoviruses [ 3 , 4 ]. However, the literature on co-infection by different SARS-CoV-2 variants and potential subsequent changes in the biological properties of this pandemic virus remains limited [ 3 , 4 , 5 ]. A recent work in France by P Combes at al showed mutation profiles suggesting that a Delta/Omicron population mixture was observed in 7 nasopharyngeal swabs out of 3831 respiratory samples in a high co-circulation period of the two variants.…”