“…An example of the existence of accumulation of small RNA fragments exists in Sclerotinia sclerotiorum infected with the SsHV2-L virus, and these small RNAs derived from the virus measure approximately 22 nt, the same length as the miRs, suggesting a cleavage by a protein Dicer-like [ 51 ]. Regarding SARS-CoV-2, such an influence on protein translation has already been described [ 53 , 54 , 55 , 56 , 57 , 58 , 59 , 60 , 61 , 62 , 63 , 64 , 65 ], causing observed effects on the concentration of certain proteins, such as a dramatic decrease in hemoglobin [ 66 , 67 , 68 , 69 ]. If we assume that short RNA subsequences (about 20 nucleotides long), from the genes of the SARS-CoV-2 virus, can bind to Argonaut proteins and hybridize the mRNA of key human proteins, involved in metabolisms important as oxygen metabolism, it follows that recombinations, mutations and/or deletions observed in the SARS-CoV-2 genome (such as those which appeared in the United Kingdom, South Africa, France, etc., or spontaneously in vitro [ 70 , 71 , 72 , 73 , 74 , 75 , 76 , 77 ]) can reinforce the possible existence of RNA fragments, possibly capable of hybridizing for example the mRNA of subunits of hemoglobin, the gamma-globin ( Figure 6 ) and the beta-globin ( Figure 7 ), impacting the oxygen transport in infected patients.…”