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Microbes & Immunity                                                   Natural phage patentability in the U.S.



            Appendix

            Table A1. Comparison of claims in the application and granted form of two patents
            Patent  Application form (20210228659-A1)  Granted form (11779617-B2)     Note
            Patent 1  1.  An antibacterial composition comprising  1.  An antibacterial composition comprising at least one   Canceled SEQ ID NO1; sequence
                     at least one bacteriophage having lytic   bacteriophage having lytic activity against a P. aeruginosa  identity requirement changed from
                     activity against a P. aeruginosa strain,   strain and a pharmaceutically acceptable excipient or   90% to 99%
                     said at least one bacteriophage selected   carrier, said at least one bacteriophage being selected
                     from the bacteriophages having a genome   from the bacteriophages having a genome comprising
                     comprising a nucleotide sequence of any   a nucleotide sequence of any one of SEQ ID NOs: 2 – 7
                     one of SEQ ID NOs: 1 – 7 or a sequence   or a sequence having at least 99% identity thereto, and
                     having at least 90% identity thereto. 2 – 4.   said pharmaceutically acceptable excipient or carrier
                     (canceled)                   comprising a preservative in an amount effective to
                                                  preserve the activity of the bacteriophage.
                   5.  The composition of claim 1, comprising   2.  The composition of claim 1, comprising at least one   The phage names and sequences
                     at least one bacteriophage of Table 1.  bacteriophage selected from the group consisting   were specified
                   6. (canceled)                  of BP1777, BP1792, BP1797, BP1800, BP1902,
                                                  and BP1940, said bacteriophage having a genome
                                                  comprising the nucleotide sequence of SEQ ID NOs:
                                                  2 – 7, respectively.
                   7.  The composition of claim 1, which is lytic  3.  The composition of claim 1, which is lytic against   Unchanged
                     against antibiotic-resistant P. aeruginosa   antibiotic-resistant P. aeruginosa strains.
                     strains.
                   8.  The composition of claim 1, which is lytic  4.  The composition of claim 1, which is lytic against more  Unchanged
                     against more than 90% of all bacterial   than 90% of all bacterial strains of the LMG collection.
                     strains of the LMG collection.
                   9.  The composition of claim 1, which   5.  The composition of claim 1, wherein the   Pharmaceutically acceptable
                     further comprises a pharmaceutically   pharmaceutically acceptable excipient or carrier   excipients or carriers were
                     acceptable excipient or carrier.  comprises buffered physiological saline.  specified
                   10.  The composition of claim 1, in the   6.  The composition of claim 1, in the form of a liquid,   /
                     form of a liquid, semi-liquid, solid, or   semi-liquid, solid, or lyophilized formulation.
                     lyophilized formulation.
                   11.  The composition of claim 10, which   7.  The composition of claim 6, which comprises between   /
                     comprises between 10e4 and 10e12 PFU   10e4 and 10e12 PFU of each bacteriophage.
                     of each bacteriophage.
                   12.  A method of treatment of an infection in  8.  A method of treatment of an infection in a mammal in  The phage composition amount
                     a mammal in need thereof comprising   need thereof comprising contacting the mammal with   and sequence identity were
                     contacting the mammal with a   an effective amount of an antibacterial composition,   specified
                     composition of claim 1.      wherein said composition comprises at least one
                                                  bacteriophage having lytic activity against a
                                                  P. aeruginosa strain, said at least one bacteriophage
                                                  being selected from the bacteriophages having a
                                                  genome comprising any one of SEQ ID NOs: 2 – 7 or a
                                                  sequence having at least 99% identity thereto.
                   13.  The method of claim 12, wherein   9.  The method of claim 8, wherein the infection is an   Unchanged
                     the infection is an infection of the   infection of the respiratory tract.
                     respiratory tract.
                   14.  A method for improving the condition   10.  A method for improving the condition of a mammal   The phage composition amount
                     of a mammal by modifying the   by modifying the microbial flora in said mammal   and sequence identity were
                     microbial flora in said mammal   comprising contacting the mammal with an effective   specified
                     comprising contacting the mammal with   amount of an antibacterial composition, wherein said
                     a composition of claim 1.     composition comprises at least one bacteriophage
                                                   having lytic activity against a P. aeruginosa strain, said
                                                   at least one bacteriophage being selected from the
                                                   bacteriophages having a genome comprising any one
                                                   of SEQ ID NOs: 2 – 7 or a sequence having at least
                                                   99% identity thereto.
                                                                                                       (Cont’d...)


            Volume 2 Issue 3 (2025)                         69                               doi: 10.36922/mi.4758
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