“…Generally, the mechanism of target protection requires sustained or repeated direct interactions between the resistant protein and the target to develop antibiotic resistance, and no permanent changes are caused to the properties of the target. Common resistant proteins include tetracycline ribosomal protective protein (TRPPs; e.g., TetM, TetO), quinolone resistance protein (e.g., Qnr), antibiotic resistance (ARE) ABC-F protein (e.g., Msr, Vga, Lsa, Sal, Vml), FusB-type proteins, and cis-acting peptides (Eiamsam-ang et al, 2022;Ero et al, 2021;Slettemeås et al, 2019). TRPPs mediate the target protection against the tetracycline via the binding to the 30S ribosome subunit to obstruct the transmission of incoming aminoyl-TrNA through the extension factor Tu (EF-TU) during the extension phase of protein synthesis, which inhibits the bacterial translation (Ero et al, 2021;Founou et al, 2019).…”