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232  Susan C. Cork and Roy Halliwell

            Table 4.4b  Mode of Action of some commonly used antibacterial drugs.

            Antibacterial drug       Mode of Action        Comments
            BACTERIOCIDAL
            ß – Lactam antibiotics   Inhibition of cell wall   Low toxicity
            e.g. Penicillins, Cephalosporins synthesis
            Aminoglycosides, e.g.    Inhibition of protein   May be ototoxic and nephrotoxic
            Steptomycin, Neomycin    synthesis
            Trimethoprim             Inhibition of nucleic acid   Usually administered with
                                     synthesis             sulphamethaxazole as a ‘potentiated
                                                           sulphonamide
            Vancomycin               Inhibition of cell wall   May be used in cases of methicillin
                                     synthesis             resistant Staphylococcus aureus (MRSA)
            Polypeptides, e.g. Polymixin  Inhibition of membrane   May be nephrotoxic and neurotoxic
                                     function
            BACTERIOSTATIC
            Nitrofurans              Inhibition of protein   Relatively toxic. Broad spectrum of
                                     synthesis             activity
            Tetracyclines            Inhibition of protein   Development of resistance common,
                                     synthesis             has been widely used for prophylactic
                                                           treatment in livestock
            Chloramphenicol          Inhibition of protein   Potentially toxic. Use prohibited in food
                                     synthesis             producing animals in many countries
            Macrolides, e.g. erythromycin,  Inhibition of protein   May be effective against Mycoplasma sp.
            Tylosin                  synthesis
            Quinilones, e.g. Enrofoxican,   Inhibition of nucleic acid   May be used in combination with other
            Nalidixic acid           synthesis             drugs for treatment of mastitis
            Sulphonamides            Inhibition of nucleic acid   Effective against rapidly growing bacteria
                                     synthesis
            Nitroimidazoles, e.g.    Disruption of DNA structure  Effective against anaerobic bacteria and
            Metronidazole            and inhibition of repair  some protozoa, e.g. Giardia




            spontaneous mutations in the loci on the micro-  MuLtIPLE rESIStancE
            bial chromosome that determine susceptibility   The development of multiple resistance in bacteria
            to specific antibiotics. It is thought that the   depends on several different mechanisms. More
            presence of the antibiotic serves as a selecting   than one mechanism may operate for the same
            mechanism to suppress susceptible microor-  antibiotic. Microorganisms resistant to a certain
            ganisms and promote the growth of resistant   antibiotic (see Table 4.4b) may also be resistant to
            strains. Spontaneous mutations can also occur   other antibiotics that share a mechanism of action
            and these are transmissible vertically, that is,   or attachment. This type of ‘cross-resistance’ is
            they are passed on during bacterial replication.  most common with antibiotics that are closely
                                                     related chemically (for example, polymyxin B and
                                                     colistin, neomycin and kanamycin), but may also







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