Abstract
Acinetobacter baumannii are non-fermentative, Gram-negative bacilli that cause a large number of nosocomial infections worldwide. They are characterized by frequent multiresistance due to multiple mechanisms. As a consequence, infections caused by strains exhibiting resistance to carbapenems and, sometimes, polymyxins, are regularly observed. Sulbactam, colistin and combinations of different antimicrobials have been reported as new therapeutic approaches for infections caused by resistant A baumannii strains. This review focuses on current and potential new drugs, such as rifampin, tigecycline, antimicrobial peptides, efflux pump resistant and inhibitor drugs, and enzyme inhibitors.
MeSH terms
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Acinetobacter Infections / drug therapy*
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Acinetobacter baumannii / drug effects*
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Acinetobacter baumannii / genetics
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Acinetobacter baumannii / metabolism
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Anti-Bacterial Agents / pharmacology*
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Antimicrobial Cationic Peptides / pharmacology
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Antimicrobial Cationic Peptides / therapeutic use
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Clinical Trials as Topic
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Dipeptides / chemistry
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Dipeptides / pharmacology
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Dipeptides / therapeutic use
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Drug Resistance, Multiple, Bacterial / drug effects*
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Drug Resistance, Multiple, Bacterial / genetics
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Enzyme Inhibitors / pharmacology*
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Enzyme Inhibitors / therapeutic use
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Humans
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Minocycline / analogs & derivatives
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Minocycline / pharmacology
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Minocycline / therapeutic use
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Molecular Structure
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Rifampin / pharmacology
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Rifampin / therapeutic use
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Tigecycline
Substances
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Anti-Bacterial Agents
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Antimicrobial Cationic Peptides
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Dipeptides
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Enzyme Inhibitors
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phenylalanine arginine beta-naphthylamide
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Tigecycline
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Minocycline
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Rifampin