Merck Manual

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Dawn Merton Boothe

, DVM, PhD, Department of Anatomy, Physiology, and Pharmacology, College of Veterinary Medicine, Auburn University

Last full review/revision Nov 2015 | Content last modified Nov 2015

Bacitracins are branched, cyclic, decapeptide antibiotics. Bacitracin A is the most active of the group and the main component of the commercial bacitracin preparations used either topically or PO. These antibiotics are bactericidal. They interfere with cell membrane function, suppress cell wall formation by preventing the formation of peptidoglycan strands, and inhibit protein synthesis. Bactericidal activity requires the presence of divalent cations, such as zinc.

The spectrum of bacitracins is described as broad, but it is used primarily to treat gram-positive infections. Resistance is rare. Bacitracins are often used in combination with neomycin and polymyxins to enhance the antibacterial spectrum.

Bacitracins are not appreciably absorbed from the GI tract and are not used systemically because of their pronounced nephrotoxicity. However, they are used locally in wound powders and ointments, dermatologic preparations, eye and ear ointments, and as feed additives in swine and poultry rations for growth promotion. In antibiotic-associated pseudomembranous colitis caused by Clostridium difficile cytotoxin, bacitracin (given PO) is considered an alternative to vancomycin. Hypersensitivity reactions to bacitracins are seen occasionally.

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Systemic Pharmacotherapeutics of the Cardiovascular System
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