Published online before print October 4, 2005
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*Department of Molecular Biology and Microbiology, Biomolecular Science Center, University of Central Florida, Orlando; and
Department of Medicine, Division of Pulmonary and Critical Care Medicine and the Will Rogers Institute Pulmonary Research Laboratory, David Geffen School of Medicine at University of California Los Angeles
@ To whom correspondence should be addressed. E-mail: tganz{at}mednet.ucla.edu.
Lysozyme is a ubiquitous and abundant, cationic, antimicrobial polypeptide of leukocytes and epithelia, but its biological function in host defense is largely unexplored. To ascertain the role of lysozyme during bacterial infection of murine airways, we exposed the airways of lysozyme M-deficient (lys M-/-) mice to the pulmonary pathogen Pseudomonas aeruginosa and examined the hosts response to infection. Despite partial compensation as a result of the appearance of lysozyme P in the infected airways of lys M-/- mice, these lys M-/- mice showed decreased clearance of P. aeruginosa compared with their lys M+/- or lys M+/+ littermates. Lysozyme contributes to optimal clearance of P. aeruginosa from the murine airways.
Key Words: knockout bacteria
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