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PMID: 3943891 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Bactericidal effect of lactoferrin on Legionella pneumophila.

Infection and immunity ·Vol. 51 ·No. 2 ·1986-02-00 ·Pages 373-7

Bortner CA, Miller RD, Arnold RR

Abstract

Lactoferrin, an iron-binding protein found in mucosal secretions and in specific granules of polymorphonuclear leukocytes, has been shown to be bactericidal for a variety of organisms. In this study, the effect of lactoferrin on Legionella pneumophila was investigated. Purified human apolactoferrin was bactericidal for the Knoxville 1 strain (serogroup 1), with a 4-log decrease in viability within 2 h at 37 degrees C. Killing was dependent on the iron-free state since iron-saturated lactoferrin had no activity. Guinea pig passage of this strain did not affect its sensitivity to lactoferrin. Treatment of the cells with dilutions of the lactoferrin resulted in correspondingly reduced killing. Activity was temperature dependent; there was no loss of viability at 1 or 22 degrees C and slightly enhanced killing at 41 degrees C. Addition of Mg2+ blocked bactericidal activity. In addition, mature human milk, a lactoferrin-containing mucosal secretion, was also bactericidal for L. pneumophila. As demonstrated with the purified lactoferrin, bactericidal activity was lost when the milk was iron saturated.

MeSH Terms
Animals Dose-Response Relationship, Drug Guinea Pigs Lactoferrin/analysis,pharmacology Lactoglobulins/pharmacology Legionella/drug effects Magnesium/pharmacology Milk, Human/analysis Temperature
Chemicals
Lactoglobulins Lactoferrin Magnesium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Bortner C A
Miller R D
Arnold R R
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30 references, click to expand
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1986-02-00
Pages
373-7
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC262332
Subset
IM
Grants
NIAID NIH HHS · R01 AI16121 · United States
NIDCR NIH HHS · R01 DEO6869 · United States
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