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PMID: 6124504 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Association of type 1 pili with the ability of livers to clear Salmonella typhimurium.

Infection and immunity ·Vol. 36 ·No. 3 ·1982-06-00 ·Pages 1168-74

Leunk RD, Moon RJ

Abstract

The role of type 1 pili in the adherence of Salmonella typhimurium strain SR-11 to hepatic sinusoidal cells was investigated. An average of 66.7% of piliated organisms was cleared by perfused livers on a single pass. Mannose and alpha-methyl-D-mannoside inhibited such trapping in a dose-dependent manner. Preincubation of the bacteria, but not the liver, with either sugar also inhibited trapping, suggesting that the sugar binds to bacterial, not hepatic, receptors. Significant numbers of previously trapped bacteria could be eluted by adding mannose to the wash medium. Bacteria with reduced piliation, obtained either by growing bacteria on agar or by using a nonpiliated variant of the parent strain, were trapped to a significantly lesser extent than the parent strain. The liver appears to selectively trap heavily piliated organisms since reperfusion of bacteria through a second liver results in significantly less trapping than occurs with the first perfusion. In vivo, the nonpiliated variant strain was cleared much more slowly than the piliated parent strain. Mannose and alpha-methyl-D-mannoside, but not glucose, decreased clearance rates of piliated organisms. Cumulatively, the data suggest that type 1 pili are a major factor in hepatic clearance of S. typhimurium.

MeSH Terms
Animals Binding, Competitive Cell Adhesion Female Fimbriae, Bacterial/immunology Liver/microbiology Mannosides/metabolism Mice Salmonella typhimurium/immunology
Chemicals
Mannosides
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Leunk R D
Moon R J
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20 references, click to expand
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1982-06-00
Pages
1168-74
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC551453
Subset
IM
Grants
NIAID NIH HHS · AI 15452 · United States
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