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PMID: 1976116 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Effect of type 1 piliation on in vitro killing of Escherichia coli by mouse peritoneal macrophages.

Infection and immunity ·Vol. 58 ·No. 10 ·1990-10-00 ·Pages 3448-54

Keith BR, Harris SL, Russell PW, Orndorff PE

Abstract

Escherichia coli K-12 mutants possessing defined lesions affecting type 1 pilus production, receptor binding, or length were examined for their ability to resist killing by mouse peritoneal macrophages in vitro. Mutants were mixed pairwise at known ratios in wells containing macrophages, and after incubation, the ratio of the survivors was assayed. The difference in phagocytic killing between type 1 piliated cells and isogenic nonpiliated cells was significant, the piliated cells being approximately threefold more resistant. Pilus length had little effect upon survival, as the long-piliated mutants were no more resistant to killing than the normal-length parents. Interestingly, the receptor-binding function of type 1 pili was most important in effecting resistance, as mutants lacking the ability to bind receptor were killed as effectively as nonpiliated mutants. These data are consistent with the notion that pili actually impede killing by macrophages rather than serve as passive physical barriers to uptake.

MeSH Terms
Animals Escherichia coli/genetics,immunology,ultrastructure Female Fimbriae, Bacterial/immunology,ultrastructure In Vitro Techniques Macrophages/immunology,ultrastructure Mice Mutation Peritoneal Cavity/cytology Phagocytosis/physiology Phenotype
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Keith B R
Department of Microbiology, Pathology and Parasitology, School of Veterinary Medicine, North Carolina State University, Raleigh 27606.
Harris S L
Russell P W
Orndorff P E
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1990-10-00
Pages
3448-54
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC313676
Subset
IM
Grants
NIAID NIH HHS · AI22223 · United States
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