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PMID: 2550368 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Adhesion to and invasion of HEp-2 cells by Campylobacter spp.

Infection and immunity ·Vol. 57 ·No. 10 ·1989-10-00 ·Pages 2984-90

Konkel ME, Joens LA

Abstract

Twenty-one isolates were tested for their ability to adhere to and invade HEp-2 cells in vitro. Of the 21 organisms tested, 2 did not invade the HEp-2 cells, and 1 of these did not adhere to the epithelial cells. Campylobacter jejuni clinical isolates were more invasive than the nonclinical strains that were tested. When HEp-2 cells were treated with cytochalasin B, the invasiveness of C. jejuni was reduced, indicating active participation of the host cell in the uptake of these organisms. The number of intracellular C. jejuni isolates decreased when Campylobacter whole-cell lysates were absorbed onto HEp-2 cell monolayers. Experiments were also conducted to identify the functional sites of the antigens responsible for expression of Campylobacter invasion. Oxidation of lysates with sodium meta-periodate significantly affected its inhibitory capacity. This implies that the Campylobacter invasive ligand appears to be dependent upon an intact carbohydrate moiety.

MeSH Terms
Bacterial Adhesion/drug effects Bacteriolysis Campylobacter/drug effects,pathogenicity,physiology Campylobacter fetus/pathogenicity,physiology Cell Line Cytochalasin B/pharmacology Endopeptidase K Epithelium/microbiology Humans Periodic Acid/pharmacology Serine Endopeptidases/pharmacology Trypsin/pharmacology Tumor Cells, Cultured/microbiology Virulence/drug effects
Chemicals
Periodic Acid Cytochalasin B metaperiodate Serine Endopeptidases Trypsin Endopeptidase K
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Konkel M E
Department of Veterinary Science, University of Arizona, Tucson 85721.
Joens L A
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1989-10-00
Pages
2984-90
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC260759
Subset
IM
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