Biological characterization of Campylobacter fetus lipopolysaccharides

Lipopolysaccharides (LPS) of three strains of Campylobacter fetus (subspp. fetus and venerealis, and serotypes A and B), a bacterium of veterinary importance but also a cause of various infections in humans, were assessed for their ability to induce mitogenicity, gelation of Limulus amebocyte lysate...

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Veröffentlicht in:FEMS immunology and medical microbiology 1996-08, Vol.15 (1), p.43-50
Hauptverfasser: Moran, A.P, O'Malley, D.T, Vuopio-Varkila, J, Varkila, K, Pyhala, L, Saxen, H, Helander, I.M
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container_issue 1
container_start_page 43
container_title FEMS immunology and medical microbiology
container_volume 15
creator Moran, A.P
O'Malley, D.T
Vuopio-Varkila, J
Varkila, K
Pyhala, L
Saxen, H
Helander, I.M
description Lipopolysaccharides (LPS) of three strains of Campylobacter fetus (subspp. fetus and venerealis, and serotypes A and B), a bacterium of veterinary importance but also a cause of various infections in humans, were assessed for their ability to induce mitogenicity, gelation of Limulus amebocyte lysate, lethal toxicity in mice, and pyrogenicity in rabbits. All C. fetus LPS exhibited activities lower than those of Salmonella typhimurium LPS. LPS of C. fetus subsp. fetus serotype A had the lowest activity in all assays. Since the majority of C. fetus subsp. fetus isolated from humans are serotype A. the lower biological activities of this LPS may aid the pathogenesis of such strains. The lower activities of C. fetus LPS compared with those of S. typhimurium LPS may reflect the presence of longer fatty acid chains in the lipid A of C. fetus LPS. whereas interstrain differences in C. fetus LPS bioactivities may be related to some property influenced by composition of the saccharide moiety.
doi_str_mv 10.1111/j.1574-695X.1996.tb00357.x
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All C. fetus LPS exhibited activities lower than those of Salmonella typhimurium LPS. LPS of C. fetus subsp. fetus serotype A had the lowest activity in all assays. Since the majority of C. fetus subsp. fetus isolated from humans are serotype A. the lower biological activities of this LPS may aid the pathogenesis of such strains. 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O'Malley, D.T ; Vuopio-Varkila, J ; Varkila, K ; Pyhala, L ; Saxen, H ; Helander, I.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3443-fd0d2ef515d460bd36b197dddb46500bdd78daf851566194b803b1bc67fcf32f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>amebocyte lysate gelation</topic><topic>Animals</topic><topic>B-Lymphocytes - drug effects</topic><topic>Biocompatibility</topic><topic>Biological activity</topic><topic>Campylobacter</topic><topic>Campylobacter fetus</topic><topic>Campylobacter fetus - chemistry</topic><topic>Campylobacter fetus - metabolism</topic><topic>Campylobacter fetus subsp. fetus</topic><topic>Campylobacter fetus subsp. venerealis</topic><topic>Carbohydrates</topic><topic>characterization</topic><topic>chemical composition</topic><topic>Crustaceans</topic><topic>Endotoxin</topic><topic>endotoxins</topic><topic>Endotoxins - toxicity</topic><topic>Fatty acids</topic><topic>Fetuses</topic><topic>Gelation</topic><topic>genetic variation</topic><topic>Limulus Test - methods</topic><topic>Lipid A</topic><topic>Lipid A - chemistry</topic><topic>Lipid A - metabolism</topic><topic>Lipids</topic><topic>Lipopolysaccharide</topic><topic>Lipopolysaccharides</topic><topic>Lipopolysaccharides - analysis</topic><topic>Lipopolysaccharides - toxicity</topic><topic>Lymphocyte Activation - drug effects</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred CBA</topic><topic>Mitogenicity</topic><topic>mitogens</topic><topic>Pathogenesis</topic><topic>pyrofenicity</topic><topic>Pyrogenicity</topic><topic>pyrogens</topic><topic>Pyrogens - analysis</topic><topic>Rabbits</topic><topic>Salmonella</topic><topic>Salmonella typhimurium</topic><topic>Serotypes</topic><topic>Serotyping</topic><topic>strains</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moran, A.P</creatorcontrib><creatorcontrib>O'Malley, D.T</creatorcontrib><creatorcontrib>Vuopio-Varkila, J</creatorcontrib><creatorcontrib>Varkila, K</creatorcontrib><creatorcontrib>Pyhala, L</creatorcontrib><creatorcontrib>Saxen, H</creatorcontrib><creatorcontrib>Helander, I.M</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; 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All C. fetus LPS exhibited activities lower than those of Salmonella typhimurium LPS. LPS of C. fetus subsp. fetus serotype A had the lowest activity in all assays. Since the majority of C. fetus subsp. fetus isolated from humans are serotype A. the lower biological activities of this LPS may aid the pathogenesis of such strains. The lower activities of C. fetus LPS compared with those of S. typhimurium LPS may reflect the presence of longer fatty acid chains in the lipid A of C. fetus LPS. whereas interstrain differences in C. fetus LPS bioactivities may be related to some property influenced by composition of the saccharide moiety.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>8871115</pmid><doi>10.1111/j.1574-695X.1996.tb00357.x</doi><tpages>8</tpages></addata></record>
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identifier ISSN: 0928-8244
ispartof FEMS immunology and medical microbiology, 1996-08, Vol.15 (1), p.43-50
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Oxford University Press Journals All Titles (1996-Current); Alma/SFX Local Collection
subjects amebocyte lysate gelation
Animals
B-Lymphocytes - drug effects
Biocompatibility
Biological activity
Campylobacter
Campylobacter fetus
Campylobacter fetus - chemistry
Campylobacter fetus - metabolism
Campylobacter fetus subsp. fetus
Campylobacter fetus subsp. venerealis
Carbohydrates
characterization
chemical composition
Crustaceans
Endotoxin
endotoxins
Endotoxins - toxicity
Fatty acids
Fetuses
Gelation
genetic variation
Limulus Test - methods
Lipid A
Lipid A - chemistry
Lipid A - metabolism
Lipids
Lipopolysaccharide
Lipopolysaccharides
Lipopolysaccharides - analysis
Lipopolysaccharides - toxicity
Lymphocyte Activation - drug effects
Mice
Mice, Inbred C57BL
Mice, Inbred CBA
Mitogenicity
mitogens
Pathogenesis
pyrofenicity
Pyrogenicity
pyrogens
Pyrogens - analysis
Rabbits
Salmonella
Salmonella typhimurium
Serotypes
Serotyping
strains
Toxicity
title Biological characterization of Campylobacter fetus lipopolysaccharides
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