Modifications of Bordetella bronchiseptica core lipopolysaccharide influence immune response without affecting protective activity

Bordetella bronchiseptica produces respiratory disease primarily in mammals including humans. Although a considerably amount of research has been generated regarding lipopolysaccharide (LPS) role during infection and stimulating innate and adaptive immune response, mechanisms involved in LPS synthes...

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Publicado: 2017
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0960894X_v27_n3_p432_Sisti
http://hdl.handle.net/20.500.12110/paper_0960894X_v27_n3_p432_Sisti
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spelling paper:paper_0960894X_v27_n3_p432_Sisti2023-06-08T15:57:53Z Modifications of Bordetella bronchiseptica core lipopolysaccharide influence immune response without affecting protective activity Bordetella Glycosyltransferase Lipopolysaccharide bacterium lipopolysaccharide glycosyltransferase bacterial protein lipopolysaccharide adaptive immunity animal experiment Article bacterial gene bacterial genome BB3394 gene BB3400 gene Bordetella bronchiseptica Bordetella bronchiseptica infection chemical modification controlled study deletion mutant gene locus genetic conservation immune response in vivo study innate immunity mouse nonhuman animal biosynthesis Bordetella bronchiseptica chemistry genetics immune system immunology matrix-assisted laser desorption-ionization mass spectrometry metabolism Animals Bacterial Proteins Bordetella bronchiseptica Genes, Bacterial Glycosyltransferases Immune System Lipopolysaccharides Mice Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Bordetella bronchiseptica produces respiratory disease primarily in mammals including humans. Although a considerably amount of research has been generated regarding lipopolysaccharide (LPS) role during infection and stimulating innate and adaptive immune response, mechanisms involved in LPS synthesis are still unknown. In this context we searched in B. bronchiseptica genome for putative glycosyltransferases. We found possible genes codifying for enzymes involved in sugar substitution of the LPS structure. We decided to analyse BB3394 to BB3400 genes, closed to a previously described LPS biosynthetic locus in B. pertussis. Particularly, conservation of BB3394 in sequenced B. bronchiseptica genomes suggests the importance of this gene for bacteria normal physiology. Deletion of BB3394 abolished resistance to naive serum as described for other LPS mutants. When purified LPS was analyzed, differences in the LPS core structure were found. Particularly, a GalNA branched sugar substitution in the core was absent in the LPS obtained from BB3394 deletion mutant. Absence of GalNA in core LPS alters immune response in vivo but is able to induce protective response against B. bronchiseptica infection. © 2016 2017 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0960894X_v27_n3_p432_Sisti http://hdl.handle.net/20.500.12110/paper_0960894X_v27_n3_p432_Sisti
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Bordetella
Glycosyltransferase
Lipopolysaccharide
bacterium lipopolysaccharide
glycosyltransferase
bacterial protein
lipopolysaccharide
adaptive immunity
animal experiment
Article
bacterial gene
bacterial genome
BB3394 gene
BB3400 gene
Bordetella bronchiseptica
Bordetella bronchiseptica infection
chemical modification
controlled study
deletion mutant
gene locus
genetic conservation
immune response
in vivo study
innate immunity
mouse
nonhuman
animal
biosynthesis
Bordetella bronchiseptica
chemistry
genetics
immune system
immunology
matrix-assisted laser desorption-ionization mass spectrometry
metabolism
Animals
Bacterial Proteins
Bordetella bronchiseptica
Genes, Bacterial
Glycosyltransferases
Immune System
Lipopolysaccharides
Mice
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
spellingShingle Bordetella
Glycosyltransferase
Lipopolysaccharide
bacterium lipopolysaccharide
glycosyltransferase
bacterial protein
lipopolysaccharide
adaptive immunity
animal experiment
Article
bacterial gene
bacterial genome
BB3394 gene
BB3400 gene
Bordetella bronchiseptica
Bordetella bronchiseptica infection
chemical modification
controlled study
deletion mutant
gene locus
genetic conservation
immune response
in vivo study
innate immunity
mouse
nonhuman
animal
biosynthesis
Bordetella bronchiseptica
chemistry
genetics
immune system
immunology
matrix-assisted laser desorption-ionization mass spectrometry
metabolism
Animals
Bacterial Proteins
Bordetella bronchiseptica
Genes, Bacterial
Glycosyltransferases
Immune System
Lipopolysaccharides
Mice
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Modifications of Bordetella bronchiseptica core lipopolysaccharide influence immune response without affecting protective activity
topic_facet Bordetella
Glycosyltransferase
Lipopolysaccharide
bacterium lipopolysaccharide
glycosyltransferase
bacterial protein
lipopolysaccharide
adaptive immunity
animal experiment
Article
bacterial gene
bacterial genome
BB3394 gene
BB3400 gene
Bordetella bronchiseptica
Bordetella bronchiseptica infection
chemical modification
controlled study
deletion mutant
gene locus
genetic conservation
immune response
in vivo study
innate immunity
mouse
nonhuman
animal
biosynthesis
Bordetella bronchiseptica
chemistry
genetics
immune system
immunology
matrix-assisted laser desorption-ionization mass spectrometry
metabolism
Animals
Bacterial Proteins
Bordetella bronchiseptica
Genes, Bacterial
Glycosyltransferases
Immune System
Lipopolysaccharides
Mice
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
description Bordetella bronchiseptica produces respiratory disease primarily in mammals including humans. Although a considerably amount of research has been generated regarding lipopolysaccharide (LPS) role during infection and stimulating innate and adaptive immune response, mechanisms involved in LPS synthesis are still unknown. In this context we searched in B. bronchiseptica genome for putative glycosyltransferases. We found possible genes codifying for enzymes involved in sugar substitution of the LPS structure. We decided to analyse BB3394 to BB3400 genes, closed to a previously described LPS biosynthetic locus in B. pertussis. Particularly, conservation of BB3394 in sequenced B. bronchiseptica genomes suggests the importance of this gene for bacteria normal physiology. Deletion of BB3394 abolished resistance to naive serum as described for other LPS mutants. When purified LPS was analyzed, differences in the LPS core structure were found. Particularly, a GalNA branched sugar substitution in the core was absent in the LPS obtained from BB3394 deletion mutant. Absence of GalNA in core LPS alters immune response in vivo but is able to induce protective response against B. bronchiseptica infection. © 2016
title Modifications of Bordetella bronchiseptica core lipopolysaccharide influence immune response without affecting protective activity
title_short Modifications of Bordetella bronchiseptica core lipopolysaccharide influence immune response without affecting protective activity
title_full Modifications of Bordetella bronchiseptica core lipopolysaccharide influence immune response without affecting protective activity
title_fullStr Modifications of Bordetella bronchiseptica core lipopolysaccharide influence immune response without affecting protective activity
title_full_unstemmed Modifications of Bordetella bronchiseptica core lipopolysaccharide influence immune response without affecting protective activity
title_sort modifications of bordetella bronchiseptica core lipopolysaccharide influence immune response without affecting protective activity
publishDate 2017
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0960894X_v27_n3_p432_Sisti
http://hdl.handle.net/20.500.12110/paper_0960894X_v27_n3_p432_Sisti
_version_ 1768543191419584512