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A Novel Method of Serum Resistance by Escherichia coli That Causes Urosepsis

Uropathogenic Escherichia coli (UPEC) is the most common cause of urinary tract infection, which in some patients can develop into life-threatening urosepsis. Serum resistance is a key virulence trait of strains that cause urosepsis. Recently, we identified a novel method of serum resistance in pati...

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Autores principales: Coggon, Carrie F., Jiang, Andrew, Goh, Kelvin G. K., Henderson, Ian R., Schembri, Mark A., Wells, Timothy J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6020292/
https://www.ncbi.nlm.nih.gov/pubmed/29946047
http://dx.doi.org/10.1128/mBio.00920-18
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author Coggon, Carrie F.
Jiang, Andrew
Goh, Kelvin G. K.
Henderson, Ian R.
Schembri, Mark A.
Wells, Timothy J.
author_facet Coggon, Carrie F.
Jiang, Andrew
Goh, Kelvin G. K.
Henderson, Ian R.
Schembri, Mark A.
Wells, Timothy J.
author_sort Coggon, Carrie F.
collection PubMed
description Uropathogenic Escherichia coli (UPEC) is the most common cause of urinary tract infection, which in some patients can develop into life-threatening urosepsis. Serum resistance is a key virulence trait of strains that cause urosepsis. Recently, we identified a novel method of serum resistance in patients with Pseudomonas aeruginosa lung infections, where patients possessed antibodies that inhibited complement-mediated killing (instead of protecting against infection). These inhibitory antibodies were of the IgG2 subtype, specific to the O-antigen component of lipopolysaccharide (LPS) and coated the bacterial surface, preventing bacterial lysis by complement. As this mechanism could apply to any Gram-negative bacterial infection, we hypothesized that inhibitory antibodies may represent an uncharacterized mechanism of serum resistance in UPEC. To test this, 45 urosepsis patients with paired blood culture UPEC isolates were screened for serum titers of IgG2 specific for their cognate strain’s LPS. Eleven patients had sufficiently high titers of the antibody to inhibit serum-mediated killing of UPEC isolates by pooled healthy control sera. Depletion of IgG or removal of O-antigen restored sensitivity of the isolates to the cognate patient serum. Importantly, the isolates from these 11 patients were more sensitive to killing by serum than isolates from patients with no inhibitory antibodies. This suggests the presence of inhibitory antibodies may have allowed these strains to infect the bloodstream. The high prevalence of patients with inhibitory antibodies (24%) suggests that this phenomenon is an important mechanism of UPEC serum resistance. LPS-specific inhibitory antibodies have now been identified against three Gram-negative pathogens that cause disparate diseases.
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spelling pubmed-60202922018-06-29 A Novel Method of Serum Resistance by Escherichia coli That Causes Urosepsis Coggon, Carrie F. Jiang, Andrew Goh, Kelvin G. K. Henderson, Ian R. Schembri, Mark A. Wells, Timothy J. mBio Observation Uropathogenic Escherichia coli (UPEC) is the most common cause of urinary tract infection, which in some patients can develop into life-threatening urosepsis. Serum resistance is a key virulence trait of strains that cause urosepsis. Recently, we identified a novel method of serum resistance in patients with Pseudomonas aeruginosa lung infections, where patients possessed antibodies that inhibited complement-mediated killing (instead of protecting against infection). These inhibitory antibodies were of the IgG2 subtype, specific to the O-antigen component of lipopolysaccharide (LPS) and coated the bacterial surface, preventing bacterial lysis by complement. As this mechanism could apply to any Gram-negative bacterial infection, we hypothesized that inhibitory antibodies may represent an uncharacterized mechanism of serum resistance in UPEC. To test this, 45 urosepsis patients with paired blood culture UPEC isolates were screened for serum titers of IgG2 specific for their cognate strain’s LPS. Eleven patients had sufficiently high titers of the antibody to inhibit serum-mediated killing of UPEC isolates by pooled healthy control sera. Depletion of IgG or removal of O-antigen restored sensitivity of the isolates to the cognate patient serum. Importantly, the isolates from these 11 patients were more sensitive to killing by serum than isolates from patients with no inhibitory antibodies. This suggests the presence of inhibitory antibodies may have allowed these strains to infect the bloodstream. The high prevalence of patients with inhibitory antibodies (24%) suggests that this phenomenon is an important mechanism of UPEC serum resistance. LPS-specific inhibitory antibodies have now been identified against three Gram-negative pathogens that cause disparate diseases. American Society for Microbiology 2018-06-26 /pmc/articles/PMC6020292/ /pubmed/29946047 http://dx.doi.org/10.1128/mBio.00920-18 Text en Copyright © 2018 Coggon et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Observation
Coggon, Carrie F.
Jiang, Andrew
Goh, Kelvin G. K.
Henderson, Ian R.
Schembri, Mark A.
Wells, Timothy J.
A Novel Method of Serum Resistance by Escherichia coli That Causes Urosepsis
title A Novel Method of Serum Resistance by Escherichia coli That Causes Urosepsis
title_full A Novel Method of Serum Resistance by Escherichia coli That Causes Urosepsis
title_fullStr A Novel Method of Serum Resistance by Escherichia coli That Causes Urosepsis
title_full_unstemmed A Novel Method of Serum Resistance by Escherichia coli That Causes Urosepsis
title_short A Novel Method of Serum Resistance by Escherichia coli That Causes Urosepsis
title_sort novel method of serum resistance by escherichia coli that causes urosepsis
topic Observation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6020292/
https://www.ncbi.nlm.nih.gov/pubmed/29946047
http://dx.doi.org/10.1128/mBio.00920-18
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