Systemic antibody response to Clostridium difficile in colonized patients with and without symptoms and matched controls
1 Centre for Infectious Diseases, University of Edinburgh College of Medicine and Veterinary Medicine, The Chancellor's Building, 49 Little France Crescent, Edinburgh EH16 4SB, UK 2 Geriatric Medicine Unit, University of Edinburgh College of Medicine and Veterinary Medicine, Edinburgh EH16 4SB,...
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creator | Sanchez-Hurtado, Karla Corretge, Maria Mutlu, Esvet McIlhagger, Rowan Starr, John M Poxton, Ian R |
description | 1 Centre for Infectious Diseases, University of Edinburgh College of Medicine and Veterinary Medicine, The Chancellor's Building, 49 Little France Crescent, Edinburgh EH16 4SB, UK
2 Geriatric Medicine Unit, University of Edinburgh College of Medicine and Veterinary Medicine, Edinburgh EH16 4SB, UK
Correspondence Ian R. Poxton i.r.poxton{at}ed.ac.uk
Received 23 October 2007
Accepted 30 January 2008
It has been proposed that patients who develop Clostridium difficile -associated disease (CDAD) do so because they are unable to mount an adequate immune response. Serum was collected from three groups of elderly in-patients: (i) cases ( n =21) of CDAD, being toxin A/B-positive; (ii) carriers ( n =21) asymptomatic for CDAD (no diarrhoea) but at least toxin or culture positive; and (iii) controls ( n =26) asymptomatic for CDAD and negative for both C. difficile toxin and culture. The age and gender of each group were compared, and the colonizing strains were ribotyped and toxinotyped. Serum antibodies (IgG and IgM) were measured by ELISA using different antigen preparations: EDTA extract (containing cell-surface proteins and carbohydrates), guanidine hydrochloride extract (surface-layer proteins), aqueous phenol-extracted lipocarbohydrate (LC); crude toxin (dialysis culture supernatant) and purified toxin A. LPS from Escherichia coli was used as a control antigen. Antibodies were also tested for toxin neutralization on tissue monolayers and for binding to EDTA-extracted antigens by Western blotting. IgG antibody measurements to cytomegalovirus (CMV) were included as an indicator of potential immunosenescence. Results showed that the patient groups were well matched by age and gender, and the colonizing strains were similar in cases and carriers, being predominantly ribotype 001 and toxinotype 0. By ELISA, IgG levels to most of the antigens were highest in the cases and lowest in the controls, with the exception of antibodies to the LC, which were higher in the controls than the cases. Levels in the carriers tended to be of intermediate level or similar to the controls. For all antigens, the levels of IgM were not significantly different among cases, carriers and controls. Serum from all groups was able to neutralize the cytotoxic action of toxin on both Vero and Caco2 cells, and all to a similar extent. Western blots showed an overall higher level of IgG antibodies to the EDTA-extracted antigens in the cases. The results of the CMV ELISA showed that specific IgG w |
doi_str_mv | 10.1099/jmm.0.47713-0 |
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2 Geriatric Medicine Unit, University of Edinburgh College of Medicine and Veterinary Medicine, Edinburgh EH16 4SB, UK
Correspondence Ian R. Poxton i.r.poxton{at}ed.ac.uk
Received 23 October 2007
Accepted 30 January 2008
It has been proposed that patients who develop Clostridium difficile -associated disease (CDAD) do so because they are unable to mount an adequate immune response. Serum was collected from three groups of elderly in-patients: (i) cases ( n =21) of CDAD, being toxin A/B-positive; (ii) carriers ( n =21) asymptomatic for CDAD (no diarrhoea) but at least toxin or culture positive; and (iii) controls ( n =26) asymptomatic for CDAD and negative for both C. difficile toxin and culture. The age and gender of each group were compared, and the colonizing strains were ribotyped and toxinotyped. Serum antibodies (IgG and IgM) were measured by ELISA using different antigen preparations: EDTA extract (containing cell-surface proteins and carbohydrates), guanidine hydrochloride extract (surface-layer proteins), aqueous phenol-extracted lipocarbohydrate (LC); crude toxin (dialysis culture supernatant) and purified toxin A. LPS from Escherichia coli was used as a control antigen. Antibodies were also tested for toxin neutralization on tissue monolayers and for binding to EDTA-extracted antigens by Western blotting. IgG antibody measurements to cytomegalovirus (CMV) were included as an indicator of potential immunosenescence. Results showed that the patient groups were well matched by age and gender, and the colonizing strains were similar in cases and carriers, being predominantly ribotype 001 and toxinotype 0. By ELISA, IgG levels to most of the antigens were highest in the cases and lowest in the controls, with the exception of antibodies to the LC, which were higher in the controls than the cases. Levels in the carriers tended to be of intermediate level or similar to the controls. For all antigens, the levels of IgM were not significantly different among cases, carriers and controls. Serum from all groups was able to neutralize the cytotoxic action of toxin on both Vero and Caco2 cells, and all to a similar extent. Western blots showed an overall higher level of IgG antibodies to the EDTA-extracted antigens in the cases. The results of the CMV ELISA showed that specific IgG was detected in more cases (78 %) than carriers and controls (both 65 %), but this difference in seropositivity was not significant. The conclusion is that, during symptomatic infection, patients respond to protein antigens of C. difficile in a manner typical of a secondary antibody response, with no evidence that an inability to respond predisposes to the appearance of symptoms.
Abbreviations: AP, alkaline phosphatase; CDAD, Clostridium difficile -associated disease; CMV, cytomegalovirus; LC, lipocarbohydrate; SLP, surface-layer protein.</description><identifier>ISSN: 0022-2615</identifier><identifier>EISSN: 1473-5644</identifier><identifier>DOI: 10.1099/jmm.0.47713-0</identifier><identifier>PMID: 18480328</identifier><language>eng</language><publisher>England: Soc General Microbiol</publisher><subject>Aged ; Aged, 80 and over ; Animals ; Antibodies, Bacterial - biosynthesis ; Antibodies, Bacterial - blood ; Antibodies, Viral - blood ; Antigens, Bacterial - immunology ; Bacterial Toxins - immunology ; Caco-2 Cells ; Carrier State - immunology ; Case-Control Studies ; Chlorocebus aethiops ; Clostridium ; Clostridium difficile ; Clostridium difficile - immunology ; Clostridium Infections - complications ; Clostridium Infections - immunology ; Cytomegalovirus ; Cytomegalovirus - immunology ; Cytomegalovirus Infections - complications ; Cytomegalovirus Infections - immunology ; Escherichia coli ; Feces - microbiology ; Female ; Humans ; Immunoglobulin G - biosynthesis ; Immunoglobulin G - blood ; Immunoglobulin M - biosynthesis ; Immunoglobulin M - blood ; Male ; Vero Cells</subject><ispartof>Journal of medical microbiology, 2008-06, Vol.57 (6), p.717-724</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-926e560ab5ca51906c80a006271eaa39b71f9b1099994bb718195242efdd04013</citedby><cites>FETCH-LOGICAL-c393t-926e560ab5ca51906c80a006271eaa39b71f9b1099994bb718195242efdd04013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3746,3747,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18480328$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sanchez-Hurtado, Karla</creatorcontrib><creatorcontrib>Corretge, Maria</creatorcontrib><creatorcontrib>Mutlu, Esvet</creatorcontrib><creatorcontrib>McIlhagger, Rowan</creatorcontrib><creatorcontrib>Starr, John M</creatorcontrib><creatorcontrib>Poxton, Ian R</creatorcontrib><title>Systemic antibody response to Clostridium difficile in colonized patients with and without symptoms and matched controls</title><title>Journal of medical microbiology</title><addtitle>J Med Microbiol</addtitle><description>1 Centre for Infectious Diseases, University of Edinburgh College of Medicine and Veterinary Medicine, The Chancellor's Building, 49 Little France Crescent, Edinburgh EH16 4SB, UK
2 Geriatric Medicine Unit, University of Edinburgh College of Medicine and Veterinary Medicine, Edinburgh EH16 4SB, UK
Correspondence Ian R. Poxton i.r.poxton{at}ed.ac.uk
Received 23 October 2007
Accepted 30 January 2008
It has been proposed that patients who develop Clostridium difficile -associated disease (CDAD) do so because they are unable to mount an adequate immune response. Serum was collected from three groups of elderly in-patients: (i) cases ( n =21) of CDAD, being toxin A/B-positive; (ii) carriers ( n =21) asymptomatic for CDAD (no diarrhoea) but at least toxin or culture positive; and (iii) controls ( n =26) asymptomatic for CDAD and negative for both C. difficile toxin and culture. The age and gender of each group were compared, and the colonizing strains were ribotyped and toxinotyped. Serum antibodies (IgG and IgM) were measured by ELISA using different antigen preparations: EDTA extract (containing cell-surface proteins and carbohydrates), guanidine hydrochloride extract (surface-layer proteins), aqueous phenol-extracted lipocarbohydrate (LC); crude toxin (dialysis culture supernatant) and purified toxin A. LPS from Escherichia coli was used as a control antigen. Antibodies were also tested for toxin neutralization on tissue monolayers and for binding to EDTA-extracted antigens by Western blotting. IgG antibody measurements to cytomegalovirus (CMV) were included as an indicator of potential immunosenescence. Results showed that the patient groups were well matched by age and gender, and the colonizing strains were similar in cases and carriers, being predominantly ribotype 001 and toxinotype 0. By ELISA, IgG levels to most of the antigens were highest in the cases and lowest in the controls, with the exception of antibodies to the LC, which were higher in the controls than the cases. Levels in the carriers tended to be of intermediate level or similar to the controls. For all antigens, the levels of IgM were not significantly different among cases, carriers and controls. Serum from all groups was able to neutralize the cytotoxic action of toxin on both Vero and Caco2 cells, and all to a similar extent. Western blots showed an overall higher level of IgG antibodies to the EDTA-extracted antigens in the cases. The results of the CMV ELISA showed that specific IgG was detected in more cases (78 %) than carriers and controls (both 65 %), but this difference in seropositivity was not significant. The conclusion is that, during symptomatic infection, patients respond to protein antigens of C. difficile in a manner typical of a secondary antibody response, with no evidence that an inability to respond predisposes to the appearance of symptoms.
Abbreviations: AP, alkaline phosphatase; CDAD, Clostridium difficile -associated disease; CMV, cytomegalovirus; LC, lipocarbohydrate; SLP, surface-layer protein.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Animals</subject><subject>Antibodies, Bacterial - biosynthesis</subject><subject>Antibodies, Bacterial - blood</subject><subject>Antibodies, Viral - blood</subject><subject>Antigens, Bacterial - immunology</subject><subject>Bacterial Toxins - immunology</subject><subject>Caco-2 Cells</subject><subject>Carrier State - immunology</subject><subject>Case-Control Studies</subject><subject>Chlorocebus aethiops</subject><subject>Clostridium</subject><subject>Clostridium difficile</subject><subject>Clostridium difficile - immunology</subject><subject>Clostridium Infections - complications</subject><subject>Clostridium Infections - immunology</subject><subject>Cytomegalovirus</subject><subject>Cytomegalovirus - immunology</subject><subject>Cytomegalovirus Infections - complications</subject><subject>Cytomegalovirus Infections - immunology</subject><subject>Escherichia coli</subject><subject>Feces - microbiology</subject><subject>Female</subject><subject>Humans</subject><subject>Immunoglobulin G - biosynthesis</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulin M - biosynthesis</subject><subject>Immunoglobulin M - blood</subject><subject>Male</subject><subject>Vero Cells</subject><issn>0022-2615</issn><issn>1473-5644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtr3DAURkVpaaZJl90WrZqVJ1cPW9YyDElaCHSRZi1kWc4oWJYryaSTXx_NA7Ls6j44fFzuQegbgTUBKa-evV_DmgtBWAUf0Ipwwaq64fwjWgFQWtGG1GfoS0rPAEQwJj-jM9LyFhhtV-jfwy5l653BesquC_0OR5vmMCWLc8CbMaQcXe8Wj3s3DM640WI3YRPGMLlX2-NZZ2ennPCLy9uS0h-asGScdn7OwafD0utstgU3YcoxjOkCfRr0mOzXUz1Hj7c3fzY_q_vfd7821_eVYZLlStLG1g3orja6JhIa04IGaKggVmsmO0EG2e0_ISXvytQSWVNO7dD3wIGwc_TjmDvH8HexKSvvkrHjqCcblqQElJ8IKv4LUmibVvC2gNURNDGkFO2g5ui8jjtFQO0vUcWJAnVwoqDw30_BS-dt_06fJBTg8ghs3dP2xUWrnuxUlMTQubAPq4VqlCjy3gBZ3ZeX</recordid><startdate>20080601</startdate><enddate>20080601</enddate><creator>Sanchez-Hurtado, Karla</creator><creator>Corretge, Maria</creator><creator>Mutlu, Esvet</creator><creator>McIlhagger, Rowan</creator><creator>Starr, John M</creator><creator>Poxton, Ian R</creator><general>Soc General Microbiol</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T5</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20080601</creationdate><title>Systemic antibody response to Clostridium difficile in colonized patients with and without symptoms and matched controls</title><author>Sanchez-Hurtado, Karla ; Corretge, Maria ; Mutlu, Esvet ; McIlhagger, Rowan ; Starr, John M ; Poxton, Ian R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-926e560ab5ca51906c80a006271eaa39b71f9b1099994bb718195242efdd04013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Animals</topic><topic>Antibodies, Bacterial - biosynthesis</topic><topic>Antibodies, Bacterial - blood</topic><topic>Antibodies, Viral - blood</topic><topic>Antigens, Bacterial - immunology</topic><topic>Bacterial Toxins - immunology</topic><topic>Caco-2 Cells</topic><topic>Carrier State - immunology</topic><topic>Case-Control Studies</topic><topic>Chlorocebus aethiops</topic><topic>Clostridium</topic><topic>Clostridium difficile</topic><topic>Clostridium difficile - immunology</topic><topic>Clostridium Infections - complications</topic><topic>Clostridium Infections - immunology</topic><topic>Cytomegalovirus</topic><topic>Cytomegalovirus - immunology</topic><topic>Cytomegalovirus Infections - complications</topic><topic>Cytomegalovirus Infections - immunology</topic><topic>Escherichia coli</topic><topic>Feces - microbiology</topic><topic>Female</topic><topic>Humans</topic><topic>Immunoglobulin G - biosynthesis</topic><topic>Immunoglobulin G - blood</topic><topic>Immunoglobulin M - biosynthesis</topic><topic>Immunoglobulin M - blood</topic><topic>Male</topic><topic>Vero Cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sanchez-Hurtado, Karla</creatorcontrib><creatorcontrib>Corretge, Maria</creatorcontrib><creatorcontrib>Mutlu, Esvet</creatorcontrib><creatorcontrib>McIlhagger, Rowan</creatorcontrib><creatorcontrib>Starr, John M</creatorcontrib><creatorcontrib>Poxton, Ian R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sanchez-Hurtado, Karla</au><au>Corretge, Maria</au><au>Mutlu, Esvet</au><au>McIlhagger, Rowan</au><au>Starr, John M</au><au>Poxton, Ian R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Systemic antibody response to Clostridium difficile in colonized patients with and without symptoms and matched controls</atitle><jtitle>Journal of medical microbiology</jtitle><addtitle>J Med Microbiol</addtitle><date>2008-06-01</date><risdate>2008</risdate><volume>57</volume><issue>6</issue><spage>717</spage><epage>724</epage><pages>717-724</pages><issn>0022-2615</issn><eissn>1473-5644</eissn><abstract>1 Centre for Infectious Diseases, University of Edinburgh College of Medicine and Veterinary Medicine, The Chancellor's Building, 49 Little France Crescent, Edinburgh EH16 4SB, UK
2 Geriatric Medicine Unit, University of Edinburgh College of Medicine and Veterinary Medicine, Edinburgh EH16 4SB, UK
Correspondence Ian R. Poxton i.r.poxton{at}ed.ac.uk
Received 23 October 2007
Accepted 30 January 2008
It has been proposed that patients who develop Clostridium difficile -associated disease (CDAD) do so because they are unable to mount an adequate immune response. Serum was collected from three groups of elderly in-patients: (i) cases ( n =21) of CDAD, being toxin A/B-positive; (ii) carriers ( n =21) asymptomatic for CDAD (no diarrhoea) but at least toxin or culture positive; and (iii) controls ( n =26) asymptomatic for CDAD and negative for both C. difficile toxin and culture. The age and gender of each group were compared, and the colonizing strains were ribotyped and toxinotyped. Serum antibodies (IgG and IgM) were measured by ELISA using different antigen preparations: EDTA extract (containing cell-surface proteins and carbohydrates), guanidine hydrochloride extract (surface-layer proteins), aqueous phenol-extracted lipocarbohydrate (LC); crude toxin (dialysis culture supernatant) and purified toxin A. LPS from Escherichia coli was used as a control antigen. Antibodies were also tested for toxin neutralization on tissue monolayers and for binding to EDTA-extracted antigens by Western blotting. IgG antibody measurements to cytomegalovirus (CMV) were included as an indicator of potential immunosenescence. Results showed that the patient groups were well matched by age and gender, and the colonizing strains were similar in cases and carriers, being predominantly ribotype 001 and toxinotype 0. By ELISA, IgG levels to most of the antigens were highest in the cases and lowest in the controls, with the exception of antibodies to the LC, which were higher in the controls than the cases. Levels in the carriers tended to be of intermediate level or similar to the controls. For all antigens, the levels of IgM were not significantly different among cases, carriers and controls. Serum from all groups was able to neutralize the cytotoxic action of toxin on both Vero and Caco2 cells, and all to a similar extent. Western blots showed an overall higher level of IgG antibodies to the EDTA-extracted antigens in the cases. The results of the CMV ELISA showed that specific IgG was detected in more cases (78 %) than carriers and controls (both 65 %), but this difference in seropositivity was not significant. The conclusion is that, during symptomatic infection, patients respond to protein antigens of C. difficile in a manner typical of a secondary antibody response, with no evidence that an inability to respond predisposes to the appearance of symptoms.
Abbreviations: AP, alkaline phosphatase; CDAD, Clostridium difficile -associated disease; CMV, cytomegalovirus; LC, lipocarbohydrate; SLP, surface-layer protein.</abstract><cop>England</cop><pub>Soc General Microbiol</pub><pmid>18480328</pmid><doi>10.1099/jmm.0.47713-0</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aged, 80 and over Animals Antibodies, Bacterial - biosynthesis Antibodies, Bacterial - blood Antibodies, Viral - blood Antigens, Bacterial - immunology Bacterial Toxins - immunology Caco-2 Cells Carrier State - immunology Case-Control Studies Chlorocebus aethiops Clostridium Clostridium difficile Clostridium difficile - immunology Clostridium Infections - complications Clostridium Infections - immunology Cytomegalovirus Cytomegalovirus - immunology Cytomegalovirus Infections - complications Cytomegalovirus Infections - immunology Escherichia coli Feces - microbiology Female Humans Immunoglobulin G - biosynthesis Immunoglobulin G - blood Immunoglobulin M - biosynthesis Immunoglobulin M - blood Male Vero Cells |
title | Systemic antibody response to Clostridium difficile in colonized patients with and without symptoms and matched controls |
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