Evaluation of commercial slides for detection of immunoglobulin G against Bartonella henselae by indirect immunofluorescence
Four commercial slides were compared with in-house slides for the detection of immunoglobulin G (IgG) against Bartonella henselae in 58 healthy persons from a rural region by an indirect immunofluorescence assay. MRL-BA slides (MRL Diagnostics, USA) and Virion slides (Virion, Switzerland) with agar-...
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Veröffentlicht in: | European journal of clinical microbiology & infectious diseases 1997-09, Vol.16 (9), p.648-652 |
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description | Four commercial slides were compared with in-house slides for the detection of immunoglobulin G (IgG) against Bartonella henselae in 58 healthy persons from a rural region by an indirect immunofluorescence assay. MRL-BA slides (MRL Diagnostics, USA) and Virion slides (Virion, Switzerland) with agar-derived Bartonella henselae showed IgG titers of > or = 1:256 in 44.8% and 51.7%, respectively, whereas Bion slides (Bios, Germany), MRL-Vero slides (MRL Diagnostics), and in-house slides with cell-associated Bartonella henselae showed such titers in 3.4%, 5.1% and 3.4%, respectively. The MRL-Vero slides (Bartonella IgG substrate slides, MRL Diagnostics) were further evaluated with 26 patients with cat scratch disease, 20 patients with lymphadenopathy not due to cat scratch disease, 100 blood donors from an urban area, and 120 blood donors from a mixed urban/rural area. In our mixed urban/rural population the IgG titer of 1:256 had a sensitivity of 84.6% and a specificity of 93.4% for the serodiagnosis of cat scratch disease. Seroprevalence was higher in blood donors from the mixed area (50.8%) than from the urban area (37%). MRL-Vero slides were considered useful for the serodiagnosis of cat scratch disease by indirect immunofluorescence and have replaced our in-house system. However, patients with low IgG titers should be retested three to four weeks after initial sampling to demonstrate a possible rise of IgG titers in paired sera. |
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MRL-BA slides (MRL Diagnostics, USA) and Virion slides (Virion, Switzerland) with agar-derived Bartonella henselae showed IgG titers of > or = 1:256 in 44.8% and 51.7%, respectively, whereas Bion slides (Bios, Germany), MRL-Vero slides (MRL Diagnostics), and in-house slides with cell-associated Bartonella henselae showed such titers in 3.4%, 5.1% and 3.4%, respectively. The MRL-Vero slides (Bartonella IgG substrate slides, MRL Diagnostics) were further evaluated with 26 patients with cat scratch disease, 20 patients with lymphadenopathy not due to cat scratch disease, 100 blood donors from an urban area, and 120 blood donors from a mixed urban/rural area. In our mixed urban/rural population the IgG titer of 1:256 had a sensitivity of 84.6% and a specificity of 93.4% for the serodiagnosis of cat scratch disease. Seroprevalence was higher in blood donors from the mixed area (50.8%) than from the urban area (37%). MRL-Vero slides were considered useful for the serodiagnosis of cat scratch disease by indirect immunofluorescence and have replaced our in-house system. However, patients with low IgG titers should be retested three to four weeks after initial sampling to demonstrate a possible rise of IgG titers in paired sera.</description><identifier>ISSN: 0934-9723</identifier><identifier>EISSN: 1435-4373</identifier><identifier>DOI: 10.1007/bf01708554</identifier><identifier>PMID: 9352257</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Antibodies, Bacterial - analysis ; Antibody Specificity ; Antigens, Bacterial - analysis ; Antigens, Bacterial - immunology ; Bacterial diseases ; Bartonella henselae - immunology ; Biological and medical sciences ; Cat-Scratch Disease - epidemiology ; Cat-Scratch Disease - immunology ; Cat-Scratch Disease - microbiology ; Evaluation Studies as Topic ; Fluorescent Antibody Technique, Indirect ; Human bacterial diseases ; Humans ; Immunoglobulin G - analysis ; Infectious diseases ; Medical sciences ; Reagent Kits, Diagnostic ; Rickettsial diseases ; Tropical bacterial diseases</subject><ispartof>European journal of clinical microbiology & infectious diseases, 1997-09, Vol.16 (9), p.648-652</ispartof><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2827287$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9352257$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ZBINDEN, R</creatorcontrib><creatorcontrib>MICHAEL, N</creatorcontrib><creatorcontrib>SEKULOVSKI, M</creatorcontrib><creatorcontrib>VON GRAEVENITZ, A</creatorcontrib><creatorcontrib>NADAL, D</creatorcontrib><title>Evaluation of commercial slides for detection of immunoglobulin G against Bartonella henselae by indirect immunofluorescence</title><title>European journal of clinical microbiology & infectious diseases</title><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><description>Four commercial slides were compared with in-house slides for the detection of immunoglobulin G (IgG) against Bartonella henselae in 58 healthy persons from a rural region by an indirect immunofluorescence assay. MRL-BA slides (MRL Diagnostics, USA) and Virion slides (Virion, Switzerland) with agar-derived Bartonella henselae showed IgG titers of > or = 1:256 in 44.8% and 51.7%, respectively, whereas Bion slides (Bios, Germany), MRL-Vero slides (MRL Diagnostics), and in-house slides with cell-associated Bartonella henselae showed such titers in 3.4%, 5.1% and 3.4%, respectively. The MRL-Vero slides (Bartonella IgG substrate slides, MRL Diagnostics) were further evaluated with 26 patients with cat scratch disease, 20 patients with lymphadenopathy not due to cat scratch disease, 100 blood donors from an urban area, and 120 blood donors from a mixed urban/rural area. In our mixed urban/rural population the IgG titer of 1:256 had a sensitivity of 84.6% and a specificity of 93.4% for the serodiagnosis of cat scratch disease. Seroprevalence was higher in blood donors from the mixed area (50.8%) than from the urban area (37%). MRL-Vero slides were considered useful for the serodiagnosis of cat scratch disease by indirect immunofluorescence and have replaced our in-house system. However, patients with low IgG titers should be retested three to four weeks after initial sampling to demonstrate a possible rise of IgG titers in paired sera.</description><subject>Antibodies, Bacterial - analysis</subject><subject>Antibody Specificity</subject><subject>Antigens, Bacterial - analysis</subject><subject>Antigens, Bacterial - immunology</subject><subject>Bacterial diseases</subject><subject>Bartonella henselae - immunology</subject><subject>Biological and medical sciences</subject><subject>Cat-Scratch Disease - epidemiology</subject><subject>Cat-Scratch Disease - immunology</subject><subject>Cat-Scratch Disease - microbiology</subject><subject>Evaluation Studies as Topic</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Immunoglobulin G - analysis</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Reagent Kits, Diagnostic</subject><subject>Rickettsial diseases</subject><subject>Tropical bacterial diseases</subject><issn>0934-9723</issn><issn>1435-4373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0D1LBDEQBuAgip4fjb2QQuxW83nZlCp6Cgc2Wh_Z7OTMkU002RUO_PGuuNpaTfE-7zAMQqeUXFJC1FXjCFWkllLsoBkVXFaCK76LZkRzUWnF-AE6LGVDRlwrtY_2NZeMSTVDn3cfJgym9yni5LBNXQfZehNwCb6Fgl3KuIUe7C_xXTfEtA6pGYKPeIHN2vhYenxjcp8ihGDwK8QCwQButtjH1uexPhVdGFKGYiFaOEZ7zoQCJ9M8Qi_3d8-3D9XyafF4e72sNnxO-8pJK2tigTRz0YLUmre1BS1szW0rmVatsiAabZ1u5pICcbUUoIxgRDqmJD9CFz9733J6H6D0q86PF4yXRkhDWSnNlZyz_yH9RpSqEZ5NcGg6aFdv2Xcmb1fTX8f8fMpNsSa4bKL15Y-xmilWK_4FgOSIsQ</recordid><startdate>19970901</startdate><enddate>19970901</enddate><creator>ZBINDEN, R</creator><creator>MICHAEL, N</creator><creator>SEKULOVSKI, M</creator><creator>VON GRAEVENITZ, A</creator><creator>NADAL, D</creator><general>Springer</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19970901</creationdate><title>Evaluation of commercial slides for detection of immunoglobulin G against Bartonella henselae by indirect immunofluorescence</title><author>ZBINDEN, R ; MICHAEL, N ; SEKULOVSKI, M ; VON GRAEVENITZ, A ; NADAL, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j361t-f5c580ce0b64de5993d8ce94c83cd5297d7ce4b9cf9b651e0f854e7a4205f2753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Antibodies, Bacterial - analysis</topic><topic>Antibody Specificity</topic><topic>Antigens, Bacterial - analysis</topic><topic>Antigens, Bacterial - immunology</topic><topic>Bacterial diseases</topic><topic>Bartonella henselae - immunology</topic><topic>Biological and medical sciences</topic><topic>Cat-Scratch Disease - epidemiology</topic><topic>Cat-Scratch Disease - immunology</topic><topic>Cat-Scratch Disease - microbiology</topic><topic>Evaluation Studies as Topic</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Immunoglobulin G - analysis</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Reagent Kits, Diagnostic</topic><topic>Rickettsial diseases</topic><topic>Tropical bacterial diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ZBINDEN, R</creatorcontrib><creatorcontrib>MICHAEL, N</creatorcontrib><creatorcontrib>SEKULOVSKI, M</creatorcontrib><creatorcontrib>VON GRAEVENITZ, A</creatorcontrib><creatorcontrib>NADAL, D</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Bacteriology Abstracts (Microbiology B)</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>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of clinical microbiology & infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ZBINDEN, R</au><au>MICHAEL, N</au><au>SEKULOVSKI, M</au><au>VON GRAEVENITZ, A</au><au>NADAL, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of commercial slides for detection of immunoglobulin G against Bartonella henselae by indirect immunofluorescence</atitle><jtitle>European journal of clinical microbiology & infectious diseases</jtitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><date>1997-09-01</date><risdate>1997</risdate><volume>16</volume><issue>9</issue><spage>648</spage><epage>652</epage><pages>648-652</pages><issn>0934-9723</issn><eissn>1435-4373</eissn><abstract>Four commercial slides were compared with in-house slides for the detection of immunoglobulin G (IgG) against Bartonella henselae in 58 healthy persons from a rural region by an indirect immunofluorescence assay. MRL-BA slides (MRL Diagnostics, USA) and Virion slides (Virion, Switzerland) with agar-derived Bartonella henselae showed IgG titers of > or = 1:256 in 44.8% and 51.7%, respectively, whereas Bion slides (Bios, Germany), MRL-Vero slides (MRL Diagnostics), and in-house slides with cell-associated Bartonella henselae showed such titers in 3.4%, 5.1% and 3.4%, respectively. The MRL-Vero slides (Bartonella IgG substrate slides, MRL Diagnostics) were further evaluated with 26 patients with cat scratch disease, 20 patients with lymphadenopathy not due to cat scratch disease, 100 blood donors from an urban area, and 120 blood donors from a mixed urban/rural area. In our mixed urban/rural population the IgG titer of 1:256 had a sensitivity of 84.6% and a specificity of 93.4% for the serodiagnosis of cat scratch disease. Seroprevalence was higher in blood donors from the mixed area (50.8%) than from the urban area (37%). MRL-Vero slides were considered useful for the serodiagnosis of cat scratch disease by indirect immunofluorescence and have replaced our in-house system. However, patients with low IgG titers should be retested three to four weeks after initial sampling to demonstrate a possible rise of IgG titers in paired sera.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>9352257</pmid><doi>10.1007/bf01708554</doi><tpages>5</tpages></addata></record> |
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subjects | Antibodies, Bacterial - analysis Antibody Specificity Antigens, Bacterial - analysis Antigens, Bacterial - immunology Bacterial diseases Bartonella henselae - immunology Biological and medical sciences Cat-Scratch Disease - epidemiology Cat-Scratch Disease - immunology Cat-Scratch Disease - microbiology Evaluation Studies as Topic Fluorescent Antibody Technique, Indirect Human bacterial diseases Humans Immunoglobulin G - analysis Infectious diseases Medical sciences Reagent Kits, Diagnostic Rickettsial diseases Tropical bacterial diseases |
title | Evaluation of commercial slides for detection of immunoglobulin G against Bartonella henselae by indirect immunofluorescence |
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