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Type b Capsule Inhibits Ingestion of Haemophilus influenzae by Murine Macrophages: Studies with Isogenic Encapsulated and Unencapsulated Strains
Phagocytosis may be important in clearing Haemophilus influenzae from the bloodstream. To define the effect of type b capsule on phagocytosis, binding and ingestion by macrophages was measured for 5 isogenic sets of capsule-sufficient strains (clinical isolates and type b transformants of capsule-de...
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Published in: | The Journal of infectious diseases 1992-07, Vol.166 (1), p.178-182 |
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description | Phagocytosis may be important in clearing Haemophilus influenzae from the bloodstream. To define the effect of type b capsule on phagocytosis, binding and ingestion by macrophages was measured for 5 isogenic sets of capsule-sufficient strains (clinical isolates and type b transformants of capsule-deficient mutants) and capsule-deficient mutants (strains lacking a 9-kb EcoRI fragment of chromosomal DNA associated with type b capsule expression). Capsule-sufficient strains were not bound in the absence of serum, whereas capsule-deficient strains were bound and ingested (1.8–5.1 organisms/macrophage; 59%–97% ingested). In the presence of nonimmune serum, capsule-sufficient strains were largely bound but not ingested (4.7–7.2 organisms/macrophage; 7%–21%ingested), whereas capsule-deficient strains were nearly all ingested (6.2–10.5 organisms/macrophage; 93%–97% ingested). Strains resisting ingestion caused persistent bacteremia 24 h after intravenous challenge in mice and were more likely than readily ingested strains to cause persistent bacteremia or death in infant rats. Thus, type b capsule inhibits ingestion by macrophages; resistance to ingestion maybe an important virulence determinant of type b organisms. |
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To define the effect of type b capsule on phagocytosis, binding and ingestion by macrophages was measured for 5 isogenic sets of capsule-sufficient strains (clinical isolates and type b transformants of capsule-deficient mutants) and capsule-deficient mutants (strains lacking a 9-kb EcoRI fragment of chromosomal DNA associated with type b capsule expression). Capsule-sufficient strains were not bound in the absence of serum, whereas capsule-deficient strains were bound and ingested (1.8–5.1 organisms/macrophage; 59%–97% ingested). In the presence of nonimmune serum, capsule-sufficient strains were largely bound but not ingested (4.7–7.2 organisms/macrophage; 7%–21%ingested), whereas capsule-deficient strains were nearly all ingested (6.2–10.5 organisms/macrophage; 93%–97% ingested). Strains resisting ingestion caused persistent bacteremia 24 h after intravenous challenge in mice and were more likely than readily ingested strains to cause persistent bacteremia or death in infant rats. Thus, type b capsule inhibits ingestion by macrophages; resistance to ingestion maybe an important virulence determinant of type b organisms.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/166.1.178</identifier><identifier>PMID: 1607693</identifier><language>eng</language><publisher>United States: The University of Chicago Press</publisher><subject>Agglutination Tests ; Animals ; Bacteremia ; Bacteremia - immunology ; Bacteria ; Bacterial Capsules - immunology ; Bacterial Outer Membrane Proteins - analysis ; Blood ; Blotting, Southern ; Cells, Cultured ; Concise Comunications ; DNA, Bacterial - analysis ; Haemophilus Infections - immunology ; Haemophilus influenzae ; Haemophilus influenzae - chemistry ; Haemophilus influenzae - genetics ; Haemophilus influenzae - immunology ; Humans ; Ingestion ; Inoculation ; Macrophages ; Macrophages - immunology ; Male ; Mice ; Nucleic Acid Hybridization ; Phagocytosis ; Virulence</subject><ispartof>The Journal of infectious diseases, 1992-07, Vol.166 (1), p.178-182</ispartof><rights>Copyright 1992 The University of Chicago</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-ce063529089b704eb7060ec088ba2374c99842e81d2b8c9859cb6961e09fc6503</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/30112252$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/30112252$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,58213,58446</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1607693$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Noel, Gary J.</creatorcontrib><creatorcontrib>Hoiseth, Susan K.</creatorcontrib><creatorcontrib>Edelson, Paul J.</creatorcontrib><title>Type b Capsule Inhibits Ingestion of Haemophilus influenzae by Murine Macrophages: Studies with Isogenic Encapsulated and Unencapsulated Strains</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>Phagocytosis may be important in clearing Haemophilus influenzae from the bloodstream. To define the effect of type b capsule on phagocytosis, binding and ingestion by macrophages was measured for 5 isogenic sets of capsule-sufficient strains (clinical isolates and type b transformants of capsule-deficient mutants) and capsule-deficient mutants (strains lacking a 9-kb EcoRI fragment of chromosomal DNA associated with type b capsule expression). Capsule-sufficient strains were not bound in the absence of serum, whereas capsule-deficient strains were bound and ingested (1.8–5.1 organisms/macrophage; 59%–97% ingested). In the presence of nonimmune serum, capsule-sufficient strains were largely bound but not ingested (4.7–7.2 organisms/macrophage; 7%–21%ingested), whereas capsule-deficient strains were nearly all ingested (6.2–10.5 organisms/macrophage; 93%–97% ingested). Strains resisting ingestion caused persistent bacteremia 24 h after intravenous challenge in mice and were more likely than readily ingested strains to cause persistent bacteremia or death in infant rats. Thus, type b capsule inhibits ingestion by macrophages; resistance to ingestion maybe an important virulence determinant of type b organisms.</description><subject>Agglutination Tests</subject><subject>Animals</subject><subject>Bacteremia</subject><subject>Bacteremia - immunology</subject><subject>Bacteria</subject><subject>Bacterial Capsules - immunology</subject><subject>Bacterial Outer Membrane Proteins - analysis</subject><subject>Blood</subject><subject>Blotting, Southern</subject><subject>Cells, Cultured</subject><subject>Concise Comunications</subject><subject>DNA, Bacterial - analysis</subject><subject>Haemophilus Infections - immunology</subject><subject>Haemophilus influenzae</subject><subject>Haemophilus influenzae - chemistry</subject><subject>Haemophilus influenzae - genetics</subject><subject>Haemophilus influenzae - immunology</subject><subject>Humans</subject><subject>Ingestion</subject><subject>Inoculation</subject><subject>Macrophages</subject><subject>Macrophages - immunology</subject><subject>Male</subject><subject>Mice</subject><subject>Nucleic Acid Hybridization</subject><subject>Phagocytosis</subject><subject>Virulence</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><recordid>eNqFkUtv1DAUhS0EKkNhzwbJK3aZ-hG_2KFR2xlpKhbTCsTGcpybjkvGCXEimP4KfjKGVC07NvaVz_nule9B6C0lS0oMPwuxqUM6o1Iu6ZIq_QwtqOCqkJLy52hBCGMF1ca8RK9SuiOElFyqE3RCJVHS8AX6dX3sAVd45fo0tYA3cR-qMKZc3EIaQxdx1-C1g0PX70M7JZxHthPEe5exI76ahhABXzk_ZIPLzAe8G6c6QMI_wrjHm9TdQgwen0f_d4YbocYu1vgmwr9Pu3FwIabX6EXj2gRvHu5TdHNxfr1aF9tPl5vVx23huRZj4YFILpgh2lSKlJAPScATrSvHuCq9MbpkoGnNKu2NFsZX0kgKxDReCsJP0fu5bz9036f8VXsIyUPbugjdlKzieVtElP81UsmZVFpmI5mNeRUpDdDYfggHNxwtJfZPWnZOKxPSUpvTysi7h95TdYD6CZjjedLv0tgNjzInlDImWNaLWQ9phJ-Puhu-Wam4Enb95avdcrb6vDMiF78BfZisKg</recordid><startdate>19920701</startdate><enddate>19920701</enddate><creator>Noel, Gary J.</creator><creator>Hoiseth, Susan K.</creator><creator>Edelson, Paul J.</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><scope>BSCLL</scope><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>C1K</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19920701</creationdate><title>Type b Capsule Inhibits Ingestion of Haemophilus influenzae by Murine Macrophages: Studies with Isogenic Encapsulated and Unencapsulated Strains</title><author>Noel, Gary J. ; Hoiseth, Susan K. ; Edelson, Paul J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-ce063529089b704eb7060ec088ba2374c99842e81d2b8c9859cb6961e09fc6503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Agglutination Tests</topic><topic>Animals</topic><topic>Bacteremia</topic><topic>Bacteremia - immunology</topic><topic>Bacteria</topic><topic>Bacterial Capsules - immunology</topic><topic>Bacterial Outer Membrane Proteins - analysis</topic><topic>Blood</topic><topic>Blotting, Southern</topic><topic>Cells, Cultured</topic><topic>Concise Comunications</topic><topic>DNA, Bacterial - analysis</topic><topic>Haemophilus Infections - immunology</topic><topic>Haemophilus influenzae</topic><topic>Haemophilus influenzae - chemistry</topic><topic>Haemophilus influenzae - genetics</topic><topic>Haemophilus influenzae - immunology</topic><topic>Humans</topic><topic>Ingestion</topic><topic>Inoculation</topic><topic>Macrophages</topic><topic>Macrophages - immunology</topic><topic>Male</topic><topic>Mice</topic><topic>Nucleic Acid Hybridization</topic><topic>Phagocytosis</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Noel, Gary J.</creatorcontrib><creatorcontrib>Hoiseth, Susan K.</creatorcontrib><creatorcontrib>Edelson, Paul J.</creatorcontrib><collection>Istex</collection><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>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Noel, Gary J.</au><au>Hoiseth, Susan K.</au><au>Edelson, Paul J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Type b Capsule Inhibits Ingestion of Haemophilus influenzae by Murine Macrophages: Studies with Isogenic Encapsulated and Unencapsulated Strains</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>1992-07-01</date><risdate>1992</risdate><volume>166</volume><issue>1</issue><spage>178</spage><epage>182</epage><pages>178-182</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><abstract>Phagocytosis may be important in clearing Haemophilus influenzae from the bloodstream. To define the effect of type b capsule on phagocytosis, binding and ingestion by macrophages was measured for 5 isogenic sets of capsule-sufficient strains (clinical isolates and type b transformants of capsule-deficient mutants) and capsule-deficient mutants (strains lacking a 9-kb EcoRI fragment of chromosomal DNA associated with type b capsule expression). Capsule-sufficient strains were not bound in the absence of serum, whereas capsule-deficient strains were bound and ingested (1.8–5.1 organisms/macrophage; 59%–97% ingested). In the presence of nonimmune serum, capsule-sufficient strains were largely bound but not ingested (4.7–7.2 organisms/macrophage; 7%–21%ingested), whereas capsule-deficient strains were nearly all ingested (6.2–10.5 organisms/macrophage; 93%–97% ingested). Strains resisting ingestion caused persistent bacteremia 24 h after intravenous challenge in mice and were more likely than readily ingested strains to cause persistent bacteremia or death in infant rats. Thus, type b capsule inhibits ingestion by macrophages; resistance to ingestion maybe an important virulence determinant of type b organisms.</abstract><cop>United States</cop><pub>The University of Chicago Press</pub><pmid>1607693</pmid><doi>10.1093/infdis/166.1.178</doi><tpages>5</tpages></addata></record> |
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subjects | Agglutination Tests Animals Bacteremia Bacteremia - immunology Bacteria Bacterial Capsules - immunology Bacterial Outer Membrane Proteins - analysis Blood Blotting, Southern Cells, Cultured Concise Comunications DNA, Bacterial - analysis Haemophilus Infections - immunology Haemophilus influenzae Haemophilus influenzae - chemistry Haemophilus influenzae - genetics Haemophilus influenzae - immunology Humans Ingestion Inoculation Macrophages Macrophages - immunology Male Mice Nucleic Acid Hybridization Phagocytosis Virulence |
title | Type b Capsule Inhibits Ingestion of Haemophilus influenzae by Murine Macrophages: Studies with Isogenic Encapsulated and Unencapsulated Strains |
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