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Passive Protection of Mice against Group A Streptococcal Pharyngeal Infection by Lipoteichoic Acid
Previous studies have shown that lipoteichoic acid (LTA) of group A streptococci plays a central role in the adherence of these organisms to epithelial cells. In this study, intranasal instillation of purified LTA but not deacylated LTA in mice blocked colonization and prevented death after intranas...
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Published in: | The Journal of infectious diseases 1994-02, Vol.169 (2), p.319-323 |
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creator | Dale, James B. Baird, Robert W. Courtney, Harry S. Hasty, David L. Bronze, Michael S. |
description | Previous studies have shown that lipoteichoic acid (LTA) of group A streptococci plays a central role in the adherence of these organisms to epithelial cells. In this study, intranasal instillation of purified LTA but not deacylated LTA in mice blocked colonization and prevented death after intranasal challenge infection with group A streptococci. Bacteria pretreated with rabbit antisera against LTA also failed to colonize or infect mice after intranasal challenge. In vitro studies showed that LTA and M protein inhibited adherence of type 24 streptococci to mouse pharyngeal cells. Passive intranasal administration of purified type 24 M protein protected mice from death after challenge infection with type 24 streptococci but had no significant effect on pharyngeal colonization. Surface LTA and M protein may mediate adherence of streptococci to mouse pharyngeal cells, and blocking adherence with LTA prevents colonization and infection in this animal model. |
doi_str_mv | 10.1093/infdis/169.2.319 |
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In this study, intranasal instillation of purified LTA but not deacylated LTA in mice blocked colonization and prevented death after intranasal challenge infection with group A streptococci. Bacteria pretreated with rabbit antisera against LTA also failed to colonize or infect mice after intranasal challenge. In vitro studies showed that LTA and M protein inhibited adherence of type 24 streptococci to mouse pharyngeal cells. Passive intranasal administration of purified type 24 M protein protected mice from death after challenge infection with type 24 streptococci but had no significant effect on pharyngeal colonization. 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In this study, intranasal instillation of purified LTA but not deacylated LTA in mice blocked colonization and prevented death after intranasal challenge infection with group A streptococci. Bacteria pretreated with rabbit antisera against LTA also failed to colonize or infect mice after intranasal challenge. In vitro studies showed that LTA and M protein inhibited adherence of type 24 streptococci to mouse pharyngeal cells. Passive intranasal administration of purified type 24 M protein protected mice from death after challenge infection with type 24 streptococci but had no significant effect on pharyngeal colonization. Surface LTA and M protein may mediate adherence of streptococci to mouse pharyngeal cells, and blocking adherence with LTA prevents colonization and infection in this animal model.</description><subject>Animal models</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Antibodies, Bacterial - immunology</subject><subject>Antigens, Bacterial</subject><subject>Bacteria</subject><subject>Bacterial Adhesion</subject><subject>Bacterial diseases</subject><subject>Bacterial Outer Membrane Proteins</subject><subject>Bacterial Proteins - immunology</subject><subject>Biological and medical sciences</subject><subject>Carrier Proteins</subject><subject>Epithelial cells</subject><subject>Experimental bacterial diseases and models</subject><subject>Fatty acids</subject><subject>Female</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Lipopolysaccharides - immunology</subject><subject>Major Articles</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Microbial colonization</subject><subject>Nasal Mucosa - immunology</subject><subject>Nasal Mucosa - microbiology</subject><subject>Receptors</subject><subject>Streptococcal infections</subject><subject>Streptococcal Infections - microbiology</subject><subject>Streptococcal Infections - prevention & control</subject><subject>Streptococcus</subject><subject>Streptococcus pyogenes - cytology</subject><subject>Streptococcus pyogenes - immunology</subject><subject>Streptococcus pyogenes - pathogenicity</subject><subject>Teichoic Acids - immunology</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNqFkM1vEzEUxC0EKqFw54LkA-K26Xv2rh0fQwRtpa2IVL7Ui-V4va1Lst7aDqL_PUZZwpGTLf1mRvOGkNcIcwTFz_zQdz6doVBzNueonpAZNlxWQiB_SmYAjFW4UOo5eZHSPQDUXMgTcrJAEFLUM7JZm5T8T0fXMWRnsw8DDT298tZRc2v8kDI9j2E_0iW9ztGNOdhgrdnS9Z2Jj8OtK9_LoZ-sm0fa-rEkeXsXvKVL67uX5Flvtsm9mt5T8uXjh8-ri6r9dH65WraVrbHOFRqOWA5pJBhWWvZqYUTXd8aZhjGGApiSsrTeWN5xBdJyWTd1A52QnWKMn5J3h9wxhoe9S1nvfLJuuzWDC_ukpeAlW_5fiEJIWQtZhHAQ2hhSiq7XY_S7crZG0H_214f9i0Nppsv-xfJmyt5vdq47GqbBC387cZPKin00gy0Bf2U1SBQL8S_mPuUQj5gDIlcIhVcH7lN2v47cxB-69JaNvvh-o6--rtqb9vq9_sZ_A3BkpsM</recordid><startdate>19940201</startdate><enddate>19940201</enddate><creator>Dale, James B.</creator><creator>Baird, Robert W.</creator><creator>Courtney, Harry S.</creator><creator>Hasty, David L.</creator><creator>Bronze, Michael S.</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><scope>BSCLL</scope><scope>IQODW</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>19940201</creationdate><title>Passive Protection of Mice against Group A Streptococcal Pharyngeal Infection by Lipoteichoic Acid</title><author>Dale, James B. ; Baird, Robert W. ; Courtney, Harry S. ; Hasty, David L. ; Bronze, Michael S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-1a311169570a2367f98a6dfdaea52221602977676bc3d3907c3745450d67d9223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Antibodies, Bacterial - immunology</topic><topic>Antigens, Bacterial</topic><topic>Bacteria</topic><topic>Bacterial Adhesion</topic><topic>Bacterial diseases</topic><topic>Bacterial Outer Membrane Proteins</topic><topic>Bacterial Proteins - immunology</topic><topic>Biological and medical sciences</topic><topic>Carrier Proteins</topic><topic>Epithelial cells</topic><topic>Experimental bacterial diseases and models</topic><topic>Fatty acids</topic><topic>Female</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Lipopolysaccharides - immunology</topic><topic>Major Articles</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microbial colonization</topic><topic>Nasal Mucosa - immunology</topic><topic>Nasal Mucosa - microbiology</topic><topic>Receptors</topic><topic>Streptococcal infections</topic><topic>Streptococcal Infections - microbiology</topic><topic>Streptococcal Infections - prevention & control</topic><topic>Streptococcus</topic><topic>Streptococcus pyogenes - cytology</topic><topic>Streptococcus pyogenes - immunology</topic><topic>Streptococcus pyogenes - pathogenicity</topic><topic>Teichoic Acids - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dale, James B.</creatorcontrib><creatorcontrib>Baird, Robert W.</creatorcontrib><creatorcontrib>Courtney, Harry S.</creatorcontrib><creatorcontrib>Hasty, David L.</creatorcontrib><creatorcontrib>Bronze, Michael S.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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>Dale, James B.</au><au>Baird, Robert W.</au><au>Courtney, Harry S.</au><au>Hasty, David L.</au><au>Bronze, Michael S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Passive Protection of Mice against Group A Streptococcal Pharyngeal Infection by Lipoteichoic Acid</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>1994-02-01</date><risdate>1994</risdate><volume>169</volume><issue>2</issue><spage>319</spage><epage>323</epage><pages>319-323</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><coden>JIDIAQ</coden><abstract>Previous studies have shown that lipoteichoic acid (LTA) of group A streptococci plays a central role in the adherence of these organisms to epithelial cells. In this study, intranasal instillation of purified LTA but not deacylated LTA in mice blocked colonization and prevented death after intranasal challenge infection with group A streptococci. Bacteria pretreated with rabbit antisera against LTA also failed to colonize or infect mice after intranasal challenge. In vitro studies showed that LTA and M protein inhibited adherence of type 24 streptococci to mouse pharyngeal cells. Passive intranasal administration of purified type 24 M protein protected mice from death after challenge infection with type 24 streptococci but had no significant effect on pharyngeal colonization. Surface LTA and M protein may mediate adherence of streptococci to mouse pharyngeal cells, and blocking adherence with LTA prevents colonization and infection in this animal model.</abstract><cop>Chicago, IL</cop><pub>The University of Chicago Press</pub><pmid>8106764</pmid><doi>10.1093/infdis/169.2.319</doi><tpages>5</tpages></addata></record> |
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source | Oxford University Press:Jisc Collections:Oxford Journal Archive: Access period 2024-2025 |
subjects | Animal models Animals Antibodies Antibodies, Bacterial - immunology Antigens, Bacterial Bacteria Bacterial Adhesion Bacterial diseases Bacterial Outer Membrane Proteins Bacterial Proteins - immunology Biological and medical sciences Carrier Proteins Epithelial cells Experimental bacterial diseases and models Fatty acids Female Infections Infectious diseases Lipopolysaccharides - immunology Major Articles Medical sciences Mice Mice, Inbred BALB C Microbial colonization Nasal Mucosa - immunology Nasal Mucosa - microbiology Receptors Streptococcal infections Streptococcal Infections - microbiology Streptococcal Infections - prevention & control Streptococcus Streptococcus pyogenes - cytology Streptococcus pyogenes - immunology Streptococcus pyogenes - pathogenicity Teichoic Acids - immunology |
title | Passive Protection of Mice against Group A Streptococcal Pharyngeal Infection by Lipoteichoic Acid |
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