The role of antibodies to Bacillus anthracis and anthrax toxin components in inhibiting the early stages of infection by anthrax spores

Divisions of Bacteriology 1 and Pathology 2 , US Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702-5011, USA Author for correspondence: Susan Welkos. Tel: +1 301 619 4930. Fax: +1 301 619 2152. e-mail: welkos{at}ncisun1.ncifcrf.gov Vaccines which are efficacio...

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Veröffentlicht in:Microbiology (Society for General Microbiology) 2001-06, Vol.147 (6), p.1677-1685
Hauptverfasser: Welkos, Susan, Little, Stephen, Friedlander, Arthur, Fritz, David, Fellows, Patricia
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container_end_page 1685
container_issue 6
container_start_page 1677
container_title Microbiology (Society for General Microbiology)
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creator Welkos, Susan
Little, Stephen
Friedlander, Arthur
Fritz, David
Fellows, Patricia
description Divisions of Bacteriology 1 and Pathology 2 , US Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702-5011, USA Author for correspondence: Susan Welkos. Tel: +1 301 619 4930. Fax: +1 301 619 2152. e-mail: welkos{at}ncisun1.ncifcrf.gov Vaccines which are efficacious against anthrax, such as the human vaccine, Anthrax Vaccine Absorbed (AVA), contain the protective antigen (PA) component of the anthrax toxins as the major protective immunogen. Although AVA protects against inhalational anthrax, the immune responses to and role in protection of PA and possibly other antigens have yet to be fully elucidated. Sera from animals immunized with a toxin-producing, unencapsulated live vaccine strain of Bacillus anthracis have been reported to have anti-spore activities associated with the antitoxin humoral response. The authors performed studies to determine whether anti-PA antibody (Ab)-containing preparations stimulated spore uptake by phagocytes and suppressed the germination of spores in vitro . AVA- and PA-immune sera from several species enhanced the phagocytosis by murine peritoneal macrophages of spores of the virulent Ames and the Sterne vaccine strains. Antitoxin Abs appeared to contribute significantly, although not solely, to the enhanced uptake. Rabbit antisera to PA purified from either Sterne or a PA-producing pX01-cured recombinant, affinity-purified anti-PA IgG, and monkey antisera to AVA were used to assess the role of anti-PA Abs. Rabbit anti-PA Abs promoted the uptake of spores of the PA-producing strains Sterne, Ames and RP42, a mutant of Sterne producing only PA, but not of the pX01- Sterne-1 strain, Ames strain, or RP4, a mutant of Sterne with deletions in the loci encoding PA and the oedema factor (EF) toxin component and producing only the lethal factor toxin component. Rabbit anti-PA and monkey anti-AVA Abs also significantly inhibited spore germination in vitro compared to preimmune serum or medium. Spore-associated proteins recognized by anti-PA Abs were detected by electron microscopy and confirmed by immunoblotting of spore coat extracts. Thus, the anti-PA Ab-specific immunity induced by AVA has anti-spore activity and might have a role in impeding the early stages of infection with B. anthracis spores. Keywords: antitoxin antibody, protective antigen, vaccines, phagocytosis Abbreviations: AVA, Anthrax Vaccine Adsorbed; BHI, brain heart infusion; EF, (o)edema factor; H, heat-activated, ungerminated; H
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Tel: +1 301 619 4930. Fax: +1 301 619 2152. e-mail: welkos{at}ncisun1.ncifcrf.gov Vaccines which are efficacious against anthrax, such as the human vaccine, Anthrax Vaccine Absorbed (AVA), contain the protective antigen (PA) component of the anthrax toxins as the major protective immunogen. Although AVA protects against inhalational anthrax, the immune responses to and role in protection of PA and possibly other antigens have yet to be fully elucidated. Sera from animals immunized with a toxin-producing, unencapsulated live vaccine strain of Bacillus anthracis have been reported to have anti-spore activities associated with the antitoxin humoral response. The authors performed studies to determine whether anti-PA antibody (Ab)-containing preparations stimulated spore uptake by phagocytes and suppressed the germination of spores in vitro . AVA- and PA-immune sera from several species enhanced the phagocytosis by murine peritoneal macrophages of spores of the virulent Ames and the Sterne vaccine strains. Antitoxin Abs appeared to contribute significantly, although not solely, to the enhanced uptake. Rabbit antisera to PA purified from either Sterne or a PA-producing pX01-cured recombinant, affinity-purified anti-PA IgG, and monkey antisera to AVA were used to assess the role of anti-PA Abs. Rabbit anti-PA Abs promoted the uptake of spores of the PA-producing strains Sterne, Ames and RP42, a mutant of Sterne producing only PA, but not of the pX01- Sterne-1 strain, Ames strain, or RP4, a mutant of Sterne with deletions in the loci encoding PA and the oedema factor (EF) toxin component and producing only the lethal factor toxin component. Rabbit anti-PA and monkey anti-AVA Abs also significantly inhibited spore germination in vitro compared to preimmune serum or medium. 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Psychology ; Goats ; Guinea Pigs ; Haplorhini ; Humans ; Immune Sera ; Immunoblotting ; Immunoglobulin G - immunology ; Macrophages, Peritoneal - immunology ; Macrophages, Peritoneal - microbiology ; Mice ; Microbiology ; Microscopy, Immunoelectron ; Phagocytosis ; protective antigen ; Rabbits ; Spores, Bacterial - immunology ; Spores, Bacterial - ultrastructure ; Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies</subject><ispartof>Microbiology (Society for General Microbiology), 2001-06, Vol.147 (6), p.1677-1685</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c506t-46438e5021b862da2838c8b7fac3ba69dd52f5693d71acc73ccd496fbe9481683</citedby><cites>FETCH-LOGICAL-c506t-46438e5021b862da2838c8b7fac3ba69dd52f5693d71acc73ccd496fbe9481683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=5692070$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11390699$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Welkos, Susan</creatorcontrib><creatorcontrib>Little, Stephen</creatorcontrib><creatorcontrib>Friedlander, Arthur</creatorcontrib><creatorcontrib>Fritz, David</creatorcontrib><creatorcontrib>Fellows, Patricia</creatorcontrib><title>The role of antibodies to Bacillus anthracis and anthrax toxin components in inhibiting the early stages of infection by anthrax spores</title><title>Microbiology (Society for General Microbiology)</title><addtitle>Microbiology</addtitle><description>Divisions of Bacteriology 1 and Pathology 2 , US Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702-5011, USA Author for correspondence: Susan Welkos. Tel: +1 301 619 4930. Fax: +1 301 619 2152. e-mail: welkos{at}ncisun1.ncifcrf.gov Vaccines which are efficacious against anthrax, such as the human vaccine, Anthrax Vaccine Absorbed (AVA), contain the protective antigen (PA) component of the anthrax toxins as the major protective immunogen. Although AVA protects against inhalational anthrax, the immune responses to and role in protection of PA and possibly other antigens have yet to be fully elucidated. Sera from animals immunized with a toxin-producing, unencapsulated live vaccine strain of Bacillus anthracis have been reported to have anti-spore activities associated with the antitoxin humoral response. The authors performed studies to determine whether anti-PA antibody (Ab)-containing preparations stimulated spore uptake by phagocytes and suppressed the germination of spores in vitro . AVA- and PA-immune sera from several species enhanced the phagocytosis by murine peritoneal macrophages of spores of the virulent Ames and the Sterne vaccine strains. Antitoxin Abs appeared to contribute significantly, although not solely, to the enhanced uptake. Rabbit antisera to PA purified from either Sterne or a PA-producing pX01-cured recombinant, affinity-purified anti-PA IgG, and monkey antisera to AVA were used to assess the role of anti-PA Abs. Rabbit anti-PA Abs promoted the uptake of spores of the PA-producing strains Sterne, Ames and RP42, a mutant of Sterne producing only PA, but not of the pX01- Sterne-1 strain, Ames strain, or RP4, a mutant of Sterne with deletions in the loci encoding PA and the oedema factor (EF) toxin component and producing only the lethal factor toxin component. Rabbit anti-PA and monkey anti-AVA Abs also significantly inhibited spore germination in vitro compared to preimmune serum or medium. Spore-associated proteins recognized by anti-PA Abs were detected by electron microscopy and confirmed by immunoblotting of spore coat extracts. Thus, the anti-PA Ab-specific immunity induced by AVA has anti-spore activity and might have a role in impeding the early stages of infection with B. anthracis spores. Keywords: antitoxin antibody, protective antigen, vaccines, phagocytosis Abbreviations: AVA, Anthrax Vaccine Adsorbed; BHI, brain heart infusion; EF, (o)edema factor; H, heat-activated, ungerminated; HRP, horseradish peroxidase; LF, lethal factor; PA, protective antigen</description><subject>Animals</subject><subject>Anthrax - immunology</subject><subject>Anthrax - microbiology</subject><subject>Anthrax - prevention &amp; control</subject><subject>anthrax toxin</subject><subject>Anthrax Vaccines - immunology</subject><subject>Antibodies, Bacterial - analysis</subject><subject>Antibodies, Bacterial - immunology</subject><subject>Antigens, Bacterial - immunology</subject><subject>Bacillus anthracis</subject><subject>Bacillus anthracis - immunology</subject><subject>Bacterial Toxins - immunology</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Cells, Cultured</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Goats</subject><subject>Guinea Pigs</subject><subject>Haplorhini</subject><subject>Humans</subject><subject>Immune Sera</subject><subject>Immunoblotting</subject><subject>Immunoglobulin G - immunology</subject><subject>Macrophages, Peritoneal - immunology</subject><subject>Macrophages, Peritoneal - microbiology</subject><subject>Mice</subject><subject>Microbiology</subject><subject>Microscopy, Immunoelectron</subject><subject>Phagocytosis</subject><subject>protective antigen</subject><subject>Rabbits</subject><subject>Spores, Bacterial - immunology</subject><subject>Spores, Bacterial - ultrastructure</subject><subject>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies</subject><issn>1350-0872</issn><issn>1465-2080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc2OFCEUhYnROOPoE5gYFsbERekFqvhZ6sS_ZBI345oARXVhqqAFOk4_ga8tnS5Hd664B7577iUHoecE3hBQ6i0ApYRK0ZFedLwjXIgH6JL0fOgoSHjYajZAB1LQC_SklO8A7RHIY3RBCFPAlbpEv25nj3NaPE4TNrEGm8bgC64JvzcuLMuhnK7n3MSpGjd114i7ELFL6z5FH2vBTYU4BxtqiDtcm683eTniUs2uOTb_ECfvakgR2-O9T9mn7MtT9GgyS_HPtvMKffv44fb6c3fz9dOX63c3nRuA167nPZN-AEqs5HQ0VDLppBWTccwarsZxoNPAFRsFMc4J5tzYKz5Zr3pJuGRX6NXZd5_Tj4MvVa-hOL8sJvp0KFqAVKRn5L8gkZT2jNIGsjPociol-0nvc1hNPmoC-hSU_hOUbkFprk9Bta4Xm_3Brn7827Ml04CXG2CKM8uUTWwJ3HPtjxQENOz1GZvDbv4Zstc7H9fQdrEhtZXdPzN_A8h5qys</recordid><startdate>20010601</startdate><enddate>20010601</enddate><creator>Welkos, Susan</creator><creator>Little, Stephen</creator><creator>Friedlander, Arthur</creator><creator>Fritz, David</creator><creator>Fellows, Patricia</creator><general>Soc General Microbiol</general><general>Society for General Microbiology</general><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>C1K</scope><scope>7X8</scope></search><sort><creationdate>20010601</creationdate><title>The role of antibodies to Bacillus anthracis and anthrax toxin components in inhibiting the early stages of infection by anthrax spores</title><author>Welkos, Susan ; Little, Stephen ; Friedlander, Arthur ; Fritz, David ; Fellows, Patricia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c506t-46438e5021b862da2838c8b7fac3ba69dd52f5693d71acc73ccd496fbe9481683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Anthrax - immunology</topic><topic>Anthrax - microbiology</topic><topic>Anthrax - prevention &amp; control</topic><topic>anthrax toxin</topic><topic>Anthrax Vaccines - immunology</topic><topic>Antibodies, Bacterial - analysis</topic><topic>Antibodies, Bacterial - immunology</topic><topic>Antigens, Bacterial - immunology</topic><topic>Bacillus anthracis</topic><topic>Bacillus anthracis - immunology</topic><topic>Bacterial Toxins - immunology</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Cells, Cultured</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Goats</topic><topic>Guinea Pigs</topic><topic>Haplorhini</topic><topic>Humans</topic><topic>Immune Sera</topic><topic>Immunoblotting</topic><topic>Immunoglobulin G - immunology</topic><topic>Macrophages, Peritoneal - immunology</topic><topic>Macrophages, Peritoneal - microbiology</topic><topic>Mice</topic><topic>Microbiology</topic><topic>Microscopy, Immunoelectron</topic><topic>Phagocytosis</topic><topic>protective antigen</topic><topic>Rabbits</topic><topic>Spores, Bacterial - immunology</topic><topic>Spores, Bacterial - ultrastructure</topic><topic>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Welkos, Susan</creatorcontrib><creatorcontrib>Little, Stephen</creatorcontrib><creatorcontrib>Friedlander, Arthur</creatorcontrib><creatorcontrib>Fritz, David</creatorcontrib><creatorcontrib>Fellows, Patricia</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>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Microbiology (Society for General Microbiology)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Welkos, Susan</au><au>Little, Stephen</au><au>Friedlander, Arthur</au><au>Fritz, David</au><au>Fellows, Patricia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The role of antibodies to Bacillus anthracis and anthrax toxin components in inhibiting the early stages of infection by anthrax spores</atitle><jtitle>Microbiology (Society for General Microbiology)</jtitle><addtitle>Microbiology</addtitle><date>2001-06-01</date><risdate>2001</risdate><volume>147</volume><issue>6</issue><spage>1677</spage><epage>1685</epage><pages>1677-1685</pages><issn>1350-0872</issn><eissn>1465-2080</eissn><abstract>Divisions of Bacteriology 1 and Pathology 2 , US Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702-5011, USA Author for correspondence: Susan Welkos. Tel: +1 301 619 4930. Fax: +1 301 619 2152. e-mail: welkos{at}ncisun1.ncifcrf.gov Vaccines which are efficacious against anthrax, such as the human vaccine, Anthrax Vaccine Absorbed (AVA), contain the protective antigen (PA) component of the anthrax toxins as the major protective immunogen. Although AVA protects against inhalational anthrax, the immune responses to and role in protection of PA and possibly other antigens have yet to be fully elucidated. Sera from animals immunized with a toxin-producing, unencapsulated live vaccine strain of Bacillus anthracis have been reported to have anti-spore activities associated with the antitoxin humoral response. The authors performed studies to determine whether anti-PA antibody (Ab)-containing preparations stimulated spore uptake by phagocytes and suppressed the germination of spores in vitro . AVA- and PA-immune sera from several species enhanced the phagocytosis by murine peritoneal macrophages of spores of the virulent Ames and the Sterne vaccine strains. Antitoxin Abs appeared to contribute significantly, although not solely, to the enhanced uptake. Rabbit antisera to PA purified from either Sterne or a PA-producing pX01-cured recombinant, affinity-purified anti-PA IgG, and monkey antisera to AVA were used to assess the role of anti-PA Abs. Rabbit anti-PA Abs promoted the uptake of spores of the PA-producing strains Sterne, Ames and RP42, a mutant of Sterne producing only PA, but not of the pX01- Sterne-1 strain, Ames strain, or RP4, a mutant of Sterne with deletions in the loci encoding PA and the oedema factor (EF) toxin component and producing only the lethal factor toxin component. Rabbit anti-PA and monkey anti-AVA Abs also significantly inhibited spore germination in vitro compared to preimmune serum or medium. Spore-associated proteins recognized by anti-PA Abs were detected by electron microscopy and confirmed by immunoblotting of spore coat extracts. Thus, the anti-PA Ab-specific immunity induced by AVA has anti-spore activity and might have a role in impeding the early stages of infection with B. anthracis spores. Keywords: antitoxin antibody, protective antigen, vaccines, phagocytosis Abbreviations: AVA, Anthrax Vaccine Adsorbed; BHI, brain heart infusion; EF, (o)edema factor; H, heat-activated, ungerminated; HRP, horseradish peroxidase; LF, lethal factor; PA, protective antigen</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>11390699</pmid><doi>10.1099/00221287-147-6-1677</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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ispartof Microbiology (Society for General Microbiology), 2001-06, Vol.147 (6), p.1677-1685
issn 1350-0872
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subjects Animals
Anthrax - immunology
Anthrax - microbiology
Anthrax - prevention & control
anthrax toxin
Anthrax Vaccines - immunology
Antibodies, Bacterial - analysis
Antibodies, Bacterial - immunology
Antigens, Bacterial - immunology
Bacillus anthracis
Bacillus anthracis - immunology
Bacterial Toxins - immunology
Bacteriology
Biological and medical sciences
Cells, Cultured
Fundamental and applied biological sciences. Psychology
Goats
Guinea Pigs
Haplorhini
Humans
Immune Sera
Immunoblotting
Immunoglobulin G - immunology
Macrophages, Peritoneal - immunology
Macrophages, Peritoneal - microbiology
Mice
Microbiology
Microscopy, Immunoelectron
Phagocytosis
protective antigen
Rabbits
Spores, Bacterial - immunology
Spores, Bacterial - ultrastructure
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies
title The role of antibodies to Bacillus anthracis and anthrax toxin components in inhibiting the early stages of infection by anthrax spores
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