Passive administration of monoclonal antibodies to Anthrolysin O prolong survival in mice lethally infected with <it>Bacillus anthracis</it>

<p>Abstract</p> <p>Background</p> <p><it>Bacillus anthracis </it>has two major virulence factors: a tripartite toxin that produces lethal and edema toxins and a polyglutamic acid capsule. A recent report suggested that a toxin belonging to the cholesterol de...

Full description

Bibliographic Details
Main Authors: Rest Richard F, Rivera Johanna, Nakouzi Antonio, Casadevall Arturo
Format: Article
Language:English
Published: BMC 2008-09-01
Series:BMC Microbiology
Online Access:http://www.biomedcentral.com/1471-2180/8/159
_version_ 1818690036748517376
author Rest Richard F
Rivera Johanna
Nakouzi Antonio
Casadevall Arturo
author_facet Rest Richard F
Rivera Johanna
Nakouzi Antonio
Casadevall Arturo
author_sort Rest Richard F
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p><it>Bacillus anthracis </it>has two major virulence factors: a tripartite toxin that produces lethal and edema toxins and a polyglutamic acid capsule. A recent report suggested that a toxin belonging to the cholesterol dependant cytolysin (CDC) family, anthrolysin O (ALO) was a new virulence factor for <it>B. anthracis </it>but subsequent studies have questioned its relevance in pathogenesis. In this study, we examined the immunogenicity of recombinant anthrolysin O (rALO) in mice.</p> <p>Results</p> <p>BALB/c mice immunized with rALO and boosted after two weeks, produce sera with strong Ab responses with a predominance of IgG1 and IgG2a. Five hybridomas to rALO were recovered representing the IgM, IgG1, and IgG2b isotypes. Passive administration of 3 of the five monoclonal antibodies (mAbs) to rALO prior to infection with lethal intravenous (i.v.) <it>B. anthracis </it>Sterne strain infection in mice was associated with enhanced average survival and a greater likelihood of surviving infection. A combination of two mAbs to ALO was more effective than either mAb separately. One mAb (64F8) slowed the toxicity of rALO for J774.16 macrophage-like cells.</p> <p>Conclusion</p> <p>Our results suggest that ALO contributes to the virulence of <it>B. anthracis </it>Sterne strain in this infection model and that Ab response to ALO may contribute to protection in certain circumstances.</p>
first_indexed 2024-12-17T12:19:37Z
format Article
id doaj.art-a9cb915793f54295b71e939bdedec4f0
institution Directory Open Access Journal
issn 1471-2180
language English
last_indexed 2024-12-17T12:19:37Z
publishDate 2008-09-01
publisher BMC
record_format Article
series BMC Microbiology
spelling doaj.art-a9cb915793f54295b71e939bdedec4f02022-12-21T21:49:02ZengBMCBMC Microbiology1471-21802008-09-018115910.1186/1471-2180-8-159Passive administration of monoclonal antibodies to Anthrolysin O prolong survival in mice lethally infected with <it>Bacillus anthracis</it>Rest Richard FRivera JohannaNakouzi AntonioCasadevall Arturo<p>Abstract</p> <p>Background</p> <p><it>Bacillus anthracis </it>has two major virulence factors: a tripartite toxin that produces lethal and edema toxins and a polyglutamic acid capsule. A recent report suggested that a toxin belonging to the cholesterol dependant cytolysin (CDC) family, anthrolysin O (ALO) was a new virulence factor for <it>B. anthracis </it>but subsequent studies have questioned its relevance in pathogenesis. In this study, we examined the immunogenicity of recombinant anthrolysin O (rALO) in mice.</p> <p>Results</p> <p>BALB/c mice immunized with rALO and boosted after two weeks, produce sera with strong Ab responses with a predominance of IgG1 and IgG2a. Five hybridomas to rALO were recovered representing the IgM, IgG1, and IgG2b isotypes. Passive administration of 3 of the five monoclonal antibodies (mAbs) to rALO prior to infection with lethal intravenous (i.v.) <it>B. anthracis </it>Sterne strain infection in mice was associated with enhanced average survival and a greater likelihood of surviving infection. A combination of two mAbs to ALO was more effective than either mAb separately. One mAb (64F8) slowed the toxicity of rALO for J774.16 macrophage-like cells.</p> <p>Conclusion</p> <p>Our results suggest that ALO contributes to the virulence of <it>B. anthracis </it>Sterne strain in this infection model and that Ab response to ALO may contribute to protection in certain circumstances.</p>http://www.biomedcentral.com/1471-2180/8/159
spellingShingle Rest Richard F
Rivera Johanna
Nakouzi Antonio
Casadevall Arturo
Passive administration of monoclonal antibodies to Anthrolysin O prolong survival in mice lethally infected with <it>Bacillus anthracis</it>
BMC Microbiology
title Passive administration of monoclonal antibodies to Anthrolysin O prolong survival in mice lethally infected with <it>Bacillus anthracis</it>
title_full Passive administration of monoclonal antibodies to Anthrolysin O prolong survival in mice lethally infected with <it>Bacillus anthracis</it>
title_fullStr Passive administration of monoclonal antibodies to Anthrolysin O prolong survival in mice lethally infected with <it>Bacillus anthracis</it>
title_full_unstemmed Passive administration of monoclonal antibodies to Anthrolysin O prolong survival in mice lethally infected with <it>Bacillus anthracis</it>
title_short Passive administration of monoclonal antibodies to Anthrolysin O prolong survival in mice lethally infected with <it>Bacillus anthracis</it>
title_sort passive administration of monoclonal antibodies to anthrolysin o prolong survival in mice lethally infected with it bacillus anthracis it
url http://www.biomedcentral.com/1471-2180/8/159
work_keys_str_mv AT restrichardf passiveadministrationofmonoclonalantibodiestoanthrolysinoprolongsurvivalinmicelethallyinfectedwithitbacillusanthracisit
AT riverajohanna passiveadministrationofmonoclonalantibodiestoanthrolysinoprolongsurvivalinmicelethallyinfectedwithitbacillusanthracisit
AT nakouziantonio passiveadministrationofmonoclonalantibodiestoanthrolysinoprolongsurvivalinmicelethallyinfectedwithitbacillusanthracisit
AT casadevallarturo passiveadministrationofmonoclonalantibodiestoanthrolysinoprolongsurvivalinmicelethallyinfectedwithitbacillusanthracisit