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Yersinia pestis IS1541 transposition provides for escape from plague immunity.
Cornelius, Claire A; Quenee, Lauriane E; Elli, Derek; Ciletti, Nancy A; Schneewind, Olaf.
Afiliação
  • Cornelius CA; Department of Microbiology, University of Chicago, 920 East 58th Street, Chicago, IL 60637, USA. oschnee@bsd.uchicago.edu
Infect Immun ; 77(5): 1807-16, 2009 May.
Article em En | MEDLINE | ID: mdl-19237527
Yersinia pestis is perhaps the most feared infectious agent due to its ability to cause epidemic outbreaks of plague disease in animals and humans with high mortality. Plague infections elicit strong humoral immune responses against the capsular antigen (fraction 1 [F1]) of Y. pestis, and F1-specific antibodies provide protective immunity. Here we asked whether Y. pestis generates mutations that enable bacterial escape from protective immunity and isolated a variant with an IS1541 insertion in caf1A encoding the F1 outer membrane usher. The caf1A::IS1541 insertion prevented assembly of F1 pili and provided escape from plague immunity via F1-specific antibodies without a reduction in virulence in mouse models of bubonic or pneumonic plague. F1-specific antibodies interfere with Y. pestis type III transport of effector proteins into host cells, an inhibitory effect that was overcome by the caf1A::IS1541 insertion. These findings suggest a model in which IS1541 insertion into caf1A provides for reversible changes in envelope structure, enabling Y. pestis to escape from adaptive immune responses and plague immunity.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peste / Proteínas de Bactérias / Yersinia pestis / Elementos de DNA Transponíveis Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Infect Immun Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peste / Proteínas de Bactérias / Yersinia pestis / Elementos de DNA Transponíveis Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Infect Immun Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Estados Unidos