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1.
Microbes Infect ; 8(8): 2075-81, 2006 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16781179

RESUMO

Buruli ulcer, a disease caused by Mycobacterium ulcerans, is emerging as an increasingly important cause of morbidity throughout the world, for which surgery is the only efficient treatment to date. The aim of this work was to identify potential vaccine candidates in an experimental model of mouse infection. In BALB/c mice infected with M. ulcerans subcutaneously, Hsp65 appeared to be an immunodominant antigen eliciting both humoral and cellular responses. However, vaccination of mice with a DNA vector encoding Mycobacterium leprae Hsp65 only poorly limited the progression of M. ulcerans infection. In contrast, a substantial degree of protection was conferred by subcutaneous vaccination with BCG, suggesting that BCG antigens that are conserved in M. ulcerans, such as TB10.4, the 19 kDa antigen, PstS3 and Hsp70, may be interesting to consider as subunit vaccines in future prospects.


Assuntos
Proteínas de Bactérias/imunologia , Vacinas Bacterianas/imunologia , Chaperoninas/imunologia , Infecções por Mycobacterium não Tuberculosas/prevenção & controle , Mycobacterium leprae/imunologia , Mycobacterium ulcerans/imunologia , Úlcera Cutânea/prevenção & controle , Vacinas de DNA/imunologia , Animais , Anticorpos Antibacterianos/sangue , Chaperonina 60 , Modelos Animais de Doenças , Feminino , Interferon gama/biossíntese , Camundongos , Camundongos Endogâmicos BALB C , Infecções por Mycobacterium não Tuberculosas/microbiologia , Mycobacterium bovis/imunologia , Mycobacterium ulcerans/crescimento & desenvolvimento , Úlcera Cutânea/microbiologia , Linfócitos T/imunologia , Cauda/microbiologia
2.
Cell Microbiol ; 7(7): 935-43, 2005 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15953026

RESUMO

Mycobacterium ulcerans was first identified as the causative agent of Buruli ulcer; this cutaneous tissue-destructive process represents the third most important mycobacterial disease in humans after tuberculosis and leprosy. More recently other life traits were documented. M. ulcerans is mainly detected in humid tropical zones as part of a complex ecosystem comprising algae, aquatic insect predators of the genus Naucoris, and very likely their vegetarian preys. Coelomic plasmatocytes could be the first cells of Naucoris cimicoides to be involved in the infection process, acting as shuttle cells that deliver M. ulcerans to the salivary glands as suggested by both in vitro and in vivo approaches. Furthermore, a key element for the early and long-term establishment of M. ulcerans in Naucoridae is demonstrated by the fact that only mycolactone toxin-producing M. ulcerans isolates are able to invade the salivary glands, a site where they proliferate. Later, the raptorial legs of Naucoris are covered by M. ulcerans-containing material that displays features of biofilms.


Assuntos
Toxinas Bacterianas/biossíntese , Heterópteros/microbiologia , Mycobacterium ulcerans/fisiologia , Animais , Toxinas Bacterianas/toxicidade , Biofilmes/crescimento & desenvolvimento , Extremidades/microbiologia , Macrolídeos , Camundongos , Camundongos Endogâmicos BALB C , Infecções por Mycobacterium não Tuberculosas/patologia , Infecções por Mycobacterium não Tuberculosas/transmissão , Mycobacterium ulcerans/crescimento & desenvolvimento , Glândulas Salivares/microbiologia
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