Influência das proteínas Yops de Yersinia pseudotuberculosis na resposta imune humoral murina
Data
2006-06-19
Autores
Maia, José Mário Lourenço [UNESP]
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Editor
Universidade Estadual Paulista (Unesp)
Resumo
As proteínas Yops. formam uma família de proteínas secretadas por Yersinia spp que incluem efetores intracelulares (seis efetores foram identificados: YopE, YopH, YopM, YpkA/YopO, YopJ/YopP e YopT) e vários componentes do aparato de secreção-translocação que são liberado pela bactéria sob quelação de Ca2+. As .Yops. efetoras têm sido relacionadas a uma série de propriedades de virulência, incluindo resistência à fagocitose, citotoxicidade e desfosforilação de proteínas do hospedeiro. Porém, a interação das .Yops. de Yersinia com a resposta imune específica do hospedeiro não está bem esclarecida. O objetivo deste estudo foi investigar o papel imunomodulador das Yops secretadas por amostras de Yersinia pseudotuberculosis sobre a produção de anticorpos e autoanticorpos por linfócitos B. Para tanto camundongos foram infectados com uma amostra selvagem de Y. pseudotuberculosis (YpIII) e com amostras mutantes, defectivas na secreção de determinadas .Yops. efetoras (YopH, YopE, YopM, YpkA e YopJ). Foram obtidas células esplênicas destes animais, e as células secretoras de imunoglobulinas inespecíficas e específicas (anti-Yersinia e anti-.Yops.) foram quantificadas através do teste ELISPOT. A presença de anticorpos específicos anti-Yersinia e anti-.Yops. no soro dos animais infectados foi analisada através do teste ELISA. A presença de auto-anticorpos séricos foi analisada através do teste DOT-BLOT. Não se observou nenhuma diferença entre o número de células secretoras de imunoglobulinas (Igs) inespecíficas dos animais inoculados com a amostra selvagem, YpIIIpIB102 (wt), em relação aos controles. Já a amostra YpIII pIB522, embora defectiva na secreção de YopE, provocou uma redução dos linfócitos B secretores de IgG2a, IgM e IgA. A única ativação observada ocorreu para o isotipo IgG2a (aumento de 1,7 vezes)...
The Yops proteins form a protein family secreted by Yersinia spp that includes intracellular effectors (six effectors had been identified: YopE , YopH, YopM, YpkA/YopO, YopJ/YopP and YopT) and some components of the secretion-translocation apparatus that are released by the bacteria under Ca2+ quelation. The Yops effectors have been related to a series of virulence properties, including resistance to phagocytosis, citotoxicity and desfosforilation of host proteins. However, the interaction of the Yersinia Yops with the host specific immune response is not well defined. The objective of this study was to investigate the immunomodulatory role of the Yops secreted by strains of Yersinia pseudotuberculosis on the production of antibodies and autoantibodies by splenic B lymphocytes. To this end, mice were infected with wild-type Y. pseudotuberculosis (YpIII) or with mutant strains, unable to secrete specific Yops (YopH, YopE, YopM, YpkA and YopJ). Spleen cells were obtained, and the cells secreting nonspecific and specific immunoglobulins (anti-Yersinia and anti-Yops) was quantified by the ELISPOT technique. The presence of anti-Yersinia and anti- .Yops. specific antibodies in infected mice serum was investigated by ELISA and the presence of autoantibodies by DOT-BLOT assay. It was not observed neither difference between the number of nonspecific Igs-secreting cells of the animals infected with YpIIIpIB102 (wt) in relation to the controls. The strain YpIII pIB522, although defective in YopE secretion, provoked a reduction in the B lymphocytes secreting IgG2a, IgM and IgA. The unique activation observed was that of IgG2a isotype (an increase of 1.7-fold) on the 7th day post infection. The YopH- strain, YpIII pIB29, provoked an increase in the number of IgG1-, IgG2a- and IgG3- secreting cells (between 1.4 to 2.4-fold), on the 7th and 14th days post infection... (Complete abstract, click electronic address below)
The Yops proteins form a protein family secreted by Yersinia spp that includes intracellular effectors (six effectors had been identified: YopE , YopH, YopM, YpkA/YopO, YopJ/YopP and YopT) and some components of the secretion-translocation apparatus that are released by the bacteria under Ca2+ quelation. The Yops effectors have been related to a series of virulence properties, including resistance to phagocytosis, citotoxicity and desfosforilation of host proteins. However, the interaction of the Yersinia Yops with the host specific immune response is not well defined. The objective of this study was to investigate the immunomodulatory role of the Yops secreted by strains of Yersinia pseudotuberculosis on the production of antibodies and autoantibodies by splenic B lymphocytes. To this end, mice were infected with wild-type Y. pseudotuberculosis (YpIII) or with mutant strains, unable to secrete specific Yops (YopH, YopE, YopM, YpkA and YopJ). Spleen cells were obtained, and the cells secreting nonspecific and specific immunoglobulins (anti-Yersinia and anti-Yops) was quantified by the ELISPOT technique. The presence of anti-Yersinia and anti- .Yops. specific antibodies in infected mice serum was investigated by ELISA and the presence of autoantibodies by DOT-BLOT assay. It was not observed neither difference between the number of nonspecific Igs-secreting cells of the animals infected with YpIIIpIB102 (wt) in relation to the controls. The strain YpIII pIB522, although defective in YopE secretion, provoked a reduction in the B lymphocytes secreting IgG2a, IgM and IgA. The unique activation observed was that of IgG2a isotype (an increase of 1.7-fold) on the 7th day post infection. The YopH- strain, YpIII pIB29, provoked an increase in the number of IgG1-, IgG2a- and IgG3- secreting cells (between 1.4 to 2.4-fold), on the 7th and 14th days post infection... (Complete abstract, click electronic address below)
Descrição
Palavras-chave
Yersinia pseudotuberculosis - Teses, Linfocitos - Teses, Imunoglobulinas - Teses, Yops, B-Lymphocytes, Immunoglobulin
Como citar
MAIA, José Mário Lourenço. Influência das proteínas Yops de Yersinia pseudotuberculosis na resposta imune humoral murina. 2006. 57 f. Dissertação (mestrado) - Universidade Estadual Paulista, Faculdade de Ciências Farmacêuticas, 2006.