Interaction of human complement factor H variants Tyr(402) and His(402) with Leptospira spp.

Autor(es)

Silva, Aldacilene Souza ^[1] ; Castiblanco Valencia, Monica Marcela ^[1] ; Cianciarullo, Aurora Marques ^[2] ; Vasconcellos, Silvio Arruda ^[3] ; Barbosa, Angela Silva ^[4] ; Isaac, Lourdes ^[1]

Afiliação do(s) autor(es)

^[1] Univ Sao Paulo, Inst Ciencias Biomed, Dept Imunol, BR-05508900 Sao Paulo - Brazil

^[2] Inst Butantan, Lab Genet, Sao Paulo - Brazil

^[3] Univ Sao Paulo, Fac Med Vet & Zootecnia, BR-05508900 Sao Paulo - Brazil

^[4] Inst Butantan, Lab Bacteriol, Sao Paulo - Brazil

• Tipo de documento: Artigo Científico
• Fonte: FRONTIERS IN IMMUNOLOGY; v. 2, 2011.
• Citações Web of Science: 0

Resumo

Leptospirosis is a zoonosis caused by pathogenic bacteria from the genus Leptospira. The disease represents a serious public health problem in underdeveloped tropical countries. Leptospires infect hosts through small abrasions in the skin or mucous membranes and they rapidly disseminate to target organs. The capacity of some pathogenic leptospiral strains to acquire the negative complement regulators factor H (FH) and C4b binding protein correlates with their ability to survive in human serum. In this study we assessed the functional consequences of the age macular degeneration-associated polymorphism FH His(402) or FH Tyr(402) on FH Leptospira interactions. In binding assays using sub-saturating amounts of FH, the FH Tyr(402) variant interacted with all the strains tested more strongly than the FH His(402) variant. At higher concentrations, differences tended to disappear. We then compared cofactor activities displayed by FH His(402) and FHTyr(402) bound to the surface of L. mterrogans. Both variants exhibit similar activity as cofactors for Factor I-mediated cleavage of C3b, thus indicating that they do not differ in their capacity to regulate the complement cascade. (AU)

• Processo FAPESP: 10/50043-0 - Sistema complemento e patogenicidade de leptospiras: mecanismos de ativação e escape identificação de ligantes bacterianos, caracterização de proteases e estabelecimento de modelo murino in vivo
• Beneficiário: Lourdes Isaac
• Modalidade de apoio: Auxílio à Pesquisa - Temático
• Processo FAPESP: 09/05979-0 - Resposta inflamatória e expressão gênica dependente do componente C5 em lesão hepática de camundongo
• Beneficiário: Lourdes Isaac
• Modalidade de apoio: Auxílio à Pesquisa - Regular