Leishmania amazonensis META2 protein confers protection against heat shock and oxidative stress
Tipo
Artigo
Data de publicação
2011
Periódico
Experimental Parasitology
Citações (Scopus)
11
Autores
Ramos C.S.
Yokoyama-Yasunaka J.K.U.
Guerra-Giraldez C.
Price H.P.
Mortara R.A.
Smith D.F.
Uliana S.R.B.
Yokoyama-Yasunaka J.K.U.
Guerra-Giraldez C.
Price H.P.
Mortara R.A.
Smith D.F.
Uliana S.R.B.
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Resumo
The META cluster of Leishmania amazonensis contains both META1 and META2 genes, which are upregulated in metacyclic promastigotes and encode proteins containing the META domain. Previous studies defined META2 as a 48.0-kDa protein, which is conserved in other Leishmania species and in Trypanosoma brucei. In this work, we demonstrate that META2 protein expression is regulated during the Leishmania life cycle but constitutive in T. brucei. META2 protein is present in the cytoplasm and flagellum of L. amazonensis promastigotes. Leishmania META2-null replacement mutants are more sensitive to oxidative stress and, upon heat shock, assume rounded morphology with shortened flagella. The increased susceptibility of null parasites to heat shock is reversed by extra-chromosomal expression of the META2 gene. Defective Leishmania promastigotes exhibit decreased ability to survive in macrophages. By contrast, META2 expression is decreased by 80% in RNAi-induced T. brucei bloodstream forms with no measurable effect on survival or resistance to heat shock. © 2010 Elsevier Inc.