Schistosoma mansoni: Evaluation of an RNAi-based treatment targeting HGPRTase gene


Autoria(s): Pereira, T. C.; Pascoal, V. D. B.; Marchesini, R. B.; Maia, Ivan de Godoy; Magalhaes, L. A.; Zanotti-Magalhaes, E. M.; Lopes-Cendes, I.
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/04/2008

Resumo

Hypoxanthine-guanine phosphoribosyltransferase (HGPRTase) is an essential gene of the parasite Schistosoma mansoni and it is well conserved in its hosts (mouse and human) at the protein but not at the RNA level. This feature prompted us to assess RNA interference (RNAi) to combat schistosomiasis. Small interfering RNAs (siRNAs) were Produced against HGPRTase, injected in infected mice and the number of worms was counted six days after injection. The total number of parasites was reduced by approximately 27% after treatment. RT-PCR analyzes showed a significant reduction in parasite target mRNA but not in host's homologue. The use of low doses of molecules did not oversaturate si- or miRNA pathways as mice survival rates were not affected by siRNAs. This is the first successful in vivo demonstration of a RNAi-based treatment against schistosomiasis. We believe that improvements in molecule delivery and an increase on siRNA dose could rapidly eliminate parasite. (c) 2007 Elsevier B.V. All rights reserved.

Formato

619-623

Identificador

http://dx.doi.org/10.1016/j.exppara.2007.11.017

Experimental Parasitology. San Diego: Academic Press Inc. Elsevier B.V., v. 118, n. 4, p. 619-623, 2008.

0014-4894

http://hdl.handle.net/11449/17977

10.1016/j.exppara.2007.11.017

WOS:000254885000026

Idioma(s)

eng

Publicador

Academic Press Inc. Elsevier B.V.

Relação

Experimental Parasitology

Direitos

closedAccess

Palavras-Chave #Schistosoma mansoni #Trematode #hypoxanthine-guanine #phosphoribosyltransferase
Tipo

info:eu-repo/semantics/article