Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.1/7217
Título: Shikimate and folate pathways in the protozoan parasite, Perkinsus olseni
Autor: Elandalloussi, L. M.
Rodrigues, P. M.
Afonso, R.
Leite, R. B.
Nunes, Patrícia A.
Cancela, Leonor
Data: 2005
Editora: Elsevier
Resumo: We have exploited the experimental accessibility of the protozoan parasite Perkinsus olseni and its simitarities to apicomplexan parasites to investigate the influence of specific drugs on its proliferation. For this purpose, shikiniate and folate pathways present in attractive target for parasitic therapy given their major differences with mammalian pathways. Glyphosate a potent inhibitor of the shikiniate pathway enzyme EPSP synthase inhibited the in vitro proliferation of P. olseni in adose-dependent manner and this effect was reversed by addition of chorismate, indicating the presence of a shikimate pathway. However. this effect was not antagonised by p-aminoben/oate or folic acid. Furthermore, antagonism was observed, via pyrimethamine to glyphosate inhibitory effect. suggesting that the shikimate pathway is not essential for the biosynthesis of folate precursors and is therefore crucial for another pathway downstream from chorismate, In addition, sulfadiazine, a well known inhibitor of dihydropteorate synthase, an enzyme of the folate biosynthetic pathway, had no inhibitory effect on P. olseni proliferation. In view of these results, the parasite does not appear to require the folate biosynthesis pathway for its survival and is most likely able to use exogenous folate. Even though pyrimethamine was found to inhibit P. atlantieus growth. this inhibitory effect could not be reversed co-addition of folic acid. Therefore we prpose that the effect of pyrimethamine observed in this study results from the inhibation of a target by other than n observed in this study results from the inhibation of a target been shown co-addition of folic acid. Therefore, we propose that the effect of other than dillydrofolate reductase. Similarly, proguanil target is likely to be separate from DHFR since only its metabolite cycloguanil has been shown to have inhibitory properties on DHFR. (c) 2005 Elsevier B.V. All rights reserved.
Peer review: yes
URI: http://hdl.handle.net/10400.1/7217
DOI: https://dx.doi.org/10.1016/j.molbiopara.2005.03.014
ISSN: 0166-6851
Aparece nas colecções:ISE2-Artigos (em revistas ou actas indexadas)



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