Identification of Sodium-Ion–Dependent Neurotransmitter Transporters among Protozoa Parasite Genomes: Structure, Function and Prospects for Drug Discovery
Author Correspondence author
Genomics and Applied Biology, 2015, Vol. 6, No. 5 doi: 10.5376/gab.2015.06.0005
Received: 30 Mar., 2015 Accepted: 22 May, 2015 Published: 01 Jun., 2015
Falade and Otarigho, Identification of Sodium-Ion–Dependent Neurotransmitter Transporters among Protozoa Parasite Genomes: Structure, Function and Prospects for Drug Discovery, Genomics and Applied Biology, Vol.6, No.5, 1-11 (doi: 10.5376/gab.2015.06.0005)
Insect-transmitted pathogenic protozoa cause widespread and debilitating diseases in man and his domestic livestock. Malaria, leishmaniasis and trypanosomiasis cause significant morbidity and mortality. A few members of the group, e.g. Toxoplasma gondii, are also important in disease of immunocompromised individuals. There are no vaccines against these diseases and most of the available drug treatments are toxic and/or ineffective making drug development a priority. The genomes of many of these protozoan parasites have recently been sequenced, allowing rational design of targeted therapies. Sodium-ion-dependent neurotransmitter transporters play important roles in the physiology of many organisms including protozoan parasites making them ideal candidates as therapeutic targets. In the present study, the analysis of 25 genera of eukaryotic pathogen genomes is described. We show the existence within their genomes of genes encoding putative homologues of sodium-ion-dependent neurotransmitter transporters. Excluding T. gondii, we discovered that all protozoan parasites we examined lack genes that encode for sodium-ion-dependent neurotransmitter transporters. Therefore T. gondii sodium-ion-dependent neurotransmitter transporter homologues may represent a parasite specific novel target for drug discovery. Furthermore, sequence alignment and evolutionary differences between humans and T. gondii may allow pathogen-specific targeting of the transporter homologues identified.
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. Mofolusho O. Falade
. Benson Otarigho
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