TY - JOUR
T1 - Toxoplasma gondii is capable of exogenous folate transport
T2 - A likely expansion of the BT1 family of transmembrane proteins
AU - Massimine, Kristen M.
AU - Doan, Lanxuan T.
AU - Atreya, Chloé A.
AU - Stedman, Timothy T.
AU - Anderson, Karen S.
AU - Joiner, Keith A.
AU - Coppens, Isabelle
N1 - Funding Information:
Apicomplexan homologs to Leishmania tarentolae FT5 ( AAM77209 ) and L. major BT1 ( AAF64060 ) were identified through BLAST analysis. Preliminary Toxoplasma genomic and/or cDNA sequence data was accessed via http://ToxoDB.org and/or http://www.tigr.org/tdb/t_gondii/ . Genomic data were provided by The Institute for Genomic Research, and by the Sanger Center (Wellcome Trust). Cryptosporidium data was found in GenBank™ ( EAL37224 and CAD98492 for Cryptosporidium hominus and Cryptosporidium parvum , respectively). Plasmodium sp. data was accessed via http://PlasmoDB.org [19] . Once ORFs were identified in the various Apicomplexan genomes, the BT1 regions of these putative genes were identified within the conserved domain database ( http://www.ncbi.nlm.nih.gov/Structure/cdd/wrpsb.cgi ). Sequences were edited to exclude non-BT1 areas and the remaining BT1 regions were aligned and shaded with BioEdit software. Percent identity was calculated by DNAstar software.
Funding Information:
Preliminary genomic and/or cDNA sequence data was accessed via http://ToxoDB.org and/or http://www.tigr.org/tdb/t_gondii/ . Genomic data were provided by The Institute for Genomic Research (supported by the NIH grant #AI05093), and by the Sanger Center (Wellcome Trust). EST sequences were generated by Washington University (NIH grant #1R01AI045806-01A1).
Funding Information:
This work was supported by an American Heart Association Grant (0230079) awarded to I.C., an NIH Grant to K.S.A. (AI 44630) and a RO1 entitled Mechanism Based Drug Selection and Design (AI46416) to K.A.J. K.M.M. was supported by a T32 GM07324 Institutional National Research Service to William Sessa and a T32 AI07404 Interdisciplinary Parasitology Training Grant. C.E.A. was supported by the NIH MSTP (GMO7205).
PY - 2005/11
Y1 - 2005/11
N2 - Folates are key elements in eukaryotic biosynthetic processes. The protozoan parasite Toxoplasma gondii possesses the enzymes necessary for de novo folate synthesis and has been suggested to lack alternative mechanisms for folate acquisition. In this paper, we present a different view by providing evidence that Toxoplasma is capable of salvaging exogenous folates. By monitoring uptake of radiolabeled folates by parasites in axenic conditions, our studies revealed a common folate transporter that has a high affinity for folic acid. Transport of this compound across the parasite plasma membrane is rapid, biphasic, temperature dependent, bi-directional, concentration dependent and specific. In addition, morphological evidence demonstrates that fluorescent methotrexate, a folate analog, is internalized by Toxoplasma and shows localization reminiscent to the mitochondrion. The presence of putative folate transporter genes in the Toxoplasma genome, which are homologous to the BT1 family of proteins, suggests that Toxoplasma may encode proteins involved in folate transport. Interestingly, genome analysis suggests that the BT1 family of proteins exists not only in Toxoplasma, but in other Apicomplexan parasites as well. Altogether, our results not only have implications for current therapeutic regimens against T. gondii, but they also allude that the folate transport mechanism may represent a novel Apicomplexan target for the development of new drugs.
AB - Folates are key elements in eukaryotic biosynthetic processes. The protozoan parasite Toxoplasma gondii possesses the enzymes necessary for de novo folate synthesis and has been suggested to lack alternative mechanisms for folate acquisition. In this paper, we present a different view by providing evidence that Toxoplasma is capable of salvaging exogenous folates. By monitoring uptake of radiolabeled folates by parasites in axenic conditions, our studies revealed a common folate transporter that has a high affinity for folic acid. Transport of this compound across the parasite plasma membrane is rapid, biphasic, temperature dependent, bi-directional, concentration dependent and specific. In addition, morphological evidence demonstrates that fluorescent methotrexate, a folate analog, is internalized by Toxoplasma and shows localization reminiscent to the mitochondrion. The presence of putative folate transporter genes in the Toxoplasma genome, which are homologous to the BT1 family of proteins, suggests that Toxoplasma may encode proteins involved in folate transport. Interestingly, genome analysis suggests that the BT1 family of proteins exists not only in Toxoplasma, but in other Apicomplexan parasites as well. Altogether, our results not only have implications for current therapeutic regimens against T. gondii, but they also allude that the folate transport mechanism may represent a novel Apicomplexan target for the development of new drugs.
KW - Apicomplexa
KW - BT1
KW - Folate metabolism
KW - Folic acid
KW - Intracellular parasitism
KW - Membrane transporter
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UR - http://www.scopus.com/inward/citedby.url?scp=25844443569&partnerID=8YFLogxK
U2 - 10.1016/j.molbiopara.2005.07.006
DO - 10.1016/j.molbiopara.2005.07.006
M3 - Article
C2 - 16159678
AN - SCOPUS:25844443569
SN - 0166-6851
VL - 144
SP - 44
EP - 54
JO - Molecular and Biochemical Parasitology
JF - Molecular and Biochemical Parasitology
IS - 1
ER -