Transport of inorganic phosphate in Leishmania infantum and compensatory regulation at low inorganic phosphate concentration

Biochimica et Biophysica Acta - General Subjects

Volumn 1830, Issue 3, 2013, Pages 2683-2689

  Russo Abrahao T ^a   Alves Bezerra, M ^a,b   Majerowicz, D ^a,b   Freitas Mesquita, A L ^a   Dick, C F ^a   Gondim, K C ^a,b   Meyer Fernandes, J R ^a  

^a FEDERAL UNIVERSITY OF RIO DE JANEIRO   (Brazil)

^b Instituto Nacional de Ciencia e Tecnologia em Entomologia Molecular   (Brazil)

Author keywords

Leishmania infantum; Pi starvation; Pi transporter

Indexed keywords

8 BENZYLOXY 2 METHYLIMIDAZO[1,2 A]PYRIDINE 3 ACETONITRILE; BAFILOMYCIN A1; CARBONYL CYANIDE 4 (TRIFLUOROMETHOXY)PHENYLHYDRAZONE; CARRIER PROTEIN; HYDROGEN PHOSPHATE COTRANSPORTER; IONOPHORE; NIGERICIN; PHOSPHATE; POTASSIUM ION; PROTON; RNA; SODIUM PHOSPHATE COTRANSPORTER; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; ENVIRONMENTAL FACTOR; GENE EXPRESSION REGULATION; GENE SEQUENCE; GENOME ANALYSIS; INHIBITION KINETICS; LEISHMANIA INFANTUM; MICHAELIS MENTEN KINETICS; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; PHOSPHATE TRANSPORT; PRIORITY JOURNAL; REGULATORY MECHANISM; SACCHAROMYCES CEREVISIAE; TRANSCRIPTION REGULATION; TRANSPORT KINETICS;

AMINO ACID SEQUENCE; BIOLOGICAL TRANSPORT; CARBONYL CYANIDE P-TRIFLUOROMETHOXYPHENYLHYDRAZONE; CULTURE MEDIA; ENZYME INHIBITORS; GENE EXPRESSION REGULATION; IMIDAZOLES; KINETICS; LEISHMANIA INFANTUM; MACROLIDES; MOLECULAR SEQUENCE DATA; NIGERICIN; PHOSPHATES; PHOSPHORUS RADIOISOTOPES; PHYLOGENY; PROTON IONOPHORES; PROTON-PHOSPHATE SYMPORTERS; PROTOZOAN PROTEINS; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SODIUM-PHOSPHATE COTRANSPORTER PROTEINS; SODIUM-POTASSIUM-EXCHANGING ATPASE; VACUOLAR PROTON-TRANSLOCATING ATPASES;

EID: 84873581452     PISSN: 03044165     EISSN: 18728006     Source Type: Journal    
DOI: 10.1016/j.bbagen.2012.11.017     Document Type: Article

References (45)

1. I.A. Rodrigues, B.A. Da-Silva, A.L.S. Santos, A.B. Vermelho, C.S. Alviano, and P.M. Dutra A new experimental culture medium for cultivation of Leishmania amazonensis: its efficacy for the continuous in vitro growth and differentiation of infective promastigote forms Parasitol. Res. 106 2010 1249 1252
2. K.S. Calabrese, V.M.C.L. Cortada, M.E.C. Dorval, M.A.A. Souza Lima, E.T. Oshiro, C.S.F. Souza, and M. Silva-Almeida Leishmania (Leishmania) infantum/chagasi: histopathological aspects of the skin in naturally infected dogs in two endemic areas Exp. Parasitol. 124 2010 253 257
3. A.H. Lopes, T. Souto-Padrón, F.A. Dias, M.T. Gomes, G.C. Rodrigues, and L.T. Zimmermann Trypanosomatids: odd organisms, devastating diseases Open Parasitol. J. 4 2010 30 59
4. S.M. Gossage, M.E. Rogers, and P.A. Bates Two separate growth phases during the development of Leishmania in sand flies: implications for understanding the life cycle Int. J. Parasitol. 33 2003 1027 1034
5. D.P. Vieira, R. Paletta-Silva, E.M. Saraiva, A.H. Lopes, and J.R. Meyer-Fernandes Leishmania chagasi: an ecto-3′-nucleotidase activity modulated by inorganic phosphate and its possible involvement in parasite-macrophage interaction Exp. Parasitol. 127 3 2011 702 707
6. D.M. Dwyer, and M. Gottlieb Surface membrane localization of 3′- and 5′-nucleotidase activities in Leishmania donovani promastigotes Mol. Biochem. Parasitol. 10 1984 139 150
7. A. Debrabant, M. Gottlieb, and D.M. Dwyer Isolation and characterization of the gene encoding the surface membrane 3′-nucleotidase/nuclease of Leishmania donovani Mol. Biochem. Parasitol. 71 1995 199551 199563
8. R. Paletta-Silva, D.P. Vieira, R. Vieira-Bernardo, D. Majerowicz, K.C. Gondim, M.A. Vannier-Santos, A.H. Lopes, and J.R. Meyer-Fernandes Leishmania amazonensis: characterization of an ecto-3′-nucleotidase activity and its possible role in virulence Exp. Parasitol. 129 2011 277 283
9. R. Paletta-Silva, R. Vieira-Bernardo, D. Cosentino-Gomes, and J.R. Meyer-Fernandes Leishmania amazonensis: inhibition of 3′-nucleotidase activity by Cu2 + ions Exp. Parasitol. 131 1 2012 63 68
10. B.L. Persson, J. Petersson, U. Fristedt, R. Weinander, A. Berhe, and J. Pattison Phosphate permeases of Saccharomyces cerevisiae: structure, function and regulation Biochim. Biophys. Acta 1422 3 1999 255 272
11. Y. Tasaki, Y. Kamiya, A. Azwan, T. Hara, and T. Joh Gene expression during Pi deficiency in Pholiota nameko: accumulation of mRNAs for two transporters Biosci. Biotechnol. Biochem. 66 2002 790 800
12. M.G. Lamarche, B.L. Wanner, S. Crépin, and J. Harel The phosphate regulon and bacterial virulence: a regulatory network connecting phosphate homeostasis and pathogenesis FEMS Microbiol. Rev. 32 3 2008 461 473
13. Y. Tamai, A. Toh-e, and Y. Oshima Regulation of inorganic phosphate transport systems in Saccharomyces cerevisiae J. Bacteriol. 164 1985 964 968
14. P.F. De Gouvêa, F.M. Soriani, I. Malavazi, M. Savoldi, M.H. Goldman, and O. Loss Functional characterization of the Aspergillus fumigatus PHO80 homologue Fungal Genet. Biol. 45 2008 1135 1146
15. R.M. Harris, D.C. Webb, S.M. Howitt, and G.B. Cox Characterization of PitA and PitB from Escherichia coli J. Bacteriol. 183 2001 5008 5014
16. K.J. Saliba, R.E. Martin, A. Bröer, R.I. Henry, C.S. McCarthy, and M.J. Downie Sodium-dependent uptake of inorganic phosphate by the intracellular malaria parasite Nature 443 2006 582 585
17. C.F. Dick, A.L.A. Dos-Santos, D. Majerowicz, K.C. Gondim, C. Caruso-Neves, I.V. Silva, A. Vieyra, and J.R. Meyer-Fernandes Na(+)-dependent and Na(+)-independent mechanisms for inorganic phosphate uptake in Trypanosoma rangeli Biochem. Biophys. Acta 1820 7 2012 1001 1008
18. C. Auesukaree, T. Homma, H. Tochio, M. Shirakawa, Y. Kaneko, and S. Harashima Intracellular phosphate serves as a signal for the regulation of the PHO pathway in Saccharomyces cerevisiae J. Biol. Chem. 279 2004 17289 17294
19. B.L. Persson, A. Berhe, U. Fristedt, P. Martinez, J. Pattison, J. Petersson, and R. Weinander Phosphate permeases of Saccharomyces cerevisiae Biochim. Biophys. Acta 1365 1-2 1998 23 30 (Review)
20. +-coupled phosphate transporter in Saccharomyces cerevisiae Mol. Gen. Genet. 258 1998 628 638
21. C. Auesukaree, T. Homma, Y. Kaneko, and S. Harashima Transcriptional regulation of phosphate-responsive genes in low-affinity phosphate-transporter- defective mutants in Saccharomyces cerevisiae Biochem. Biophys. Res. Commun. 306 4 2003 843 850
22. F. Lundh, J.M. Mouillon, D. Samyn, K. Stadler, Y. Popova, and J.O. Lagerstedt Molecular mechanisms controlling phosphate-induced downregulation of the yeast Pho84 phosphate transporter Biochemistry 48 2009 4497 4505
23. Y. Oshima The phosphatase system in Saccharomyces cerevisiae Genes Genet. Syst. 72 1997 323 334
24. H.P. De Koning, C.J. Watson, L. Sutcliffe, and S.M. Jarvis Differential regulation of nucleoside and nucleobase transporters in Crithidia fasciculate and Trypanosoma brucei brucei Mol. Biochem. Parasitol. 106 2000 93 107
25. 2 + release from acidocalcisomes of Trypanosoma brucei Biochem. J. 315 1996 265 270
26. N.R. Chintagari, A. Mishra, L. Su, Y. Wang, S. Ayalew, S.D. Hartson, and L. Liu Vacuolar ATPase regulates surfactant secretion in rat alveolar type II cells by modulating lamellar body calcium PLoS One 5 2 2010 1 14
27. +-ATPase regulates intracellular pH in Leishmania mexicana amazonensis Mol. Biochem. Parasitol. 119 2002 225 236
28. L.F. Kneipp, M.L. Rodrigues, C. Holandino, F.F. Esteves, T. Souto-Padrón, and C.S. Alviano Ectophosphatase activity in conidial forms of Fonsecaea pedrosoi is modulated by exogenous phosphate and influences fungal adhesion to mammalian cells Microbiology 150 10 2004 3355 3362
29. S.A. Gomes, A.L. Fonseca-de-Souza, B.A. Silva, T. Kiffer-Moreira, J.R. Santos-Mallet, A.L. Santos, and J.R. Meyer-Fernandes Trypanosoma rangeli: differential expression of cell surface polypeptides and ecto-phosphatase activity in short and long epimastigote forms Exp. Parasitol. 112 4 2006 253 262
30. S.F. Altschul, T.L. Madden, A.A. Schäffer, J. Zhang, Z. Zhang, W. Miller, and D.J. Lipman Gapped BLAST and PSI-BLAST: a new generation of protein database search programs Nucleic Acids Res. 25 1997 3389 3402
31. E. Birney, M. Clamp, and R. Durbin GeneWise and Genomewise Genome Res. 14 5 2004 988 995
32. S. Brunak, J. Engelbrecht, and S. Knudsen Prediction of human mRNA donor and acceptor sites from the DNA sequence J. Mol. Biol. 220 1991 49 65
33. S.M. Hebsgaard, P.G. Korning, N. Tolstrup, J. Engelbrecht, P. Rouzé, and S. Brunak Splice site prediction in Arabidopsis thaliana pre-mRNA by combining local and global sequence information Nucleic Acids Res. 24 1996 3439 3452
34. M.G. Reese Application of a time-delay neural network to promoter annotation in the Drosophila melanogaster genome Comput. Chem. 26 2001 51 56
35. A. Krogh, B. Larsson, G. von Heijne, and E.L. Sonnhammer Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes J. Mol. Biol. 305 2001 567 580
36. K. Tamura, J. Dudley, M. Nei, and S. Kumar MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0 Mol. Biol. Evol. 24 2007 1596 1599
37. S. Rozen, and H. Skaletsky Primer3 on the WWW for general users and for biologist programmers Methods Mol. Biol. 132 2000 365 386
38. M. Brenndörfer, and M. Boshart Selection of reference genes for mRNA quantification in Trypanosoma brucei Mol. Biochem. Parasitol. 172 2010 52 55
39. X. Huang, and A. Madan CAP3: a DNA sequence assembly program Genome Res. 9 1999 68 877
40. O. Norgard, J.T. Kvaloy, R.K. Farmen, and R. Heikkila Error propagation in relative real-time reverse transcription polymerase chain reaction quantification models: the balance between accuracy and precision Anal. Biochem. 356 2006 182 193
41. M.J. Burns, G.J. Nixon, C.A. Foy, and N. Harris Standardisation of data from realtime quantitative PCR methods - evaluation of outliers and comparison of calibration curves BMC Biotechnol. 5 2005 31
42. C.F. Dick, A.L.A. Dos-Santos, A.L. Fonseca-de-Souza, J. Rocha-Ferreira, and J.R. Meyer-Fernandes Trypanosoma rangeli: differential expression of ecto-phosphatase activities in response to inorganic phosphate starvation Exp. Parasitol. 124 2010 386 393
43. R.A. Zvyagilskaya, F. Lundh, D. Samyn, J. Pattison-Granberg, J.M. Mouillon, and Y. Popova Characterization of the Pho89 phosphate transporter by functional hyperexpression in Saccharomyces cerevisiae FEMS Yeast Res. 8 2008 685 696
44. S. Jiang, S.A. Anderson, C.D. Winget, and A.J. Mukkada Plasma membrane K +/H +-ATPase from Leishmania donovani J. Cell. Physiol. 159 1994 60 66
45. M. Bun-Ya, M. Nishimura, S. Harashima, and Y. Oshima The PHO84 gene of Saccharomyces cerevisiae encodes an inorganic phosphate transporter Mol. Cell. Biol. 11 6 1991 3229 3238