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Instituto de Parasitología y Biomedicina
"López - Neyra"
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[ Staff | Summary of Research | Funding Agencies | Publications | Doctoral Theses | Patents | Teaching]



ABC GENES IN PROTOZOAN PARASITES

 

SUMMARY OF RESEARCH


 

ABC GENES IN PROTOZOAN PARASITES

 

Our group is included at the Department of Biochemistry and Molecular Pharmacology, Instituto de Parasitología "Lopez-Neyra", Spanish Research Council. The group has experience in the area of Biology and Molecular and Cellular Pharmacology of the protozoan parasites of the family Trypanosomatidae, specifically Trypanosoma cruzi and Leishmania.









 

Mechanisms of drug resistance in parasites. Search for drug resistance markers.

 

Presently, we are focusing on the study of miltefosine(hexadecylphosphocholine) (MIL) resistance, the first oral drug active visceral leishmaniasis. We have found that miltefosine resistant parasites are deficient in the inward-directed translocation across the plasma membrane of both MIL and glycerophospholipids, independently of their polar head group, in a process that is protein, energy and temperature dependent, without modification of drug metabolism or endocytic activity. Recently, we have described in Leishmania donovani that resistance to MIL and other phospholipid derivatives can be mediated through a mutation in the MIL transporter (LdMT), a new member of the P-type ATPase aminophospholipid translocase subfamily expressed at the plasma membrane. LdMT mediates the translocation of MIL and glycerophospholipids in Leishmania. Transfection experiments demonstrated that LdMT was able to rescue inward translocation and thus to increase uptake of MIL in resistant parasites. The absence of deletions or rearrangements at the LdMT locus in resistant parasites and the presence of similar expression levels in both mutant and wild-type lines suggested the presence of stable mutations of the gene in the MIL resistant parasites. PCR-based approach identified single but different point mutations in both alleles that are able to inactivate LdMT function. Similarly, in Leishmania resistant lines obtained by mutagenesis, we observed not only a similar phenotype but also a similar genetic basis for the acquisition of resistance: inactivating point mutations within LdMT. Also, we have found that the sensitivity to MIL in Leishmania was directly related with the level of expression of LdMT. We have obtained double knock-out for LdMT and these experiments support that LdMT is essential for the uptake and potency of MIL in L. donovani. Also, the intracellular forms of the parasite obtained from the above mutants, shows similar resistance level to MIL. Thus, these results suggest that the generation of MIL-resistant clinical isolates bearing specific mutations in LdMT is likely to occur. Our results represent the first description of one phospholipid transporter in parasites, whose biological role was related with the maintenance of lipid asymmetry at the plasma membrane. We have established a direct correlation between the sensitivity of these Leishmania species and their drug accumulation profile. Interestingly, L. braziliensis, refractory to the activity of the drug, is unable to accumulate MIL compared with other Leishmania species, indicating that MIL will be only useful in geographical areas where sensitive species are prevalent. We continue with the functional characterization of LdMT and its involvement in phospholipid trafficking. We are interested to know the minimal complex for the functionality of this transporter; if it is required another accessory protein for the transport and activity of LdMT. Considering that aminophospholipid translocase subfamily in Leishmania include 4 different transporters, we will continue with the functional characterization of other members of this subfamily. Considering the increasing problem of drug resistance in Leishmania, we shall explore possible molecular mechanisms of resistance to different leishmanicidal drugs, among others: alkyl-lysophospholipids (miltefosine), sitamaquine and paramomycin, using pharmacoproteomic analysis. This study will give us knowledge of drug resistance markers that could be used in clinical samples with therapeutic failure. All this information will be used to drug design that will be crucial for the control of Leishmaniasis which incidence represents a World Health problem in addition to have a great impact in the economy of the populations affected.









 

Functional characterization of ABC (ATP-binding cassette) transporters.

 

The ABC superfamily of transporters is thought to be one of the largest protein families present throughout evolution. They transport a range of structurally unrelated compounds using ATP hydrolysis as their energy source. These transporters are composed of two transmembrane domains and two nucleotide binding domains that contain the conserved Walker A and Walker B motifs as well as the ABC signature. This superfamily include 7 different subfamilies: ABCA, ABCB, ABCC, ABCD, ABCE, ABCF y ABCG; these subfamilies are divided into half-transporters, which contain one ATPase domain and one transmembrane domain (ABCD and ABCG subfamilies, and some members of the ABCB subfamily) and full transporters which contain paired modules in tandem (ABCA, ABCB and ABCC subfamilies). The ABCE and ABCF subfamilies contain proteins, which have ATP-binding domains that are clearly derived from others ABC transporters, but have no transmembrane domain and are not know to be involved in any membrane transport functions. In last years, we have been characterizing the functionality of some of these subfamilies in the protozoan parasites Leishmania and Trypanosoma cruzi. Thus, the Leishmania Pgp-MDR1 transporter (included in the ABCB subfamily) is responsible of a multidrug resistant phenotype to different structurally and functionality unrelated drugs. Additionally, this transporter is able to translocate different glycerophospholipids, whose function could be related with a floppase activity energy-dependent, consequently conferring resistance to different phospholipid analogues such as alkyl-lysophospholipids. Similarly, we have characterized the ABCA subfamily in Leishmania and T. cruzi; this subfamily appears to be involved in lipid movements across the plasma membrane of the parasite since overexpression reduces the accumulation of fluorescent phospholipid analogues. Also, this activity may influence the vesicular trafficking, since secreted acid phosphatase (SAP) activity was significantly lower in parasites overexpressing this transporter, as well as the infectivity of parasites. Recently, we are interested in the functional characterization of the half transporters included in the subfamily ABCG in the parasites Leishmania and Trypanosoma brucei. The ABCG or White subfamily of transporters is the latest drug efflux ABC transporters discovered. Among the subfamily, ABCG2 is a well-know efflux ABC transporter identified by different approaches, receiving different and equivalent names such as placenta-specific ABC (ABCP), a breast cancer resistance protein (BCRP) and a mitoxantrone resistance associated protein (MXR). The members of this subfamily have the ATPase catalytic domain located N-terminal to the transmembrane domain. It is generally accepted that ABC half-transporters function as homo- or heterodimers. The members of this subfamily ABCG2 has been shown to be amplified and overexpressed in human cancer cells resistance to different hydrophobic drugs such as mitoxantrone, topotecan,daunorubicin, doxorubicin, methotrexate, camptothecins, flavopiridol, among others. In Leishmania, the ABCG subfamily includes at least 4 different transporters; the overexpression of ABCG15 and ABCG36 in Leishmania confers resistance to hydrophobic drugs such as miltefosine, edelfosine and perifosine. As described in mammalian cells, ABCG transporters function as floppases, able to translocate fluorescent phospholipid analogues. We continue with the characterization of ABCG transporters and its involvement on lipid trafficking and their influence in the biology of the protozoan parasites Leishmania and Trypanosoma brucei.









 

Reversal agents of drug resístance phenotype mediated by ABC transporters in Leishmania and tumoral cells.

 

During last years, we have been interested on the search of new natural compounds able to modulate the activity of ABC transporters both in Leishmania parasites and cancer cells overexpressing the P-glycoprotein MDR1. Among the active compounds identified in plant extracts of the Celastraceae family are sesquiterpenes, which constitute a wide family of natural compounds with a considerable range of bioactive properties and with potential clinical application as MDR reversal agents in cancer cells and in the protozoan parasite Leishmania. We have characterized a total of 58 and 79 different dihydro-beta-agarofuran sesquiterpenes as reversal agents of Leishmania and cancer MDR phenotype, respectively. The results have allowed us to identify the most potent sesquiterpenes and to assess the specific interaction with the P-glycoprotein. Similar experiments using MRP (ABCC) and BCRP (ABCG)-expressing cells showed that sesquiterpenes do not modify the activities of these ABC transporters. Direct molecular interaction of active sesquiterpenes with plasma membranes from cells overexpressing P-glycoprotein and purified protein, and photoaffinity labelling confirm that sesquiterpenes interact with transmembrane domains of P-glycoprotein. Moreover, the identification of P-glycoprotein as the cellular target of sesquiterpenes and the knowledge about their molecular mechanism of action has stimulated us to start the studies directed to a computer-assisted quantitative-structrural activity relationship model (QSAR) that will allow the rational design of new reversal agents more potents and less toxics. Moreover, we continue the characterization of the mechanism of action of sesquiterpenes in Leishmania and mammalian cells such as: influence on protein expression levels, activity on cytochrome P450, and induction of apoptosis on MDR overexpressing cells. Additionally, we have started the search for reversal natural compounds specific for ABCC (MRP) and ABCG (BCRP) transporters of Leishmania and cancer cells.









 


FUNDING AGENCIES LAST 5 YEARS

- ABORDAJE MEDIANTE TECNICAS OMICAS DE LA MODULACION DE LAS CELULAS HOSPEDADORAS POR LEISHMANIA SU IMPLICACION EN LA SENSIBILIDAD A FARMACOS.. PROYECTO, PN2018 - Proyectos I+D+i «Retos Investigación», Ref: RTI-2018-097210-B-I00, (2019 - 2021).

 

 

PUBLICATIONS LAST 5 YEARS

-José Ignacio Manzan; Ana Perea-Martínez; Raquel García-Hernández; Eduardo Andrés-León; Laura C. Terrón-Camero; José Antonio Poveda; Francisco Gamarro, Modulation of cholesterol pathways in clinical isolates of Leishmania infantum-Infected Human Macrophages., Frontiers in cellular and infection microbiology, 2022, Vol. 12: 878711-878711, ARTÍCULO, Id:887851

-Perea-Martínez, Ana; García-Hernández, Raquel; Manzano, Jose Ignacio; Gamarro, Francisco, Transcriptomic analysis in human macrophages infected with therapeutic failure clinical isolates of Leishmania infantum, ACS Infectious Diseases, 2022, Vol. 8: 800-810, ARTÍCULO, Id:887570

-Raquel García-Hernández; José Ignacio Manzano; Ana Perea-Martínez; Francisco Gamarro, New insights on drug resistant clinical isolates of Leishmania infantum-infected human macrophages as determined by comparative transcriptome analyses, OMICS A Journal of Integrative Biology, 2022, Vol. 26: 165-177, ARTÍCULO, Id:887569

-Sánchez-Fernández, E.M.; García-Hernández, R.; Gamarro, F.; Arroba, A.I.; Aguilar-Diosdado, M.; Padrón, J.M.; García Fernández, J.M.; Mellet, C.O., Synthesis of sp2-Iminosugar Selenoglycolipids as Multitarget Drug Candidates with Antiproliferative, Leishmanicidal and Anti-Inflammatory Properties, Molecules, 2021, Vol. 26: 24-7501, ARTÍCULO, Id:868221

-Klug, D.M.; Mavrogiannaki, E.M.; Forbes, K.C.; Silva, L.; Diaz-Gonzalez, R.; Pérez-Moreno, G.; Ceballos-Pérez, G.; Garcia-Hernández, R.; Bosch-Navarrete, C.; Cordón-Obras, C.; Gómez-Liñán, C.; Saura, A.; Momper, J.D.; Martinez-Martinez, M.S.; Manzano, P.; Syed, A.; El-Sakkary, N.; Caffrey, C.R.; Gamarro, F.; Ruiz-Perez, L.M.; Gonzalez Pacanowska, D.; Ferrins, L.; Navarro, M.; Pollastri, M.P., Lead Optimization of 3,5-Disubstituted-7-Azaindoles for the Treatment of Human African Trypanosomiasis, Journal of Medicinal Chemistry, 2021, Vol. 64: 9404-9430, ARTÍCULO, Id:852597

-Dana M. Klug; Rosario Diaz-Gonzalez; Travis J. DeLano; Eftychia M. Mavrogiannaki; Melissa J. Buske; Raeann M. Dalton; John K. Fisher; Katherine M. Schneider; Vivian Hilborne; Melanie G. Fritsche; , Quillon J. Simpson; Westley F. Tear; William G. Devine; Guiomar Pérez-Moreno; Gloria Ceballos-Pérez; Raquel García-Hernández; Cristina Bosch-Navarrete; Luis Miguel Ruiz-Pérez; Francisco Gamarro; Dolores González-Pacanowska; Maria Santos Martinez-Martinez; Pilar Manzano-Chinchon; Miguel Navarro; Michael P. Pollastri; Lori Ferrins., Structure-property studies of an imidazoquinoline chemotype with antitrypanosomal activity, RSC Medicinal Chemistry, 2020, Vol. 11: 950-959, ARTÍCULO, Id:840926

-Klug, D.M.; Tschiegg, L.; Diaz, R.; Rojas-Barros, D.; Perez-Moreno, G.; Ceballos, G.; García-Hernández, R.; Martinez-Martinez, M.S.; Manzano, P.; Ruiz, L.M.; Caffrey, C.R.; Gamarro, F.; Pacanowska, D.G.; Ferrins, L.; Navarro, M.; Pollastri, M.P., Hit-to-Lead Optimization of Benzoxazepinoindazoles As Human African Trypanosomiasis Therapeutics, Journal of Medicinal Chemistry, 2020, Vol. 63: 2527-2546, ARTÍCULO, Id:804253

-Tear WF; Bag S; Diaz-Gonzalez R; Ceballos-Pérez G; Rojas-Barros DI; Cordon-Obras C; Pérez-Moreno G; García-Hernández R; Martinez-Martinez MS; Ruiz-Perez LM; Gamarro F; Gonzalez Pacanowska D; Caffrey CR; Ferrins L; Manzano P; Navarro M; Pollastri MP, Selectivity and Physicochemical Optimization of Repurposed Pyrazolo[1,5-b]pyridazines for the Treatment of Human African Trypanosomiasis, Journal of Medicinal Chemistry, 2020, Vol. 63: 756-783, ARTÍCULO, Id:779338

-Manzano, J.I.; Cueto-Díaz, E.J.; Olías-Molero, A.I.; Perea, A.; Herraiz, T.; Torrado, J.J.; Alunda, J.M.; Gamarro, F.; Dardonville, C., Discovery and Pharmacological Studies of 4-Hydroxyphenyl-Derived Phosphonium Salts Active in a Mouse Model of Visceral Leishmaniasis, Journal of Medicinal Chemistry, 2019, Vol. 62: 10664-10675, ARTÍCULO, Id:781226

-Sánchez-Fernández, E.M.; García-Moreno, M.I.; Arroba, A.I.; Aguilar-Diosdado, M.; Padrón, J.M.; García-Hernández, R.; Gamarro, F.; Fustero, S.; Sánchez-Aparicio, J.E.; Masgrau, L.; García Fernández, J.M.; Ortiz Mellet, C., Synthesis of polyfluoroalkyl sp2-iminosugar glycolipids and evaluation of their immunomodulatory properties towards anti-tumor, anti-leishmanial and anti-inflammatory therapies, European Journal of Medicinal Chemistry, 2019, Vol. 182: 111604, ARTÍCULO, Id:770525

-Sánchez-Fernández, E.M.; Isabel García-Moreno, M.; García-Hernández, R.; Padrón, J.M.; García Fernández, J.M.; Gamarro, F.; Ortiz Mellet, C., Thiol-ene "click" synthesis and pharmacological evaluation of C-glycoside sp2-iminosugar glycolipids, Molecules, 2019, Vol. 24: 16-2882, ARTÍCULO, Id:770478

-Arsène, S.; Gómez-Pérez, V.; Escarcena, R.; Abengózar, M.Á.; García-Hernández, R.; Nácher-Vázquez, M.; San Feliciano, A.; Gamarro, F.; Rivas, L.; Olmo, E.d., Imidazo[2,1-a]isoindole scaffold as an uncharted structure active on Leishmania donovani, European Journal of Medicinal Chemistry, 2019, Vol. 182: 111568, ARTÍCULO, Id:770430

-Manzano, J.I.; Konstantinovi¿, J.; Scaccabarozzi, D.; Perea, A.; Pavi¿, A.; Cavicchini, L.; Basilico, N.; Gamarro, F.; ?olaja, B.A., 4-Aminoquinoline-based compounds as antileishmanial agents that inhibit the energy metabolism of Leishmania, European Journal of Medicinal Chemistry, 2019, Vol. 180: 28-40, ARTÍCULO, Id:767431

-Camacho, E.; González-de la Fuente, S.; Rastrojo, A.; Peiró-Pastor, R.; Solana, J.C.; Tabera, L.; Gamarro, F.; Carrasco-Ramiro, F.; Requena, J.M.; Aguado, B., Complete assembly of the Leishmania donovani (HU3 strain) genome and transcriptome annotation, Scientific Reports, 2019, Vol. 9: 1-6127, ARTÍCULO, Id:763038

-Klug DM; Diaz-Gonzalez R; Pérez-Moreno G; Ceballos-Pérez G; García-Hernández R; Gomez-Pérez V; Ruiz-Pérez LM; Rojas-Barros DI; Gamarro F; González-Pacanowska D; Martínez-Martínez MS; Manzano P; Ferrins L; Caffrey CR; Navarro M; Pollastri MP, Evaluation of a class of isatinoids identified from a high-throughput screen of human kinase inhibitors as anti-Sleeping Sickness agents, PLoS Neglected Tropical Diseases, 2019, Vol. 13: e00071292-e0007129, ARTÍCULO, Id:742826

-Perandrés-López, R.; Sánchez-Cañete, M.P.; Gamarro, F.; Castanys, S., Functional role of highly conserved residues of the N-terminal tail and first transmembrane segment of a P4-ATPase, Biochemical Journal, 2018, Vol. 475: 887-899, ARTÍCULO, Id:718909

-Perea, A.; Manzano, J.I.; Kimura, Y.; Ueda, K.; Castanys, S.; Gamarro, F., Leishmania LABCG2 transporter is involved in ATP-dependent transport of thiols, Biochemical Journal, 2018, Vol. 475: 87-97, ARTÍCULO, Id:718799

-Rastrojo, A.; García-Hernández, R.; Vargas, P.; Camacho, E.; Corvo, L.; Imamura, H.; Dujardin, J.C.; Castanys, S.; Aguado, B.; Gamarro, F.; Requena, J.M., Genomic and transcriptomic alterations in Leishmania donovani lines experimentally resistant to antileishmanial drugs, International Journal for Parasitology: Drugs and Drug Resistance, 2018, Vol. 8: 246-264, ARTÍCULO, Id:717071


 

 

DOCTORAL THESES LAST 5 YEARS

 

 

 


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