NUTRITIONAL-REQUIREMENTS OF WILD-TYPE AND FOLATE TRANSPORT-DEFICIENT LEISHMANIA-DONOVANI FOR PTERINS AND FOLATES

被引:41
作者
BECK, JT [1 ]
ULLMAN, B [1 ]
机构
[1] OREGON HLTH SCI UNIV,DEPT BIOCHEM & MOLEC BIOL,PORTLAND,OR 97201
关键词
Folate; Genetics; Leishmania; Mutant; Pterin; Transport;
D O I
10.1016/0166-6851(90)90147-E
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The nutritional requirements for folates and pterins were assessed for two strains of Leishmania donovani promastigotes, a wild-type (D1700) parental strain and a mutant derivative (MTXA5) which possesses a markedly diminished capacity to transport both [3H]folate and [3H]methotrexate (MTX) [14]. Both L. donovani strains have an absolute growth requirement for an exogenous pterin, since their proliferation could not be sustained in completely defined medium lacking either a pterin or a folate. Supplementation of the growth medium by many of a spectrum of folates and pterins could support growth of the wild-type cell line. Surprisingly, however, the MTXA5 strain could not thrive in folate-deficient medium fortified with any of the pterins that promoted wild-type cell division, including biopterin and neopterin. The relationship between the incapacity of MTXA5 cells to transport folate and methotrexate and their inability to multiply in folate-deficient medium supplemented with pterins was evaluated using genetic approaches. First, an independently generated MTX-resistant mutant, MTXB4, was isolated in 1 mM MTX. The phenotype of the MTXB4 cells was like that of MTXA5 cells since they were unable to transport [3H]MTX and [3H]folate or grow in folate-deficient medium supplemented with pterins. Second, three revertants of the MTXA5 cells were selected for their ability to grow in 1 μM biopterin. All three revertants had regained [3H]folate and [3H]MTX transport capability concomitant with growth sensitivity to methotrexate toxicity. These observations provide genetic evidence that the competence of L. donovani to transport [3H]folate and [3H]MTX and the capability of the organisms to utilize pterins as a nutritional factor are influenced by a common genetic locus. © 1990.
引用
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页码:221 / 230
页数:10
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  • [1] Amand, Sulphonamides: Structure-activity relationships and mechanism of action, Handbook of Experimental Pharmacology, 64, pp. 25-54, (1983)
  • [2] Rollo, Inhibitors of dihydrofolate reductase as antiprotozoal agents, Handbook of Experimental Pharmacology, 64, pp. 293-308, (1983)
  • [3] Scholer, Leiner, Richie, Sulphonamides and sulphones, Handbook of Experimental Pharmacology, 68, pp. 123-206, (1984)
  • [4] Ferone, Dihydrofolate reductase inhibitors, Handbook of Experimental Pharmacology, 68, pp. 207-221, (1984)
  • [5] Campbell, Rew, Chemotherapy of Parasitic Diseases, (1986)
  • [6] David, Feuerman, Cutaneous leishmaniasis treated with trimethoprim-sulfamethoxazole, Harefuah, 92, pp. 305-307, (1977)
  • [7] Kandil, Treatment of cutaneous leishmaniasis with trimethoprim-sulfamethoxazole combination, Dermatologica, 146, pp. 303-309, (1973)
  • [8] Murphy, Bong, Co-trimoxazole for systemic leishmaniasis, Lancet, 1, pp. 323-324, (1981)
  • [9] Mattock, Peters, The experimental chemotherapy of leishmaniasis, II. The activity in tissue culture of some antiparasitic and anti-microbial compounds in clinical use, 69, pp. 359-371, (1975)
  • [10] El-On, Jacobs, Witztum, Greenblatt, Development of topical treatment for cutaneous leishmaniasis caused by Leishmania major in experimental animals, Antimicrob. Agents Chemother., 26, pp. 745-751, (1984)