Antileishmanial effect of mevastatin is due to interference with sterol metabolism

• Published in: Parasitology research (1987) 2015-10, Vol.114 (10), p.3873-3883
• Main Authors: Dinesh, Neeradi, Soumya, Neelagiri, Singh, Sushma
• Format: Article
• Language: English
• Subjects: Acyl Coenzyme A - chemistry; Acyl Coenzyme A - genetics; Acyl Coenzyme A - metabolism; Biomedical and Life Sciences; Biomedicine; Cell Line; Dosage and administration; Enzyme Inhibitors - chemistry; Enzyme Inhibitors - pharmacology; Health aspects; Host-parasite relationships; Identification and classification; Immunology; Kinetics; Leishmania donovani - chemistry; Leishmania donovani - drug effects; Leishmania donovani - enzymology; Leishmania donovani - metabolism; Leishmaniasis; Leishmaniasis, Visceral - parasitology; Lovastatin - analogs & derivatives; Lovastatin - chemistry; Lovastatin - pharmacology; Medical Microbiology; Metabolism; Microbiology; Original Paper; Prevention; Protozoan Proteins - chemistry; Protozoan Proteins - genetics; Protozoan Proteins - metabolism; Statins; Sterols; Sterols - metabolism
• ISSN: 0932-0113; 1432-1955
• DOI: 10.1007/s00436-015-4618-5

Visceral leishmaniasis (VL) is one of the most severe forms of leishmaniasis which is fatal if left untreated. Sterol biosynthetic pathway in Leishmania is currently being explored for its therapeutic potential. In the present study, we have evaluated the antileishmanial efficacy of mevastatin, a known inhibitor of 3-hydroxy-3-methyl glutaryl-CoA reductase (HMGR) enzyme. Mevastatin inhibited Leishmania donovani promastigotes and intracellular amastigotes with an 50 % inhibitory concentration (IC 50 ) value of 23.8 ± 4.2 and 7.5 ± 1.1 μM, respectively, without exhibiting toxicity towards host cell line. Mevastatin also inhibited recombinant L. donovani HMGR ( Ld HMGR) enzyme activity with an IC 50 value of 42.2 ± 3.0 μM. Kinetic analysis revealed that the inhibition of recombinant Ld HMGR activity by mevastatin was competitive with HMG-CoA. Mevastatin-treated parasites exhibited 66 % reduction in ergosterol levels with respect to untreated parasites. Incubation of mevastatin-treated L. donovani promastigotes with ergosterol resulted in revival of cell growth, whereas cholesterol supplementation failed to cause reversal in cell death. To further prove the specificity of mevastatin for HMGR enzyme, HMGR-overexpressing parasites were used which showed almost threefold resistance to mevastatin. It also induced morphological changes in the parasite accompanied by lipid body accumulation. Hence, antileishmanial effect of mevastatin was due to the inhibition of HMGR, which eventually leads to reduction in ergosterol levels and hence parasite death. The present study may have implications in the treatment of visceral form of leishmaniasis.