Fungal Metabolites and Leishmaniasis: A Review

Nighat Fatima *

Department of Pharmacy, COMSATS Institute of Information Technology, Abbottabad, Pakistan.

Syed Aun Muhammad

Institute of Molecular Biology and Biotechnology, Bahauddin Zakariya University, Multan, Pakistan.

Amara Mumtaz

Department of Chemistry, COMSATS Institute of Information Technology, Abbottabad, Pakistan.

Hina Tariq

Department of Pharmacy, COMSATS Institute of Information Technology, Abbottabad, Pakistan.

Irum Shahzadi

Department of Environmental Sciences, COMSATS Institute of Information Technology, Abbottabad, Pakistan.

Muhammad Soaib Said

Department of Pharmacy, COMSATS Institute of Information Technology, Abbottabad, Pakistan.

Muhammad Dawood

Department of Pharmacy, COMSATS Institute of Information Technology, Abbottabad, Pakistan.

*Author to whom correspondence should be addressed.


Abstract

Among the most neglected tropical diseases in the world, one is leishmaniasis, which is caused by parasites that belongs to protozoans of the genus Leishmania. Leishmaniasis can be controlled profoundly by using chemotherapeutic agents which includes pentavalent antimonials, paromomycin, pentamidine, amphotericin B and miltefosine, as it depends greatly on it. The only oral drug used with high cure rate is miltefosine used for the treatment of visceral leishmaniasis but its observed susceptibility decrease in countries like India where it is extensively used. Hence, the development of novel antileishmanial agents with good potency and better therapeutic profile is very necessary. Here we review diverse classes of secondary metabolites, focusing on anti-parasitic compounds, biosynthesized by fungi.

Keywords: Leishmaniasis, fungi, secondary metabolites, drug leads


How to Cite

Fatima, N., Muhammad, S. A., Mumtaz, A., Tariq, H., Shahzadi, I., Soaib Said, M. and Dawood, M. (2016) “Fungal Metabolites and Leishmaniasis: A Review”, Journal of Pharmaceutical Research International, 12(2), pp. 1–12. doi: 10.9734/BJPR/2016/26094.