Evolutionary genomics of epidemic visceral leishmaniasis in the Indian subcontinent

H. Imamura, T. Downing, F. Van den Broeck, M. J. Sanders, S. Rijal, S. Sundar, A. Mannaert, M. Vanaerschot, M. Berg, G. de Muylder, F. Dumetz, B. Cuypers, I. Maes, M. Domagalska, S. Decuypere, K. Rai, S. Uranw, N. R. Bhattarai, B. Khanal, V. K. Prajapati, S. Sharma, O. Stark, G. Schönian, H. P. De Koning, L. Settimo, B. Vanhollebeke, S. Roy, B. Ostyn, M. Boelaert, L. Maes, M. Berriman, J.-C. Dujardin,, James Cotton
March 2016
PDF Cite Project DOI publisher Hideo Imamura Jean-Claude Dujardin

Abstract

Leishmania donovani causes visceral leishmaniasis (VL), the second most deadly vector-borne parasitic disease. A recent epidemic in the Indian subcontinent (ISC) caused up to 80% of global VL and over 30,000 deaths per year. Resistance against antimonial drugs has probably been a contributing factor in the persistence of this epidemic. Here we use whole genome sequences from 204 clinical isolates to track the evolution and epidemiology of L. donovani from the ISC. We identify independent radiations that have emerged since a bottleneck coincident with 1960s DDT spraying campaigns. A genetically distinct population frequently resistant to antimonials has a two base-pair insertion in the aquaglyceroporin gene LdAQP1 that prevents the transport of trivalent antimonials. We find evidence of genetic exchange between ISC populations, and show that the mutation in LdAQP1 has spread by recombination. Our results reveal the complexity of L. donovani evolution in the ISC in response to drug treatment.

Type
Journal article
Publication
In Elife 5
James Cotton
James Cotton
Professor

My research interests are in the genomics, and particularly population genomics of parasites, particularly those that cause neglected tropical diseases