Miltefosine enhances the fitness of a non-virulent drug-resistantLeishmania infantumstrain
Author(s) -
Eline Eberhardt,
Dimitri Bulté,
Lieselotte Van Bockstal,
Magali Van den Kerkhof,
Paul Cos,
Peter Delputte,
Sarah Hendrickx,
Louis Maes,
Guy Caljon
Publication year - 2018
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dky450
Subject(s) - miltefosine , visceral leishmaniasis , biology , virulence , leishmaniasis , microbiology and biotechnology , in vivo , drug resistance , virology , infectivity , leishmania infantum , immunology , genetics , gene , virus
Miltefosine is currently the only oral drug for visceral leishmaniasis, and although deficiency in an aminophospholipid/miltefosine transporter (MT) is sufficient to elicit drug resistance, very few naturally miltefosine-resistant (MIL-R) strains have yet been isolated. This study aimed to make a detailed analysis of the impact of acquired miltefosine resistance and miltefosine treatment on in vivo infection.
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