Metabolic adaptations of Leishmania donovani in relation to differentiation, drug resistance, and drug pressure

被引:42
作者
Berg, Maya [1 ]
Vanaerschot, Manu [1 ]
Jankevics, Andris [2 ,3 ,7 ]
Cuypers, Bart [1 ]
Maes, Ilse [1 ]
Mukherjee, Sandip [4 ]
Khanal, Basudha [5 ]
Rijal, Suman [5 ]
Roy, Syamal [4 ]
Opperdoes, Fred [6 ]
Breitling, Rainer [2 ,3 ,7 ]
Dujardin, Jean-Claude [1 ,8 ]
机构
[1] Inst Trop Med, Unit Mol Parasitol, Dept Biomed Sci, B-2000 Antwerp, Belgium
[2] Univ Glasgow, Coll Med Vet & Life Sci, Inst Mol Cell & Syst Biol, Glasgow, Lanark, Scotland
[3] Univ Groningen, Groningen Bioinformat Ctr, Groningen Biomol Sci & Biotechnol Inst, Groningen, Netherlands
[4] Indian Inst Chem Biol, Kolkata, India
[5] BP Koirala Inst Hlth Sci, Dharan, Nepal
[6] Catholic Univ Louvain, Trop Dis Res Unit, de Duve Inst, B-1200 Brussels, Belgium
[7] Univ Manchester, Manchester Inst Biotechnol, Fac Life Sci, Manchester, Lancs, England
[8] Univ Antwerp, Dept Biomed Sci, B-2020 Antwerp, Belgium
关键词
PENTOSE-PHOSPHATE PATHWAY; POPULATION-STRUCTURE; GENE-EXPRESSION; PURINE SALVAGE; CHROMATOGRAPHY; MECHANISMS; REVEALS;
D O I
10.1111/mmi.12374
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
Antimonial (sodium stibogluconate, SSG) resistance and differentiation have been shown to be closely linked in Leishmania donovani, with SSG-resistant strains showing an increased capacity to generate infectious (metacyclic) forms. This is the first untargeted LC-MS metabolomics study which integrated both phenomena in one experimental design and provided insights into metabolic differences between three clinical L.donovani strains with a similar genetic background but different SSG-susceptibilities. We performed this analysis at different stages during promastigote growth and in the absence or presence of drug pressure. When comparing SSG-resistant and SSG-sensitive strains, a number of metabolic changes appeared to be constitutively present in all growth stages, pointing towards a clear link with SSG-resistance, whereas most metabolic changes were only detected in the stationary stage. These changes reflect the close intertwinement between SSG-resistance and an increased metacyclogenesis in resistant parasites. The metabolic changes suggest that SSG-resistant parasites have (i) an increased capacity for protection against oxidative stress; (ii) a higher fluidity of the plasma membrane; and (iii) a metabolic survival kit to better endure infection. These changes were even more pronounced in a resistant strain kept under Sb-III drug pressure.
引用
收藏
页码:428 / 442
页数:15
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