Quantitative proteomic analysis of amastigotes from <i>Leishmania (L</i>.<i>) amazonensis</i> LV79 and PH8 strains reveals molecular traits associated with the virulence phenotype

<div><p>Background</p><p>Leishmaniasis is an antropozoonosis caused by <i>Leishmania</i> parasites that affects around 12 million people in 98 different countries. The disease has different clinical forms, which depend mainly on the parasite genetics and on the immunologic status of the host. The promastigote form of the parasite is transmitted by an infected female phlebotomine sand fly, is internalized by phagocytic cells, mainly macrophages, and converts into amastigotes which replicate inside these cells. Macrophages are important cells of the immune system, capable of efficiently killing intracellular pathogens. However, <i>Leishmania</i> can evade these mechanisms due to expression of virulence factors. Different strains of the same <i>Leishmania</i> species may have different infectivity and metastatic phenotypes <i>in vivo</i>, and <i>w</i>e have previously shown that analysis of amastigote proteome can give important information on parasite infectivity. Differential abundance of virulence factors probably accounts for the higher virulence of PH8 strain parasites shown in this work. In order to test this hypothesis, we have quantitatively compared the proteomes of PH8 and LV79 lesion-derived amastigotes using a label-free proteomic approach.</p><p>Methodology/Principal findings</p><p>In the present work, we have compared lesion development by <i>L</i>. <i>(L</i>.<i>) amazonensis</i> PH8 and LV79 strains in mice, showing that they have different virulence <i>in vivo</i>. Viability and numbers of lesion-derived amastigotes were accordingly significantly different. Proteome profiles can discriminate parasites from the two strains and several proteins were differentially expressed.</p><p>Conclusions/Significance</p><p>This work shows that PH8 strain is more virulent in mice, and that lesion-derived parasites from this strain are more viable and more infective <i>in vitro</i>. Amastigote proteome comparison identified GP63 as highly expressed in PH8 strain, and Superoxide Dismutase, Tryparedoxin Peroxidase and Heat Shock Protein 70 as more abundant in LV79 strain. The expression profile of all proteins and of the differential ones precisely classified PH8 and LV79 samples, indicating that the two strains have proteins with different abundances and that proteome profiles correlate with their phenotypes.</p>