Laboratório de Bioquímica de Tripanosomatídeos, Instituto Oswaldo Cruz/Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
Laboratório de Biologia Molecular e Doenças Endêmicas, Instituto Oswaldo Cruz/Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
PLoS One. 2020 Dec 3;15(12):e0230545. doi: 10.1371/journal.pone.0230545. eCollection 2020.
Leishmania infantum infantum (LII) is one of the species that causes visceral leishmaniasis (VL) in the Old World, while L. infantum chagasi (LIC) is present in the New World. Few studies address biological differences or the behavior of these strains during infection. These parasites live inside cells of their hosts, continuously evading microbicidal mechanisms and modulating the immune responses of these cells. One of the mechanisms used by these protozoa involves the L-arginine metabolism. Understanding the differences between Leishmania species and establishing an improved murine model for study of leishmaniasis are matters of extreme importance. Thereby, the objectives of this work were to analyze the biological and molecular differences between two Leishmania infantum strains (LII and LIC) and the degree of susceptibility to infection of mice with different genetic backgrounds. The infectivity in vivo and in vitro of LII and LIC strains was evaluated in BALB/c and Swiss Webster mice, as well the NOS and ARG activities. The LII strain was more infective than the LIC strain both in vivo and in vitro. In animals infected by the LII and LIC strains, differences in NOS and ARG activities occurred. In vitro, promastigotes of LII isolated from BALB/c and Swiss Webster mice showed higher ARG activity than LIC promastigotes during the growth curve. However, no difference was observed in intracellular NO production by promastigotes of these strains. The ARG gene sequences were compared, and those of both strains were identical. However, despite the similarity, the strains showed different expression levels of this gene. It can be concluded that although L. chagasi strains are considered identical to L. infantum strains from a molecular point of view, these strains have different biological behavior.
婴儿利什曼原虫(LII)是旧世界引起内脏利什曼病(VL)的物种之一,而新世界存在婴儿利什曼原虫查加斯(LIC)。很少有研究涉及这些菌株在感染过程中的生物学差异或行为。这些寄生虫生活在宿主细胞内,不断逃避杀菌机制并调节这些细胞的免疫反应。这些原生动物使用的机制之一涉及 L-精氨酸代谢。了解利什曼原虫物种之间的差异并建立改良的用于研究利什曼病的小鼠模型非常重要。因此,本工作的目的是分析两种婴儿利什曼原虫株(LII 和 LIC)之间的生物学和分子差异,以及不同遗传背景的小鼠对感染的易感性程度。在 BALB/c 和瑞士 Webster 小鼠中评估了 LII 和 LIC 株的体内和体外感染性,以及 NOS 和 ARG 活性。LII 株在体内和体外均比 LIC 株更具感染力。在感染 LII 和 LIC 株的动物中,NOS 和 ARG 活性存在差异。在体外,从 BALB/c 和瑞士 Webster 小鼠分离的 LII 前鞭毛体在生长曲线中表现出比 LIC 前鞭毛体更高的 ARG 活性。然而,这些菌株的内体 NO 产生没有差异。比较了 ARG 基因序列,两种菌株的序列完全相同。然而,尽管相似,这些菌株表现出该基因的不同表达水平。可以得出结论,尽管从分子角度来看,L. chagasi 株被认为与 L. infantum 株相同,但这些菌株具有不同的生物学行为。