Pomares Christelle, Marty Pierre, Bañuls Anne Laure, Lemichez Emmanuel, Pratlong Francine, Faucher Benoît, Jeddi Fakhri, Moore Sandy, Michel Grégory, Aluru Srikanth, Piarroux Renaud, Hide Mallorie
INSERM, U1065, Centre Méditerranéen de Médecine Moléculaire, C3M, Toxines Microbiennes dans la Relation Hôte-Pathogènes, Nice, France.
Université de Nice Sophia Antipolis, Faculté de Médecine, Nice, France.
PLoS Negl Trop Dis. 2016 Jan 25;10(1):e0004303. doi: 10.1371/journal.pntd.0004303. eCollection 2016 Jan.
In the south of France, Leishmania infantum is responsible for numerous cases of canine leishmaniasis (CanL), sporadic cases of human visceral leishmaniasis (VL) and rare cases of cutaneous and muco-cutaneous leishmaniasis (CL and MCL, respectively). Several endemic areas have been clearly identified in the south of France including the Pyrénées-Orientales, Cévennes (CE), Provence (P), Alpes-Maritimes (AM) and Corsica (CO). Within these endemic areas, the two cities of Nice (AM) and Marseille (P), which are located 150 km apart, and their surroundings, concentrate the greatest number of French autochthonous leishmaniasis cases. In this study, 270 L. infantum isolates from an extended time period (1978-2011) from four endemic areas, AM, P, CE and CO, were assessed using Multi-Locus Microsatellite Typing (MLMT). MLMT revealed a total of 121 different genotypes with 91 unique genotypes and 30 repeated genotypes. Substantial genetic diversity was found with a strong genetic differentiation between the Leishmania populations from AM and P. However, exchanges were observed between these two endemic areas in which it seems that strains spread from AM to P. The genetic differentiations in these areas suggest strong epidemiological structuring. A model-based analysis using STRUCTURE revealed two main populations: population A (consisting of samples primarily from the P and AM endemic areas with MON-1 and non-MON-1 strains) and population B consisting of only MON-1 strains essentially from the AM endemic area. For four patients, we observed several isolates from different biological samples which provided insight into disease relapse and re-infection. These findings shed light on the transmission dynamics of parasites in humans. However, further data are required to confirm this hypothesis based on a limited sample set. This study represents the most extensive population analysis of L. infantum strains using MLMT conducted in France.
在法国南部,婴儿利什曼原虫导致了大量犬类利什曼病(CanL)病例、散发性人类内脏利什曼病(VL)病例以及罕见的皮肤和黏膜皮肤利什曼病(分别为CL和MCL)病例。法国南部已明确确定了几个流行地区,包括东比利牛斯省、塞文山脉(CE)、普罗旺斯(P)、滨海阿尔卑斯省(AM)和科西嘉岛(CO)。在这些流行地区内,相距150公里的尼斯市(AM)和马赛市(P)及其周边地区集中了法国本土利什曼病病例的最大数量。在本研究中,使用多位点微卫星分型(MLMT)对来自四个流行地区(AM、P、CE和CO)的270株婴儿利什曼原虫分离株进行了评估,这些分离株来自较长时间段(1978 - 2011年)。MLMT共揭示了121种不同的基因型,其中91种为独特基因型,30种为重复基因型。发现了大量的遗传多样性,来自AM和P的利什曼原虫种群之间存在强烈的遗传分化。然而,在这两个流行地区之间观察到了基因交流,似乎菌株从AM传播到了P。这些地区的遗传分化表明存在强烈的流行病学结构。使用STRUCTURE进行的基于模型的分析揭示了两个主要种群:种群A(主要由来自P和AM流行地区的样本组成,包括MON - 1和非MON - 1菌株)和种群B,仅由基本上来自AM流行地区的MON - 1菌株组成。对于四名患者,我们观察到来自不同生物样本的多个分离株,这为疾病复发和再次感染提供了见解。这些发现揭示了寄生虫在人类中的传播动态。然而,基于有限的样本集,需要进一步的数据来证实这一假设。本研究是法国使用MLMT对婴儿利什曼原虫菌株进行的最广泛的种群分析。
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