Laboratoire de Parasitologie-Mycologie à la Faculté de Pharmacie, 99-UR/08-05 Monastir, Tunisia.
Int J Parasitol. 2009 Jun;39(7):801-11. doi: 10.1016/j.ijpara.2008.11.016. Epub 2009 Jan 12.
Twenty-seven strains of Leishmania infantum from north and central Tunisia belonging to the three main MON zymodemes (the MON-typing system is based on multilocus enzyme electrophoresis (MLEE) of 15 enzymes) found in this country (MON-1, MON-24 and MON-80) and representing different pathologies (visceral, cutaneous and canine leishmaniasis) have been studied to understand the genetic polymorphism within this species. Intraspecific variation could be detected in L. infantum by the use of 14 hypervariable microsatellite markers. In addition to microsatellite repeat length variation, a high degree of allelic heterozygosity has been observed among the strains investigated, suggestive of sexual recombination within L. infantum groups. The two major clusters found by using Bayesian statistics as well as distance analysis are consistent with the classification based on isoenzymes, dividing Tunisian L. infantum into MON-1 and MON-24/MON-80. Moreover, the existence of hybrid strains between the MON-1 and the non-MON-1 populations has been shown and verified by analysis of clones of one of these strains. Substructure analysis discriminated four groups of L. infantum. The major MON-1 cluster split into two groups, one comprising only Tunisian strains and the second both Tunisian and European strains. The major MON-24 cluster was subdivided into two groups with geographical and clinical feature correlations: a dermotropic group of strains mainly from the north, and a viscerotropic group of strains from the centre of Tunisia. The four viscerotropic hybrid strains all originated from central Tunisia and were typed by MLEE as MON-24 or MON-80. To our knowledge, this is the first report describing relationships between clinical picture and population substructure of L. infantum MON-24 based on genotype data, as well as the existence of hybrids between zymodemes MON-1 and MON-24/MON-80, and proving one of these hybrid strains by molecular analysis of the parent strain and its clones.
从突尼斯北部和中部的 27 株利什曼原虫婴儿株属于该国的三种主要 MON 生物型(MON 分型系统基于 15 种酶的多位点酶电泳(MLEE))(MON-1、MON-24 和 MON-80),并代表不同的病理学(内脏、皮肤和犬利什曼病),已经研究了这种物种的遗传多态性。通过使用 14 种高变微卫星标记,可以检测到利什曼原虫婴儿株内的种内变异。除了微卫星重复长度的变化外,在所研究的菌株中观察到了高度的等位基因杂合性,表明利什曼原虫群体内存在性重组。使用贝叶斯统计和距离分析发现的两个主要聚类与基于同工酶的分类一致,将突尼斯利什曼原虫婴儿株分为 MON-1 和 MON-24/MON-80。此外,通过对其中一株的克隆分析,表明并验证了 MON-1 和非 MON-1 种群之间存在杂交株。亚结构分析区分了利什曼原虫婴儿株的四个群体。主要的 MON-1 聚类分为两组,一组仅包括突尼斯株,另一组包括突尼斯和欧洲株。主要的 MON-24 聚类分为两组,具有地理和临床特征相关性:一组主要来自北部的亲表皮株,另一组主要来自突尼斯中部的亲内脏株。四个亲内脏的杂交株均来自突尼斯中部,通过 MLEE 分型为 MON-24 或 MON-80。据我们所知,这是首次根据基因型数据描述利什曼原虫婴儿株 MON-24 的临床图片与种群亚结构之间的关系,以及 MON-1 和 MON-24/MON-80 生物型之间杂交株的存在,并通过对亲本菌株及其克隆的分子分析证明了其中一个杂交株的存在。
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