Division of Medical Zoology, Department of Infection and Immunity, Jichi Medical University, Tochigi, Japan.
Sección de Entomología, Instituto de Medicina Tropical "Daniel A. Carrión" y Departamento Académico de Microbiología Médica, Facultad de Medicina Humana, Universidad Nacional Mayor de San Marcos, Lima, Peru.
Front Cell Infect Microbiol. 2021 Feb 24;11:625001. doi: 10.3389/fcimb.2021.625001. eCollection 2021.
Approximately 20 species are known to cause cutaneous, mucocutaneous, and visceral disorders in humans. Identification of the causative species in infected individuals is important for appropriate treatment and a favorable prognosis because infecting species are known to be the major determinant of clinical manifestations and may affect treatments for leishmaniasis. Although species have been conventionally identified by multilocus enzyme electrophoresis, genetic analysis targeting kinetoplast and nuclear DNA (kDNA and nDNA, respectively) is now widely used for this purpose. Recently, we conducted countrywide epidemiological studies of leishmaniasis in Ecuador and Peru to reveal prevalent species using PCR-RFLP targeting nDNA, and identified unknown hybrid parasites in these countries together with species reported previously. Furthermore, comparative analyses of kDNA and nDNA revealed the distribution of parasites with mismatches between these genes, representing the first report of mito-nuclear discordance in protozoa. The prevalence of an unexpectedly high rate (~10%) of genetically complex strains including hybrid strains, in conjunction with the observation of mito-nuclear discordance, suggests that genetic exchange may occur more frequently than previously thought in natural populations. Hybrid strains resulting from genetic exchanges are suggested to cause more severe clinical symptoms when compared with parental strains, and to have increased transmissibility by vectors of the parental parasite species. Therefore, it is important to clarify how such genetic exchange influences disease progression and transmissibility by sand flies in nature. In addition, our aim was to identify where and how the genetic exchange resulting in the formation of hybrid and mito-nuclear discordance occurs.
已知约有 20 种物种可引起人类皮肤、黏膜和内脏疾病。鉴定感染个体中的致病物种对于适当的治疗和良好的预后很重要,因为已知感染物种是临床症状的主要决定因素,并且可能影响利什曼病的治疗。尽管传统上通过多基因酶电泳鉴定物种,但现在广泛使用针对动质体和核 DNA(分别为 kDNA 和 nDNA)的遗传分析来进行鉴定。最近,我们在厄瓜多尔和秘鲁进行了全国范围的利什曼病流行病学研究,使用针对 nDNA 的 PCR-RFLP 鉴定了流行物种,并在这些国家发现了以前未报告的未知杂交寄生虫。此外,对 kDNA 和 nDNA 的比较分析揭示了与这些基因不匹配的寄生虫的分布,这是原生动物中线粒体与核 DNA 不一致的首次报道。遗传复杂株(包括杂交株)的高流行率(约 10%)令人惊讶,加上线粒体与核 DNA 不一致的观察结果表明,在自然种群中,基因交换可能比以前认为的更为频繁。遗传交换产生的杂交菌株与亲本菌株相比,可能导致更严重的临床症状,并且与亲本寄生虫物种的媒介的传染性增加。因此,阐明这种基因交换如何影响疾病的进展以及沙蝇在自然界中的传播性非常重要。此外,我们的目的是确定导致形成杂交和线粒体与核 DNA 不一致的基因交换发生的地点和方式。