蝰科蛇类感染哺乳动物相关锥虫和一种自由生活的克氏锥虫。

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES
Wesley Arruda Gimenes Nantes , Sany Caroline Liberal , Filipe Martins Santos , Maria Augusta Dario , Lincoln Takashi Hota Mukoyama , Katrine Berres Woidella , Paula Helena Santa Rita , André Luiz Rodrigues Roque , Carina Elisei de Oliveira , Heitor Miraglia Herrera , Ana Maria Jansen
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引用次数: 0

摘要

锥虫在寄生于不同类群方面取得了巨大的进化成功,但爬行动物相对而言仍未被探索。利用先进的分子工具发现,脊椎动物宿主中的锥虫种类越来越丰富。本研究旨在鉴定 2000 年至 2022 年期间人工饲养的 Bothrops moojeni 和 Crotalus durissus 所感染的锥虫种类。研究人员采集了 106 条蛇的血液样本:其中,73 条为杜氏蝮蛇,33 条为莫氏蝮蛇。采集全血进行血液培养、血液涂片和离心,以获得血凝块,提取其 DNA 并提交巢式 PCR(18S rDNA 基因)以检测锥虫。对阳性样本进行量化,并提交给传统(桑格)和新一代测序(NGS)。仅对 C. durissus 的一个个体进行了 PCR 扩增产物的克隆。为了排除本地病媒传播的可能性,我们尝试使用 6 个 CDC-LT 型灯光诱捕器捕捉沙蝇。分子诊断结果显示,34%的蛇携带锥虫 DNA,其中 47.94% 为 C. durissus,3.9% 为 B. moojeni。克隆过程中产生的四个菌落被鉴定为一种新的 MOTU,命名为 Trypanosomatidae sp.CROT。克隆过程中产生的四个菌落被鉴定为新的 MOTU,命名为 Trypanosomatidae sp.)和一种自由生活的奇异变形虫(Neobodo sp.),并通过系统发育分析得到证实。单倍型网络将 T. cascavelli 序列分为两组:1)有袋类动物和蛇类;2)有袋类动物独有。因此,Kinetoplastea 的多样性仍被低估。蛇类有能力维持感染 T. cruzi 和 L. infantum 长达 20 年的时间,而在 C. durissus 的血液中发现 Neobodo sp.的 DNA 表明该属可以感染脊椎动物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Viperidae snakes infected by mammalian-associated trypanosomatids and a free-living kinetoplastid

Viperidae snakes infected by mammalian-associated trypanosomatids and a free-living kinetoplastid

Trypanosomatids have achieved significant evolutionary success in parasitizing various groups, yet reptiles remain relatively unexplored. The utilization of advanced molecular tools has revealed an increased richness of trypanosomatids in vertebrate hosts. The aim of this study was to identify the trypanosomatid species infecting Bothrops moojeni and Crotalus durissus kept in captivity from 2000 to 2022. Blood samples were obtained from 106 snakes: 73C. durissus and 33 B. moojeni. Whole blood was collected for hemoculture, blood smears and centrifugated to obtain the blood clot that had its DNA extracted and submitted to Nested PCR (18S rDNA gene) to detect Trypanosomatidae. Positive samples were quantified and submitted to both conventional (Sanger) and next generation sequencing (NGS). Cloning of the amplified PCR product was performed for only one individual of C. durissus. To exclude the possibility of local vector transmission, attempts to capture sandflies were conducted using six CDC-LT type light traps. Molecular diagnosis revealed that 34% of the snakes presented trypanosomatid DNA, 47.94% in C. durissus and 3.9% in B. moojeni. The cloning process generated four colonies identified as a new MOTU named Trypanosomatidae sp. CROT. The presence of DNA of five trypanosomatids (Trypanosoma cruzi TcII/VI, Trypanosoma sp. DID, Trypanosoma cascavelli, Trypanosomatidae sp. CROT, Leishmania infantum and Leishmania sp.) and one free-living kinetoplastid (Neobodo sp.) was revealed through NGS and confirmed by phylogenetic analysis. The haplotypic network divided the T. cascavelli sequences into two groups, 1) marsupials and snakes and 2) exclusive to marsupials. Therefore, the diversity of Kinetoplastea is still underestimated. Snakes have the ability to maintain infection with T. cruzi and L. infantum for up to 20 years and the DNA finding of Neobodo sp. in the blood of a C. durissus suggests that this genus can infect vertebrates.

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来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
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