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阐明克氏锥虫微环超变区类组成的多样性:在分型和 kDNA 遗传方面的新观点。

Elucidating diversity in the class composition of the minicircle hypervariable region of Trypanosoma cruzi: New perspectives on typing and kDNA inheritance.

机构信息

Unidad de Epidemiología Molecular (UEM), Instituto de Patología Experimental, Universidad Nacional de Salta-CONICET, Salta, Salta, Argentina.

Instituto de Biotecnología, Centro de Investigaciones en Ciencias Agronómicas y Veterinarias, Instituto Nacional de Tecnología Agropecuaria, Hurlingham, Buenos Aires, Argentina.

出版信息

PLoS Negl Trop Dis. 2019 Jun 27;13(6):e0007536. doi: 10.1371/journal.pntd.0007536. eCollection 2019 Jun.

Abstract

BACKGROUND

Trypanosoma cruzi, the protozoan causative of Chagas disease, is classified into six main Discrete Typing Units (DTUs): TcI-TcVI. This parasite has around 105 copies of the minicircle hypervariable region (mHVR) in their kinetoplastic DNA (kDNA). The genetic diversity of the mHVR is virtually unknown. However, cross-hybridization assays using mHVRs showed hybridization only between isolates belonging to the same genetic group. Nowadays there is no methodologic approach with a good sensibility, specificity and reproducibility for direct typing on biological samples. Due to its high copy number and apparently high diversity, mHVR becomes a good target for typing.

METHODOLOGY/PRINCIPAL FINDINGS: Around 22 million reads, obtained by amplicon sequencing of the mHVR, were analyzed for nine strains belonging to six T. cruzi DTUs. The number and diversity of mHVR clusters was variable among DTUs and even within a DTU. However, strains of the same DTU shared more mHVR clusters than strains of different DTUs and clustered together. In addition, hybrid DTUs (TcV and TcVI) shared similar percentages (1.9-3.4%) of mHVR clusters with their parentals (TcII and TcIII). Conversely, just 0.2% of clusters were shared between TcII and TcIII suggesting biparental inheritance of the kDNA in hybrids. Sequencing at low depth (20,000-40,000 reads) also revealed 95% of the mHVR clusters for each of the analyzed strains. Finally, the method revealed good correlation in cluster identity and abundance between different replications of the experiment (r = 0.999).

CONCLUSIONS/SIGNIFICANCE: Our work sheds light on the sequence diversity of mHVRs at intra and inter-DTU level. The mHVR amplicon sequencing workflow described here is a reproducible technique, that allows multiplexed analysis of hundreds of strains and results promissory for direct typing on biological samples in a future. In addition, such approach may help to gain knowledge on the mechanisms of the minicircle evolution and phylogenetic relationships among strains.

摘要

背景

克氏锥虫,引起恰加斯病的原生动物,被分为六个主要离散型单元(DTU):TcI-TcVI。这种寄生虫在其动质体 DNA(kDNA)中有大约 105 个小环超变区(mHVR)的拷贝。mHVR 的遗传多样性实际上是未知的。然而,使用 mHVR 的交叉杂交分析显示,只有属于同一遗传群的分离株之间发生杂交。目前,没有一种方法具有良好的敏感性、特异性和重现性,无法直接对生物样本进行分型。由于其高拷贝数和明显的多样性,mHVR 成为一个很好的分型靶标。

方法/主要发现:对属于六个 T. cruzi DTU 的九个菌株的 mHVR 扩增子测序,获得了约 2200 万条读长,进行了分析。DTU 之间以及同一 DTU 内的 mHVR 簇的数量和多样性是可变的。然而,同一 DTU 的菌株比不同 DTU 的菌株共享更多的 mHVR 簇,并聚集在一起。此外,杂种 DTU(TcV 和 TcVI)与亲本 DTU(TcII 和 TcIII)共享相似的 mHVR 簇比例(1.9-3.4%)。相反,TcII 和 TcIII 之间仅共享 0.2%的簇,这表明杂种中 kDNA 的双亲遗传。在低深度(20,000-40,000 个读长)测序也揭示了分析的每个菌株的 95%的 mHVR 簇。最后,该方法在不同实验重复之间显示出簇身份和丰度的良好相关性(r = 0.999)。

结论/意义:我们的工作揭示了 mHVR 在 intra 和 inter-DTU 水平上的序列多样性。这里描述的 mHVR 扩增子测序工作流程是一种可重复的技术,允许对数百个菌株进行多重分析,并有望在未来直接对生物样本进行分型。此外,这种方法可以帮助我们了解小环进化的机制以及菌株之间的系统发育关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f557/6619836/dda564511368/pntd.0007536.g001.jpg

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