鉴定宿主驯化产生的潜在 SARS-CoV-2 遗传标记。

Janusz Wiśniewski, Heng-Chang CHEN
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引用次数: 0

摘要

我们开发了一种基于 K-聚合体的管道,即使用富集 K-聚合体的病原体起源识别工具(PORT-EK),用于在比较两个宿主物种间分离物的元基因组后,识别相应宿主中富集的基因组区域。利用它,我们确定了数千个富集于美国白尾鹿和蝙蝠水库中的betacoronaviruses的K-mers,同时将它们与人类分离物进行了比较。我们展示了鹿和蝙蝠中富集的 k-mers 的不同覆盖图谱,并通过比较蝙蝠和人类分离物的病毒元基因组,揭示了富集的 k-mers 中的 148 个突变。我们观察到,遗传密码子内的第三个位置容易发生突变,导致与未发生变化的氨基酸具有相同理化性质的氨基酸发生同义突变的频率很高。最后,我们根据富集的 k-mer 计数对宿主物种的可能性进行了分类和预测。总之,PORT-EK 展示了其识别富集病毒基因组区域的可行性,揭示了冠状病毒在宿主驯化后的不同内在趋向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of potential SARS-CoV-2 genetic markers resulting from host domestication.
We developed a k-mer-based pipeline, namely the Pathogen Origin Recognition Tool using Enriched K-mers (PORT-EK) to identify genomic regions enriched in the respective hosts after the comparison of metagenomes of isolates between two host species. Using it we identified thousands of k-mers enriched in US white-tailed deer and betacoronaviruses in bat reservoirs while comparing them with human isolates. We demonstrated different coverage landscapes of k-mers enriched in deer and bats and unraveled 148 mutations in enriched k-mers yielded from the comparison of viral metagenomes between bat and human isolates. We observed that the third position within a genetic codon is prone to mutations, resulting in a high frequency of synonymous mutations of amino acids harboring the same physicochemical properties as unaltered amino acids. Finally, we classified and predicted the likelihood of host species based on the enriched k-mer counts. Altogether, PORT-EK showcased its feasibility for identifying enriched viral genomic regions, illuminating the different intrinsic tropisms of coronavirus after host domestication.
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