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物种 D 人腺病毒的计算分析提供了一种新型病毒的证据。

Computational analysis of a species D human adenovirus provides evidence of a novel virus.

机构信息

Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones en Ciencias de la Salud, Universidad Nacional de Asunción, Paraguay.

Sección Virología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.

出版信息

J Gen Virol. 2017 Nov;98(11):2810-2820. doi: 10.1099/jgv.0.000947. Epub 2017 Oct 17.

Abstract

A human adenovirus (HAdV) species D, was isolated from a hospitalised child with severe lower respiratory infection. It was initially detected in the nasopharyngeal aspirate of the child followed by conventional PCR amplification of the hexon, penton base, and fibre genes. Sanger DNA sequencing and phylogenetic analyses showed characteristics of a recombinant genome not described before. Next Generation Sequencing analysis was performed to reconstruct its complete DNA genome after viral isolation in adenocarcinoma human cell line (A549). A complete genomic sequence of 35.2 kb in length, with a G+C content of 57 % was obtained, related to HAdV-D29 (96 % identity). Imputed serology analysis demonstrated its novel type with a nucleotide sequence identity of 95.3 % (hexon loop 1) and 96 % (hexon loop 2) to HAdV-D9. The penton base gene showed a novel sequence, distantly related to HAdV-D44. The E3 and E4 regions evolved significantly from their ancestors. The fibre gene was almost identical to the knob region of HAdV-D15 but showed an unrelated shaft sequence. In conclusion the genomics of this novel HAdV, designated the HAdV-D83 [P83H9F15] prototype and bearing a new penton base gene, supports the importance of viral evolution to understand modified tissue tropism, enhanced transmission, or altered virulence.

摘要

一株人腺病毒(HAdV)D 型,从一名患有严重下呼吸道感染的住院儿童的鼻咽抽吸物中分离得到。最初在该患儿的鼻咽抽吸物中检测到该病毒,随后对其六邻体、五邻体基和纤维基因进行了常规 PCR 扩增。Sanger DNA 测序和系统发育分析显示,该病毒基因组具有以前未描述的重组特征。下一代测序分析用于在腺癌细胞系(A549)中分离病毒后重建其完整 DNA 基因组。获得了一个长度为 35.2kb 的完整基因组序列,G+C 含量为 57%,与 HAdV-D29(96%同一性)相关。推测血清学分析表明其为新型,与 HAdV-D9 的核苷酸序列同一性为 95.3%(六邻体环 1)和 96%(六邻体环 2)。五邻体基因为新型序列,与 HAdV-D44 关系较远。E3 和 E4 区从其祖先进化而来。纤维基因与 HAdV-D15 的 knob 区几乎相同,但轴序列无关。总之,该新型 HAdV 的基因组,命名为 HAdV-D83 [P83H9F15] 原型,并带有新的五邻体基,支持病毒进化对于理解改变的组织嗜性、增强的传播或改变的毒力的重要性。

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