北京地区2022-2023年急性呼吸道感染患儿新重组人腺病毒分子特征分析

IF 4.1
Yi Nan Guo, Ri De, Fang Ming Wang, Zhen Zhi Han, Li Ying Liu, Yu Sun, Yao Yao, Xiao Lin Ma, Shuang Liu, Chunmei Zhu, Dong Qu, Lin Qing Zhao
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引用次数: 0

摘要

目的:重组事件是常见的,是多种人腺病毒(hav)的主要驱动力,特别是在急性呼吸道感染(ARIs)儿童中。因此,持续监测这些事件对于有效监测和控制病毒至关重要。方法:采集2022年1月~ 2023年12月急性呼吸道感染患儿的呼吸道标本。从hadv阳性标本中扩增penton碱基、hexon和纤维基因,并测序以确定病毒类型。在分型结果不一致的情况下,将基因克隆到pGEM-T载体中以检测重组事件。利用新一代元基因组测序(mNGS)对重组hav基因组进行表征。结果:在6771份标本中,277份(4.09%,277/ 6771)hav阳性,其中157份(56.68%,157/277)成功分型,hav - b3型为优势型(91.08%,143/157),14份(5.05%,14/277)分型结果不一致,其中6份属于b种。6份标本的penton碱基基因被归为hav - b7, hexon基因和纤维基因被归为hav - b3,重组基因型为P7H3F3。它与HAdV-B114非常相似。此外,还发现了一个编码L1 52/ 55kd的部分基因,该基因起源于HAdV-B16。结论:重组蛋白P7H3F3含有HAdV-B3和HAdV-B7的同源序列,与HAdV-B114相似,并添加了HAdV-B16的同源序列。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Characterization of New Recombinant Human Adenoviruses Detected in Children with Acute Respiratory Tract Infections in Beijing, China, 2022-2023.

Objective: Recombination events are common and serve as the primary driving force of diverse human adenovirus (HAdV), particularly in children with acute respiratory tract infections (ARIs). Therefore, continual monitoring of these events is essential for effective viral surveillance and control.

Methods: Respiratory specimens were collected from children with ARIs between January 2022 and December 2023. The penton base, hexon, and fiber genes were amplified from HAdV-positive specimens and sequenced to determine the virus type. In cases with inconsistent typing results, genes were cloned into the pGEM-T vector to detect recombination events. Metagenomic next-generation sequencing (mNGS) was performed to characterize the recombinant HAdV genomes.

Results: Among 6,771 specimens, 277 (4.09%, 277/6,771) were positvie for HAdV, of which 157 (56.68%, 157/277) were successfully typed, with HAdV-B3 being the dominant type (91.08%, 143/157), and 14 (5.05%, 14/277) exhibited inconsistent typing results, six of which belonged to species B. The penton base genes of these six specimens were classified as HAdV-B7, whereas their hexon and fiber genes were classified as HAdV-B3, resulting in a recombinant genotype designated P7H3F3, which closely resembled HAdV-B114. Additionally, a partial gene encoding L1 52/55 kD was identified, which originated from HAdV-B16.

Conclusion: A novel recombinant, P7H3F3, was identified, containing sequences derived from HAdV-B3 and HAdV-B7, which is similar to HAdV-B114, along with additional sequences from HAdV-B16.

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