Ganzenmueller Tina, Wolf Magnus, Wolfram Lasse, Gkioule Charikleia, Steinbrück Lars, Heim Albert
Institute for Medical Virology, University Hospital Tuebingen, Tuebingen, Germany.
German Center for Infection Research (DZIF), Site Tuebingen, Tuebingen, Germany.
J Med Virol. 2025 Jul;97(7):e70464. doi: 10.1002/jmv.70464.
Human adenoviruses of species B (HAdV-B) can cause upper respiratory tract infections and conjunctivitis, but also severe lower respiratory tract infections (LRTI). Although HAdV-associated LRTI are non-notifiable in Germany, typing data of our Adenovirus Reference Laboratory indicated an HAdV-B3 epidemic in 2023, with 67 samples initially typed as HAdV-B3 compared to < 10/year in the previous years. Circulation of a novel, highly virulent HAdV-B3 strain was suspected and complete viral genomic sequencing performed, revealing a recombinant phylogeny of the penton gene (P), which originated from HAdV-B7, whereas hexon (H) and fiber (F) genes originated from HAdV-B3. Therefore, this virus was acknowledged by the Adenovirus Working Group as the novel recombinant genotype 114 (P7H3F3). Interestingly, BLAST search of the HAdV-B114 prototype sequence showed 99.91% identity to the old HAdV-B genome type 3a. Additionally, multiple complete adenovirus genomic sequences labeled as HAdV-B3 during the last two decades had > 99.8% identity, suggesting long-term circulation of HAdV-B114 although the recombinant phylogeny of its penton region had not been recognized. This detailed analysis of an HAdV epidemic associated with ocular and respiratory infections, including severe LRTI, led to the discovery of a novel genotype HAdV-B114, which is rather a neglected, re-emergent than an emerging virus.
B种人类腺病毒(HAdV-B)可引起上呼吸道感染和结膜炎,也可导致严重的下呼吸道感染(LRTI)。尽管在德国,与腺病毒相关的下呼吸道感染无需上报,但我们腺病毒参考实验室的分型数据显示,2023年出现了HAdV-B3疫情,有67个样本最初被分型为HAdV-B3,而前几年每年的病例数不到10例。怀疑有新型高毒力HAdV-B3毒株在传播,并进行了完整的病毒基因组测序,结果显示五聚体基因(P)的重组系统发育起源于HAdV-B7,而六邻体(H)和纤维(F)基因起源于HAdV-B3。因此,这种病毒被腺病毒工作组认定为新型重组基因型114(P7H3F3)。有趣的是,对HAdV-B114原型序列进行BLAST搜索发现,它与旧的HAdV-B基因组3a型有99.91%的同一性。此外,在过去二十年中标记为HAdV-B3的多个完整腺病毒基因组序列的同一性>99.8%,这表明HAdV-B114长期存在,尽管其五聚体区域的重组系统发育尚未被识别。对与眼部和呼吸道感染(包括严重下呼吸道感染)相关的腺病毒疫情的详细分析,导致发现了一种新型基因型HAdV-B114,它与其说是一种新出现的病毒,不如说是一种被忽视的、重新出现的病毒。