Madisch Ijad, Harste Gabi, Pommer Heidi, Heim Albert
Institut für Virologie, Medizinische Hochschule Hannover, Carl-Neuberg-Str. 1, D-30625 Hannover, Germany.
J Virol. 2005 Dec;79(24):15265-76. doi: 10.1128/JVI.79.24.15265-15276.2005.
Human adenoviruses (HAdV) are responsible for a wide spectrum of diseases. The neutralization epsilon determinant (loops 1 and 2) and the hemagglutination gamma determinant are relevant for the taxonomy of HAdV. Precise type identification of HAdV prototypes is crucial for detection of infection chains and epidemiology. epsilon and gamma determinant sequences of all 51 HAdV were generated to propose molecular classification criteria. Phylogenetic analysis of epsilon determinant sequences demonstrated sufficient genetic divergence for molecular classification, with the exception of HAdV-15 and HAdV-29, which also cannot be differentiated by classical cross-neutralization. Precise sequence divergence criteria for typing (<2.5% from loop 2 prototype sequence and <2.4% from loop 1 sequence) were deduced from phylogenetic analysis. These criteria may also facilitate identification of new HAdV prototypes. Fiber knob (gamma determinant) phylogeny indicated a two-step model of species evolution and multiple intraspecies recombination events in the origin of HAdV prototypes. HAdV-29 was identified as a recombination variant of HAdV-15 (epsilon determinant) and a speculative, not-yet-isolated HAdV prototype (gamma determinant). Subanalysis of molecular evolution in hypervariable regions 1 to 6 of the epsilon determinant indicated different selective pressures in subclusters of species HAdV-D. Additionally, gamma determinant phylogenetic analysis demonstrated that HAdV-8 did not cluster with -19 and -37 in spite of their having the same tissue tropism. The phylogeny of HAdV-E4 suggested origination by interspecies recombination between HAdV-B (hexon) and HAdV-C (fiber), as in simian adenovirus 25, indicating additional zoonotic transfer. In conclusion, molecular classification by systematic sequence analysis of immunogenic determinants yields new insights into HAdV phylogeny and evolution.
人腺病毒(HAdV)可引发多种疾病。中和ε决定簇(环1和环2)和血凝γ决定簇与HAdV的分类学相关。准确鉴定HAdV原型对于检测感染链和开展流行病学研究至关重要。生成了所有51种HAdV的ε和γ决定簇序列,以提出分子分类标准。对ε决定簇序列的系统发育分析表明,除了HAdV-15和HAdV-29(这两种病毒也无法通过经典的交叉中和法区分)外,分子分类具有足够的遗传差异。从系统发育分析中推导出了精确的分型序列差异标准(与环2原型序列的差异<2.5%,与环1序列的差异<2.4%)。这些标准也可能有助于鉴定新的HAdV原型。纤维结(γ决定簇)系统发育表明,HAdV原型起源存在两步式物种进化模型和多次种内重组事件。HAdV-29被鉴定为HAdV-15(ε决定簇)和一种推测性的、尚未分离的HAdV原型(γ决定簇)的重组变体。对ε决定簇高变区1至6的分子进化进行的亚分析表明,HAdV-D物种的亚群中存在不同的选择压力。此外,γ决定簇系统发育分析表明,尽管HAdV-8与-19和-37具有相同的组织嗜性,但它并未与它们聚类。HAdV-E4的系统发育表明,它是由HAdV-B(六邻体)和HAdV-C(纤维)之间的种间重组产生的,就像猴腺病毒25一样,这表明存在额外的人畜共患病传播。总之,通过对免疫原性决定簇进行系统序列分析进行分子分类,为HAdV的系统发育和进化提供了新的见解。