Roy Soumitra, Vandenberghe Luk H, Kryazhimskiy Sergey, Grant Rebecca, Calcedo Roberto, Yuan Xin, Keough Martin, Sandhu Arbans, Wang Qiang, Medina-Jaszek C Angelica, Plotkin Joshua B, Wilson James M
Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, USA.
PLoS Pathog. 2009 Jul;5(7):e1000503. doi: 10.1371/journal.ppat.1000503. Epub 2009 Jul 3.
Adenoviruses are important human pathogens that have been developed as vectors for gene therapies and genetic vaccines. Previous studies indicated that human infections with adenoviruses are self-limiting in immunocompetent hosts with evidence of some persistence in adenoid tissue. We sought to better understand the natural history of adenovirus infections in various non-human primates and discovered that healthy populations of great apes (chimpanzees, bonobos, gorillas, and orangutans) and macaques shed substantial quantities of infectious adenoviruses in stool. Shedding in stools from asymptomatic humans was found to be much less frequent, comparable to frequencies reported before. We purified and fully sequenced 30 novel adenoviruses from apes and 3 novel adenoviruses from macaques. Analyses of the new ape adenovirus sequences (as well as the 4 chimpanzee adenovirus sequences we have previously reported) together with 22 complete adenovirus genomes available from GenBank revealed that (a) the ape adenoviruses could clearly be classified into species corresponding to human adenovirus species B, C, and E, (b) there was evidence for intraspecies recombination between adenoviruses, and (c) the high degree of phylogenetic relatedness of adenoviruses across their various primate hosts provided evidence for cross species transmission events to have occurred in the natural history of B and E viruses. The high degree of asymptomatic shedding of live adenovirus in non-human primates and evidence for zoonotic transmissions warrants caution for primate handling and housing. Furthermore, the presence of persistent and/or latent adenovirus infections in the gut should be considered in the design and interpretation of human and non-human primate studies with adenovirus vectors.
腺病毒是重要的人类病原体,已被开发用作基因治疗和基因疫苗的载体。先前的研究表明,在免疫功能正常的宿主中,人类感染腺病毒是自限性的,有证据表明腺样组织中存在一定程度的持续性感染。我们试图更好地了解各种非人灵长类动物中腺病毒感染的自然史,发现健康的大猩猩(黑猩猩、倭黑猩猩、大猩猩和猩猩)和猕猴群体在粪便中排出大量有传染性的腺病毒。发现无症状人类粪便中的病毒排出频率要低得多,与之前报道的频率相当。我们从猿类中纯化并完全测序了30种新型腺病毒,从猕猴中纯化并完全测序了3种新型腺病毒。对新的猿腺病毒序列(以及我们之前报道的4种黑猩猩腺病毒序列)与从GenBank获得的22个完整腺病毒基因组进行分析后发现:(a)猿腺病毒可以明确地分为与人类腺病毒B、C和E种相对应的种;(b)有证据表明腺病毒之间存在种内重组;(c)各种灵长类宿主中的腺病毒在系统发育上的高度相关性为B和E病毒自然史中发生的跨物种传播事件提供了证据。非人灵长类动物中活腺病毒的高度无症状排出以及人畜共患病传播的证据,警示在处理和饲养灵长类动物时需谨慎。此外,在设计和解释使用腺病毒载体的人类和非人灵长类动物研究时,应考虑肠道中持续性和/或潜伏性腺病毒感染的存在。