Kanda Ravinder K, Coulson Tim
Department of Zoology, University of Oxford, South Parks Road, Oxford, United Kingdom.
PLoS One. 2015 Feb 18;10(2):e0117442. doi: 10.1371/journal.pone.0117442. eCollection 2015.
Endogenous retroviruses (ERV), or the remnants of past retroviral infections that are no longer active, are found in the genomes of most vertebrates, typically constituting approximately 10% of the genome. In some vertebrates, particularly in shorter-lived species like rodents, it is not unusual to find active endogenous retroviruses. In longer-lived species, including humans where substantial effort has been invested in searching for active ERVs, it is unusual to find them; to date none have been found in humans. Presumably the chance of detecting an active ERV infection is a function of the length of an ERV epidemic. Intuitively, given that ERVs or signatures of past ERV infections are passed from parents to offspring, we might expect to detect more active ERVs in species with longer generation times, as it should take more years for an infection to run its course in longer than in shorter lived species. This means the observation of more active ERV infections in shorter compared to longer-lived species is paradoxical. We explore this paradox using a modeling approach to investigate factors that influence ERV epidemic length. Our simple epidemiological model may explain why we find evidence of active ERV infections in shorter rather than longer-lived species.
内源性逆转录病毒(ERV),即过去逆转录病毒感染的残余物,现已不再活跃,存在于大多数脊椎动物的基因组中,通常占基因组的10%左右。在一些脊椎动物中,特别是在像啮齿动物这样寿命较短的物种中,发现活跃的内源性逆转录病毒并不罕见。在寿命较长的物种中,包括人类,尽管已经投入大量精力寻找活跃的ERV,但发现它们的情况却很少见;迄今为止,在人类中尚未发现。据推测,检测到活跃的ERV感染的可能性是ERV流行时间长短的一个函数。直观地说,鉴于ERV或过去ERV感染的特征是从父母传给后代的,我们可能会预期在世代时间较长的物种中检测到更多活跃的ERV,因为感染在寿命较长的物种中持续的时间应该比在寿命较短的物种中更长。这意味着,与寿命较长的物种相比,在寿命较短的物种中观察到更多活跃的ERV感染是自相矛盾的。我们使用建模方法来探索这个悖论,以研究影响ERV流行时间长短的因素。我们简单的流行病学模型或许可以解释为什么我们在寿命较短而非较长的物种中发现了活跃的ERV感染的证据。