Backbone of RNA Viruses Uncovered
Backbone of RNA Viruses Uncovered
Many human diseases, from the common cold to deadly haemorrhagic fevers, are caused by RNA viruses. Most of these viruses are thought to have originated from close relatives that infected mammals, and so the majority of virus-discovery studies have focused on mammals and birds. RNA viruses, however, are probably older than the last common ancestor of life on Earth. Detailed genetic information for RNA viruses from other classes of vertebrate is sorely needed if we are to fully understand long-term virus evolution. In a paper in Nature, Shi et al. report the discovery of previously unidentified vertebrate RNA viruses from across evolutionary timescales.
The authors analysed the viruses in 186 vertebrate species using an approach called metatranscriptomic sequencing, in which all of the RNA present in a sample is sequenced. The samples were taken from species of fish, amphibian and reptile — every vertebrate class except mammals and birds. In these samples, Shi and colleagues discovered a total of 214 viruses, dramatically increasing the number of known RNA viruses in each vertebrate class. For example, they identified more than 20 RNA viruses that infect amphibians, whereas just a few had previously been identified.
The analysis also revealed an astonishing level of biodiversity — the researchers identified previously unknown viruses in almost every RNA-virus family known to infect mammals. These include viruses highly pathogenic to humans, such as influenza virus, arenaviruses and filoviruses, that have not previously been reported in fish or amphibians.
Shi et al. used this information to construct phylogenetic trees that describe the evolutionary relationships between viruses. They found that the phylogenies of RNA viruses were broadly comparable to those of the viruses’ vertebrate hosts. This shows that RNA viruses followed a similar evolutionary trajectory to vertebrates, and have co-evolved with their hosts over millions of years. The evolution of vertebrates began more than 500 million years ago — vertebrate life then divided into several classes of fish, followed by the evolution of amphibians that moved on to land (http://www.onezoom.org). The authors’ findings indicate that mammalian RNA viruses probably originated from viruses that infected fish, and then followed vertebrates on to land.
However, the researchers also show that some viruses can infect multiple hosts, indicating that, in addition to co-evolution, viruses have made jumps between species. In fact, many virus outbreaks in humans are the result of animal-to-human transmission, as exemplified by the recent Ebola epidemic in West Africa. Most cross-species transmission events result in limited or no onwards transmission (the virus typically continues to circulate only temporarily in the new host species), and the ability of a virus to establish itself depends on a range of factors, including host divergence. Thus, transmission between animals belonging to the same vertebrate class (bats to humans, for example) is more likely than that between animals belonging to different vertebrate classes (such as reptiles to mammals). But Shi and colleagues’ phylogenies reveal that viruses regularly jump between vertebrate classes, with successful onwards transmission that can continue for millions of years.
The current study greatly expands our knowledge of vertebrate virus evolution. However, it is not without limitations. First, excluding birds and mammals, there are more than 50,000 vertebrate species. And although the current study is one of the largest of its kind, Shi et al. sampled less than 0.5% of these species. Moreover, the authors focused their sampling towards common taxa such as ray-finned fishes, and included relatively few amphibians. This means that the group’s findings represent only a minuscule fraction of the total diversity of RNA viruses. We are just scratching the surface of these viruses’ evolutionary history. Our understanding of viral evolution will continue to expand as we sample RNA viruses from across deeper evolutionary timescales.
Another limitation of the current study is that — as is typical for this type of work — new viruses are identified on the basis of genetic similarity to those that have been sequenced previously. This strategy has the potential to introduce biases. It is therefore possible that there are entire groups of viruses yet to be discovered, because they cannot be detected using similarity-based approaches.
Finally, it is becoming increasingly clear that only a tiny fraction of RNA viruses will ever infect humans, and the factors that contribute to virus emergence in humans are not fully understood. As Shi et al. show, phylogenetic analyses are a powerful tool for identifying cross-species transmissions that happened in the past. But they cannot be used to predict host jumps and virus emergence of the future — the complexity of successful cross-species transmission renders efforts to predict disease emergence by mapping non-human virus diversity ineffective. Studies that give us a more fundamental understanding of RNA-virus evolution and diversity, as Shi and colleagues work does, will be crucial to inform future surveillance efforts in humans.
It took us many decades to understand the basics of the evolutionary history of vertebrates. It will probably take even longer before we can confidently say that we are beginning to understand the enormous diversity of RNA viruses and their complex relationships with humans and other vertebrates. Shi et al. have provided an exciting starting point from which to strike out towards this goal.
This article has been republished from materials provided by Nature. Note: material may have been edited for length and content. For further information, please contact the cited source.
The evolutionary history of vertebrate RNA viruses. Mang Shi, Xian-Dan Lin, Xiao Chen, Jun-Hua Tian, Liang-Jun Chen, Kun Li, Wen Wang, John-Sebastian Eden, Jin-Jin Shen, Li Liu, Edward C. Holmes & Yong-Zhen Zhang. Nature (2018), doi:10.1038/s41586-018-0012-7.