The discovery of many new species of hepaciviruses and pegiviruses, which exhibit enormous genetic diversity, in wild rodent and bat populations might help us to understand the origins of the hepatitis C virus.
The hepatitis C virus does not give up its secrets lightly. Despite infecting about 3 out of every 100 people worldwide, a small proportion of whom consequently develop severe liver disease, the virus eluded discovery for decades. It was eventually identified in 1989 as the cause of 'non-A, non-B hepatitis'. Researchers who have since sought the origins of hepatitis C virus (HCV), as it is now known, have been frustrated in equal measure. The virus infects chimpanzees in the laboratory, but studies of wild and captive primates uncovered no evidence of an animal population that might have transmitted HCV to humans1, contrasting with the success of other surveys that exposed close relatives of HIV-1 and human malaria in great apes2. Now, however, Kapoor et al.3 and Quan et al.4, writing in mBio and Proceedings of the National Academy of Sciences, respectively, report a diverse and widespread array of HCV-like viruses in wild populations of rodents3 and bats4. Although none of these viruses can yet be claimed as the source of HCV, their discovery may represent the beginning of the end of the search for HCV's origins.
HCV belongs to the Hepacivirus genus of viruses, whose closest taxonomic neighbour is the Pegivirus genus5; the newly discovered bat and rodent viruses include members of both groups. Kapoor et al. found five provisional virus species among more than 400 blood samples from four North American rodent species. Quan and colleagues describe 11 virus lineages from around 1,700 samples taken from 58 bat species collected in Mexico, Bangladesh and sub-Saharan Africa. The most notable property of the new viruses is their exceptional genetic heterogeneity, which dwarfs the diversity of all previously known hepaciviruses and pegiviruses, including HCV, which is itself highly variable.
This diversity strongly implicates bats and rodents as natural and ancestral hosts for viruses of both genera, an idea supported by the comparatively high frequency of infection in wild animals (around 5%) and by Quan and colleagues' observations that some bats were co-infected with multiple viruses. Furthermore, all the infected bats seemed healthy when collected, which is consistent with a long evolutionary association between virus and host. But despite their already remarkable diversity, the viruses were isolated from approximately 5% of bat and less than 1% of rodent species known, and thus probably represent only a fraction of hepaciviruses and pegiviruses present in nature.
Before these reports, the hepaciviruses and pegiviruses were known as sparsely populated genera that between them contained fewer than ten species, isolated from a motley collection of hosts: humans, chimpanzees, horses, dogs, wild and captive New World primates, plus one bat pegivirus found6 in 2010. The discovery of enormous viral genetic diversity in bats and rodents presents the possibility that each of the formerly identified species arose through successful cross-species transmission of a bat or rodent virus. Indeed, it is estimated that a quarter of recently emerged human pathogens originated from rodents or bats7, and both animal groups are abundant, widely distributed and live in large numbers near human settlements or domesticated animals. This postulated cross-species transmission need not have been direct, but may have occurred through an intermediate host in even closer contact with humans — civet cats had such a role in the transfer of the SARS coronavirus to humans8, and pigs in the transfer of the Nipah virus9, both of which originate in bats.
Although none of the new hepaciviruses and pegiviruses are sufficiently genetically similar to those found in humans or other animals to be declared their immediate source, bats and rodents are now prime suspects in the hunt for the ultimate origins of HCV. Further sampling of small-mammal populations worldwide should reveal the true diversity and host range of these viruses, and may uncover viruses more similar to HCV. Three possible outcomes of such sampling can be imagined: new viruses are found but none are closely related to HCV and its origin remains unresolved (Fig. 1a); viruses more similar to HCV than to equine hepacivirus, HCV's closest known relative, are found, suggesting that all HCV strains arose from a single successful ancestral transfer to humans (Fig. 1b); or viruses are found that group within the current genetic diversity of HCV, indicating that it arose from two or more independent cross-species transmissions (Fig. 1c).
The third hypothesis is particularly intriguing as it potentially solves the enigma of 'endemic' HCV transmission: how some rural populations in central Africa and southeast Asia come to bear a range of divergent HCV strains, indicative of centuries of stable human-to-human transmission, in the absence of any consistently effective and widespread route of transmission. This riddle would be answered if the virus diversity originates not in humans but from an animal reservoir.
Although the immediate consequences of the current findings for human health seem minimal, only detailed investigation of the transmission and ecology of the new viruses in their natural hosts can elucidate their true potential for cross-species transmission. The ongoing emergence in humans of coronaviruses of probable bat origin10, ten years after the successful eradication of SARS, is a timely reminder of the potential benefits to epidemiology and public health of understanding the dynamics of infectious disease in wild animal populations.
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Pybus, O., Gray, R. The virus whose family expanded. Nature 498, 310–311 (2013). https://doi.org/10.1038/498310b
Emerging Microbes & Infections (2014)