RJ GIFFORD CVR

Virology | Evolution | Genomics

Cycloviruses - emerging human viruses?

May 17th, 2018

Advances in DNA sequencing have dramatically increased the rate at which new viruses are being identified. However, the host associations of viruses that have only been identified via sequencing are often open to question.

dong thap province Dong Thap province in Vietnam, where the 'index case' in a cluster of cyclovirus-associated acute central nervous system infections was identified.

In 2013, DNA sequences derived from mysterious viruses called ‘cycloviruses’ were detected in patients with severe neurological disease on two continents. In Vietnam, a virus named "Cyclovirus-VN" was identified in association with severe brain infections. Around the same time, a closely related virus was detected in Malawi - again via sequencing - in association with cases of unexplained paraplegia.

The authors of these studies emphasised that a causal link with disease had yet to be determined. Somewhat inevitably though, the impression has been created - at least in some quarters - that cycloviruses are emerging viruses of humans and domestic animals.


"Newly emerging viruses such as Cycloviruses, which are causing neurological problems in children in Asia, are also emerging in sewage and are spreading.". The Guardian

What is certainly true is that cycloviruses continue to be detected in human samples, as well in samples derived from other sources. In most respects, however, they remain a mystery - so are these viruses really a threat to humans?


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A flexible software system for virus genomics.

May 10th, 2018

Revolutionary advances in DNA sequencing technology have transformed the way that we research and monitor viruses.

This has been reflected in the development of a diverse range of virus genome data resources (VGDRs) - computational tools that facilitate the use of virus genome data in experimental research and public health. VGDRs are diverse - they may focus on any virus species or aspect of virus biology. Nevertheless, at their core, they typically operate on similar data types, using related computational processes. This means that in spite of the great diversity of VGDRs, there is room for the development of standardised approaches, and these can enable extensive re-use of code and vastly greater efficiency in VGDR development.

In my research group, we've been working for several years on ways to enable this. I'm delighted that we can now present GLUE a unified bioinformatics software environment for VGDR development.

Our manuscript describing GLUE is available here


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Tracing the history of primate deltaretroviruses

April 9th, 2018

Deltaretroviruses are a genus of retroviruses that have so far only been identified in primates and cattle. They include the Human T-lymphotrophic viruses (HTLVs), which are currently estimated to infect 15-20 million people worldwide.

There are four distinct HTLVs that infect humans. HTLV-1 and HTLV-2 are closely related but have very different geographic distributions. HTLV-1 can cause a rare type of lymphoma called adult T-cell leukaemia/lymphoma (ATLL), while HTLV-2 has been associated with sporadic cases of neurological disorders. HTLV-3 and HTLV-4 have only been found in isolated populations in Central Africa, and are not known to be associated with disease.



peruvian mummy HTLV-1 DNA has been recovered from mummified corpses in the Atacama desert.

The global distribution of HTLV-1 and HTLV-2 seems to reflect to historical patterns of human migration (see figure above), indicating that these viruses have an ancestral presence in the human population.

Among the lines of evidence supporting this are HTLV-1 DNA sequences recovered from 'mummies' excavated in the Atamaca desert Due to the extremely arid conditions that occur in this region, the bodies of people buried there over 1,000 years ago have remained relatively well preserved, such that DNA could be recovered (even in the early 2000s, when techniques for doing this were considerably less advanced than those available today).

The evolutionary relationships between (i) HTLV-1 DNA sequences recovered from an Atacamanian mummy, and (ii) HTLV-1 isolates obtained from infected populations in present day Chile and Japan, were observed to be consistent with a scenario in which HTLV-1 spread to South America along with the human populations that migrated from Asia to the Americas over 10,000 years ago (see figure above).

The HTLVs are closely related to viruses found in african primates, called simian T-lymphotrophic viruses (STLVs). Phylogenetic studies indicate that the various HTLVs (1-4) likely originated in separate primate-to-human transfer events. Accordingly, the deltaretroviruses found in human and non-human primates are now collectively referred to as 'primate T-lymphotrophic viruses' (PTLVs).



A recent study of PTLV sequences obtained from orangutans revealed new insights into the evolutionary history of PTLV-1 (the group of PTLVs that contains HTLV-1) in Asia. This analyses used a molecular clock based approach to estimate the timing of PTLV-1 spread, and indicated that the virus was first introduced into Australia between 3,000 and 4,000 years ago.

The study also inferred that HTLV-1 arrived in Melanesia between 2,300 to 2,700 years ago - approximately corresponding to the time when the Lapita peoples are thought to have migrated into the region.

But while it seems clear that deltaretroviruses have an association with primates that dates back thousands of years, their deeper origins have until recently remained a mystery.


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Circovirus Evolution

March 25th, 2018

My lab has recently published a paper in the journal Virus Research, describing our investigation into the evolutionary interactions between vertebrates and circoviruses. Circoviruses (family Circoviridae, genus Circovirus) are among the smallest of all known viruses. They have small, simple genomes comprised of a single, circular strand of DNA ~2000 bases in length. Their genomes encode two major proteins: replication-associated protein (Rep) and capsid (Cap).

These viruses remain a bit of a mystery - they are not very widely studied and are difficult to grow in cell culture. However, over the past decade it's become apparent they are extremely widespread in the environment, being among the most commonly detected viruses in metagenomic samples.

corella Beak and feather disease virus has recently caused a wave of corella deaths in Western Australia.

Two pathogenic circoviruses have been described. First, there is “beak and feather disease virus” (BFDV), which is associated with serious disease in psittacine birds (parrots and their relatives). BFDV, which was first identified in captive birds, poses a significant threat to some endangered parrot species

Secondly, there is porcine circovirus 2 (PCV-2), which is thought to cause post-weaning multisystemic wasting syndrome (PMWS), an emerging disease of domestic swine Symptoms of PMWS are poor growth rate and/or acute malnutrition and weight loss. The emergence of PCV-2 as a pathogen appears linked - in an as-yet-undetermined way - to the modern swine production process.

We previously demonstrated that sequences derived from circoviruses occur in animal genomes. These endogenous circoviral elements (CVe) provide something akin to a fossil record for circoviruses. Like fossils, CVe sequences provide a retrospective source of information about evolution, allowing us to make inferences about the long term interactions between circoviruses and the species groups they infect.

In this study we performed a comprehensive survey of CVe in published vertebrate genome sequences.

Recovering the Circovirus fossil record

A Weddel seal A Weddell seal (*Leptonychotes weddellii*). Pinnipeds are one of the carnivore groups in which CVe are highly duplicated.

We identified nearly 200 CVe in vertebrate genomes. This number is possibly a little misleading, as most of these sequences are part of single, large group of highly duplicated elements found in carnivore genomes. All of these CVe derive from a small number of germline incorporation events (possibly just one), and seem to have have been duplicated in carnivore genomes by mechanisms associated with non-LTR retrotransposons (the prime suspect being LINE-1

We think that the 200-odd CVe we find in published genome sequences represent at least 19 distinct occasions in which genetic material derived from a circovirus was incorporated into the vertebrate germline. However, this is a conservative estimate - the number could be much higher, perhaps double.

We also established that CVe were inserted into the germline of songbirds, parrots, snakes, and fish many millions of years ago, before the major speciation events in these vertebrate groups. Knowing this allows us to show how incredibly ancient these CVe are - ranging from ~50 million years old for the elements in birds, mammals, and fish, to ~100 million years old for the element in snakes.

Among these demonstrably ancient CVe, one identified in cyprinid fish was among the most intriguing. It has an unusual structure, comprising several genomes arranged end-to-end. It's not too hard to imagine how these tandem genome structures could have been generated as a consequence of the rolling circle mechanism of DNA replication used by these viruses.

More surprisingly, this CVe is closely related to a contemporary circovirus that infects common barbel (Barbus barbus), called barbel circovirus (BarbCV). Indeed, the similarity was so close we wondered if the BarbCV genome sequence might actually be derived from this CVe (i.e. it’s actually a PCR artifact However, this seems unlikely, not only because the genome of BarbCV is intact (whereas the CVe in cyprinids are somewhat degraded), but also because some of the researchers who reported BarbCV have also described CVe in the Indian rohu (Labeo rohita), so it seems more than likely they’re aware of this possibility and have ruled it out.

Parrots The stunning scarlet macaw (*Ara macao*) - one of the parrot species in which we found endogenous circoviral elements.

The upshot of all this is it looks like BarbCV is the modern version of a fish circovirus that circulated over 39 million years ago. Given how rapidly circoviruses can evolve, it is striking that the ancient virus looks so similar to the modern one. Along the same lines, we describe CVe in the genomes of songbirds (order Passeriformes) that are over 38 million years old, and appear to represent the ancestors of modern circoviruses infecting birds.

Interestingly, ancient CVe (30-60 million years old) were also identified in the genomes of psittaciform birds (parrots). This one seemed to have been incorporated into the germline separately from the one in songbirds, and seemed more remotely related to modern avian circoviruses such as BFDV. Could it be that parrots have - over the course of evolution - been afflicted by a lineage of circoviruses that is distinct from the one found in other birds? More speculatively (much more), could this be why parrots seem to be afflicted far more seriously by BFDV infection than other avian species?

A baby Tasmanian devil A baby Tasmanian devil. Endogenous circoviral elements in marsupial genomes indicate circoviruses have been infecting Australian mammals for millennia.

Another interesting CVe was identified in the Ryukyu mouse (Mus caroli). This sequence grouped convincingly with carnivore circovirus (CarCV) in evolutionary trees, and because it is easy to imagine that most zoonotic infections of large-bodied mammals might have originated in smaller ones, it is tempting to think that this demonstrates a rodent origin for carnivore circoviruses. However, the fact of the matter is that at this point we can’t yet draw any firm conclusions here. Nevertheless, the robust grouping of the Ryukyu mouse CVe with a modern virus infecting dogs suggests that these two sequences could be the first representatives of a larger sub-lineage of mammalian circoviruses.

In addition, the CVe in the Ryuku mouse has apparently been generated quite recently - presumably after this species diverged from the domestic mouse (Mus musculus). This indicates that a broad range of species and genus-specific CVe remain to be identified in vertebrate genomes.

We identified some pairs of CVe that stood an outside chance of being very old orthologs, but were more likely to be distinct integrations. These included insertions in the genomes of frogs that would be very old indeed (>200 million years) if they could be shown to be orthologs - but again, this seems unlikely.

Hagfish An endogenous circoviral element identified in the genome of a hagfish (pictured) was found to be nearly as alien as its host.

Another pair of possible (but unlikely) orthologs was identified in marsupials. While CVe in the Tasmanian devil and koala genomes may not be orthologs of one another, they could nevertheless be old enough to predate the arrival of placental mammals in Australia. This would indicating that circoviruses were present in Australian marsupials ancestrally, and were not introduced to the continent by placental mammals.

Finally, we identified sequences in the genome of the inshore hagfish that appeared to be derived from a highly divergent circovirus-related lineage. Hagfish are basal vertebrates - in other words, they branched off the vertebrate tree early in evolution. The CVe we identify in the hagfish genome presumably derive from a circovirus lineage that infects these species. It will be interesting to see if any related virus sequences turn up in metagenomic samples.

Directions for future research

Understanding circovirus ecology & evolution

We have a lot left to learn about circoviruses. For example, to reduce disease risks, we really need to understand why some circovirus infections are asymptomatic, whereas others cause severe disease. Studies of porcine circoviruses implicate the modern swine production process in the emergence of circovirus disease, but through what mechanism precisely?

A baby Tasmanian devil pig being vaccinated against porcine circovirus infection. Current vaccine

are based on whole, inactivated virus, or the Cap protein.)

Once again, we can expect to gain a great deal of insight into this question (as well as other aspects of circovirus ecology and evolution) simply by investigating the distribution and diversity of contemporary circoviruses using the stupendous power of next-generation sequencing.

A limitation of our study is the lack of statistical support for some of the internal branching patterns of the Circovirus tree. In addition, there are many CVe that we are not yet able to date, or for which we are only able to provide one age bound (i.e. a minimum or maximum). However, further sampling of CVe and circoviruses may resolve these issues, making it possible to calibrate the timeline of circovirus evolution in greater detail, and with greater precision.

Role of RNA elements in circovirus replication

Geese A recent study examined RNA secondary structure in the goose circovirus genome.

Our study allowed us to calibrate the long-term evolution of some circovirus lineages. This in turn allowed us to demonstrate that the protein-coding sequences of these viruses have changed remarkably little in millions of years. This is surprising when we consider the capacity of viruses to evolve extremely rapidly. Also, if circoviral proteins aren't changing much, how have circoviruses been able to adapt so that they could counter host defences, and infect new hosts?

Possibly, the answer lies in the non-coding regions of circovirus genomes, which appear much less conserved. Interestingly, a recent study indicated the presence of conserved secondary structures within the non-coding region of the goose circovirus genome. These structures appeared to be conserved despite the underlying sequences being highly variable, which suggests they could be functional elements in circovirus replication.

I'm intrigued by the notion that circovirus adaptation might be characterised by rapid evolution in non-coding sequences while the core protein components of the replication cycle remain largely unchanged.


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Parvovirus Metagenomics

March 24th, 2018

Parvoviruses (family Parvoviridae) are small, single-stranded DNA viruses. Several pathogenic parvoviruses of medical and veterinary importance have been identified.

We recently published the findings of a field study in which we describe our investigation into parvoviruses circulating among wild and domestic animals in Brazil. Genomic analysis of these novel viruses provided insights into general aspects of parvovirus ecology and evolution.



We performed metagenomic analysis of animal samples obtained at several distinct sites in Brazil (see map at bottom of page), encompassing Pernambuco, São Paulo, Paraná and Rio Grande do Sul states. Sampling was carried out by a team comprised of PhD students and posdocs from Brazilian universities.

Brazil has a great diversity and abundance of wildlife, and is consequently considered a hotspot for the potential emergence of novel zoonotic viruses. Moreover, many rural communities in Brazil live in close proximity to wildlife species, as can be appreciated in the photo below, taken near a sampling site in Isla de Marajó in the North of Brazil.



In our study, we sampled both wild and domestic animals. Among wild animals, we focussed in particular on species that might be considered likely vectors of human and/or domestic animal viruses.

What did we learn?

We identified eight parvovirus species in total (six of which have not been described previously). The novel parvovirus species were identified in songbirds, marsupials and rodents. None of the infections were associated with obvious disease symptoms in sampled animals.

Tetraparvoviruses

white eared opossum A white-eared opossum captured in the study is carefully sampled before being released.

We detected strains of ungulate tetraparvovirus 1 —a virus in the genus Tetraparvovirus—in cattle from the South of Brazil, demonstrating that this virus is present in cattle populations in South America. It’s presence in farmed cattle in South America, as well as domestic yak in Asia indicates it circulates widely among bovids and is likely to be present in cattle populations throughout the world.

We also recovered the genome of a novel tetraparvovirus from a white-eared opossum. Assuming the genome sequence we recovered from this sample is indeed derived from a parvovirus that infects opossum, it represents the first example of a marsupial tetraparvovirus.

A dependoparvovirus in a New World bat

bat samples Vampire bats were among the species sampled.

The "Dependoparvovirus" genus of parvoviruses have attracted interest as potential gene therapy vectors We provide the first report of a dependoparvovirus in a New World bat—the vampire bat (Desmodus rotundus). The grouping of this novel virus in phylogenetic trees was consistent with an ancestral origin in bats for the Dependoparvovirus genus, as has been proposed previously. However, as sampling remains quite limited, we should perhaps withhold judgement on this for now. Further sampling of Dependoparvovirus diversity (including paleoviruses as well as contemporary viruses) should allow the evolutionary history of the genus to be reconstructed in greater detail, and with greater confidence.

Parvovirus ecology

Besides simply documenting novel parvoviruses, our study offered some revealing insights into the natural biology of parvoviruses in vertebrate species.

sampling viruses in brazil Members of the sampling team at work in the field.

We used phylogenetic approaches to reconstruct the evolutionary relationships between the novel parvoviruses described in our study, and those that have been described previously.

We found that viruses from particular host species often grouped together in phylogenies. For example, we recovered identified viruses closely related to the "minute virus of mice" (MVM) in several species of sigmodontine rodent - otherwise known as “New World mice”.

Similarly, we identified a novel aveparvovirus in songbirds, suggesting viruses belonging to the Aveparvovirus genus may circulate widely among wild birds, as well as in poultry. We also identified rodent bocaparvoviruses (genus Bocaparvovirus) that were closely related to bocaparvoviruses recently reported in brown rats in China.

Together, our findings suggest that groups of closely related parvoviruses circulate widely among species in the same order or class, with the barriers to cross-species transmission within these groups being much lower than between them. These kinds of dynamics have previously been described for parvoviruses infecting carnivores.


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