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Viola, B.

Publications and source records attributed to Viola, B..

6 recordsLinked to original sources

A Method to Analyze Low-Quality Archaic Human Genomes and its Application to the Teshik-Tash 1 Neandertal

The Teshik-Tash 1 child whose remains were found in Uzbekistan represents the southeastern-most extent of the known Neandertal range, providing an important link with the better studied Caucasus and Altai Mountain ranges. However, due to poor DNA preservation, studying the genetics of Teshik Tash 1 has remained elusive. Here we present analyses of the nuclear DNA from the Teshik-Tash 1, from extracts that are highly contaminated with present-day human DNA. To achieve this, we developed a new computational method, admixslug, that jointly models contamination and population relationships, in order to infer the relationship of a target individual from which only low-quality nuclear DNA is available, to high-quality archaic human genomes. After validating admixslug, we show that Teshik-Tash 1 is genetically more similar to later Neandertals from Western Eurasia than to older Neandertals from the Altai Mountains. We estimate that Teshik-Tash 1 split from the Western Eurasian lineage between 80,000 and 100,000 years ago. Despite the geographical proximity of Teshik-Tash 1 to the Denisovan range, we find no evidence for Denisovan ancestry in his genome. Our results demonstrate that admixslug enables the study of archaic human specimens in cases where DNA preservation was previously considered too poor for population genetic analyses.

genetics↗

Mass mortality of southern elephant seals during multi-species outbreak of HPAI H5N1 on sub-Antarctic Heard Island

High pathogenicity avian influenza (HPAI) has spread across the sub-Antarctic, causing significant wildlife impacts. We report its first detection in an Australian external territory, Heard Island and McDonald Islands, which supports over one million breeding seabirds and seals. Drone and ground surveys (October 2025, January 2026), combined with viral genome analysis, confirmed infection with Influenza A H5N1 clade 2.3.4.4b at Heard Island. Drone surveys revealed mass mortality in southern elephant seals, with 8,573 pups (62%) recorded dead across Heard Island by the final surveys. Mortality increased at an average rate of 5.6% per day in a subset of harems, and the highest observed mortality in a harem was 97%. Based on the average (76%) mortality in the final surveys, total estimated pup mortality at Heard Island was 13,359 (from a total population of 17,364 pups), though this may be an underestimate as mortality was ongoing at this time. HPAI was detected in six of nine species tested and, we suspect, led to elevated mortality in king and gentoo penguins. Phylogenetic analysis indicates the virus was introduced from Crozet Islands, with an estimated arrival around August 2025. These data show the continued easterly spread of HPAI around the sub-Antarctic, with severe but heterogeneous impacts across taxa. Our results demonstrate the value of drones for large-scale monitoring, underscoring the need for continued and enhanced HPAI surveillance across the Southern Ocean.

ecology↗

A high-coverage genome from a 200,000-year-old Denisovan

Denisovans, an extinct sister group of Neandertals who lived in Eastern Eurasia during the Middle and Late Pleistocene, are known only from a handful of skeletal remains and limited genetic data, including the high-coverage genome of a woman who lived [~]65,000 years ago. Here, we present a second high-quality Denisovan genome, reconstructed from a molar found at Denisova Cave. It belonged to a man who lived [~]200,000 years ago in a small Denisovan group. This group mixed with early Neandertals and was then replaced by Denisovans who had mixed with later Neandertals. We show that in addition Denisovans received gene flow from hominins that diverged before the split of the ancestors of Denisovans and modern humans. The two Denisovan genomes allow us to disentangle Denisovan ancestry in present-day humans revealing contributions from at least three distinct Denisovan groups. In particular, Oceanians and South Asians independently inherited DNA from a deeply diverged Denisovan population which was likely isolated in South Asia. This supports an early migration of the ancestors of Oceanians through South Asia followed by the later arrival of the ancestors of present-day South Asians. East Asians do not share this Denisovan component in their genomes, suggesting that their ancestors arrived independently, perhaps by a northerly route. Finally, the two high-quality Denisovan genomes allow us to refine the catalogue of genetic changes that arose on the Denisovan lineage, some of which were contributed to present-day humans.

genomics↗

Archaic Adaptive Introgression in Modern Human Reproductive Genes

Modern humans and archaic hominins, namely Denisovans and Neanderthals, have been demonstrated to have a long history of admixture. Specifically, some of these admixture events have been adaptive and allowed modern humans to adapt to their new environments outside of Africa. Little research has been done on the impact of archaic introgression on genes associated with reproduction. In this study we report evidence of putative adaptive introgression of 118 genes within modern humans that have been previously associated with reproduction in mice or modern humans. From these genes we identified 11 archaic core haplotypes, three that have been positively selected. Additionally, we found that 327 archaic alleles have genome-wide significance for a variety of traits and 308 of these variants were discovered to be eQTLs regulating 176 genes. We highlight that 81% of the archaic eQTLs overlapping a core haplotype region regulate genes expressed in ovaries, prostate, testes, and vagina compared to other tissues. We also found that several of the putatively adaptively introgressed genes in our results are enriched in developmental and cancer pathways. Further, some of these genes have been associated with embryo development and reproductive-inhibiting phenotypes like preeclampsia. Lastly, we found that archaic alleles overlapping an introgressed segment on chromosome 2 are protective against prostate cancer. Taken together, our results describe how archaic haplotypes, when introduced into a modern human background, may be important in regulating development across the lifespan of an individual.

evolutionary biology↗

Exploring adaptive introgression in modern human circadian rhythm genes

Interbreeding between modern humans and archaic hominins, including Neanderthals and Denisovans, occurred as modern humans migrated outside of Africa. Here, we report on evidence of introgression from archaic hominins within genomic regions associated with circadian rhythm and chronotype using 76 worldwide modern human populations from the Human Genome Diversity Project and 1000 Genomes Project. We calculated the extent of regions indicative of adaptive introgression across the autosomes and identified regions that are suggested to be under positive selection. We tested for evidence of a latitudinal cline within 36 core haplotypes along with presenting the likely archaic donor for each of these haplotypes. We identified 265 independent segments that overlap genes described as having a circadian rhythm component or contain variants and segments previously identified as being associated with circadian rhythm or chronotype. Within these segments we found 1,729 archaically derived variants with allele frequencies of at least 40% intersecting 303 genes and intergenic segments. Seventeen of these segments show evidence of positive selection, three of which are found within our core haplotypes. We found that many of our genes are associated with the immune system or gastrointestinal function. Additionally, variants associated with complex traits such as schizophrenia and bipolar disorder are present within our adaptively introgressed regions. Lastly, genes and markers associated with sleep and chronotype phenotypes and serotonin pathways were also found in our adaptive introgression results, potentially signalling selection on genes related to seasonal light variation as modern humans migrated into new environments after leaving Africa. Author summaryAs modern humans migrated out of Africa, they encountered archaic hominins, the Neanderthals and Denisovans, and interbred with them. Signatures of these admixture events can be found in populations across the world. The result of these admixture events has shaped modern human evolution regarding high altitude adaptation, immune function, and skin and hair colour, to name a few. However, much of this information has been gathered with a focus on Eurasian populations using the 1000 Genomes Project samples. Here, we take advantage of newly published resources from 76 worldwide modern human populations to investigate how strongly a role admixture played on modern human circadian rhythm genes. Circadian rhythms have been tied to sleep-wake regulation, immune function, and digestive health. We find evidence for adaptive introgression in over 300 genes and intergenic segments. Many of these genes, like AMIGO2, are associated with complex traits such as schizophrenia and bipolar disorder or with immune system function, like JAK1. Some of these traits have been previously described before regarding archaic admixture. Interestingly, many of these associated traits are influenced by circadian rhythm oscillations, providing a new perspective on interpreting these findings.

genomics↗

A high-coverage Neandertal genome from Chagyrskaya Cave

We sequenced the genome of a Neandertal from Chagyrskaya Cave in the Altai Mountains, Russia, to 27-fold genomic coverage. We estimate that this individual lived ~80,000 years ago and was more closely related to Neandertals in western Eurasia (1,2) than to Neandertals who lived earlier in Denisova Cave (3), which is located about 100 km away. About 12.9% of the Chagyrskaya genome is spanned by homozygous regions that are between 2.5 and 10 centiMorgans (cM) long. This is consistent with that Siberian Neandertals lived in relatively isolated populations of less than 60 individuals. In contrast, a Neandertal from Europe, a Denisovan from the Altai Mountains and ancient modern humans seem to have lived in populations of larger sizes. The availability of three Neandertal genomes of high quality allows a first view of genetic features that were unique to Neandertals and that are likely to have been at high frequency among them. We find that genes highly expressed in the striatum in the basal ganglia of the brain carry more amino acid-changing substitutions than genes expressed elsewhere in the brain, suggesting that the striatum may have evolved unique functions in Neandertals.

genomics↗