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Vishnivetskaya, T.

Publications and source records attributed to Vishnivetskaya, T..

2 recordsLinked to original sources

Traits enabling persistence of living Promethearchaeota in marine sediments frozen for over 100 kyr

The phylum Promethearchaeota (formerly "Asgard" archaea), the microbial progenitors of all Eukaryotes, are abundant throughout Earths subsurface, who have been hypothesized to persist over geological timescales in stable environments with little cell division. We therefore examined the genetic adaptations of Promethearchaeota after being frozen for >100 kyr by comparing metagenome-assembled genomes (MAGs) from the Kolyma Lowland, Siberia, to MAGs from other marine and terrestrial sediments worldwide. We reconstructed 22 Promethearchaeota MAGs from 5 classes (Heimdallarchaeia, Gerdarchaeia, Lokiarchaeia, Helarachaeia and Thorarchaeia). Six MAGs from the intracellular DNA fraction were > 70% complete before and after DNA repair, and therefore likely represent living Promethearchaeota that have maintained high DNA integrity under cryogenic conditions through geological time. These 6 MAGs were also over 7 times more abundant than all other Promethearchaeota MAGs based on read recruitment. These permafrost Promethearchaeota MAGs are closely related to other non-permafrost Promethearchaeota lineages at the family or genus level and share metabolic potential and genes for DNA and protein repair with them. This suggests that the ability to survive for >100 kyr in permafrost is a trait that is widespread within the Promethearchaeota. No genes were more prevalent in our permafrost MAGs compared to Promethearchaeota MAGs from other environments. The lack of detectable genetic change since these groups were frozen is consistent with the predicted state of inactivity. Furthermore, although DNA repair mechanisms were present in the Promethearchaeota/Eukaryote lineage before the eukaryotic split, Promethearchaeota protein repair mechanisms emerged after the split, suggesting that adaptations to long term dormancy, or aeonophily, may set modern Promethearchaeota apart from eukaryotes. Collectively, our study expands the known habitat range of many subgroups of Promethearchaeota to ancient marine permafrost and suggests they may have extraordinary long-term survivability under cryogenic conditions through geological time.

microbiology↗

Systems genetic discovery of host-microbiome interactions reveals mechanisms of microbial involvement in disease

The role of the microbiome in health and disease involves complex networks of host genetics, genomics, microbes and environment. Identifying the mechanisms of these interactions has remained challenging. Systems genetics in the laboratory mouse enables data-driven discovery of network components and mechanisms of host-microbial interactions underlying multiple disease phenotypes. To examine the interplay among the whole host genome, transcriptome and microbiome, we mapped quantitative trait loci and correlated the abundance of cecal mRNA, luminal microflora, physiology and behavior in incipient strains of the highly diverse Collaborative Cross mouse population. The relationships that are extracted can be tested experimentally to ascribe causality among host and microbe in behavior and physiology, providing insight into disease. Application of this strategy in the Collaborative Cross population revealed experimentally validated mechanisms of microbial involvement in models of autism, inflammatory bowel disease and sleep disorder.\n\neTOC BlurbHost genetic diversity provides a variable selection environment and physiological context for microbiota and their interaction with host physiology. Using a highly diverse mouse population Bubier et al. identified a variety of host, microbe and potentially disease interactions.\n\nHighlights* 18 significant species-specific QTL regulating microbial abundance were identified\n* Cis and trans eQTL for 1,600 cecal transcripts were mapped in the Collaborative Cross\n* Sleep phenotypes were highly correlated with the abundance of B.P. Odoribacter\n* Elimination of sleep-associated microbes restored normal sleep patterns in mice.

genetics↗