@article {4868, title = {An Antarctic worm and its soil ecosystem: A review of an emerging research program in ecological genomics}, journal = {Applied Soil Ecology}, volume = {193}, year = {2024}, month = {01/2024}, pages = {105110}, abstract = {

Relationships between the evolution of species and their ecosystems can be difficult to accurately assess due to the high number of confounding biological variables (e.g., biotic interactions among community members and the resulting complex relationships between genetic pathways and organism phenotypes). Thus, progress in ecological genomics by making inferences about fundamental ecological patterns and processes is hampered by high biodiversity and subsequent complex biotic interactions. Study systems that are naturally low in biological and ecological complexity, and strongly structured by abiotic drivers, can serve as models for bridging the gap between controlled mesocosm experiments and natural ecosystems. The terrestrial ecosystems of the Antarctic dry valleys have low biodiversity and constrained ecological complexity, primarily because ecological communities are so strongly shaped by physical, rather than biological, factors. The harsh constraints of the physical environment on organismal evolution and the structure of ecological communities make this an optimal natural system for disentangling the influence of specific environmental parameters on genotype/phenotype and gene by environment interactions. This work reviews the biology, evolution, and ecology of an emerging model organism, the free-living nematode Plectus murrayi, in a model ecosystem, the McMurdo Dry Valleys (MDVs) of Antarctica. In the MDVs, habitat suitability, including nutrient availability, has been shown to drive organismal (nematode) life history evolution, including growth and reproduction, primarily by way of changes in the expression of developmental genes. Changes in growth rates and reproductive schedules are accomplished primarily through alterations of nuclear rRNA gene copy number. The predicted and observed responses to natural experiments have been replicated in the laboratory, providing a synthesis of field observations and experimental evolution. Studying such natural model systems as this could fill several persistent knowledge gaps in our understanding of how genetic variation, genomic architecture, and gene regulation drive the genotype-phenotype paradigm, and the consequent effects of these drivers on ecosystem structure and functioning.

}, keywords = {LTER-MCM, ecological amplitude, ecological succession, elemental stoichiometry, extreme environments, life history evolution, model systems}, issn = {09291393}, doi = {10.1016/j.apsoil.2023.105110}, url = {https://www.sciencedirect.com/science/article/pii/S0929139323003086}, author = {Xue, Xia and Thompson, Andrew R. and Adams, Byron J.} } @article {4833, title = {Ecological stoichiometry drives the evolution of soil nematode life history traits}, journal = {Soil Biology and Biochemistry}, volume = {177}, year = {2023}, month = {02/2023}, pages = {108891}, abstract = {

Ecological stoichiometry is a useful theoretical framework for understanding the sources and controls on nutrient availability that structure the composition and diversity of biotic communities. One such relationship is that organismal development rate is positively linked to cellular Phosphorus (P). We hypothesized that P availability, relative to other nutrients, e.g., nitrogen and carbon, would drive the evolution of traits associated with organismal growth and development. We examined the effects of P availability both in situ and in vitro, on free-living soil nematodes. We found that P-deficient environments produce predictable changes in the ecology and evolution of important life history traits. Our results identify altered rRNA gene copy number and subsequent changes in gene expression and protein synthesis as mechanisms by which P-deficiency influences these traits. These findings have important implications for explaining soil ecological and evolutionary patterns across multiple levels of organization, including the structure and functioning of organisms, populations, communities, and ecosystems.

}, keywords = {LTER-MCM, elemental stoichiometry, growth rate hypothesis, life history theory, molecular evolution, nematoda, rRNA}, doi = {10.1016/j.soilbio.2022.108891}, url = {https://www.sciencedirect.com/science/article/pii/S0038071722003480}, author = {Xue, Xia and Bishwo N. Adhikari and Ball, Becky and John E. Barrett and Miao, Jinxin and Perkes, Ammon and Martin, Mac and Breana L. Simmons and Diana H. Wall and Byron Adams} } @article {4840, title = {Temperature response of metabolic activity of an Antarctic nematode}, journal = {Biology}, volume = {12}, year = {2023}, month = {01/2023}, pages = {109}, abstract = {

Because of climate change, the McMurdo Dry Valleys of Antarctica (MCM) have experienced an increase in the frequency and magnitude of summer pulse warming and surface ice and snow melting events. In response to these environmental changes, some nematode species in the MCM have experienced steady population declines over the last three decades, but Plectus murrayi, a mesophilic nematode species, has responded with a steady increase in range and abundance. To determine how P. murrayi responds to increasing temperatures, we measured metabolic heat and CO2 production rates and calculated O2 consumption rates as a function of temperature at 5 \°C intervals from 5 to 50 \°C. Heat, CO2 production, and O2 consumption rates increase approximately exponentially up to 40 \°C, a temperature never experienced in their polar habitat. Metabolic rates decline rapidly above 40 \°C and are irreversibly lost at 50 \°C due to thermal stress and mortality. Caenorhabditis elegans, a much more widespread nematode that is found in more temperate environments reaches peak metabolic heat rate at just 27 \°C, above which it experiences high mortality due to thermal stress. At temperatures from 10 to 40 \°C, P. murrayi produces about 6 times more CO2 than the O2 it consumes, a respiratory quotient indicative of either acetogenesis or de novo lipogenesis. No potential acetogenic microbes were identified in the P. murrayi microbiome, suggesting that P. murrayi is producing increased CO2 as a byproduct of de novo lipogenesis. This phenomenon, in conjunction with increased summer temperatures in their polar habitat, will likely lead to increased demand for carbon and subsequent increases in CO2 production, population abundance, and range expansion. If such changes are not concomitant with increased carbon inputs, we predict the MCM soil ecosystems will experience dramatic declines in functional and taxonomic diversity.

}, keywords = {LTER-MCM, Antarctica, carbon cycling, climate change, nematode, respiration rates, soil temperature}, doi = {10.3390/biology12010109}, url = {https://www.mdpi.com/2079-7737/12/1/109}, author = {Robinson, Colin Michael and Hansen, Lee D. and Xue, Xia and Adams, Byron J.} } @article {4836, title = {A draft mitogenome of Plectus murrayi}, journal = {Journal of Nematology}, volume = {54}, year = {2022}, month = {02/2022}, abstract = {

Plectus murrayi is a free-living microbivorous nematode endemic to Antarctic soils. Our draft assembly of its mitogenome was 15,656 bp long, containing 12 protein-coding, eight transfer RNA (tRNA), and two ribosomal RNA (rRNA) genes. Mitophylogenomic analyses extend our understanding of mitochondrial evolution in Nematoda

}, keywords = {LTER-MCM, Antarctica, genome decay, genomics, mitochondrial genome, MitoZ, phylogeny}, doi = {10.2478/jofnem-2022-0035}, url = {https://www.sciendo.com/article/10.2478/jofnem-2022-0035https://www.sciendo.com/pdf/10.2478/jofnem-2022-0035}, author = {Xue, Xia and Adams, Byron J. and Dilman, Adler R.} } @article {4583, title = {Genome analysis of Plectus murrayi, a nematode from continental Antarctica}, journal = {G3 Genes|Genomes|Genetics}, year = {2021}, month = {01/2021}, abstract = {

Plectus murrayi is one of the most common and locally abundant invertebrates of continental Antarctic ecosystems. Because it is readily cultured on artificial medium in the laboratory and highly tolerant to an extremely harsh environment, Plectus murrayi is emerging as a model organism for understanding the evolutionary origin and maintenance of adaptive responses to multiple environmental stressors, including freezing and desiccation. The de novo assembled genome of Plectus murrayi contains 225.741 million base pairs and a total of 14,689 predicted genes. Compared to Caenorhabditis elegans, the architectural components of Plectus murrayi are characterized by a lower number of protein-coding genes, fewer transposable elements, but more exons, than closely related taxa from less harsh environments. We compared the transcriptomes of lab-reared Plectus murrayi with wild-caught Plectus murrayi and found genes involved in growth and cellular processing were up-regulated in lab-cultured Plectus murrayi, while a few genes associated with cellular metabolism and freeze tolerance were expressed at relatively lower levels. Preliminary comparative genomic and transcriptomic analyses suggest that the observed constraints on P. murrayi genome architecture and functional gene expression, including genome decay and intron retention, may be an adaptive response to persisting in a biotically simplified, yet consistently physically harsh environment.

}, keywords = {LTER-MCM, gene loss, genome architecture, genome assembly, genome decay, Plectus murrayi}, doi = {10.1093/g3journal/jkaa045}, url = {https://academic.oup.com/g3journal/advance-article/doi/10.1093/g3journal/jkaa045/6044189}, author = {Xue, Xia and Suvorov, Anton and Fujimoto, Stanley and Dilman, Adler R. and Byron Adams} } @phdthesis {4363, title = {Genomics and transcriptomics of Antarctic nematodes reveal drivers of life history evolution and genome evolution}, volume = {Ph.D.}, year = {2018}, school = {Brigham Young University}, type = {doctoral}, address = {Provo, UT}, abstract = {

Elemental stoichiometry defines a critical understanding of the relationship between\ nutrient availability and usage throughout different levels of the biological community. We\ found there is a link between available phosphorus (P), cellular phosphorus, and nematode development as postulated by the growth rate hypothesis (GRH). I predicted that in a P-poor environment, cellular RNA concentrations would be lower than they are in P-rich environment, and thus the 18srRNA expression level will have reduced. To most efficiently regulate the\ uptake of limited P, I predicted that nematodes in P-poor environments would decrease the number of copies of the 18s rRNA gene in their genome. I measured life history traits as well as rRNA gene expression and gene copy number. We found that elemental stoichiometry predicts evolutionary changes consistent with the Growth Rate Hypothesis. We sequenced and assembled a draft genome of P. murrayi. Although we expected to find genes responsible for stress tolerance, we hypothesized that in response to strong selection pressure associated with living in\ a simplified ecosystem, over time the genome of P. murrayi should have undergone significant decay (gene loss) relative to species in ecosystems structured more strongly by biotic interactions. We found significantly fewer genes in P. murrayi. To compare patterns of gene expression between two highly divergent Antarctic nematode species, we sequenced and assembled the transcriptomes of S. lindsayae and P. murrayi. Under laboratory conditions at 4\  ̊C, S. lindsayae had significantly lower rates of gene expression but expressed a significantly larger number of genes. We speculate that the differences in gene expression are correlated with life history traits (developmental rates) while the differences in the number of genes expressed can be explained\ by their different genetic systems (S. lindsayae is amphimictic, P. murrayi is parthenogenic) and the soil environments to which they are adapted. Since we previously showed that differences in available P content can influence the evolution of gene expression via gene copy number, and that this ultimately influences growth rate, we wondered how much of this response is driven by genetics versus how strongly these patterns are driven by temperature. To better understand this, we maintained wild type populations of P. murrayi in P-rich and P-poor conditions at 5\  ̊C, 10\  ̊C and 15 ̊C in the laboratory for over 40 generations and sequenced the transcriptomes prepared from each treatment group. We found that nutrient levels played an important role in gene expression when the temperature is optimal for P. murrayi culturing and that temperature is more important in gene expression when the available P is limited. This work underscores the utility of using principles of elemental stoichiometry coupled with genomic and transcriptomics research tools to make and test predictions about life history evolution. The results of my work also\ inform inferences about the ways in which nutrient availability also drives the organization of trophic interactions and ultimately ecosystems.

}, keywords = {LTER-MCM, Antarctic nematodes, Caenorhabditis elegans, genome evolution, growth rate hypothesis, Plectus murrayi, Scottnema lindsayae, transcriptome}, url = {https://search.proquest.com/docview/2081899003}, author = {Xue, Xia and Byron Adams} }