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Gibbs, J.

Publications and source records attributed to Gibbs, J..

10 recordsLinked to original sources

Ecological and evolutionary impacts of urbanization: applying a causal modeling framework

As the fastest-growing form of land use, urbanization drives profound environmental change that reshapes biodiversity. Studies often characterize biodiversity patterns along urban-rural gradients with statistical models that include one or more generic indices of urbanization. Such models may be useful for prediction, but they do not permit explicit tests of causal hypotheses by which urbanization mediates ecological and evolutionary processes. Here, we show how a graphical causal modeling framework with directed acyclic graphs (DAGs) can be used to design clear conceptual models and inform appropriate statistical analysis to better evaluate mechanistic hypotheses about the effects of urbanization on biodiversity. We first introduce the basic structure of DAGs and illustrate their value with simulated datasets. We then apply the framework to a case study on coat color variation in eastern gray squirrels (Sciurus carolinensis) along an urbanization gradient in Syracuse, New York, USA. We show how statistical models ungrounded in causal assumptions are difficult to interpret and can lead to misleading conclusions about mechanisms in urban ecology and evolution. In contrast, DAGs - by making causal assumptions transparent - help researchers identify appropriate control variables for statistical models to estimate the effects of interest. When applied to our case study, statistical models informed by a DAG revealed a surprising finding: although squirrel melanism was more prevalent in urban than rural populations, the prevalence of melanism was constrained by components of environmental change common to cities, namely roads, forest loss, and predator activity, contrary to expectations. Managing biodiversity in an increasingly urbanized world will require a mechanistic understanding of how urbanization impacts biodiversity patterns; graphical causal models such as DAGs can provide a powerful approach to do so.

evolutionary biology↗

Syncytia Formation Promotes Virus Resistance to Interferon and Neutralizing Antibodies

SARS-CoV-2, like many viruses, generates syncytia but the role of syncytia formation in viral evolution remains unknown. Using SARS-CoV-2 and SARS-CoV-2 Spike (S) replacement vesicular stomatitis (VSV), we show that S-mediated syncytia impair the antiviral effects of interferons in cultured cells, human lung cell cultures, and hACE2 transgenic mice. Amino acid substitutions that modulate syncytia formation in Delta- and Omicron-encoded S have parallel effects on viral interferon resistance. S-mediated syncytia compromise antibody-mediated virus neutralization in cultured cells. We recapitulate interferon and neutralizing antibody resistance in syncytia generated by the orthoreovirus p14 fusion-associated small transmembrane (FAST) protein in VSV, influenza virus, and seasonal coronavirus OC43 infections. These findings explain selection of SARS-CoV-2 fusogenic variants in humans and, more generally, the evolution of fusogenic viruses driven by adaptive and innate immunity.

microbiology↗

A century of sampling at an ecological preserve reveals declining diversity of wild bees

We analyzed the wild bee community from 1921 to 2018 at a nature preserve in southern Michigan, USA using museum records and found significant shifts in the bee community. Across the near century of records, species richness peaked in the 1970s and 1980s. There was an intensive bee survey completed by F.C. Evans in 1972 and 1973. We attempted to replicate his effort in 2017 and 2018, and again found a significant decline in species richness and evenness. There was also evidence of declining abundance in many of the more common species. We also conducted traits analyses using neural networks, revealing that oligolectic ground-nesting bees and cleptoparasitic bees were more likely to be extirpated whereas polylectic cavity-nesting bees were more likely to have persisted. Additionally, larger body size was associated with increased probability of local extirpation for polylectic cavity-nesting species. Larger phenological range was associated with increased chances of persistence for polylectic species, while it was associated with extirpation for oligolectic ground-nesting species. Species in the contemporary samples also had a more southerly overall distribution compared to the historic one. Open Research StatementData used for analyses in this manuscript, including Evans original dataset from 1972/1973 with updated species nomenclature, will be permanently archived at the USDA Ag Data Commons after the acceptance of this manuscript and will be citable and accessible here: https://data.nal.usda.gov/dataset/century-sampling-ecological-preserve-reveals-declining-diversity-wild-bees. Complete instructions on how to access all data referenced in this manuscript can be found in Appendix S1.

ecology↗

Parallel evolution of urban-rural clines

Urbanization is the dominant trend of global land use change. The replicated nature of environmental change associated with urbanization should drive parallel evolution, yet insight into the repeatability of evolutionary processes in urban areas has been limited by a lack of multi-city studies. Here we leverage community science data on coat color in >60,000 eastern gray squirrels (Sciurus carolinensis) across 43 North American cities to test for parallel clines in melanism, a genetically based trait associated with thermoregulation and crypsis. We show the prevalence of melanism was positively associated with urbanization as measured by impervious cover. Urban-rural clines in melanism were strongest in the largest cities with extensive forest cover and weakest or absent in cities with warmer winter temperatures, where thermal selection likely limits the prevalence of melanism. Our results suggest that novel traits can evolve in a highly repeatable manner among urban areas, modified by factors intrinsic to individual cities, including their size, land cover, and climate.

evolutionary biology↗

Relationship Between Inter-individual Variation in Circadian Rhythm and Sociality: A case Study Using Halictid Bees

The bee family Halictidae is considered to be an optimal model for the study of social evolution due to its remarkable range of social behaviors. Past studies in circadian rhythms suggest that social species may express more diversity in circadian behaviors than solitary species. However, these previous studies did not make appropriate taxonomic comparisons. To further explore the link between circadian rhythms and sociality, we examine four halictid species with different degrees of sociality, three social species of Lasioglossum, one from Greece and two from Puerto Rico, and a solitary species of Systropha from Greece. Based on our previous observations, we hypothesized that species with greater degree of sociality will show greater inter-individual variation in circadian rhythms than solitary species. We observed distinct differences in their circadian behavior that parallel differences across sociality, where the most social species expressed the highest inter-individual variation. We predict that circadian rhythm differences will be informative of sociality across organisms.

animal behavior and cognition↗

Pollinator habitat plantings benefit wild, native bees, but do not necessarily favor rare species

O_LIInstalling pollinator habitat is a ubiquitous conservation tool, but little is known about which pollinator taxa require support, or which benefit from habitat installations. C_LIO_LIWe studied the response of rare and common bees to pollinator habitat enhancement. We used independent regional datasets to designate bee species as common or rare based on their rank according to one of three metrics: a) site occurrence frequency, b) local relative abundance, and c) geographic range size. We asked whether the abundance or richness of rare and common bees were greater in pollinator habitat, relative to old-field controls. Because we used an arbitrary, quantile-based cutoff to categorize species rarity, we conducted sensitivity analysis and controlled for rarity classification errors with a null model. With this null model, we determined whether rare and/or common species responded to pollinator habitat disproportionately, compared to the expectation for typical bee species. C_LIO_LIWe found that the number of individuals and of species designated as rare based on local relative abundance was greater in pollinator habitat enhancements. The number of individuals from bee species designated as rare based on site occurrence was lower in pollinator habitat enhancements, but the number of species was not clearly different between habitat types. We did not find a clear positive nor negative effect of habitat enhancement for species designated rare based on geographic range size. For all three rarity metrics, common species increased in abundance and richness in pollinator habitat relative to controls. Null models indicated that in most cases, neither rare nor common species disproportionately benefited from pollinator habitat. C_LIO_LISynthesis and Applications: Our results suggest that pollinator habitat can lead to an increase in the abundance and richness of bees, including species that are rare and that are common. However, rare species appeared to respond differently than typical species, and depending on how species were classified as rare, could display muted or even negative responses to habitat enhancement. Targeting rare species with specific floral resources or unique habitat types may lead to better outcomes for rare and threatened species. C_LI

ecology↗

Evoked and spontaneous pain assessment during tooth pulp injury

Injury of the tooth pulp is excruciatingly painful and yet the receptors and neural circuit mechanisms that transmit this form of pain remain poorly defined in both the clinic and preclinical rodent models. Easily quantifiable behavioral assessment in the rodent orofacial area remains a major bottleneck in uncovering molecular mechanisms that govern inflammatory pain in the tooth. Here we use a dental pulp injury model in the mouse and expose the tooth pulp to the outside environment, a procedure we have previously shown produces pulpal inflammation. We demonstrate here with RNAscope technology in the trigeminal ganglion of injured mice, an upregulation of genes that contribute to the inflammatory pain state. Using both evoked and spontaneous measures of pain in the orofacial area, including application of von Frey Hair filaments and pain feature detection with the mouse grimace scale, we reveal a differential timeline of induction of spontaneous pain versus mechanical allodynia following pulpal injury. This work demonstrates that tooth pain can be easily assessed in freely behaving mice using approaches common for other types of pain assessment. Harnessing these assays in the orofacial area during gene manipulation should assist in uncovering mechanisms for tooth pulp inflammation and other forms of trigeminal pain.

neuroscience↗

Discovery Of UFO Proteins: Human-Virus Chimeric Proteins Generated During Influenza Virus Infection

Influenza A virus (IAV) is a threat to mankind because it generates yearly epidemics and poorly predictable sporadic pandemics with catastrophic potential. IAV has a small RNA genome composed of 8 mini-chromosomes (segments) that constitute a 5UTR followed by a coding region and a 3UTR. Transcription of IAV RNA into mRNA depends on host mRNA, as the viral polymerase cleaves 5m7G-capped nascent transcripts to use as primers to initiate viral mRNA synthesis. We hypothesized that captured host transcripts bearing AUG could drive the expression of upstream ORFs in the viral segments, a phenomenon that would depend on the translatability of the viral 5UTRs. Here we report the existence of this mechanism, which generates host-virus chimeric proteins. We label these proteins as Upstream Flu ORFs (UFO). Depending on the frame, two types of host-virus UFO proteins are made: canonical viral proteins with human-derived N term extensions or novel uncharacterized proteins. Here we show that both types are made during IAV infection. Sequences that enable chimeric protein synthesis are conserved across IAV strains, indicating that selection allowed the expansion of the proteome diversity of IAV in infected cells to include multiple human-virus proteins.

microbiology↗

A comprehensive assessment of benign genetic variability for neurodegenerative disorders

1AbstractOver the last few years, as more and more sequencing studies have been performed, it has become apparent that the identification of pathogenic mutations is, more often than not, a complex issue. Here, with a focus on neurodegenerative diseases, we have performed a survey of coding genetic variability that is unlikely to be pathogenic.\n\nWe have performed whole-exome sequencing in 478 samples derived from several brain banks in the United Kingdom and the United States of America. Samples were included when subjects were, at death, over 60 years of age, had no signs of neurological disease and were subjected to a neuropathological examination, which revealed no evidence of neurodegeneration. This information will be valuable to studies of genetic variability as a causal factor for neurodegenerative syndromes. We envisage it will be particularly relevant for diagnostic laboratories as a filter step to the results being produced by either genome-wide or gene-panel sequencing. We have made this data publicly available at www.alzforum.org/exomes/hex.

genomics↗

Influenza A Virus Negative Strand RNA is Translated for CD8+ T Cell Immunosurveillance

To probe the limits of CD8+ T cell immunosurveillance, we inserted the model peptide SIINFEKL into influenza A virus (IAV) negative strand gene segments. Although IAV genomic RNA is widely considered as non-coding, there is a conserved, relatively long open reading frame present in the genomic strand of segment eight, encoding a potential protein termed NEG8. The biosynthesis of NEG8 from IAV has yet to be demonstrated. While we failed to detect NEG8 protein expression in IAV infected cells, cell surface Kb-SIINFEKL complexes are generated when SIINFEKL is genetically appended to the predicted COOH-terminus of NEG8, as shown by activation of OT-I T cells in vitro and in vivo. Moreover, recombinant IAV encoding SIINFEKL embedded in the negative strand of the NA-stalk coding sequence also activates OT-I T cells in vivo. Together, our findings demonstrate both the translation of sequences on the negative strand of a single stranded RNA virus and its relevance anti-viral immunosurveillance.\n\nSignificanceEvery gene encodes complementary information on the opposite strand that can potentially be used for immunosurveillance. In this study, we show that the influenza A virus \"non-coding\" strand translated into polypeptides during a viral infection of either cultured cells or mice that can be recognized by CD8+ T cells. Our findings raise the possibility that influenza virus uses its negative strand to generate proteins useful to the virus. More generally, it adds to a growing literature showing that immunosurveillance extends to gene sequences generally thought not to be converted into proteins. The relevance of translating this \"dark\" information extends from viral immunity to cancer immunotherapy and autoimmunity.

immunology↗