The Grizzly, December 4, 1981

Dealing With Financial Pressure • EcBA Department Interviews for New Positions • Freshman Relates Pre-Collegiate Experiences in Japan • Union Evaluation Prompts Improvement • Campus-wide Planning Meeting Sets Competitive Goals for UC • Residents Fix Up Curtis Hall • Lucas Named To PaCIE • \u27Messiah\u27 Rehearsal Open to Public • Jarvis and Rutherford in Last Coffeehouse • Best Albums of 1981 • Senior Poet Honored Nationally • New Wrestlers Lead the Way • Girls B-Ball Prime for Opener • Baseball Team Has New Skipper • Men\u27s Swimmers Take Third Place • Hoopsters Off to Slow Start • Gymnasts Pleasing • Women\u27s Swim Team Prepares for Tough Schedule • Mike Fagan All-MAChttps://digitalcommons.ursinus.edu/grizzlynews/1069/thumbnail.jp

A Systematically Improved High Quality Genome and Transcriptome of the Human Blood Fluke Schistosoma mansoni

Schistosomiasis is one of the most prevalent parasitic diseases, affecting millions of people in developing countries. Amongst the human-infective species, Schistosoma mansoni is also the most commonly used in the laboratory and here we present the systematic improvement of its draft genome. We used Sanger capillary and deep-coverage Illumina sequencing from clonal worms to upgrade the highly fragmented draft 380 Mb genome to one with only 885 scaffolds and more than 81% of the bases organised into chromosomes. We have also used transcriptome sequencing (RNA-seq) from four time points in the parasite's life cycle to refine gene predictions and profile their expression. More than 45% of predicted genes have been extensively modified and the total number has been reduced from 11,807 to 10,852. Using the new version of the genome, we identified trans-splicing events occurring in at least 11% of genes and identified clear cases where it is used to resolve polycistronic transcripts. We have produced a high-resolution map of temporal changes in expression for 9,535 genes, covering an unprecedented dynamic range for this organism. All of these data have been consolidated into a searchable format within the GeneDB (www.genedb.org) and SchistoDB (www.schistodb.net) databases. With further transcriptional profiling and genome sequencing increasingly accessible, the upgraded genome will form a fundamental dataset to underpin further advances in schistosome research

Формирование эмоциональной культуры как компонента инновационной культуры студентов

Homozygosity has long been associated with rare, often devastating, Mendelian disorders1 and Darwin was one of the first to recognise that inbreeding reduces evolutionary fitness2. However, the effect of the more distant parental relatedness common in modern human populations is less well understood. Genomic data now allow us to investigate the effects of homozygosity on traits of public health importance by observing contiguous homozygous segments (runs of homozygosity, ROH), which are inferred to be homozygous along their complete length. Given the low levels of genome-wide homozygosity prevalent in most human populations, information is required on very large numbers of people to provide sufficient power3,4. Here we use ROH to study 16 health-related quantitative traits in 354,224 individuals from 102 cohorts and find statistically significant associations between summed runs of homozygosity (SROH) and four complex traits: height, forced expiratory lung volume in 1 second (FEV1), general cognitive ability (g) and educational attainment (nominal p<1 × 10−300, 2.1 × 10−6, 2.5 × 10−10, 1.8 × 10−10). In each case increased homozygosity was associated with decreased trait value, equivalent to the offspring of first cousins being 1.2 cm shorter and having 10 months less education. Similar effect sizes were found across four continental groups and populations with different degrees of genome-wide homozygosity, providing convincing evidence for the first time that homozygosity, rather than confounding, directly contributes to phenotypic variance. Contrary to earlier reports in substantially smaller samples5,6, no evidence was seen of an influence of genome-wide homozygosity on blood pressure and low density lipoprotein (LDL) cholesterol, or ten other cardio-metabolic traits. Since directional dominance is predicted for traits under directional evolutionary selection7, this study provides evidence that increased stature and cognitive function have been positively selected in human evolution, whereas many important risk factors for late-onset complex diseases may not have been

Genetic mechanisms of critical illness in COVID-19.

Host-mediated lung inflammation is present1, and drives mortality2, in the critical illness caused by coronavirus disease 2019 (COVID-19). Host genetic variants associated with critical illness may identify mechanistic targets for therapeutic development3. Here we report the results of the GenOMICC (Genetics Of Mortality In Critical Care) genome-wide association study in 2,244 critically ill patients with COVID-19 from 208 UK intensive care units. We have identified and replicated the following new genome-wide significant associations: on chromosome 12q24.13 (rs10735079, P = 1.65 × 10-8) in a gene cluster that encodes antiviral restriction enzyme activators (OAS1, OAS2 and OAS3); on chromosome 19p13.2 (rs74956615, P = 2.3 × 10-8) near the gene that encodes tyrosine kinase 2 (TYK2); on chromosome 19p13.3 (rs2109069, P = 3.98 ×  10-12) within the gene that encodes dipeptidyl peptidase 9 (DPP9); and on chromosome 21q22.1 (rs2236757, P = 4.99 × 10-8) in the interferon receptor gene IFNAR2. We identified potential targets for repurposing of licensed medications: using Mendelian randomization, we found evidence that low expression of IFNAR2, or high expression of TYK2, are associated with life-threatening disease; and transcriptome-wide association in lung tissue revealed that high expression of the monocyte-macrophage chemotactic receptor CCR2 is associated with severe COVID-19. Our results identify robust genetic signals relating to key host antiviral defence mechanisms and mediators of inflammatory organ damage in COVID-19. Both mechanisms may be amenable to targeted treatment with existing drugs. However, large-scale randomized clinical trials will be essential before any change to clinical practice

Increasing frailty is associated with higher prevalence and reduced recognition of delirium in older hospitalised inpatients: results of a multi-centre study

Purpose: Delirium is a neuropsychiatric disorder delineated by an acute change in cognition, attention, and consciousness. It is common, particularly in older adults, but poorly recognised. Frailty is the accumulation of deficits conferring an increased risk of adverse outcomes. We set out to determine how severity of frailty, as measured using the CFS, affected delirium rates, and recognition in hospitalised older people in the United Kingdom. Methods: Adults over 65 years were included in an observational multi-centre audit across UK hospitals, two prospective rounds, and one retrospective note review. Clinical Frailty Scale (CFS), delirium status, and 30-day outcomes were recorded. Results: The overall prevalence of delirium was 16.3% (483). Patients with delirium were more frail than patients without delirium (median CFS 6 vs 4). The risk of delirium was greater with increasing frailty [OR 2.9 (1.8–4.6) in CFS 4 vs 1–3; OR 12.4 (6.2–24.5) in CFS 8 vs 1–3]. Higher CFS was associated with reduced recognition of delirium (OR of 0.7 (0.3–1.9) in CFS 4 compared to 0.2 (0.1–0.7) in CFS 8). These risks were both independent of age and dementia. Conclusion: We have demonstrated an incremental increase in risk of delirium with increasing frailty. This has important clinical implications, suggesting that frailty may provide a more nuanced measure of vulnerability to delirium and poor outcomes. However, the most frail patients are least likely to have their delirium diagnosed and there is a significant lack of research into the underlying pathophysiology of both of these common geriatric syndromes

The Importance of Motherhood among Women in the Contemporary United States

We contribute to feminist and gender scholarship on cultural notions of motherhood by analyzing the importance of motherhood among mothers and non-mothers. Using a national probability sample (N = 2,519) of U.S. women ages 25-45, we find a continuous distribution of scores measuring perceptions of the importance of motherhood among both groups. Employing OLS multiple regression, we examine why some women place more importance on motherhood, focusing on interests that could compete with valuing motherhood (e.g., education, work success, leisure), and controlling for characteristics associated with becoming a mother. Contrary to cultural schemas that view mother and worker identities as competing, we find that education level is not associated with the importance of motherhood for either group and that valuing work success is positively associated with valuing motherhood among mothers. Consistent with feminist explanations for delayed fertility, valuing leisure is negatively associated with valuing motherhood for non-mothers

'The Hand on the Doorknob': Visit Agenda Setting by Complex Patients and Their Primary Care Physicians

Choosing which issues to discuss in the limited time available during primary care visits is an important tasks for complex patients with chronic conditions

Strategic national approach for improving the conservation management of insects and allied invertebrates in Australia

Despite progress in recent decades, the conservation management of insects and allied invertebrates in Australia is challenging and remains a formidable task against a background of poor taxonomic and biological knowledge, limited resources (funds and scientific expertise) and a relatively low level of community engagement, education and awareness. In this review, we propose a new, strategic national approach for the conservation of insects and allied invertebrates in Australia to complement and build on existing actions and increase awareness with the general public and government. A review of all species listed under relevant State and Territory Acts, national legislation (EPBC Act) and on international lists (IUCN Red List) indicated that of the 285 species currently listed under these conservation schedules, 10 (3%) are considered extinct, 204 (72%) threatened (Critically Endangered, Endangered or Vulnerable) and 71 (25%) are classified as other (Threatened, Near Threatened, Rare or Least Concern). Comparison of the geographic ranges of listed species in relation to bioregions (IBRA regions) shows a striking discordance in spatial representation across the Australian landscape, reflecting an ad hoc approach to threatened species conservation and the concentration of invertebrate biologists in urban centres of temperate coastal Australia. There is a positive relationship between the number of threatened species and extent of protection according to the National Reserve System within each IBRA region, exemplifying the anomaly in spatial representativeness of listed species. To overcome these shortfalls, we propose a novel educational, regional approach based on selecting, for each of the 89 IBRA regions, a relatively small set of ‘flagship taxa’ (threatened species and/or ‘iconic’ species of high scientific/social value), which are then promoted and/or nominated for listing by the scientific community. Such species could be adopted by local community groups whereby a community‐based regional approach would ensure spatial representativeness of insect conservation across the entire Australian continent. This novel approach may ultimately provide a better strategy for the conservation management of habitats and threatened ecological communities, reducing extinction risk of threatened species and addressing key threatening processes. Members of the Australian entomological community are strongly encouraged to nominate candidate taxa as flagship species for wider promotion and/or listing nationally under the EPBC Act.The authors, as members of the Australian Entomological Society Conservation Committee, gratefully acknowledge the Australian Entomological Society for financial support towards the preparation of this paper