Zinc is an essential nutrient for humans; however, a sensitive biomarker to assess zinc status has not been identified. The objective of this study was to determine the reliability and sensitivity of zinc transporter and metallothionein (MT) genes in peripheral blood mononuclear cells (PBMCs) to zinc exposure ex vivo and to habitual zinc intake in human subjects. In study 1, human PBMCs were cultured for 24 h with 0-50 µM ZnSO4 with or without 5 µM N,N,N’,N’-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN) and mRNA expression of SLC30A1-10, SLC39A1-14, MT1 subtypes (A, B, E, F, G, H, L, M, and X), MT2A, MT3, and MT4 mRNA was determined. In study 2, 54 healthy male and female volunteers (31.9 ± 13.8 y, BMI 25.7 ± 2.9 kg/m2) completed a Food Frequency Questionnaire, blood was collected, PBMCs were isolated, and mRNA expression of selected zinc transporters and metallothionein isoforms was determined. Study 1: MT1E, MT1F, MT1G, MT1H, MT1L, MT1M, MT1X, MT2A, and SLC30A1 increased with increased with increasing concentrations of zinc and declined with the addition of TPEN. Study 2: Average daily zinc intake was 16.0 ± 5.3 mg/d (range: 9–31 mg/d) and plasma zinc concentrations were 101.4 ± 18.0 μg/dL (range: 68-153 μg/dL). PBMC MT2A was positively correlated with dietary zinc intake (r=0.306, P=0.03) and total zinc intake (r=0.382, P<0.01), whereas plasma zinc was not (P>0.05 for both). Findings suggest that MT2A mRNA in PBMCs reflects dietary zinc intake in healthy adults and may be a component in determining zinc status.

Previous studies have stressed the role of a child's family environment for future political participation. This field of research has, however, overlooked that children within the same family have different experiences depending on their birth order. First-borns spend their first years of life without having to compete over their parents' attention and resources, while their younger siblings are born into potential rivalry. We examine differences in turnout depending on birth order, using unique population-wide individual level register data from Sweden and Norway that enables precise within-family estimates. We consistently find that higher birth order entails lower turnout, and that the turnout differential with respect to birth order is stronger when turnout is lower. The link between birth order and turnout holds when we use data from four other, non-Nordic countries. This birth order effect appears to be partly mediated by socio-economic position and attitudinal predispositions.

Advances in the fabrication and characterization of polymeric nanomaterials has greatly advanced the miniaturization of soft actuators, creating materials capable of replicating the functional physical behavior previously limited to the macroscale. Here, we demonstrate how a reversible shape-memory polymer actuation can be generated in a single micro/nano object, where the shape change during actuation of an individual fiber can be dictated by programming using an AFM-based method. Electrospinning was used to prepare poly(ε-caprolactone) micro-/nanofibers, which were fixed and crosslinked on a structured silicon wafer. The programming as well as the observation of recovery and reversible displacement of the fiber were performed by vertical three point bending, using an AFM testing platform introduced here. A plateau tip was utilized to improve the stability of the fiber contact and working distance, enabling larger deformations and greater rbSMPA performance. Values for the reversible elongation of εrev = 3.4 ± 0.1% and 10.5 ± 0.1% were obtained for a single micro (d = 1.0 ± 0.2 μm) and nanofiber (d = 300 ± 100 nm) in cyclic testing between the temperatures 10 and 60 °C. The reversible actuation of the nanofiber was successfully characterized for 10 cycles. The demonstration and characterization of individual shape-memory nano and microfiber actuators represents an important step in the creation of miniaturized robotic devices capable of performing complex physical functions at the length scale of cells and structural component of the extracellular matrix.

OBJECTIVES/GOALS: To determine the prevalence of myocardial diastolic dysfunction (DD) and association of serum concentration of the cardiac biomarker serum soluble ST2 in HIV-infected as compared to uninfected Tanzanian adults at the time of HIV diagnosis. METHODS/STUDY POPULATION: In this cross-sectional study we consecutively enrolled HIV-infected participants and uninfected controls at a large, referral HIV clinic in Mwanza, Tanzania. Standardized history, physical examination, echocardiography and serum samples were obtained. The primary outcome was prevalence of myocardial diastolic dysfunction in HIV-infected as compared to uninfected adults. The secondary outcome was the association of baseline serum sST2 concentration with diastolic dysfunction prevalence. Regression models were used to quantify the associations. RESULTS/ANTICIPATED RESULTS: We enrolled 388 HIV-infected, ART naïve and 461 HIV-uninfected controls. Participants with HIV had a higher prevalence of DD (OR = 2.44, p = 0.001, controlled for age, sex, hypertension and BMI) and more severe dysfunction (66.7% vs 42.5%, p = 0.056) at an earlier age. Baseline serum sST2 concentration was significantly associated with DD in HIV-infected but not uninfected participants (p = 0.04 and 0.90, respectively). More HIV-infected adults with concurrent DD exceeded the threshold of 35ng/mL as compared to controls (15.7% vs 5.3%, p<0.0001). Additionally, a significant population level shift to higher sST2 concentration was observed in HIV-infected adults with dysfunction as compared to both HIV-infected without and HIV-uninfected adults with dysfunction (Kolmogrov-Smirnov test: p = 0.02 and 0.04). DISCUSSION/SIGNIFICANCE OF IMPACT: In a large population of HIV-infected adults in sub-Saharan Africa, HIV infection is associated with myocardial diastolic dysfunction. This dysfunction is associated with higher sST2 concentrations. Therefore, we conclude that the sST2 pathway may provide insight into the pathophysiologic mechanisms of dysfunction in HIV-infected adults.

Amazona lilacina is a threatened species endemic to Ecuador, existing across a patchwork of mangroves, lowland coastal forests, agricultural and community owned land. The species was described in 2014 and listed as ‘Endangered’ on the IUCN Red List, however, full assessment of the population was lacking. Using a combination of field observations, roost surveys and community questionnaires, conducted over the last 20 years, we provide up-to-date information on the species’ Extent of Occurrence, estimate its global population size, and evaluate its level of threat. Our results suggest the species occurs across an area of 19,890 km2 in three distinct geographically isolated subpopulations. Roost surveys across the range estimate the minimum remaining population at 741–1,090 individuals and we present evidence to suggest a 60% decline over the past 19 years in one part of the species’ range. We conducted community questionnaires with 427 people from 52 communities. The presence of pet parrots was reported in 37 communities, including 17 communities which reported pet A. lilacina. From this we predict that over half of all communities within our study area keep parrots as pets and at least 96 communities keep A. lilacina. Our findings justify an IUCN Red Listing of at least ‘Endangered’ for this species and highlight the need for conservation support. In order to assess population health in more detail, further research is required to assess genetic diversity and roost dynamics, and to identify areas that may be important for feeding and nesting throughout the range. As many of these areas are likely to overlap with community owned land, we suggest that future conservation actions should revolve around, and be led by, these communities.