2,597 research outputs found
Another Corn Rootworm Management Tool Fails: Assessing the Status of Western Corn Rootworms Laying Eggs in Soybeans
A variant of western com rootworm that lays eggs in crops other than com was recognized in east-central Illinois as early as 1987 (Steffey et al. 1992), although at the time we believed we were witnessing the phenomenon of extended diapause. Thereafter, the problem with com rootworm larvae damaging com planted after soybean in east-central Illinois and northwestern Indiana increased in frequency and severity during the early 1990s and emerged as a full-blown crisis in 1995. Since then, entomologists throughout the Com Belt have watched warily as the problem spread throughout northern Indiana and into southern Michigan and western Ohio. The spread of the problem westward and northward in Illinois has occurred relatively slowly. However, we annually add counties to the list of counties threatened by the new variant of western corn rootworm
Tropomodulin’s Actin-Binding Abilities Are Required to Modulate Dendrite Development
There are many unanswered questions about the roles of the actin pointed end capping and actin nucleation by tropomodulins (Tmod) in regulating neural morphology. Previous studies indicate that Tmod1 and Tmod2 regulate morphology of the dendritic arbor and spines. Tmod3, which is expressed in the brain, had only a minor influence on morphology. Although these studies established a defined role of Tmod in regulating dendritic and synaptic morphology, the mechanisms by which Tmods exert these effects are unknown. Here, we overexpressed a series of mutated forms of Tmod1 and Tmod2 with disrupted actin-binding sites in hippocampal neurons and found that Tmod1 and Tmod2 require both of their actin-binding sites to regulate dendritic morphology and dendritic spine shape. Proximity ligation assays (PLAs) indicate that these mutations impact the interaction of Tmod1 and Tmod2 with tropomyosins Tpm3.1 and Tpm3.2. This impact on Tmod/Tpm interaction may contribute to the morphological changes observed. Finally, we use molecular dynamics simulations (MDS) to characterize the structural changes, caused by mutations in the C-terminal helix of the leucine-rich repeat (LRR) domain of Tmod1 and Tmod2 alone and when bound onto actin monomers. Our results expand our understanding of how neurons utilize the different Tmod isoforms in development
Recommended from our members
Variations in Community Prevalence and Determinants of Recreational and Utilitarian Walking in Older Age
Background:. Regular walking is critical to maintaining health in older age. We examined influences of individual and community factors on walking habits in older adults. Methods:. We analyzed walking habits among participants of a prospective cohort study of 745 community-dwelling men and women, mainly aged 70 years or older. We estimated community variations in utilitarian and recreational walking, and examined whether the variations were attributable to community differences in individual and environmental factors. Results:. Prevalence of recreational walking was relatively uniform while prevalence of utilitarian walking varied across the 16 communities in the study area. Both types of walking were associated with individual health and physical abilities. However, utilitarian walking was also strongly associated with several measures of neighborhood socioeconomic status and access to amenities while recreational walking was not. Conclusions:. Utilitarian walking is strongly influenced by neighborhood environment, but intrinsic factors may be more important for recreational walking. Communities with the highest overall walking prevalence were those with the most utilitarian walkers. Public health promotion of regular walking should take this into account
Expressions 2010
https://openspace.dmacc.edu/expressions/1026/thumbnail.jp
Recommended from our members
Increased wind risk from sting-jet windstorms with climate change
Extra-tropical cyclones dominate autumn and winter weather over western Europe. The strongest cyclones, often termed windstorms, have a large socio-economic impact on landfall due to strong surface winds and coastal storm surges. Climate model integrations have predicted a future increase in the frequency of, and potential damage from, European windstorms and yet these integrations cannot properly represent localised jets, such as sting jets, that may significantly enhance damage. Here we present the first prediction of how the climatology of sting-jet-containing cyclones will change in a future warmer climate, considering the North Atlantic and Europe. A proven sting-jet precursor diagnostic is applied to 13-year present-day and future (2100) climate integrations from the Met Office Unified Model in its Global Atmosphere 3.0 configuration. The present-day climate results are consistent with previously-published results from a reanalysis dataset (with around 32\% of cyclones exhibiting the sing-jet precursor), lending credibility to the analysis of the future-climate integration. The proportion of cyclones exhibiting the sting-jet precursor in the future-climate integration increases to 45\%. Furthermore, while the proportion of explosively-deepening storms increases only slightly in the future climate, the proportion of those storms with the sting-jet precursor increases by 60\%. The European resolved-wind risk associated with explosively-deepening storms containing a sting-jet precursor increases substantially in the future climate; in reality this wind risk is likely to be further enhanced by the release of localised moist instability, unresolved by typical climate models
Evidence for Dose-Additive Effects of Pyrethroids on Motor Activity in Rats
BACKGROUND: Pyrethroids are neurotoxic insecticides used in a variety of indoor and outdoor applications. Previous research characterized the acute dose-effect functions for 11 pyrethroids administered orally in corn oil (1 mL/kg) based on assessment of motor activity. OBJECTIVES: We used a mixture of these 11 pyrethroids and the same testing paradigm used in single-compound assays to test the hypothesis that cumulative neurotoxic effects of pyrethroid mixtures can be predicted using the default dose-addition theory. METHODS: Mixing ratios of the 11 pyrethroids in the tested mixture were based on the ED30 (effective dose that produces a 30% decrease in response) of the individual chemical (i.e., the mixture comprised equipotent amounts of each pyrethroid). The highest concentration of each individual chemical in the mixture was less than the threshold for inducing behavioral effects. Adult male rats received acute oral exposure to corn oil (control) or dilutions of the stock mixture solution. The mixture of 11 pyrethroids was administered either simultaneously (2 hr before testing) or after a sequence based on times of peak effect for the individual chemicals (4, 2, and 1 hr before testing). A threshold additivity model was fit to the single-chemical data to predict the theoretical dose-effect relationship for the mixture under the assumption of dose additivity. RESULTS: When subthreshold doses of individual chemicals were combined in the mixtures, we found significant dose-related decreases in motor activity. Further, we found no departure from the predicted dose-additive curve regardless of the mixture dosing protocol used. CONCLUSION: In this article we present the first in vivo evidence on pyrethroid cumulative effects supporting the default assumption of dose addition.Fil: Wolansky, Marcelo Javier. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Biológica; ArgentinaFil: Gennings, Chris. Solveritas; Estados UnidosFil: DeVito, Michael J.. U.S. Environmental Protection Agency; Estados UnidosFil: Crofton, Kevin M.. U.S. Environmental Protection Agency; Estados Unido
Global gene expression analysis of human erythroid progenitors
This article is available open access through the publisher’s website. Copyright @ 2011 American Society of Hematology. This article has an erratum: http://bloodjournal.hematologylibrary.org/content/118/26/6993.3.Understanding the pattern of gene expression during erythropoiesis is crucial for a synthesis of erythroid developmental biology. Here, we isolated 4 distinct populations at successive erythropoietin-dependent stages of erythropoiesis, including the terminal, pyknotic stage. The transcriptome was determined using Affymetrix arrays. First, we demonstrated the importance of using defined cell populations to identify lineage and temporally specific patterns of gene expression. Cells sorted by surface expression profile not only express significantly fewer genes than unsorted cells but also demonstrate significantly greater differences in the expression levels of particular genes between stages than unsorted cells. Second, using standard software, we identified more than 1000 transcripts not previously observed to be differentially expressed during erythroid maturation, 13 of which are highly significantly terminally regulated, including RFXAP and SMARCA4. Third, using matched filtering, we identified 12 transcripts not previously reported to be continuously up-regulated in maturing human primary erythroblasts. Finally, using transcription factor binding site analysis, we identified potential transcription factors that may regulate gene expression during terminal erythropoiesis. Our stringent lists of differentially regulated and continuously expressed transcripts containing many genes with undiscovered functions in erythroblasts are a resource for future functional studies of erythropoiesis. Our Human Erythroid Maturation database is available at https://cellline.molbiol.ox.ac.uk/eryth/index.html.National Health Service
Blood and Transplant, National Institute for Health Research
Biomedical Research Center Program, and National Institute for
Health Research
A Simple Whole-Plasmid PCR Method to Construct High-Diversity Synthetic Phage Display Libraries
Phage display technology utilises peptide and antibody libraries with very high diversities to select ligands with specific binding properties. The production of such libraries can be labour intensive and technically challenging and whilst there are commercial sources of libraries, the exploitation of the resulting binders is constrained by ownership of the libraries. Here, a peptide library of ~ 1 × 109 variants for display on gene VIII was produced alongside three VHH antibody libraries with similar diversity, where 12mer, 16mer or 21mer CDR3s were introduced into the highly stable cAbBCII10 scaffold displayed on gene III. The cloning strategy used a simple whole-plasmid PCR method and type IIS restriction enzyme assembly that facilitate the seamless insertion of diversity into any suitable phage coat protein or antibody scaffold. This method reproducibly produced 1 × 109 variants from just 10 transformations and the four libraries had relatively low bias with 82 to 86% of all sequences present as single copies. The functionality of both peptide and antibody libraries were demonstrated by selection of ligands with specific binding properties by biopanning. The peptide library was used to epitope map a monoclonal antibody. The VHH libraries were pooled and used to select an antibody to recombinant human collagen type 1
In situ identification of Gram-negative bacteria in human lungs using a topical fluorescent peptide targeting lipid A
Acknowledgment to AAAS for publishing this manuscript with DOI 10.1126/scitranslmed.aal0033
https://www.science.org/doi/10.1126/scitranslmed.aal0033Respiratory infections in mechanically ventilated patients caused by Gram-negative bacteria are a major cause of
morbidity. Rapid and unequivocal determination of the presence, localization, and abundance of bacteria is criti cal for positive resolution of the infections and could be used for patient stratification and for monitoring treat ment efficacy. Here, we developed an in situ approach to visualize Gram-negative bacterial species and cellular
infiltrates in distal human lungs in real time. We used optical endomicroscopy to visualize a water-soluble optical
imaging probe based on the antimicrobial peptide polymyxin conjugated to an environmentally sensitive fluoro phore. The probe was chemically stable and nontoxic and, after in-human intrapulmonary microdosing, enabled
the specific detection of Gram-negative bacteria in distal human airways and alveoli within minutes. The results
suggest that pulmonary molecular imaging using a topically administered fluorescent probe targeting bacterial
lipid A is safe and practical, enabling rapid in situ identification of Gram-negative bacteria in humans.This work was supported by
Wellcome Trust, the Department of Health Healthcare Innovation Challenge Fund
(HICF-0510-069), and the Engineering and Physical Sciences Research Council Interdisciplinary
Research Collaboration “Proteus” (EP/K03197X/1). The GMP activities were supported by the
National Institute for Health Research (NIHR) BRC GMP Unit at Guy’s and St. Thomas’ NHS
Foundation Trust and NIHR Biomedical Research Centre based at Guy’s and St. Thomas’ NHS
Foundation Trust and King’s College London
Moments of the B Meson Inclusive Semileptonic Decay Rate using Neutrino Reconstruction
We present a measurement of the composition of B meson inclusive semileptonic
decays using 9.4 fb^-1 of e^+e^- data taken with the CLEO detector at the
Upsilon(4S) resonance. In addition to measuring the charged lepton kinematics,
the neutrino four-vector is inferred using the hermiticity of the detector. We
perform a maximum likelihood fit over the full three-dimensional differential
decay distribution for the fractional contributions from the B -> X_c l nu
processes with X_c = D, D*, D**, and nonresonant X_c, and the process B -> X_u
l nu. From the fit results we extract the first and second moments of the M_X^2
and q^2 distributions with minimum lepton-energy requirements of 1.0 GeV and
1.5 GeV. We find = 0.456 +- 0.014 +- 0.045 +- 0.109
(GeV/c^2)^2 with a minimum lepton energy of 1.0 GeV and =
0.293 +- 0.012 +- 0.033 +- 0.048 (GeV/c^2)^2 with minimum lepton energy of 1.5
GeV. The uncertainties are from statistics, detector systematic effects, and
model dependence, respectively. As a test of the HQET and OPE calculations, the
results for the M^X_c moment as a function of the minimum lepton energy
requirement are compared to the predictions.Comment: 26 pages postscript, als available through
http://w4.lns.cornell.edu/public/CLNS/, Submitted to PRD (back-to-back with
following preprint hep-ex/0403053
- …