Tamara Kotevska, Ljubomir Stefanov, Honeyland, North Macedonia, 2019, 87’

Review of Tamara Kotevska, Ljubomir Stefanov, Honeyland, North Macedonia, 2019, 87’.Recensione di Tamara Kotevska, Ljubomir Stefanov, Honeyland, North Macedonia, 2019, 87’

16th RAI Film Festival 2019 | Bristol (UK), 27-30 March 2019

Review of the 16th RAI Film Festival 2019 | Bristol (UK), 27-30 March 2019.Recensione del 16th RAI Film Festival 2019 | Bristol (UK), 27-30 March 2019

Human mobility networks and persistence of rapidly mutating pathogens

Rapidly mutating pathogens may be able to persist in the population and reach an endemic equilibrium by escaping hosts' acquired immunity. For such diseases, multiple biological, environmental and population-level mechanisms determine the dynamics of the outbreak, including pathogen's epidemiological traits (e.g. transmissibility, infectious period and duration of immunity), seasonality, interaction with other circulating strains and hosts' mixing and spatial fragmentation. Here, we study a susceptible-infected-recovered-susceptible model on a metapopulation where individuals are distributed in subpopulations connected via a network of mobility flows. Through extensive numerical simulations, we explore the phase space of pathogen's persistence and map the dynamical regimes of the pathogen following emergence. Our results show that spatial fragmentation and mobility play a key role in the persistence of the disease whose maximum is reached at intermediate mobility values. We describe the occurrence of different phenomena including local extinction and emergence of epidemic waves, and assess the conditions for large scale spreading. Findings are highlighted in reference to previous works and to real scenarios. Our work uncovers the crucial role of hosts' mobility on the ecological dynamics of rapidly mutating pathogens, opening the path for further studies on disease ecology in the presence of a complex and heterogeneous environment.Comment: 29 pages, 7 figures. Submitted for publicatio

The R18 polyarginine peptide is more effective than the TAT-NR2B9c (NA-1) peptide when administered 60 minutes after permanent middle cerebral artery occlusion in the rat

We examined the dose responsiveness of polyarginine R18 (100, 300, and 1000 nmol/kg) when administered 60 minutes after permanent middle cerebral artery occlusion (MCAO).The TAT-NR2B9c peptide, which is known to be neuroprotective in rodent and nonhuman primate stroke models, served as a positive control. At 24 hours afterMCAO, there was reduced total infarct volume in R18 treated animals at all doses, but this reduction only reached statistical significance at doses of 100 and 1000 nmol/kg. The TAT-NR2B9c peptide reduced infarct volume at doses of 300 and 1000 nmol/kg, but not to a statistically significant extent, while the 100 nmol/kg dose was ineffective.The reduction in infarct volume with R18 and TAT-NR2B9c peptide treatments was mirrored by improvements in one or more functional outcomes (namely, neurological score, adhesive tape removal, and rota-rod), but not to a statistically significant extent. These findings further confirm the neuroprotective properties of polyarginine peptides and for R18 extend its therapeutic time window and dose range, as well as demonstrating its greater efficacy compared to TAT-NR2B9c in a severe stroke model.The superior neuroprotective efficacy of R18 over TAT-NR2B9c highlights the potential of this polyarginine peptide as a lead candidate for studies in human stroke

Experimental and Computational Study of the New Gaseous Molecules OMnF and OMnF[Sub 2]

The new gaseous species OMnF and OMnF2 were identified and studied by high-temperature Knudsen Cell Mass Spectrometry. Their thermochemical atomization energies were derived through the study of several all-gas equilibria in the temperature range 1735–1913 K. FTIR matrix isolation experiments together with ab initio and density functional calculations were performed to determine the molecular parameters, bond distances, and vibrational frequencies of OMnF(g) and OMnF2(g) . The results allowed us to evaluate a set of thermal functions for the new species that were used in the evaluation of the equilibrium data. The proposed atomization energies and enthalpies of formation are DaH0 + (OMnF,g)5(90365) kJ mol21, DfH298.15 + (OMnF,g)5(229765) kJ mol21, and DaH0 + (OMnF2 ,g)5(1470670) kJ mol21, DfH298.15 + (OMnF2 ,g)5(2789670) kJ mol21

Loop bounds on non-standard neutrino interactions

We reconsider the bounds on non-standard neutrino interactions with matter which can be derived by constraining the four-charged-lepton operators induced at the loop level. We find that these bounds are model dependent. Naturalness arguments can lead to much stronger constraints than those presented in previous studies, while no completely model-independent bounds can be derived. We will illustrate how large loop-contributions to four-charged-lepton operators are induced within a particular model that realizes gauge invariant non-standard interactions and discuss conditions to avoid these bounds. These considerations mainly affect the $\mathcal O(10^{-4})$ constraint on the non-standard coupling strength \eps_{e\mu}, which is lost. The only model-independent constraints that can be derived are $\mathcal O(10^{-1})$. However, significant cancellations are required in order to saturate this bound.Comment: Minor changes, version to be published in JHEP. 17 pages, 3 Axodraw figures, REVTeX

Legacy of wood charcoal production on subalpine forest structure and species composition

Land-use legacy on forest dynamics at both stand and landscape scale can last for centuries, affecting forest structure and species composition. We aimed to disentangle the history of the charcoal production legacies that historically shaped Mont Avic Natural Park (Aosta Valley, Italy) forests by integrating LiDAR, GIS, anthracological, and field data at the landscape scale. We adopted different geostatistical tools to relate geographic layers from various data sources. The overexploitation due to intensive charcoal production to fuel mining activities shaped the current forests by homogenising their structure and species composition into dense and young stands with a reduction in late seral species such as Norway spruce (Picea abies) and an increase in pioneer species such as Mountain pine (Pinus uncinata). The multidisciplinary and multi-scale framework adopted in this study stresses the role of historical landscape ecology in evaluating ecosystem resilience to past anthropogenic disturbances. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13280-022-01750-y

Poly-arginine peptides reduce infarct volume in a permanent middle cerebral artery rat stroke model

Background: We recently reported that poly-arginine peptides have neuroprotective properties both in vitro and in vivo. In cultured cortical neurons exposed to glutamic acid excitotoxicity, we demonstrated that neuroprotective potency increases with polymer length plateauing at R15 to R18 (R = arginine resides). In an in vivo study in rats, we also demonstrated that R9D (R9 peptide synthesised with D-isoform amino acids) administered intravenously at a dose of 1000 nmol/kg 30 min after permanent middle cerebral artery occlusion (MCAO) reduces infarct volume. Based on these positive in vitro and in vivo findings, we decided to examine the neuroprotective efficacy of the L-isoform poly-arginine peptides, R12, R15 and R18 when administered at a dose of 1000 nmol/kg 30 min after permanent MCAO in the rat. Results: At 24 h post-MCAO, there was reduced total infarct volume for R12 (12.8 % reduction) and R18 (20.5 % reduction), but this reduction only reached statistical significance for R18. Brain slice analysis revealed significantly reduced injury in coronal slices 4 and 5 for R18, and slice 5 for R12. The R15 peptide had no effect on infarct volume. Peptide treatment did not reveal any statistical significant improvement in functional outcomes. Conclusion: While these findings confirm the in vivo neuroprotective properties of poly-arginine peptides, additional dose studies are required particularly in less severe transient MCAO models so as to further assess the potential of these agents as a stroke therapy

Crystal structure of the DNA-binding domain of Myelin-gene Regulatory Factor

Myelin-gene Regulatory Factor (MyRF) is one of the master transcription factors controlling myelin formation and development in oligodendrocytes which is crucial for the powerful brain functions. The N-terminal of MyRF, which contains a proline-rich region and a DNA binding domain (DBD), is auto-cleaved from the ER membrane, and then enters the nucleus to participate in transcription regulation of the myelin genes. Here we report the crystal structure of MyRF DBD. It shows an Ig-fold like architecture which consists of two antiparallel β-sheets with 7 main strands, packing against each other, forming a β-sandwich. Compared to its homolog, Ndt80, MyRF has a smaller and less complex DBD lacking the helices and the big loops outside the core. Structural alignment reveals that MyRF DBD possess less interaction sites with DNA than Ndt80 and may bind only at the major groove of DNA. Moreover, the structure reveals a trimeric assembly, agreeing with the previous report that MyRF DBD functions as a trimer. The mutant that we designed based on the structure disturbed trimer formation, but didn't affect the auto-cleavage reaction. It demonstrates that the activation of self-cleavage reaction of MyRF is independent of the presence of its N-terminal DBD homotrimer. The structure reported here will help to understand the molecular mechanism underlying the important roles of MyRF in myelin formation and development

RooHammerModel: interfacing the HAMMER software tool with the HistFactory package

Recent $B$-physics results have sparkled great interest in the search for beyond-the-Standard-Model (BSM) physics in $b\to c\ell \bar{\nu}$ transitions. The need to analyse in a consistent manner big datasets for these searches, using high-statistics Monte-Carlo (MC) samples, led to the development of HAMMER, a software tool which enables to perform a fast morphing of MC-derived templates to include BSM effects and/or alternative parameterisations of long-distance effects, avoiding the need to re-generate simulated samples. This note describes the development of RooHammerModel, an interface between this tool and the commonly-used data-fitting framework HistFactory. The code is written in C++ and admits an alternative usage in standalone RooFit analyses. In this document, the structure and functionality of the user interface are explained. Information of a public repository where it can be accessed is provided, as well as validation and performance studies of the interface. The methods developed in the construction of RooHammerModel can provide specific information for alternative future attempts to interface HAMMER with other data-fitting frameworks