Molecular phylogenetics of Dipsacaceae reveals parallel trends in seed dispersal syndromes

Phylogenetic relationships among 17 taxa of Dipsacaceae were inferred from nucleotide sequence variation in both the internal transcribed spacer (ITS) regions of nuclear ribosomal DNA and the chloroplast trnL (UAA) intron sequences. The combined phylogenetic analysis, carried out by using two taxa from Valerianaceae as an outgroup yielded a single most parsimonious tree, in which Dipsacaceae are divided into two major clades: one including Lomelosia and Pycnocomon, both in a sister group relationship with a clade containing Pterocephalus, Scabiosa and Sixalix; the other including Pseudoscabiosa, Succisa and Succisella is sister group to Knautia, Pterocephalidium, Dipsacus and Cephalaria. The results obtained here greatly differ from previous ones based on classical morphology, but are congruent with recent findings on epicalyx differentiation and with pollen characters. In particular, our results would confirm on molecular grounds the recently restricted circumscription for Scabioseae proposed by other authors. Our phylogenetic hypothesis indicates that adaptations to seed dispersal have been a very strong driving force in Dipsacaceae evolution, with similar selective pressures causing the onset of similar epicalyx shapes and dispersal modes in a parallel fashion in various taxa. For this reason, the gross morphology of the involucel is deceptive in inferring relationships

Stellar limits on scalars from electron-nucleus bremsstrahlung

We revisit stellar energy-loss bounds on the Yukawa couplings $g_{\rm B,L}$ of baryophilic and leptophilic scalars $\phi$. The white-dwarf luminosity function yields $g_{\rm B}\lesssim 7 \times 10^{-13}$ and $g_{\rm L}\lesssim 4 \times 10^{-16}$, based on bremsstrahlung from ${}^{12}{\rm C}$ and ${}^{16}{\rm O}$ collisions with electrons. In models with a Higgs portal, this also implies a bound on the scalar-Higgs mixing angle $\sin \theta \lesssim 2 \times 10^{-10}$. Our new bounds apply for $m_\phi\lesssim {\rm 1~keV}$ and are among the most restrictive ones, whereas for $m_\phi\lesssim 0.5\,{\rm eV}$ long-range force measurements dominate. Besides a detailed calculation of the bremsstrahlung rate for degenerate and semi-relativistic electrons, we prove with a simple argument that non-relativistic bremsstrahlung by the heavy partner is suppressed relative to that by the light one by their squared-mass ratio. This large reduction was overlooked in previous much stronger bounds on $g_{\rm B}$. In an Appendix, we provide fitting formulas (few percent precision) for the bremsstrahlung emission of baryophilic and leptophilic scalars as well as axions for white-dwarf conditions, i.e., degenerate, semi-relativistic electrons and ion-ion correlations in the ``liquid'' phase.Comment: 22 pages + appendices, 7 figure

Towards Digital Twin Implementation for Assessing Production Line Performance and Balancing

The optimization of production processes has always been one of the cornerstones for manufacturing companies, aimed to increase their productivity, minimizing the related costs. In the Industry 4.0 era, some innovative technologies, perceived as far away until a few years ago, have become reachable by everyone. The massive introduction of these technologies directly in the factories allows interconnecting the resources (machines and humans) and the entire production chain to be kept under control, thanks to the collection and the analyses of real production data, supporting the decision making process. This article aims to propose a methodological framework that, thanks to the use of Industrial Internet of Things—IoT devices, in particular the wearable sensors, and simulation tools, supports the analyses of production line performance parameters, by considering both experimental and numerical data, allowing a continuous monitoring of the line balancing and performance at varying of the production demand. A case study, regarding a manual task of a real manufacturing production line, is presented to demonstrate the applicability and the effectiveness of the proposed procedure

Variability and Nativeness in the Mediterranean Taxa: Divergence and Phylogeography of Genista etnensis (Fabaceae) Inferred from Nuclear and Plastid Data

Genista etnensis is a remarkable and well-known tree endemic to Sicily, Sardinia, and Corsica (Mediterranean Basin). Nevertheless, its morphological variability and its native status throughout its range need to be further investigated. In this study, we aim to clarify some aspects of this infraspecific variability by molecular means. Sequences of one nuclear and five plastid markers were analyzed under maximum parsimony by using TCS software. Plastid data were also timecalibrated under a Bayesian Inference framework. Plastid data revealed strong isolation between the populations from the Cyrno-Sardinian biogeographical province, which are also the most diverse and presumably the most archaic, and those from Sicily and Southern Italy (in this latter area, the species is naturalized). The calibration analysis indicates that the last common ancestor between G. etnensis and its sister group G. fasselata dates back to the middle Pliocene or slightly later, when sclerophyllous Mediterranean vegetation spread, whereas G. etnensis itself might have originated in the middle Pleistocene. The current, rather unusual distribution of G. etnensis could be explained by long-range seed dispersal from the western part of the range or by anthropogenic introduction into Sicily, with extinctions of transported haplotypes in the region of origin. Interestingly, the Vesuvius population, introduced from Sicily in recent times and locally naturalized, shows private genotypes, and was richer in both genotypes and haplotypes than the Sicilian ones

The Tat Protein of HIV-1 Prevents the Loss of HSV-Specific Memory Adaptive Responses and Favors the Control of Viral Reactivation

The development of therapeutic strategies to control the reactivation of the Herpes Simplex Virus (HSV) is an unaddressed priority. In this study, we evaluated whether Tat, a HIV-1 protein displaying adjuvant functions, could improve previously established HSV-specific memory responses and prevent viral reactivation. To this aim, mice were infected with non-lethal doses of HSV-1 and, 44 days later, injected or not with Tat. Mice were then monitored to check their health status and measure memory HSV-specific cellular and humoral responses. The appearance of symptoms associated with HSV-reactivation was observed at significantly higher frequencies in the control group than in the Tat-treated mice. In addition, the control animals experienced a time-dependent decrease in HSV-specific Immunoglobulin G (IgG), while the Tat-treated mice maintained antibody titers over time. IgG levels were directly correlated with the number of HSV-specific CD8+ T cells, suggesting an effect of Tat on both arms of the adaptive immunity. Consistent with the maintenance of HSV-specific immune memory, Tat-treated mice showed a better control of HSV-1 re-infection. Although further studies are necessary to assess whether similar effects are observed in other models, these results indicate that Tat exerts a therapeutic effect against latent HSV-1 infection and re-infection by favoring the maintenance of adaptive immunity

Constitutive Differential Features of Type 2 Transglutaminase in Cells Derived from Celiac Patients and from Healthy Subjects

Type 2 transglutaminase (TG2) is a ubiquitous enzyme able to modify gliadin peptides introduced into the organism through the diet. By means of its catalytic activity, TG2 seems to have an important pathogenetic role in celiac disease (CD), an inflammatory intestinal disease caused by the ingestion of gluten-containing cereals. A strong autoimmune response to TG2 characterizes CD development. Anti-TG2 antibodies specifically derange the uptake of the α-gliadin peptide 31-43 by control, but not by celiac dermal fibroblasts, underlying some different constitutive features regarding TG2 in healthy and celiac subjects. Our aim was to investigate whether these differences depended on a different TG2 subcellular distribution and whether peptide 31-43 differentially regulated TG2 expression and activity in cells of the two groups of subjects. We found that TG2 was more abundantly associated with membranes of celiac fibroblasts than of control cells, in particular with the early endosomal and autophagic compartments. We also found that peptide 31-43 differentially affected TG2 expression and activity in the two groups of cells, activating TG2 more in control than in celiac cells and inducing TG2 expression in celiac cells, but not in control ones. The different TG2 subcellular localization and the different way the peptide 31-43 modulates TG2 activity and availability into control and CD cells suggested that TG2 is involved in the definition of a constitutive CD cellular phenotype, thus having an important and still undefined role in CD pathogenesis

Polydatin Induces Differentiation and Radiation Sensitivity in Human Osteosarcoma Cells and Parallel Secretion through Lipid Metabolite Secretion

Osteosarcoma is a bone cancer characterized by the production of osteoid tissue and immature bone from mesenchymal cells. Osteosarcoma mainly affects long bones (femur is most frequently site) and occur in children and young adults with greater incidence. Here, we investigated the role accomplished by polydatin, a natural antioxidative compound, in promoting osteogenic differentiation alone or after radiation therapy on osteosarcoma cells. In vitro, polydatin significantly induced cell cycle arrest in S-phase and enhanced bone alkaline phosphatase activity. Moreover, the differentiation process was paralleled by the activation of Wnt-β-catenin pathway. In combination with radiotherapy, the pretreatment with polydatin promoted a radiosensitizing effect on osteosarcoma cancer cells as demonstrated by the upregulation of osteogenic markers and reduced clonogenic survival of tumor cells. Additionally, we analyzed, by mass spectrometry, the secretion of sphingolipid, ceramides, and their metabolites in osteosarcoma cells treated with polydatin. Overall, our results demonstrate that polydatin, through the secretion of sphingolipids and ceramide, induced osteogenic differentiation, alone and in the presence of ionizing therapy. Future investigations are needed to validate the use of polydatin in clinical practice as a potentiating agent of radiotherapy-induced anticancer effects