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In this study, a new and very quick method to depolymerize PET plastics is reported. The depolymerization experiments were conducted using a type-IV deep eutectic solvent containing ZnCl2 and urea, and a microwave oven as reactor. Different combinations of power and reaction times were employed while keeping the total energy constant. Successful conversions were obtained carrying out the process at 180 W for 2 min and 360 W for 1 min, whereas at higher powers and shorter times, an inclusion likely occurs of some solvent into the structure of the recovered PET flakes, as suggested by the porosity of the flakes, imaged by SEM microscopy. The flakes increase their crystalline character during the treatment, as indicated by the appearance of narrow diffraction peaks in the XRD patterns, at variance with the broad signals observed in the case of the pristine amorphous polymer. The NMR analysis of the supernatant liquid above the partially solubilized PET shows the presence of terephthalic acid peaks. The infrared spectra of the solid powder achieved upon the acidic treatment of the extract reveal the presence of C=O stretching peaks and the absence of typical CH2 wagging absorptions that satisfactorily comply with the presence of terephthalic acid.

Within the framework of plant biostimulation, a pivotal role is played by the achievement of low-cost, easily prepared nanoparticles for priming purposes. Therefore, in this report, two different synthetic strategies are described to engineer zinc oxide nanoparticles with an inulin coating. In both protocols, i.e., two-step and gel-like one-pot protocols, nanoparticles with a highly pure ZnO kernel are obtained when the reaction is carried out at T ≥ 40 °C, as ascertained by XRD and ATR/FTIR studies. However, a uniformly dispersed, highly homogeneous coating is achieved primarily when different temperatures, i.e., 60 °C and 40 °C, are employed in the two phases of the step-wise synthesis. In addition, a different binding mechanism, i.e., complexation, occurs in this case. When the gel-like process is employed, a high degree of coverage by the fructan is attained, leading to micrometric coated aggregates of nanometric particles, as revealed by SEM investigations. All NPs from the two-step synthesis feature electronic bandgaps in the 3.25–3.30 eV range in line with previous studies, whereas the extensive coating causes a remarkable 0.4 eV decrease in the bandgap. Overall, the global analysis of the investigations indicates that the samples synthesized at 60 °C and 40 °C are the best suited for biostimulation. Proof-of-principle assays upon Vicia faba seed priming with Zn5 and Zn5@inu indicated an effective growth stimulation of seedlings at doses of 100 mgKg−1, with concomitant Zn accumulation in the leaves.

Small interfering RNAs (siRNAs) are particularly attractive among the frontier drugs due to their high specificity of action, activity on disease-inducing genes, and small molecular weight, thus being one of the most studied agents for gene therapy. However, siRNAs are prone to fast enzymatic degradation in the bloodstream, as well as other limitations that challenge their clinical translation. Nanoparticle (NP) delivery of siRNA has been proposed as a potential solution, overcoming their intrinsic limitations. In this regard, the siRNA delivery by magnetic nanoparticles is of particular interest because, being susceptible to external magnetic fields, it may be guided remotely, maximizing transfection efficiency and minimizing side effects. In addition, magnetic NPs would also allow a theranostic combination of drug delivery, magnetic resonance imaging, and hyperthermia. In this work we have studied the uptake of a model therapeutic siRNA by iron-doped hydroxyapatite nanoparticles (FeHA NPs), which are known to have excellent biocompatibility and magnetic susceptibility. We discovered that FeHA NPs stabilized by citrate (Cit-FeHA NPs) uptake siRNA by adsorption quickly and with high efficiency (ca. 90%) without altering nanoparticles physicochemical properties or colloidal stability. SiRNA-loaded Cit-FeHA NPs are able to slowly release their payload, with a sustained release of 45 days without siRNA degradation. Our work is therefore the preliminary validation of the suitability of FeHA NPs for magnetically guided delivery of therapeutic siRNAs.

Innovative applications of high-resolution airborne imaging are explored for detecting grapevine diseases. Driven by the motivation to enhance early disease detection, the method’s effectiveness lies in its capacity to identify isolated cases of grapevine yellows (Flavescence dorée and Bois Noir) and trunk disease (Esca complex), crucial for preventing the disease from spreading to unaffected areas. Conducted over a 17 ha vineyard in the Forlì municipality in Emilia-Romagna (Italy), the aerial survey utilized a photogrammetric camera capturing centimeter-level resolution images of the whole area in 17 minutes. These images were then processed through an automated analysis leveraging RGB-based spectral indices (Green–Red Vegetation Index—GRVI, Green–Blue Vegetation Index—GBVI, and Blue–Red Vegetation Index—BRVI). The analysis scanned the 1.24 · 109 pixels of the orthomosaic, detecting 0.4% of the vineyard area showing evidence of disease. The instances, density, and incidence maps provide insights into symptoms’ spatial distribution and facilitate precise interventions. High specificity (0.96) and good sensitivity (0.56) emerged from the ground field observation campaign. Statistical analysis revealed a significant edge effect in symptom distribution, with higher disease occurrence near vineyard borders. This pattern, confirmed by spatial autocorrelation and non-parametric tests, likely reflects increased vector activity and environmental stress at the vineyard margins. The presented pilot study not only provides a reliable detection tool for grapevine diseases but also lays the groundwork for an early warning system that, if extended to larger areas, could offer a valuable system to guide on-the-ground monitoring and facilitate strategic decision-making by the authorities.

Halyomorpha halys is an invasive polyphagous pest with a high negative impact on fruit orchards and other agricultural crops in the USA. In Italy, it was first detected in 2012 in Emilia Romagna, a northern region that is among the major European tree fruit production areas. A specific monitoring programme using active techniques was carried out in pear orchards and adjacent uncultivated areas between 2014 and 2016 to assess the abundance, seasonality and impact of H. halys and other phytophagous Heteroptera in the field. It emerged that just a few years after first discovery, this invasive species already largely outnumbers all the other Heteroptera and that it is a season-long pest for pear crops. Severe yield losses are reported in different farms, especially on the orchard borders, with more than 50% deformed fruits. Mirids are mostly found in the grassy areas and crops, and the other phytophagous Heteroptera, only occasionally detected in the orchard trees, occur mainly on hedges and other crops. Our survey demonstrates for the first time the great damaging potential of H. halys as a new key pest of orchards in southern Europe. The study also identified the patterns of seasonal abundance of adults and nymphs in the orchards and their uncultivated surroundings, providing baseline data for the development of specific strategies for sustainable management.

The master regulator of MHC-II gene transcription, class II transactivator (CIITA), acts as a potent inhibitor of human T cell leukemia virus type 2 (HTLV-2) replication by blocking the activity of the viral Tax-2 transactivator. Here, we show that this inhibitory effect takes place at the nuclear level and maps to the N-terminal 1-321 region of CIITA, where we identified a minimal domain, from positions 64-144, that is strictly required to suppress Tax-2 function. Furthermore, we show that Tax-2 specifically cooperates with cAMP response element binding protein-binding protein (CBP) and p300, but not with p300/CBP-associated factor, to enhance transcription from the viral promoter. This finding represents a unique difference with respect to Tax-1, which uses all three coactivators to transactivate the human T cell leukemia virus type I LTR. Direct sequestering of CBP or p300 is not the primary mechanism by which CIITA causes suppression of Tax-2. Interestingly, we found that the transcription factor nuclear factor Y, which interacts with CIITA to increase transcription of MHC-II genes, exerts a negative regulatory action on the Tax-2-mediated HTLV-2 LTR transactivation. Thus, CIITA may inhibit Tax-2 function, at least in part, through nuclear factor Y. These findings demonstrate the dual defensive role of CIITA against pathogens: it increases the antigen-presenting function for viral determinants and suppresses HTLV-2 replication in infected cells.