Development and characterization of environmentally friendly composites from poly(butylene succinate) (PBS) and almond shell flour with different compatibilizers

[EN] This work reports the enhancement of the properties of poly (butylene succinate) (PBS) composites containing 30 wt% almond shell flour (ASF) by using different compatibilizer families: epoxy, maleic anhydride and acrylic. With regard to the epoxy compatibilizers, epoxidized linseed oil (ELO) and epoxidized soybean oil (ESBO) were used. Two maleic anhydride-derived compatibilizers, namely, maleinized linseed oil (MLO) and dodecenyl succinic anhydride (DDSA) were used. Finally, two acrylic monomers, namely methyl methacrylate (MMA) and acrylic acid (AA) were employed. Uncompatibilized and compatibilized PBS/ASF composites were characterized in terms of their mechanical properties, morphology, thermal behaviour and thermomechanical performance. The obtained results suggest that all three vegetable oil-derived compatibilizers (ELO, ESBO and MLO) give a remarkable increase in ductile properties while poor compatibilization is obtained with the acrylic monomers. These vegetable-oil derived compatibilizers could represents an interesting environmentally friendly solution to compatibilizing polyester-type polymers and their composites with lignocellulosic materials.This work was supported by the Ministry of Economy and Competitiveness (MINECO) grant numbers MAT2014-59242-C2-1-R and MAT2017-84909-C2-2-R. L. Quiles-Carrillo acknowledges Generalitat Valenciana (GV) for financial support through a FPI grant (ACIF/2016/182) and the Spanish Ministry of Education, Culture, and Sports (MECD) for his FPU grant (FPU15/03812).Liminana, P.; Garcia-Sanoguera, D.; Quiles-Carrillo, L.; Balart, R.; Montanes, N. (2018). Development and characterization of environmentally friendly composites from poly(butylene succinate) (PBS) and almond shell flour with different compatibilizers. Composites Part B Engineering. 144:153-162. https://doi.org/10.1016/j.compositesb.2018.02.031S15316214

A feature-rich transmission spectrum for WASP-127b

WASP-127b is one of the lowest density planets discovered to date. With a sub-Saturn mass ($M_{\rm p}=0.18 \pm 0.02 M_J$) and super-Jupiter radius ($R_{\rm p}= 1.37 \pm 0.04 R_J$), it orbits a bright G5 star, which is about to leave the main-sequence. We aim to explore WASP-127b's atmosphere in order to retrieve its main atmospheric components, and to find hints for its intriguing inflation and evolutionary history. We used the ALFOSC spectrograph at the NOT telescope to observe a low resolution ($R\sim330$, seeing limited) long-slit spectroscopic time series during a planetary transit, and present here the first transmission spectrum for WASP-127b. We find the presence of a strong Rayleigh slope at blue wavelengths and a hint of Na absorption, although the quality of the data does not allow us to claim a detection. At redder wavelengths the absorption features of TiO and VO are the best explanation to fit the data. Although higher signal-to-noise ratio observations are needed to conclusively confirm the absorption features, WASP-127b seems to posses a cloud-free atmosphere and is one of the best targets to perform further characterization studies in the near future.Comment: Accepted for Publication A&A Letters, May 22nd, 201

Single-cell analysis of upper airway cells reveals host-viral dynamics in influenza infected adults [preprint]

Influenza virus infections are major causes of morbidity and mortality. Research using cultured cells, bulk tissue, and animal models cannot fully capture human disease dynamics. Many aspects of virus-host interactions in a natural setting remain unclear, including the specific cell types that are infected and how they and neighboring bystander cells contribute to the overall antiviral response. To address these questions, we performed single-cell RNA sequencing (scRNA-Seq) on cells from freshly collected nasal washes from healthy human donors and donors diagnosed with acute influenza during the 2017-18 season. We describe a previously uncharacterized goblet cell population, specific to infected individuals, with high expression of MHC class II genes. Furthermore, leveraging scRNA-Seq reads, we obtained deep viral genome coverage and developed a model to rigorously identify infected cells that detected influenza infection in all epithelial cell types and even some immune cells. Our data revealed that each donor was infected by a unique influenza variant and that each variant was separated by at least one unique non-synonymous difference. Our results demonstrate the power of massively-parallel scRNA-Seq to study viral variation, as well as host and viral transcriptional activity during human infection

SARS-CoV-2 Receptor ACE2 Is an Interferon-Stimulated Gene in Human Airway Epithelial Cells and Is Detected in Specific Cell Subsets across Tissues

There is pressing urgency to understand the pathogenesis of the severe acute respiratory syndrome coronavirus clade 2 (SARS-CoV-2), which causes the disease COVID-19. SARS-CoV-2 spike (S) protein binds angiotensin-converting enzyme 2 (ACE2), and in concert with host proteases, principally transmembrane serine protease 2 (TMPRSS2), promotes cellular entry. The cell subsets targeted by SARS-CoV-2 in host tissues and the factors that regulate ACE2 expression remain unknown. Here, we leverage human, non-human primate, and mouse single-cell RNA-sequencing (scRNA-seq) datasets across health and disease to uncover putative targets of SARS-CoV-2 among tissue-resident cell subsets. We identify ACE2 and TMPRSS2 co-expressing cells within lung type II pneumocytes, ileal absorptive enterocytes, and nasal goblet secretory cells. Strikingly, we discovered that ACE2 is a human interferon-stimulated gene (ISG) in vitro using airway epithelial cells and extend our findings to in vivo viral infections. Our data suggest that SARS-CoV-2 could exploit species-specific interferon-driven upregulation of ACE2, a tissue-protective mediator during lung injury, to enhance infection

Single cell profiling of COVID-19 patients: an international data resource from multiple tissues

In late 2019 and through 2020, the COVID-19 pandemic swept the world, presenting both scientific and medical challenges associated with understanding and treating a previously unknown disease. To help address the need for great understanding of COVID-19, the scientific community mobilized and banded together rapidly to characterize SARS-CoV-2 infection, pathogenesis and its distinct disease trajectories. The urgency of COVID-19 provided a pressing use-case for leveraging relatively new tools, technologies, and nascent collaborative networks. Single-cell biology is one such example that has emerged over the last decade as a powerful approach that provides unprecedented resolution to the cellular and molecular underpinnings of biological processes. Early foundational work within the single-cell community, including the Human Cell Atlas, utilized published and unpublished data to characterize the putative target cells of SARS-CoV-2 sampled from diverse organs based on expression of the viral receptor ACE2 and associated entry factors TMPRSS2 and CTSL (Muus et al., 2020; Sungnak et al., 2020; Ziegler et al., 2020). This initial characterization of reference data provided an important foundation for framing infection and pathology in the airway as well as other organs. However, initial community analysis was limited to samples derived from uninfected donors and other previously-sampled disease indications. This report provides an overview of a single-cell data resource derived from samples from COVID-19 patients along with initial observations and guidance on data reuse and exploration

SMART-1 Impact Ground-based campaign

Based on predictions of impact magnitude and cloud ejecta dynamics, we organized a SMART-1 ground-based observation campaign to perform coordinated measurements of the impact. Results from the coordinated multi-site campaign will be discussed