Genetic Engineering of Bacteriophages Against Infectious Diseases

Bacteriophages (phages) are the most abundant and widely distributed organisms on Earth, constituting a virtually unlimited resource to explore the development of biomedical therapies. The therapeutic use of phages to treat bacterial infections (“phage therapy”) was conceived by Felix d’Herelle nearly a century ago. However, its power has been realized only recently, largely due to the emergence of multi-antibiotic resistant bacterial pathogens. Progress in technologies, such as high-throughput sequencing, genome editing, and synthetic biology, further opened doors to explore this vast treasure trove. Here, we review some of the emerging themes on the use of phages against infectious diseases. In addition to phage therapy, phages have also been developed as vaccine platforms to deliver antigens as part of virus-like nanoparticles that can stimulate immune responses and prevent pathogen infections. Phage engineering promises to generate phage variants with unique properties for prophylactic and therapeutic applications. These approaches have created momentum to accelerate basic as well as translational phage research and potential development of therapeutics in the near future

Materials design towards sport textiles with low-friction and moisture-wicking dual functions

In the field of sportswear, the structure and morphology of textiles are of great importance to achieve good moisture transport and low friction, which are two critical comfort-related properties. To improve these properties, dual-layer nanofibrous nonwoven mats were studied in this work. Core–shell nanofibers with a polyacrylonitrile (PAN)-rich core and a poly(vinylidene fluoride) (PVDF)-rich shell were fabricated by single-spinneret electrospinning and used as the inner layer of the dual-layer mats, while thick base-treated Cellulose Acetate (CA) nanofibrous mats were used as the outer layer. The core-located PAN and a small amount of PAN on the PAN/PVDF nanofiber surface ensure good moisture transport through the nanofibrous mats. The synergistic combination of a considerably hydrophobic PAN/PVDF inner layer and a highly hydrophilic CA outer layer induces a strong push–pull effect, resulting in efficient moisture transport from the inner to the outer layer. Furthermore, the fluorine-rich PVDF shell of the inner layer touches the human skin and provides a lubricating effect to enhance comfortability. This design provides a promising route for sports textiles with both good moisture-wicking and low friction

Tailoring surface hydrophilicity of porous electrospun nanofibers to enhance capillary and push-pull effects for moisture wicking

In this article, liquid moisture transport behaviors of dual-layer electrospun nanofibrous mats are reported for the first time. The dual-layer mats consist of a thick layer of hydrophilic polyacrylonitrile (PAN) nanofibers with a thin layer of hydrophobic polystyrene (PS) nanofibers with and without interpenetrating nanopores, respectively. The mats are coated with polydopamine (PDOPA) to different extents to tailor the water wettability of the PS layer. It is found that with a large quantity of nanochannels, the porous PS nanofibers exhibit a stronger capillary effect than the solid PS nanofibers. The capillary motion in the porous PS nanofibers can be further enhanced by slight surface modification with PDOPA while retaining the large hydrophobicity difference between the two layers, inducing a strong push–pull effect to transport water from the PS to the PAN layer

Diverse Feature Blend Based on Filter-Bank Common Spatial Pattern and Brain Functional Connectivity for Multiple Motor Imagery Detection

Motor imagery (MI) based brain-computer interface (BCI) is a research hotspot and has attracted lots of attention. Within this research topic, multiple MI classification is a challenge due to the difficulties caused by time-varying spatial features across different individuals. To deal with this challenge, we tried to fuse brain functional connectivity (BFC) and one-versus-the-rest filter-bank common spatial pattern (OVR-FBCSP) to improve the robustness of classification. The BFC features were extracted by phase locking value (PLV), representing the brain inter-regional interactions relevant to the MI, whilst the OVR-FBCSP is used to extract the spatial-frequency features related to the MI. These diverse features were then fed into a multi-kernel relevance vector machine (MK-RVM). The dataset with three motor imagery tasks (left hand MI, right hand MI, and feet MI) was used to assess the proposed method. Experimental results not only showed that the cascade structure of diverse feature fusion and MK-RVM achieved satisfactory classification performance (average accuracy: 83.81%, average kappa: 0.76), but also demonstrated that BFC plays a supplementary role in the MI classification. Moreover, the proposed method has a potential to be integrated into multiple MI online detection owing to the advantage of strong time-efficiency of RVM

Neuropeptide Y-Positive Neurons in the Dorsomedial Hypothalamus Are Involved in the Anorexic Effect of Angptl8

Angiopoietin-like protein 8 (Angptl8), a recently identified member of the angiopoietin-like protein family (ANGPTLs), is a 22-kDa peptide synthesized in the liver. It participates in lipid metabolism by inhibiting lipoprotein lipase (LPL) activity, consequently increasing the triglyceride levels. Despite evidence that Angptl8 is involved in feeding control, the underlying mechanisms are unclear. Central and peripheral injections of Angptl8 significantly decreased food intake. Angptl8 was widely expressed in appetite-related nuclei, including the paraventricular nucleus (PVN), the dorsomedial hypothalamus (DMH), the ventromedial hypothalamus, and the arcuate nucleus (ARC) in the hypothalamus. Peripheral Angptl8 administration decreased c-Fos-positive neurons in the DMH. Central Angptl8 administration decreased c-Fos-positive neurons in the DMH and PVN but increased these neurons in the ARC. Angptl8 inhibited appetite via neuropeptide Y (NPY) neurons in the DMH. Furthermore, the chronic administration of Angptl8 decreased body weight gain and altered adipose tissue deposits. Nevertheless, neither peripheral nor central Angptl8 influenced the brown adipose tissue (BAT) morphology or uncoupling protein 1 (Ucp-1) expression in BAT. Taken together, these data suggested that Angptl8 modulates appetite and energy homeostasis