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Abstract Background Branched-chain amino acids (BCAAs), including leucine, isoleucine, and valine, are essential amino acids for mammals. Maternal BCAAs during pregnancy have been associated with newborn development. Meanwhile, BCAAs have been tightly linked with insulin resistance and diabetes in recent years. Diabetes in pregnancy is a common metabolic disorder. The current study aims to assess the circulating BCAA levels in pregnant women with diabetes and their relationship with neonatal development. Methods The serum concentrations of BCAAs and their corresponding branched-chain α-keto acids (BCKAs) catabolites in 33 pregnant women with normal glucose tolerance, 16 pregnant women with type 2 diabetes before pregnancy (PDGM), and 15 pregnant women with gestational diabetes mellitus (GDM) were determined using a liquid chromatography system coupled to a mass spectrometer. The data were tested for normal distribution and homogeneity of variance before statistical analysis. Correlations were computed with the Pearson correlation coefficient. Results The maternal serum BCAAs and BCKAs levels during late pregnancy were higher in women with PGDM than those in healthy women. Meanwhile, the circulating BCAAs and BCKAs showed no significant changes in women with GDM compared with those in healthy pregnant women. Furthermore, the circulating BCAA and BCKA levels in women with PGDM were positively correlated with the weight of the newborn. The circulating leucine level in women with GDM was positively correlated with the weight of the newborn. BCAA and BCKA levels in healthy pregnant women showed no correlation with newborn weight. Conclusions The serum BCAAs in pregnant women with diabetes, which was elevated in PGDM but not GDM, were positively correlated with newborn weight. These findings highlight potential approaches for early identification of high-risk individuals and interventions to reduce the risk of adverse pregnancy outcomes.

Tamm-plasmon-polariton (TPP) has strong light absorption and polarization-independence, shows potential application in the optical biosensors. However, with the weak field confinement of the distributed Bragg reflector (DBR), the sensitivity enhancement of TPP biosensors require defect layers or nano-materials with strong light absorption. Herein, we propose a novel TPP biosensor by using one-dimensional topological photonic crystal (1D TPhC) as DBR, the working wavelength is 633 nm, where 1D TPhC is composed by two 1D photonic crystals (1D PhCs) with different topological invariants. The strong field confinement of 1D TPhC is employed to improve the light absorption of TPP, and enhance the susceptibility of the biosensor to the analyte. Since TPP is polarization-independent, it has superior sensing performance in both transverse electric (TE) and transverse magnetic (TM) polarization modes. The sensitivity and Figure of Merit (FOM) are 2.6553 × 104 RIU−1 (1.3349 × 104 RIU−1) and 3.1238 × 107 RIU−1deg−1 (6.6745 × 108 RIU−1deg−1) for TM(TE)-polarization mode. The proposed TPP biosensor without defect layer, doesn’t need consider the thickness and position of the sensing medium layer, shows high operational flexibility. Besides, with the protection of the topological edge state, this biosensor has high tolerance to the thickness deviations, which can reduce the requirements on fabrication. It is anticipated that the proposed TPP biosensor has excellent sensing performances, possesses great potentials in environmental monitoring, biological detection, etc.

Background: Chlorothalonil and acetamiprid are chemical pesticides commonly used in agricultural production and have been shown to have negative effects on bee’s fitness. Despite many studies have revealed that honey bee (Apis mellifera L.) larvae are posting a high risk on exposure to pesticides, but the toxicology information of chlorothalonil and acetamiprid on bee larvae remain limited.Results: The no observed adverse effect concentration (NOAEC) of chlorothalonil and acetamiprid for honey bee larvae were 4 μg/mL and 2 μg/mL, respectively. Except for CarE, the enzymic activities of GST and P450 were not influenced by chlorothalonil at NOAEC, while chronic exposure to acetamiprid slightly increased the activities of the three tested enzymes at NOAEC. Further, the exposed larvae showed significantly higher expression of genes involved in a series of different toxicologically relevant process following, including caste development (Tor (GB44905), InR-2 (GB55425), Hr4 (GB47037), Ac3 (GB11637) and ILP-2 (GB10174)), immune system response (abaecin (GB18323), defensin-1 (GB19392), toll-X4 (GB50418)), and oxidative stress response (P450, GSH, GST, CarE).Conclusion: Our results suggest that the exposure to chlorothalonil and acetamiprid, even at concentrations below the NOAEC, showed potentially effects on bee larvae’s fitness, and more important synergistic and behavioral effects that can affect larvae fitness should be explored in the further.

This paper proposes a multifrequency seamless dual-link handover scheme based on beamforming for the high-speed railway (HSR) communication, i.e., when the train travels to the edge of overlapping area of the adjacent two cells, a gain beam is assigned to the overlapping area by the target base station (BS) using a beamforming technique to cover the entire region to enhance the received signal strength (RSS) and handover opportunity. The switching antenna is allowed to handover multiple times to improve the traditional scheme and reduce the handover failure probability (HFP) greatly. In the process of signal reception, considering the impact of the intercell cochannel interference on the RSS, the proposed scheme uses signal to interference ratio (SIR) instead of the RSS to indicate the received signal quality to optimize handover mode. The handover success probability (HSP) is analyzed to describe the relationship between train location and the probability. We also establish a probabilistic model and corresponding handover algorithm for the proposed scheme to complete the handover operations and theoretically analyze a series of indexes including handover trigger probability (HTP), HFP, communication interruption probability (CIP), and HSP. Theoretical and experimental results show that the proposed scheme can effectively improve the HTP and HSP and greatly reduce the HFP and the CIP.

Non-alcoholic fatty liver disease (NAFLD) is a major public health problem in many countries. Berberine (BBR) is an effective therapeutic agent in alleviating NAFLD. Berberrubine (BRB) is one of the main active metabolites of BBR, which shows significant anti-obesity and antihypoglycemic effects. However, whether BRB is responsible for the in vivo therapeutic effect and the underlying mechanism of BRB on NAFLD have not been elucidated. In this study, the ability of BRB to ameliorate NAFLD, together with its molecular mechanism, was investigated. The results showed that BRB treatments could significantly improve hepatic steatosis and insulin resistance in high-fat diet (HFD)–fed mice and oleic acid (OA)–treated HepG2 cells. Meanwhile, BBR and BRB treatment similarly prevented lipid accumulation by regulating the protein expression of ATGL, GK, PPARα, CPT-1, ACC1, FAS, and CD36. In addition, compared with BBR, BRB could maintain glucose homeostasis via GLUT2, GSK3β, and G6Pase in HFD-fed mice. Furthermore, the components of the gut microbiota in mice were analyzed by 16S rRNA gene sequencing. BBR and BRB treatment could greatly modify the structure and composition of gut microbiota. At the genus level, BBR and BRB treatment decreased Lactobacillus and Romboutsia, while BBR increased beneficial bacteria, such as Akkermansia and Bacteroides, and BRB increased beneficial bacteria, such as Ileibacterium and Mucispirillum. Altogether, both BRB and BBR were active in alleviating NAFLD in vivo and BRB might be used as a functional material to treat NAFLD clinically.

Ascosphaera apis and some Aspergillus species are the main pathogenic fungi of honey bee, and A. apis is the pathogen of chalkbrood disease. However, the infection mechanism of them is incompletely known and it is still unclear whether other factors impact their pathogenesis. In this study, Aspergillus tubingensis were obtained from the chalkbrood bee samples for the first time. Our results showed that A. tubingensis could promote the accumulation of the spores of A. apis. Pathogenicity test found that inoculation of the spores of the two fungi alone or their combination could induce disease characterization of chalkbrood and stonebrood but the extent was less than those in field. To further identify other pathogens impacted the pathogenesis, we found several honey bee viruses presented in the pathogenic fungi A. apis and A. tubingensis, which were different from previous reported. Our results indicated that acute bee paralysis virus (ABPV) and chronic bee paralysis virus (CBPV) could replicate in these two fungi and increased in titer with the going of cultivation time. In addition, CBPV could not only transmit vertically to the next generation by spores, but also spread horizontally to different fungi through hyphal anastomosis. These results suggested that the honey bee chalkbrood contained the other pathogenic fungi besides A. apis, the interactions between different pathogens of chalkbrood microbial communities may influence the prevalence of chalkbrood. Moreover, the discovery of honey bee viruses and their transmission mode in these two fungi enhanced the potential of exploring fungi virus as valuable factors that cause fungal disease outbreak.

The treatment of cancer of unknown primary (CUP) is a huge challenge for clinicians. Gene expression profiling can help identify the tissue origin of tumors by detecting the expression levels of specific genes in tumor tissues. Herein, we report four CUP cases. All of them have been successfully identified with the corresponding primary tumor sites through gene expression profiling analysis. Then all patients received accurate treatment, providing reference to guide therapeutic decisions to treat CUP tumors in the future.

To solve the conflict when multi-user packets are transmitted in a shared wireless link, a novel frameless slotted-ALOHA protocol is proposed. Signature codes are used to help the receiver identify the set of transmitting users, and successive interference cancellation technology is employed to recover conflicting packets. Thus, the information in the conflicting slot can be reused to reduce the number of retransmissions. Taking the number of backlogged users in each slot as a system state, a Markov chain model is established to analyze the protocol, in which the state transition probabilities are obtained based on the binomial distribution of packets sent in a slot. Under the maximum number of detectable conflicting users, the best value is taken, traffic balance equations are obtained, and the expressions of throughput, average number of backlogged users, average successful transmission probability and average memory size are derived. Finally, a numerical simulation is carried out to accurately analyze the influence of the first transmission probability of the packets on various performance indexes and the effectiveness of the theoretical analysis is further verified by the simulation results.

Chinese sacbrood virus (CSBV) is a serious threat to eastern honeybees (Apis cerana), especially larvae. However, the pathological mechanism of this deadly disease remains unclear. Here, we employed mRNA and small RNA (sRNA) transcriptome approach to investigate the microRNAs (miRNAs) and small interfering RNAs (siRNAs) expression changes of A. cerana larvae infected with CSBV under natural condition. We found that serine proteases involved in immune response were down-regulated, while the expression of siRNAs targeted to serine proteases were up-regulated. In addition, CSBV infection also affected the expression of larvae cuticle proteins such as larval cuticle proteins A1A and A3A, resulting in increased susceptibility to CSBV infection. Together, our results provide insights into sRNAs that they are likely to be involved in regulating honeybee immune response.

Honey bee viruses are one of the most important pathogens that have contributed to the decrease in honey bee colony health. To analyze the infection dynamics of honey bee viruses, quantification of viral gene expression by RT-qPCR is necessary. However, suitable reference genes have not been reported from viral and RNAi studies of honey bee. Here, we evaluated the expression of 11 common reference genes (ache2, rps18, β-actin, tbp, tif, rpl32, gadph, ubc, α-tubulin, rpl14, and rpsa) from Apis mellifera (Am) and Apis cerana (Ac) under Israeli acute paralysis virus (IAPV), chronic bee paralysis virus (CBPV), and Chinese sacbrood virus (CSBV) infection as well as dsRNA-PGRP-SA treatment, and we confirmed their validation by evaluating the levels of the defensin 1 and prophenoloxidase (ppo) genes during viral infection. Our results showed that the expression of selected genes varied under different viral infections. ache2, rps18, β-actin, tbp, and tif can be used to normalize expression levels in Apis mellifera under IAPV infection, while the combination of actin and tif is suitable for CBPV-infected experiments. The combination of rpl14, tif, rpsa, ubc, and ache2 as well as more reference genes is suitable for CSBV treatment in Apis cerana. Rpl14, tif, rps18, ubc, and α-tubulin were the most stable reference genes under dsRNA treatment in Apis mellifera. Furthermore, the geNorm and NormFinder algorithms showed that tif was the best suitable reference gene for these four treatments. This study screened and validated suitable reference genes for the quantification of viral levels in honey bee, as well as for RNAi experiments.

We report the infestation of small hive beetle, Aethina tumida, in a honeybee, Apis cerana, in South China. This is the first record for domestic Chinese honey bee infested with small hive beetle.

We investigate a framework of local field, quality factor and lifetime for tunable graphene nanoribbon plasmonic-photonic absorbers and study the second order and third order nonlinear optical response of surface plasmons. The energy exchange of plasmonic-photonic absorber occurs in two main ways: one way is the decay process of intrinsic loss for each resonant mode and another is the decay process of energy loss between graphene surface plasmon (GSP) mode and the external light field. The quality factor and lifetime of the plasmonic-photonic absorber can be obtained with using the coupled mode theory (CMT) and finite difference time domain (FDTD) method, which are effectively tunable with changing Fermi energy, carrier mobility and superstrate refractive index. The evolutions of total energy and lifetime of GSP are also shown, which are helpful for the study of micro processes in a two-dimensional material plasmonic-photonic absorber. The strongly localized fundamental field induces a desired increase of second harmonic (SH) wave and third harmonic (TH) wave. The manipulation of the quality factor and lifetime of the GSP makes graphene an excellent platform for tunable two-dimensional material plasmonic-photonic devices to realize the active control of the photoelectric/photothermal energy conversion process and higher harmonic generation.

In this paper, we consider a novel cooperative underlay cognitive radio network based on non-orthogonal multiple access (CR-NOMA) with adaptive relay selection and power allocation. In secondary networks, dedicated relay assistance and user assistance are used to achieve communication between the base station and the far (and near) user. Here, a two-stage adaptive relay selection and power allocation strategy is proposed to maximize the achievable data rate of the far user while ensuring the service quality of near user. Furthermore, the closed-form expressions of outage probability of two secondary users are derived, respectively, under interference power constraints, revealing the impact of transmit power, number of relays, interference threshold and target data rate on system outage probability. Numerical results and simulations validate the advantages of the established cooperation and show that the proposed adaptive relay selection and power allocation strategy has better outage performance.

Although it had been reported that Israeli acute paralysis virus (IAPV) can cause systemic infection in honey bees, little is known about how it establishes this infection and results in the typical symptoms, paralysis and trembling. Here, we used our previously constructed IAPV infectious clone to investigate viral loads in different tissues of honey bees and further identify the relation between tissue tropism and paralytic symptoms. Our results showed that tracheae showed a greater concentration of viral abundance than other tissues. The abundance of viral protein in the tracheae was positively associated with viral titers, and was further confirmed by immunological and ultrastructural evidence. Furthermore, higher viral loads in tracheae induced remarkable down-regulation of succinate dehydrogenase and cytochrome c oxidase genes, and progressed to causing respiratory failure of honey bees, resulting in the appearance of typical symptoms, paralysis and body trembling. Our results showed that paralysis symptoms or trembling was actually to mitigate tachypnea induced by IAPV infection due to the impairment of honey bee tracheae, and revealed a direct causal link between paralysis symptoms and tissue tropism. These findings provide new insights into the understanding of the underlying mechanism of paralysis symptoms of honey bees after viral infection and have implications for viral disease prevention and specific therapeutics in practice.

A volumetric ablation model for EPDM (ethylene- propylene-diene monomer) is established in this paper. This model considers the complex physicochemical process in the porous structure of a char layer. An ablation physics model based on a porous structure of a char layer and another model of heterogeneous volumetric ablation char layer physics are then built. In the model, porosity is used to describe the porous structure of a char layer. Gas diffusion and chemical reactions are introduced to the entire porous structure. Through detailed formation analysis, the causes of the compact or loose structure in the char layer and chemical vapor deposition (CVD) reaction between pyrolysis gas and char layer skeleton are introduced. The Arrhenius formula is adopted to determine the methods for calculating carbon deposition rate C which is the consumption rate caused by thermochemical reactions in the char layer, and porosity evolution. The critical porosity value is used as a criterion for char layer porous structure failure under gas flow and particle erosion. This critical porosity value is obtained by fitting experimental parameters and surface porosity of the char layer. Linear ablation and mass ablation rates are confirmed with the critical porosity value. Results of linear ablation and mass ablation rate calculations generally coincide with experimental results, suggesting that the ablation analysis proposed in this paper can accurately reflect practical situations and that the physics and mathematics models built are accurate and reasonable.

A novel type of macromolecular prodrug delivery system is reported in this research. The N-galactosylated-chitosan-5-fluorouracil acetic acid conjugate (GC-FUA) based nanoparticle delivery system was evaluated in vitro and in vivo. Biocompatibility of GC-FUA-NPs was screened by BSA adsorption test and hemolysis activity examination in vitro. Cytotoxicity and cellular uptake study in HepG2 and A549 cells demonstrated that compared to free 5-Fu, the GC-FUA-NPs play great function in killing cancer cells for the cell endocytosis mediated by asialoglycoprotein receptor (ASGPR), which overexpresses on the cell surface. Pharmacokinetics study further illustrated that the drug-loaded nanoparticles has a much longer half-time than free 5-Fu in blood circulation in Sprague–Dawley (SD) rats. Tissue distribution was investigated in Kunming mice, and the result showed that the GC-FUA-NPs have a long circulation effect. The obtained data suggested that GC-FUA-NP is a very promising drug delivery system for efficient treatment of hepatocellular carcinoma.

Honey bee viruses are associated with honey bee colony decline. Israeli acute paralysis virus (IAPV) is considered to have a strong impact on honey bee survival. Phylogenetic analysis of the viral genomes from several regions of the world showed that various IAPV lineages had substantial differences in virulence. Chronic bee paralysis virus (CBPV), another important honey bee virus, can induce two significantly different symptoms. However, the infection characteristics and pathogenesis of IAPV and CBPV have not been completely elucidated. Here, we constructed infectious clones of IAPV and CBPV using a universal vector to provide a basis for studying their replication and pathogenesis. Infectious IAPV and CBPV were rescued from molecular clones of IAPV and CBPV genomes, respectively, that induced typical paralysis symptoms. The replication levels and expression proteins of IAPV and CBPV in progeny virus production were confirmed by qPCR and Western blot. Our results will allow further dissection of the role of each gene in the context of viral infection while helping to study viral pathogenesis and develop antiviral drugs using reverse genetics systems.

Infection and transmission of honey bee viruses pose a serious threat to the pollination services of crops and wild plants, which plays a vital role in agricultural economy and ecology. RNA interference (RNAi) is an effective defense mechanism against commonly occurring viral infections of animals and plants. However, recent studies indicate that the effects of RNAi on the honey bee can induce additional impacts and might not always be effective in suppressing the virus. Moreover, the RNAi responses differed in relation to the developmental stage of the insect and the target tissue used, even though the same method of delivery was used. These results indicate that further analysis and field experiments should be performed to characterize the varying effectiveness of RNAi-based methods for treating honey bee viral infections. In this review, we provide an overview of the current knowledge and the recent progress in RNAi-based anti-viral treatments for honey bees, focusing in particular highlight the role of the dsRNA-delivery method used and its effect on RNAi efficiency and demonstrate the potential practical value of this tool for controlling the virus. We conclude studying the gene function and disease control of honey bee by RNAi technology requires a complex consideration from physiology, genetics to environment.

Honey bees are essential to the functioning of terrestrial ecosystems. However, despite no single factor being blamed for losses of honey bee colonies in Europe and the USA, viruses have been considered as a major driver. Moreover, a virus vector can enhance the titer and virulence of virus such as Varroa destructor can change the virulence of the deformed wing virus. Here, we report molecular evidence for aphid lethal paralysis virus (ALPV) infecting Vespa velutina, which is an important predator of honey bees, especially of Apis cerana. Viral replication and phylogenetic analysis indicated that ALPV can not only replicate in V. velutina and A. cerana, but ALPV from A. cerana (ALPV-Ac) was also significantly associated with that of V. velutina (ALPV-Vv), though distinct from those of Apis mellifera (ALPV-Am). The host state posterior probability displayed that V. velutina is the main viral reservoir between V. velutina and A. cerana. Our results show ALPV had expanded host diversity resulting in potential impacts on the health of pollinators, even on the pollination ecosystem. We suggest further studies should investigate potential risks and impacts on pollinator populations of hornets. These results should have an impact conservation efforts focused on sustaining native pollinator abundance and diversity, and therefore, the crucial ecosystem services that they provide.

As the authors of the title paper [...]

A numerical methodology has been developed to simulate the overall ablation process of the insulator material named ethylene-propylene-diene monomer. Special attention is focused on the char layers of ethylene-propylene-diene monomer formed in different ablation environments by analyzing the characters of the char layers, which was defined as an uneven porous medium. An overall ablation model has been developed to describe the simultaneous thermo-chemical ablation and particle erosion of ethylene-propylene-diene monomer using porous medium equation methodology. A total of six calculations of one kind of ethylene-propylene-diene monomer material have been performed to obtain the theory erosion properties in two lab-scale solid rocket motors, and all the submodels of overall ablation model have been validated.

Glycyrrhhizic acid (GA), including 18α-glycyrrhizic acid (18α-GA) and 18β-glycyrrhizic acid (18β-GA), is the main active ingredient of licorice. GA is generally considered an effective pharmacological strategy protecting against hepatic disease; however, the optimal compatibility proportion of 18α-GA and 18β-GA against alcoholic liver disease (ALD) and the underlying mechanism are not well established. Hence, this study was designed to explore the optimal compatibility proportion of 18α-GA and 18β-GA against ALD, followed by investigating the underlying mechanisms. SD rats were administered 40% ethanol once a day, accompanied by treatment with different proportions of 18α-GA and 18β-GA for four weeks. Then all rats were anesthetized with chloral hydrate and blood samples were taken from the abdominal aorta for biochemical assay. Livers were also collected and the liver function, lipid profile, ROS production, and mRNA and protein levels of related genes involved in lipid metabolism were assessed. The results showed that 18α-GA and 18β-GA, particularly at a proportion of 4:6, significantly reduced liver damage, lipid accumulation, and oxidative stress in ethanol-induced rats, as indicated by the decreased levels of alanine aminotransferase (ALT) and aminotransferase (AST) in serum, improvement of liver histopathological changes, regulation of total cholesterol (TC), total triglyceride (TG), high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C), and modulation of superoxide dismutase (SOD), glutathione (GSH), and malonaldehyde (MDA). Moreover, the combination treatment with 18α-GA and 18β-GA substantially reduced the mRNA and protein levels of sterol regulatory element-binding protein-1c (SREBP-1c) and acetyl-coal carboxylase (ACC); meanwhile, increased levels of peroxisome proliferators activated receptor-α (PPAR-α) and carnitine palmitoy transferase-1 (CTP-1) in the liver tissues of ethanol-induced rats. In conclusion, our results indicated that the optimal compatibility proportion of 18α-GA and 18β-GA protecting against ALD was 4:6, and the mechanism was associated with the regulation of oxidative stress and lipid metabolism.

Slickwater-based fracturing fluid has recently garnered significant attention as the major fluid for volumetric fracturing; however, lots of challenges and limitations such as low viscosity, poor salt tolerance, and possible formation damage hinder the application of the conventional simple slickwaterbased fracturing fluid. In addition, nanomaterials have proven to be potential solutions or improvements to a number of challenges associated with the slickwater. In this paper, molybdenum disulfide (MoS2) nanosheets were chemically synthesized by hydrothermal method and applied to improve the performance of conventional slickwater-based fracturing fluid. Firstly, the microstructure characteristics and crystal type of the MoS2 nanosheets were analyzed by SEM, EDS, TEM, XPS, and Raman spectroscopy techniques. Then, a series of evaluation experiments were carried out to compare the performance of MoS2 nanosheet-modified slickwater with the conventional slickwater, including rheology, drag reduction, and sand suspension. Finally, the enhanced imbibition capacity and potential mechanism of the nanosheet-modified slickwater were systematically investigated. The results showed that the selfsynthesized MoS2 nanosheets displayed a distinct ultrathin flake-like morphology and a lateral size in the range of tens of nanometers. In the nano-composites, each MoS2 nanosheet plays the role of crosslinking point, so as to make the spatial structure of the entire system more compact. Moreover, nanosheet-modified slickwater demonstrates more excellent properties in rheology, drag reduction, and sand suspension. The nanosheet-modified slickwater has a higher apparent viscosity after shearing 120 min under 90 °C and 170 s-1. The maximum drag reduction rate achieved 76.3% at 20 °C, and the sand settling time of proppants with different mesh in the nano-composites was prolonged. Spontaneous imbibition experiments showed that the gel-breaking fluid of nanosheet-modified slickwater exhibited excellent capability of oil-detaching, and increase the oil recovery to ~35.43%. By observing and analyzing the interfacial behavior of MoS2 nanosheets under stimulated reservoir conditions, it was found that the presence of an interfacial tension gradient and the formation of a climbing film may play an essential role in the spontaneous imbibition mechanism. This work innovatively uses two-dimensional MoS2 nanosheets to modify regular slickwater and confirms the feasibility of flake-like nanomaterials to improve the performance of slickwater. The study also reveals the underlying mechanism of enhanced imbibition efficiency of the nano-composites. [ABSTRACT FROM AUTHOR]