Explore the vast range of titles available.

Superparaelectrics are considered promising candidate materials for achieving superior energy storage capabilities. However, due to the complicated local structural design, simultaneously achieving high recoverable energy density ( W rec ) and energy storage efficiency ( η ) under high electric fields remains a challenge in bulk superparaelectrics. Here, we propose utilizing entropy engineering to disrupt long-range ferroic orders into local polymorphic distortion disorder with multiple BO 6 tilt types and diverse heterogeneous polarization configurations. This strategy reduces the switching barriers, thereby facilitating the emergence of superparaelectric behaviors with ideal polarization forms. Furthermore, it enables high polarization response, negligible remnant polarization, delayed polarization saturation, and enhanced breakdown electric fields ( E b ) in high-entropy superparaelectrics. Consequently, an extraordinary W rec of 15.48 J cm –3 and an ultrahigh η of 90.02% are achieved at a high E b of 710 kV cm –1 , surpassing the comprehensive energy storage performance of previously reported bulk superparaelectrics. This work demonstrates that entropy engineering is a viable strategy for designing high-performance superparaelectrics. High-entropy superparaelectrics with locally diverse ferroic distortion simultaneously achieve ultrahigh energy density and ultrahigh energy storage efficiency under large electric fields.

Th17 cells play important roles in anti-infective responses. The 15 kDa excretory/secretory protein of Haemonchus contortus (HcES-15) has been identified as a promising immune-protective antigen against H. contortus infection capable of up-regulating IL-17, IL-4 and IL-10 production. To obtain the peptides that primarily induce the Th17 immune response, we amplified and expressed the peptides ES15-1, ES15-2 and ES15-3 from HcES-15. In vitro studies demonstrated that ES15-1 stimulated transcriptional activation of the STAT3/RORγt signaling pathway and induced IL-17 production in goat peripheral blood mononuclear cells (PBMCs). In vivo studies, flow cytometric analysis revealed that subcutaneous injection of PLGA-encapsulated ES15-1 peptide (PLGA-ES15-1, 50 μg) significantly enhanced Th17 cell differentiation in the spleens of BALB/c mouse. Consistent with these findings, ELISA quantification demonstrated that ES15-1 treatment significantly increased serum levels of pro-inflammatory cytokine (IL-17, IL-1, IL-6, and TNF-α). In goat immune protection studies, goats ( n  = 6) were subcutaneously immunized with 500 μg of PLGA-ES15-1 on days 0 and 14, followed by infection with H. contortus infective third-stage larvae (iL3s) 1 week post-second immunization. ES15-1 significantly enhanced serum levels of pro-inflammatory cytokines (IL-17, IL-1, IL-6, TNF-α). At autopsy, vaccinated goats exhibited 69.0% ( p  < 0.001) reduction of fecal egg counts (FEC) and 50.54% ( p  < 0.05) reduction of worm burdens versus controls. Our findings suggested that peptide ES15-1 enhanced Th17 responses through regulation of the STAT3/RORγt pathway, conferring a certain immune protection against H. contortus infection.

Background Previous studies indicated that infection with Haemonchus contortus is host-specific (goat: susceptible host; gerbil: paratenic host; mouse: resistant host). Neutrophils play an essential role in host defense against parasitic infection through phagocytic engulfment, reactive oxygen species (ROS) generation, and neutrophil extracellular traps (NETs) formation. NETs are large web-like complexes consisting of a DNA scaffold decorated with various proteins components, including histones, myeloperoxidase, and elastase. They are released through both ROS-dependent and ROS-independent pathways. Previous studies have demonstrated both constraints and effectiveness of NETs in helminths. However, the roles of NETs in anti-infection of H. contortus in different hosts are still unclear. Methods To assess host-specific variations in NETs release, neutrophils isolated from goats, gerbils, and mice were co-cultured with Haemonchus contortus third-stage larvae (HcL3), followed by quantitative analysis of NETs formation using the PicoGreen® fluorescence assay. Subsequently,  H. contortus  excretory–secretory proteins (HcESPs) were co-cultured with neutrophils isolated from each host species. NETs release and ROS production were then quantitatively assessed using PicoGreen® fluorescence intensity and oxidation-sensitive dichlorodihydrofluorescein diacetate (DCFH-DA) fluorescence. In addition, the neutrophil’s phagocytic ability for FITC-dextran was evaluated by flow cytometric analysis. Finally, to elucidate the signaling pathways involved in HcESP-induced NETs release in goat neutrophils, four specific inhibitors were employed for pretreatment prior to stimulation. Results Our results demonstrate that in vitro stimulation with HcL3 triggers NETs formation. The release of NETs exhibits significant host-specific variation, specifically, neutrophils from mice showed the highest NETs release, followed by gerbils, and a minimal response in goats. Moreover, HcESP treatment markedly inhibited ROS generation and phagocytic capacity in neutrophils from all three host species. Intriguingly, HcESPs exerted host-specific modulation of NETs release, with inhibition observed in goats, enhancement in mice, and context-dependent modulation in gerbils. Mechanistic investigations revealed that the NETs suppression in goats neutrophils involved both nicotinamide adenine dinucleotide phosphate (NADPH) oxidase- and neutrophil elastase-dependent pathways. Conclusions Our results demonstrate that HcESPs significantly inhibit NETs formation in goat neutrophils through dual modulation of NADPH oxidase and neutrophil elastase activity. This finding highlights these two enzymes as promising molecular targets for anti-helminthic vaccine development. Graphical abstract

Ticks are an important type of pathogen transmission vector, and pathogens not only cause serious harm to livestock but can also infect humans. Because of the roles that ticks play in disease transmission, reducing tick pathogen infectivity has become increasingly important and requires the identification and characterization of these pathogens and their interaction mechanisms. In this study, we determined the miRNA expression profile of Hemaphysalis longicornis infected with Theileria orientalis, predicted the target genes of miRNAs involved in this infection process, and investigated the role of miRNA target recognition during host–pathogen interactions. The results showed that longipain is a target gene of miR-5309, which was differentially expressed at different developmental stages and in various tissues in the control group. However, the miR-5309 level was reduced in the infection group. Analysis of the interaction between miRNA and the target gene showed that miR-5309 negatively regulated the expression of the longipain protein during the infection of H. longicornis with T. orientalis. To verify this inference, we compared longipain with the blocking agent orientalis. In this study, the expression of longipain was upregulated by the inhibition of miR-5309 in ticks, and the ability of the antibody produced by the tick-derived protein to attenuate T. orientalis infection was verified through animal immunity and antigen–antibody binding tests. The results showed that expression of the longipain + GST fusion protein caused the cattle to produce antibodies that could be successfully captured by ticks, and cellular immunity was subsequently activated in the ticks, resulting in a subtractive effect on T. orientalis infection. This research provides ideas for the control of ticks and tickborne diseases and a research basis for studying the mechanism underlying the interaction between ticks and pathogens.

In the original publication [...]

Background The gram-negative Coxiella burnetii bacterium is the pathogen that causes Q fever. The bacterium is transmitted to animals via ticks, and manure, air, dead infected animals, etc. and can cause infection in domestic animals, wild animals, and humans. Xinjiang, the provincial-level administrative region with the largest land area in China, has many endemic tick species. The infection rate of C. burnetii in ticks in Xinjiang border areas has not been studied in detail. Results For the current study, 1507 ticks were collected from livestock at 22 sampling sites in ten border regions of the Xinjiang Uygur Autonomous region from 2018 to 2019. C. burnetii was detected in 205/348 (58.91%) Dermacentor nuttalli ; in 110/146 (75.34%) D. pavlovskyi ; in 66/80 (82.50%) D. silvarum ; in 15/32 (46.90%) D. niveus ; in 28/132 (21.21%) Hyalomma rufipes ; in 24/25 (96.00%) H. anatolicum ; in 219/312 (70.19%) H. asiaticum ; in 252/338 (74.56%) Rhipicephalus sanguineus ; and in 54/92 (58.70%) Haemaphysalis punctata . Among these samples, C. burnetii was detected in D. pavlovskyi for the first time. The infection rate of Rhipicephalus was 74.56% (252/338), which was the highest among the four tick genera sampled, whereas the infection rate of H. anatolicum was 96% (24/25), which was the highest among the nine tick species sampled. A sequence analysis indicated that 63 16S rRNA sequences could be found in four newly established genotypes: MT498683.1 ( n  = 18), MT498684.1 ( n  = 33), MT498685.1 ( n  = 6), and MT498686.1 ( n  = 6). Conclusions This study indicates that MT498684.1 might represent the main C. burnetii genotype in the ticks in Xinjiang because it was detected in eight of the tick species studied. The high infection rate of C. burnetii detected in the ticks found in domestic animals may indicate a high likelihood of Q fever infection in both domestic animals and humans.

Bartonella are gram-negative intracellular bacteria; certain species of Bartonella can cause diseases in mammals and humans. Ticks play a major role in the transmission of Bartonella . Xinjiang is the largest province in China according to land area and has one-third of the tick species in China; the infection rate of Bartonella in ticks in the Xinjiang border areas has not been studied in detail. Therefore, this study investigated tick infections by Bartonella in Xinjiang border areas, and the purpose of the study was to fill in gaps in information regarding the genetic diversity of tick infections by Bartonella in Xinjiang. We tested 1,549 tick samples from domestic animals (sheep and cattle) for Bartonella using ribC -PCR. Positive samples from the ribC -PCR assay for Bartonella spp. were further subjected to PCR assays targeting the ITS, rpoB and gltA genes followed by phylogenetic analyses. Bartonella DNA was detected in 2.19% (34/1,549) of tick samples, and the ITS, rpoB and gltA genes of ribC gene-positive samples were amplified to identify nine samples of Bartonella melophagi . In this study, molecular analysis was used to assess the presence and genetic diversity of B. melophagi in ticks collected from sheep and cattle from Xinjiang, China. This study provides new information on the presence and identity of B. melophagi in ticks from sheep and cattle.

High blood pressure frequently occurs in the setting of acute stroke and is associated with worse prognoses. However, it is still uncertain whether initiating blood pressure-lowering therapy in the prehospital phase after stroke onset can enhance outcomes for patients with undifferentiated acute stroke. We conducted a search of the PubMed, Embase, and Cochrane databases to identify randomized controlled trials investigating prehospital blood pressure lowering interventions for presumed ultra-acute stroke (within <6 hours). The primary outcome analyzed was the 90-day modified Rankin Scale (mRS), while mortality was considered a secondary outcome. This meta-analysis included four studies with a total of 3912 patients. The pooled data revealed no significant difference in poor functional outcomes at 90 days (RR = 0.97, 95% CI: 0.92-1.02) or mortality rates (RR = 1.02, 95% CI: 0.90-1.15) between the group receiving blood pressure lowering treatment and the control or placebo group. In patients with ultra-acute presumed stroke, prehospital blood pressure lowering treatment within 6 hours of stroke did not improve clinical outcomes (PROSPERO: CRD42024557505).

MicroRNAs act as mRNA posttranscriptional regulators, playing important roles in cell differentiation, transcriptional regulation, growth and development. In this study, microRNA expression profiles of Hyalomma anatolicum anatolicum ticks at different developmental stages were detected by high-throughput sequencing and functionally assessed. In total, 2,585,169, 1,252,678, 1,558,217 and 1,155,283 unique reads were obtained from eggs, larvae, nymphs and adults, respectively, with 42, 46, 45 and 41 conserved microRNAs in these stages, respectively. Using eggs as a control, 48, 43 and 39 microRNAs were upregulated and 3, 10 and 9 downregulated in larvae, nymphs and adults, respectively. microRNA-1 (miR-1) was expressed in high abundance throughout Ha. anatolicum development, with an average of nearly one million transcripts, and it is highly conserved among tick species. Quantitative real-time PCR (qPCR) showed that miR-1 expression gradually increased with tick development, reaching the highest level at engorgement. Differential tissue expression was detected, with significantly higher levels in the salivary glands and epidermis than in the midgut. Inhibition assays showed no significant change in body weight or spawning time or amount between experimental and control groups, but there was a significant difference (p<0.01) in engorgement time. With miR-1 inhibition, ticks displayed obvious deformities during later development. To more fully explain the microRNA mechanism of action, the miR-1 family was analyzed regarding target gene; members acting on Hsp60 include miR-5, miR-994, miR-969, and miR-1011, which jointly play a role. Therefore, microRNAs are critical for normal tick development, and the primary structure of the mature sequence of miR-1 is highly conserved. Nonetheless, different developmental stages and tissues show different expression patterns, with a certain role in prolonging feeding. miR-1, together with other family members, regulates mRNA function and may be used as a molecular marker for species origin and evolution analysis and internal reference gene selection.

The application of high-resolution analog-to-digital conversion devices in wireless seismic data acquisition equipment causes massive invalid noise and seismic signals to be generated during long-term seismic acquisition, and the subsequent processing of massive data will occupy a lot of system resources. To address the above issues, we employ the STM32F4 as the core to integrate an improved environmental dynamic threshold P-wave picking algorithm for continuous vibration data acquisition. During data storage, only the relevant vibration signals are preserved to minimize the storage of irrelevant data and enhance work efficiency. The research results indicate that embedding a vibration identification algorithm inside the microcontroller can quickly and effectively identify seismic data, filter out invalid noise signals, reduce data volume, and improve work efficiency.