Foot and mouth disease virus (FMDV) is a highly contagious pathogen propagating among cloven-hoofed animals. As a major immunogenic protein, VP1 plays a pivotal role in the induction of neutralizing ...antibodies, which therefore is an ideal target for developing subunit vaccines. In current study, four prokaryotic expression clones (rV4C, rC4V, rV5F and rF5V) were constructed by fusing truncated calreticulin (CRT) (120–250 aa or 120–308 aa) at the N/C terminal of vp1 gene, and co-expressed with chaperone trigger factor 16 (Tf16) in E.coli, respectively. The soluble recombinant CRT-fused VP1 proteins could form into homogeneous reactive polymers with average hydrodynamic diameters around 100 nm according to the dynamic light scattering (DLS) data. Immunization of guinea pigs with 10 μg purified CRT-fused VP1 proteins induced high levels of antibodies against naked-VP1 through indirect ELISA. Sandwich ELISA showed that only rC4V could elicit the same level of antibody against FMD virus as commercial inactivated vaccine after booster. The lymphocyte cytokines secretion of immunized rC4V was higher than the other CRT-fused VP1 proteins in guinea pigs. These results showed that the soluble CRT-fused VP1 proteins, especially rC4V, expressed with Tf16 in E. coli might have potential to be used as subunit vaccine candidate against FMDV.
A Bi2WO6/BiVO4 composite photocatalytic material was synthesized by the hydrothermal method, and achieved the effective degradation of oxytetracycline (OTC) and tetracycline (TC) under visible light. ...The compositions, structures, chemical states and optoelectronic properties of Bi2WO6, BiVO4 and Bi2WO6/BiVO4 composites were characterized by systematic characterization. The results show that the existence of the heterojunction interface facilitates the separation of photogenerated carriers. Compared with the pure catalyst of Bi2WO6 and BiVO4, the Bi2WO6/BiVO4 composite material significantly improves the degradation efficiency of OTC and TC. The degradation rate is 6.22 and 3.02 times higher than that of Bi2WO6 and BiVO4, respectively. Through the free radical quenching experiments, it is known that photogenerated holes (h+) and superoxide anion free radicals (·O2−) are the main active substances in the degradation of OTC. By analyzing the process of photocatalytic degradation of OTC, there are mainly six intermediates during the process. Their possible degradation pathways are also inferred in this paper.
The frequency of the pathogenic allele of the autosomal recessive deafness gene GJB2 varies among different populations in the world, and accumulates to a sufficiently high frequency in certain ...population. The purpose of this study is to investigate the origin and evolution of GJB2 pathogenic alleles in Chinese deaf patients. Children with non‐syndromic hearing loss, and their parents, from 295 families were recruited. Customized capture probes targeted at 943 single nucleotide polymorphisms (SNPs) related to GJB2 gene were designed for sequencing of genomic DNA in blood samples. Haplotypes carrying pathogenic allele were analyzed through linkage disequilibrium block building, ancestry tracing, and extended haplotype heterozygosity calculation. Two pathogenic GJB2 alleles, c.235delC (18.41%) and c.109G > A (15.57%), were observed in 867 donors. For c.235delC allele, three different core haplotypes with one major haplotype (97.32%) were found, and their core SNPs were 100% conserved. For c.109G > A allele, six different haplotypes with one major haplotype (93.28%) were found and the major c.109G > A allele evolved from a specific ancestral haplotype. Geographical origins of donors carrying GJB2 c.109G > A and c.235delC core haplotypes centered between Qinghai and Neimenggu. GJB2 c.235delC has long‐range linkage disequilibrium. No positive selection signature was found for GJB2 c.235delC or c.109G > A in the studied population. In conclusion, we discovered a single origin of GJB2 c.235delC allele and multiple independent origins of GJB2 c.109G > A allele. Alternative to positive selection or multiple independent recurrent mutation event, population bottleneck effect might account for the observed high population frequency of these pathogenic alleles.
A single origin of GJB2 c.235delC allele and multiple, independent origin of c.109G > A allele in Chinese non‐syndromic hearing loss population.
The origin of A-type granites is purely circumstantial. Granitic complexes are quite common and generally composed of different type granites. I- and A-type granite association in a granitic complex ...is often described in the literature. Here we present a granitic complex, i.e. the Pitou complex in southern Jiangxi province, South China that is composed of different varieties of A-type granites. Detailed zircon LA-ICP-MS UPb chronology and in situ Hf isotope, mineral chemistry and whole-rock element and SrNd isotope data of this granitic complex are used to explore their origin and to further constrain the geodynamics of Mesozoic magmatism in South China. Our new data indicate that the Pitou complex was emplaced during the Late Triassic (237 Ma) (central to northern part) and Early Jurassic (188–185 Ma) (southern part), respectively and that both the Late Triassic and Early Jurassic granites belong to A-type but show contrasting origins. The Late Triassic granites show an association of alkali-feldspar granite-syenogranite-monzogranite and the rock type of the Early Jurassic granites is alkali-feldspar granite. All the granites are composed mainly of K-feldspar, quartz, plagioclase and biotite (ferri-biotite or annite) with biotite occurring as anhedral crystal, interstitial to quartz and feldspar. Both the Late Triassic and Early Jurassic granites have high SiO2 (>70 wt%) and total alkalis (K2O + Na2O > 8 wt%) with high FeOT/(FeOT + MgO) and low Mg#. They are enriched in rare earth elements (except Eu) and depleted in Sr and Ba. They display Zr + Y + Ce + Nb >350 ppm, 10,000 × Ga/Al >2.6 and have high zircon saturation temperatures (>800 °C). Biotites in the granites are Fe-rich with very low Fe3+/Fe2+, indicating fairly reducing conditions. However, the Late Triassic and Early Jurassic granites also show some geochemical differences. The Late Triassic granites have lower FeOT/(FeOT + MgO) and higher Mg# than the Early Jurassic granites, with the Mg# of the former consistent with pure crustal melts and the Mg# of the latter much lower than pure crustal melts. In addition, the Late Triassic granites have lower zircon saturation temperatures (up to 843 °C, average 823 °C) than the Early Jurassic granites (up to 946 °C, average 875 °C). Furthermore, the Late Triassic granites have high 87Sr/86Sr (t) (0.7132–0.7226) and negative εNd (t) (−10.3 to −10.9) and εHf (t) (in situ zircon) (−11.5 to −11.6) that are similar to those of the early Paleozoic granitoids in the region whereas the Early Jurassic granites have low 87Sr/86Sr (t) (down to 0.7034) and positive εNd (t) (up to +3.0) and εHf (t) (in situ zircon) (up to +8.3) that are similar to those of the Early Jurassic gabbroic rocks in the region. Geochemical data and major element modeling suggest that the Late Triassic A-type granites were formed by shallow (ca. 15–20 km depth) dehydration melting of the early Paleozoic granitoids triggered by intraplating of basaltic magmas and the Early Jurassic A-type granites were produced by extensive fractionation (ca. 90% to 95%) from gabbroic magmas by removal of plagioclase, amphibole, K-feldspar, clinopyroxene and magnetite. We further suggest the origin of the Late Triassic A-type granites was related to the transtension of the regional NE–trending strike-slip faults caused by the early Indosinian continental collisions and the Early Jurassic A-type granites were emplaced in a back-arc extensional setting coupled with the slab rollback and subsequent slab break-off of the subducted Palaeo-Pacific plate. Our new data confirm that the early Mesozoic magmatism in South China was controlled by continental collisions during the Late Permian to Triassic amalgamation in Southeast Asia whereas the late Mesozoic magmatism was related to the northwestward subduction of the Palaeo-Pacific plate. A transition in the dominant tectonic regime from the Tethyan to the Pacific tectonic domain most likely took place during the Rhaetian.
•The Pitou granitic complex emplaced during the Late Triassic and Early Jurassic.•Both Late Triassic and Early Jurassic granites are A-type but show contrasting origin.•Late Triassic granites formed by shallow dehydration melting of Paleozoic granitoids.•Early Jurassic granites formed by extensive fractionation from gabbroic magmas.•Origin of both A-type granites suggests different geodynamic mechanisms.
An abrupt decrease in egg production and quality in laying hens can be brought on by the avian adenovirus known as the egg drop syndrome virus (EDSV). So far, there are no efficient commercial ...diagnostic approaches for EDSV. In the present study, we first purified two monoclonal antibodies (mAbs 5G4 and 6G6) specifically against the EDSV fibre protein. The mAb 5G4 was then employed as capture antibody. Additionally, the detection antibody 6G6 (HRP-6G6) was conjugated with horseradish peroxidase. Consequently, based on these two mAbs, we developed a sandwich enzyme-linked immunosorbent assay (ELISA) for EDSV detection. Specificity evaluation demonstrated that only EDSV gave a positive result while other avian viruses showed negative results. Sensitivity investigation showed that the limit of detection of EDSV was 10
2.9
TCID
50
/ml and the limit of detection of the purified His-Fiber was 5 ng/ml. Furthermore, the screening of samples from infected chickens showed that this method was very effective and could be applied to the detection of EDSV in infected samples. In summary, the sandwich enzyme-linked immunosorbent assay developed here provides an efficient, sensitive, and large-scale method for the specific diagnosis of EDSV.
A sandwich ELISA was developed to detect EDSV using the mAbs 5G4 and HRP-6G6.
The sandwich ELISA maintained high specificity and sensitivity.
The sandwich ELISA had equivalent consistency with real-time PCR assay.
African swine fever (ASF) is a devastating disease, which is causing huge economic losses in China. Therefore, it is urgent to provide a rapid, highly specific and sensitive diagnostic method for the ...detection of African swine fever virus (ASFV), the ASF infectious agent. In this study, a novel quantitative real‐time polymerase chain reaction (qPCR) assay with lyophilized powder reagents (LPR), targeting the major structural protein p72 gene, was established for the detection of ASFV. This assay had many advantages, such as saving time and money, good sensitivity and repeatability. The sensitivity of this assay was 100 copies/μl of ASFV plasmid templates, and the assay showed 10‐fold greater sensitivity than a qPCR assay recommended by OIE. Furthermore, specificity analysis showed that qPCR with LPR for ASFV had no cross‐reactivity with other important swine pathogens. In clinical diagnoses of 218 blood samples of domestic pigs in China, the positive rate of the diagnosis of ASFV by qPCR with the LPR and commercial kit reached 80.73% (176/218) and 76.61% (167/218) respectively. The coincidence rate between the two assays is 92.20% (201/218), and kappa value is 0.768 (p < .0001) by SPSS analysis. The overall agreement between the two assays was 95.87% (209/218). Further Pearson correlation and linear regression analysis showed a significant correlation between the two assays with an R2 value of 0.9438. The entire procedure, from specimen processing to result reporting, can be completed within 2 hr. Our results demonstrated that the qPCR‐LPR assay is a good laboratory diagnostic tool for sensitive and efficient detection of ASFV.
The superposition of quantum states, quantified by coherence, is a fundamental feature to distinguish quantum mechanics from classical theories. Estimations of coherence with perfectly characterised ...devices have been well‐studied. However, imperfections or malfunctions of realistic measurement devices might nullify the characterization. Device‐independent (DI) tests allow to witness and quantify the quantum feature of a system, such as entanglement, without trusting the implementation devices. Although DI test is a powerful tool in many quantum information tasks, it generally requires nonlocal settings. Little is known if single party coherence can be witnessed and estimated via untrusted devices. In this work, coherence witnesses and estimations with untrusted devices are systematically studied. First, a no‐go theorem for detecting existences of single party coherence via a DI or semi DI means is proven. A general prepare‐and‐measure semi DI scheme for witnessing and estimating the amount of coherence is then proposed. How to estimate the relative entropy and the l1 norm of single party coherence with analytical and numerical approaches is shown. As coherence is an essential resource for tasks such as quantum random number generation and quantum key distribution, it is expected that this result may shed light on designing new quantum cryptographic schemes.
The problems of coherence witnesses and estimations with untrusted measurement devices are systematically examined. Fully device‐independent protocols or semi‐quantum games fail in witnessing single party coherence. Instead, a prepare‐and‐measure scenario could be applied. All coherent states could be witnessed with this method, and measures of the relative entropy of coherence and the l1 norm of coherence are estimated.
Pseudorabies virus (PRV) was isolated from some human cases recently and the infected patients manifested respiratory dysfunction and acute neurological symptoms. However, no effective drug or ...vaccine, preventing the progression of PRV infection, is available. Nectin-1 was the only reported receptor for PRV cell entry both swine and human origin, representing an excellent target to block PRV infection, and especially its transmission from pigs to humans. A PRV-gD specific mAbs (10B6) was isolated from hybridomas and its neutralizing activities in vitro and in vivo were determined. 10B6 exhibited effective neutralizing activities in vitro with IC50 = 2.514 μg/ml and 4.297 μg/ml in the presence and absence of complement. And in vivo, 10B6 provided 100% protection against PRV lethal challenge with a dose of 15 mg/kg. Further, 10B6 could bind to a conserved epitope, 316QPAEPFP322, locating in gD pro-fusion domain, and finally blocks the binding of PRV-gD to nectin-1. Moreover, 10B6 showed an effective inhibition on PRV cell-attachment in a cell type-independent manner and could also block the virus spreading among cells. 10B6 exhibited effectively neutralizing activities to Chinese PRV variant strain in vitro and in vivo by blocking gD binding to nectin-1, implied both prophylactic and therapeutic interventions against PRV infections.
•A PRV-gD specific mAbs (10B6) was isolated.•10B6 exhibited effective neutralizing activities in vitro and in vivo.•10B6 blocked the binding between PRV gD and nectin-1 to neutralize virus.•A linear neutralizing epitope of PRV-gD (316QPAEPFP322) was firstly reported.
