Lignite-steel slag constructed wetland with multi-functionality and effluent reuse.

Constructed wetlands (CWs) are widely used to treat wastewater, while innovative studies are needed to support resource conservation, enhance multi-functionality, and improve the effectiveness of effluent usage. This study assessed the potential of CW's multiple functions by combining low-rank coal (lignite) and industrial waste (steel slag) in different configurations as CW substrates. The results of scanning electron microscope (SEM), energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), and metagenomic sequencing showed that the experimental treatment with lignite and steel slag mixtures had the highest multi-functionality, including efficient nutrient removal and carbon sequestration, as well as hydroponic crop production. Lignite and steel slag were mixed to form lignite-steel slag particle clusters, where Ca2+ dissolved on the surface of steel slag was combined with PO43- in wastewater to form Ca3(PO4)2 precipitation for phosphorus removal. A biofilm grew on the surface of lignite in this cluster, and OH- released from steel slag promoted lignite to release fulvic acid, which provided a carbon source for heterotrophic microorganisms and promoted denitrification. Moreover, fulvic acid enhanced carbon sequestration in CWs by increasing the biomass of Phragmites australis. The effluent from lignite-steel slag CW increased cherry tomato yield and quality while saving N and P applications. These results provide new ideas for the "green" and economic development of CW technology.

[Effects of chitosan oligosaccharide on bone metabolism and IKK/NF-κB pathway in rats with osteoporosis and periodontitis].

PURPOSE: To investigate the effects of chitosan oligosaccharide on bone metabolism and IKK/NF-κB pathway in mice with osteoporosis and periodontitis. METHODS: Thirty rats were randomly divided into 3 groups, with 10 rats in each group. They were divided into control group, ovariectomized periodontitis group and chitosan oligosaccharide treatment group. Except for the control group, the other two groups were ovariectomized and smeared with Porphyromonas gingivalis fluid to establish the model of osteoporosis with periodontitis. Four weeks after ligation, the rats in chitosan oligosaccharide treatment group were gavaged with 200 mg/kg chitosan oligosaccharide, and the other two groups were gavaged with equal volume of normal saline once a day for 90 days. The periodontal tissues of each group were observed before administration, and the bone mineral density of rats was detected by dual energy X-ray animal bone mineral density and body composition analysis system. After 90 days of administration, the bone mineral density was detected again. After administration, blood was collected from tail vein, and the contents of serum alkaline phosphatase (ALP), bone Gla protein (BGP) and tartrate resistant acid phosphatase 5b (TRACP5b) were measured by enzyme-linked immunodeficient assay. The gingival index and periodontal attachment loss of rats in each group were obtained by visual examination and exploratory examination. The maxilla was removed, and the distance from the enamel cementum boundary to the alveolar crest was measured to obtain alveolar bone absorption value. H-E staining was used to observe the pathology of maxilla in each group. RT-PCR and Western blot were used to detect the nuclear factors in periodontal tissue of rats in each group. SPSS 22.0 software package was used for statistical analysis. RESULTS: Before administration, the gums of the control group were pink without bleeding, and the gums of the other two groups were red and swollen with slight bleeding. After administration, compared with the control group, the bone mineral density, serum ALP, BGP of ovariectomized periodontitis group decreased significantly(P＜0.05); while TRACP5b, gingival index, loss of periodontal attachment and alveolar bone resorption, NF-κB and IKK mRNA and protein expression in periodontal tissue increased significantly(P＜0.05). Compared with the ovariectomized periodontitis group, the bone mineral density, serum ALP, BGP were significantly increased(P＜0.05); while TRACP5b, gingival index, periodontal attachment loss and alveolar bone resorption, NF-κB and IKK mRNA and protein expression in periodontal tissue were significantly decreased (P＜0.05). In the ovariectomized periodontitis group, the periodontal tissue combined with epithelium was separated from the tooth surface, the dental pocket was obvious and deep, and the height of alveolar bone decreased. Although dental pocket could be observed in the periodontal tissue of rats treated with chitosan oligosaccharide, it was not obvious, and new bone appeared around the alveolar bone. CONCLUSIONS: Chitosan oligosaccharide can induce biochemical indexes of bone metabolism to become normal, alleviate the symptoms of periodontitis, this may be related to the inhibition of IKK/NF-κB pathway by chitosan oligosaccharide.

Identification of Neuropeptides as Potential Crosstalks Linking Down Syndrome and Periodontitis Revealed by Transcriptomic Analyses.

BACKGROUND: This bioinformatics study was aimed to investigate the relationship between periodontitis (PD) and Down Syndrome (DS) regarding potential crosstalk genes, related neuropeptides, and biological processes. METHODS: Data for PD (GSE23586, GSE10334 and GSE16134) and DS (GSE35665) were downloaded from NCBI Gene Expression Omnibus (GEO). Following normalization and merging of PD data, differential expression analysis was performed (p value < 0.05 and ∣log FC | ≥0.5). The common deregulated genes between PD and DS were considered as crosstalk genes. The significantly differentially expressed genes were used to construct the coexpression network and to further identify coexpression gene modules. To acquire the significant modules, the significant expression level of genes in the module was used to analyze the enrichment of genes in each module. Neuropeptides were assessed from NeuroPedia database. Neuropeptide genes and crosstalk genes were merged and mapped into PPI network, and the correlation coefficient (Spearman) was determined for the crosstalk genes. RESULTS: 138 crosstalk genes were predicted. According to the functional enrichment analysis, these genes significantly regulated different biological processes and pathways. In enrichment analysis, the significant module of DS was pink module, and turquoise module was significant in PD. Four common crosstalk genes were acquired, i.e., CD19, FCRL5, FCRLA, and HLA-DOB. In the complex network, INS and IGF2 interacted with CASP3 and TP53, which commonly regulated the MAPK signaling pathway. Moreover, the results showed that TP53 interacted with IGF2 and INS inducing the dysregulation of PI3K-Akt signaling pathway. UBL was positively correlated with crosstalk genes in both diseases. LEP was revealed to be both a neuropeptide and crosstalk gene and was positively correlated with other crosstalk genes. CONCLUSION: Different crosstalk genes, related neuropeptides, and biological pathways and processes were revealed between PD and DS, which can serve as a theoretical basis for future research.

Ultrafiltration of up-flow biological activated carbon effluent: Extracellular polymer biofouling mechanism and mitigation using pre-ozonation with H2O2 backwashing.

Biofouling is a key problem in membrane filtration, and extracellular polymer substances (EPS) play a key role in biofouling. Biofouling contributes to membrane fouling during ultrafiltration of up-flow biological activated carbon filter (UBACF) effluent. EPS are released when pollutants get attached with membrane surface and when pollutants are in solution phase from cell lysis and by cell secretions. In our study of EPS + humic acid (HA) prepared as the effluent pollutants for ultrafiltration, we found that EPS increased the interfacial forces between the pollutants and the membrane, resulting in membrane fouling. In the early stages of filtration, the main contribution of EPS to membrane fouling was to bond with organic colloids, which led to an increase in the pollutant particle size and zeta potential. This increased the short-range Lewis acid-base (AB) forces from -4.89 nN to -12.59 nN and accelerated the formation of a cake layer. In the late stage of filtration, the EPS increased both the AB and London-van der Waals (LW) forces, thus accelerating membrane fouling. In order to mitigate biofouling, we developed a method of pretreating the effluent with 0.4 mg/L ozone prior to ultrafiltration and backwashing with 8 mg/L H2O2 to sterilize bacteria attached to the membrane surface. This method not only changed the characteristics of the EPS, but also inactivated bacteria by disinfection with H2O2, thereby reducing the amount of EPS. The proposed method provided a long-term stable operation guarantee for ultrafiltration of UBACF effluent.

Thermally Triggered, Cell-Specific Enzymatic Glyco-Editing: In Situ Regulation of Lectin Recognition and Immune Response on Target Cells.

In situ glyco-editing on the cell surface can endow cellular glycoforms with new structures and properties; however, the lack of cell specificity and dependence on cells' endogenous functions plague the revelation of cellular glycan recognition properties and hamper the application of glyco-editing in complicated authentic biosystems. Herein, we develop a thermally triggered, cell-specific glyco-editing method for regulation of lectin recognition on target live cells in both single- and cocultured settings. The method relies on the aptamer-mediated anchoring of microgel-encapsulated neuraminidase on target cells and subsequent thermally triggered enzyme release for localized sialic acid (Sia) trimming. This temperature-based enzyme accessibility modulation strategy exempts genetic or metabolic engineering operations and, thus for the first time, enables tumor-specific desialylation on complicated tissue slices. The proposed method also provides an unprecedented opportunity to potentiate the innate immune response of natural killer cells toward target tumor cells through thermally triggered cell-specific desialylation, which paves the way for in vivo glycoimmune-checkpoint-targeted cancer therapeutic intervention.

Okubasca Dworakowska (Hemiptera: Cicadellidae: Typhlocybinae: Empoascini) elevated to separate genus status with description of two new species from China.

Okubasca Dworakowska, 1982, formerly treated as a subgenus of Empoasca Walsh, 1862, is elevated to status as a separate genus. Two new species of Okubasca from China are described and illustrated: Okubasca convoluta Yu Yang sp. nov.; Okubasca paracalvata Yu Yang sp. nov. Okubasca convoluta is similar to O. okubella in having the aedeagal shaft about as long as the preatrium but differs in having the aedeagus of uniform thickness in lateral view, the anal tube process straight and the face mostly black. Okubasca paracalvata resembles Okubasca calvata in aedeagal shape, but differs in having a lamellar swelling and a small tooth on the dorsal side of the aedeagus, and the vertex anterior margin rounded.

[Treatment of mandibular first premolars with complex root canals: report of 2 cases].

Mandibular first premolars have complex root canals. Double root canals and three root canals usually happen. Clinicians should be aware of the normal anatomy of root canal system and vigilant about the possibility of canal variation. In this paper, two cases of mandibular first premolars with double (2-2,Verlucci) and three(1-3,Verlucci) root canals were reported. The root canal type and its incidence were discussed. Clinicians should carefully explore to confirm the existence of variation and avoid missed canals, which are necessary for a successful root canal therapy.

[Double root canal of all mandibular incisors: report of one case and review of the literature].

Mandibular incisors are the smallest human permanent teeth with complex root canals. Double root canal, lateral branch of root canal, apical ramification or apical furcation usually happen, which make the clinical therapy more difficult. In this paper, a case of mandibular incisors with double root canals was reported, the root canal type and its incidence were discussed.