Background: Since January 2020, coronavirus disease 2019 has spread rapidly and developing the pandemic model around the world. Data have been needed on the clinical characteristics of the affected patients in an imported cases as model in island outside Wuhan. Methods:We conducted a retrospective study included all 168 confirmed cases of Covidconfirmed by real-time RT-PCR and were analysed for demographic, clinical, radiological and laboratory data.Results: Of 168 patients, 160 have been discharged, 6 have died and 2 remain hospitalized. The median age was 51.0 years and 51.8% were females. 129 (76.8%) patients were imported cases, and 118 (70.2%), 51 (30.4%) and 52 (31%) of patients lived in Wuhan or traveled to Wuhan, had contact with Covid-19 patients, or had contact with Wuhan residents, respectively. The most common symptoms at onset of illness were fever (65.5%), dry cough (48.8%) and expectoration (32.1%). On admission, ground-glass opacity was the most common radiologic finding on chest computed tomography (60.2%). The elderly people with diabetes, hypertension and CVD are more likely to develop severe cases. Follow-up of 160 discharged patients found that 20 patients (12.5%) had a positive RT-PCR test results of pharyngeal swabs or anal swabs or fecal.

Sivelestat sodium (SIV), a neutrophil elastase inhibitor, is mainly used for the clinical treatment of acute respiratory distress syndrome (ARDS) or acute lung injury (ALI). However, studies investigating the effects of SIV treatment of ALI are limited. Therefore, this study investigated the potential molecular mechanism of the protective effects of SIV against ALI. Human pulmonary microvascular endothelial cells (HPMECs) were stimulated with tumor necrosis factor α (TNF-α), and male Sprague-Dawley rats were intratracheally injected with Klebsiella pneumoniae (KP) and treated with SIV, ML385, and anisomycin (ANI) to mimic the pathogenetic process of ALI in vitro and in vivo, respectively. The levels of inflammatory cytokines and indicators of oxidative stress were assessed in vitro and in vivo. The wet/dry (W/D) ratio of lung tissues, histopathological changes, inflammatory cells levels in bronchoalveolar lavage fluid (BALF), and survival rates of rats were analyzed. The JNK/NF-κB (p65) and Nrf2/HO-1 levels in the HPMECs and lung tissues were analyzed by western blot and immunofluorescence analyses. Administration of SIV reduced the inflammatory factors levels, intracellular reactive oxygen species (ROS) production, and malondialdehyde (MDA) levels and increased the levels of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) in lung tissues. Meanwhile, SIV alleviated pathological injuries, decreased the W/D ratio, and inflammatory cell infiltration in lung tissue. In addition, SIV also inhibited the activation of JNK/NF-κB signaling pathway, promoted nuclear translocation of Nrf2, and upregulated the expression of heme oxygenase 1 (HO-1). However, ANI or ML385 significantly reversed these changes. SIV effectively attenuated the inflammatory response and oxidative stress. Its potential molecular mechanism was related to the JNK/NF-κB activation and Nrf2/HO-1 signaling pathway inhibition. This further deepened the understanding of the protective effects of SIV against ALI.

Background: Reduning (RDN) is a common Chinese medicine preparation with antibacterial, antiinflammatory, antiviral and immunomodulatory effects in respiratory infectious diseases. Clinically, it is used in combination with antibiotics, but its synergistic effect and mechanism in treating severe pneumonia remain unclear.Methods: A rat model of severe pneumonia and an in vitro coculture model consisting of A549 and THP-1 cells were used to observe the synergistic effect of RDN on severe pneumonia. The inflammatory cytokines were tested by enzyme-linked immunosorbent assay (ELISA). The localization of Aryl hydrocarbon receptor (AhR) in A549 cells was observed by immunofluorescence, and the interaction of AhR and signal transducer and activator of transcription 3 (STAT3) proteins was observed by co-immunoprecipitation.AhR-Src tyrosine kinase (Src)-STAT3 pathway in rats and A549 cells were examined by Western Blot. Histopathological changes were observed by Hematoxylin-eosin (HE) staining, X-ray and survival rates were used to evaluate the effects of paclitaxel on severe pneumonia rats.Results: RDN regulation of Src-STAT3-interleukin 10 (IL-10) signaling pathway activation and macrophage polarization were mediated through the nuclear receptor AhR. The expression of AhR was significantly increased after RDN treatment, and this effect was accompanied by STAT3 expression increasing. Coimmunoprecipitation confirmed an interaction between AhR and STAT3 and upregulated IL-10 expression. Silencing AhR decreased Src, STAT3, and IL-10 expression. RDN activated AhR and increased Src, STAT3, and IL-10 expression. In addition, RDN regulated the polarization of macrophages RDN combined with cefmetazole sodium significantly reduced the pulmonary bacterial load, alleviated lung injury, and reduced o inflammatory factors expression, improving their survival.Conclusions: RDN can synergistically enhance the effect of cefmetazole sodium treatment in severe pneumonia, and the mechanism may involve increasing the expression level of IL-10 mediated through the AhR-Src-STAT3 pathway, driving the polarization of macrophages, and attenuating the cytokine storm to control inflammation in severe pneumonia.

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To combat severe intersymbol interference incurred by multipath propagation of sound waves in the underwater acoustic environment, we introduce an iterative equalization and decoding scheme by iteratively exchanging soft information between a low-density parity check (LDPC) decoder and a decision feedback equalizer. We apply extrinsic information transfer (EXIT) charts to analyze performance of LDPC codes over the acoustic multipath channel. Furthermore, using differential evolution technique, we develop an EXIT-aided method to optimize LDPC codes for the underwater acoustic channel. Design examples are presented for two different realizations of the underwater acoustic channel that are generated by an acoustic ray tracing model. Computer simulations show that the optimized LDPC codes outperform its regular counterpart or Turbo codes under the same coding rate and block length, with gains of 1.0 and 0.8 dB, respectively, at the bit error rate of 10 −5 .

This paper simulates and analyzes numerically the dispersion characteristics of the waves propagating in the shallow-ocean overlying a semi-infinite elastic solid. The analytical solution of the acoustic field in the shallow-ocean, excited by an explosive point source in the solid bottom, is derived by using the theories for sound propagation in liquid and solid. The time-domain waveforms of transient acoustic field are simulated with the above analytical solution. The dispersion characteristics of the transient acoustic field are analyzed by using the smoothed pseudo Wigner-Ville distribution.

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In this article, a quick and sensitive photoelectrochemical biosensing platform was successfully fabricated for microRNA (miRNA)-155 detection based on the rutile titanium dioxide facet heterostructure (FH-TiO2). Nanosheets with different crystal faces (111) and (101) exposed are assembled on rutile TiO2 nanorods (TiO2 NRs) to serve as a TiO2 facet heterostructure (FH-TiO2) platform. In this assay, double-stranded specific nuclease was used to remove the double strands formed by the target RNA and probe DNA and release the target DNA for the next cycle so that the subsidiary DNA (S1) can hybridize with the residual base strands of probe DNA, which will introduce the SiO2 nanoparticles attached to the electrode surface. Infinitesimal targets could initiate huge change in the electrode signal via an enzyme-assisted target cycling procedure. A satisfactory performance with a linear range (0.1 pM to 10 nM) and the detection limit (0.025 pM, LOD = 3*σ/S) was obtained for the miRNA-155 detection, implying a promising application in the biological analysis of related diseases and clinical diagnosis.