Canine distemper virus (CDV)-neutralizing activities of an anti-CDV canine-derived single-chain variable antibody fragment 4-15 (scFv 4-15) screened by phage display technology.

Canine distemper virus (CDV) is a highly contagious pathogen that causes severe diarrhea, fever and vomiting in domestic dogs, posing a serious threat to the dog breeding industry. Currently, there are no effective therapeutic agents for emergency treatment despite the availability of vaccines against CDV infection. Single-chain fragment variable (scFv) antibody has been demonstrated to effectively inhibit virus infections, suggesting a potential candidate as a therapeutic agent for canine distemper. In this study, a phage-displayed scFv library was constructed from the peripheral blood lymphocytes of dog immunized intramuscularly with live-attenuated CDV vaccine, and was subjected to four rounds of pannings against CDV. Subsequent indirect enzyme-linked immunosorbent assay screening revealed high-affinity scFv antibodies specific to CDV, and indirect immunofluorescence assay screening revealed CDV-neutralizing activity of scFv antibodies. Our results showed that a scFv antibody 4-15 (scFv 4-15) with high-affinity binding to CDV and neutralizing activity against CDV was obtained, which displayed effective therapeutic potential in vivo for dogs challenged with a lethal dose of CDV. Conclusively, the scFv 4-15 with high-affinity binding and neutralizing activity to CDV that was obtained by phage display technology provides a promising candidate for the therapeutic agents against CDV infection.

Up-regulated lncRNA CYLD as a ceRNA of miR-2383 facilitates bovine viral diarrhea virus replication by promoting CYLD expression to counteract RIG-I-mediated type-I IFN production.

Bovine viral diarrhea virus (BVDV) is one of the most important pathogens of cattle, causing numerous economic losses to the cattle industry. To date, many potential mechanisms of BVDV evading or subverting innate immunity are still unknown. In this study, an lnc-CYLD/miR-2383/CYLD axis involved in BVDV-host interactions was screened from RNA-seq-based co-expression networks analysis of long noncoding RNAs, microRNAs and mRNAs in BVDV-infected bovine cells, and underlying mechanisms of lnc-CYLD/miR-2383/CYLD axis regulating BVDV replication were explored. Results showed that BVDV-induced up-regulation of the lnc-CYLD competed for binding to the miR-2383, and then promoted CYLD expression, thereby inhibiting RIG-I-mediated type-I interferon (IFN) production, which was subsequently confirmed by treatment with lnc-CYLD overexpression and miR-2383 inhibitor. However, miR-2383 transfection and small interfering RNA-mediated lnc-CYLD knockdown inhibited CYLD expression and enhanced RIG-I-mediated type-I IFN production, inhibiting BVDV replication. In addition, interaction relationship between lnc-CYLD and miR-2383, and colocalization relationship of lnc-CYLD, miR-2383 and CYLD were confirmed by dual-luciferase assay and in situ hybridization assay. Conclusively, up-regulation of the lnc-CYLD as a competing endogenous RNA binds to the miR-2383 to reduce inhibitory effect of the miR-2383 on the CYLD expression, playing an important role in counteracting type-I IFN-dependent antiviral immunity to facilitate BVDV replication.

Synergistic effect, kinetic and thermodynamics parameters analyses of co-gasification of municipal solid waste and bituminous coal with CO2.

Co-gasification of municipal solid waste (MSW) with bituminous coal (BC) is an attractive alternative to realize the harmless disposal and energy harvesting of MSW. In this work, co-gasification characteristics and synergistic interaction of MSW and BC with CO2 atmosphere are studied by thermogravimetric method, including analyses of thermodynamics, kinetic parameters and reaction mechanism function. Results indicate that MSW gasification process can be divided into four main stages, and that of BC has only three main stages. Gasification temperature of coal char is much higher than that of MSW char, and addition of MSW can significantly improve the gasification reactivity of BC. Besides, a significant synergistic effect is observed for all the blends in char gasification stage. Based on three kinetic methods of Flynn-Wall-Ozawa (Xie et al., 2018), Starink (Zhang et al., 2019a) and Friedman, the minimum average activation energy Ea (184.13 kJ/mol) is obtained when the blend ratio of BC is 40% which might be an optimal option for co-gasification of the blends. The average values of the enthalpy, the Gibbs function and the entropy changes for sample 60MSW40BC are 176.82 kJ/mol, 257.89 kJ/mol and -89.16 J/mol·K, respectively. According to the Malek method, F6, A1 and D7 models are probably more suitable to describe three main stages of sample 60MSW40BC CO2 co-gasification.