Rabbit Anti-NDV HN protein polyclonal antibody

A water-soluble polysaccharide known as Paulownia fortunei flower polysaccharide (PFFPS) was isolated from the flowers of Paulownia fortunei. Gel permeation chromatography (GPC) analysis showed that approximately 92.5% of PFFPS fractions had molecular weights under 500 kDa. High performance liquid chromatograph (HPLC) analysis revealed that PFFPS was composed of 10 monosaccharides, including galactose (28.61%), rhamnose (18.09%), glucose (15.21%), and arabinose (15.91%). Fourier transform infrared (FT-IR) spectra revealed the specific absorption peaks of the polysaccharide. Using in vivo tests in chickens, we found that even very low doses of PFFPS could significantly promote the development of the immune organs, increase the quantity of leukocytes and the ratio of lymphocytes, and improve antibody titers against Newcastle disease virus (NDV). In addition, PFFPS also increased the concentrations of IL-2 and IFIV-gamma, as well as the content of SIgA in the duodenum. Furthermore, PFFPS was found to be able to relieve immunosuppression caused by cyclophosphamide (CTX). This study therefore suggests that PFFPS may be a valuable component of new immunopotentiator and/or adjuvant for the livestock and poultry industries. (C) 2019 Published by Elsevier B.V.

The Chinese tree shrew holds a great potential as a viable animal model in biomedical research, especially for infectious diseases and neuropsychiatric disorders. A thorough understanding of the innate immunity, which represents the first line that defends the host against viral infection, of the Chinese tree shrew, is needed. However, the progress is hindered by the lack of a proper cell line for research usage. In this study, we established a cell line that is applicable to the study of tree shrew innate immune responses against viral infections. The Chinese tree shrew primary renal cells (TSPRCs) were immortalized by simian virus 40 large T antigen (SV40LT) transduction, and the immortalized cells were termed TSR6 (tree shrew renal cell #6). TSR6 showed a similar morphology to TSPRCs and expressed the epithelial cell-specific marker cytokeratin 18 (KRT18). In addition, TSR6 could be transfected by transfection reagent and was suitable for CRISPR/Cas9-mediated gene editing. Infection of Newcastle disease virus (NDV) or herpes simplex virus 1 (HSV-1) in TSR6 induced the mRNA expression of tree shrew interferon- (tIFNB1) and myxovirus resistance protein 1 (tMx1) in a dose- and time-dependent manner. Collectively, we successfully established a tree shrew renal cell line and demonstrated that this cell line was suitable for the study of the innate immune response to viral infections.