Mumps virus (MuV) has high tropism to the testis and may lead to male infertility. Sertoli cells are the major targets of MuV infection. However, the mechanisms by which MuV infection impairs male fertility and Sertoli cell function remain unclear. The present study elucidated the effect of MuV infection on the blood‐testis barrier (BTB). The transepithelial electrical resistance of MuV‐infected mouse Sertoli cells was monitored, and the expression of major proteins of the BTB was examined. We demonstrated that MuV infection disrupted the BTB by reducing the levels of occludin and zonula occludens 1. Sertoli cells derived from Tlr2–/– and Tnfa–/– mice were analyzed for mediating MuV‐induced impairment. TLR2‐mediated TNF‐α production by Sertoli cells in response to MuV infection impaired BTB integrity. MuV‐impaired BTB was not observed in Tlr2–/– and Tnfa–/– Sertoli cells. Moreover, an inhibitor of TNF‐α, pomalidomide, prevents the disruption of BTB in response to MuV infection. FITC‐labeled biotin tracing assay confirmed that BTB permeability and spermatogenesis were transiently impaired by MuV infection in vivo. These findings suggest that the disruption of the BTB could be one of the mechanisms underlying MuV‐impaired male fertility, in which TNF‐α could play a critical role.—Wu, H., Jiang, X., Gao, Y., Liu, W., Wang, F., Gong, M., Chen, R., Yu, X., Zhang, W., Gao, B., Song, C., Han, D. Mumps virus infection disrupts blood‐testis barrier through the induction of TNF‐α in Sertoli cells. FASEB J. 33, 12528–12540 (2019). http://www.fasebj.org

Our initial experience showed that combined CT-guided (125)I radioactive seed implantation and GP chemotherapy are effective and safe for treating advanced NCSLC.

This paper examines the effects of seed size and the depth of sand burial on seed germination and seedling development for Pinus thunbergii. Parl. Seeds from 20- to 30-year old trees grown in the coastal area of Yantai were divided into three size categories (large, medium, and small). The seeds were sown in pots with different depth of sand, and their germination and seedling growth during the first month were investigated. Results showed that large seeds possessed the highest 1000-seed weight and soluble sugar concentration. Large and medium seeds had a higher germination rate, germination index, vigor index, and seedling biomass than small seeds. With the increase in seed size, root mass ratio, root/shoot ratio, specific root length, and specific root area decreased, whereas leaf mass ratio increased. Sand burial depth significantly influenced seed germination and seedling growth, and the highest germination rate and seedling biomass were achieved with 2–3 cm sand burial. We also found that seedling biomass was positively related to germination rate, germination index, and vigor index, but was negatively related to mean germination time. Moreover, seedling biomass was negatively correlated with root mass ratio and root/shoot ratio, but positively correlated with leaf mass ratio, specific root length, and specific root area. The results suggest that seed size and sand burial depth are key factors in the regeneration of the coastal P. thunbergii forest.

Application of plant artificial cultivation substrates lead to alteration of rhizosphere environment. Whether this alteration could lead to root microbiome variation was limitedly investigated. This work aims to determine the diversity shifts in the root microbiome of cucumber under different plant cultivation substrates and predict corresponding function of these different root bacterial microbiota. Cucumber root samples cultivated with two artificial cultivation substrates and greenhouse soils were prepared. Subsequently, high throughput sequencing and bioinformatics analysis were applicated to compare the root bacterial diversity of cucumber cultivated in different substrates and their corresponding function. In total, 311,039 sequences were obtained, and they were annotated to 42 operational taxonomic units (OTUs), belonging to 28 genera, 18 families, 12 orders, four classes, and three phyla. The α and β diversity of samples from the two cultivation substrates and greenhouse soils were significantly different. Only 2–3 bacterial species were found to be discrepancy between cucumber root samples from artificial cultivation substrates and from greenhouse soils. The relative abundance of genus Asticcacaulis, Methylophilus, Massilia, Dyella, and Devosia in samples of artificial cultivation substrates was significantly higher than that of soils, while the relative abundance of genus Phenylobacterium, Noviherbaspirillum, and Arenimonas was significantly lower than that of soils. Besides, compared to cucumber root bacterial community cultivated in soils, the abundance of synthetic pathways for flavonoids and flavonols, bile acids, indole alkaloids, lactose, and neolactose increased by 41.6-, 28.7-, 5.9-, and 5.5-fold, respectively, in the bacterial community of the substrate 1-cultivated roots, and the abundance of clavulanic acid, receptor interaction, sesquiterpenoid, bile acid, flavonoid and flavonol, indole alkaloid, lactose, and neolactose synthetic pathways increased by 42.3-, 32.4-, 32.4-, 13.9-, 10.3-, 6.3-, and 5.2-fold, respectively, in the bacterial community of the substrate two-cultivated roots. This paper verified the diversity shifts in the root microbiome of cucumber under different plant cultivation substrates. Besides, the corresponding function difference of these different root bacterial microbiota was predicted. This work would provide theoretical support for discovering microbial resources and building artificial microbial flora.