A secreted ribonuclease effector from Verticillium dahliae localizes in the plant nucleus to modulate host immunity

The arms race between fungal pathogens and plant hosts involves recognition of fungal effectors to induce host immunity. Although various fungal effectors have been identified, the effector functions of ribonucleases are largely unknown. Herein, we identified a ribonuclease secreted by Verticillium dahliae (VdRTX1) that translocates into the plant nucleus to modulate immunity. The activity of VdRTX1 causes hypersensitive response (HR)‐related cell death in Nicotiana benthamiana and cotton. VdRTX1 possesses a signal peptide but is unlikely to be an apoplastic effector because its nuclear localization in the plant is necessary for cell death induction. Knockout of VdRTX1 significantly enhanced V. dahliae virulence on tobacco while V. dahliae employs the known suppressor VdCBM1 to escape the immunity induced by VdRTX1. VdRTX1 homologs are widely distributed in fungi but transient expression of 24 homologs from other fungi did not yield cell death induction, suggesting that this function is specific to the VdRTX1 in V. dahliae. Expression of site‐directed mutants of VdRTX1 in N. benthamiana leaves revealed conserved ligand‐binding sites that are important for VdRTX1 function in inducing cell death. Thus, VdRTX1 functions as a unique HR‐inducing effector in V. dahliae that contributes to the activation of plant immunity.     

Depression compromises antiviral innate immunity via the AVP-AHI1-Tyk2 axis

Depression is a serious public-health issue. Recent reports have suggested higher susceptibility to viral infections in depressive patients. However, how depression affects antiviral innate immune signaling remains unknown. Here, we revealed a reduction in expression of Abelson helper integration site 1 (AHI1) in the peripheral blood mononuclear cells (PBMCs) and macrophages from the patients with major depressive disorder (MDD), which leads to attenuated antiviral immune response. We found that depression-related arginine vasopressin (AVP) induces reduction of AHI1 in macrophages. Further studies demonstrated that AHI1 is a critical stabilizer of basal type-I-interferon (IFN-I) signaling. Mechanistically, AHI1 recruits OTUD1 to deubiquitinate and stabilize Tyk2, while AHI1 reduction downregulates Tyk2 and IFN-I signaling activity in macrophages from both MDD patients and depression model mice. Interestingly, we identified a clinical analgesic meptazinol that effectively stimulates AHI1 expression, thus enhancing IFN-I antiviral defense in depression model mice. Our study promotes the understanding of the signaling mechanisms of depression-mediated antiviral immune dysfunction, and reveals meptazinol as an enhancer of antiviral innate immunity in depressive patients.Subject terms: Innate immunity, Ubiquitylation, Cell signalling     

湘潭锰矿废弃地不同林龄栾树人工林碳储量变化趋势

对湘潭锰矿区废弃地植被恢复区的3年生、5年生和9年生栾树林,进行了不同时间序列栾树林生物量和碳储量的时空变化研究。结果表明:随着林龄的增长,林木和各器官生物量增加,树干生物量所占比例逐渐增大,林下植被层生物量随林龄增长而增加,且以草本植被为主;不同林龄栾树人工林乔木层碳含量在0.51—0.53gC/g之间,并高于林下植被层碳含量;不同林龄林地土壤层碳含量变化范围为0.01—0.03gC/g,同一林龄不同深度土层碳含量没有显著差异,相同深度不同林龄土层碳含量存在差异;3年生、5年生和9年生栾树碳储量分别为:1.66、18.32和49.87t/hm2,随林龄增长而增加,其中树干碳储量贡献率最大,所占比例由3年生的27.71%增长到9年生的43.43%;不同林龄栾树林生态系统总碳储量分别为77.76、101.63和149.86t/hm2,其中土壤层碳储量变化范围为76.09—99.93t/hm2,占总储量的66.68%—97.85%,死地被物层碳储量为0.01—0.04t/hm2,占总储量0.001%—0.02%,植被层碳储量为1.67—49.89t/hm2,占总碳储量的2.15%—33.29%,植被层中乔木层为1.66—49.87t/hm2,占植被层碳储量的99%以上。各林龄栾树林生态系统碳储量空间分布序列为土壤层植被层死地被物层。研究结果可为我国矿区植被恢复地的森林资源和碳汇管理提供科学依据。     

湘南某矿区蔬菜中Pb、Cd污染状况及健康风险评估

通过采集湘南某矿区周边农田中种植的蔬菜和对应耕作层土壤样品,探究了农田蔬菜Pb、Cd的污染状况,蔬菜和土壤重金属含量之间的相关性,蔬菜中重金属对人体的健康风险。结果表明:(1)污染区土壤重金属污染非常严重,叶菜类蔬菜重金属超出了食品卫生标准限值,但是果菜类蔬菜中重金属没有超出食品卫生标准限值。(2)不同蔬菜不同器官所含Pb、Cd有明显差异;不同种类蔬菜Pb、Cd含量不同,一般是叶菜类果菜类;同种蔬菜不同部位重金属含量的顺序也不同,一般为根茎叶果,或根叶茎果。(3)二类蔬菜中重金属Pb、Cd的富集系数顺序为叶菜类果菜类。(4)蔬菜中Pb、Cd含量与土壤中相对应元素含量均无显著相关性。(5)就农产品安全性而言,果菜类蔬菜比叶菜类蔬菜更适合在此矿区栽培。     

数理统计方法优化单细胞蛋白发酵培养基研究

采用正交试验和中心组合设计相结合的数理统计方法,在２Ｌ发酵罐中对紫云英汁液培养单细胞蛋白发酵培养基进行筛选、优化,试验结果表明较优培养基为：初糖２．３％,酵母粉０．１６％,ＫＨ_２ＰＯ_４０．２％,ＭｇＳＯ_４０．０５％。酵母浓度最高达１０．４６ｇ／Ｌ,基质生长得率为０．５５ｇ菌体／ｇ基质,基质转化率为８３％。研究结果同时说明采用数理统计方法设计实验,工作量小,效率高,结果准确。     

Lithocholic acid inhibits dendritic cell activation by reducing intracellular glutathione via TGR5 signaling

Dendritic cells (DCs) are the major antigen-presenting cells and play an important role in autoimmune uveitis. Emerging evidence suggests that bile acids (BAs) regulate DCs maturation. However, the underlying mechanisms by which BAs regulate the function of DCs still need to be clarified. Here, we demonstrate that lithocholic acid (LCA) inhibits the production of pro-inflammatory cytokines and the expression of surface molecules in bone marrow-derived dendritic cells (BMDCs). LCA attenuates the severity of EAU by modulating the maturation of splenic CD11C⁺MHCII^high DCs. Notably, Takeda G-protein coupled receptor 5 (TGR5) deficiency partially reverses the inhibitory effect of LCA on DCs in vitro and in vivo. TGR5 activation also downregulates the NF-κB and MAPK pathways by inhibiting glutathione production and inducing oxidative stress in DCs, which leads to apoptosis and autophagy in DCs. In addition, LCA or INT-777 treatment increases the TGR5 expression in monocyte-derived dendritic cells (MD-DCs) of patients with active BD, whereas both LCA and TGR5 agonists inhibit the activation of MD-DCs. These results suggest that LCA and TGR5 agonists might be potential therapeutic drugs for the treatment of autoimmune uveitis.