JQ-1 ameliorates schistosomiasis liver granuloma in mice by suppressing male and female reproductive systems and egg development of Schistosoma japonicum

Schistosomiasis is a serious and widespread parasitic disease caused by infection with Schistosoma. Because the parasite’s eggs are primarily responsible for schistosomiasis dissemination and pathogenesis, inhibiting egg production is a potential approach to control the spread and severity of the disease. The bromodomain and extra-terminal (BET) proteins represent promising targets for the development of epigenetic drugs against Schistosoma. JQ-1 is a selective inhibitor of the BET protein family. In the present study, JQ-1 was applied to S. japonicum in vitro. By using laser confocal scanning microscopy and EdU incorporation assays, we showed that application of JQ-1 to worms in vitro affected egg laying and the development of both the male and female reproductive systems. JQ-1 also inhibited the expression of the reproductive-related genes SjPlk1 and SjNanos1 in S. japonicum. Mice infected with S. japonicum were treated with JQ-1 during egg granuloma formation. JQ-1 treatment significantly reduced the size of the liver granulomas and levels of serum alanine aminotransferase and aspartate aminotransferase in mice and suppressed both egg laying and the development of male and female S. japonicum reproductive systems in vivo. Moreover, the mRNA expression levels of some proinflammatory cytokines were decreased in the parasites. Our findings suggest that JQ-1 treatment attenuates S. japonicum egg–induced hepatic granuloma due at least in part to suppressing the development of the reproductive system and egg production of S. japonicum. These findings further suggest that JQ-1 or other BET inhibitors warrant additional study as a new approach for the treatment or prevention of schistosomiasis.     

Two Magnaporthe appressoria‐specific (MAS) proteins,MoMas3 and MoMas5, are required for suppressing host innate immunity and promoting biotrophic growth in rice cells

In the devastating rice blast fungus Magnaporthe oryzae, six Magnaporthe appressoria‐specific (MAS) proteins are encoded by MoGAS1, MoGAS2 and MoMAS3–MoMAS6. MoGAS1 and MoGAS2 were previously characterized as M. oryzae virulence factors; however, the roles of the other four genes are unknown. Here, we found that, although the loss of any MAS gene did not affect appressorial formation or vegetative growth, ∆Momas3 and ∆Momas5 mutant strains (but not the others) were reduced in virulence on susceptible CO‐39 rice seedlings. Focusing on ∆Momas3 and ∆Momas5 mutant strains, we found that they could penetrate host leaf surfaces and fill the first infected rice cell but did not spread readily to neighbouring cells, suggesting they were impaired for biotrophic growth. Live‐cell imaging of fluorescently labelled MoMas3 and MoMas5 proteins showed that during biotrophy, MoMas3 localized to the apoplastic compartment formed between fungal invasive hyphae and the plant‐derived extra‐invasive hyphal membrane while MoMas5 localized to the appressoria and the penetration peg. The loss of either MoMAS3 or MoMAS5 resulted in the accumulation of reactive oxygen species (ROS) in infected rice cells, resulting in the triggering of plant defences that inhibited mutant growth in planta. ∆Momas3 and ∆Momas5 biotrophic growth could be remediated by inhibiting host NADPH oxidases and suppressing ROS accumulation. Thus, MoMas3 and MoMas5 are novel virulence factors involved in suppressing host plant innate immunity to promote biotrophic growth.     

Three new red neutral and ionic iridium(III) complexes based on the same main ligand and auxiliary ligand but with different counterions for solution-processed organic light-emitting diodes

Three new neutral and ionic phosphorescent iridium(III) complexes were successfully prepared using 1-(6-methoxynaphthalen-2-yl)isoquinoline as the main ligand, while the auxiliary ligand was 2-(2-1H-imidazolyl)pyridine. Three complexes (Ir1, Ir2, Ir3) showed red emission, peaking at 610, 609, and 615 nm, respectively, and they exhibited good solubility and excellent photophysical properties in different solvents, which is suitable to prepare organic light-emitting diodes (OLEDs) by solution method. Among the three OLEDs prepared by iridium(III) complexes using the solution method, the device based on Ir2 possessed better electroluminescent properties, and its maximum brightness, current efficiency (CE), power efficiency (PE), and the maximum external quantum efficiency (EQE) were 507.2 cd m⁻², 0.14 cd A⁻¹, 0.06 lm W⁻¹, and 0.14%. respectively, proving that the three complexes have a certain of potential for OLEDs applications and are expected to expand the applications of iridium(III) complexes for OLEDs.     

抗虫辣椒叶片对斜纹夜蛾幼虫相关生理生化指标的影响

为明确朝天椒(品种：BLTY2)叶片饲喂的斜纹夜蛾Spodoptera litura幼虫生长发育受到抑制的关键原因,本研究以人工饲料及牛角椒（品种：FXBX）叶片饲喂的斜纹夜蛾幼虫为对照,通过比较3种食料饲喂后斜纹夜蛾幼虫相关生理生化指标的变化,分析BLTY 2辣椒叶片饲喂所致的斜纹夜蛾幼虫生长发育异常的原因。结果表明,朝天椒辣椒叶片饲喂的斜纹夜蛾幼虫生长发育速率滞后于牛角椒辣椒叶片及人工饲料饲喂的斜纹夜蛾幼虫,且每头幼虫的发育时长均显著延长（P<0.05）。饲喂后第1天、第3天、第4天、第5天、第6天和第7天,饲喂BLTY 2辣椒叶片的斜纹夜蛾幼虫体内保幼激素（JH）含量均显著高于其他2种食料饲喂的斜纹夜蛾幼虫（P<0.05）。饲喂后第3天、第4天、第5天和第7天,饲喂BLTY 2辣椒叶片的斜纹夜蛾幼虫体内蜕皮激素（Ecd）含量均显著高于其他2种食料饲喂的斜纹夜蛾幼虫（P<0.05）。3种食料饲喂后斜纹夜蛾幼虫体内的几丁质酶（CHT）活性变化差异较大,而2种辣椒叶片饲喂后斜纹夜蛾幼虫体内的组织蛋白酶（CTS）活性变化趋势相似,且不同于人工饲料饲喂的斜纹夜蛾幼虫体内的CTS活性变化趋势。由此可见,BLTY 2辣椒主要干扰斜纹夜蛾幼虫体内JH与Ecd的含量抑制其生长发育。本研究结果可为筛选具有抗虫活性的植物次生代谢物质奠定基础。     

北京地区热力景观格局及典型城市景观的热环境效应

城市热环境是城市生态环境中的一个重要指标,将景观生态学理论融入到热环境研究中,尝试探讨北京地区热力景观格局及城市公园、道路景观的热环境效应。地表温度反演是分析热力景观格局及典型城市景观热环境效应的前提,论文以北京地区为例,首先利用两景ASTER影像数据采用TES算法定量反演地表温度。通过半变异函数分析地表温度空间异质性,确定最大采样尺度,然后在景观统计软件Fragstats中,计算不同粒度下的景观格局指数,分析热力景观格局及其尺度效应。通过景观斑块特征分析和缓冲区分析,探讨公园景观斑块、道路景观廊道特征的热环境效应。总体上公园景观对应的平均温度随着公园面积、边界长度的增加而减小,随着公园周长面积比增大而增大;随着距离公园渐远,地表温度升高,且升温趋势变缓。随着道路密度增加,道路平均温度显著升高,标准差显著降低,道路密度等级与道路平均温度的相关系数达到0.8021;随着距离道路中心线距离增加,缓冲区内的平均温度略有下降,但变化微弱。因此,应充分重视公园景观在缓解城市热环境方面的作用,合理布局城市道路。     

猪链球菌2型唾液酸合成酶neu B基因敲除突变株的构建及其生物学特性

利用同源重组基因敲除方法构建猪链球菌2型强毒株05ZYH33唾液酸合成酶neuB基因敲除突变株。PCR和Southern杂交结果均显示neuB基因在1株转化重组体中完全被壮观霉素抗性基因替代, 表明neuB基因敲除突变体构建成功。生物学特性鉴定显示, 突变体与强毒株在菌落形态、溶血活性以及染色特性方面均无明显差异; 电镜检查发现突变体表面结构组分与强毒株有显著差异, 荚膜明显变薄, 质地更加紧密; 小鼠致病性试验结果显示, 突变体毒力显著减弱。研究结果提示菌体荚膜中的唾液酸对于猪链球菌2型侵袭和致病具有重要作用。     

The structural dynamics of full-length divisome transmembrane proteins FtsQ,FtsB, and FtsL in FtsQBL complex formation

FtsQBL is a transmembrane protein complex in the divisome of Escherichia coli that plays a critical role in regulating cell division. Although extensive efforts have been made to investigate the interactions between the three involved proteins, FtsQ, FtsB, and FtsL, the detailed interaction mechanism is still poorly understood. In this study, we used hydrogen-deuterium exchange mass spectrometry to investigate these full-length proteins and their complexes. We also dissected the structural dynamic changes and the related binding interfaces within the complexes. Our data revealed that FtsB and FtsL interact at both the periplasmic and transmembrane regions to form a stable complex. Furthermore, the periplasmic region of FtsB underwent significant conformational changes. With the help of computational modeling, our results suggest that FtsBL complexation may bring the respective constriction control domains (CCDs) in close proximity. We show that when FtsBL adopts a coiled-coil structure, the CCDs are fixed at a vertical position relative to the membrane surface; thus, this conformational change may be essential for FtsBL’s interaction with other divisome proteins. In the FtsQBL complex, intriguingly, we show only FtsB interacts with FtsQ at its C-terminal region, which stiffens a large area of the β-domain of FtsQ. Consistent with this, we found the connection between the α- and β-domains in FtsQ is also strengthened in the complex. Overall, the present study provides important experimental evidence detailing the local interactions between the full-length FtsB, FtsL, and FtsQ protein, as well as valuable insights into the roles of FtsQBL complexation in regulating divisome activity.     

Detection and Quantification of Fusarium oxysporum f. sp. niveum Race 1 in Plants and Soil by Real-time PCR

Fusarium wilt caused by Fusarium oxysporum f. sp. niveum (Fon) is the most serious soil-borne disease in the world and has become the main limiting factor of watermelon production. Reliable and quick detection and quantification of Fon are essential in the early stages of infection for control of watermelon Fusarium wilt. Traditional detection and identification tests are laborious and cannot efficiently quantify Fon isolates. In this work, a real-time polymerase chain reaction (PCR) assay has been described to accurately identify and quantify Fon in watermelon plants and soil. The FONRT-18 specific primer set which was designed based on identified specific sequence amplified a specific 172 bp band from Fon and no amplification from the other formae speciales of Fusarium oxysporum tested. The detection limits with primers were 1.26 pg/μl genomic DNA of Fon, 0.2 pg/ng total plant DNA in inoculated plant, and 50 conidia/g soil. The PCR assay could also evaluate the relationships between the disease index and Fon DNA quantity in watermelon plants and soil. The assay was further used to estimate the Fon content in soil after disinfection with CaCN₂. The real-time PCR method is rapid, accurate and reliable for monitoring and quantification analysis of Fon in watermelon plants and soil. It can be applied to the study of disease diagnosis, plant-pathogen interactions, and effective management.