植原体引起雪花木小叶病在中国的首次报道

2022年首次在广州市发现园林植物雪花木小叶病病株, 采用分子生物学技术对其进行植原体的种类鉴定。以雪花木叶片总DNA为模板, 利用植原体16S rRNA通用引物P1/P7进行PCR扩增, 获得广东雪花木小叶病植原体(BLL-GD2022)16S rRNA基因片段(1 811 bp, GenBank登录号为OQ625536)。16S rRNA序列相似性显示, BLL-GD2022与16SrVI组植原体株系的相似性最高, 为97.05%~99.83%, 其中与隶属于16SrVI-D亚组的10个植原体株系相似性为99.21%~99.83%。系统进化分析显示, BLL-GD2022与16SrVI组各植原体株系聚类在一个大分支, 其中与16SrVI-D亚组成员聚类在一个小分支, 亲缘关系最近。基于16S rRNA序列的iPhyClassifier限制性内切酶虚拟RFLP分析表明, BLL-GD2022与16SrVI-D亚组的参考株系Brinjal little leaf phytoplasma (GenBank登录号为X83431)的酶切图谱一致, 相似系数为1.00。基于上述研究结果, 明确广州市雪花木小叶病植原体隶属16SrVI-D亚组成员。本研究首次在园林植物雪花木上检测到植原体, 通过16S rRNA序列分析明确为16SrVI-D亚组成员, 为开展16SrVI-D亚组植原体在蔬菜、花卉和园林植物的发生监测及病害防控提供科学依据。     

茭虾共作对土壤氮磷含量和茭白干物质积累及氮磷钾吸收分配的影响

为探究茭白种养模式的施肥策略,设置茭虾共作（ZC）、茭白单作（Z） 2个处理,研究茭虾共作对土壤氮磷含量、茭白产量和茭白干物质积累及氮磷钾吸收分配的影响。2021-2022年的研究结果显示,茭虾共作模式较茭白单作模式采茭期土壤中全氮、全磷、速效磷的含量分别提高了10.85%~38.89%、5.45%~13.79%、6.19%~61.79%,净茭产量提高了5.10%~19.54%,采茭期茭白茎、叶、净茭的干物质积累量分别增加14.41%~16.58%、10.28%~15.15%、10.57%~21.45%。2021年茭虾共作处理较茭白单作处理在采茭期叶的氮含量显著增加了25.74%,但在孕茭期茎中磷含量显著减少了16.76%;2022年氮肥减量、减量投喂下,茭虾共作处理较茭白单作处理在孕茭期茎的氮含量显著减少了23.75%,在分蘖期叶中磷含量显著减少了12.08%,2 a全生育期同一器官的钾含量在2个处理间差异不显著。对于养分积累,2021年茭虾共作处理在分蘖期叶的氮、磷、钾积累量较茭白单作处理分别减少26.04%、27.27%、30.11%,但在采茭期茎的氮、钾积累量和叶的氮、磷积累量较茭白单作处理分别增加18.80%、38.41%和44.77%、35.71%;2022年在氮肥减量、饲料减量投喂下,茭虾共作处理在采茭期叶的磷积累量和茎的钾积累量较茭白单作处理显著增加30.0%和30.77%。关于养分分配,2种处理的茭白在孕茭期和采茭期氮素的分配均以茎、叶为主,而磷、钾元素的分配均以茎为主,茎分配比例在42%~66%。对于养分转运,2021年2种处理茭白的根、茎、叶在氮、磷转运上大多为表现为“库”器官,而在钾转运上大多表现为“源”器官;2022年氮肥减量、减量投喂下,茭白的根、茎、叶在氮、磷、钾转运量上大多表现为“源”器官。因此,在茭虾共作模式中适当减少肥料、饲料的投入,能促进形成合理的源库关系,有利于茭白产量的形成。     

CJD交流电力测功机的研制

介绍了自行研制的CJD交流电力测功机的结构、工作原理以及系统控制的实现过程.运行结果表明,该CJD交流电力测功机具有结构简单,稳定性、可靠性好,使用方便,适用性广等特点,节能效果显著,能量反馈效率最高可达到74%.     

杨树主要病虫害的防治

近年来病虫害已严重威胁到杨树生长。为了及时和系统地控制杨树病虫害,有效地减少病虫害所产生的损失,通过调查,并结合我公司原料林基地杨树病虫害防治的试验和经验,对杨树病虫害防治措施进行了总结和记述。     

木荷幼苗在林窗不同生境中的形态响应与生物量分配

对从林窗边缘到林窗中央环境梯度上3种不同生境的木荷幼苗的主要形态因子和生物量进行了测定,结果表明,3种生境下木荷幼苗的形态数量指标表现出极显著的差异,从林窗边缘到林窗中央,随着光照等环境条件的改善,其生长量和生物量逐渐增加。生物量的分配格局基本相似,但叶和主茎生物量表现出显著的差异,林窗边缘处,木荷幼苗将生物量相对多地分配到地上叶构件上,林窗中央处,则相对多地分配到地上主茎上。研究显示,木荷幼苗具有喜光能耐阴的特性。运用非线性幂函数拟合了不同生境木荷幼苗生物量模型,回归模型较好地反映了生物量随苗高、地径的变化趋势,可作为环境条件类似的木荷幼苗生物量预测的依据。     

绝对定量分析不同条锈病抗性小麦品种根际细菌群落结构

[目的]分析不同条锈病抗性小麦品种根际细菌群落的结构和功能差异,为开发防治小麦条锈病的环境友好方案提供理论基础和创新思路.[方法]以同一地块中对条锈病具有不同抗性的4个小麦品种(抗病品种贵农19和华麦1223,感病品种002和I19)为研究材料,采集不同抗性小麦品种根际土壤样品,采用绝对定量扩增子分析技术,研究抗病和感病小麦品种根际细菌的群落结构和功能.[结果]同一地块的4个小麦品种条锈病病情指数具有明显差异.4个小麦品种根际土壤细菌群落结构绝对定量分析表明,感病与抗病小麦品种的根际细菌群落分别聚类成独立的两类.感病小麦品种根际细菌群落丰度和多样性显著高于抗病小麦品种根际细菌群落(P<0.05).坐标分析(PCoA)表明,所有小麦品种根际细菌群落按照抗病性不同分为两组;细菌群落功能分析表明,抗病小麦品种根际细菌群落具有更多的氨基酸和抗生素分泌功能.[结论]条锈病抗性对小麦根际细菌群落的影响超过小麦不同品种间遗传变异的影响.通过分析和挖掘不同条锈病抗性小麦品种的根际细菌群落,可开发出环境友好的小麦条锈病生物防治菌剂.     

大豆作为前作植物对油菜根肿病发生的影响

为了解前作大豆对后茬油菜根肿病的影响,采用大田轮作试验和实时荧光定量PCR检测法,研究大豆、白菜、油菜分别作为前作,调查后茬油菜根肿病的发生和土壤中休眠孢子含量,比较分析了不同前作的根系分泌物对休眠孢子萌发的影响,结果表明前作大豆,后茬油菜根肿病的发病率和病情指数分别为34.00%和19.26、土壤休眠孢子含量为1.45×106个/克土壤,显著低于前作为油菜、白菜和撂荒对照的相应量。大豆、油菜和白菜根系分泌物均可刺激根肿菌休眠孢子萌发。与根肿菌休眠孢子共培6 d后,大豆根系分泌物培养的休眠孢子萌发率为29.82%,显著高于白菜（15.52%）、油菜根系分泌物（14.83%）和营养液（6.48%）培养下的萌发率。据此推测,前作种植大豆,后茬油菜根肿病发生和危害减轻,原因应与大豆根系分泌物刺激根肿菌休眠孢子萌发,产生的游动孢子因缺少寄主植物而死亡,导致诱发病害的初侵染源（土壤中休眠孢子含量）减少有关。     

Minimally modified low-density lipoprotein up-regulates endothelin receptors in mouse mesenteric artery through p38 MAPK pathway

AIMTo investigate whether minimally modified low-density lipoprotein (mmLDL) affects the quantity and activity of endothelin （ET） type A (ET_A) and type B (ET_B) receptors in mouse mesenteric artery by activating p38 mitogen-activated protein kinase (MAPK) inflammatory pathway. METHODSThe KM mice were divided into normal saline (NS) group (injection of NS via caudal vein), mmLDL group (injection of mmLDL via caudal vein), LDL group (injection of LDL via caudal vein), mmLDL+SB 203580 group (injection of mmLDL via caudal vein and intraperitoneal injection of p38 MAPK pathway specific inhibitor SB 203580) and mmLDL+DMSO group (injection of mmLDL via caudal vein and intraperitoneal injection of DMSO). Mesenteric artery ring segment vasoconstriction dose-response curves affected by sarafotoxin 6c (S6c) and ET-1 were recorded by the myography system. The mRNA levels of ET_B receptor, ET_A receptor and interleukin-6 (IL-6) were detected by RT-qPCR. The protein levels of ET_B receptor, ET_A receptor, IL-6, p38 MAPK, p-p38 MAPK, NF-κB and p-NF-κB were determined by Western blot. The serum concentration of IL-6 was measured by ELISA. RESULTSThe contractile responses of the blood vessel segments to S6c and ET-1 were significantly increased by mmLDL (P<0.01). The mRNA and protein expression levels of ET_A receptor, ET_B receptor, and IL-6 significantly increased (P<0.01). The protein levels of p-p38 MAPK and p-NF-κB were significantly increased (P<0.01). The serum level of IL-6 was significantly increased (P<0.01). These effects of mmLDL were inhibited by p38 MAPK inhibitor SB 203580. CONCLUSION mmLDL increses the serum concentration of IL-6, up-regulates the expression of IL-6, ET_A receptor and ET_B receptor in mouse mesenteric artery, and enhances the vasoconstriction function medi?ated by ET_A and ET_B receptors, which is related to the activation of p38 MAPK inflammatory pathway and downstream NF-κB pathway.     

Effects of apelin-13 on oxidative stress induced by high uric acid in adipocytes

AIM: To study the effects of apelin-13 on oxidative stress induced by high uric acid in 3T3-L1 adipocytes and its underlying mechanisms. METHODS: 3T3-L1 adipocytes were stimulated with uric acid at 10 mg/dL for 48 h. Some of the adipocytes were administered with 1 μmol/L apelin-13 in the presence of uric acid at 10 mg/dL. The adipocytes stimulated with 100 μmol/L H₂O₂ were served as positive controls. The intracellular reactive oxygen species (ROS) concentrations were detected by flow cytometry. The biochemical kits were used to measure the activities of superotide dismutase (SOD), glutathione peroxidase (GSH-Px), catalase (CAT) and NADPH oxidase (NOX) activity, and the content of malondialdehyde (MDA) in the cell lysate and the supernatant. The mRNA levels of renin-angiotensin system (RAS) components, including angiotensinogen (AGT), angiotensin-converting enzyrne1 (ACE1), angiotensin II type 1 receptor (AT1R) and AT2R, as well as angiotensin II receptor -like 1 (APJ) were measured by real-time PCR. The concentrations of angiotensin II (AngⅡ) in the cell lysate and the supernatant were measured by ELISA. RESULTS: Adipocytes stimulated with uric acid at 10 mg/dL had lower activities of antioxidant enzymes (SOD, GSH-PX and CAT) and higher levels of NOX activity and MDA content (P < 0.05). Accordingly, the intracellular ROS levels were found to be dramatically increased. However, apelin-13 administration attenuated uric acid-induced oxidative stress in the 3T3-L1 adipocytes. Uric acid at 10 mg/dL upregulated the mRNA expression of local RAS, enhanced AngⅡ concentrations both in the cell lysate and the supernatant, and down-regulated the mRNA level of APJ in the adipocytes (P < 0.05). Conversely, apelin-13 partially reversed these parameters. CONCLUSION: Apelin-13 attenuates oxidative stress induced by uric acid, may be via down-regulation of local RAS expression in the 3T3-L1 adipocytes.