鸡Ii结合Rab5a和Rab7b分子的分析

本研究旨在探明鸡恒定链（invariant chain，Ii）与内吞体转运蛋白Rab5a和Rab7b结合的结构域和在细胞内共定位的特征。首先，用PCR和基因突变技术将Ii胞浆区与跨膜区[Ii_{（Cyt-Tra）}]、Ii CLIP （class Ⅱ-associated invariant chain peptide）-三聚体区[Ii_{（CLIP-TRIM）}]和Ii突变体[Ii_{（M81-87aa）}、Ii_{（M91-99aa）}和Ii_{（M81-99aa）}]分别插入pET-32a和pEGFP-C1构建相应的原核和真核重组质粒。其次，将构建的含有绿色荧光蛋白的重组质粒与实验室保存的含有红色荧光Rab5a和Rab7b的重组质粒共转染至人胚胎肾细胞系293 T，观察它们的共定位。将构建的原核重组质粒进行表达和纯化，最后用拉下法和免疫印迹检测Ii与Rab5a和Rab7b的结合域。结果表明，成功构建Ii结构域及Ii突变体的重组质粒。Ii_{（Cyt-Tra）}及Ii突变体均能与Rab5a和Rab7b在细胞内共定位，而Ii_{（CLIP-TRIM）}与空载体却不能。Ii的胞浆区和跨膜区是与Rab5a和Rab7b结合的功能结构域，而不是CLIP与三聚体区。综上所述，鸡Ii与Rab5a和Rab7b共定位和结合的区域是其胞浆区和跨膜区，而不是内质网腔区。这些结果提示Rab分子参与了Ii在胞内细胞器的转运机制，为进一步研究Ii及其载体在细胞内的转运机制和功能提供了新的途径。     

茎用芥菜新品种1年2代繁育研究初报

为了探索福建省茎用芥菜1年2代繁育技术，选择6个茎用芥菜品种，分别进行冬春季正常繁育和夏秋季高山加代繁育的2代繁育试验，并对比各品种2代繁育的生育期、株高、株幅和种子产量。结果表明：所有参试茎用芥菜品种只要通过打破种子休眠、衔接好2代繁育的播种期都能完成1周年2代繁育，夏秋季高山加代繁育的全生育期比冬春季正常繁育平均缩短约50 d；冬春季繁育比夏秋季高山加代繁育株高增加31.2%～132.9%，株幅增加1.5%～21.8%，所有参试品种冬春季繁育的种子产量都极显著高于相应夏秋季高山加代繁育，种子产量增加17.8%～153.6%。     

Development of a linear mixed-effects individual-tree basal area increment model for masson pine in Hunan Province,South-central China

ABSTRACT

An individual-tree basal area increment model was developed for masson pine based on 26276 observations of 13,138 trees in 987 sample plots from the 7th (2004), 8th (2009), and 9th (2014) Chinese National Forest Inventory in Hunan Province, South-central China. The model was built using a linear mixed-effects approach with sample plots included as random effects since the data have a hierarchical stochastic structure and biased estimates of the standard error of parameter estimates could be a consequence of applying ordinary least square (OLS) for regression. In addition, within-plot heteroscedasticity and autocorrelation were also considered. The final mixed-effects model was determined according to the Akaike information criterion (AIC), Bayesian information criterion (BIC), log-likelihood (Loglik), and the likelihoodratio test (LRT). The results revealed that initial diameter (DBH), the sum of the basal area (m²/ha) in trees with DBHs larger than the DBH of the subject tree (BAL), number of trees per hectare (NT), and elevation (EL) had a significant impact on individual-tree basal area increment. The mixed-effects model performed much better than the basic model produced using OLS. Additionally, the variance structure of the model errors was successfully modeled using the power function. However, the autocorrelation structures were not defined because there was no autocorrelation amongst the data. It is believed that the final model will contribute to the scientific management of the masson pine.     

Site‐specific management is crucial to managing Mikania micrantha

Increasingly, weeds have been taking on global distributions. With the proliferation of invasive weeds has come the challenge of managing these species over broad geographical regions, with diverse habitats and political jurisdictions. Here, we review the management of Mikania micrantha Kunth (Asteraceae; mile‐a‐minute) throughout its invaded range, extending through most of the Pacific islands and southern and south‐east Asia. Context matters when determining the best course of action for managing M. micrantha, as it has invaded a large variety of agricultural and natural systems. In Queensland, Australia and Florida, USA, M. micrantha has been targeted in relatively successful eradication campaigns, highlighting the importance of early detection and rapid response methods, while elsewhere in its invaded range, populations are either still increasing or showing limited signs of decline. An inter‐regional approach to research and management should incorporate successful management strategies employed throughout the invaded range including, but not limited to, chemical and cultural control practices, manual and mechanical control, classical biological control using the rust fungus Puccinia spegazzinii, plant–plant competition and integrated approaches utilising two or more control methods concurrently. Additional knowledge of M. micrantha genetics is required to determine if management approaches could be fine‐tuned for particular populations. Countries bordering the Mekong River formed a network in 2011 to co‐ordinate the management of invasive species such as M. micrantha. Expanding such a collaborative approach to other regions could further reduce populations of M. micrantha and limit its spread.     

牛星状病毒EvaGreen实时荧光定量PCR检测方法的建立及应用

牛星状病毒(BAstV)是我国新发的犊牛腹泻病原,本试验的目的是建立检测BAstV的Real-time PCR方法。根据BAstV流行株的ORF1a基因序列设计引物,通过优化反应条件和体系,成功建立基于EvaGreen检测BAstV的Real-time PCR方法。结果表明,该检测方法的Ct值与标准品模板在1.36×10¹~1.36×10⁸拷贝/μL线性关系良好,相关系数R²=0.999,扩增效率为93.79%;该方法可特异性检出BAstV,对犊牛腹泻其他相关病原呈阴性;最低检测下限为13.6拷贝/μL;批间和批内的变异系数均小于2%,重复性好。对2017年9月至2019年5月采自河南省的221份犊牛腹泻样本进行检测,BAstV的检出率为18.1%(40/221),采样场阳性率为100.0%(14/14)。本试验所建方法灵敏度高、特异性强、稳定性好,为BAstV的检测和流行病学调查提供了有力手段。     

植物病原镰刀菌产生的毒素种类及其危害

镰刀菌(Fusarium spp.)是多种重要农作物的病原体，不仅可造成农作物产量和品质的严重损失还可在离体培养条件下或植物寄主体内产生一系列被称为镰刀菌毒素的次生代谢产物。这些毒素一方面作为致病因子与镰刀菌对宿主植物的致病力密切相关，另一方面可导致家畜生产性能下降和相关病症的出现，进而影响农业生态系统并对人类健康造成威胁。鉴于镰刀菌毒素对农作物生产的影响及其对家畜和人类的毒性作用，目前已有较多关于镰刀菌侵染粮食作物后产生毒素种类的研究，但关于镰刀菌侵染豆科牧草后产生的毒素种类以及毒素在镰刀菌对豆科牧草致病力方面作用的研究则较少。本文对引起主要粮食和饲料作物病害的常见镰刀菌物种产生的主要毒素，以及这些毒素对植物、家畜和人类的危害进行了综述，并对豆科牧草中镰刀菌毒素的研究前景及意义进行了展望。     

番茄褪绿病毒在湖南省首次发生

2016年7月在湖南省蔬菜病害调查中发现,4种茄科蔬菜表现出叶脉间褪绿、叶片黄化等症状,疑似被番茄褪绿病毒(Tomato chlorosis virus,To CV)感染,同时叶片背面聚集了大量烟粉虱。采用To CV热激蛋白(heat shock protein 70,HSP70)序列的特异性引物对采集的番茄、茄子、辣椒、马铃薯样品和烟粉虱样品进行RT-PCR检测,均扩增出目标条带,且扩增序列与北京番茄To CV分离物(KC887999.1)部分序列相似度为99.0%,确认采集样品被To CV感染。4种茄科蔬菜To CV的感染率达70%~100%;发病叶片上烟粉虱的带毒率为66.7%~87.5%;鉴定出烟粉虱的生物类型为MED烟粉虱。这是湖南省首次确认该病毒,需要引起关注和加强防范。     

Replication of neurovirulent equine herpesvirus type 1 (EHV-1) in CD172a+ monocytic cells

Equine herpesvirus type 1 (EHV-1) is responsible for respiratory disorders, abortion and myeloencephalopathy (EHM) in horses. Two pathotypes of EHV-1 strains are circulating in the field: neurovirulent (N) and non-neurovirulent (NN). For both strains, CD172a⁺ monocytic cells are one of the main carrier cells of EHV-1 during primary infection, allowing the virus to invade the horse’s body. Recently, we showed that EHV-1 NN strains showed a restricted and delayed replication in CD172a⁺ cells. Here we characterize the in vitro replication kinetics of two EHV-1 N strains in CD172a⁺ cells and investigate if the replication of these strains is similarly silenced as shown for EHV-1 NN strains. We found that EHV-1 N replication was restricted to 7–8% in CD172a⁺ cells compared to 100% in control RK-13 cells. EHV-1 N replication was not delayed in CD172a⁺ cells but virus production was significant lower (10^3.0 TCID₅₀/10⁵ inoculated cells) than in RK-13 cells (10^8.5 TCID₅₀/10⁵ inoculated cells). Approximately 0.04% of CD172a⁺ cells produced and transmitted infectious EHV-1 to neighbour cells compared to 65% of RK-13 cells. Unlike what we observed for the NN strain, pretreatment of CD172a⁺ cells with histone deacetylases inhibitors (HDACi) did not influence the replication of EHV-1 N strains in these cells. Overall, these results show that the EHV-1 replication of N strains in CD172a⁺ cells differs from that observed for NN strains, which may contribute to their different pathogeneses in vivo.