辣椒传入中国的途径与传播路径

通过考证认为，一年生辣椒(Capsicum annuum L.)于16世纪80年代从日本传入中国，最早的传入点是浙江。以浙江为起点，向北、西、南3个方向传播。向北方向，经江苏传到山东，虽然江苏没有接受辣椒，但山东很快接受并把辣椒当作花椒的替代品，名称由番椒变成了秦椒；再以山东为中心，继续向河北、辽宁传播，东北的辣椒是闯关东的山东人传播的；向西传到了天津、山西、河南、北京、甘肃、内蒙古，形成华北传播路线。向西方向，从浙江沿长江西上，安徽、江西、湖北没有接受，但湖南很快接受了辣椒，并以湖南为中心，向贵州、四川、云南、广东、广西、陕西等地传播，形成影响最大的长江传播路线，新疆的辣椒是在左宗棠收复新疆时由湖南军人传过去的。向南传播的速度非常缓慢，传到江西、福建的时间都较晚。从荷兰传入台湾的灌木辣椒(Capsicum frutescens L.)和从印度尼西亚雅加达传入台湾的中国辣椒(Capsicum chinense Jacq.)，经福建传到海南和云南。     

香蕉TGA转录因子家族的鉴定及枯萎病菌胁迫下的表达分析

尖孢镰刀菌（Fusarium oxysporum f. sp. Cubense, Foc）引起的香蕉枯萎病是我国香蕉的主要病害之一,严重影响香蕉的产量和品质。TGA防御反应基因在香蕉应对尖孢镰刀菌胁迫的应答转录调控过程中至关重要。本研究以拟南芥TGA转录因子家族成员蛋白为查询序列,在香蕉基因组数据库中Blast筛选出TGA转录因子家族成员,并对该家族成员进行生物信息学分析。共鉴定得到9个香蕉TGA家族成员,分别命名为MaTGA1~MaTGA9;香蕉TGA家族蛋白富含酸性氨基酸,大部分蛋白以α螺旋为主;亚细胞定位主要在细胞核内。进化树分析表明,香蕉MaTGA转录因子家族的9个成员可分为Class Ⅰ和Class Ⅱ两类,基因结构及功能结构域的分布情况也呈现出高度一致。进一步通过RT-qPCR分析发现,MaTGA2、MaTGA3和MaTGA8在香蕉枯萎病菌侵染后的‘威廉斯’（易感病）及‘南天黄’（抗病）中均显著下调表达,MaTGA1、MaTGA6、MaTGA7和MaTGA9均呈现先下降后上升的趋势;然而MaTGA4和MaTGA5仅在‘威廉斯’中上调表达,以上结果表明MaTGA2、MaTGA3和MaTGA8在香蕉抗枯萎病中发挥重要的生物学功能。本研究结果为香蕉TGA转录因子功能挖掘奠定理论基础。     

Projecting future habitat quality of three midwestern reservoir fishes under warming conditions

Rising temperatures caused by climate change are likely to affect cool‐water and warm‐water fishes differently. Yet, forecasts of anticipated temperature effects on fishes of different thermal guilds are lacking, especially in freshwater ecosystems. Towards this end, we used spatially explicit, growth rate potential (GRP) models to project changes in seasonal habitat quality for a warm‐water piscivore (largemouth bass Micropterus salmoides), a cool‐water piscivore (walleye Sander vitreus) and a hybrid piscivore (saugeye S. vitreus × S. canadensis) in two Midwestern reservoirs. We assessed habitat quality for two periods (early and middle 21st century) under two realistic greenhouse gas emission scenarios (a mid‐century emissions peak and a rapid continuous increase in emissions). Largemouth bass were projected to experience enhanced or slightly reduced habitat during all seasons, and throughout the mid‐21st century. By contrast, walleye habitat was projected to decline with anticipated warming, except during the spring in the smaller of our two study reservoirs and during the fall in the larger of our two study reservoirs. Saugeye habitat was projected to either increase modestly or decline slightly during the spring and fall and declines in habitat quality and quantity that were smaller than those for walleye were identified during summer. Collectively, our findings indicate that climate warming will differentially alter habitat suitability for reservoir piscivores, favouring warm‐water species over cool‐water species. We expect these changes in habitat quality to impact the dynamics of reservoir fish populations to varying degrees necessitating the consideration of climate when making future management decisions.     

艾纳香内生真菌抗细菌和炭疽菌的活性研究

为获得丰富的艾纳香内生真菌资源,筛选出抗性生防菌株,用于活性次生代谢产物的发现,通过水琼脂法对海南产艾纳香进行内生真菌分离,通过ITS序列分析,对其进行鉴定和分析。采用滤纸片法评价内生真菌发酵产物对细菌的抑制活性,采用平板对峙培养法评价艾纳香内生真菌对植物炭疽菌的拮抗作用。本研究共分离鉴定出191株内生真菌,分属于27属,45种,其中优势菌属为Diaporthe、Paraphoma、Ectophoma、Penicillium、Talaromyces、Hypoxylon、Phomopsis、Colletotrichum和Fusarium。抗细菌活性结果显示,Clonostachys、Fusarium和Diapothe属活性较强。抗炭疽病菌试验显示,Talaromyces、Ectophoma和Penicillium属活性较强。本研究初步探讨了海南产艾纳香内生真菌种类的多样性,并首次对其进行了抗病原菌活性筛查,获得的活性菌株可作为微生物源菌剂开发的重要材料。     

水杨酸对盐胁迫下豇豆幼苗生长发育的影响

在300 mmol/L Na Cl胁迫条件下,研究了水杨酸对豇豆[Vigna unguiculata(L.)Walp]幼苗生长发育的影响。结果表明,经水杨酸处理的豇豆幼苗株高、茎粗明显提高,促进了幼苗的形态构建。并且幼苗的超氧化物歧化酶和过氧化物酶活性均显著高于对照,丙二醛含量和电解质渗透率显著或明显降低;水杨酸在适宜的施用浓度范围内能够缓解豇豆幼苗的盐害症状,提高抗盐能力,对豇豆幼苗的生长有一定的促进作用,当水杨酸的处理浓度为100~150 mg/L时,作用效果最明显。     

Effect of bacteria isolates in powdery mildew control in flowering dogwoods (Cornus florida L.)

Five bacterial isolates collected from dogwood leaves were evaluated for powdery mildew control in shadehouse and greenhouse environments by using foliar sprays and/or root drenching. Two isolates displayed superior bioactivity and suppressed powdery mildew similar to conventional fungicide thiophanate methyl (Cleary’s 3336F^®). The two bacteria disrupted powdery mildew spore germination and ruptured spore membranes causing spore lyses. Bacterial filtrates without bacterial cells were also effective in suppressing powdery mildew and disrupting spore germination and suggested the involvement of secondary metabolites. The two biocontrol agents (BCAs) colonized roots endophytically and promoted plant growth.     

柳蛎盾蚧危害与丁香防御蛋白活力的关系

在柳蛎盾蚧的未危害期(5月末)、危害盛期(6月末)、危害弱期(7月末)、危害末期(8月末),测定高抗类[什锦丁香等7种(品种)]、中抗类[西南丁香等3种(品种)]、易感类[紫丁香等2种]、高感类(红丁香)13种(品种)丁香叶中的POD,SOD,CAT,PPO,PAL,TI和CI 7种防御蛋白的活性.结果表明:危害时期,丁香种(品种)对丁香防御蛋白活力有极显著影响(P＜0.01).POD活性,在危害盛期,在高抗、中抗类丁香中均显著升高(P＜0.05),而在易感、高感类中应激滞后,即分别在危害弱期和危害末期升高.CAT在易感类和高感类丁香防御上起主导作用,其活性在危害盛期显著升高,而中抗和高抗类未见明显变化.SOD活性,在危害盛期高抗类丁香中无显著变化,而其余3类则显著降低.PPO活性在未危害期的高低与抗性相关,在虫害盛期诱导表达的强弱也与抗性相关;PAL活性未能反映抗性品种间的差异.TI和CI活性,在未危害期的高低与其抗虫性无明显相关性,在危害盛期的升高幅度与抗虫性呈正相关.综上所述,PPO在未危害期的活力可作为筛选丁香抗虫种(品种)的指标,危害盛期POD,PPO,TI和CI活性升高的幅度与丁香抗虫性呈正相关.     

A filter-assisted culture method for isolation of Treponema spp. from bovine digital dermatitis and their identification by MALDI-TOF MS

Digital dermatitis (DD) is a major infectious foot disease of cattle worldwide. Some DD stages are associated with lameness, and the disease has significant economic and animal welfare consequences. The pathogenesis of the disease is not yet fully understood, but Treponema spp. have been associated consistently with clinical cases. Isolation of these fastidious bacteria is difficult and cumbersome. We describe an improved method enabling the culturing of the 3 Treponema spp. (T. pedis, T. phagedenis, and T. medium) from bovine foot specimens derived from DD lesions, using a combination of membrane filtering and subsequent growth on selective agar media. The entire procedure from sampling to verification of individual Treponema spp. takes up to 24 d. In addition, we established a MALDI-TOF MS–based identification method to be applied for confirmation of the different Treponema spp. This scheme provides an unambiguous, simple, and straightforward identification procedure for DD-associated Treponema spp.     

Validation of a multiplex PCR assay to detect Babesia spp. and Anaplasma marginale in cattle in Uruguay in the absence of a gold standard test

Detection of bovine Babesia spp. and Anaplasma marginale is based on the reading of Giemsa-stained blood or organ smears, which can have low sensitivity. Our aim was to improve the detection of bovine Babesia spp. and A. marginale by validating a multiplex PCR (mPCR). We used 466 samples of blood and/or organs of animals with signs and presumptive autopsy findings of babesiosis or anaplasmosis. The primers in our mPCR amplified the rap-1a gene region of Babesia bovis and B. bigemina, and the msp-5 region of A. marginale. We used a Bayesian model with a non-informative priori distribution for the prevalence estimate and informative priori distribution for estimation of sensitivity and specificity. The sensitivity and specificity for smear detection of Babesia spp. were 68.6% and 99.1%, and for A. marginale 85.6% and 98.8%, respectively. Sensitivity and specificity for mPCR detection for Babesia spp. were 94.2% and 97.1%, and for A. marginale 95.2% and 92.7%, respectively. Our mPCR had good accuracy in detecting Babesia spp. and A. marginale, and would be a reliable test for veterinarians to choose the correct treatment for each agent.     

Detection of bacterial contamination and DNA quantification in stored blood units in 2 veterinary hospital blood banks

Blood transfusions in veterinary medicine have become increasingly more common and are now an integral part of lifesaving and advanced treatment in small and large animals. Important risks associated with transfusion of blood products include the transmission of various infectious diseases. Several guidelines suggest what infectious agents to screen for in canine and feline transfusion medicine. However, while the risk of bacterial contamination of blood products during storage and administration has not been documented in veterinary medicine, it has emerged as a cause of morbidity and mortality in human transfusion medicine. Clinical experience shows that the majority of blood component bacterial contaminations are caused by only a few species. Unlike other types of bacteria, psychrotolerant species like Pseudomonas spp. and Serratia spp. can proliferate during the storage of blood units at 4°C from a very low titer at the time of blood collection to a clinically significant level (> 10⁵ CFU/mL) causing clinical sepsis resulting from red blood cell concentrate transfusions in human medicine. The purpose of this report was to describe the detection and quantification procedures applied in 4 cases of bacterial contamination of canine and feline blood units, which suggest the need for further investigations to optimize patients’ safety in veterinary transfusion medicine.