钼镉联合胁迫对山羊肾脏细胞凋亡相关基因表达的影响

本研究以波尔山羊为实验动物,旨在观察钼镉联合胁迫对山羊肾脏细胞凋亡相关基因表达的影响。选用63头健康波尔山羊随机分成7组,每组3个重复,选用七钼酸铵([(NH4)6Mo7O24·4H2O])作为实验钼源,氯化镉(Cd Cl2)作为实验镉源,按每kg山羊体质量添加钼、镉对照组(Mo 0 mg/kg+Cd 0 mg/kg),低镉低钼组(Mo 15mg/kg+Cd 0.5 mg/kg),低镉中钼组(Mo 30 mg/kg+Cd 0.5 mg/kg),低镉高钼组(Mo 45 mg/kg+Cd 0.5 mg/kg),高镉低钼组(Mo 15 mg/kg+Cd 1.0 mg/kg),高镉中钼组(Mo 30 mg/kg+Cd 1.0 mg/kg),高镉高钼组(Mo 45 mg/kg+Cd1.0 mg/kg),实验期50 d。并于当天、第25、50天每组各剖杀3头山羊取肾组织进行相关实验,观察不同剂量钼、镉对山羊肾脏细胞凋亡相关基因表达等的影响。结果显示,与对照组相比,在实验第25、50天时,实验组山羊肾脏bcl-2 mRNA表达量下降(P0.01),bax mRNA、caspase-3 mRNA和cytc mRNA表达量上升(P0.05或P0.01);山羊钼镉联合胁迫导致肾线粒体抗氧化功能降低、自由基含量升高,导致细胞促凋亡基因表达量上升,抗凋亡基因的表达量下降,提示钼镉联合胁迫对山羊肾脏有明显损伤。     

Note: A comparison of molecular diagnostic procedures for the detection of aster yellows phytoplasmas (16Sr-I) in leafhopper vectors

Different molecular procedures were compared for the detection of aster yellows phytoplasmas (AYP) in the leafhopper vectorsMacrosteles quadripunctulatus (Kirschbaum),Euscelidius variegatus (Kirschbaum) andEuscelis incisus (Kirschbaum). Polymerase chain reaction (PCR) with universal and group-specific primers designed on the 16S-rDNA sequence was most sensitive in nested assays. A dot-blot procedure with an oligoprobe designed on the 16S-rDNA was less sensitive and consistent to detect phytoplasmas in total insect DNA, but consistently detected amplicons from direct PCR. The dot-blot assay with a probe based on a phytoplasma plasmid sequence detected AYP in most vector specimens and did not react with DNAs from leafhoppers infected by flavescence dorée and psyllids infected by apple proliferation phytoplasmas. This last assay is almost devoid of contamination risks, faster and cheaper compared to PCR, therefore it has to be preferred for field-scale analysis of leafhopper populations. http://www.phytoparasitica.org posting Feb. 24, 2004.     

An in vitro study of hematopoietic progenitor cells from peripheral blood of rabbits

The purpose of this study was to isolate and cultivate a subpopulation of pluripotent stem cells (PSCs) from the peripheral blood of rabbits, which are frequently used in veterinary research as an animal model. Pluripotent stem cells, as described in human beings, are fibroblast-like cells that exhibit a CD34 marker, specific from other hematopoietic stem cells. Commonly used human commercial media has been researched for culturing rabbit PSCs. These findings allow us to contemplate the direct application of this simple and standardized methodology in several areas of study, such as of the pharmacological effect of many drugs on hematopoietic cells, veterinary practice, and even the study of new strategies in cellular therapy for some human diseases.     

Molecular characterization of Pseudomonas syringae isolates from fruit trees and raspberry in Serbia

Infection of fruit trees by Pseudomonas syringae is a potentially serious problem that may limit the establishment and sustained productivity of pome and stone fruit orchards in Serbia. To estimate possible diversity of Pseudomonas syringae fruit trees strains, we collected a set of strains in several areas of Serbia. The samples were taken from infected orchards with raspberry, plum, cherry, sour cherry, peach, pear and apple trees. Genetic diversity of P. syringae strains isolated from fruit trees was determined by using SpeI macrorestriction analysis of genomic DNAs by pulsed-field gel electrophoresis (PFGE) and REP-PCR. Molecular analysis showed that most of isolates had unique profiles, with the exception of isolates from plum and cherry that displayed profiles identical to each other and similar to P. syringae pv. morsprunorum. The study presented here clearly demonstrates the discriminative power of molecular techniques in enabling a detailed analysis of the genetic variations between strains of P. syringae from different pome and stone fruit hosts in Serbia.     

翘嘴鲌淀山湖和兴凯湖群体的胚胎发育及染色体核型比较

为了解翘嘴鲌(Culter alburnus)南、北不同地理群体在繁殖和染色体核型方面的差异性,以翘嘴鲌南方(上海淀山湖)群体和北方(黑龙江兴凯湖)群体为研究对象,在上海地区同时进行了翘嘴鲌两个群体的人工繁育、胚胎发育观察和染色体组成比较。结果显示,翘嘴鲌南方淀山湖群体的受精卵呈灰黄色,有黏性,为黏性卵,卵径为(1.11±0.05)mm;北方兴凯湖群体的受精卵呈青灰色,无黏性,为浮性卵,卵径为(1.21±0.03)mm。两个群体的相对繁殖力和受精率无明显差异。在(25±1)℃的水温条件下,两个群体的胚胎均可以在24 h内出膜,且胚胎发育特征及时序无明显差异。北方兴凯湖群体仔鱼的出膜后体长为(5.77±0.29)mm,极显著大于南方淀山湖群体[(3.40±0.14)mm](P<0.01)。两个群体的染色体数目均为2n=48,其中南方淀山湖群体的核型公式为2n=24m+20sm+4st,染色体臂数NF=88;北方兴凯湖群体的核型公式为2n=22sm+26m, NF=96。研究表明,翘嘴鲌南方淀山湖与北方兴凯湖群体在受精卵的特征及染色体核型上存在一定的差异,且北方兴凯湖水系翘嘴鲌可以在...     

RADIX: rhizoslide platform allowing high throughput digital image analysis of root system expansion

Background

Phenotyping of genotype-by-environment interactions in the root-zone is of major importance for crop improvement as the spatial distribution of a plant’s root system is crucial for a plant to access water and nutrient resources of the soil. However, so far it is unclear to what extent genetic variations in root system responses to spatially varying soil resources can be utilized for breeding applications. Among others, one limiting factor is the absence of phenotyping platforms allowing the analysis of such interactions.

Results

We developed a system that is able to (a) monitor root and shoot growth synchronously, (b) investigate their dynamic responses and (c) analyse the effect of heterogeneous N distribution to parts of the root system in a split-nutrient setup with a throughput (200 individual maize plants at once) sufficient for mapping of quantitative trait loci or for screens of multiple environmental factors. In a test trial, 24 maize genotypes were grown under split nitrogen conditions and the response of shoot and root growth was investigated. An almost double elongation rate of crown and lateral roots was observed under high N for all genotypes. The intensity of genotype-specific responses varied strongly. For example, elongation of crown roots differed almost two times between the fastest and slowest growing genotype. A stronger selective root placement in the high-N compartment was related to an increased shoot development indicating that early vigour might be related to a more intense foraging behaviour.

Conclusion

To our knowledge, RADIX is the only system currently existing which allows studying the differential response of crown roots to split-nutrient application to quantify foraging behaviour in genome mapping or selection experiments. In doing so, changes in root and shoot development and the connection to plant performance can be investigated.

     

Epidemiology of Haemophilus somnus infection in dairy cattle in Quebec.

Serological studies on Haemophilus somnus infection were carried out on 1795 cattle from 231 dairy herds in the province of Quebec. An epidemiological investigation was done in each of the dairy operations. Seroreactivity rate and mean log2 titer for all the sera were 55.4% and 4.1620 respectively. Cattle from eastern regions of Quebec demonstrated the lowest prevalence of H. somnus agglutinins. The percentage of seroreactor animals was 60.3 in herds of 100 cattle or more in comparison to 53.2 in herds of smaller size. About 75% of the animals from 16 herds in which one or more cattle showed nervous manifestations of undetermined origin over a one year period had antibodies to H. somnus. Herds in which respiratory diseases occurred had 59.6% seroreactor animals and herds in which weak calf syndrome was diagnosed over a one year period had 61.4% seroreactor animals. In 87 herds located within 20 km of feedlots, 61.8% of the sera had titers and the mean log2 titer was 4.4813.     

巨大/胶冻样类芽孢杆菌对印度芥菜修复Cd污染土壤的影响

采用盆栽试验方法,研究了接种巨大芽孢杆菌和胶冻样类芽孢杆菌的混合发酵液对印度芥菜修复Cd污染土壤的影响。结果表明,接种混合菌发酵液可显著增加印度芥菜的生物量,接种20d、接种量为50ml时,总生物量较对照组增加了50.44%;在接种30d时,50ml混合菌发酵液处理的印度芥菜地上部P、K的含量显著高于对照组,分别增加了48.84%和74.90%,同时接种50ml混合菌发酵液可显著提高根际和非根际土壤中有效态Cd含量,使其较对照分别增加了39.29%和32.52%。接种混合菌发酵液可促进印度芥菜对土壤Cd的吸收,接种40d接种量为50ml时Cd吸收总量较对照组显著增加了60.36%。综上所述,接种混合菌发酵液50ml时,可促进印度芥菜的生长,增加土壤有效态Cd含量,从而提高了印度芥菜对Cd污染土壤的修复效率。     

Microbial indicators for soil quality

The living soil is instrumental to key life support functions (LSF) that safeguard life on Earth. The soil microbiome has a main role as a driver of these LSF. Current global developments, like anthropogenic threats to soil (e.g., via intensive agriculture) and climate change, pose a burden on soil functioning. Therefore, it is important to dispose of robust indicators that report on the nature of deleterious changes and thus soil quality. There has been a long debate on the best selection of biological indicators (bioindicators) that report on soil quality. Such indicators should ideally describe organisms with key functions in the system, or with key regulatory/connecting roles (so-called keystone species). However, in the light of the huge functional redundancy in most soil microbiomes, finding specific keystone markers is not a trivial task. The current rapid development of molecular (DNA-based) methods that facilitate deciphering microbiomes with respect to key functions will enable the development of improved criteria by which molecular information can be tuned to yield molecular markers of soil LSF. This review critically examines the current state-of-the-art in molecular marker development and recommends avenues to come to improved future marker systems.