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21.
Kazuhiro Kawai Tomohito Hayashi Yoshio Kiku Tomoyuki Chiba Hajime Nagahata Hidetoshi Higuchi Tetsu Obayashi Seigo Itoh Ken Onda Sachiko Arai Reiichiro Sato Toshio Oshida 《Animal Science Journal》2013,84(12):805-807
Somatic cell counts (SCC) measurements are typically performed using quantitative methods, such as the Breed method (Breed) and the Fossomatic method (FSCC). The DeLaval cell counter (DCC) developed recently is a quantitative somatic cell counter with a low initial cost and superior portability. However, since the DCC was specifically developed for measuring SCC of ≤ 4 × 106 cells/mL milk from bulk tanks or individual cows, its reliability for estimating SCC that exceed this concentration has not yet been clarified. This study therefore examined whether it is possible to accurately measure SCC by diluting milk samples with initial SCC of 4 × 106 cells/mL, as seen in clinical mastitis milk. We collected milk samples from 99 quarters of 99 Holstein cows with clinical mastitis. These milk samples were diluted 10‐fold with saline and thoroughly mixed before performing SCC measurement with the DCC. The correlation coefficients of SCC measured by the FSCC, Breed and DCC methods indicated strong correlations between each pair of methods. The findings showed that DCC can be used to identify bovine clinical mastitis milk and is useful as a quantitative SCC measurement device on farm sites. 相似文献
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23.
西瓜花叶病毒对四倍体西瓜叶片细胞超微结构的影响 总被引:1,自引:0,他引:1
为研究西瓜花叶病毒(WMV)对四倍体西瓜功能叶片细胞超微结构的影响,用透射电镜观察四倍体西瓜受WMV侵染后功能叶片细胞超微结构的变化。结果表明,WMV侵染四倍体西瓜后,四倍体西瓜叶片细胞叶绿体肿胀、片层模糊不清、叶绿体外膜产生异形增生物等;细胞内嗜锇颗粒增加,有大量的风轮状内含体出现,产生大量的束丝包裹病毒粒子;有高尔基体出现,线粒体数目增加,细胞核核膜部分边缘被破坏,核仁融解等。与正常四倍体西瓜叶片细胞相比,WMV对四倍体西瓜叶片细胞超微结构破坏严重,影响四倍体西瓜正常生长。 相似文献
24.
Jeleel O. Agboola Emma Teuling Peter A. Wierenga Harry Gruppen Johan W. Schrama 《Aquaculture Nutrition》2019,25(4):783-797
The rigid cell walls of microalgae may hinder their utilization in fish feeds. The current experiment assessed the correlation between the accessibility of microalgae nutrients and their in vivo digestibility in African catfish. Nannochloropsis gaditana biomass was subjected to physical or mechanical treatments to weaken its cell wall; untreated—no disruption treatment (UNT), pasteurization (PAS), freezing (FRO), freeze‐drying (FRD), cold pasteurization (L40) and bead milling (BEM). Six experimental diets formulated from differently treated and untreated microalgae (at 30% diet inclusion level) were tested on growth performance and apparent nutrient digestibility (ADCs) in juvenile African catfish. A basal diet (REF) containing no microalgae was used as reference diet. Results showed that biomass gain and feed conversion ratio of fish fed L40 and BEM diets increased by 13% and 11%, respectively, relative to the UNT diet. Additionally, FRD, FRO, L40 and BEM cell wall disruption treatments improved protein digestibility by 0.5%, 5.9%, 8.4% and 16.3%, respectively, compared to the UNT treatment. There was a positive correlation between accessibility of microalgal nutrients and their digestibility in African catfish. Nutrient digestibility of microalgae was dependent on extent of cell disruption. Also, the impact of cell disruption on nutrient digestibility of microalgae differs between African catfish and Nile tilapia. 相似文献
25.
选用(28±1)d断奶和平均体重为(6.16±0.13)kg的长白×约克夏仔猪96头,按体重相近原则随机分为6个处理,试验日粮分别在基础日粮中添加浓度为0%、0.3%、0.6%、0.9%、1.2%和1.5%的谷氨酰胺。试验期21d。结果表明,随着谷氨酰胺的添加量增加,仔猪血中红细胞、血小板数目逐渐增加,而白细胞、嗜酸白细胞数目逐渐减少。且随着断奶后时间的延长,仔猪自身免疫力和合成谷氨酰胺能力的加强,这种影响逐渐减小,到断奶后第21天,处理组间各指标均差异不显著(P>0.05)。谷氨酰胺的最佳添加剂量为1.2%。 相似文献
26.
Suying Hou Guoquan Chen Wenji Wang Liqun Xia Zhiwen Wang Yishan Lu 《Journal of fish diseases》2020,43(5):571-581
Nocardia seriolae, a Gram-positive bacterium, is the main pathogen of fish nocardiosis. Protein NlpC/P60 is a cell-wall peptidase and a potential virulence factor of N. seriolae. Subcellular localization research revealed that both NlpC/P60-GFP and NlpC/P60Δsig-GFP fusion proteins were evenly distributed in the whole cell of fathead minnow (FHM) cells. Furthermore, typical apoptotic features, such as nuclear pyrosis and apoptotic bodies, were observed in the transfected FHM cells and grouper spleen cells by the overexpression of protein NlpC/P60. Then, quantitative assays of mitochondrial membrane potential (ΔΨm) value, caspase-3 activity and apoptosis-related gene (Bax, BNIP3, TNF1 and TNF6) mRNA expression were conducted. The results showed that ΔΨm was decreased, caspase-3 was significantly activated, and the mRNA expression of pro-apoptotic genes (Bax and BNIP3) and tumour necrosis factors (TNF1 and TNF6) was up-regulated in NlpC/P60-overexpressed cells. Taken together, the results indicated that the protein NlpC/P60 of N. seriolae might involve in apoptosis regulation. This study may lay the foundation for further study on the function of N. seriolae NlpC/P60 and promote the understanding of the virulence factors and pathogenic mechanism of N. seriolae. 相似文献
27.
针对传统的细胞力学研究方法的非无损性,不能对细胞力学参数连续、长期监测的特点,研制出一种基于石英晶体压电效应的简易型细胞力学测试仪。该测试仪以STM32 103C8 为核心,设计有石英晶体在液相环境下的起振电路、稳定振荡电路,采用了频率/电压转换电路。系统实现了对石英晶体频率变化的高精度采集,对与传感器耦合的界面层(细胞)的质量、粘弹性和表面应力多参数敏感,能对细胞黏附过程和细胞力学性能进行动态监测。通过整机在细胞培养液环境下的实验,验证了测试仪系统的可行性与稳定性。 相似文献
28.
S Rowe;JK House;RN Zadoks; 《Australian veterinary journal》2024,102(1-2):5-10
Mastitis is the major disease affecting milk production of dairy cattle, and milk is an obvious substrate for the detection of both the inflammation and its causative infectious agents at quarter, cow, or herd levels. In this review, we examine the use of milk to detect inflammation based on somatic cell count (SCC) and other biomarkers, and for the detection of mastitis pathogens through culture-based and culture-free methods. 相似文献
29.
Ki-Soo Park Yong-Soon Lee Kyung-Sun Kang 《Journal of veterinary science (Suw?n-si, Korea)》2006,7(4):343-348
Mesenchymal stem cells (MSCs) have the capabilities for self-renewal and differentiation into cells with the phenotypes of bone, cartilage, neurons and fat cells. These features of MSCs have attracted the attention of investigators for using MSCs for cell-based therapies to treat several human diseases. Because bone marrow-derived cells, which are a main source of MSCs, are not always acceptable due to a significant drop in their cell number and proliferative/differentiation capacity with age, human umbilical cord blood (UCB) cells are good substitutes for BMCs due to the immaturity of newborn cells. Although the isolation of hematopoietic stem cells from UCB has been well established, the isolation and characterization of MSCs from UCB still need to be established and evaluated. In this study, we isolated and characterized MSCs. UCB-derived mononuclear cells, which gave rise to adherent cells, exhibited either an osteoclast or a mesenchymal-like phenotype. The attached cells with mesenchymal phenotypes displayed fibroblast-like morphologies, and they expressed mesenchym-related antigens (SH2 and vimentin) and periodic acid Schiff activity. Also, UCB-derived MSCs were able to transdifferentiate into bone and 2 types of neuronal cells, in vitro. Therefore, it is suggested that the MSCs from UCB might be a good alternative to bone marrow cells for transplantation or cell therapy. 相似文献
30.
应用Crispr/Cas9基因编辑技术敲除MDCK细胞中的Annexin A2基因,并验证其是否为ε毒素在MDCK细胞表面的受体。根据Crispr/Cas9靶点设计原则设计靶点,构建PALentiCRISPR v2重组质粒。借助Crispr/Cas9技术,将构建好的质粒转染至MDCK细胞中,用嘌呤霉素筛选敲除Annexin A2蛋白的MDCK细胞株,并通过测序和Western blot验证敲除效果。通过细胞毒性试验验证MDCK细胞膜表面的Annexin A2蛋白是否为ε毒素的受体蛋白。测序结果和Western blot结果表明,通过Crispr/Cas9技术成功敲除了MDCK细胞的Annexin A2基因,但细胞毒性试验结果表明,敲除Annexin A2基因并不能减弱ε毒素对MDCK细胞的毒性。结果表明,Annexin A2蛋白不是ε毒素在MDCK细胞表面的受体,研究结果为今后MDCK细胞其他蛋白的敲除提供了试验方法,构建的Annexin A2基因敲除的MDCK细胞也为Annexin A2蛋白引起的其他疾病的研究奠定了基础。 相似文献