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We tried to identify the bacteria and explore the mechanism of the bacteria's pathogenicity via housekeeping gene gyrB and in vitro organ culture (IVOC) of ileum and intramuscular injection. Microscope, electron microscope and scanning electron microscope were also used to observe and the structure, pathogen of M12 and changes of infected tissues. The results showed that M12 was short gram-negative bacteria, and both ends of it were obtuse and the size without flagellum was (0.6 to 1.6) μm×(0.6 to 0.7)μm while length of flagellum was about 2 to 3 times of the length of bacteria.It had 100.0% similarity with Aeromonas caviae from GenBank. IVOC test observed M12' adhesion in intestinal epithelial cell, resulting in formulation of biofilm structure and damage in intestinal epithelial cell. Histopathologic examination showed that M12 could cause damage in intestine, liver, lung, kidney, muscle tissue of rabbit.The assay would offer references for researching the pathogenic mechanism of Aeromonas caviae. 相似文献
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为了在体外细胞水平模拟多浪绵羊肌肉生长发育过程,本研究以多浪绵羊为试验动物,采用胶原酶和胰酶两步酶消化法分离多浪绵羊骨骼肌卫星细胞(satellite cells,SCs),并利用差速贴壁的方法纯化分离得到的SCs。利用免疫荧光技术检测SCs标记基因Desmin、Pax7和MyoD1的表达情况,鉴定分离得到的SCs。采用血清撤离的方法诱导SCs向成肌方向分化。通过显微镜观察和成肌分化标记基因肌球蛋白重链(myosin heavy chain,MHC)的免疫荧光,检测肌管的形成情况。通过对SCs标记基因Desmin、Pax7和MyoD1的免疫荧光鉴定,确认本研究成功分离得到多浪绵羊SCs。采用血清撤离的方法诱导SCs成肌分化,显微镜观察和MHC免疫荧光可以明显观察和检测到肌管的形成。本研究对多浪绵羊SCs成功地进行了分离和鉴定,并建立了体外培养条件下多浪绵羊SCs的成肌诱导分化。 相似文献
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Alban L Boes J Kreiner H Petersen JV Willeberg P 《Preventive veterinary medicine》2008,87(3-4):340-357
Increasing demands for cost-effectiveness in surveillance for human health hazards from animal origins can be met by introducing risk-based principles. This e.g. implies targeting subpopulations with higher risk of infection compared to the whole population. Furthermore, historical data from surveillance can be collated and used to assess future risk of infection. To demonstrate the effectiveness of combining these two approaches, we used a model called “Discounting historical evidence”. It depends mainly on the annual risk of introduction (PIntro) and the surveillance system sensitivity (SSe) (ability to detect infection if present). The model implies simulations that reiterate for a number of years. For each year the output is updated with the confidence on absence in infection. Trichinella spiralis infection in pigs is used as an example. In Denmark, more than 20 million pigs are tested annually. Despite more than 70 years of testing no pigs have been found positive for Trichinella. Hence, PIntro is low. SSe can be estimated from the maximum number of infected carcasses expected under the specified design prevalence, and the sensitivity of the test applied. According to our assessment, the current prevalence of Trichinella in Danish pigs is less than one case per million, which we interpret as negligible risk. Based on this, a risk-based surveillance programme for Trichinella is designed that targets all out-door reared pigs as well as all sows and boars (current total 610,000 slaughtered annually). These subpopulations are judged to have higher risk of getting Trichinella. Again, SSe and PIntro are estimated and the model results show that risk-based surveillance can be applied without jeopardizing human health. Finally, we incorporate wildlife surveys and test quality assurance in the programme. The results of the simulation model were included in an application to the European Commission concerning Denmark's status as a region with negligible risk of Trichinella. In July 2007, the European Commission granted status as “negligible risk” to Danish pigs and pork. 相似文献