首页> 外文期刊>American Journal of Infectious Diseases and Microbiology >Epidemiological Studies ,Molecular Diagnosis of Anaplasma Marginale in Cattle and Biochemical Changes Associated with it in Kaliobia Governorate
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Epidemiological Studies ,Molecular Diagnosis of Anaplasma Marginale in Cattle and Biochemical Changes Associated with it in Kaliobia Governorate

机译:牛Mar缘无性病的流行病学研究,分子诊断以及与之相关的生化变化

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This investigation is performed on 100 cattle in Kaliobia governorate Egypt aged from 1- 6years severity of illness increase with age , these animals suffered from fever (41°C) enlargement lymph node and drop in milk yield emaciation in progressive stages , cattle producers first notice the anemic anaplasmosis – infected animal when it becomes weak and lag behind the herd when these animals were subjected to microscopic examination the degree of parasitaema was recorded as the percentage of infected red blood cells in each blood smear 100 microscopic field wear examined .We report the detection of anaplasma marginale by PCR in blood samples obtained from cattle supposed to be infected. The assay employs primers specific for the gene encoding anaplasma marginale specific PCR using primers derived from msp5 gene .The PCR products for 26 positive samples were subjected to sequence (Labtechnology, Egypt) and BLAST analysis was used for identification of the genomic DNA of these parasites. changes associated with anaplasma marginale in these cattle particular emphasis to the oxidative stress the reduce TAC level may reflect adecrease in antioxidant capacity and CBC change . Blood collected from all animals on EDTA to microscopic examination and PCR to determine type of anaplasma.
机译:这项研究是在埃及卡里奥比亚省的100头牛上进行的,这些牛的病情严重程度随着年龄的增长在1至6岁之间增加,这些动物患有发烧(41°C)淋巴结肿大和逐步减产的乳汁脱落,奶牛生产者首先注意到贫血性贫血-当感染的动物变得虚弱并在显微镜下检查时落后于畜群时,寄生虫的程度记录为在每次血液涂片100次显微镜现场检查中感染的红细胞的百分比。我们报告了通过PCR检测应感染牛的血液样本中的无缘无核质样。该检测方法使用了源自msp5基因的引物,对编码无缘无核小体特异性PCR的基因具有特异性的引物。对26个阳性样品的PCR产物进行了测序(Labtechnology,Egypt),并使用BLAST分析鉴定了这些寄生虫的基因组DNA。 。这些牛与无体无缘种相关的变化特别强调氧化应激,TAC水平的降低可能反映了抗氧化能力和CBC变化的减少。在EDTA上从所有动物收集的血液进行显微镜检查和PCR,以确定无性体类型。

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