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首页> 外文期刊>Journal of Clinical Microbiology >A 16S rRNA-based PCR assay for detection and identification of granulocytic Ehrlichia species in dogs, horses, and cattle.
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A 16S rRNA-based PCR assay for detection and identification of granulocytic Ehrlichia species in dogs, horses, and cattle.

机译:一种基于16S rRNA的PCR检测试剂盒,用于检测和鉴定狗,马和牛的粒细胞埃希氏菌。

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摘要

A PCR-based assay was developed for detecting DNA of granulocytic ehrlichiae in blood samples from dogs, horses, and cattle, Primers were designed from 16S rRNA sequence information to specifically amplify DNA from a newly identified Swedish Ehrlichia species. The 16S rRNA nucleotide sequence of this Swedish species differs in only two and three positions from the sequences of Ehrlichia phagocytophila and Ehrlichia equi, respectively, which were also amplified by this PCR system. For evaluation, PCR results were compared with microscopic examination of stained blood smears for the detection of granulocytes containing ehrlichiae (morulae). Thirty-four of 36 microscopically positive samples were also positive by PCR, and 6 microscopically negative samples were negative by PCR as well. Six samples, in which morulae-like structures had been seen, were negative by PCR, also at a lower annealing temperature and when a reamplification of the first PCR products was performed. The identities of the PCR products from some canine and equine isolates were verified by direct DNA sequencing and were found to be identical with the Ehrlichia sequence found in these animal species that had been obtained earlier. The sequences of a segment of approximately 600 nucleotides from two bovine isolates were identical to that of E. phagocytophila, whereas the sequence of another bovine isolate differed in two positions from that of E. phagocytophila and in three positions from the sequences of the canine and equine isolates. Serum samples were analyzed by indirect fluorescent-antibody testing. Seventy-three percent of the animals which were positive by microscopy and PCR also had positive antibody titers. However, it was not possible to rely on a single serological result for diagnosis of present infection. It was, therefore, concluded that PCR was the most reliable method, useful in the clinical laboratory for specific and early diagnosis of granulocytic ehrlichiosis in animals.
机译:已开发出一种基于PCR的检测方法,用于检测狗,马和牛的血样中的粒状嗜酸杆菌DNA,并根据16S rRNA序列信息设计了引物,以特异性扩增新鉴定的瑞典埃希氏菌属物种的DNA。该瑞典物种的16S rRNA核苷酸序列分别与嗜血埃里希氏菌和马埃里希氏菌的序列仅相差两个和三个位置,后者也通过此PCR系统扩增。为了进行评估,将PCR结果与显微镜检查的血涂片进行了比较,以检测含有埃希氏菌(桑ula)的粒细胞。 PCR检测的36例镜检阳性样品中有34例也是阳性的,PCR检测的6例镜检阴性样品也均为阴性。当在较低的退火温度下并且在进行第一PCR产物的再扩增时,六个样品中已经看到桑样结构的样品通过PCR是阴性的。通过直接DNA测序验证了来自某些犬和马分离株的PCR产物的身份,发现它们与早先获得的这些动物物种中的埃希氏菌序列相同。来自两个牛分离株的大约600个核苷酸的片段的序列与嗜吞噬性大肠杆菌的序列相同,而另一个牛分离株的序列在两个位置不同于噬菌性大肠杆菌,在三个位置与犬和猫的序列不同。马分离株。通过间接荧光抗体测试分析血清样品。在显微镜和PCR呈阳性的动物中,有73%的抗体滴度也呈阳性。但是,不可能依靠单一的血清学结果来诊断当前的感染。因此,得出的结论是,PCR是最可靠的方法,在临床实验室中可用于动物的粒细胞埃希氏菌病的特异性和早期诊断。

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