首页> 外文OA文献 >Definitive differentiation between single and mixed mycobacterial infections in red deer (Cervus elaphus) by a combination of duplex amplification of p34 and f57 sequences and Hpy188I enzymatic restriction of duplex amplicons.
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Definitive differentiation between single and mixed mycobacterial infections in red deer (Cervus elaphus) by a combination of duplex amplification of p34 and f57 sequences and Hpy188I enzymatic restriction of duplex amplicons.

机译:通过对p34和f57序列进行双链扩增和对双链扩增子进行Hpy188I酶促酶解结合,可以确定马鹿单枝和混合分枝杆菌感染之间的明确区别。

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摘要

Severe emaciation and mortalities suggestive of mycobacterial infections were recently reported for both adult and young wild red deer (Cervus elaphus) in the southeastern part of Belgium. In deer, tuberculous lesions are not pathognomonic of Mycobacterium bovis infection due to gross and microscopic similarities with lesions caused by Mycobacterium avium subsp. paratuberculosis or M. avium subsp. avium. The aim of this study was to improve molecular methods for the species-specific identification of M. bovis, M. avium subsp. avium, and M. avium subsp. paratuberculosis in mycobacterial infections of deer. DNA banding patterns were assessed prior to and after Hpy188I restriction of f57-upstream (us)-p34 duplex amplicons. The duplex f57-us-p34 PCR differentiated M. bovis from M. avium subsp. paratuberculosis and M. avium subsp. avium infections, whereas the restriction step differentiated single M. avium subsp. paratuberculosis or M. avium subsp. avium infections from mixed M. avium subsp. paratuberculosis/M. avium subsp. avium infections. The endonuclease Hpy188I cleaves DNA between nucleotides N and G in the unique TCNGA sequence. This restriction site was found at position 168 upstream of the us-p34 initiation codon in all M. avium subsp. avium strains tested, regardless of their origin and the results of IS901 PCR. In contrast, the restriction site was abrogated in all M. avium subsp. paratuberculosis strains tested, independent of their origin, Mycobactin J dependency, and IS900 PCR results. Consequently, a two-step strategy, i.e., duplex us-p34-f57 PCR and Hpy188I restriction, allowed us to exclude M. bovis infection and to identify single (M. avium subsp. paratuberculosis or M. avium subsp. avium) or mixed (M. avium subsp. paratuberculosis/M. avium subsp. avium) infections in wild red deer in Belgium. Accordingly, we propose to integrate, in a functional molecular definition of M. avium subsp. paratuberculosis, the absence of the Hpy188I restriction site from the us-p34 amplicon.
机译:最近,比利时东南部的成年和幼年野马鹿(鹿)的严重消瘦和死亡提示有分枝杆菌感染。在鹿中,由于与鸟分枝杆菌亚种引起的病变具有总体和微观相似性,因此结核性病变不是牛分枝杆菌感染的病原学。副结核病或鸟分枝杆菌亚种阿维姆这项研究的目的是改进分子方法,以鉴定牛分枝杆菌,鸟分枝杆菌亚种。 avium和M. avium subsp。结核分支杆菌感染了鹿的分枝杆菌。在Hpy188I限制f57上游(美国)-p34双链扩增子的之前和之后,评估了DNA条带模式。双重f57-us-p34 PCR区分了牛分枝杆菌和鸟分枝杆菌亚种。副结核病和鸟分枝杆菌亚种。禽感染,而限制步骤区分了单个禽分枝杆菌亚种。副结核病或鸟分枝杆菌亚种混合禽鸟支原体亚种的禽鸟感染。副结核病鸟亚种禽感染。内切核酸酶Hpy188I在独​​特的TCNGA序列中的核苷酸N和G之间切割DNA。在所有鸟分枝杆菌亚种中us-p34起始密码子上游168位发现了该限制性酶切位点。不论其来源和IS901 PCR的结果如何,均应测试禽杆菌菌株。相反,在所有鸟分枝杆菌亚种中限制位点都被取消。测试了副结核病菌株,与它们的来源,Mycobactin J依赖性和IS900 PCR结果无关。因此,分两步进行的策略,即双链us-p34-f57 PCR和Hpy188I限制,使我们可以排除牛分枝杆菌感染,并鉴定出单一的(鸟分枝杆菌副结核菌副杆菌或鸟分枝杆菌副孢子菌)或混合的。在比利时的野生马鹿中感染了(M. avium副结核亚种/ M。avium副病毒)。因此,我们建议将鸟分枝杆菌亚种的功能分子定义整合进去。副结核病,没有来自us-p34扩增子的Hpy188I限制性酶切位点。

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