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首页> 外文期刊>Journal of Veterinary Diagnostic Investigation >Diagnosis of Avian bornavirus infection in psittaciformes by serum antibody detection and reverse transcription polymerase chain reaction assay using feather calami.
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Diagnosis of Avian bornavirus infection in psittaciformes by serum antibody detection and reverse transcription polymerase chain reaction assay using feather calami.

机译:通过羽毛抗体检测血清抗体并进行逆转录聚合酶链反应分析,可诊断鹦鹉形虫中的禽痘病毒。

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Avian bornavirus (ABV) is the causative agent of proventricular dilatation disease (PDD), a highly devastating and contagious disease of psittacines (parrots and parakeets), which has resulted in the death of many captive birds. Accurate diagnosis of bornavirus infection is therefore important for the identification and isolation of infected birds. The current study showed that nonvascular contour (chest) feather calami provide a ready and minimally invasive source of RNA for the detection of ABV by reverse transcription polymerase chain reaction (RT-PCR). Storage of the feathers at room temperature for at least a month did not affect the results. Serological analysis by enzyme-linked immunosorbent assay (ELISA) showed that identification of anti-bornaviral nucleoprotein P40 antibodies can identify many birds with a past or present infection. The presence of anti-avian bornaviral P24 phosphoprotein and P16 matrix protein antibodies was quite variable, rendering these antibodies less useful for diagnosis of ABV infection. The significance of the present findings is that the use of nonvascular feathers as a source of RNA allows sample collection under conditions where storage of other samples would be difficult. Serum detection by ELISA of anti-P40 antibodies allows the identification of infected birds when RT-PCR fails.
机译:禽流感病毒(ABV)是引起前列腺癌(鹦鹉和长尾小鹦鹉)高度毁灭性和传染性的小肠扩张疾病(PDD)的病原体,导致许多圈养鸟类死亡。因此,准确诊断出Boravirus感染对于鉴定和分离受感染的鸟类很重要。当前的研究表明,非血管轮廓(胸)羽毛cal鱼提供了一种现成的且微创的RNA来源,可用于通过逆转录聚合酶链反应(RT-PCR)检测ABV。将羽毛在室温下存放至少一个月不会影响结果。通过酶联免疫吸附测定(ELISA)进行的血清学分析表明,鉴定抗新生儿病毒核蛋白P40抗体可以鉴定出许多有过去或现在感染的鸟类。抗禽流感病毒P24磷蛋白和P16基质蛋白抗体的存在是非常可变的,这使得这些抗体在诊断ABV感染中的作用较小。本研究结果的意义在于,使用非血管羽毛作为RNA的来源可以在难以保存其他样品的条件下收集样品。通过ELISA检测抗P40抗体的血清,可以在RT-PCR失败时鉴定出感染的禽鸟。

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