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Detection of humoral immunity to mycobacteria causing leprosy in Eurasian red squirrels (Sciurus vulgaris) using a quantitative rapid test

机译:用定量快速试验检测欧亚红松鼠(Sciurus vulgaris)在欧亚红松鼠(Sciurus vulgaris)中的体液疫苗

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Eurasian red squirrels (Sciurus vulgaris, ERS) in the British Isles are a recently discovered natural host for Mycobacterium leprae and Mycobacterium lepromatosis. Infected squirrels can develop skin lesions or carry the bacteria without showing clinical signs. Until now the clinical diagnosis of leprosy could only be confirmed in squirrels by isolating DNA of leprosy bacilli from carcasses or by establishing the presence of acid-fast bacilli in skin sections of carcasses with clinical signs. In this study, we assessed the performance of a field-friendly diagnostic test for detection of M. leprae/M. lepromatosis infection in ERS. This up-converting phosphor lateral flow assay (UCP-LFA) is well established for detection of M. leprae specific anti-phenolic glycolipid-I antibodies (PGL-I) IgM antibodies in humans and associated with bacterial load. Assessment was performed on serum and blood drops from live squirrels and body cavity fluid samples from dead squirrels. Clinically diseased squirrels showed significantly higher PGL-I levels than healthy animals or subclinically infected individuals (p0.0001), both in serum and whole blood drop samples. Subclinically, infected animals were identified using molecular methods to detect the presence of leprosy bacilli DNA in punch biopsy tissue samples. In body cavity fluids, PGL-I levels antibody levels were lower than in serum or blood drops. This study shows that the PGL-I UCP-LFAs presented here allows a field-friendly serological confirmation of M. leprae infection in clinically diseased live ERS. For surveillance purposes, the combination of clinical assessment, PGL-I UCP-LFAs, and molecular methods allow the identification of both diseased animals and subclinically infected animals.
机译:英国群岛的欧亚红松鼠(Sciurus vulgaris,Ers)是最近发现的菌杆菌和乳杆菌的分枝杆菌的天然宿主。受感染的松鼠可以在不显示临床症状的情况下培养皮肤病变或携带细菌。到目前为止,Leprosy的临床诊断只能通过从尸体中分离出胡培芽孢杆菌的DNA或通过建立具有临床症状的皮肤部分的酸快杆菌的存在来在血松中确认。在这项研究中,我们评估了用于检测M. Leprae / M的现场友好诊断试验的性能。 Lepromatosis ins in in。该上转换磷光体横向流动测定(UCP-LFA)是为了检测人类中的M.Leprae特异性抗酚醛糖脂-i抗体(PGL-1)IgM抗体并与细菌载荷相关。从死鼠的活鼠和体腔液体样品上对血清和血液滴进行评估。临床患病的鼠鼠显着高于PGL-I水平,而不是健康的动物或亚透明的个体(P <0.0001),无论是血清和全血滴样品。亚透视上,使用分子方法鉴定受感染的动物,以检测冲头活检组织样品中麻风杆菌DNA的存在。在体腔液中,PGL-I水平抗体水平低于血清或血液滴。本研究表明,这里呈现的PGL-I UCP-LFA允许在临床患者中患上M.Seprae感染的野外型血清学确认。对于监视目的,临床评估,PGL-I UCP-LFA和分子方法的组合允许鉴定患病动物和亚透明感染的动物。

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