采用ELISA法检测肠炎沙门菌和鼠伤寒沙门菌悬浮液中的非特异性抗体,对沙门氏菌病进行血清诊断,用于流行病学监测

W. Rastawicki, N. Rokosz-Chudziak, K. Śmietańska, Urszula Roguska
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引用次数: 0

摘要

沙门氏菌病的诊断通常是通过粪便培养进行的,然而在许多实验室中,用于检测两种主要沙门氏菌血清型LPS抗原混合物的人血清抗体的ELISA被开发出来。我们提出了用血清样品中肠炎沙门氏菌(血清型D)和鼠伤寒沙门氏菌(血清型B)悬液吸收非特异性抗体的方法,作为ELISA法诊断沙门氏菌病的有效方法。这种简单、经济、有效的吸收方法可用于流行病学调查。方法:采用ELISA法检测肠炎沙门氏菌LPS、鼠伤寒沙门氏菌LPS和两种血清型LPS的1:1混合抗原。采集14例沙门氏菌病患者的血清样本,用从肠炎沙门氏菌、鼠伤寒沙门氏菌和两种血清型(B+D型)的混合物中获得的20%细菌悬浮液进行吸收。用ELISA法分别检测非吸收血清和特定吸收后血清的三种抗原。结果:14份非吸收血清中IgA、IgG和IgM三种LPS抗原ELISA检测均呈高阳性。用沙门氏菌B悬浮液吸收14份样品中的13份,导致沙门氏菌B抗原抗体水平显著降低,但沙门氏菌B + D和沙门氏菌D抗原水平仅略有下降。另一方面,与沙门氏菌D悬浮液吸收相同的血清,引起血清D、B和B + D抗原抗体水平显著降低。这样的检测结果清楚地表明,这13份血清样本来自肠炎沙门氏菌(血清组D)感染的患者,而从鼠伤寒沙门氏菌(血清组B)感染的1份血清样本中获得的体液反应情况与此相反。提出的工作证明了非特异性抗体与肠炎沙门氏菌和鼠伤寒沙门氏菌悬浮液的吸收在ELISA进行沙门氏菌病血清诊断中的有用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Absorption of non-specific antibodies with Salmonella Enteritidis and Salmonella Typhimurium suspensions from tested serum samples as a useful method in serodiagnosis of salmonellosis carried out by ELISA for epidemiological surveillance
Introduction: Diagnosis of salmonellosis is usually made by stool culture however in many laboratories ELISA for the detection of human serum antibodies against mixture of LPS antigens of the two predominant serovars of Salmonella was developed. We present the method of absorbing non-specific antibodies with S. Enteritidis (serovars D) and S. Typhimurium (serovars B) suspensions from serum samples as a useful method in serodiagnosis of salmonellosis carried out by ELISA. This simple, cost-efficient and effective method of absorption may be used in the epidemiological investigations. Methods: We used in-house ELISA three different antigens: LPS of the S. Enteritidis, LPS of the S. Typhimurium and 1:1 mixture of LPS of both serovars. Serum samples collected from 14 patients with salmonellosis, were absorbed with 20% bacterial suspensions obtained from S. Enteritidis, S. Typhimurium and mixture of both serovars (serovars B+D). The non-absorbed sera and sera after particular absorptions were tested separately in ELISA with all three antigens. Results: The all 14 non-absorbed serum samples showed a high positive results in the IgA, IgG and IgM ELISA with all three LPS antigens. Absorption of the 13 from 14 tested samples with the Salmonella B suspension resulted in a significant decrease in the level of antibodies to Salmonella B antigen, but only a very slight decrease in the levels of Salmonella B + D and Salmonella D antigen. On the other hand, the absorption of the same sera with Salmonella D suspension, caused a significant decrease in the level of antibodies for serovars D, B and B + D antigens. Such a test result clearly shows that the 13 serum samples were obtained from patients with an infection caused by S. Enteritidis (serogroup D). A opposite picture of the humoral response was obtained in the case of one serum sample obtained from a subject with an infection caused by S. Typhimurium (serogroup B). Conclusions: The presented work demonstrates the usefulness of absorption of non-specific antibodies with S. Enteritidis and S. Typhimurium suspensions in serodiagnosis of salmonellosis carried out by ELISA.
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