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尽管接种了针对肠炎沙门氏菌和鼠伤寒沙门氏菌的疫苗,但鸡白痢/鸡伤寒快速平板凝集试验仍具有高特异性。

High specificity of the Pullorum/Gallinarum rapid plate agglutination test despite vaccinations against Enteritidis and Typhimurium.

作者信息

Ter Veen Christiaan, Feberwee Anneke, Augustijn Marieke, de Wit Sjaak

机构信息

Royal GD, Deventer, OV, the Netherlands.

Veterinary Faculty, Utrecht University, Utrecht, the Netherlands.

出版信息

Avian Pathol. 2022 Feb;51(1):19-25. doi: 10.1080/03079457.2021.1990854. Epub 2021 Nov 4.

Abstract

In Europe, monitoring of breeding stock for Pullorum (SP) or a Gallinarum (SG) infections is compulsory at the point of lay. Vaccinations against Enteritidis (SE) and Typhimurium (ST) are increasingly administered in Europe. These vaccines might induce cross-reactions in the rapid plate agglutination (RPA) SP/SG test due to shared O-antigens, possibly resulting in a lower test specificity. The extent to which the specificity of SP/SG serological tests is influenced by SE and/or ST vaccinations in the field has not been reported. In this paper, we report the diagnostic and flock specificity of the commercially available RPA SP/SG test using 1:2-1:16 serum dilutions on four panels of sera: SPF sera, field sera from flocks of varying age and SE/ST vaccination status, and reference sera from an international proficiency testing scheme. The results showed that the use of live SE/ST vaccines did not influence the specificity of the RPA SP/SG test. Inactivated vaccines showed a drop of the diagnostic specificity to 96.54% and a flock specificity of 34.1% when the 1:2 serum dilution was used. The 1:8 serum dilution showed a diagnostic specificity of 99.41% and a flock specificity of 86.4%. In conclusion, the use of SE/ST vaccines has either no effect or a modest effect on the specificity of the RPA SP/SG test used to monitor flocks. The main factors are the type of vaccine, and the serum dilution used for testing and a cut-off.

摘要

在欧洲,产蛋时必须对种禽进行鸡白痢(SP)或禽霍乱(SG)感染监测。欧洲越来越多地接种针对肠炎沙门氏菌(SE)和鼠伤寒沙门氏菌(ST)的疫苗。由于存在共同的O抗原,这些疫苗可能会在快速平板凝集(RPA)SP/SG试验中引发交叉反应,可能导致试验特异性降低。现场SE和/或ST疫苗接种对SP/SG血清学检测特异性的影响程度尚未见报道。在本文中,我们报告了使用1:2至1:16血清稀释度的市售RPA SP/SG试验在四组血清上的诊断特异性和群体特异性:无特定病原体(SPF)血清、来自不同年龄和SE/ST疫苗接种状态鸡群的现场血清,以及来自国际能力验证计划的参考血清。结果表明,使用SE/ST活疫苗不会影响RPA SP/SG试验的特异性。当使用1:2血清稀释度时,灭活疫苗的诊断特异性降至96.54%,群体特异性为34.1%。1:8血清稀释度显示诊断特异性为99.41%,群体特异性为86.4%。总之,SE/ST疫苗的使用对用于监测鸡群的RPA SP/SG试验的特异性要么没有影响,要么影响较小。主要因素是疫苗类型、用于检测的血清稀释度和临界值。

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