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运用Ceditest® O型口蹄疫病毒和口蹄疫病毒非结构蛋白酶联免疫吸附测定法检测乌干达特定家畜和野生动物物种中抗口蹄疫病毒抗体

Application of the Ceditest® FMDV type O and FMDV-NS enzyme-linked immunosorbent assays for detection of antibodies against Foot-and-mouth disease virus in selected livestock and wildlife species in Uganda.

作者信息

Ayebazibwe Chrisostom, Mwiine Frank Norbert, Balinda Sheila Nina, Tjørnehøj Kirsten, Alexandersen Soren

机构信息

Ministry of Agriculture, Animal Industry and Fisheries, Entebbe, Uganda.

出版信息

J Vet Diagn Invest. 2012 Mar;24(2):270-6. doi: 10.1177/1040638711435807.

Abstract

Diagnosis and control of Foot-and-mouth disease virus (FMDV) requires rapid and sensitive diagnostic tests. Two antibody enzyme-linked immunosorbent assay (ELISA) kits, Ceditest® FMDV-NS for the detection of antibodies against the nonstructural proteins of all FMDV serotypes and Ceditest® FMDV type O for the detection of antibodies against serotype O, were evaluated under African endemic conditions where the presence of multiple serotypes and the use of nonpurified vaccines complicate serological diagnosis. Serum samples from 218 African buffalo, 758 cattle, 304 goats, and 88 sheep were tested using both kits, and selected samples were tested not only in serotype-specific ELISAs for antibodies against primarily FMDV serotype O, but also against other serotypes. The FMDV-NS assay detected far more positive samples (93%) than the FMDV type O assay (30%) in buffalo (P < 0.05), with predominant antibodies against the South African Territories (SAT) serotypes, while the seroprevalence was generally comparable in cattle with antibodies against serotype O elicited by infection and/or vaccination. However, some districts had higher seroprevalence using the FMDV type O assay indicating vaccination without infection, while 1 cattle herd with antibodies against the SAT serotypes had far more positive samples (85%) using the FMDV-NS versus the FMDV type O (10%), consistent with the latter test's lower sensitivity for antibodies against SAT serotypes. Based on the current investigation, the FMDV type O ELISA may be limited by the presence of SAT serotypes. The FMD NS assay worked well as a screening test for antibodies against all FMDV serotypes present in Uganda; however, as long as nonpurified vaccines are applied in the region, this test cannot be used to differentiate between vaccinated and infected animals.

摘要

口蹄疫病毒(FMDV)的诊断与防控需要快速且灵敏的诊断检测方法。在非洲流行地区,对两种抗体酶联免疫吸附测定(ELISA)试剂盒进行了评估,其中Ceditest® FMDV - NS试剂盒用于检测针对所有口蹄疫病毒血清型非结构蛋白的抗体,Ceditest® FMDV O型试剂盒用于检测针对O型血清型的抗体。该地区存在多种血清型,且使用的是非纯化疫苗,这使得血清学诊断变得复杂。使用这两种试剂盒对来自218头非洲水牛、758头牛、304只山羊和88只绵羊的血清样本进行了检测,并且选取的样本不仅在针对主要口蹄疫病毒O型血清型抗体的血清型特异性ELISA中进行了检测,还针对其他血清型进行了检测。在水牛中,FMDV - NS检测法检测出的阳性样本(93%)远多于FMDV O型检测法(30%)(P < 0.05),主要是针对南非地区(SAT)血清型的抗体,而在牛中,通过感染和/或接种疫苗产生的针对O型血清型抗体情况下,血清阳性率总体相当。然而,一些地区使用FMDV O型检测法时血清阳性率较高,表明是接种疫苗而非感染所致,而有一个牛群针对SAT血清型的抗体检测中,使用FMDV - NS检测法的阳性样本(85%)远多于FMDV O型检测法(10%),这与后者对SAT血清型抗体检测灵敏度较低一致。基于当前调查,FMDV O型ELISA可能受SAT血清型存在的限制。FMD NS检测法作为针对乌干达存在的所有口蹄疫病毒血清型抗体的筛查检测方法效果良好;然而,只要该地区使用非纯化疫苗,此检测方法就无法用于区分接种疫苗和感染的动物。

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