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首页> 外文期刊>Vaccine >Secretory IgA as an indicator of oro-pharyngeal foot-and-mouth disease virus replication and as a tool for post vaccination surveillance
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Secretory IgA as an indicator of oro-pharyngeal foot-and-mouth disease virus replication and as a tool for post vaccination surveillance

机译:分泌型IgA可作为口咽口蹄疫病毒复制的指标,并可作为预防接种后监测的工具

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A serotype-specific ELISA was developed to detect foot-and-mouth disease virus (FMDV) specific IgA antibody in the saliva of cattle, and the method was evaluated for its feasibility in detecting serotype O FMDV carrier animals, particularly amongst vaccinated cattle that had subsequently become sub-clinically infected. For this purpose, saliva samples were collected from naive cattle (n = 173), FMDV challenged cattle (n = 10), FMDV vaccinated cattle (n = 40) and FMDV vaccinated-and-challenged cattle (n = 40). A subset of 29 cattle was sampled for 105-168 days after challenge. The FMDV infection status of each of the cattle was determined by virus isolation and RT-PCR tests on oesophago-pharyngeal fluids and the ability of the IgA test to detect viral infection and persistence was compared to an ELISA for the detection of serum antibodies against the 3ABC non-structural proteins of FMDV. Eleven out of twelve vaccinated cattle that were shown to be persistently infected with FMDV up to or beyond 28 days post challenge, were also detected by the IgA test on saliva. With some modification and further validation, this test could be useful in post-vaccination surveillance to help confirm the absence of sub-clinical infection in order to regain the FMD-free status of a region or country.
机译:开发了一种血清型特异性ELISA来检测牛唾液中的口蹄疫病毒(FMDV)特异性IgA抗体,并评估了该方法在检测O型FMDV血清型携带动物中的可行性,尤其是在已接种牛随后被亚临床感染。为此,从幼稚牛(n = 173),FMDV激发牛(n = 10),FMDV接种牛(n = 40)和FMDV接种挑战牛(n = 40)中收集唾液样品。在攻击后105-168天取样了29只牛的子集。通过病毒分离和食管咽液的RT-PCR测试确定每只牛的FMDV感染状况,并将IgA测试检测病毒感染和持久性的能力与ELISA进行比较,以检测针对牛的FMDV血清抗体。 FMDV的3ABC非结构蛋白。通过对唾液进行IgA检测,还发现了在攻击后28天或之后持续感染FMDV的12头接种牛中的11头。经过一些修改和进一步的验证,该测试可用于疫苗接种后的监测,以帮助确认不存在亚临床感染,从而恢复一个地区或国家的无口蹄疫状态。

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