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虹鳟鱼在感染病毒性出血性败血症病毒(VHSV)后能持续产生针对重组 G 蛋白片段的抗体。

Rainbow trout surviving infections of viral haemorrhagic septicemia virus (VHSV) show lasting antibodies to recombinant G protein fragments.

机构信息

INIA, SGIT - Dept Biotecnología Crt, Coruña Km 7, 28040 Madrid, Spain.

出版信息

Fish Shellfish Immunol. 2011 Mar;30(3):929-35. doi: 10.1016/j.fsi.2011.01.021. Epub 2011 Feb 2.

Abstract

Rainbow trout antibodies (Abs) binding to recombinant fragments (frgs) derived from the protein G of the viral haemorrhagic septicemia virus (VHSV)-07.71 strain, could be detected by ELISA (frg-ELISA) in sera from trout surviving laboratory-controlled infections. Abs were detected not only by using sera from trout infected with the homologous VHSV isolate but also with the VHSV-DK-201433 heterologous isolate, which had 13 amino acid changes. Sera from healthy trout and/or from trout surviving infectious haematopoietic necrosis virus (IHNV) infection, were used to calculate cut-off absorbances to differentiate negative from positive sera. Specific anti-VHSV Abs could then be detected by using any of the following frgs: frg11 (56-110), frg15 (65-250), frg16 (252-450) or G21-465. While high correlations were found among the ELISA values obtained with the different frgs, no correlations between any frg-ELISA and complement-dependent 50% plaque neutralization test (PNT) titres could be demonstrated. Between 4 and 10 weeks after VHSV infection, more trout sera were detected as positives by using heterologous frg-ELISA rather than homologous PNT. Furthermore, the percentage of positive sera detected by frg11-ELISA increased with time after infection to reach 100%, while those detected by complement-dependent PNT decreased to 29.4%, thus confirming that the lack of neutralizing Abs does not mean the lack of any anti-VHSV Abs in survivor trout sera. Preliminary results with sera from field samples suggest that further refinements of the frg-ELISA could allow detection of anti-VHSV trout Abs in natural outbreaks caused by different heterologous VHSV isolates. The homologous frg-ELISA method could be useful to follow G immunization attempts during vaccine development and/or to best understand the fish Ab response during VHSV infections. The viral frgs approach might also be used with other fish species and/or viruses.

摘要

虹鳟鱼的抗体(Abs)可以与从病毒性出血性败血症病毒(VHSV)-07.71 株的蛋白 G 衍生的重组片段(frgs)结合,通过 ELISA(frg-ELISA)在实验室控制感染后存活的虹鳟血清中检测到。Abs 不仅可以使用感染同源 VHSV 分离株的虹鳟血清检测到,也可以使用具有 13 个氨基酸变化的 VHSV-DK-201433 异源分离株检测到。使用来自健康虹鳟鱼和/或感染传染性造血坏死病毒(IHNV)后存活的虹鳟鱼的血清来计算区分阴性和阳性血清的截止吸光度值。然后可以使用以下任何 frgs 检测到特异性抗 VHSV Abs:frg11(56-110)、frg15(65-250)、frg16(252-450)或 G21-465。虽然不同 frgs 获得的 ELISA 值之间存在高度相关性,但未能证明任何 frg-ELISA 与补体依赖性 50%噬菌斑中和试验(PNT)滴度之间存在相关性。在 VHSV 感染后 4 至 10 周内,使用异源 frg-ELISA 检测到更多的虹鳟血清呈阳性,而不是同源 PNT。此外,frg11-ELISA 检测到的阳性血清百分比随着感染后时间的增加而增加,达到 100%,而补体依赖性 PNT 检测到的阳性血清百分比降低至 29.4%,这证实了幸存者虹鳟血清中缺乏中和 Abs 并不意味着缺乏任何抗 VHSV Abs。对来自野外样本的血清的初步结果表明,对 frg-ELISA 的进一步改进可以在由不同异源 VHSV 分离株引起的自然暴发中检测到抗 VHSV 虹鳟 Abs。同源 frg-ELISA 方法可用于疫苗开发期间 G 免疫尝试的跟踪和/或在 VHSV 感染期间更好地了解鱼类 Ab 反应。病毒 frgs 方法也可用于其他鱼类和/或病毒。

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