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

机译:彩虹鳟鱼幸存感染病毒出血性血症病毒(VHSV)显示持久抗体对重组G蛋白片段

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摘要

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.
机译:虹鳟鱼抗体(ABS)与来自病毒出血性败血症病毒(VHSV)-07.71菌株的蛋白质G的重组片段(FRG)结合,可以通过鳟鱼幸存实验室受控感染的血清中的ELISA(FRG-ELISA)检测到血清中的蛋白质。不仅通过使用与同源VHSV分离物感染的鳟鱼的鼠李检测到ABS,还检测到具有VHSV-DK-201433的异源分离物,其具有13个氨基酸的变化。来自健康鳟鱼的血清和/或来自鳟鱼幸存的传染病病毒(IHNV)感染,用于计算截止光学吸光度,从阳性血清中区分阴性。然后可以使用以下任何一种FRGS检测特异性抗VHSV ABS:FRG11(56-110),FRG15(65-250),FRG16(252-450)或G21-465。虽然在用不同的FRG获得的ELISA值中发现高相关性,但可以证明任何FRG-ELISA和补体依赖性50%斑块中和试验(PNT)滴度之间没有相关性。在VHSV感染后4至10周之间,通过使用异源FRG-ELISA而不是同源PNT,将更多的鳟鱼血清检测为阳性。此外,FRG11-ELISA检测的正血清的百分比随着感染后的时间而增加,达到100%,而通过补体依赖性PNT检测的那些减少至29.4%,从而证实缺乏中和ABS缺乏意味着缺乏任何缺陷在幸存者鳟鱼血清中的抗VHSV ABS。来自田间样品的血清的初步结果表明FRG-ELISA的进一步改进可以允许检测由不同异源VHSV分离株引起的天然爆发中的抗VHSV鳟鱼腹肌。同源FRG-ELISA方法可用于在疫苗发育期间遵循G免疫尝试和/或最佳地了解VHSV感染期间的鱼AB反应。病毒FRGS方法也可以与其他鱼类和/或病毒一起使用。

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