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Characterization of the M2e antibody response following highly pathogenic H5N1 avian influenza virus infection and reliability of M2e ELISA for identifying infected among vaccinated chickens

机译:高致病性H5N1禽流感病毒感染后M2e抗体反应的表征以及在疫苗接种的鸡中鉴定感染的M2e ELISA的可靠性

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A surveillance method able to differentiate between vaccinated and infected poultry is required for those countries that practice vaccination against highly pathogenic avian influenza H5N1. The external domain of the M2 protein (M2e) of influenza virus is a potentially useful differentiating-infected from vaccinated animals (DIVA) antigen but little is known about the M2e antibody response and factors influencing its detection. In this study, the M2e antibody response was characterized in layer birds vaccinated and challenged with an Indonesian H5N1 virus isolate, using a single M2e peptide or four-branched multiple antigenic peptide form of M2e (MAP-M2e) as antigens in two separate ELISAs. Anti-M2e antibodies were absent in chicks with high level of maternal haemagglutination inhibition antibodies and also in all layers vaccinated once, twice or three times with an inactivated commercial H5N1 vaccine. In contrast, anti-M2e antibodies were detected in vaccinated layers challenged with H5N1 virus and their presence was associated with virus isolation and an increase in haemagglutination inhibition titres. The number of birds that developed M2e antibodies, as well as the strength and duration of the M2e antibody response were strongly influenced by the length of the interval between vaccination and challenge. Birds challenged at six weeks after vaccination all developed M2e antibodies by 14 days that lasted until at least 56 days after infection. In birds challenged at two weeks after vaccination, only a proportion of birds developed M2e antibodies by 14 days that lasted only until 28 days post-infection. Both single M2e peptide and MAP-M2e ELISAs had high diagnostic specificity but the diagnostic sensitivity of MAP-M2e ELISA was significantly higher and more effective in detecting M2e antibody in immune and infected birds. The results show that MAP-M2e ELISA would be useful for surveillance in countries using vaccination to control highly pathogenic avian influenza H5N1.
机译:对于那些针对高致病性禽流感H5N1进行疫苗接种的国家,需要一种能够区分接种疫苗的家禽和感染的家禽的监视方法。流感病毒的M2蛋白(M2e)的外部结构域可能与疫苗接种的动物(DIVA)抗原有区别,但对于M2e抗体反应和影响其检测的因素知之甚少。在这项研究中,在单独的ELISA中使用单个M2e肽或M2e的四支多抗原肽形式的M2e(MAP-M2e)作为抗原,在接种了印度尼西亚H5N1病毒分离株并对其进行了攻击的鸡中表征了M2e抗体反应。具有高水平母体血凝抑制抗体的雏鸡中不存在抗M2e抗体,并且在所有层中均使用灭活的商业H5N1疫苗接种了一次,两次或三次。相反,在用H5N1病毒攻击的疫苗接种层中检测到抗M2e抗体,它们的存在与病毒分离和血凝抑制滴度的增加有关。产生M2e抗体的禽鸟的数量以及M2e抗体应答的强度和持续时间受疫苗接种和攻击之间间隔时间的长短影响很大。接种疫苗后六周攻击的鸟类在14天之前都产生了M2e抗体,这种抗体持续到感染后至少56天。在接种疫苗后两周受到攻击的禽鸟中,只有一部分禽鸟在14天之前发展出M2e抗体,这种抗体仅持续到感染后28天。单个M2e肽和MAP-M2e ELISA都具有较高的诊断特异性,但MAP-M2e ELISA的诊断敏感性显着更高,并且在免疫和感染禽类中检测M2e抗体更为有效。结果表明,MAP-M2e ELISA对使用疫苗接种控制高致病性禽流感H5N1的国家进行监测非常有用。

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