首页> 外文期刊>Virology Journal >Comparative efficacy of experimental inactivated and live-attenuated chimeric porcine circovirus (PCV) 1-2b vaccines derived from PCV1 and PCV2b isolates originated in China
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Comparative efficacy of experimental inactivated and live-attenuated chimeric porcine circovirus (PCV) 1-2b vaccines derived from PCV1 and PCV2b isolates originated in China

机译:源自中国的PCV1和PCV2b分离株的实验灭活和减毒活的嵌合猪圆环病毒(PCV)1-2b疫苗的比较功效

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Background Porcine circovirus type-2b (PCV2b) is recognized as the etiological agent of the various clinical manifestations of porcine circovirus-associated disease (PCVAD). Previous studies have demonstrated effectiveness of chimeric PCV1-2 vaccines against PCV2b challenge. In this study, the efficacy of inactivated and live-attenuated (2?×?10 3.5 or 2?×?10 4.0 50?% tissue culture infective dose [TCID 50 ] dose) chimeric PCV1-2b vaccines was compared side-by-side in conventional pigs. Methods Twenty-seven non-PCV2 viremic pigs without PCV2-specific antibody were randomly divided into six groups, including four vaccinated and challenged groups, a nonvaccinated challenged group, and a mock group. All pigs except those in the mock group were challenged at 28?days post vaccination (DPV) using PCV2b. Results Both inactivated and live-attenuated chimeric PCV1-2b vaccines induced a robust antibody responses, and significantly decreased microscopic lesion and lower viral loads in serum or superficial inguinal lymph nodes (SILN) compared with that in the nonvaccinated challenged group. PCV2 antibody titers decreased after 7?days post challenge (DPC) in pigs administered the inactivated PCV1-2b vaccine and they were lower than those in pigs inoculated with live-attenuated PCV1-2b on the day of necropsy. Moreover, no viremia was present in pigs inoculated with live-attenuated PCV1-2b vaccine at 21 DPC regardless of the dose difference. Conclusions The results demonstrated that both inactivated and live-attenuated chimeric PCV1-2b vaccines were effective to induce protective immunity against PCV2b infection.
机译:背景技术猪圆环病毒2b型(PCV2b)被认为是猪圆环病毒相关疾病(PCVAD)各种临床表现的病原体。先前的研究表明嵌合PCV1-2疫苗可抵抗PCV2b攻击。在这项研究中,灭活和减毒(2?×?10 3.5 或2?×?10 4.0 50?%组织培养感染剂量[TCID < sub> 50 ]剂量)嵌合PCV1-2b疫苗在常规猪中并排比较。方法将27只无PCV2特异性抗体的非PCV2病毒血症猪随机分为6组,包括4个接种和挑战组,1个未接种挑战组和一个模拟组。除模拟组中的猪外,所有其他猪均在接种后28天使用PCV2b攻击。结果与未接种疫苗的攻击组相比,灭活和减毒活的嵌合PCV1-2b疫苗均能产生强大的抗体应答,并显着降低血清或浅表腹股沟淋巴结(SILN)的微观病变并降低病毒载量。接种灭活PCV1-2b疫苗的猪在攻击后7天(DPC)后PCV2抗体滴度降低,并且比尸检当天接种减毒活PCV1-2b的猪的PCV2抗体滴度低。此外,无论剂量差异如何,在21 DPC接种减毒的PCV1-2b减毒活疫苗的猪中均无病毒血症。结论结果表明,灭活和减毒的嵌合PCV1-2b疫苗均可有效诱导针对PCV2b感染的保护性免疫。

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