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经典猪瘟E2(CSF-E2)亚单位疫苗在预防病毒传播中的效果及母源抗体干扰在猪场实际应用中的影响评估。

Evaluation of classical swine fever E2 (CSF-E2) subunit vaccine efficacy in the prevention of virus transmission and impact of maternal derived antibody interference in field farm applications.

作者信息

Chen Jing-Yuan, Wu Chi-Ming, Chen Zeng-Weng, Liao Chih-Ming, Deng Ming-Chung, Chia Min-Yuan, Huang Chienjin, Chien Maw-Sheng

机构信息

Graduate Institute of Veterinary Pathobiology, College of Veterinary Medicine, National Chung Hsing University, 145 Xingda Road, Taichung, 40227, Taiwan, Republic of China.

Animal Technology Laboratories, Agricultural Technology Research Institute, No. 52, Kedong 2nd Rd., Zhunan Township, Miaoli County, 350401, Taiwan, Republic of China.

出版信息

Porcine Health Manag. 2021 Jan 11;7(1):9. doi: 10.1186/s40813-020-00188-6.

Abstract

BACKGROUND

Classical swine fever (CSF) is one of the most devastating pig diseases that affect the swine industry worldwide. Besides stamping out policy for eradication, immunization with vaccines of live attenuated CSF or the CSF-E2 subunit is an efficacious measure of disease control. However, after decades of efforts, it is still hard to eliminate CSF from endemically affected regions and reemerging areas. Most of previous studies demonstrated the efficacy of different CSF vaccines in laboratories under high containment conditions, which may not represent the practical performance in field farms. The inadequate vaccine efficacy induced by unrestrained factors may lead to chronic or persistent CSF infection in animals that develop a major source for virus shedding among pig populations. In this study, a vaccination-challenge-cohabitation trial on specific-pathogen-free (SPF) pigs and long-term monitoring of conventional sows and their offspring were used to evaluate the efficacy and the impact of maternally derived antibody (MDA) interference on CSF vaccines in farm applications.

RESULTS

The trials demonstrated higher neutralizing antibody (NA) titers with no clinical symptoms and significant pathological changes in the CSF-E2 subunit vaccine immunized group after CSFV challenge. Additionally, none of the sentinel pigs were infected during cohabitation indicating that the CSF-E2 subunit vaccine could provoke adequately acquired immunity to prevent horizontal transmission. In field farm applications, sows immunized with CSF-E2 subunit vaccine revealed an average of higher and consistent antibody level with significant reduction of CSF viral RNA detection via saliva monitoring in contrast to those of live attenuated CSF vaccine immunized sows possessing diverse antibody titer distributions and higher viral loads. Furthermore, early application of the CSF-E2 subunit vaccine in 3-week-old piglets illustrated no MDA interference on primary immunization and could elicit consistent and long-lasting adequate antibody response suggesting the flexibility of CSF-E2 subunit vaccine on vaccination program determination.

CONCLUSIONS

The CSF-E2 subunit vaccine demonstrated significant efficacy and no MDA interference for immunization in both pregnant sows and piglets. These advantages provide a novel approach to avoid possible virus shedding in sow population and MDA interference in piglets for control of CSF in field farm applications.

摘要

背景

经典猪瘟(CSF)是影响全球养猪业的最具毁灭性的猪病之一。除了扑杀根除政策外,使用减毒活CSF疫苗或CSF-E2亚单位疫苗进行免疫接种是疾病控制的有效措施。然而,经过数十年的努力,在地方流行区和重新出现疫情的地区仍难以消除CSF。以前的大多数研究在高隔离条件下的实验室中证明了不同CSF疫苗的效力,这可能无法代表猪场的实际性能。不受控制的因素导致的疫苗效力不足可能导致动物出现慢性或持续性CSF感染,而这些动物成为猪群中病毒传播的主要来源。在本研究中,对无特定病原体(SPF)猪进行了疫苗接种-攻毒-同居试验,并对常规母猪及其后代进行了长期监测,以评估CSF疫苗在猪场应用中的效力以及母源抗体(MDA)干扰的影响。

结果

试验表明,CSFV攻毒后,CSF-E2亚单位疫苗免疫组的中和抗体(NA)滴度较高,无临床症状,也无明显病理变化。此外,在同居期间没有哨兵猪被感染,这表明CSF-E2亚单位疫苗可以激发充分获得性免疫以防止水平传播。在猪场应用中,与接种减毒活CSF疫苗的母猪相比,接种CSF-E2亚单位疫苗的母猪平均抗体水平更高且更一致,通过唾液监测发现CSF病毒RNA检测显著减少,而接种减毒活CSF疫苗的母猪抗体滴度分布多样且病毒载量更高。此外,在3周龄仔猪中早期应用CSF-E2亚单位疫苗表明,MDA对初次免疫没有干扰,并且可以引发持续且持久的充分抗体反应,这表明CSF-E2亚单位疫苗在疫苗接种程序确定方面具有灵活性。

结论

CSF-E2亚单位疫苗在妊娠母猪和仔猪免疫中显示出显著效力且无MDA干扰。这些优势为在猪场应用中控制CSF提供了一种新方法,可避免母猪群体中可能的病毒传播以及仔猪中的MDA干扰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa32/7798205/db0bddeb87c0/40813_2020_188_Fig1_HTML.jpg

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