Heterologous prime-boost immunization of two-component vaccine candidate PWDVax protected pigs against F18 enterotoxigenic Escherichia coli post-weaning diarrhea.

IF 2.9 3区 医学 Q3 IMMUNOLOGY
Infection and Immunity Pub Date : 2025-04-08 Epub Date: 2025-03-12 DOI:10.1128/iai.00406-24
Chongyang Zhang, Siqi Li, Ipshita Upadhyay, Sai Simah Reddy Vakamalla, Kathyrn L Lauder, Chance Hansen, Kristen Ann Massey, Courtney Hayes, Nicole L Herndon, Weiping Zhang
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引用次数: 0

Abstract

Post-weaning diarrhea (PWD) is associated predominantly with enterotoxigenic Escherichia coli (ETEC) and continuously causes significant economic losses to swine producers worldwide. Currently, there are no effective countermeasures against this significant swine disease. Challenges persist in developing vaccines against PWD since ETEC strains produce heterogeneous virulence factors, including F4 (K88) and F18 fimbria and heat-labile toxin (LT), heat-stable toxin type I (STa), heat-stable toxin II (STb), and Shiga toxin type 2e (Stx2e, also causes edema disease). An effective PWD vaccine would induce broadly protective immunity, ideally against two fimbriae and four toxins. In this study, by applying a novel epitope- and structure-based multiepitope-fusion-antigen (MEFA) vaccinology platform, we created a monomeric polyvalent fimbria-toxin protein (fimbria-toxin MEFA) and a holotoxin-structured protein to target PWD virulence determinants (F4 and F18 fimbriae and LT, STa, STb, and Stx2e toxins) and developed a two-component multivalent PWD vaccine candidate, PWDVax. We further applied a heterologous prime-boost immunization strategy and assessed vaccine protection against F18 ETEC-associated PWD. Piglets, after being primed intramuscularly with a fimbria-toxin MEFA monomer protein and boosted orally with live Escherichia coli bacteria producing GM1-binding holotoxin-structured fimbria-toxin MEFA, developed IgG and secretory IgA responses to the target fimbriae and toxins. Challenged with an F18ac ETEC strain, the immunized piglets were protected against watery diarrhea (87.5%) or any diarrhea (66.7%). These data indicated that PWDVax protects against F18 ETEC-associated PWD and can become an effective PWD vaccine. The two-component vaccine and heterologous prime-boost immunization strategy may be instructive for developing neonatal vaccines in general.IMPORTANCEEnterotoxigenic Escherichia coli (ETEC)-associated post-weaning diarrhea (PWD) is a global swine disease, remains a major threat to pig health and well-being, and causes significant economic losses. Currently, there are no effective vaccines available against this disease because of challenges including heterogeneity among ETEC strains (or virulence factors) and difficulties in inducing protective immunity against some key virulence determinants. PWDVax, a two-component PWD vaccine candidate, unprecedentedly targeted two ETEC fimbriae (F4 and F18) and four toxins (LT, STa, STb, and Stx2e), the virulence factors associated with nearly all PWD clinical cases. Under a heterologous prime-boost immunization schedule, it induced broad systemic and mucosal antigen-specific antibodies but also protected weaned piglets against F18 ETEC diarrhea. This makes PWDVax potentially an effective vaccine to protect against PWD, particularly the current F18 ETEC-associated severe PWD outbreaks in the United States. Additionally, the two-component vaccine and heterologous prime-boost immunization strategy may also facilitate the development of effective neonatal vaccines for humans.

双组份候选疫苗PWDVax的异源预增强免疫保护猪免受F18肠毒素大肠杆菌断奶后腹泻。
断奶后腹泻(PWD)主要与产肠毒素大肠杆菌(ETEC)有关,并不断给世界各地的养猪户造成重大经济损失。目前,对这一重大猪病尚无有效的防治措施。由于ETEC菌株产生异质毒力因子,包括F4 (K88)和F18菌膜以及热不稳定毒素(LT)、热不稳定毒素I型(STa)、热不稳定毒素II型(STb)和志贺毒素2e型(Stx2e,也引起水肿病),因此开发针对PWD的疫苗仍然存在挑战。一种有效的PWD疫苗将诱导广泛的保护性免疫,理想情况下针对两种菌膜和四种毒素。本研究利用基于表位和结构的多表位融合抗原(MEFA)疫苗学平台,构建了针对PWD毒力决定因子(F4和F18菌膜以及LT、STa、STb和Stx2e毒素)的单体多价菌膜毒素蛋白(MEFA)和全毒素结构蛋白),并开发了一种双组分多价PWD候选疫苗PWDVax。我们进一步应用了异源免疫策略,并评估了疫苗对F18 etec相关PWD的保护作用。在仔猪肌内注入一种纤维毒素MEFA单体蛋白,并口服产生gm1结合全毒素结构的纤维毒素MEFA的活大肠杆菌后,仔猪对目标纤维和毒素产生IgG和分泌IgA反应。接种F18ac ETEC菌株后,免疫仔猪无水样腹泻(87.5%),无腹泻(66.7%)。这些数据表明PWDVax对F18 etec相关的PWD具有保护作用,可以成为一种有效的PWD疫苗。双组分疫苗和异源免疫策略可能对一般新生儿疫苗的开发具有指导意义。产肠毒素大肠杆菌(ETEC)相关的断奶后腹泻(PWD)是一种全球性的猪疾病,仍然是猪健康和福祉的主要威胁,并造成重大的经济损失。目前,由于ETEC菌株(或毒力因子)之间的异质性以及难以诱导针对某些关键毒力决定因素的保护性免疫等挑战,尚无针对该疾病的有效疫苗。PWDVax是一种双组分的PWD候选疫苗,前所未有地靶向两种ETEC菌膜(F4和F18)和四种毒素(LT、STa、STb和Stx2e),这四种毒力因子几乎与所有PWD临床病例相关。在异源启动-增强免疫计划下,它诱导广泛的全身和粘膜抗原特异性抗体,但也保护断奶仔猪免受F18 ETEC腹泻。这使得PWDVax有可能成为预防PWD的有效疫苗,特别是目前在美国爆发的F18 etec相关的严重PWD。此外,双组分疫苗和异源启动-增强免疫策略也可能促进人类有效新生儿疫苗的开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Infection and Immunity
Infection and Immunity 医学-传染病学
CiteScore
6.00
自引率
6.50%
发文量
268
审稿时长
3 months
期刊介绍: Infection and Immunity (IAI) provides new insights into the interactions between bacterial, fungal and parasitic pathogens and their hosts. Specific areas of interest include mechanisms of molecular pathogenesis, virulence factors, cellular microbiology, experimental models of infection, host resistance or susceptibility, and the generation of innate and adaptive immune responses. IAI also welcomes studies of the microbiome relating to host-pathogen interactions.
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