口服疫苗诱导的抗ospa抗体的母体转移保护Peromyscus sps免受蜱传播的伯氏疏螺旋体。

IF 2.8 3区 医学 Q3 IMMUNOLOGY
Infection and Immunity Pub Date : 2025-06-10 Epub Date: 2025-05-19 DOI:10.1128/iai.00216-25
Jose F Azevedo, Greg Joyner, Suman Kundu, Kamalika Samanta, Maria Gomes-Solecki
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引用次数: 0

摘要

被动免疫保护的效果和持续时间取决于母体抗体水平和转移效率。我们研究了用表达重组外表面蛋白A (OspA)的大肠埃希菌口服接种白斑过omyscus leucopus dams是否能诱导母鼠转移抗OspA抗体并保护幼崽免受伯氏疏螺旋体的攻击。接种疫苗直到繁殖配对(i),直到分娩(ii),直到幼崽2周大(iii)。幼犬在4周龄时感染由肩胛骨伊蚊传播的伯氏疏螺旋体。测定母鼠和幼崽血清中抗ospa IgG的含量;在幼犬体内定量检测伯氏体IgG。用flaB定量PCR法测定蜱虫攻击后4周幼鼠组织中伯氏疏螺旋体的负荷,用心脏组织培养法测定伯氏疏螺旋体的生存能力。在繁殖前接种疫苗的幼崽血清抗ospa抗体较低,不能预防蜱传播的伯氏疏螺旋体感染。然而,当母鼠的疫苗接种延长到分娩和幼崽2周龄时,出现了显著的抗ospa抗体转移和对伯氏疏螺旋体感染的保护。这可以通过对伯氏疏螺旋体PepVF抗体的缺失,心脏和膀胱组织中不存在伯氏疏螺旋体flaB DNA,以及出生后90周安乐死的小狗心脏组织培养物中不存在flaB来证明。我们发现,在美国,接种过疫苗的白斑弓形虫将抗ospa抗体传递给后代,可以阻止蜱虫在该螺旋体的主要宿主中传播和伯氏疏螺旋体的感染动态。这项研究有助于我们理解基于库靶向外表面蛋白A疫苗的干预措施是如何阻断来自受感染的肩胛骨棘虫蜱的伯氏疏螺旋体传播的,这可能会破坏这种螺旋体的动物循环并降低莱姆病的发病率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Maternal transfer of oral vaccine induced anti-OspA antibodies protects <i>Peromyscus</i> spp. from tick-transmitted <i>Borrelia burgdorferi</i>.

Maternal transfer of oral vaccine induced anti-OspA antibodies protects <i>Peromyscus</i> spp. from tick-transmitted <i>Borrelia burgdorferi</i>.

Maternal transfer of oral vaccine induced anti-OspA antibodies protects <i>Peromyscus</i> spp. from tick-transmitted <i>Borrelia burgdorferi</i>.

Maternal transfer of oral vaccine induced anti-OspA antibodies protects Peromyscus spp. from tick-transmitted Borrelia burgdorferi.

The efficacy and duration of passive immunity protection depend on maternal antibody levels and transfer efficiency. We investigated whether oral vaccination of Peromyscus leucopus dams with recombinant outer surface protein A (OspA)-expressing Escherichia coli could induce maternal transfer of anti-OspA antibodies and protect pups from Borrelia burgdorferi challenge. Dams were vaccinated until breeding pairs were created (i), until parturition (ii), and until pups were 2 weeks old (iii). Pups were challenged with nymphal Ixodes scapularis-transmitted B. burgdorferi at ~4 weeks of age. Anti-OspA IgG was quantified in dams and pups, and anti-B. burgdorferi IgG was quantified in pups. B. burgdorferi burden was assessed by flaB quantitative PCR in pups' tissues ~4 weeks after tick challenge, and viability of B. burgdorferi was assessed by culture of the heart tissue. P. leucopus pups born to dams vaccinated until breeding had low serologic anti-OspA antibody and were not protected from tick-transmitted B. burgdorferi infection. However, when dams' vaccination extended until parturition and until pups were 2 weeks old, significant anti-OspA antibody transfer and protection from B. burgdorferi infection occurred. This was evidenced by the absence of antibody to B. burgdorferi PepVF, absence of B. burgdorferi flaB DNA in heart and bladder tissues, and absence of flaB in culture from heart tissues from pups euthanized >9 weeks after birth. We show that the transfer of anti-OspA antibodies from vaccinated P. leucopus dams to offspring prevents tick transmission and infection dynamics of B. burgdorferi in the major reservoir host of this spirochete in the USA.IMPORTANCEThis study contributes to our understanding of how interventions based in reservoir-targeted outer surface protein A vaccines designed to block transmission of B. burgdorferi from infected Ixodes scapularis ticks may disrupt the enzootic cycle of this spirochete and reduce incidence of Lyme disease.

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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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