Department of Internal Medicine, Center for Experimental and Molecular Medicine, Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
Division of Infectious Diseases, Department of Internal Medicine, Academic Medical Center, Amsterdam, The Netherlands.
Sci Rep. 2021 Feb 26;11(1):4775. doi: 10.1038/s41598-021-84130-y.
BB0405 is a surface exposed Borrelia burgdorferi protein and its vaccination protected mice against B. burgdorferi infection. As BB0405 is highly conserved across different B. burgdorferi sensu lato species, we investigated whether vaccination with recombinant BB0405 or through intradermal bb0405 DNA tattoo vaccination could provide protection against different Borrelia species, specifically against Borrelia afzelii, the predominant B. burgdorferi sensu lato genospecies causing Lyme borreliosis across Eurasia. We immunized C3H/HeN mice with recombinant BB0405 or with a codon-optimized bb0405 DNA vaccine using the pVAC plasmid and immunized corresponding control groups mice with only adjuvant or empty vectors. We subsequently subjected these immunized mice to a tick challenge with B. afzelii CB43-infected Ixodes ricinus nymphs. Upon vaccination, recombinant BB0405 induced a high total IgG response, but bb0405 DNA vaccination did not elicit antibody responses. Both vaccine formulations did not provide protection against Borrelia afzelii strain CB43 after tick challenge. In an attempt to understand the lack of protection of the recombinant vaccine, we determined expression of BB0405 and showed that B. afzelii CB43 spirochetes significantly and drastically downregulate the expression of BB0405 protein at 37 °C compared to 33 °C, where as in B. burgdorferi B31 spirochetes expression levels remain unaltered. Vaccination with recombinant BB0405 was previously shown to protect against B. burgdorferi sensu stricto. Here we show that vaccination with either recombinant BB0405 (or non-immunogenic bb0405 DNA), despite being highly conserved among B. burgdorferi sl genospecies, does not provide cross-protection against B. afzelii, mostly likely due to downregulation of this protein in B. afzelii in the mammalian host.
BB0405 是一种暴露于表面的伯氏疏螺旋体蛋白,其疫苗接种可保护小鼠免受伯氏疏螺旋体感染。由于 BB0405 在不同的伯氏疏螺旋体亚种中高度保守,我们研究了用重组 BB0405 或通过皮内 bb0405 DNA 纹身疫苗接种是否可以提供针对不同的伯氏疏螺旋体物种的保护,特别是针对伯氏疏螺旋体 afzelii,这是造成欧亚大陆莱姆病的主要伯氏疏螺旋体亚种。我们用重组 BB0405 或用优化密码子的 bb0405 DNA 疫苗(使用 pVAC 质粒)免疫 C3H/HeN 小鼠,并给相应的对照组小鼠用仅佐剂或空载体免疫。随后,我们用 B. afzelii CB43 感染的 Ixodes ricinus 若虫对这些免疫小鼠进行 tick 挑战。接种后,重组 BB0405 诱导了高总 IgG 反应,但 bb0405 DNA 疫苗接种没有引起抗体反应。在 tick 挑战后,两种疫苗制剂都不能提供对伯氏疏螺旋体 afzelii 株 CB43 的保护。为了了解重组疫苗缺乏保护作用的原因,我们测定了 BB0405 的表达情况,并表明与 33°C 相比,伯氏疏螺旋体 afzelii CB43 旋体在 37°C 时显著且急剧地下调 BB0405 蛋白的表达,而伯氏疏螺旋体 B31 旋体的表达水平保持不变。先前的研究表明,用重组 BB0405 疫苗接种可预防伯氏疏螺旋体 sensu stricto。在这里,我们表明,用重组 BB0405(或非免疫原性的 bb0405 DNA)接种疫苗,尽管在伯氏疏螺旋体亚种中高度保守,但不能提供对伯氏疏螺旋体 afzelii 的交叉保护,这很可能是由于该蛋白在伯氏疏螺旋体 afzelii 在哺乳动物宿主中下调所致。