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Live Attenuated Borrelia burgdorferi Targeted Mutants in an Infectious Strain Background Protect Mice from Challenge Infection

机译:活的减毒伯氏疏螺旋体靶向突变株在传染性菌株背景下保护小鼠免受挑战性感染。

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摘要

Borrelia burgdorferi, B. garinii, and B. afzelii are all agents of Lyme disease in different geographic locations. If left untreated, Lyme disease can cause significant and long-term morbidity, which may continue after appropriate antibiotic therapy has been administered and live bacteria are no longer detectable. The increasing incidence and geographic spread of Lyme disease are renewing interest in the vaccination of at-risk populations. We took the approach of vaccinating mice with two targeted mutant strains of B. burgdorferi that, unlike the parental strain, are avirulent in mice. Mice vaccinated with both strains were protected against a challenge with the parental strain and a heterologous B. burgdorferi strain by either needle inoculation or tick bite. In ticks, the homologous strain was eliminated but the heterologous strain was not, suggesting that the vaccines generated a response to antigens that are produced by the bacteria both early in mammalian infection and in the tick. Partial protection against B. garinii infection was also conferred. Protection was antibody mediated, and reactivity to a variety of proteins was observed. These experiments suggest that live attenuated B. burgdorferi strains may be informative regarding the identification of protective antigens produced by the bacteria and recognized by the mouse immune system in vivo. Further work may illuminate new candidates that are effective and safe for the development of Lyme disease vaccines.
机译:伯氏疏螺旋体,加氏芽孢杆菌和afzelii都是在不同地理位置的莱姆病病原体。如果不加以治疗,莱姆病可能会导致严重的长期发病,这种疾病可能会在进行适当的抗生素治疗后继续存在,并且无法检测到活细菌。莱姆病的发病率和地域分布的不断增长,使人们对高危人群的疫苗接种产生了新的兴趣。我们采用了两种针对性的B. burgdorferi突变菌株为小鼠接种疫苗的方法,与亲本菌株不同,该菌株在小鼠中无毒。接种两种菌株的小鼠均可以通过针头接种或tick咬保护免受亲本菌株和异源伯氏疏螺旋体的攻击。在tick中,消除了同源菌株,但没有消除异源,表明疫苗在哺乳动物感染的早期和the中均对细菌产生的抗原产生了反应。还提供了针对加里氏芽孢杆菌感染的部分保护。保护是抗体介导的,并且观察到对多种蛋白质的反应性。这些实验表明,活的减毒的伯氏疏螺旋体菌株在体内鉴定由细菌产生并由小鼠免疫系统识别的保护性抗原方面可能是有益的。进一步的工作可能会为开发莱姆病疫苗的有效和安全的新候选人提供启发。

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