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Outer membrane vesicles of Shigella boydii type 4 induce passive immunity in neonatal mice

机译:波氏志贺氏菌4型的外膜囊泡诱导新生小鼠被动免疫

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Like most other Gram-negative bacteria, Shigella releases outer membrane vesicles (OMVs) into the surrounding environment during growth. In this study, we have exploited OMVs of Shigella as a protective immunogen in a mice model against Shigellosis. Distinctive vesicle secretion was noticed from different Shigella strains. Among them, Shigella boydii type 4 (BCH612) was secreting relatively higher amounts. We immunized female adult mice orally with 32 μg of purified Shigella boydii type 4 (BCH612) OMVs four times at 1-week intervals. Antibodies against these vesicles were detected in immunized sera until 120 days, indicating a persistent immune response. To observe whether the passive immunity had been transferred to the neonates, the immunized female mice were mated and the offspring were challenged orally, with wild-type homologous and heterologous Shigella strains. All offspring of immunized mothers survived the challenge with homologous strain BCH612 and up to 81% protective efficacy was noted against heterologous strains Shigella dysenteriae 1, Shigella flexneri 2a, Shigella flexneri 3a, Shigella flexneri 6 and Shigella sonnei. Our results exhibited for the first time that oral immunization of adult female mice with purified OMVs of Shigella, without any adjuvant, conferred passive protection to their offspring against shigellosis. These findings will contribute to the future development of a potential non-living vaccine candidate against shigellosis.
机译:像大多数其他革兰氏阴性细菌一样,志贺氏菌在生长过程中将外膜囊泡(OMV)释放到周围环境中。在这项研究中,我们已经利用志贺氏菌的OMV作为抗志贺氏菌病小鼠模型中的一种保护性免疫原。从不同的志贺氏菌菌株中观察到独特的囊泡分泌。其中,波氏志贺氏菌4型(BCH612)分泌的相对较高。我们以32克纯化的博伊氏志贺氏菌4型(BCH612)OMV口服免疫雌性成年小鼠,间隔1周四次。在免疫血清中检测到针对这些囊泡的抗体,直到120天为止,表明存在持续的免疫反应。为了观察被动免疫是否已转移至新生儿,将经免疫的雌性小鼠进行交配,并用野生型同源和异源志贺氏菌菌株对后代进行口服攻击。免疫母亲的所有后代均在同源菌株BCH612的攻击下存活下来,并且针对异源痢疾志贺氏菌1型,弗氏志贺氏菌2a,弗氏志贺氏菌3a,弗氏志贺氏菌6和索内氏志贺氏菌具有高达81%的保护效力。我们的结果首次显示,用志贺氏菌纯化的OMV口服免疫成年雌性小鼠,没有任何佐剂,可以赋予其后代抵抗志贺氏菌病的被动保护。这些发现将有助于潜在的针对志贺氏菌病的无生命疫苗的未来发展。

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