家兔假结核耶尔森氏菌野生和突变菌株的实验感染。

H Najdenski, A Vesselinova, E Golkocheva, S Garbom, H Wolf-Watz
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引用次数: 11

摘要

本实验采用野生型假结核耶尔森菌pIB102和2个零突变株yopK和ypkA对家兔进行了口腔感染实验,目的是探讨假结核耶尔森菌突变株作为活载体疫苗的可能性。这三种菌株的感染过程表现为暂时性高热、白细胞增多伴粒细胞增多、中度单核细胞增多和短暂性淋巴细胞减少,在突变株感染中表现得更好。在yopK感染中观察到短期细菌播散到脑和内脏。在感染的初始阶段,白细胞对杀菌活性的抵抗力增强,随后在yopK菌株中发现敏感性增加,对小鼠的ypkA毒性分别降低至少70倍和20倍。yopK的衰减水平伴随着显著的耶尔森氏菌特异性IgG和IgM抗体应答。野生型感染后在脑组织、肺和小肠均可见炎性灶,而yopK突变株感染后仅在脑组织和肠系膜淋巴结可见炎性灶。感染后在感染动物的脑和脾脏中发现突变灶。突变株感染兔淋巴组织的形态学变化与诱导免疫发生一致。这些数据表明,基因构建的yopK零突变株具有使该菌株适合用作传递异源抗原的活载体疫苗的特性。
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Experimental infections with wild and mutant Yersinia pseudotuberculosis strains in rabbits.
Experimental oral infections of rabbits with a wild-type Yersinia pseudotuberculosis strain (pIB102), and two null-mutants (yopK and ypkA) were carried out with the aim to explore the possibility to use mutant strains of Y. pseudotuberculosis as live carrier vaccine strains. The infectious process of the three strains proceed with passing hyperthermia, leucocytosis with granulocytosis, moderate monocytosis and a transient lymphopenia, better demonstrated at mutant strain infections. Short-term bacterial dissemination into the brain and viscera was observed at yopK infection. An augmented resistance to bactericidal activity of leucocytes at the initial phase of infection was followed by an increased sensitivity discovered earlier in case of yopK strain accompanied by at least 70- and 20-fold, respectively, for ypkA lower virulence for mice. The level of attenuation of yopK was accompanied by significant Yersinia specific IgG and IgM antibody response. Inflammatory foci were found by morphological examination in brain, lung and small intestines after infection with the wild-type strain, while such foci were only observed in brain and mesenterial lymph nodes after infection with the yopK mutant. After infection with the ypkA mutant foci were found in brain and spleen of the infected animals. Morphological changes in the lymphatic tissue of rabbits infected with mutant strains were consistent with induction of immunogenesis. The data suggest that genetically constructed yopK null-mutant exhibits characteristics that makes the strain suitable to be used as a live carrier vaccine to deliver heterologous antigens.
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