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Cell-wall deficient L. monocytogenes L-forms feature abrogated pathogenicity

机译:细胞壁缺乏单核细胞增生李斯特氏菌L型具有致病性消失的特点

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摘要

Stable L-forms are cell wall-deficient bacteria which are able to multiply and propagate indefinitely, despite the absence of a rigid peptidoglycan cell wall. We investigated whether L-forms of the intracellular pathogen L. monocytogenes possibly retain pathogenicity, and if they could trigger an innate immune response. While phagocytosis of L. monocytogenes L-forms by non-activated macrophages sometimes resulted in an unexpected persistence of the bacteria in the phagocytes, they were effectively eliminated by IFN-γ preactivated or bone marrow-derived macrophages (BMM). These findings were in line with the observed down-regulation of virulence factors in the cell-wall deficient L. monocytogenes. Absence of Interferon-β (IFN-β) triggering indicated inability of L-forms to escape from the phagosome into the cytosol. Moreover, abrogated cytokine response in MyD88-deficient dendritic cells (DC) challenged with L. monocytogenes L-forms suggested an exclusive TLR-dependent host response. Taken together, our data demonstrate a strong attenuation of Listeria monocytogenes L-form pathogenicity, due to diminished expression of virulence factors and innate immunity recognition, eventually resulting in elimination of L-form bacteria from phagocytes.
机译:稳定的L型是细胞壁缺陷型细菌,尽管没有刚性肽聚糖细胞壁,但它们仍可以无限繁殖和繁殖。我们调查了细胞内病原体单核细胞增生李斯特氏菌的L型是否可能保留致病性,以及它们是否可以触发先天性免疫应答。尽管未激活的巨噬细胞吞噬单核细胞增生李斯特氏菌L型有时会导致细菌在吞噬细胞中意外地持久存在,但可以通过IFN-γ预激活或骨髓衍生的巨噬细胞(BMM)有效地消除细菌。这些发现与在细胞壁缺陷的单核细胞增生李斯特氏菌中观察到的毒力因子的下调一致。缺乏干扰素-β(IFN-β)触发表明L型无法从吞噬体逃逸到细胞质中。此外,在单核细胞增生李斯特氏菌L型攻击的MyD88缺陷树突状细胞(DC)中废除的细胞因子应答提示了独家的TLR依赖性宿主应答。两者合计,我们的数据表明,由于毒力因子的表达减少和先天免疫识别,导致单核细胞增生李斯特氏菌L型致病性大大减弱,最终导致从吞噬细胞中消除L型细菌。

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