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Francisella philomiragia Infection and Lethality in Mammalian Tissue Culture Cell Models, Galleria mellonella, and BALB/c Mice

机译:哺乳动物组织培养细胞模型,梅勒商业街廊和BALB / c小鼠中的感染和致死性

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Francisella (F.) philomiragia is a Gram-negative bacterium with a preference for brackish environments that has been implicated in causing bacterial infections in near-drowning victims. The purpose of this study was to characterize the ability of F. philomiragia to infect cultured mammalian cells, a commonly used invertebrate model, and, finally, to characterize the ability of F. philomiragia to infect BALB/c mice via the pulmonary (intranasal) route of infection. This study shows that F. philomiragia infects J774A.1 murine macrophage cells, HepG2 cells and A549 human Type II alveolar epithelial cells. However, replication rates vary depending on strain at 24 h. F. philomiragia infection after 24 h was found to be cytotoxic in human U937 macrophage-like cells and J774A.1 cells. This is in contrast to the findings that F. philomiragia was non-cytotoxic to human hepatocellular carcinoma cells, HepG2 cells and A549 cells. Differential cytotoxicity is a point for further study. Here, it was demonstrated that F. philomiragia grown in host-adapted conditions (BHI, pH 6.8) is sensitive to levofloxacin but shows increased resistance to the human cathelicidin LL-37 and murine cathelicidin mCRAMP when compared to related the Francisella species, F. tularensis subsp. novicida and F. tularensis subsp. LVS . Previous findings that LL-37 is strongly upregulated in A549 cells following F. tularensis subsp. novicida infection suggest that the level of antimicrobial peptide expression is not sufficient in cells to eradicate the intracellular bacteria. Finally, this study demonstrates that F. philomiragia is lethal in two in vivo models; Galleria mellonella via hemocoel injection, with a LD_(50)of 1.8 × 10~(3), and BALB/c mice by intranasal infection, with a LD_(50)of 3.45 × 10~(3). In conclusion, F. philomiragia may be a useful model organism to study the genus Francisella , particularly for those researchers with interest in studying microbial ecology or environmental strains of Francisella . Additionally, the Biosafety level 2 status of F. philomiragia makes it an attractive model for virulence and pathogenesis studies.
机译:弗朗西斯菌(F.)philomiragia是革兰氏阴性细菌,偏爱微咸的环境,该环境与导致接近溺水的受害者引起细菌感染有关。这项研究的目的是表征费氏念珠菌感染培养的哺乳动物细胞(一种常用的无脊椎动物模型)的能力,并最终表征费氏念珠菌通过肺(鼻内)感染BALB / c小鼠的能力。感染途径。该研究表明,费氏疟原虫感染了J774A.1鼠巨噬细胞,HepG2细胞和A549人II型肺泡上皮细胞。但是,复制速度根据24小时的应变而有所不同。发现在人U937巨噬细胞样细胞和J774A.1细胞中,F. philomiragia感染在24小时后具有细胞毒性。这与费氏杆菌对人肝癌细胞,HepG2细胞和A549细胞无细胞毒性的发现相反。差异细胞毒性是进一步研究的重点。在这里,已证明在适应宿主的条件下(BHI,pH 6.8)生长的费氏念珠菌对左氧氟沙星敏感,但与相关弗朗西斯菌种F.相比,对人cathelicidin LL-37和小鼠cathelicidin mCRAMP的抵抗力增强。 tularensis亚种Novicida和Tularensis亚种LVS。先前的发现LL.37在F. tularensis亚种之后的A549细胞中强烈上调。 Novicida感染表明,抗菌肽在细胞中的表达水平不足以根除细胞内细菌。最后,这项研究表明,费氏疟原虫在两种体内模型中具有致死性。 LD_(50)为1.8×10〜(3)的血红素注射法注射梅勒菌体,LD_(50)为3.45×10〜(3)的经鼻内感染的BALB / c小鼠。总而言之,对于研究弗朗西斯菌属的人来说,费城镰刀菌可能是一种有用的模式生物,特别是对于那些对弗朗西斯菌的微生物生态学或环境菌株感兴趣的研究人员而言。此外,费城菌的生物安全性2级状态使其成为毒力和发病机理研究的有吸引力的模型。

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