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Temperature-dependence of yadBC phenotypes in Yersinia pestis

机译:yersinia pestis中YADBC表型的温度依赖性

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YadB and YadC are putative trimeric autotransporters present only in the plague bacterium Yersinia pestis and its evolutionary predecessor, Yersinia pseudotuberculosis. Previously, yadBC was found to promote invasion of epithelioid cells by Y. pestis grown at 37 °C. In this study, we found that yadBC also promotes uptake of 37 °C-grown Y. pestis by mouse monocyte/macrophage cells. We tested whether yadBC might be required for lethality of the systemic stage of plague in which the bacteria would be pre-adapted to mammalian body temperature before colonizing internal organs and found no requirement for early colonization or growth over 3 days. We tested the hypothesis that YadB and YadC function on ambient temperature-grown Y. pestis in the flea vector or soon after infection of the dermis in bubonic plague. We found that yadBC did not promote uptake by monocyte/macrophage cells if the bacteria were grown at 28 °C, nor was there a role of yadBC in colonization of fleas by Y. pestis grown at 21 °C. However, the presence of yadBC did promote recoverability of the bacteria from infected skin for 28 °C-grown Y. pestis. Furthermore, the gene for the proinflammatory chemokine CXCL1 was upregulated in expression if the infecting Y. pestis lacked yadBC but not if yadBC was present. Also, yadBC was not required for recoverability if the bacteria were grown at 37 °C. These findings imply that thermally induced virulence properties dominate over effects of yadBC during plague but that yadBC has a unique function early after transmission of Y. pestis to skin.
机译:YADB和YADC是推定的三聚体自耦运动员,只存在于瘟疫菌Yersinia Pestis及其进化前任yersinia假冒ublosis。此前,发现YADBC促进在37℃下培养的瘟疫侵袭上皮细胞。在这项研究中,我们发现YADBC还通过小鼠单核细胞/巨噬细胞促进了37°C-生长的Y.Pestis的摄取。我们测试了瘟疫的系统阶段的致死性是否可能需要,其中细菌将在殖民化内器官之前预先适应哺乳动物体温,发现不需要早期定植或增长超过3天。我们测试了yadb和YADC在环境温度生长的Y. Pestis在糊状物中的假设或在泡泡中感染后不久的作用。我们发现,如果细菌在28℃下生长,YADBC没有促进单核细胞/巨噬细胞的摄取,也不是YADBC在21℃下生长的紫杉c的殖民化中的作用。然而,Yabbc的存在确实促进了细菌的可回收性来自受感染的皮肤28°C-生长的Y.Pestis。此外,如果感染Y.Pestis缺乏YADBC,则表达临炎趋化因子CXCL1的基因在表达中令人抑制,但如果存在YADBC,则缺乏yaDBC。此外,如果在37℃下生长细菌,则不需要yaDBC。这些发现意味着热诱导的毒力特性在瘟疫期间占据YADBC的影响,但YADBC在y.pestis对皮肤传播后早期具有独特的功能。

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