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炭疽样生物体蜡样芽胞杆菌 G9241 的抗病毒因子是 Certhrax。

Certhrax Is an Antivirulence Factor for the Anthrax-Like Organism Bacillus cereus Strain G9241.

机构信息

Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.

Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA

出版信息

Infect Immun. 2018 May 22;86(6). doi: 10.1128/IAI.00207-18. Print 2018 Jun.

Abstract

G9241 caused a life-threatening anthrax-like lung infection in a previously healthy human. This strain harbors two large virulence plasmids, pBCXO1 and pBC210, that are absent from typical isolates. The pBCXO1 plasmid is nearly identical to pXO1 from and carries genes (, , and ) for anthrax toxin components (protective antigen [called PA1 in G9241], lethal factor [LF], and edema factor [EF], respectively). The plasmid also has an intact hyaluronic acid capsule locus. The pBC210 plasmid has a tetrasaccharide capsule locus, a gene for a PA1 homolog called PA2 (), and a gene () for Certhrax, an ADP-ribosyltransferase toxin that inactivates vinculin. LF, EF, and Certhrax require PA for entry into cells. In this study, we asked what role PA1, PA2, LF, and Certhrax play in the pathogenicity of G9241. To answer this, we generated isogenic deletion mutations in the targeted toxin gene components and then assessed the strains for virulence in highly G9241-susceptible (A/J) and moderately G9241-sensitive (C57BL/6) mice. We found that full virulence of G9241 required PA1 and LF, while PA2 contributed minimally to pathogenesis of G9241 but could not functionally replace PA1 as a toxin-binding subunit Surprisingly, we discovered that Certhrax attenuated the virulence of G9241; i.e., a Δ Δ mutant strain was more virulent than a Δ mutant strain following subcutaneous inoculation of A/J mice. Moreover, the enzymatic activity of Certhrax contributed to this phenotype. We concluded that Certhrax acts as an antivirulence factor in the anthrax-like organism G9241.

摘要

G9241 在一名既往健康的个体中引发了危及生命的类似炭疽的肺部感染。该菌株携带两个大型毒力质粒,pBCXO1 和 pBC210,而这两个质粒在典型的菌株中是不存在的。pBCXO1 质粒与炭疽杆菌的 pXO1 几乎完全相同,携带炭疽毒素成分(保护性抗原[在 G9241 中称为 PA1]、致死因子[LF]和水肿因子[EF])的基因。该质粒还具有完整的透明质酸荚膜基因座。pBC210 质粒具有四糖荚膜基因座、一个称为 PA2 的 PA1 同源基因()和一个 Certhrax 基因(),Certhrax 是一种 ADP-核糖基转移酶毒素,可使 vinculin 失活。LF、EF 和 Certhrax 需要 PA 才能进入细胞。在这项研究中,我们想知道 PA1、PA2、LF 和 Certhrax 在 G9241 致病性中的作用。为了回答这个问题,我们在靶向毒素基因成分中生成了基因缺失突变体,然后评估了这些菌株在高度易感(A/J)和中度易感(C57BL/6)小鼠中的毒力。我们发现 G9241 的完全毒力需要 PA1 和 LF,而 PA2 对 G9241 发病机制的贡献很小,但不能作为毒素结合亚基替代 PA1。出乎意料的是,我们发现 Certhrax 减弱了 G9241 的毒力;即在 A/J 小鼠皮下接种后,ΔΔ 突变株比 Δ 突变株的毒力更强。此外,Certhrax 的酶活性促成了这种表型。我们得出结论,Certhrax 作为一种抗毒力因子在类似炭疽的生物体 G9241 中起作用。

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