Freie Universität Berlin, Institute of Biology-Microbiology, D-14195, Berlin, Germany.
Center for Biotechnology, Bielefeld University, D-33594, Bielefeld, Germany.
Free Radic Biol Med. 2021 Dec;177:120-131. doi: 10.1016/j.freeradbiomed.2021.10.024. Epub 2021 Oct 19.
Staphylococcus aureus has to cope with oxidative and electrophile stress during host-pathogen interactions. The TetR-family repressor GbaA was shown to sense electrophiles, such as N-ethylmaleimide (NEM) via monothiol mechanisms of the two conserved Cys55 or Cys104 residues in vitro. In this study, we further investigated the regulation and function of the GbaA repressor and its Cys residues in S. aureus COL. The GbaA-controlled gbaAB-SACOL2595-97 and SACOL2592-nmrA-2590 operons were shown to respond only weakly 3-10-fold to oxidants, electrophiles or antibiotics in S. aureus COL, but are 57-734-fold derepressed in the gbaA deletion mutant, indicating that the physiological inducer is still unknown. Moreover, the gbaA mutant remained responsive to disulfide and electrophile stress, pointing to additional redox control mechanisms of both operons. Thiol-stress induction of the GbaA regulon was strongly diminished in both single Cys mutants, supporting that both Cys residues are required for redox-sensing in vivo. While GbaA and the single Cys mutants are reversible oxidized under diamide and allicin stress, these thiol switches did not affect the DNA binding activity. The repressor activity of GbaA could be only partially inhibited with NEM in vitro. Survival assays revealed that the gbaA mutant confers resistance under diamide, allicin, NEM and methylglyoxal stress, which was mediated by the SACOL2592-90 operon encoding for a putative glyoxalase and oxidoreductase. Altogether, our results support that the GbaA repressor functions in the defense against oxidative and electrophile stress in S. aureus. GbaA represents a 2-Cys-type redox sensor, which requires another redox-sensing regulator and an unknown thiol-reactive ligand for full derepression of the GbaA regulon genes.
金黄色葡萄球菌在宿主-病原体相互作用过程中必须应对氧化应激和亲电应激。TetR 家族抑制剂 GbaA 已被证明可通过体外两个保守半胱氨酸残基 Cys55 或 Cys104 的单硫醇机制感应亲电试剂,如 N-乙基马来酰亚胺 (NEM)。在这项研究中,我们进一步研究了 GbaA 抑制剂及其 Cys 残基在金黄色葡萄球菌 COL 中的调控和功能。GbaA 控制的 gbaAB-SACOL2595-97 和 SACOL2592-nmrA-2590 操纵子在金黄色葡萄球菌 COL 中仅对氧化剂、亲电试剂或抗生素表现出弱的 3-10 倍响应,但在 gbaA 缺失突变体中被 57-734 倍去抑制,表明生理诱导剂仍未知。此外, gbaA 突变体仍对二硫键和亲电应激有反应,表明这两个操纵子还有其他氧化还原调控机制。在两个单一 Cys 突变体中,GbaA 调节子的硫醇应激诱导均大大减弱,支持这两个 Cys 残基在体内均需要进行氧化还原感应。虽然 GbaA 和单一 Cys 突变体在二酰胺和大蒜素应激下均可被可逆氧化,但这些硫醇开关不会影响 DNA 结合活性。体外实验中,NEM 只能部分抑制 GbaA 的抑制活性。生存实验表明, gbaA 突变体能在二酰胺、大蒜素、NEM 和甲基乙二醛应激下产生抗性,这是由编码潜在的醛糖酶和氧化还原酶的 SACOL2592-90 操纵子介导的。总的来说,我们的结果支持 GbaA 抑制剂在金黄色葡萄球菌的氧化应激和亲电应激防御中发挥作用。GbaA 代表一种 2-Cys 型氧化还原传感器,其需要另一个氧化还原感应调节剂和未知的硫醇反应配体来完全解除 GbaA 调节子基因的抑制。