Department of Biological Science and Technology, School of Biological Science and Technology, National Chiao Tung University, Hsinchu, Taiwan, Republic of China.
School of Chinese Medicine, China Medical University, Taichung, Taiwan, Republic of China.
PLoS One. 2019 Feb 28;14(2):e0212909. doi: 10.1371/journal.pone.0212909. eCollection 2019.
In Klebsiella pneumoniae CG43S3, deletion of the response regulator gene rcsB reduced the capsular polysaccharide amount and survival on exposure to acid stress. A comparison of the pH 4.4-induced proteomes between CG43S3 and CG43S3ΔrcsB revealed numerous differentially expressed proteins and one of them, YfdX, which has recently been reported as a periplasmic protein, was absent in CG43S3ΔrcsB. Acid survival analysis was then conducted to determine its role in the acid stress response. Deletion of yfdX increased the sensitivity of K. pneumoniae CG43S3 to a pH of 2.5, and transforming the mutant with a plasmid carrying yfdX restored the acid resistance (AR) levels. In addition, the effect of yfdX deletion was cross-complemented by the expression of the periplasmic chaperone HdeA. Furthermore, the purified recombinant protein YfdX reduced the acid-induced protein aggregation, suggesting that YfdX as well as HdeA functions as a chaperone. The following promoter activity measurement revealed that rcsB deletion reduced the expression of yfdX after the bacteria were subjected to pH 4.4 adaptation. Western blot analysis also revealed that YfdX production was inhibited by rcsB deletion and only the plasmid expressing RcsB or the nonphosphorylated form of RcsB, RcsBD56A, could restore the YfdX production, and the RcsB-mediated complementation was no longer observed when the sensor kinase RcsD gene was deleted. In conclusion, this is the first study demonstrating that YfdX may be involved in the acid stress response as a periplasmic chaperone and that RcsB positively regulates the acid stress response partly through activation of yfdX expression. Moreover, the phosphorylation status of RcsB may affect the YfdX expression under acidic conditions.
在肺炎克雷伯氏菌 CG43S3 中,响应调节基因 rcsB 的缺失减少了荚膜多糖的量,并降低了在暴露于酸应激时的存活率。CG43S3 和 CG43S3ΔrcsB 之间的 pH4.4 诱导的蛋白质组比较揭示了许多差异表达的蛋白质,其中一种名为 YfdX 的蛋白质最近被报道为周质蛋白,在 CG43S3ΔrcsB 中不存在。然后进行了酸存活分析以确定其在酸应激反应中的作用。yfdX 的缺失增加了肺炎克雷伯氏菌 CG43S3 对 pH2.5 的敏感性,并且用携带 yfdX 的质粒转化突变体恢复了酸抗性 (AR) 水平。此外,yfdX 缺失的效应可通过周质伴侣 HdeA 的表达进行交叉互补。此外,纯化的重组蛋白 YfdX 减少了酸诱导的蛋白质聚集,表明 YfdX 以及 HdeA 作为伴侣发挥作用。随后的启动子活性测量显示,rcsB 缺失减少了细菌适应 pH4.4 后 yfdX 的表达。Western blot 分析还表明,rcsB 缺失抑制了 YfdX 的产生,只有表达 RcsB 或非磷酸化形式的 RcsB(RcsBD56A)的质粒才能恢复 YfdX 的产生,并且当传感器激酶 RcsD 基因缺失时,RcsB 介导的互补作用不再观察到。总之,这是第一项研究表明,YfdX 可能作为周质伴侣参与酸应激反应,并且 RcsB 通过激活 yfdX 的表达来正向调节酸应激反应。此外,RcsB 的磷酸化状态可能会影响酸性条件下的 YfdX 表达。