Huillet Eugénie, Bridoux Ludovic, Wanapaisan Pagakrong, Rejasse Agnès, Peng Qi, Panbangred Watanalai, Lereclus Didier
Micalis Institute, INRA, AgroParisTech, Université Paris-Saclay, Jouy-en-Josas, France.
Department of Biotechnology, Faculty of Science, Mahidol University, Bangkok, Thailand.
PLoS One. 2017 Oct 9;12(10):e0184975. doi: 10.1371/journal.pone.0184975. eCollection 2017.
The Gram-positive pathogen Bacillus cereus is able to grow in chains of rod-shaped cells, but the regulation of chaining remains largely unknown. Here, we observe that glucose-grown cells of B. cereus ATCC 14579 form longer chains than those grown in the absence of glucose during the late exponential and transition growth phases, and identify that the clhAB2 operon is required for this chain lengthening phenotype. The clhAB2 operon is specific to the B. cereus group (i.e., B. thuringiensis, B. anthracis and B. cereus) and encodes two membrane proteins of unknown function, which are homologous to the Staphylococcus aureus CidA and CidB proteins involved in cell death control within glucose-grown cells. A deletion mutant (ΔclhAB2) was constructed and our quantitative image analyses show that ΔclhAB2 cells formed abnormal short chains regardless of the presence of glucose. We also found that glucose-grown cells of ΔclhAB2 were significantly wider than wild-type cells (1.47 μm ±CI95% 0.04 vs 1.19 μm ±CI95% 0.03, respectively), suggesting an alteration of the bacterial cell wall. Remarkably, ΔclhAB2 cells showed accelerated autolysis under autolysis-inducing conditions, compared to wild-type cells. Overall, our data suggest that the B. cereus clhAB2 operon modulates peptidoglycan hydrolase activity, which is required for proper cell shape and chain length during cell growth, and down-regulates autolysin activity. Lastly, we studied the transcription of clhAB2 using a lacZ transcriptional reporter in wild-type, ccpA and codY deletion-mutant strains. We found that the global transcriptional regulatory protein CodY is required for the basal level of clhAB2 expression under all conditions tested, including the transition growth phase while CcpA, the major global carbon regulator, is needed for the high-level expression of clhAB2 in glucose-grown cells.
革兰氏阳性病原菌蜡样芽孢杆菌能够以杆状细胞链的形式生长,但其链形成的调控机制在很大程度上仍不清楚。在此,我们观察到,在指数生长后期和过渡生长阶段,蜡样芽孢杆菌ATCC 14579在葡萄糖存在下生长的细胞比在无葡萄糖条件下生长的细胞形成更长的链,并确定clhAB2操纵子是这种链延长表型所必需的。clhAB2操纵子是蜡样芽孢杆菌属(即苏云金芽孢杆菌、炭疽芽孢杆菌和蜡样芽孢杆菌)所特有的,编码两个功能未知的膜蛋白,它们与金黄色葡萄球菌中参与葡萄糖生长细胞内细胞死亡控制的CidA和CidB蛋白同源。构建了一个缺失突变体(ΔclhAB2),我们的定量图像分析表明,无论有无葡萄糖,ΔclhAB2细胞都会形成异常短链。我们还发现,ΔclhAB2在葡萄糖存在下生长的细胞比野生型细胞明显更宽(分别为1.47μm±CI95% 0.04和1.19μm±CI95% 0.03),这表明细菌细胞壁发生了改变。值得注意的是,与野生型细胞相比,ΔclhAB2细胞在自溶诱导条件下表现出自溶加速。总体而言,我们的数据表明,蜡样芽孢杆菌clhAB2操纵子调节肽聚糖水解酶活性,这是细胞生长过程中正常细胞形状和链长度所必需的,并下调自溶素活性。最后,我们使用lacZ转录报告基因在野生型、ccpA和codY缺失突变体菌株中研究了clhAB2的转录。我们发现,全局转录调节蛋白CodY在所有测试条件下,包括过渡生长阶段,都是clhAB2基础水平表达所必需的,而主要的全局碳调节因子CcpA是葡萄糖生长细胞中clhAB2高水平表达所必需的。