Wang Bobo, Li Bo, Liang Ying, Li Jing, Gao Lang, Chen Lin, Duan Kangmin, Shen Lixin
Key Laboratory of Resources Biology and Biotechnology in Western China, Ministry of Education, Faculty of Life Sciences, Northwest University, Xi'an, 710069, China.
Key Laboratory of Resources Biology and Biotechnology in Western China, Ministry of Education, Faculty of Life Sciences, Northwest University, Xi'an, 710069, China; Department of Oral Biology; Department of Medical Microbiology, University of Manitoba, 780 Bannatyne Ave., Winnipeg, MB, R3E 0W2, Canada.
Microb Pathog. 2016 Feb;91:5-17. doi: 10.1016/j.micpath.2015.11.003. Epub 2015 Nov 17.
Pseudomonas aeruginosa is an important human pathogen which adapts to changing environment, such as temperature variations and entering host by regulating their gene expression. Here, we report that gene PA0011 in P. aeruginosa PAO1, which encodes a 2-OH-lauroytransferase participating in lipid A biosynthesis, is involved in carbapenem resistance and virulence in a temperature-regulated manner in PAO1. The expression of PA0011 was higher at an environment temperature (21 °C) than that at a body temperature (37 °C). The inactivation of PA0011 rendered increased antibiotic susceptibility and decreased virulence both in vivo and in vitro. The impaired integrity and the decreased stability of the outer membrane were the cause of the increased susceptibility of PAO1(Δ0011) to carbapenem and many other common antibiotics. The reduced endotoxic activity of lipopolysaccharide (LPS) contributed to the decreased virulence both at 21 °C and 37 °C in PAO1 (Δ0011). In addition, we have found that PA0011 repressed the expression of TTSS virulence factors both at transcriptional and translational levels, similar to the effect of O antigen of LPS but unlike any effect of its homologue reported in other bacteria. The effect of PA0011 on resistance to many antibiotics including carbapenem and virulence in P. aeruginosa makes it a target for novel antimicrobial therapies.
铜绿假单胞菌是一种重要的人类病原体,它通过调节基因表达来适应不断变化的环境,如温度变化以及进入宿主。在此,我们报告铜绿假单胞菌PAO1中的基因PA0011,其编码一种参与脂多糖A生物合成的2-羟基月桂酰转移酶,在PAO1中以温度调节的方式参与碳青霉烯类耐药性和毒力。PA0011在环境温度(21°C)下的表达高于体温(37°C)下的表达。PA0011的失活导致体内外抗生素敏感性增加和毒力降低。外膜完整性受损和稳定性降低是PAO1(Δ0011)对碳青霉烯类和许多其他常用抗生素敏感性增加的原因。脂多糖(LPS)内毒素活性降低导致PAO1(Δ0011)在21°C和37°C时毒力均降低。此外,我们发现PA0011在转录和翻译水平上均抑制III型分泌系统(TTSS)毒力因子的表达,这与LPS的O抗原的作用相似,但不同于其他细菌中报道的其同源物的任何作用。PA0011对铜绿假单胞菌对包括碳青霉烯类在内的多种抗生素的耐药性和毒力的影响使其成为新型抗菌治疗的靶点。