Tomlin Kerry L, Malott Rebecca J, Ramage Gordon, Storey Douglas G, Sokol Pamela A, Ceri H
Department of Biological Sciences, University of Calgary, 2500 University Drive N.W., Calgary, Alberta, Canada T2N 1N4.
Appl Environ Microbiol. 2005 Sep;71(9):5208-18. doi: 10.1128/AEM.71.9.5208-5218.2005.
Biofilm formation in Burkholderia cenocepacia has been shown to rely in part on acylhomoserine lactone-based quorum sensing. For many other bacterial species, it appears that both the initial adherence and the later stages of biofilm maturation are affected when quorum sensing pathways are inhibited. In this study, we examined the effects of mutations in the cepIR and cciIR quorum-sensing systems of Burkholderia cenocepacia K56-2 with respect to biofilm attachment and antibiotic resistance. We also examined the role of the cepIR system in biofilm stability and structural development. Using the high-throughput MBEC assay system to produce multiple equivalent biofilms, the biomasses of both the cepI and cepR mutant biofilms, measured by crystal violet staining, were less than half of the value observed for the wild-type strain. Attachment was partially restored upon providing functional gene copies via multicopy expression vectors. Surprisingly, neither the cciI mutant nor the double cciI cepI mutant was deficient in attachment, and restoration of the cciI gene resulted in less attachment than for the mutants. Meanwhile, the cciR mutant did show a significant reduction in attachment, as did the cciR cepIR mutant. While there was no change in antibiotic susceptibility with the individual cepIR and cciIR mutants, the cepI cciI mutant biofilms were more sensitive to ciprofloxacin. A significant increase in sensitivity to removal by sodium dodecyl sulfate was seen for the cepI and cepR mutants. Flow cell analysis of the individual cepIR mutant biofilms indicated that they were both structurally and temporally impaired in attachment and development. These results suggest that biofilm structural defects might be present in quorum-sensing mutants of B. cenocepacia that affect the stability and resistance of the adherent cell mass, providing a basis for future studies to design preventative measures against biofilm formation in this species, an important lung pathogen of cystic fibrosis patients.
已证明洋葱伯克霍尔德菌生物膜的形成部分依赖于基于酰基高丝氨酸内酯的群体感应。对于许多其他细菌物种而言,当群体感应途径受到抑制时,生物膜的初始黏附及生物膜成熟的后期阶段似乎都会受到影响。在本研究中,我们研究了洋葱伯克霍尔德菌K56-2的cepIR和cciIR群体感应系统中的突变对生物膜附着及抗生素抗性的影响。我们还研究了cepIR系统在生物膜稳定性和结构发育中的作用。使用高通量MBEC检测系统生成多个等效生物膜,通过结晶紫染色测量,cepI和cepR突变体生物膜的生物量均不到野生型菌株观察值的一半。通过多拷贝表达载体提供功能基因拷贝后,黏附得以部分恢复。令人惊讶的是,cciI突变体和cciI cepI双突变体在黏附上均无缺陷,并且cciI基因的恢复导致黏附比突变体更少。同时,cciR突变体确实显示出黏附显著减少,cciR cepIR突变体也是如此。虽然单个cepIR和cciIR突变体的抗生素敏感性没有变化,但cepI cciI突变体生物膜对环丙沙星更敏感。cepI和cepR突变体对十二烷基硫酸钠去除的敏感性显著增加。对单个cepIR突变体生物膜的流动细胞分析表明,它们在附着和发育方面在结构和时间上均受损。这些结果表明,洋葱伯克霍尔德菌的群体感应突变体中可能存在生物膜结构缺陷,这会影响黏附细胞团的稳定性和抗性,为未来研究设计针对该物种生物膜形成的预防措施提供了基础,该物种是囊性纤维化患者重要的肺部病原体。