IBB - Institute for Biotechnology and Bioengineering, Centre for Biological and Chemical Engineering, IST, Lisbon, Portugal.
Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6, 2780-156 Oeiras, Portugal.
Microbiology (Reading). 2011 Nov;157(Pt 11):3124-3137. doi: 10.1099/mic.0.050989-0. Epub 2011 Aug 11.
Burkholderia cepacia complex (Bcc) bacteria are opportunistic pathogens infecting hosts such as cystic fibrosis (CF) patients. Long-term Bcc infection of CF patients' airways has been associated with emergence of phenotypic variation. Here we studied two Burkholderia multivorans clonal isolates displaying different morphotypes from a chronically infected CF patient to evaluate trait development during lung infection. Expression profiling of mucoid D2095 and non-mucoid D2214 isolates revealed decreased expression of genes encoding products related to virulence-associated traits and metabolism in D2214. Furthermore, D2214 showed no exopolysaccharide production, lower motility and chemotaxis, and more biofilm formation, particularly under microaerophilic conditions, than the clonal mucoid isolate D2095. When Galleria mellonella was used as acute infection model, D2214 at a cell number of approximately 7 × 10⁶ c.f.u. caused a higher survival rate than D2095, although 6 days post-infection most of the larvae were dead. Infection with the same number of cells by mucoid D2095 caused larval death by day 4. The decreased expression of genes involved in carbon and nitrogen metabolism may reflect lower metabolic needs of D2214 caused by lack of exopolysaccharide, but also by the attenuation of pathways not required for survival. As a result, D2214 showed higher survival than D2095 in minimal medium for 28 days under aerobic conditions. Overall, adaptation during Bcc chronic lung infections gave rise to genotypic and phenotypic variation among isolates, contributing to their fitness while maintaining their capacity for survival in this opportunistic human niche.
洋葱伯克霍尔德菌复合群(Bcc)细菌是机会性病原体,感染囊性纤维化(CF)等宿主。CF 患者气道中长期的 Bcc 感染与表型变异的出现有关。在这里,我们研究了从慢性感染 CF 患者中分离出的两株具有不同形态的伯克霍尔德菌多维多利亚种克隆株,以评估在肺部感染过程中特征的发展。粘液型 D2095 和非粘液型 D2214 分离株的表达谱分析表明,D2214 中与毒力相关性状和代谢相关的基因表达降低。此外,与克隆粘液型 D2095 相比,D2214 不产生胞外多糖,运动性和趋化性较低,生物膜形成能力较强,特别是在微需氧条件下。当使用大蜡螟作为急性感染模型时,D2214 的细胞数约为 7×106 c.f.u. 导致比 D2095 更高的存活率,尽管在感染后 6 天,大多数幼虫都死了。用相同数量的细胞感染粘液型 D2095 导致幼虫在第 4 天死亡。参与碳氮代谢的基因表达下调可能反映了 D2214 缺乏胞外多糖导致的代谢需求降低,但也反映了不需要生存的途径的衰减。结果,D2214 在有氧条件下的最小培养基中 28 天的存活率高于 D2095。总的来说,Bcc 慢性肺部感染过程中的适应导致了分离株之间的基因型和表型变异,有助于其在维持生存能力的同时适应这种机会性人类生态位。