Wand Matthew E, Bock Lucy J, Sutton J Mark
Public Health England, National Infection Service, Porton Down, Salisbury, Wiltshire, SP4 0JG, UK.
J Med Microbiol. 2017 Jul;66(7):959-964. doi: 10.1099/jmm.0.000530. Epub 2017 Jul 21.
This study aimed to understand the impact on virulence and fitness of mutations in specific genes found after adaptation of Klebsiella pneumoniae to colistin. Isolates with an increase in their inhibitory concentration (MIC) to colistin of 32- to >128-fold were shown to have mutations in mgrB, phoPQ and pmrAB, all known regulators of pathways affecting membrane lipid content. When these strains were used in studies in Galleria mellonella there was no clear correlation between mutations in specific genes per se and loss of virulence. Strains which showed sequence duplication in the HAMP-domain of PmrB showed reduced virulence but strains with point mutations in pmrAB showed no decrease in virulence. Similarly, specific mutations in mgrB in individual strains showed either loss of virulence or no effect/increased virulence. This study suggests that the impact on virulence may be independent of the colistin resistance mechanism and reflects differences in individual strain backgrounds.
本研究旨在了解肺炎克雷伯菌适应黏菌素后发现的特定基因突变对其毒力和适应性的影响。对黏菌素的抑制浓度(MIC)增加32至>128倍的分离株显示在mgrB、phoPQ和pmrAB中存在突变,这些都是影响膜脂含量途径的已知调节因子。当这些菌株用于大蜡螟研究时,特定基因本身的突变与毒力丧失之间没有明显的相关性。在PmrB的HAMP结构域中显示序列重复的菌株毒力降低,但pmrAB中存在点突变的菌株毒力没有降低。同样,个别菌株中mgrB的特定突变显示出毒力丧失或无影响/毒力增加。本研究表明,对毒力的影响可能独立于黏菌素耐药机制,并且反映了个别菌株背景的差异。