Zhang Ping, Wright John A, Osman Ahmed A, Nair Sean P
Department of Microbial Diseases, UCL Eastman Dental Institute, University College LondonLondon, United Kingdom.
Immunology Catalyst, GlaxoSmithKline plcStevenage, United Kingdom.
Front Microbiol. 2017 May 31;8:1001. doi: 10.3389/fmicb.2017.01001. eCollection 2017.
can undergo phenotypic switching between a normal colony phenotype (NCP) and a small colony variant (SCV). The SCV phenotype confers increased antibiotic resistance and the capacity to persist within human tissues and cells, and because these cells can revert back to the NCP they cause chronic and/or recurrent infections that are very difficult to treat. A complete picture of the genetic events that can lead to phenotypic switching in is currently lacking. We describe the selection of an SCV with a previously unreported genetic alteration leading to an ochre mutation of . In addition to the known mechanisms of phenotypic switching between the SCV and the NCP we describe a previously unreported mechanism involving tRNA ochre suppressors arising. The ochre suppressor strains had wild-type growth rates and restored antibiotic sensitivity, similar to the wild-type strain. However, whilst they had increased virulence compared to the SCV parent strain, their virulence was not restored to that of the NCP parental strain. These findings establish that phenotypic switching between the NCP and SCV states can give rise to strains with different pathogenic potential.
可在正常菌落表型(NCP)和小菌落变体(SCV)之间发生表型转换。SCV表型赋予更高的抗生素抗性以及在人体组织和细胞内持续存在的能力,并且由于这些细胞可恢复为NCP,它们会引发非常难以治疗的慢性和/或复发性感染。目前尚缺乏关于可导致 表型转换的遗传事件的完整情况。我们描述了一种具有先前未报道的遗传改变导致 发生赭石型突变的SCV的筛选。除了已知的SCV和NCP之间表型转换机制外,我们还描述了一种先前未报道的涉及产生tRNA赭石型抑制子的机制。赭石型抑制菌株具有野生型生长速率并恢复了抗生素敏感性,类似于野生型菌株。然而,虽然它们与SCV亲本菌株相比毒力有所增加,但其毒力并未恢复到NCP亲本菌株的水平。这些发现表明,NCP和SCV状态之间的表型转换可产生具有不同致病潜力的菌株。