Tavares Débora A, Simões Alexandra S, Bootsma Hester J, Hermans Peter Wm, de Lencastre Hermínia, Sá-Leão Raquel
Laboratory of Molecular Microbiology of Human Pathogens, Instituto de Tecnologia Química e Biológica (ITQB) António Xavier, Universidade Nova de Lisboa (UNL), Oeiras, Portugal.
BMC Genomics. 2014 Oct 6;15(1):863. doi: 10.1186/1471-2164-15-863.
Pneumococcus is a major human pathogen and the polysaccharide capsule is considered its main virulence factor. Nevertheless, strains lacking a capsule, named non-typeable pneumococcus (NT), are maintained in nature and frequently colonise the human nasopharynx. Interest in these strains, not targeted by any of the currently available pneumococcal vaccines, has been rising as they seem to play an important role in the evolution of the species. Currently, there is a paucity of data regarding this group of pneumococci. Also, questions have been raised on whether they are true pneumococci. We aimed to obtain insights in the genetic content of NT and the mechanisms leading to non-typeability and to genetic diversity.
A collection of 52 NT isolates representative of the lineages circulating in Portugal between 1997 and 2007, as determined by pulsed-field gel electrophoresis and multilocus sequence typing, was analysed. The capsular region was sequenced and comparative genomic hybridisation (CGH) using a microarray covering the genome of 10 pneumococcal strains was carried out. The presence of mobile elements was investigated as source of intraclonal variation. NT circulating in Portugal were found to have similar capsular regions, of cps type NCC2, i.e., having aliB-like ORF1 and aliB-like ORF2 genes. The core genome of NT was essentially similar to that of encapsulated strains. Also, competence genes and most virulence genes were present. The few virulence genes absent in all NT were the capsular genes, type-I and type-II pili, choline-binding protein A (cbpA/pspC), and pneumococcal surface protein A (pspA). Intraclonal variation could not be entirely explained by the presence of prophages and other mobile elements.
NT circulating in Portugal are a homogeneous group belonging to cps type NCC2. Our observations support the theory that they are bona-fide pneumococcal isolates that do not express the capsule but are otherwise essentially similar to encapsulated pneumococci. Thus we propose that NT should be routinely identified and reported in surveillance studies.
肺炎球菌是一种主要的人类病原体,多糖荚膜被认为是其主要毒力因子。然而,缺乏荚膜的菌株,即不可分型肺炎球菌(NT),在自然界中存在,并经常定植于人类鼻咽部。由于这些菌株似乎在该物种的进化中起重要作用,因此对这些未被目前任何可用肺炎球菌疫苗靶向的菌株的兴趣日益增加。目前,关于这组肺炎球菌的数据很少。此外,对于它们是否是真正的肺炎球菌也存在疑问。我们旨在深入了解NT的基因内容以及导致不可分型和遗传多样性的机制。
分析了一组52株NT分离株,这些分离株代表了1997年至2007年间在葡萄牙流行的谱系,通过脉冲场凝胶电泳和多位点序列分型确定。对荚膜区域进行了测序,并使用覆盖10株肺炎球菌菌株基因组的微阵列进行了比较基因组杂交(CGH)。研究了移动元件的存在作为克隆内变异的来源。发现葡萄牙流行的NT具有相似的荚膜区域,属于cps NCC2型,即具有aliB样开放阅读框1和aliB样开放阅读框2基因。NT的核心基因组与有荚膜菌株的核心基因组基本相似。此外,感受态基因和大多数毒力基因也存在。所有NT中缺失的少数毒力基因是荚膜基因、I型和II型菌毛、胆碱结合蛋白A(cbpA/pspC)和肺炎球菌表面蛋白A(pspA)。克隆内变异不能完全由原噬菌体和其他移动元件的存在来解释。
在葡萄牙流行的NT是属于cps NCC2型的同质群体。我们的观察结果支持这样一种理论,即它们是真正的肺炎球菌分离株,不表达荚膜,但在其他方面与有荚膜肺炎球菌基本相似。因此,我们建议在监测研究中应常规鉴定和报告NT。