Novartis Vaccines and Diagnostics, Siena, Italy.
PLoS One. 2011;6(6):e21269. doi: 10.1371/journal.pone.0021269. Epub 2011 Jun 22.
The Streptococcus pneumoniae pilus-1 is encoded by pilus islet 1 (PI-1), which has three clonal variants (clade I, II and III) and is present in about 30% of clinical pneumococcal isolates. In vitro and in vivo assays have demonstrated that pilus-1 is involved in attachment to epithelial cells and virulence, as well as protection in mouse models of infection. Several reports suggest that pilus-1 expression is tightly regulated and involves the interplay of numerous genetic regulators, including the PI-1 positive regulator RlrA. In this report we provide evidence that pilus expression, when analyzed at the single-cell level in PI-1 positive strains, is biphasic. In fact, the strains present two phenotypically different sub-populations of bacteria, one that expresses the pilus, while the other does not. The proportions of these two phenotypes are variable among the strains tested and are not influenced by genotype, serotype, growth conditions, colony morphology or by the presence of antibodies directed toward the pilus components. Two sub-populations, enriched in pilus expressing or not expressing bacteria were obtained by means of colony selection and immuno-detection methods for five strains. PI-1 sequencing in the two sub-populations revealed the absence of mutations, thus indicating that the biphasic expression observed is not due to a genetic modification within PI-1. Microarray expression profile and western blot analyses on whole bacterial lysates performed comparing the two enriched sub-populations, revealed that pilus expression is regulated at the transcriptional level (on/off regulation), and that there are no other genes, in addition to those encoded by PI-1, concurrently regulated across the strains tested. Finally, we provide evidence that the over-expression of the RrlA positive regulator is sufficient to induce pilus expression in pilus-1 negative bacteria. Overall, the data presented here suggest that the observed biphasic pilus expression phenotype could be an example of bistability in pneumococcus.
肺炎链球菌菌毛-1 由菌毛岛 1(PI-1)编码,其具有三个克隆变体(I 类、II 类和 III 类),存在于约 30%的临床肺炎链球菌分离株中。体外和体内试验表明,菌毛-1 参与了与上皮细胞的附着和毒力,以及在感染的小鼠模型中的保护作用。有几项报告表明,菌毛-1 的表达受到严格调控,涉及许多遗传调节剂的相互作用,包括 PI-1 阳性调节剂 RlrA。在本报告中,我们提供了证据表明,在 PI-1 阳性菌株中在单细胞水平上分析时,菌毛表达呈双峰。事实上,这些菌株存在两种表型上不同的细菌亚群,一种表达菌毛,另一种不表达菌毛。这两种表型的比例在测试的菌株中是可变的,不受基因型、血清型、生长条件、菌落形态或针对菌毛成分的抗体的影响。通过对 5 株菌进行菌落选择和免疫检测方法,获得了两种富集表达菌毛或不表达菌毛的细菌亚群。对这两个亚群进行 PI-1 测序,发现没有突变,因此表明观察到的双峰表达不是由于 PI-1 内的遗传修饰所致。对两个富集亚群进行全菌裂解物的微阵列表达谱和 Western blot 分析,结果表明菌毛表达受转录水平(开/关调控)调控,并且除了 PI-1 编码的基因外,在测试的菌株中没有其他基因同时受到调控。最后,我们提供了证据表明,RrlA 阳性调节剂的过度表达足以诱导菌毛-1 阴性细菌表达菌毛。总之,这里提出的数据表明,观察到的双峰菌毛表达表型可能是肺炎链球菌中双稳定性的一个例子。