McEllistrem M Catherine, Ransford Jennifer V, Khan Saleem A
Division of Infectious Diseases, University of Pittsburgh School of Medicine, PA 15213-2582, USA.
J Clin Microbiol. 2007 Jan;45(1):97-101. doi: 10.1128/JCM.01658-06. Epub 2006 Nov 8.
An increasing proportion of children with acute otitis media due to Streptococcus pneumoniae have serotype 3 infections since licensure of the seven-valent pneumococcal conjugate vaccine. These serotype 3 strains are genetically related by molecular subtyping. During otitis media with effusion and recurrent otitis media, biofilms commonly develop. Pneumococcal in vitro biofilms are comprised of phase variants that differ in colony morphology. By using a representative strain of the mucoid serotype 3 clone, rough phase variants with a diverse array of mutations were detected in biofilms formed in vitro. Most phase variants had mutations in the cps3D gene, the first gene of the capsular operon. Eleven had single nucleotide polymorphisms (SNPs) in the cps3D gene, one had an SNP in the -10 promoter, and three had large deletions in the cps3D gene. Reversion to the mucoid phenotype was associated with reversion of the mutation in the cps3D gene. Unlike the phase variants detected in the nasopharynx, which have at least 20% of the parental amount of capsule, the in vitro biofilm-associated phase variants had < or =12% of the parental amount of capsule, as determined by capsule enzyme-linked immunosorbent assays. Using real-time reverse transcription-PCR, we determined that capsule expression in the phase variants was likely regulated at multiple levels. These in vitro phase variation data, which underscore the plasticity of the pneumococcus, need to be confirmed with in vivo analyses of the middle ear mucosa during otitis media.
自七价肺炎球菌结合疫苗获批以来,由肺炎链球菌引起的急性中耳炎患儿中,感染血清型3的比例不断增加。这些血清型3菌株通过分子亚型分析具有遗传相关性。在中耳积液和复发性中耳炎期间,生物膜通常会形成。肺炎球菌体外生物膜由菌落形态不同的相变变体组成。通过使用黏液样血清型3克隆的代表性菌株,在体外形成的生物膜中检测到具有多种突变的粗糙相变变体。大多数相变变体在荚膜操纵子的第一个基因cps3D基因中发生了突变。11个在cps3D基因中有单核苷酸多态性(SNP),1个在-10启动子中有SNP,3个在cps3D基因中有大片段缺失。向黏液样表型的回复与cps3D基因中突变的回复相关。与在鼻咽部检测到的相变变体不同,后者具有至少20%的亲本荚膜量,通过荚膜酶联免疫吸附测定确定,体外生物膜相关的相变变体具有≤12%的亲本荚膜量。使用实时逆转录PCR,我们确定相变变体中的荚膜表达可能在多个水平受到调控。这些体外相变变异数据强调了肺炎球菌的可塑性,需要通过对中耳炎期间中耳黏膜的体内分析来证实。