Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
J Clin Microbiol. 2012 Apr;50(4):1326-30. doi: 10.1128/JCM.05182-11. Epub 2012 Jan 11.
Streptococcus pneumoniae is a major cause of bacteremia, meningitis, pneumonia, sinusitis, and acute otitis media in children. Although optochin susceptibility, bile solubility, and Quellung testing are the standards for identifying and differentiating pneumococci, there are several reports of nontypeable pneumococci that give inconsistent results with one or more of these tests. We characterized 52 isolates previously labeled as nontypeable pneumococci. Microbiological methods included repeating the Quellung reaction using a new and expanded group of antisera, optochin susceptibility and bile solubility tests, and automated Vitek 2 identification. Molecular methods included PCR detection of ply and psaA genes, multilocus sequence typing (MLST), 16S rRNA gene sequencing, and pyrosequencing. Of the 52 isolates, 38 (73%) were optochin susceptible, were psaA and ply positive, and could be serotyped by the Quellung reaction. The remaining 14 isolates, isolated from patients with otitis media (n = 6), bacteremia (n = 6), meningitis (n = 1), and pneumonia (n = 1), underwent further analysis. Three of these 14 isolates were nontypeable due to autoagglutination but were pneumococci by all tests and represented pneumococcal sequence types previously recognized by MLST. The 11 remaining isolates were optochin resistant, and 6 of these were bile soluble. Three of 11 were both psaA and ply positive and clustered with pneumococci by MLST (2 were bile soluble); 8 lacked psaA (5 ply positive, 4 bile soluble) and likely belonged to other Streptococcus species. In conclusion, few isolates were truly nontypeable by Quellung reaction, and MLST and the presence of psaA proved useful in distinguishing between atypical pneumococci and other streptococcal species.
肺炎链球菌是儿童菌血症、脑膜炎、肺炎、鼻窦炎和急性中耳炎的主要病因。虽然 Optochin 敏感性、胆汁溶解和 Quellung 检测是鉴定和区分肺炎链球菌的标准,但有几报告称,一些非典型肺炎链球菌对这些测试中的一种或多种测试的结果不一致。我们对之前标记为非典型肺炎链球菌的 52 株分离株进行了特征描述。微生物学方法包括使用新的和扩展的抗血清组重复 Quellung 反应、Optochin 敏感性和胆汁溶解试验以及自动化 Vitek 2 鉴定。分子方法包括 ply 和 psaA 基因的 PCR 检测、多位点序列分型(MLST)、16S rRNA 基因测序和焦磷酸测序。在这 52 株分离株中,38 株(73%)对 Optochin 敏感,psaA 和 ply 阳性,并且可以通过 Quellung 反应进行血清分型。其余 14 株分离株,来自中耳炎(n=6)、菌血症(n=6)、脑膜炎(n=1)和肺炎(n=1)患者,进一步分析。这 14 株分离株中的 3 株由于自凝而无法分型,但通过所有测试均被鉴定为肺炎链球菌,代表 MLST 先前认可的肺炎链球菌序列型。其余 11 株分离株对 Optochin 耐药,其中 6 株对胆汁溶解。这 11 株分离株中的 3 株 psaA 和 ply 均阳性,通过 MLST 聚类为肺炎链球菌(2 株对胆汁溶解);8 株缺乏 psaA(5 株 ply 阳性,4 株对胆汁溶解),可能属于其他链球菌种。总之,很少有分离株通过 Quellung 反应真正无法分型,MLST 和 psaA 的存在有助于区分非典型肺炎链球菌和其他链球菌种。