Morrison K E, Lake D, Crook J, Carlone G M, Ades E, Facklam R, Sampson J S
Division of Bacterial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, U.S. Department of Health and Human Services, Atlanta, Georgia 30333, USA.
J Clin Microbiol. 2000 Jan;38(1):434-7. doi: 10.1128/JCM.38.1.434-437.2000.
The gene encoding the pneumococcal surface adhesin A (PsaA) protein, psaA, was confirmed in all Streptococcus pneumoniae serotypes by a newly developed PCR (psaA PCR) assay. Eighty-nine of the 90 serotypes amplified produced an 838-bp fragment; the exception was a serotype 16F strain acquired from the American Type Culture Collection (ATCC). Analysis of 20 additional 16F strains from the United States and Brazil showed that the gene was amplified in all 16F strains, implying that the serotype 16F ATCC strain must be a variant. The specificity of the assay was verified by the lack of signal from analysis of heterologous bacterial species (n = 30) and genera (n = 14), including viridans group streptococci. The potential of the assay for clinical application was shown by its ability to detect pneumococci in culture-positive nasopharyngeal specimens. Demonstration of psaA in all 90 serotypes and lack of amplification of heterologous organisms suggest that this assay could be a useful tool for detection of pneumococci and diagnosis of disease.
通过一种新开发的聚合酶链反应(psaA PCR)检测方法,在所有肺炎链球菌血清型中均证实了编码肺炎球菌表面黏附素A(PsaA)蛋白的基因psaA。90种血清型中有89种扩增出了一个838碱基对的片段;例外的是从美国典型培养物保藏中心(ATCC)获得的一株16F血清型菌株。对另外20株来自美国和巴西的16F菌株进行分析表明,所有16F菌株中该基因均能扩增,这意味着ATCC的16F血清型菌株必定是一个变种。通过对包括草绿色链球菌在内的异源细菌种(n = 30)和属(n = 14)进行分析未发现信号,验证了该检测方法的特异性。该检测方法在培养阳性的鼻咽标本中检测肺炎球菌的能力表明了其临床应用潜力。在所有90种血清型中均证实了psaA的存在,且异源生物体未扩增,这表明该检测方法可能是检测肺炎球菌和疾病诊断的有用工具。