Evaluation and Improvement of Real-Time PCR Assays Targeting lytA, ply, and psaA Genes for Detection of Pneumococcal DNA

Evaluation and Improvement of Real-Time PCR Assays Targeting lytA, ply, and psaA Genes for Detection of Pneumococcal DNA

Maria da Gloria S. Carvalho;Maria Lucia Tondella;Karen McCaustland;Luciana Weidlich;Lesley McGee;Leonard W. Mayer;Arnold Steigerwalt;Melissa Whaley;Richard R. Facklam;Barry Fields;George Carlone;Edwin W. Ades;Ron Dagan;Jacquelyn S. Sampson;Maria da Gloria S. Carvalho;Maria Lucia Tondella;Karen McCaustland;Luciana Weidlich;Lesley McGee;Leonard W. Mayer;Arnold Steigerwalt;Melissa Whaley;Richard R. Facklam;Barry Fields;George Carlone;Edwin W. Ades;Ron Dagan;Jacquelyn S. Sampson;
Journal of clinical microbiology 2007 Vol. 45 pp. 2460-2466
144
carvalho2007journalevaluation

Abstract

The accurate diagnosis of pneumococcal disease has frequently been hampered not only by the difficulties in obtaining isolates of the organism from patient specimens but also by the misidentification of pneumococcus-like viridans group streptococci (P-LVS) as Streptococcus pneumoniae . This is especially critical when the specimen comes from the respiratory tract. In this study, three novel real-time PCR assays designed for the detection of specific sequence regions of the lytA , ply , and psaA genes were developed ( lytA -CDC, ply -CDC, and psaA , respectively). These assays showed high sensitivity (

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112782
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10.1128/JCM.02498-06
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