Direct detection of methicillin-resistant Staphylococcus aureus in sputum specimens from patients with hospital-associated pneumonia using a novel multilocus PCR assay

• Published in: Pathogens (Basel) 2015-04, Vol.4 (2), p.199-209
• Main Authors: Huang, Zeng-Guang, Zheng, Xing-Zheng, Guan, Jing, Xiao, Shu-Nian, Zhuo, Chao
• Format: Article
• Language: English
• Subjects: Fluorescence; Hospitals; Identification; mecA gene; MRSA; nuc gene; Pathogens; Pneumonia; Respiratory tract; Staphylococcus aureus; Staphylococcus infections; Ventilators
• ISSN: 2076-0817; 2076-0817
• DOI: 10.3390/pathogens4020199

Methicillin-resistant Staphylococcus aureus (MRSA) is a significant cause of hospital-associated pneumonia (HAP). The rapid identification of MRSA would be beneficial for early diagnosis. The study aimed to evaluate a multilocus, fluorescence-based PCR assay based on the detection of mecA and nuc genes for identification of S. aureusin lower respiratory tract (LRT) specimens. Sensitivity and specificity of the PCR assay were analyzed. Clinical evaluation for the assay was performed using LRT specimens from patients with HAP, and the sensitivity, specificity, positive and negative predictive values (PPV and NPV) were evaluated in comparison with semi-quantitative culture methods. The result showed the assay provided positive identification of all MRSA reference strains with a limit of detection for MRSA of 4 × 103 CFU/mL. Compared with semi-quantitative culture, the sensitivity, specificity, PPV and NPV were 100%, 89.6%, 75.0%, and 100%, respectively. A positive correlation between MRSA bacterial colonies and PCR copy number was found. The specificity and PPV reached 96.6% and 89.7% respectively, if the PCR copy number reached a definite positive threshold of 5.96 × 105. It suggested that this novel multilocus, fluorescence-based PCR assay proved to be a fast, sensitive and specific tool for direct detection of MRSA from LRT specimens.