One of the S. aureus isolates that was positive for mecA gene by pentaplex PCR was found to be sensitive to oxacillin by the conventional MIC method. The diagnostic accuracy of a pentaplex PCR for 16S rRNA and femA genes was determined using 230 clinical isolates and found to have 100% sensitivity, specificity, and positive and negative predictive values. Selleck GSK1904529A However, the pentaplex PCR for the mecA gene detection showed 97.6% of sensitivity, 99.3% of specificity, and 98.8% of positive and 98.6% of negative predictive values in detecting methicillin-resistant staphylococci. Discussion The present study is believed to be the first to develop a combined molecular Selleck Lazertinib test for the rapid identification and discrimination
of the Staphylococcus genus from others, with simultaneous discrimination of methicillin-resistant from -susceptible staphylococcal strains, S. aureus from CoNS, and concomitant detection of PVL genes. Although there are numerous reports on PCR assays for the detection of methicillin resistance [15–17], only a few of them have incorporated internal controls in their assays to rule out false-negative results [18, 19]. According to guidelines for Molecular Diagnostic Methods for Infectious Diseases [20], incorporation of an internal control in the reaction is essential for the diagnostic test to exclude VX-809 price false-negative results or the presence of inhibitors
[21]. In the present study, the inclusion of a 759-bp internal control in the pentaplex PCR assay helped us
to rule out false-negative results or PCR inhibitors. To deal with applicability and accuracy, we further applied our pentaplex PCR assay to test a total of 53 MRSA, 125 MSSA, 22 methicillin-sensitive CoNS, and 30 methicillin-resistant Casein kinase 1 CoNS from routine clinical specimens obtained from Hospital Universiti Sains Malaysia. The Staphylococcus genus consists of at least 35 unique species, and only a few have been recovered from humans [6]. Previously published staphylococcal genus specific primers [22, 23] do not target wholly conserved regions in the staphylococcal 16S rRNA gene, which results in misdetection of some important CoNS. Therefore, we designed a new conserved Staphylococcus genus-specific primer and included it in our new pentaplex PCR assay, which allowed us to detect most species and strains of staphylococci (Table 1). The pentaplex PCR was found to be 100% sensitive and specific in detecting 16S rRNA genes among staphylococcal strains. Another gene, femA, has been characterized as essential for the expression of methicillin resistance in S. aureus and is universally present only in S. aureus isolates. This gene has been implicated in cell wall metabolism and is present in large amounts in actively growing cultures [24]. Specific primers for femA were designed and used in the pentaplex PCR to survey various staphylococcal isolates from our culture collection. All 178 S.