Evaluation of a fourth-generation latex agglutination test for the identification of Staphylococcus aureus

• Published in: European Journal of Clinical Microbiology & Infectious Diseases
• Main Authors: Andriesse, G. I., Elberts, S., Vrolijk, A., Verhulst, C., Kluytmans, J. A. J. W.
• Format: Text
• Language: English
• Published: Springer-Verlag 2010
• Subjects: Article; Pasteur; DML
• Online Access: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022149; http://www.ncbi.nlm.nih.gov/pubmed/20941519; https://doi.org/10.1007/s10096-010-1080-2

In this study, we evaluated a fourth-generation agglutination assay (Staph Plus; DiaMondiaL[DML]) for the rapid identification of Staphylococcus aureus. First, comparison with three third-generation assays (Slidex Staph Plus, bioMérieux; Staphaurex Plus, Murex Diagnostics; Pastorex Staph-Plus, Sanofi Diagnostics Pasteur) was performed on a predefined strain collection: 265 coagulase-negative staphylococci (CNS), 266 methicillin-resistant S. aureus (MRSA) and 262 methicillin-susceptible S. aureus (MSSA) strains (“strain study”). Second, patient material-derived strains (883 CNS, 847 MSSA and 135 MRSA) were tested concurrently with both the DML and Slidex assays (“daily practice study”). In the strain study, the overall sensitivity and specificity of the DML, Slidex, Staphaurex and Pastorex assays were 99.2% and 100%, 98.1% and 100%, 95.2% and 100%, and 98.2% and 98.8%, respectively. Using the respective tests, the result was indeterminate in 0.0%, 0.6%, 0.4% and 1.5% of the strains. Overall, the sensitivity of the DML and Slidex assays were comparable in both sub-studies. However, in MRSA strains, the sensitivity of the DML assay was significantly lower than the Slidex assay. The specificity of the Slidex assay was significantly higher than the DML assay. However, the percentage of indeterminate results was much higher for the Slidex than the DML assay. In conclusion, the presumptive identification of S. aureus by the DML assay proved to be equal to third-generation latex agglutination assays.