DOI QR코드

DOI QR Code

Methicillin-resistant Staphylococcus aureus in Nasal Surveillance Swabs at an Intensive Care Unit: An Evaluation of the LightCycler MRSA Advanced Test

  • Huh, Hee Jin (Department of Laboratory Medicine, Dongguk University Ilsan Hospital) ;
  • Kim, Eu Suk (Department of Internal Medicine, Seoul National University Bundang Hospital) ;
  • Chae, Seok Lae (Department of Laboratory Medicine, Dongguk University Ilsan Hospital)
  • Published : 2012.11.01

Abstract

Background: We compared the LightCycler MRSA advanced test (Roche Diagnostics, Germany) with enrichment culture methods to evaluate the relative diagnostic performance of the LightCycler MRSA advanced test for active surveillance in a high-prevalence setting. Methods: A total of 342 nasal swab specimens were obtained from patients in the intensive care unit at admission and on the seventh day for follow-up. The results of LightCycler MRSA advanced test were compared to those of the enrichment culture. For discrepant results, mecA gene PCR was performed. Results: For the detection of methicillin-resistant Staphylococcus aureus (MRSA), the LightCycler MRSA advanced test showed 98.5% sensitivity and 78.6% specificity and had positive and negative predictive values of 75.0% and 98.8%, respectively. A total of 46 samples had discrepant results between the LightCycler MRSA advanced test and enrichment culture. Of the 44 specimens that were positive in the LightCycler MRSA advanced test but negative by enrichment culture, mecA genes were detected in 37 specimens. In addition, of the original 44 cases, 21 patients had a history of MRSA colonization or infection within the last month; of those 21 specimens, 20 were positive for mecA gene as shown by PCR. Seven mecA-negative discrepant specimens comprised 3 methicillin-sensitive S. aureus-culture positive and only 2 patients had MRSA infections. Conclusions: Despite its low specificity and positive predictive value, the LightCycler MRSA advanced test could serve as a rapid test for patients colonized with MRSA.

Keywords

References

  1. Cosgrove SE, Qi Y, Kaye KS, Harbarth S, Karchmer AW, Carmeli Y. The impact of methicillin resistance in Staphylococcus aureus bacteremia on patient outcomes: mortality, length of stay, and hospital charges. Infect Control Hosp Epidemiol 2005;26:166-74. https://doi.org/10.1086/502522
  2. Muto CA, Jernigan JA, Ostrowsky BE, Richet HM, Jarvis WR, Boyce JM, et al. SHEA guideline for preventing nosocomial transmission of multidrug-resistant strains of Staphylococcus aureus and enterococcus. Infect Control Hosp Epidemiol 2003;24:362-86. https://doi.org/10.1086/502213
  3. Salgado CD, Farr BM, Calfee DP. Community-acquired methicillin-resistant Staphylococcus aureus: a meta-analysis of prevalence and risk factors. Clin Infect Dis 2003;36:131-9. https://doi.org/10.1086/345436
  4. Wertheim HF, Melles DC, Vos MC, van Leeuwen W, van Belkum A, Verbrugh HA, et al. The role of nasal carriage in Staphylococcus aureus infections. Lancet Infect Dis 2005;5:751-62. https://doi.org/10.1016/S1473-3099(05)70295-4
  5. Park BG and Lee MK. Nasal Carriage of Methicillin-Resistant Staphylococcus aureus among Healthcare Workers and Community Students in 1997 and 2006. Korean J Nosocomial Infect Control 2007;12:85-90.
  6. Park SH, Jang YH, Sung H, Kim MN, Kim JS, Park YJ. Performance evaluation of BD GeneOhm MRSA PCR assay for detection of nasal colonization of methicillin-resistant Staphylococcus aureus at endemic intensive care units. Korean J Lab Med 2009;29:439-47. https://doi.org/10.3343/kjlm.2009.29.5.439
  7. Diederen B, van Duijn I, van Belkum A, Willemse P, van Keulen P, Kluytmans J. Performance of CHROMagar MRSA medium for detection of methicillin-resistant Staphylococcus aureus. J Clin Microbiol 2005;43:1925-7. https://doi.org/10.1128/JCM.43.4.1925-1927.2005
  8. Nahimana I, Francioli P, Blanc DS. Evaluation of three chromogenic media (MRSA-ID, MRSA-Select and CHROMagar MRSA) and ORSAB for surveillance cultures of methicillin-resistant Staphylococcus aureus. Clin Microbiol Infect 2006;12:1168-74. https://doi.org/10.1111/j.1469-0691.2006.01534.x
  9. Boyce JM and Havill NL. Comparison of BD GeneOhm methicillin-resistant Staphylococcus aureus (MRSA) PCR versus the CHROMagar MRSA assay for screening patients for the presence of MRSA strains. J Clin Microbiol 2008;46:350-1. https://doi.org/10.1128/JCM.02130-07
  10. Reischl U, Linde HJ, Metz M, Leppmeier B, Lehn N. Rapid identification of methicillin-resistant Staphylococcus aureus and simultaneous species confirmation using real-time fluorescence PCR. J Clin Microbiol 2000;38:2429-33.
  11. Huletsky A, Giroux R, Rossbach V, Gagnon M, Vaillancourt M, Bernier M, et al. New real-time PCR assay for rapid detection of methicillin-resistant Staphylococcus aureus directly from specimens containing a mixture of staphylococci. J Clin Microbiol 2004;42:1875-84. https://doi.org/10.1128/JCM.42.5.1875-1884.2004
  12. Safdar N, Narans L, Gordon B, Maki DG. Comparison of culture screening methods for detection of nasal carriage of methicillin-resistant Staphylococcus aureus: a prospective study comparing 32 methods. J Clin Microbiol 2003;41:3163-6. https://doi.org/10.1128/JCM.41.7.3163-3166.2003
  13. Peterson LR, Liesenfeld O, Woods CW, Allen SD, Pombo D, Patel PA, et al. Multicenter evaluation of the LightCycler methicillin-resistant Staphylococcus aureus (MRSA) advanced test as a rapid method for detection of MRSA in nasal surveillance swabs. J Clin Microbiol 2010;48:1661-6. https://doi.org/10.1128/JCM.00003-10
  14. Paule SM, Hacek DM, Kufner B, Truchon K, Thomson RB Jr, Kaul KL, et al. Performance of the BD GeneOhm methicillin-resistant Staphylococcus aureus test before and during high-volume clinical use. J Clin Microbiol 2007;45:2993-8. https://doi.org/10.1128/JCM.00670-07
  15. Bischof LJ, Lapsley L, Fontecchio K, Jacosalem D, Young C, Hankerd R, et al. Comparison of chromogenic media to BD GeneOhm methicillinresistant Staphylococcus aureus (MRSA) PCR for detection of MRSA in nasal swabs. J Clin Microbiol 2009;47:2281-3. https://doi.org/10.1128/JCM.02256-08
  16. Kim OS, Yoon SW, Kang YJ, Kim YK, Lee NY, Lee JH, et al. Rate of nasal colonization of Methicillin-Resistant Staphylococcus aureus at admission to a medical intensive care unit. Korean J Nosocomial Infect Control 2007;12:42-9.
  17. de San N, Denis O, Gasasira MF, De Mendonca R, Nonhoff C, Struelens MJ. Controlled evaluation of the IDI-MRSA assay for detection of colonization by methicillin-resistant Staphylococcus aureus in diverse mucocutaneous specimens. J Clin Microbiol 2007;45:1098-101. https://doi.org/10.1128/JCM.02208-06
  18. Rossney AS, Herra CM, Fitzgibbon MM, Morgan PM, Lawrence MJ, O'Connell B. Evaluation of the IDI-MRSA assay on the SmartCycler realtime PCR platform for rapid detection of MRSA from screening specimens. Eur J Clin Microbiol Infect Dis 2007;26:459-66. https://doi.org/10.1007/s10096-007-0303-7
  19. Martineau F, Picard FJ, Lansac N, Menard C, Roy PH, Ouellette M, et al. Correlation between the resistance genotype determined by multiplex PCR assays and the antibiotic susceptibility patterns of Staphylococcus aureus and Staphylococcus epidermidis. Antimicrob Agents Chemother 2000;44:231-8. https://doi.org/10.1128/AAC.44.2.231-238.2000
  20. Donnio PY, Oliveira DC, Faria NA, Wilhelm N, Le Coustumier A, de Lencastre H. Partial excision of the chromosomal cassette containing the methicillin resistance determinant results in methicillin-susceptible Staphylococcus aureus. J Clin Microbiol 2005;43:4191-3. https://doi.org/10.1128/JCM.43.8.4191-4193.2005
  21. Farley JE, Stamper PD, Ross T, Cai M, Speser S, Carroll KC. Comparison of the BD GeneOhm methicillin-resistant Staphylococcus aureus (MRSA) PCR assay to culture by use of BBL CHROMagar MRSA for detection of MRSA in nasal surveillance cultures from an at-risk community population. J Clin Microbiol 2008;46:743-6. https://doi.org/10.1128/JCM.02071-07
  22. Donnio PY, Fevrier F, Bifani P, Dehem M, Kervegant C, Wilhelm N, et al. Molecular and epidemiological evidence for spread of multiresistant methicillin-susceptible Staphylococcus aureus strains in hospitals. Antimicrob Agents Chemother 2007;51:4342-50. https://doi.org/10.1128/AAC.01414-06
  23. Drews SJ, Willey BM, Kreiswirth N, Wang M, Ianes T, Mitchell J, et al. Verification of the IDI-MRSA assay for detecting methicillin-resistant Staphylococcus aureus in diverse specimen types in a core clinical laboratory setting. J Clin Microbiol 2006;44:3794-6. https://doi.org/10.1128/JCM.01509-06

Cited by

  1. Frequency Distribution of Hospital-Acquired MRSA Nasal Carriage Among Hospitalized Patients in West of Iran vol.6, pp.6, 2012, https://doi.org/10.5812/jjm.9076
  2. The Prevalence and Significance of Methicillin-Resistant Staphylococcus aureus Colonization at Admission in the General ICU Setting: A Meta-Analysis of Published Studies* vol.42, pp.2, 2012, https://doi.org/10.1097/ccm.0b013e3182a66bb8
  3. Whole genome SNP typing to investigate methicillin-resistant Staphylococcus aureus carriage in a health-care provider as the source of multiple surgical site infections vol.153, pp.1, 2016, https://doi.org/10.1186/s41065-016-0017-x
  4. Evaluation of the novel artus C. difficile QS-RGQ, VanR QS-RGQ and MRSA/SA QS-RGQ assays for the laboratory diagnosis of Clostridium difficile infection (CDI), and for vancomycin-resistant enterococci vol.36, pp.5, 2017, https://doi.org/10.1007/s10096-016-2867-6
  5. Methicillin-resistant Staphylococcus aureus nasal colonization and infection in an intensive care unit of a university hospital in China vol.46, pp.9, 2018, https://doi.org/10.1177/0300060518777812
  6. Duration of Contact Precautions for Acute-Care Settings vol.39, pp.2, 2012, https://doi.org/10.1017/ice.2017.245