Journal List > Korean J Clin Microbiol > v.14(1) > 1038234

Lee, Suh, Jeon, and Kim: Prevalence and Clinical Characteristics of Mupirocin-Resistant Staphylococcus aureus

Abstract

Background

Nasal colonization with methicillin-resistant Staphylococcus aureus (MRSA) is a known risk factor for nosocomialtransmission and infection. In an effort to mitigate this problem, topical mupirocin has been widely used for clearing nasal carriage of MRSA. However, mupirocin resistance has become a worldwide concern due to increased use of the antibiotic. The aims of this study were to evaluate the clinical characteristics and prevalence of mupirocin resistance among clinical isolates of staphylococci and to investigate antimicrobial susceptibility.

Methods

A total of 175 S. aureus specimens recovered over a 4-month period from various body sites were tested for resistance to mupirocin and other antibiotics using the Vitek2 automated system. The presence of the mupA gene was assessed in isolates exhibiting resistance to mupirocin and in other selected organisms. The clinical characteristics of the isolates were also reviewed.

Results

Of the 175 S. aureus isolates, 9.1% (16/175) were resistant to mupirocin, with 1.7% (3/175) having high-level resistance (HR) and 7.4% (13/175) having low-level resistance (LR). Patients with HR-mupirocin-resistant S. aureus had a longer duration of hospitalization (P=0.026). Of the 13 LR-mupirocin-resistant S. aureus strains, 11 had identical antibiogram patterns. The mupA gene was detected only among HR isolates.

Conclusion

The rate of mupirocin resistance in the S. aureus isolates was high. The spread of mupirocin-resistant S. aureus may be due to nosocomial infection.

REFERENCES

1. Muder RR, Brennen C, Wagener MM, Vickers RM, Rihs JD, Hancock GA, et al. Methicillin-resistant staphylococcal colonization and infection in a longterm care facility. Ann Intern Med. 1991; 114:107–12.
crossref
2. Klevens RM, Edwards JR, Tenover FC, McDonald LC, Horan T, Gaynes R. National Nosocomial Infections Surveillance System. Changes in the epidemiology of methicillin-resistant Staphylococcus aureus in intensive care units in US hospitals, 1992-2003. Clin Infect Dis. 2006; 42:389–91.
crossref
3. Lee K, Chang CL, Lee NY, Kim HS, Hong SK, Cho HC. Korean nationwide surveillance of antimicrobial. resistance group. Korean nationwide surveillance of antimicrobial resistance of bacteria in 1998. Yonsei Med J. 2000; 41:497–506.
4. Boyce JM. Methicillin-resistant Staphylococcus aureus. Detection, epidemiology, and control measures. Infect Dis Clin North Am. 1989; 3:901–13.
5. Huang SS and Platt R. Risk of methicillin-resistant Staphylococcus aureus infection after previous infection or colonization. Clin Infect Dis. 2003; 36:281–5.
6. Yang JA, Park DW, Sohn JW, Yang IS, Kim KH, Kim MJ. Molecular analysis of isoleucyl-tRNA synthetase mutations in clinical isolates of methicillin-resistant Staphylococcus aureus with low-level mupirocin resistance. J Korean Med Sci. 2006; 21:827–32.
crossref
7. Yanagisawa T, Lee JT, Wu HC, Kawakami M. Relationship of protein structure of isoleucyl-tRNA synthetase with pseudomonic acid resistance of Escherichia coli. A proposed mode of action of pseudomonic acid as an inhibitor of isoleucyl-tRNA synthetase. J Biol Chem. 1994; 269:24304–9.
crossref
8. Rahman M, Noble WC, Cookson B, Baird D, Coia J. Mupirocin-resistant Staphylococcus aureus. Lancet. 1987; 2(8555):387–8.
crossref
9. Bradley SF, Ramsey MA, Morton TM, Kauffman CA. Mupirocin resistance: clinical and molecular epidemiology. Infect Control Hosp Epidemiol. 1995; 16:354–8.
crossref
10. Riley TV, Carson CF, Bowman RA, Mulgrave L, Golledge CL, Pearman JW, et al. Mupirocin-resistant methicillin-resistant Staphylococcus aureus in Western Australia. Med J Aust. 1994; 161:397–8.
11. Yun HJ, Lee SW, Yoon GM, Kim SY, Choi S, Lee YS, et al. Prevalence and mechanisms of low- and high-level mupirocin resistance in staphylococci isolated from a Korean hospital. J Antimicrob Chemother. 2003; 51:619–23.
crossref
12. Gilbart J, Perry CR, Slocombe B. High-level mupirocin resistance in Staphylococcus aureus: evidence for two distinct isoleucyl-tRNA synthetases. Antimicrob Agents Chemother. 1993; 37:32–8.
crossref
13. Pérez-Roth E, López-Aguilar C, Alcoba-Florez J, Méndez-Alvarez S. High-level mupirocin resistance within methicillin-resistant Staphylococcus aureus pandemic lineages. Antimicrob Agents Chemother. 2006; 50:3207–11.
14. Hodgson JE, Curnock SP, Dyke KG, Morris R, Sylvester DR, Gross MS. Molecular characterization of the gene encoding high-level mupirocin resistance in Staphylococcus aureus J2870. Antimicrob Agents Chemother. 1994; 38:1205–8.
crossref
15. Kim EC, Jung HJ, Oh MD, Lee HJ, Oh HS, Choe KW. Epidemiological typing of methicillin-resistant Staphylococcus aureus outbreak isolates by pulsed-field gel electrophoresis and antibiogram. Yonsei Med J. 1998; 39:587–94.
16. Yoo JI, Shin ES, Cha JO, Lee JK, Jung YH, Lee KM, et al. Clonal dissemination and mupA gene polymorphism of mupirocin-resistant Staphylococcus aureus isolates from longterm-care facilities in South Korea. Antimicrob Agents Chemother. 2006; 50:365–7.
17. Boyce JM. Preventing staphylococcal infections by eradicating nasal carriage of Staphylococcus aureus: proceeding with caution. Infect Control Hosp Epidemiol. 1996; 17:775–9.
crossref
18. Baird D and Coia J. Mupirocin-resistant. staphylococcus aureus. Lancet. 1987; 2:387–8.
19. Walker ES, Vasquez JE, Dula R, Bullock H, Sarubbi FA. Mupirocin-resistant, methicillin-resistant Staphylococcus aureus: does mupirocin remain effective? Infect Control Hosp Epidemiol. 2003; 24:342–6.
20. Harbarth S, Dharan S, Liassine N, Herrault P, Auckenthaler R, Pittet D. Randomized, placebo-controlled, double-blind trial to evaluate the efficacy of mupirocin for eradicating carriage of methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 1999; 43:1412–6.
21. Wise R and Johnson J. Mupirocin resistance. Lancet. 1991; 338(8766):578.
22. Orrett FA. The emergence of mupirocin resistance among clinical isolates of methicillin-resistant Staphylococcus aureus in Trinidad: a first report. Jpn J Infect Dis. 2008; 61:107–10.
23. Jones JC, Rogers TJ, Brookmeyer P, Dunne WM Jr, Storch GA, Coopersmith CM, et al. Mupirocin resistance in patients colonized with methicillin-resistant Staphylococcus aureus in a surgical intensive care unit. Clin Infect Dis. 2007; 45:541–7.
crossref
24. Song W, Lee TJ, Kim SJ, Park MJ, Lee KM. Methicillin-resistant staphylococcus aureus infections in intensive care unit (ICU) patients: relation to nasal carriage of patients or ICU personnels. Korean J Clin Microbiol. 2001; 4:45–51.
25. Ko KS, Park S, Peck KR, Shin EJ, Oh WS, Lee NY, et al. Molecular characterization of methicillin-resistant Staphylococcus aureus spread by neonates transferred from primary obstetrics clinics to a tertiary care hospital in Korea. Infect Control Hosp Epidemiol. 2006; 27:593–7.
26. Okuma K, Iwakawa K, Turnidge JD, Grubb WB, Bell JM, O'Brien FG, et al. Dissemination of new methicillin-resistant Staphylococcus aureus clones in the community. J Clin Microbiol. 2002; 40:4289–94.
27. Malaviolle X, Nonhoff C, Denis O, Rottiers S, Struelens MJ. Evaluation of disc diffusion methods and Vitek 2 automated system for testing susceptibility to mupirocin in Staphylococcus aureus. J Antimicrob Chemother. 2008; 62:1018–23.
crossref

Fig. 1.
Bands of mupA gene in 3 high-level resistance of mupirocin. Lane 1, patient No. 162; Lane 2, patient No. 192; Lane 3, patient No. 195; Lane 4, PCR size marker.
kjcm-14-18f1.tif
Table 1.
Distribution of mupirocin MICs among 175 strains of Staphylococcus aureus
Mupirocin resistance MIC (μg/mL) No. of isolate (%)
Susceptible <2 150 (85.7)
  4 9 (5.1)
Low-level resistant 64 13 (7.4)
High-level resistant ≥512 3 (1.7)
Total   175 (100)

Abbreviation: MIC, minimal inhibitory concentration.

Table 2.
Clinical characteristics of 175 strains of Staphylococcus aureus
    Mupirocin susceptible (N=159) Mupirocin LR (N=13) Mupirocin HR (N=3)
Hospital stay, median days (range) 6 (1∼1,670) 6 (2∼60) 55 (24∼222)
Specimens, N (%)      
 Sputum 69 (39.4) 59 (85.5) 9 (13.0) 1 (1.4)
 Urine 17 (9.7) 17 (100.0) 0 (0.0) 0 (0.0)
 Blood 30 (17.1) 28 (93.3) 1 (3.3) 1 (3.3)
 Wound 38 (21.7) 35 (92.1) 2 (5.3) 1 (2.6)
 Others 21 (12.0) 20 (95.2) 1 (4.8) 0 (0.0)
Total 175 (100.0) 159 (90.9) 13 (7.4) 3 (1.7)
Place, N (%)      
 ICU 48 (27.4) 44 (91.7) 3 (6.2) 1 (2.1)
 GW 95 (54.3) 84 (88.4) 9 (9.5) 2 (2.1)
 OPD 11 (6.3) 11 (100.0) 0 (0.0) 0 (0.0)
 ED 21 (12.0) 20 (95.2) 1 (7.7) 0 (0.0)
Total 175 (100.0) 159 (90.9) 13 (7.4) 3 (1.7)

Abbreviations: LR, low-level resistant; HR, high-level resistant; ICU, intensive care unit; GW, general ward; OPD, outpatient department; ED, emergency department.

Table 3.
Antimicrobial resistance profile of 108 MRSA strain
Antimicrobial No. (%)
Ciprofloxacin 88 (81.5)
Clindamycin 95 (87.9)
Erythromycin 96 (88.9)
Fusidic acid 74 (68.5)
Nitrofurantoin 6 (5.6)
Gentamicin 89 (82.4)
Arbekacin 0 (0.0)
Linezolid 0 (0.0)
Penicillin G 108 (100)
Quinupristin-Dafopristin 0 (0.0)
Rifampin 7 (6.5)
Teicoplanin 0 (0.0)
Tetracycline 92 (85.2)
Trimethoprim-sulfamethoxazole 9 (8.3)
Telithromycin 87 (80.6)
Tigecycline 0 (0.0)
Vancomycin 0 (0.0)
Table 4.
Epidemiologic and clinical features of the sixteen mupirocin-resistant Staphylococcus aureus
No. MR Antibiogram Specimen Place Hospita stay (days) Primary diagnosis
4 HR LQVT Blood ICU 222 COPD
8 LR LQRTsVT Sputum GW 6 COPD
10 LR LQRTsVT Ascitic fluid GW 24 Duodenal ulcer
15 LR GLQRTsVT Sputum ICU 5 SAH
55 LR LQRTsVT Sputum ED 2 COPD
65 LR LQRTsVT Sputum GW 30 Gangrene of toe
66 LR LQRTsVT Wound GW 2 Sacral sore
79 LR LQRTsVT Sputum GW 4 ESRD
92 LR LQVT Sputum GW 9 Pneumothorax
99 LR LQRTsVT Sputum GW 60 Aplastic anemia
100 LR LQRTsVT Sputum ICU 4 Septic shock
106 LR LQRTsVT Blood GW 4 ESRD
107 HR CLQRTsV T Wound GW 24 Sacral sore
109 HR CiCELQRTs TeVT Sputum GW 55 SAH
153 LR LQRTsVT Wound GW 35 Open wound of ankle and foot
169 LR LQRTsVT Sputum ICU 23 Spine fracture

Type of antibiogram: LQVT (susceptible to linezolid, quinupristin-dafopristin, vancomycin, teicoplanin), LQRTsVT (susceptible to linezolid, quinupristin-dafopristin, rifampin, trimethoprim-sulfamethoxazole, vancomycin, teicoplanin), GLQRTsVT (susceptible to gentamicin, linezolid, quinupristin-dafopristin, rifampin, trimethoprim-sulfamethoxazole, vancomycin, teicoplanin), CiCELQRTsTeVT (susceptible to ciprofloxacin, clindamycin, erythromycin, linezolid, quinupristin-dafopristin, rifampin, trimethoprim-sulfamethoxazole, tetracycline, vancomycin, teicoplanin).

Abbreviations: MR, mupirocin resistance; LR, low-level resistant, HR, high-level resistant; ICU, intensive care unit; GW, general word; ED, emergency department; COPD, chronic obstructive pulmonary disease; SAH, subarachnoidal hemorrhage; ESRD, end-stage renal disease.

TOOLS
Similar articles