Volume 17, Number 10—October 2011
Antimicrobial Ointments and Methicillin-Resistant Staphylococcus aureus USA300
We tested 259 methicillin-resistant Staphylococcus aureus isolates and 2 USA300 ATCC type strains for susceptibility to bacitracin and neomycin contained in over-the-counter antibacterial ointments. Resistance to both bacitracin and neomycin was found only in USA300. The use of over-the counter antimicrobial drugs may select for the USA300 clone.
Community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) is rapidly spreading worldwide. MRSA USA300 is a clone of increasing public health concern among rapidly disseminating CA-MRSA strains in the United States (1). MRSA USA300 is designated as sequence type (ST) 8 by multilocus sequence typing (MLST) and possesses staphylococcal cassette chromosome mec (SCCmec) type IVa. Although the rapid dissemination of the USA300 clone may occur because of a high virulence level that arises from the production of Panton-Valentine leukocidin (PVL) or an existing arginine catabolic mobile element (ACME) (2), there is no conclusive evidence to support this hypothesis (3). Furthermore, the hypothesis cannot account for the rapid dissemination of MRSA in countries where USA300 clones are not the dominant clones (most European countries, South Korea, and Japan) (4–6). In most European countries, the dominant CA-MRSA clone is the European clone (ST80, SCCmec type IV, PVL positive and ACME negative) (1,4). In South Korea, only 1 isolate was a USA300 clone among 138 MRSA isolates collected from patients with bacteremia and soft tissue infection (5). In Japan, the MRSA USA300 clone is rare (6).
In many cases, soft tissue infection acquired in communities was treated by using over–the-counter (OTC) drugs called triple-antibiotic ointment (TAO), e.g., Neosporin (polymyxin B [PL-B] sulfate, 5,000 units/g; bacitracin, 400 units/g; and neomycin, 3.5 mg/g) and Polysporin triple ointment (PL-B sulfate, 10,000 units/g; bacitracin, 500 units/g; and gramicidin 0.25 mg/g). These ointments contain antimicrobial drugs at concentrations far exceeding their MICs among S. aureus strains (16–32 μg/mL [equivalent to 124–248 unit/mL] for PL-B, <1–64 units/mL for bacitracin, and <1–>128 μg/mL for neomycin) (7,8). It is hypothesized that CA-MRSA cases in the United States were under the selective pressure of TAOs.
In this study, we tested the susceptibilities of MRSA isolates, including the USA300 clone, to the antimicrobial drugs in TAOs. We also considered the possible role of TAOs in spreading the USA300 clone.
We selected 222 MRSA isolates that were not classified as the New York/Japan (NY/JP) clone on the basis of the absence of SCCmec kdpC (9). In addition, 37 NY/JP clone-like isolates were used. A total of 259 MRSA isolates were tested in our study. Of these 259 isolates, 227 were collected during 2004–2010 at Nagoya Medical Center, and 32 isolates were collected in 2006–2009 at Kyoto University Hospital, including 9 USA300 outbreak isolates (6). Details of isolates used in this study are shown in Table 1. ATCC BAA1556 (USA300 FPR3757) (American Type Culture Collection, Manassas, VA, USA) and ATCC BAA1717 (USA300-HOU-MR TCH1516) strains were also used in our study. Susceptibilities to bacitracin and neomycin were tested by the Kirby-Bauer disk diffusion method (Becton Dickinson, Franklin Lakes, NJ, USA). MICs of bacitracin, neomycin, and PL-B for USA300 strains were determined by the agar dilution method according to the Clinical and Laboratory Standard Institute M07-A8 guidelines (10). To observe interaction among these 3 antimicrobial drugs, a double-disk synergy test was performed with modification by using ATCC BAA1717 (11).
SCCmec were determined according to the method of Hisata et al. (12). Isolates possessing both PVL and arcA (13) were analyzed by pulsed-field gel electrophoresis as described in our previous study (9). Moreover, USA300 isolates were genotyped by MLST (www.mlst.net) and staphylococcal protein A (spa) typing (www.spaserver.ridom.de).
Nineteen of the 259 isolates harbored both the PVL and the arcA gene. Of these 19 isolates, 18 had been collected from Kyoto University Hospital and 1 from Nagoya Medical Center (Table 2). All 19 PVL- and ACME-positive isolates were determined to be ST8 by MLST. These isolates showed USA300 PFGE patterns identical to ATCC BAA1556 and were of SCCmec type IVa. SCCmec elements of other isolates were determined as type I (n = 4), IIa (n = 37), IIb (n = 52), II untypeable (n = 14), IV (n = 104), and V (n = 9). The SCCmec element of the remaining 20 isolates could not be identified.
The 18 USA300 isolates collected from Kyoto University Hospital showed the same spa type (t008). However, the 1 USA300 isolate collected from Nagoya Medical Center was of spa t190.
ATCC BAA1717 and 9 USA300 isolates collected during 2007–2009 at Kyoto University Hospital were resistant to both bacitracin and neomycin. The USA300 isolate detected at Nagoya Medical Center in 2004 was bacitracin resistant and neomycin susceptible. The other 9 USA300 isolates and ATCC BAA1556 were susceptible to both drugs (Table 2). Highlander et al. (14) found that the bacitracin- and aminoglycoside-resistant genes were located on pUSA300-HOU-MR, a plasmid typically observed in the USA300 strain TCH1516. The resistance to bacitracin and neomycin may depend on the presence of the plasmid and may be absent in some USA300 clones.
On the other hand, nearly all MRSA isolates that were determined to be a type other than USA300 were susceptible to bacitracin. One isolate was determined to have intermediate resistance to bacitracin. Also, 11 (4.5%) of the 240 MRSA isolates not deemed to be USA300 were resistant to neomycin, while 132 (55%) demonstrated intermediate resistance (Table 2). A study performed in the 1990s reported that most MRSA strains were susceptible to bacitracin, and many were resistant to neomycin (8). Our findings were consistent with the previous study.
MICs of bacitracin, neomycin, and PL-B were 400 units/mL, 128 μg/mL, and 400 units/mL, respectively, among most USA300 isolates with resistance to both bacitracin and neomycin (Table 2). The concentrations of neomycin and PL-B in the TAOs were ≈10 to 30× higher than the MICs of both drugs. In addition, neomycin and PL-B were observed to be weakly synergistic (Figure). However, Bearden et al. reported that despite containing antimicrobial drugs at concentrations far exceeding their MICs among MRSA, PL-B and neomycin ointment, or PL-B and gramicidin ointment exhibited deficient bactericidal activity in time-kill assays (15). Bacitracin may thus be required for sufficient bactericidal activity. Acquiring resistance to bacitracin and neomycin may be essential for survival under the selective pressure of TAOs. If so, bacitracin resistance should be considered a key characteristic of the USA300 clone.
TAOs containing bacitracin, neomycin, and PL-B are widely used in the United States; thus, bacitracin- and neomycin-resistant strains may be selected by the selective pressure of the TAOs. Although bacitracin and neomycin ointments are also available as OTC drugs in Japan, use of the ointments is not widespread. As a result, the selective pressure that leads to bacitracin and neomycin resistance is weak in Japan.
The emergence of MRSA USA300 depends partly on the virulence of MRSA USA300, but it may be influenced by usage of OTC drugs. In each country, susceptibilities of MRSA USA300 to bacitracin and neomycin should be thoroughly investigated, and relationships between the dissemination of MRSA USA300 and the usage of OTC drugs should be clarified. Such an investigation will provide valuable information regarding the emergence of organisms resistant to OTC topical antibiotics and likely a warning against the indiscriminate use of antimicrobial drugs. Further studies are required to validate these findings.
Dr Suzuki is a senior researcher at Aichi Prefectural Institute of Public Health, Japan. His research interests include the molecular epidemiology of Staphylococcus aureus.
We thank Editage for editing this manuscript for language.
This study was supported by grant H21-Shinkou-Ippan-008 from the Ministry of Health, Labour, and Welfare of Japan.
- David MZ, Daum RS. Community-associated methicillin-resistant Staphylococcus aureus: epidemiology and clinical consequences of an emerging epidemic. Clin Microbiol Rev. 2010;23:616–87.
- Diep BA, Stone GG, Basuino L, Graber CJ, Miller A, des Etages SA, The arginine catabolic mobile element and staphylococcal chromosomal cassette mec linkage: convergence of virulence and resistance in the USA300 clone of methicillin-resistant Staphylococcus aureus. J Infect Dis. 2008;197:1523–30.
- Montgomery CP, Boyle Vavra S, Daum RS. The arginine catabolic mobile element is not associated with enhanced virulence in experimental invasive disease caused by the community-associated methicillin-resistant Staphylococcus aureus USA300 genetic background. Infect Immun. 2009;77:2650–6.
- Otter JA, French GL. Molecular epidemiology of community-associated meticillin-resistant Staphylococcus aureus in Europe. Lancet Infect Dis. 2010;10:227–39.
- Park C, Lee DG, Kim SW, Choi SM, Park SH, Chun HS, Predominance of community-associated methicillin-resistant Staphylococcus aureus strains carrying staphylococcal chromosome cassette mec type IVA in South Korea. J Clin Microbiol. 2007;45:4021–6.
- Nagao M, Iinuma Y, Suzuki M, Matsushima A, Takakura S, Ito Y, First outbreak of methicillin-resistant Staphylococcus aureus USA300 harboring the Panton-Valentine leukocidin genes among Japanese healthcare workers and hospitalized patients. Am J Infect Control. 2010;38:e37–9.
- Duwe AK, Rupar CA, Horsman GB, Vas SI. In vitro cytotoxicity and antibiotic activity of polymyxin B nonapeptide. Antimicrob Agents Chemother. 1986;30:340–1.
- Maple PA, Hamilton Miller JM, Brumfitt W. World-wide antibiotic resistance in methicillin-resistant Staphylococcus aureus. Lancet. 1989;1:537–40.
- Suzuki M, Tawada Y, Kato M, Hori H, Mamiya N, Hayashi Y, Development of a rapid strain differentiation method for methicillin-resistant Staphylococcus aureus isolated in Japan by detecting phage-derived open-reading frames. J Appl Microbiol. 2006;101:938–47.
- Clinical and Laboratory Standards Institute. Methods for dilution antimicrobial susceptibility test for bacteria that grow aerobically; approved standard. 8th ed. CLSI document M07-A8. Wayne (PA): The Institute; 2009.
- Leclercq R, Bingen E, Su QH, Lambert Zechovski N, Courvalin P, Duval J. Effects of combinations of beta-lactams, daptomycin, gentamicin, and glycopeptides against glycopeptide-resistant enterococci. Antimicrob Agents Chemother. 1991;35:92–8.
- Hisata K, Kuwahara Arai K, Yamanoto M, Ito T, Nakatomi Y, Cui L, Dissemination of methicillin-resistant staphylococci among healthy Japanese children. J Clin Microbiol. 2005;43:3364–72.
- Zhang K, McClure JA, Elsayed S, Louie T, Conly JM. Novel multiplex PCR assay for simultaneous identification of community-associated methicillin-resistant Staphylococcus aureus strains USA300 and USA400 and detection of mecA and Panton-Valentine leukocidin genes, with discrimination of Staphylococcus aureus from coagulase-negative staphylococci. J Clin Microbiol. 2008;46:1118–22.
- Highlander SK, Hulten KG, Qin X, Jiang H, Yerrapragada S, Mason EO Jr, Subtle genetic changes enhance virulence of methicillin resistant and sensitive Staphylococcus aureus. BMC Microbiol. 2007;7:99.
- Bearden DT, Allen GP, Christensen JM. Comparative in vitro activities of topical wound care products against community-associated methicillin-resistant Staphylococcus aureus. J Antimicrob Chemother. 2008;62:769–72.
Suggested citation for this article: Suzuki M, Yamada K, Nagao M, Aoki E, Matsumoto M, Hirayama T, et al. Antimicrobial ointments and methicillin-resistant Staphylococcus aureus USA300. Emerg Infect Dis [serial on the Internet]. 2011 Oct [date cited]. http://dx.doi.org/10.3201/eid1710.101365
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