Presence and Molecular Epidemiology of Virulence Factors in Methicillin-Resistant Staphylococcus aureus Strains Colonizing and Infecting Soldiers

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1 JOURNAL OF CLINICAL MICROBIOLOGY, Apr. 2009, p Vol. 47, No /09/$ doi: /jcm Copyright 2009, American Society for Microbiology. All Rights Reserved. Presence and Molecular Epidemiology of Virulence Factors in Methicillin-Resistant Staphylococcus aureus Strains Colonizing and Infecting Soldiers Michael W. Ellis, 1 * Matthew E. Griffith, 1 James H. Jorgensen, 2 Duane R. Hospenthal, 1 Katrin Mende, 3 and Jan E. Patterson 2,4,5 Department of Medicine (Infectious Diseases), Brooke Army Medical Center, Fort Sam Houston, San Antonio, Texas 1 ; Departments of Pathology 2 and Medicine 4 (Infectious Diseases), University of Texas Health Science Center, San Antonio, Texas; Infectious Disease Clinical Research Program, Uniformed Services University of the Health Sciences, Bethesda, Maryland 3 ; and South Texas Veterans Health Care System, San Antonio, Texas 5 Received 8 December 2008/Returned for modification 19 January 2009/Accepted 4 February 2009 Methicillin-resistant Staphylococcus aureus (MRSA) has emerged as an important cause of skin and softtissue infections (SSTI). The understanding of the molecular epidemiology and virulence of MRSA continues to expand. From January 2005 to December 2005, we screened soldiers for MRSA nasal colonization, administered a demographic questionnaire, and monitored them prospectively for SSTI. All MRSA isolates underwent molecular analysis, which included pulsed-filed gel electrophoresis (PFGE) and PCR for Panton-Valentine leukocidin (PVL), the arginine catabolic mobile element (ACME), and the staphylococcal cassette chromosome mec (SCCmec). Of the 3,447 soldiers screened, 134 (3.9%) had MRSA colonization. Of the 3,066 (89%) who completed the study, 39 developed culture-confirmed MRSA abscesses. Clone USA300 represented 53% of colonizing isolates but was responsible for 97% of the abscesses (P < 0.001). Unlike colonizing isolates, isolates positive for USA300, PVL, ACME, and type IV SCCmec were significantly associated with MRSA abscess isolates. As determined by multivariate analysis, risk factors for MRSA colonization were a history of SSTI and a history of hospitalization. Although various MRSA strains may colonize soldiers, USA300 is the most virulent when evaluated prospectively, and PVL, ACME, and type IV SCCmec are associated with these abscesses. Downloaded from Methicillin-resistant Staphylococcus aureus (MRSA) has emerged as a cause of infections in persons within the general community (community-associated methicillin-resistant Staphylococcus aureus [CA-MRSA]) (14, 31). Diseases caused by CA-MRSA range from cutaneous infection to life-threatening systemic illness (13, 14, 28, 31); however, the majority of disease manifests as suppurative skin and soft-tissue infections (SSTI) (13, 14, 28, 31, 32). CA-MRSA is of particular importance to the military, as soldiers are counted among the epidemiological groups who appear to be particularly at risk (10, 11). Pulsed-field type USA300 appears to have eclipsed other pulsed-field types, as nearly all recently reported MRSA outbreaks in the community have involved USA300 (13, 20, 28, 31, 33). Indeed, large analyses of clinical isolates obtained in metropolitan areas and university-affiliated emergency departments have demonstrated that USA300 is the predominant cause of MRSA SSTI in these settings (14, 21, 24, 31). Additionally, in some regions, USA300 is emerging as a hospitalassociated pathogen (24, 37, 39). The factors responsible for * Corresponding author. Mailing address: Uniformed Services University of the Health Sciences, Department of Medicine (Infectious Diseases), 4301 Jones Bridge Road, Bethesda, MD Phone: (301) Fax: (301) michael.w.ellis@us.army.mil. Present address: Department of Medicine (Infectious Diseases), Uniformed Services University of the Health Sciences, Bethesda, MD Published ahead of print on 11 February USA300 s emergence as a significant pathogen remain unclear. USA300 does possess numerous genetic factors that are believed to augment its virulence, including Panton-Valentine leukocidin (PVL) and the arginine catabolic mobile element (ACME) (4, 5, 13, 20, 31, 42). Much of the clinical research on MRSA infections in the general community is limited to the retrospective analysis of clinical isolates. No large prospective investigations have been conducted to validate the observations that USA300 appears to be the most virulent MRSA clone. During 2005, a cluster-randomized, double-blind, placebocontrolled trial was undertaken at Fort Sam Houston, TX, in which participants with MRSA nares colonization received intranasal mupirocin or placebo in an attempt to decrease colonization and subsequent SSTI (10). This investigation demonstrated no decrease in infection rate in either the mupirocin-treated individuals or within the larger study group (10). We evaluated molecular and epidemiological data obtained in that trial to identify risk factors for MRSA colonization and to prospectively describe which MRSA pulsed-field types were responsible for colonization and which pulsed-field types went on to cause subsequent infection, and to determine the presence of PVL and ACME in colonizing and abscess-causing isolates. MATERIALS AND METHODS Study participants. Study participants were U.S. Army personnel enrolled in the Health Care Specialist Course from 10 January 2005 to 16 December on September 24, 2018 by guest 940

2 VOL. 47, 2009 MRSA MOLECULAR EPIDEMIOLOGY AND VIRULENCE IN SOLDIERS 941 TABLE 1. Comparison of colonizing and abscess-causing MRSA isolates f PFT No. (%) of colonizing isolates positive for: No. (%) of abscess isolates positive for: PVL ACME Type IV SCCmec Overall PVL ACME Type IV SCCmec Overall USA (87) 57 (80) 70 (99) 71 (53) 38 (100) 34 (90) 38 (100) 38 (97) a USA800 1 (2) 6 (13) 33 (73) 45 (34) 0 (0) 0 (0) 1 (100) 1 (3) USA600 0 (0) 0 (0) 12 (100) 12 (9) 0 (0) 0 (0) 0 (0) 0 (0) Other b 2 (33) 1 (17) 4 (67) 6 (5) 0 (0) 0 (0) 0 (0) 0 (0) Total 65 (49) 64 (48) 119 (89) 134 (100) 38 (97) c 34 (87) d 39 (100) e 39 (100) a For the association of USA300 with soft-tissue abscesses and colonizing PFTs, P b Other PFTs included USA100 (n 1), USA400 (n 1), USA700 (n 1), USA1100 (n 1), and two nontyped isolates. c For the association of PVL positivity with soft-tissue abscesses and colonizing PFTs, P d For the association of ACME positivity with soft-tissue abscesses and colonizing PFTs, P e For the association of type IV SCCmec positivity with soft-tissue abscesses and colonizing PFTs, P f Percentages may not total 100 due to rounding. PFT, pulsed-field type. This is a 16-week course held at Fort Sam Houston, TX, which trains soldiers to become combat medics. The first 14 weeks of the course are conducted entirely outside of a health care setting. Soldiers were enrolled into the trial on the first day of their training after giving informed consent. The Brooke Army Medical Center Institutional Review Board approved the protocol (ClinicalTrials.gov; number NCT ). Specimen collection and identification. Following enrollment, soldiers had their anterior nares cultured on the first day of training and again 8 to 10 weeks later. Cultures were obtained using BBL CultureSwabs with Stuart s transport media (BD, Sparks, MD). Specimens were transported to the clinical microbiology laboratory and plated onto selective culture media, BBL CHROMagar Staph aureus and BBL CHROMagar MRSA media (BD Diagnostics, Sparks, MD). Isolates were identified by the characteristic colony morphology and color specific to these medium types (12). Both plates were incubated and examined for growth at 24 h per the manufacturer s specifications. MRSA plates were read a second time at 48 h, also according to the manufacturer s specifications. During a 16-week period following enrollment, participants were observed prospectively to assess for clinical skin and soft-tissue abscesses. For any illness that occurred during this time, participants were seen in the same health care system, thus allowing the complete capture of all clinical infections. SSTI were identified by a daily review of clinic records and administrative codes from the International Classification of Diseases, ninth revision (17a). Health care providers were blinded to nares culture results. Anterior nares cultures were not performed at the time when participants presented with skin and soft-tissue abscesses. Wound culture isolates from abscesses were processed by the Brooke Army Medical Center clinical microbiology laboratory according to their standard protocols. We defined MRSA colonization as any study participant with MRSA recovered on the anterior nares screening culture, and we defined an MRSA skin and soft-tissue abscess as any incised, drained, and cultured abscess that yielded MRSA. Laboratory methods. Antimicrobial susceptibility testing was performed on all isolates obtained during the study using the disk diffusion method (2). All isolates underwent molecular characterization by pulsed-field gel electrophoresis (PFGE) following SmaI digestion. PFGE findings were resolved and analyzed using Molecular Analyst software (Bio-Rad, Hercules, CA). Results were interpreted and grouped into pulsed-field types using established criteria (25, 41). All isolates underwent PCR in duplicate to detect PVL (23), ACME (5), and SCCmec (35). Statistical methods. Prior to conducting our analyses, we screened the data for missing or out-of-range values, sparse cell frequency counts, and the sample size/number of cells ratio. There were no missing data points or empty cells, and the sample size was greater than five times the number of cells for all analyses. We then examined the associations of colonizing and abscess MRSA isolates with pulsed-field types, the presence of PVL, the presence of ACME, the presence of type SCCmec, and antimicrobial susceptibility, using the 2 contingency test and Fisher s exact test where indicated. To evaluate the impact of epidemiological variables on MRSA colonization, we performed 2 contingency tests. Multivariate analysis for significant variable associations was assessed using logistic regression with a type I error rate of Since these MRSA isolates were derived from an intervention trial, we also analyzed only the placebo-arm isolates using a Bonferroni correction for multiple comparisons to adjust for an inflated type I error rate. We used SPSS statistical software, version 14.0 (SPSS, Chicago, IL), for our analysis. RESULTS Characteristics of colonization isolates. Of the 4,003 eligible soldiers, 3,447 (86%) participated in the study and 556 declined (10). At the initial nasal culture, 134 (3.9%) of the participants were found to have nasal colonization with MRSA, and 1,316 (38%) were colonized with methicillin-susceptible Staphylococcus aureus (MSSA). Seventy-one (53%) of the 134 MRSA-colonized participants were colonized with the USA300 pulsed-field type (Table 1.). USA800 was the second most common pulsed-field type, found in 45 participants (34%), and USA600 accounted for colonization in 12 participants (9%). Pulsed-field types colonizing only one participant each included USA100, USA400, USA700, and USA1100. Two isolates possessed undefined PFGE clonal types. Of the 134 subjects colonized with MRSA, 65 (49%) carried a PVLpositive strain, 64 (48%) carried an ACME-positive strain, and 119 (89%) carried a type IV SCCmec-positive strain (Table 1). USA300 was more highly associated with PVL than the other colonizing MRSA pulsed-field types, as PVL was found in 62 of 71 (87%) USA300 colonizing isolates and only 3 of 63 (5%) other colonizing pulsed-field types (P 0.001). Similarly, ACME was found in 57 of 71 (80%) USA300 colonizing isolates and only 7 of 63 (11%) other colonizing pulsed-field types (P 0.001). Of the 3,447 participants who enrolled, 3,066 (89%) were available for follow-up. At the second nasal culture, 78 (2.5%) of the 3,066 participants were found to have nasal colonization with MRSA. Thirty-five (45%) of the 78 MRSA-colonized participants were colonized with the USA300 pulsed-field type. USA800 was the second most common pulsed-field type, found in 30 participants (39%), and USA600 accounted for colonization in 7 participants (9%). Other pulsed-field types included USA100 (one participant) and USA400 (four participants), and we could not determine the pulsed-field type of one isolate. Characteristics of MRSA abscess isolates. Of the 3,066 participants who completed the investigation, 39 developed culture-proven MRSA soft-tissue abscesses. USA300 caused a significant number of infections, as 38 of the 39 (97%) isolates

3 942 ELLIS ET AL. J. CLIN. MICROBIOL. TABLE 2. Potential risk factors identified for colonization with MRSA after univariate analysis e Risk factor % (no.) MRSA colonized (n 134) % (no.) not MRSA colonized (n 3,313) P value Antimicrobial use in the past 6 mo 55 (73) 44 (1,448) 0.02 a Antimicrobial use at time of nasal culture 2 (3) 1 (46) 0.55 Lived with a person with chronic illness b in the prior yr 14 (19) 13 (437) 0.33 Lived with person who worked in/was a patient in a hospital 29 (39) 29 (944) 0.88 in the prior yr Lived with a nursing home resident in the prior yr 6 (7) 5.0 (166) 0.78 Hospitalized in the prior yr 19 (25) 9 (291) a Worked in a health care facility in the prior yr 15 (20) 14 (457) 0.65 Lived with children under 16 yr old in the prior yr 56 (75) 53 (1,763) 0.53 History of SSTI in the past 6 mo 13 (18) 5 (162) a Reported avg of less than one daily shower c 1 (1) 1 (20) 0.43 Reported a history of sharing towels 8 (10) 9 (295) 0.56 Reported a history of sharing soap 8 (11) 10 (331) 0.24 Participated in contact sports in the prior yr d 28 (37) 27 (885) 0.59 a The association was statistically different from results for colonized subjects (P 0.05) and was included in multivariate analysis. b Defined as someone with asthma, chronic obstructive pulmonary disease, a history of organ transplant, vascular disease, diabetes, or someone receiving dialysis. c Average number of daily showers taken during basic training. d Defined as football, wrestling, lacrosse, or soccer. e Percentages may not total 100 due to rounding. cultured from the MRSA abscesses were USA300 (P 0.001) (Table 1). One abscess was caused by a USA800 strain. PVL was present in 38 of 39 (97%) abscess isolates overall, and of the USA300 abscess isolates, 38 of 38 (100%) were PVL positive. Of the 39 participants who developed MRSA abscesses, 11 participants had the identical MRSA strain recovered from the anterior nares at either the initial or terminal nasal screening culture. Of these 11 isolates, 10 were USA300 and 1 was USA800. The remaining 28 participants did not have MRSA nares colonization detected at either sampling. Comparison between colonizing and abscess isolates. There was a significant difference between the colonizing pulsed-field types and the MRSA abscess pulsed-field types, as USA300 was more likely to be associated with abscess development than with colonization (P 0.001) (Table 1). In terms of virulence and resistance properties, there were significant differences between colonizing isolates and the MRSA abscess isolates in terms of PVL positivity (65 of 134 [49%] and 38 of 39 [97%]; P 0.001), ACME positivity (64 of 134 [48%] and 34 of 39 [87%]; P 0.001), and type IV SCCmec positivity (119 of 134 [89%] and 39 of 39 [100%]; P 0.03) (Table 1). Additionally, 66 of 134 colonizing isolates, and 20 of 39 abscess isolates, were from the placebo arm of the trial. When only these placebo-arm isolates were analyzed, there were significant differences between colonizing isolates and the MRSA abscess isolates for USA300 (33 of 66 [50%] and 19 of 20 [95%]; P 0.001), for PVL positivity (28 of 66 [42%] and 19 of 20 [95%]; P 0.001), and for ACME positivity (27 of 66 [41%] and 17 of 20 [85%]; P 0.001). Finally, in the treated patients who were colonized with MRSA at the initial screening, there were two MRSA abscesses in the placebo group and three MRSA abscesses in the mupirocin group. All five abscesses were USA300, and all abscess isolates had the same PFGE pattern as the participant s colonizing isolate. Risk factors for MRSA colonization. After bivariate correlational analysis, MRSA-colonized participants were more likely to have received antibiotics in the past 6 months, were more likely to have been hospitalized in the prior year, and were more likely to have a history of previous SSTI in the past 6 months (Table 2). After multivariate analysis using logistic regression, the significant risk factors for MRSA colonization were a history of SSTI and a history of hospitalization (Table 3). Of the 134 participants with MRSA colonization, 18 (13%) reported a history of SSTI within the prior 6 months. Of these 18 participants, 11 initially were colonized with USA300, and 7 initially were colonized with a non-usa300 pulsed-field type (5 with USA800 and 2 with USA600). The association for having a history of SSTI between USA300-colonized participants and non-usa300-colonized participants was not statistically significant. Of the 134 MRSA-colonized participants, 25 (19%) reported a history of admission to a hospital in the prior year. The causes for the admission of these MRSA-colonized participants were the following: respiratory tract infection, 12; orthopedic injury, 7; SSTI, 3; cholecystectomy, 1; pelvic inflammatory disease, 1; and concussion, 1. The initial colonization results of these 25 participants were the following: USA300, 12; USA800, 12; and USA600, 1. The association of having a history of hospital admission between USA300-colonized participants and non-usa300-colonized participants was not statistically significant. Antimicrobial susceptibility results. MRSA susceptibilities by pulsed-field type and whether the isolates were colonizing or abscess strains are described in Table 4. Clindamycin sus- TABLE 3. Results of multivariate analysis using logistic regression on the risk factors for colonization with MRSA Risk factor % (no.) positive for risk factor Multivariate analysis odds ratio (95% confidence interval) P value Antimicrobial use in 55 (73) 0.98 ( ) 0.93 the past 6 mo Hospitalization in the 19 (25) 2.0 ( ) prior yr SSTI in the past 6 mo 13 (18) 2.1 ( ) 0.02

4 VOL. 47, 2009 MRSA MOLECULAR EPIDEMIOLOGY AND VIRULENCE IN SOLDIERS 943 TABLE 4. Number of MRSA isolates that were susceptible to selected antimicrobial agents d No. of susceptible isolates/total no. (%) Antimicrobial Colonizing Abscess USA300 USA800 USA600 Other PFT a Overall USA300 USA800 Overall Vancomycin 71/71 (100) 45/45 (100) 12/12 (100) 6/6 (100) 134/134 (100) 38/38 (100) 1/1 (100) 39/39 (100) Rifampin (rifampicin) 71/71 (100) 45/45 (100) 12/12 (100) 6/6 (100) 134/134 (100) 38/38 (100) 1/1 (100) 39/39 (100) TMP-SMX 71/71 (100) 45/45 (100) 12/12 (100) 6/6 (100) 134/134 (100) 38/38 (100) 1/1 (100) 39/39 (100) Tetracycline 66/71 (93) 43/45 (96) 12/12 (100) 5/6 (83) 126/134 (94) 38/38 (100) 1/1 (100) 39/39 (100) Ciprofloxacin 39/71 (55) 33/45 (73) 12/12 (100) 3/6 (50) 87/134 (65) 22/38 (58) 1/1 (100) 23/39 (59) Linezolid 71/71 (100) 45/45 (100) 12/12 (100) 6/6 (100) 134/134 (100) 38/38 (100) 1/1 (100) 39/39 (100) Clindamycin b,c 62/71 (87) 38/45 (84) 12/12 (100) 5/6 (83) 117/134 (87) 38/38 (100) 1/1 (100) 39/39 (100) Erythromycin 3/71 (4) 7/45 (16) 9/12 (75) 2/6 (33) 21/134 (16) 2/38 (5) 0/1 (0) 2/39 (5) Mupirocin 71/71 (100) 45/45 (100) 12/12 (100) 6/6 (100) 134/134 (100) 38/38 (100) 1/1 (100) 39/39 (100) a Other PFT isolates included USA100 (n 1), USA400 (n 1), USA700 (n 1), USA1100 (n 1), and two nontyped isolates. b For the association of clindamycin susceptibility to abscess isolates, P (95% confidence interval, 0.69 to 0.82). c Four of 39 (10%) abscess isolates showed inducible clindamycin resistance (USA300, 3 of 38, 8% ; USA800, 1 of 1 100% ). Twenty-two of 134 colonizing isolates showed inducible clindamycin resistance (USA300, 4 of % ; USA800, 17 of 45 38% ; USA600, 0 of 12; other PFTs, 1 of 6 17% ). d Percentages may not total 100 due to rounding. PFT, pulsed-field type; TMP-SMX, trimethoprim-sulfamethoxazole. ceptibility was more likely to be found in abscess isolates than in colonizing isolates (P 0.02). DISCUSSION In this prospective investigation, we have demonstrated that although many MRSA strains may be circulating within a population, USA300 is the most likely pulsed-field type to cause skin and soft-tissue abscesses. Additionally, this study strengthens the notion that PVL and ACME are important virulence factors for MRSA for soft-tissue abscess development. Prior investigations have identified USA300 as a particularly virulent pulsed-field type, causing the majority of reported MRSA infections in community settings (13, 20, 21, 24, 28, 31). USA300 also is emerging as a significant hospital-associated pathogen (24, 36, 37, 39). Additionally, Montgomery et al. recently have shown, in a necrotizing pneumonia model in rats, that USA300 demonstrated greater virulence and lethality than a comparator strain, USA400 (30). Our findings prospectively support the concept that USA300 is the most virulent clone, as it was the pulsed-field type most responsible for infections among those strains that were found to be colonizing soldiers. Although it comprised little more than half of the colonizing isolates in our participants (53%), it was responsible for a significantly disproportionate number (97%) of skin and soft-tissue abscesses (P 0.001). As with other S. aureus strains, USA300 possesses numerous purported virulence determinants, including exotoxins, adhesins, proteases, lipases, and accessory gene regulation, but it is unclear if there is one factor that makes USA300 so pathogenic (4 7, 30). The overall fitness and virulence of USA300 most likely is due to a multitude of factors acting in concert. Two important virulence determinants appear to be PVL and ACME. Because PVL often is found in CA-MRSA infections, many authors posit that it is a cornerstone of CA-MRSA s pathogenicity, in particular that of the USA300 clone (1, 13, 20, 28, 29, 42). There is considerable clinical evidence that points to PVL s importance. In a cumulative total of 150 isolates from three large studies, PVL was found in all of the CA-MRSA isolates studied (8, 21, 42). In an investigation conducted by Moran et al., 213 of 218 MRSA isolates tested possessed PVL (31). In our study, PVL was found in only 49% of colonizing isolates but in 97% of abscess isolates (P 0.001). PVL is a bicomponent exotoxin that causes dermal necrosis and possesses particular cytolytic activity against neutrophils and monocytes (38), and whether caused by MRSA or MSSA, it is associated with suppurative cutaneous disease and necrotizing infections (15, 19, 45). In one report of surgically drained community-associated soft-tissue abscesses, PVL was found in 89% of 48 MSSA isolates tested (19). Likewise, in an investigation of purulent SSTI in university-affiliated emergency departments, 23 of 55 (42%) MSSA isolates tested possessed PVL (31). Although PVL commonly is found in S. aureus isolates responsible for suppurative infections, currently it is found in fewer than 15% of colonizing MRSA isolates in the general community (17). The overall significance of PVL in experimental animal models has yet to be clearly determined. In a murine model conducted by Voyich et al., PVL did not appear to be a significant factor in the formation of skin abscesses (43). However, Labandeira-Rey et al. found in a murine pneumonia model that PVL appears to be an important virulence determinant in the development of necrotizing pneumonia (22). In our investigation, ACME was detected in 48% of colonizing isolates and 87% of skin and soft-tissue abscess isolates (P 0.001). ACME, which is found adjacent to SCCmec, recently has been noted to be a potentially important virulence factor (5, 6). ACME appears to have been horizontally acquired from Staphylococcus epidermidis and is thought to augment virulence by enhancing growth and survival on human skin (5). In a rabbit bacteremia model using isogenic USA300 strains with type IV SCCmec and ACME deletions, Diep et al. demonstrated AMCE s importance (6). In this elegant study, the deletion of ACME resulted in diminished pathogenicity, whereas the absence of type IV SCCmec did not (6). ACME may be found in MSSA and MRSA isolates, including clones other than USA300 (9, 16), but it appears to be present in nearly all USA300 isolates (6, 16). There is a strong association between ACME and USA300, but the overall significance of ACME, like that of PVL, has yet to be fully determined. It is not entirely clear what patient factors are associated

5 944 ELLIS ET AL. J. CLIN. MICROBIOL. with the acquisition of MRSA colonization within the community. Indeed, risk factors appear to vary even with gender (17). In our population, we found that MRSA-colonized participants were more likely to report a history of hospitalization and a history of SSTI. In a previous investigation, we also found that a history of SSTI had been a risk factor for colonization (11). We also noted that colonized participants were more likely to report a history of antibiotic use in the past 6 months; however, this was not statistically significant in multivariate analysis. Similarly to our findings, Hidron et al. reported that risk factors for MRSA colonization at the time of admission to an urban Atlanta hospital included antimicrobial use, a history of hospitalization, and a diagnosis of SSTI (18). Gorwitz et al. also recently reported that among men, recent health care exposure was associated with MRSA colonization (17). In contrast to our study, a recent meta-analysis demonstrated that previous antimicrobial exposure was a risk factor for MRSA colonization (40). Notably, several factors that have been postulated to increase the risk for MRSA colonization, namely the sharing of towels and soap and a history of contact sports, were not associated with MRSA colonization in our investigation (20, 33). A question raised by our study is that if USA300 is more virulent than other pulsed-field types, why is it not able to handily outcompete these other strains in the anterior nares? In this population, roughly one-half of participants were colonized with MRSA pulsed-field types other than USA300, yet these non-usa300 pulsed-field types were responsible for only one of the observed skin and soft-tissue abscesses. There are several possible explanations for this discrepancy. First, nasal colonization with USA300 may be transient, or the time between colonization and infection may be brief. Our sampling technique may have been insufficient to detect all colonization, and the limited sampling in our investigation could fail to identify this dynamic intermittent carrier state (44). Nevertheless, we were able to find that 11 of the 39 participants who developed USA300 MRSA abscesses were colonized with the same strain at either the initial or terminal anterior nares culture. Second, it also is possible that USA300 is simply not a persistent nasal colonizer or that it preferentially colonizes other anatomic sites. For example, Kazakova et al. found no nasal colonization during an outbreak investigation of USA300 abscesses among professional football players (20). Additionally, extranasal sites of colonization and environmental exposures may serve as important reservoirs for USA300 (27). Our noting a wide variety of MRSA strains in our study population is consistent with previous observations. Coombs et al. reported 22 different CA-MRSA clones circulating in Western Australia, which builds on similar findings in that nation (3, 34). The proportions of the various pulsed-field types noted in our study population were different than those noted recently by Gorwitz et al. in the National Health and Nutrition Examination Survey (NHANES) of S. aureus nasal colonization (17). In our investigation, USA300 accounted for 53% of the colonizing MRSA isolates, and there was only one USA100 clone among the group of 134 colonizing isolates. In contrast, in the NHANES S. aureus survey, among 208 colonizing MRSA isolates, 50% were USA100 and less than 20% were USA300 (17). The prevalence of USA300 in our population was more comparable to that found in the Atlanta metropolitan area, where USA300 was found in 30% of nares-colonizing isolates (18). Similarly to our investigation in which USA800 represented 34% of the colonizing isolates, Gorwitz et al. found USA800 to be the second most prevalent pulsed-field type (15.8%) (17). The high prevalence of USA800, which generally has been considered a hospital-associated clone (25), points to the changing epidemiology of MRSA within the community and further blurs the nomenclature of CA-MRSA. A limitation of our study is that it was undertaken as part of a larger intervention trial. This intervention may have altered nasal flora and potentially changed the population of isolates that led to subsequent infection. We feel that the effect likely was minimal, as our results remained significant when we analyzed only the placebo arm. Additionally, all MRSA colonizing isolates were susceptible to mupirocin. Our investigation would have been strengthened by culturing the anterior nares of participants when they presented to health care providers for skin and soft-tissue abscesses. Sampling other anatomic sites may have captured more participants who were colonized, and sampling common environmental contact areas may have identified significant fomites (26, 27). In conclusion, although many MRSA pulsed-field types may be circulating in a population, USA300 is the predominant cause of skin and soft-tissue abscesses in soldiers when evaluated prospectively. Our findings suggest that among other virulence factors, PVL and ACME play a significant role in the disease process. This work provides important additional insights into the acquisition of MRSA colonization and its impact on the development of infections. More remains to be learned about the dynamic interaction between the human host and MRSA virulence factors. ACKNOWLEDGMENTS We thank the soldiers of the 232nd Medical Battalion, Fort Sam Houston, TX. Without the spirit of volunteerism of these combat medics, this work would not have been done. We thank Cindy Kelly and Xin Yu, who contributed to the molecular analysis of this investigation. We thank Linda McDougal and Herminia de Lencastre for technical assistance. We thank Larry Price, who aided in statistical analysis. REFERENCES 1. Boyle-Vavra, S., and R. S. Daum Community-acquired methicillinresistant Staphylococcus aureus: the role of Panton-Valentine leukocidin. Lab. Investig. 87: Clinical and Laboratory Standards Institute/National Committee for Clinical Laboratory Standards Performance standards for antimicrobial disk susceptibility tests, M2 A9. Clinical and Laboratory Standards Institute, Wayne, PA. 3. Coombs, G. W., J. C. Pearson, F. G. O Brien, R. J. Murray, W. B. Grubb, and K. J. Christiansen Methicillin-resistant Staphylococcus aureus clones, Western Australia. Emerg. Infect. Dis. 12: Diep, B., H. Carleton, R. Chang, G. Sensabaugh, and F. Perdreau-Remington Roles of 34 virulence genes in the evolution of hospital and community-associated strains of methicillin-resistant Staphylococcus aureus. J. Infect. Dis. 193: Diep, B. A., S. R. Gill, R. F. Chang, T. H. Phan, J. H. Chen, M. G. Davidson, F. Lin, J. Lin, H. A. Carleton, E. F. Mongodin, G. F. Sensabaugh, and F. Perdreau-Remington Complete genome sequence of USA 300, an epidemic clone of community-acquired methicillin-resistant Staphylococcus aureus. Lancet 367: Diep, B. A., G. G. Stone, L. Bauino, C. J. Graber, A. Miller, S. des Etages, A. Jones, A. M. Pallazzolo-Balance, F. Perdreau-Remington, G. F. Sensabaugh, F. R. DeLeo, and H. F. Chambers The arginine catabolic mobile element and staphylococcal chromosomal cassette mec linkage: convergence of virulence and resistance in the USA300 clone of methicillinresistant Staphylococcus aureus. J. Infect. Dis. 197: Dinges, M. M., P. M. Orwin, and P. M. Schlievert Exotoxins of Staphylococcus aureus infections. Clin. Microbiol. Rev. 13:16 34.

6 VOL. 47, 2009 MRSA MOLECULAR EPIDEMIOLOGY AND VIRULENCE IN SOLDIERS Dufour, P., Y. Gillet, M. Bes, G. Lina, F. Vandenesch, D. Floret, J. Etienne, and H. Richet Community-acquired methicillin-resistant Staphylococcus aureus infections in France: emergence of a single clone that produces Panton-Valentine leukocidin. Clin. Infect. Dis. 35: Ellington, M. J., L. Yearwood, M. Ganner, C. East, and A. M. Kearns Distribution of the ACME-arcA gene among methicillin-resistant Staphylococcus aureus from England and Wales. J. Antimicrob. Chemother. 61: Ellis, M. W., M. E. Griffith, D. P. Dooley, J. C. McLean, J. H. Jorgensen, J. E. Patterson, K. A. Davis, J. S. Hawley, J. A. Regules, R. G. Rivard, P. J. Gray, J. M. Ceremuga, M. A. DeJoseph, and D. R. Hospenthal Targeted intranasal mupirocin to prevent community-associated methicillin-resistant Staphylococcus aureus colonization and infection in soldiers: a randomized controlled trial. Antimicrob. Agents Chemother. 51: Ellis, M. W., D. R. Hospenthal, D. P. Dooley, P. J. Gray, and C. K. Murray Natural history of community-acquired methicillin-resistant Staphylococcus aureus colonization and infection in soldiers. Clin. Infect. Dis. 39: Flayhart, D., J. F. Hindler, D. A. Bruckner, G. Hall, R. K. Shrestha, S. A. Vogel, S. S. Richter, W. Howard, R. Walther, and K. C. Carroll Multicenter evaluation of BBL CHROMagar MRSA medium for direct detection of methicillin-resistant Staphylococcus aureus from surveillance cultures of the anterior nares. J. Clin. Microbiol. 43: Francis, J. S., M. C. Doherty, U. Lopatin, C. P. Johnston, G. Sinha, T. Ross, M. Cai, N. N. Hansel, T. Perl, J. R. Ticehurst, K. Carroll, D. L. Thomas, E. Nuermberger, and J. G. Bartlett Severe community-onset pneumonia in healthy adults caused by methicillin-resistant Staphylococcus aureus carrying the Panton-Valentine leukocidin genes. Clin. Infect. Dis. 40: Fridkin, S. K., J. C. Hageman, M. Morrison, L. T. Sanza, K. Como-Sabetti, J. A. Jernigan, K. Harriman, L. H. Harrison, R. Lynfield, and M. M. Farley Methicillin-resistant Staphylococcus aureus in three communities. N. Engl. J. Med. 352: Gillet, Y., B. Issartel, P. Vanhems, P. J. C. Fournet, G. Lina, M. Bes, F. Vandenesch, Y. Piemont, N. Brousse, D. Floret, and J. Etienne Association between community-acquired Staphylococcus aureus strains carrying gene for Panton-Valentine leukocidin and highly lethal necrotizing pneumonia in young immunocompetent patients. Lancet 359: Goering, R. V., L. K. McDougal, G. E. Fosheim, K. K. Bonnstetter, D. J. Wolter, and F. C. Tenover Epidemiologic distribution of the arginine catabolic mobile element among selected methicillin-resistant Staphylococcus aureus and methicillin-susceptible Staphylococcus aureus isolates. J. Clin. Microbiol. 45: Gorwitz, R. J., D. Kruszon-Moran, S. K. McAllister, G. McQuillan, L. K. McDougal, G. E., Fosheim, B. J. Jensen, G. Killgore, F. C. Tenover, and M. J. Kuehnert Changes in the prevalence of Staphylococcus aureus nasal colonization in the United States, J. Infect. Dis. 197: a.Hart, A. C., and C. A. Hopkins ICD-9-CM: international classification of diseases, 9th revision, clinical modification, 6th ed. St. Anthony Publishing, Boston, VA. 18. Hidron, A. I., E. V. Kourbatova, J. S. Halvosa, B. J. Terrell, L. K. McDougal, F. C. Tenover, H. M. Blumberg, and M. D. King Risk factors for colonization with methicillin-resistant Staphylococcus aureus (MRSA) in patients admitted to an urban hospital: emergence of community-associated MRSA nasal carriage. Clin. Infect. Dis. 41: Issartel, B., A. Tristan, S. Lechevallier, G. Lina, B. Garin, F. Lacassin, M. Bes, F. Vandenesch, and J. Etienne Frequent carriage of Panton- Valentine leucocidin genes by Staphylococcus aureus isolates from surgically drained abscesses. J. Clin. Microbiol. 43: Kazakova, S. V., J. C. Hageman, M. Matava, A. Srinivasan, L. Phelan, B. Garfinkel, T. Boo, S. McAllister, J. Anderson, B. Jensen, D. Dodson, D. Lonsway, L. K. McDougal, M. Arduino, V. J. Fraser, G. Killgore, F. C. Tenover, S. Cody, and D. B. Jernigan A clone of methicillin-resistant Staphylococcus aureus among professional football players. N. Engl. J. Med. 352: King, M. D., B. J. Humphrey, Y. F. Wang, E. V. Kourbatova, S. M. Ray, and H. M. Blumberg Emergence of community-acquired methicillin-resistant Staphylococcus aureus USA 300 clone as the predominant cause of skin and soft-tissue infections. Ann. Intern. Med. 144: Labandeira-Rey, M., F. Couzon, S. Boisset, E. L. Brown, M. Bes, Y. Benito, E. M. Barbu, M. Hook, J. Etienne, F. Vandenesch, and M. G. Bowden Staphylococcus aureus Panton Valentine leukocidin causes necrotizing pneumonia. Science 315: Lina, G., Y. Piemont, F. Godail-Gamot, M. Bes, M. Peter, V. Gauduchon, F. Vandenesch, and J. Etienne Involvement of Panton-Valentine leukocidin-producing Staphylococcus aureus in primary skin infections and pneumonia. Clin. Infect. Dis. 29: Liu, C., C. J. Graber, M. Karr, B. A. Diep, L. Basuino, B. S. Schwartz, M. C. Enright, S. J. O Hanlon, J. C. Thomas, F. Perdreau-Remington, S. Gordon, H. Gunthorpe, R. Jacobs, P. Jensen, G. Leoung, J. S. Rumack, and H. F. Chambers A population-based study of the incidence and molecular epidemiology of methicillin-resistant Staphylococcus aureus disease in San Francisco, Clin. Infect. Dis. 46: McDougal, L. K., C. D. Steward, G. E. Killgore, J. M. Chaitram, S. K. McAllister, and F. C. Tenover Pulsed-field gel electrophoresis typing of oxacillin-resistant Staphylococcus aureus isolates from the United States: establishing a national database. J. Clin. Microbiol. 41: Mertz, D., R. Frei, B. Jaussi, A. Tietz, C. Stebler, U. Fluckiger, and A. F. Widmer Throat swabs are necessary to reliably detect carriers of Staphylococcus aureus. Clin. Infect. Dis. 45: Miller, L. G., and B. A. Diep Colonization, fomites, and virulence: rethinking the pathogenesis of community-associated methicillin-resistant Staphylococcus aureus infection. Clin. Infect. Dis. 46: Miller, L. G., F. Perdreau-Remington, G. Rieg, M. Sheherbano, J. Perlroth, A. S. Bayer, A. W. Tang, T. O. Phung, and B. Spellberg Necrotizing fasciitis caused by community-associated methicillin-resistant Staphylococcus aureus in Los Angeles. N. Engl. J. Med. 352: Moellering, R The growing menace of community-acquired methicillin-resistant Staphylcoccus aureus. Ann. Intern. Med. 144: Montgomery, C. P., S. Boyle-Vavra, P. A. Adem, J. C. Lee, A. N. Husain, J. Clasen, and R. S. Daum Comparison of community-associated methicillin-resistant Staphylococcus aureus pulsotypes USA300 and USA400 in a rat model of pneumonia. J. Infect. Dis. 198: Moran, G. J., A. Krishnadasan, R. J. Gorwitz, G. E. Fosheim, L. K. McDougal, R. B. Carey, and D. A. Talan Methicillin-resistant S. aureus infections among patients in the emergency department. N. Engl. J. Med. 355: Naimi, T. S., K. H. LeDell, K. Como-Sabetti, S. M. Borchardt, D. J. Boxrud, J. Etienne, S. K. Johnson, F. Vandenesch, S. Fridkin, C. O Boyle, R. N. Danila, and R. Lynfield Comparison of community- and health careassociated methicillin-resistant Staphylococcus aureus infection. JAMA 290: Nguyen, D. M., L. Mascola, and E. Bancroft Recurring methicillin-resistant Staphylococcus aureus in a football team. Emerg. Infect. Dis. 11: O Brien, F. G., T. T. Lim, F. N. Chong, G. W. Coombs, M. C. Enright, D. A. Robinson, A. Monk, B. Said-Salim, B. N. Kreiswirth, and W. B. Grubb Diversity among isolates of methicillin-resistant Staphylococcus aureus in Australia. J. Clin. Microbiol. 42: Oliveira, D. C., and H. de Lencastre Multiplex PCR strategy for rapid identification of structural types and variants of the mec element in methicillin-resistant Staphylococcus aureus. Antimicrob. Agents Chemother. 46: Patel, M., R. A. Kumar, A. M. Stamm, C. J. Hoesley, S. A. Moser, and K. B. Waites USA300 genotype community-associated methicillin-resistant Staphylococcus aureus as a cause of surgical site infections. J. Clin. Microbiol. 45: Popovich, K. J., R. A. Winstein, and B. Hota Are community-associated methicillin resistant Staphylococcus aureus (MRSA) strains replacing traditional nosocomial MRSA strains? Clin. Infect. Dis. 46: Prevost, G., G. Menestrina, D. A. Colin, S. Werner, S. Bronner, M. Dalla Serra, L. Moussa, M. Coraiola, A. Gravet, and H. Monteil Staphylococcal bicomponent leucotoxins, mechanism of action, impact on cells and contribution to virulence, p In G. Menestrina, M. Dalla Serra, and P. Lazarovici, (ed.), Pore-forming peptides and proteins. Taylor & Francis Group, London, United Kingdom. 39. Seybold, U., E. V. Kourbatova, J. G. Johnson, S. J. Halvosa, Y. F. Wang, M. D. King, S. M. Ray, and H. M. Blumberg Emergence of community-associated methicillin-resistant Staphylococcus aureus USA300 genotype as a major cause of health care-associated blood stream infections. Clin. Infect. Dis. 42: Tacconelli, E., G. De Angelis, M. A. Cataldo, E. Pozzi, and R. Cauda Does antibiotic exposure increase the risk of methicillin-resistant Staphylococcus aureus isolation? A systematic review and meta-analysis. J. Antimicrob. Chemother. 61: Tenover, F. C., R. D. Abreit, R. V. Goering, P. A. Mickelsen, B. E. Murray, D. H. Persing, and B. Swaminathan Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J. Clin. Microbiol. 33: Vandenesch, F., T. Naimi, M. Enright, G. Lina, G. R Ninno, H. Heffernan, N. Liassine, M. Bes, T. Greenland, M. Reverdy, and J. Etienne Community-acquired methicillin-resistant Staphylococcus aureus carrying Panton- Valentine leukocidin genes: worldwide emergence. Emerg. Infect. Dis. 9: Voyich, J. M., M. Otto, B. Mathema, K. R. Braughton, A. R. Whitney, D. Welty, R. D. Long, D. W. Dorward, D. J. Gardner, G. Lina, B. N. Kreiswirth, and F. R. DeLeo Is Panton-Valentine leukocidin the major virulence determinant in community-associated methicillin-resistant Staphylococcus aureus disease? J. Infect. Dis. 194: Wertheim, H. F., D. C. Melles, M. C. Vos, W. van Leeuwen, A. van Belkum, H. A. Verbrugh, and J. L. Nouwen The role of nasal carriage in Staphylococcus aureus infections. Lancet Infect. Dis. 5: Yamasaki, O., J. Kaneko, S. Morizane, H. Akiyama, J. Arata, S. Narita, J. Chiba, Y. Kamio, and K. Iwatsuki The association between Staphylococcus aureus strains carrying Panton-Valentine leukocidin genes and the development of deep seated follicular infection. Clin. Infect. Dis. 40: