Frequent Carriage of Panton-Valentine Leucocidin Genes by Staphylococcus aureus Isolates from Surgically Drained Abscesses

ABSTRACT Between 1 February and 15 April 2002, 95 patients were admitted to Gaston Bourret Territorial Hospital (New Caledonia, France) for drainage of community-acquired soft tissue abscesses. Staphylococcus aureus was detected in 68 cases (72%). Two-thirds of the patients with S. aureus infection had furuncles, which were located on the limbs in 82% of cases. The median interval between symptom onset and hospital admission was 5.7 days. Three-quarters of the patients were Melanesians living in tribes. Fifty-four S. aureus isolates were screened for toxin genes. Panton-Valentine leucocidin (PVL) genes were detected in 48 isolates (89%), the exfoliative toxin A gene was detected in 1 isolate, and no toxin genes were detected in 4 isolates. S. aureus nasal carriage was detected in 39.7% of patients with S. aureus infections. Two infecting S. aureus strains and two nasal carriage strains were resistant to methicillin. Comparative pulsed-field gel electrophoresis, performed in 16 cases, showed that five of six patients with PVL-positive nasal carriage strains were infected by the same strains. In contrast, 8 of 10 patients with PVL-negative nasal carriage strains were infected by PVL-positive strains. PVL genes thus appear to be a major virulence factor in both primary and secondary S. aureus skin infections.

Skin and soft tissue infections caused by Staphylococcus aureus are frequent worldwide. These infections are considered "primary" in patients with no preexisting skin lesion and "secondary" in other cases (25). Folliculitis, furuncles, and impetigo are examples of primary S. aureus infections. Furuncles are associated with S. aureus strains that produce the Panton-Valentine leucocidin (PVL) (10,18), while bullous impetigo is associated with strains that produce exfoliative toxins. Secondary skin infections can occur in patients with skin trauma, surgical incisions, skin ulcers, or eczema. These secondary infections are not generally associated with specific toxins, but the proinflammatory effects of superantigenic toxins (e.g., toxic shock syndrome toxin and staphylococcal enterotoxins) may contribute to the clinical severity of the secondary infection, especially in patients with eczema (21).
Less than 2% of the consecutive strains isolated in Strasbourg General Hospital Microbiology Laboratory, Strasbourg, France, were PVL positive (28), but that study included isolates from patients with community-and hospital-acquired infections, primary and secondary skin and soft tissue infections, and systemic infections.
Soft tissue infections are responsible for about 500 stays per annum in Gaston Bourret Territorial Hospital, New Caledonia, France. Most are abscesses that require surgical incision and drainage. This high prevalence allowed us to conduct a large prospective clinical and microbiological study of PVL in primary and secondary soft tissue abscesses caused by S. aureus. Patients with abscesses that occurred after surgery, intravenous or intramuscular injections, or indwelling catheter placement were excluded, together with patients who lived in institutions or who were hospitalized during the month preceding the current infection. Infections were considered primary when the patient noted no skin damage prior to the appearance of the abscess and secondary in other cases.

MATERIALS AND METHODS
The following data were recorded in each case: demographic characteristics, underlying conditions (diabetes mellitus, alcoholism, progressive neoplasia, steroid therapy, intravenous drug addiction, or a personal or familial history of furunculosis or abscess), hospitalization in the previous 3 months, antibiotic treatment before admission, recent skin damage (trauma, superficial wound, or puncture), clinical presentation, length of hospital stay, and number of surgical procedures. Abscess fluid was collected by swabbing drained material in the operating room. Blood cultures were performed in some cases. The anterior nares were swabbed to detect S. aureus carriage.
S. aureus identification, gene detection, and genotyping. S. aureus was identified on the basis of colony and microscopic morphology, coagulase testing with rabbit plasma (bioMérieux, Marcy l'Etoile, France), and the Staphyslide agglutination test (bioMérieux). Antimicrobial susceptibility was tested with the API ATB Staph system (bioMérieux). Strains were sent to the French National Reference Centre for Staphylococci and were grown on brain heart infusion agar or in brain heart infusion broth at 37°C overnight. Genomic DNA was used as the PCR target after extraction by a standard procedure (1); the DNA concentration was estimated spectrophotometrically (19). Sequences specific for exfoliative toxin genes (eta, etb), PVL genes (lukS-PV--lukF-PV), and accessory gene regulator alleles (agr-1 to agr-4) were detected by PCR, as described previously (13). The mecA gene, which codes for methicillin resistance, was detected by PCR, as described by Murakami et al. (22). Amplification of gyrA was used to confirm the quality of each DNA extract and the absence of PCR inhibitors (8). All PCR products were analyzed by electrophoresis through 1% agarose gels (Sigma, Saint Quentin Fallavier, France). Isolates were genotyped by pulsed-field gel electrophoresis (PFGE) by using the restriction enzyme SmaI, as described previously (11). The PFGE patterns were digitized and analyzed by using the Taxotron typing system (Institut Pasteur, France). Strain relatedness was interpreted by using published guidelines (30). Isolates that differed by no more than three fragments were considered subtypes of a given clonal type.
Statistical analysis. Categorical data were compared by the chi-square test or Fisher's exact test, while the equality of means was compared by the t test with SPSS software version 10.0 (SPSS Inc., Chicago, Ill.). P values of Ͻ0.05 were considered statistically significant. , Nocardia asteroides tendon sheath infection (n ϭ 1), and abscesses with no positive bacterial culture (n ϭ 19). The clinical and epidemiological characteristics differed significantly between patients with and without S. aureus infection (Table 1): the S. aureus group had a higher frequency of S. aureus nasal carriage (P ϭ 0.049), a possible shorter interval between symptom onset and hospitalization (5.7 days versus 10 days; P ϭ 0.117), and a higher frequency of primary infection (furuncles), while the non-S. aureus group had a higher frequency of secondary infection (P ϭ 0.001).

RESULTS
Clinical characteristics of patients with S. aureus skin abscesses. The 68 patients with S. aureus infections comprised 43 males and 25 females, with a mean age of 29.5 years (range, 1 to 80 years) ( Table 1). The patients were mainly Melanesians (51 cases; 75%) living in tribes (28 cases). Thirty-three patients (48.5%) had either a personal (21 cases) or a familial (12 cases) history of skin infections (furunculosis or abscess). Twenty-two patients noted a skin lesion before onset. Nineteen patients (27.9%) were febrile (temperature, Ͼ38°C) on hospital admission. The first sign of infection (known in 66 cases) was pain (35 cases; 52%), swelling (19 cases; 28%), or pruritus (12 cases; 18%). The mean interval between symptom onset and hospital admission was 5.7 days (median, 5 days; range, 1 to 15 days). Most infections were located on the limbs (56 cases [82%]; an upper limb in 32 cases and a lower limb in 24 cases). Three patients had multiple abscesses. S. aureus bacteremia was diagnosed in three cases; one case involved a young patient with myositis of the thigh and the right arm who required intensive care. All the infections healed after surgical drainage. More than one drainage procedure was necessary in five cases.

Bacteriology of S. aureus abscesses.
Among the 68 abscesses from which S. aureus was isolated, S. aureus was the only potential pathogen in 56 cases, while it was associated with Streptococcus pyogenes in 7 cases and with a gram-negative bacillus in 4 cases (Klebsiella oxytoca, Klebsiella pneumoniae, Proteus mirabilis, Enterobacter cloacae) and with Streptococcus agalactiae in 1 case. Only two S. aureus isolates (2.1%) were resistant to methicillin. Fifty-four of the 68 S. aureus isolates (38 from primary infections and 16 from secondary infections) were forwarded to the French Reference Centre for Staphylococci (the remaining 14 had not been stored frozen in New Caledonia). Comparative studies of the toxin gene profiles (PVL and exfoliative toxin genes) ( Table 2) showed no significant differences between isolates from primary and secondary  infections, and the 54 strains are therefore considered below as a single group. The PVL genes were detected in 48 strains (89%), none of which was methicillin resistant. The PVLpositive isolates had a diverse genetic background: 9 strains (19%) were agr group 1, 13 strains (27%) were agr group 3, and 26 strains (54%) were agr group 4. The exfoliative toxin A (eta) gene was detected in only 1 of the 54 strains, which was from a patient with an abscess of the toe and no signs of exfoliation; this isolate was susceptible to methicillin. The remaining five isolates did not harbor either the PVL genes or exfoliative toxin genes, but two were resistant to methicillin. S. aureus nasal carriage. S. aureus nasal carriage was found in 32 of the patients (33.7%), including 27 patients with S. aureus abscesses (39.7%). When the carriage population as a whole is considered, S. aureus carriage was significantly less frequent in patients recently exposed to antibiotics (44.5% versus 55.5%; P ϭ 0.017). Two of the S. aureus nasal isolates were resistant to methicillin; the two corresponding infections were not due to the same strain as the nasal isolate and occurred in patients with no classical risk factors for methicillinresistant S. aureus infection. PVL genes were less frequently detected in nasal carriage strains (6 of 21 cases tested; 28.6%) than in abscess isolates (48 of 54 cases; 89%) (P Ͻ 0.0001).
PFGE comparison of infecting and nasal carriage strains was possible in 16 cases (Fig. 1). The PFGE patterns of the infecting and the nasal carriage strains were identical in seven cases (43.7%), five of which were PVL positive. In the nine remaining cases, the PFGE patterns of the infecting and the nasal carriage strains were different: in seven cases (patients 2, 4, 5, 7, 9, 11, and 16) the nasal isolates were PVL negative and the infecting isolates were PVL positive; in one case (patient 6) the nasal and the infecting isolates were two different PVL-positive isolates; the last case (patient 1) had different PVL-negative strains from both sites. Hence, patients with nasal carriage of PVL-positive strains were frequently infected by the same strain, whereas patients carrying PVL-negative strains tended to be infected by PVL-positive strains (P ϭ 0.035).

DISCUSSION
This study involved 95 patients with community-acquired soft tissue abscesses requiring surgical drainage. Only surgically treated patients were studied, in order to avoid the risk of contamination associated with superficial sampling. S. aureus was detected in 72% of cases. Most patients had rapidly progressive primary infections (furuncles), with a median interval of only 5.7 days between symptom onset and hospital admission. PVL genes were detected in 89% of S. aureus isolates. The discrepancy with reports describing PVL as a very infrequent toxin (Ͻ2%) in S. aureus (28) is probably due to differences in patient selection (random patients versus patients with community-acquired soft tissue abscesses requiring surgical drainage) and in geographic area.
The link between PVL and severe abscesses was first described more than 70 years ago. PVL toxin was discovered by Van de Velde in 1894 (33) but was only clearly distinguished from hemolysins by its leukotoxic activity in 1932 in studies by Panton and Valentine (27), who noted an association between leucocidin (PVL) production and styes, carbuncles, and "pyaemic" infections. In 1936, Valentine reported that "S. aureus [isolates] which have succeeded in invading human tissue were found capable of producing in vitro considerable amounts of leucocidin" (31). Interest in staphylococcal leucocidin subsided for several decades, until Cribier et al. (7) demonstrated in 1992 that PVL was mainly associated with primary cutaneous infections and especially furuncles and abscesses. Cribier et al. (7) detected PVL by immunoassay in 43 S. aureus isolates from patients with skin infections. In 1999, Lina et al. (18) used PCR to screen 172 S. aureus isolates for PVL genes and confirmed the strong association with furunculosis and with necrotizing pneumonia in children and young adults. Clinical investigation made by Yamasaki et al. (36) revealed that PVL-positive S. aureus strains are involved in the development of multiple furuncles with more intense erythema, particularly in healthy young adults. The only report on the association of PVL with cutaneous abscesses included only six isolates (of which three were PVL positive) and offered no clinical information (18).
We found no difference in the prevalence of PVL genes between S. aureus isolates from primary and secondary skin infections. PVL has a dermonecrotic effect on both intact and damaged skin (35), damaging host cell membranes by the synergistic action of two classes of secretory proteins designated S and F. PVL-producing isolates produce the PVL-specific class S and F proteins (LUKS-PV and LUKF-PV). Injection of both components intradermally into rabbits induces severe inflammatory lesions, capillary dilation, chemotaxis, skin infiltration, polymorphonuclear leukocyte PMN karyorrhexis, and skin necrosis (6,35). PVL is also leukotoxic, by pore induction, for rabbit and human polymorphonuclear leukocytes and macrophages. The large number of secondary skin infections in our series may be due to frequent minor skin trauma among individuals in tribes.
The PVL genes are mainly associated with pandemic clones of true community-acquired methicillin-resistant S. aureus. This combination of PVL genes and methicillin resistance has not yet been detected in New Caledonia, even though multiple highly epidemic clones have been described on all the continents (9,10,32).
The overall nasal carriage rate of S. aureus found here (33.7%) is similar to that observed in the general population of industrialized countries (15). We found that patients with severe S. aureus skin infections were more likely than patients with non-S. aureus infections to be nasal carriers (39% and 18%, respectively), in keeping with findings presented in previous reports (12,17,23). Nasal carriage is considered a risk factor for S. aureus infection in patients undergoing surgery (34) and hemodialysis (20). In our study, in the 16 cases in which genotyping of paired nasal carriage and infecting strains was possible, genetic identity was found in seven cases, of which five were PVL positive, suggesting that subjects with nasal carriage of PVL-positive S. aureus isolates might be at risk of cutaneous infection.
Genotyping of the strains also revealed that several patients were infected with the same strain. We suspect that the transmission of strains between these patients in the closed community formed by tribes, as has been shown for other closed communities, such as an Alaskan village or sports teams (4,16,29). Moreover, PFGE typing has revealed a higher diversity among the PVL-negative strains than among the PVL-positive VOL. 43, 2005 PVL GENES IN S. AUREUS ABCESSES 3205 strains. We speculate that PVL-positive strains are more successful at spreading, as observed with PVL-positive community-acquired methicillin-resistant S. aureus (2,3,5,14,26,37). Lastly, in one case, the PFGE pattern of PVL-negative isolates (patient 10) was identical to that of a PVL-positive isolate (patient 4), suggesting that acquisition or deletion of the PVL phage occurred, in accordance with the known mobility of such elements (24). The colonizing and infecting isolates differed genetically in the other nine patients, in keeping with another study of community-acquired S. aureus pyoderma, in which the antibiotic susceptibility profiles of the infecting isolates differed from those of the nasal isolates in 51% of cases (23). In such cases, nasal carriage may simply reflect individual susceptibility to staphylococcal colonization and/or infection rather than a specific characteristic of certain strains.