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Journal of Clinical Microbiology, December 2006, p. 4436-4440, Vol. 44, No. 12
0095-1137/06/$08.00+0     doi:10.1128/JCM.01546-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Antimicrobial Susceptibility Patterns and Staphylococcal Cassette Chromosome mec Types of, as Well as Panton-Valentine Leukocidin Occurrence among, Methicillin-Resistant Staphylococcus aureus Isolates from Children and Adults in Middle Tennessee

Abdullah Kilic,^1,3 Haijing Li,¹ Charles W. Stratton,^1,2 and Yi-Wei Tang^1,2*

Departments of Medicine,¹ Pathology, Vanderbilt University Medical Center, Nashville, Tennessee 37232,² Gulhane Military Medical Academy, Ankara 06018, Turkey³

Received 25 July 2006/ Returned for modification 29 September 2006/ Accepted 11 October 2006

Top Abstract Introduction Materials and Methods Results Discussion References

 
Antimicrobial susceptibility patterns, Panton-Valentine leukocidin (PVL) occurrence, and staphylococcal cassette chromosome mec (SCCmec) types in methicillin-resistant Staphylococcus aureus (MRSA) strains isolated from children and adults at Vanderbilt University Medical Center during a 12-month period were evaluated. A total of 1,315 MRSA isolates were collected, of which 748 (36.7%) were recovered from children. Among all isolates, 448 (34.1%) were SCCmec-II, and 847 (64.4%) were SCCmec-IV. More SCCmec-IV isolates were recovered from children than SCCmec-II isolates (424 [50.1%] versus 50 [11.2%]; odds ration [OR] = 7.98; P < 0.000001). The PVL gene was detected in 93.6% of SCCmec-IV isolates, in contrast to 0.2% in SCCmec-II isolates. Within SCCmec-IV isolates, a statistically higher PVL occurrence was noticed in children (98.1%) than in adults (89.1%) (OR = 6.34; P < 0.000001). Overall, SCCmec-II strains showed greater resistance than SCCmec-IV strains to clindamycin, erythromycin, levofloxacin, gentamicin, rifampin, minocycline, and trimethoprim-sulfamethoxazole. Both SCCmec-II and SCCmec-IV strains recovered from adults were more resistant to these antibiotics than those recovered from children. SCCmec-II strains were predominantly recovered from the respiratory tract, whereas SCCmec-IV strains were predominantly recovered from skin, soft tissue, abscesses, and surgical wounds. These data indicate that SCCmec-IV MRSA isolates frequently infect children in middle Tennessee and are likely to harbor the PVL gene.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Staphylococcus aureus is a frequent and important human pathogen that causes both hospital- and community-acquired infections (3, 6, 12, 25). Since methicillin-resistant S. aureus (MRSA) was first described in 1961 in England (18), it has become an important problem in hospitals around the world (6). MRSA became a problem in many European countries in the 1960s and in the United States in the 1970s (1, 6). In contrast to hospital-acquired MRSA (HA-MRSA), community-acquired MRSA (CA-MRSA) strains are isolated from healthy people in the community and are susceptible to a number of commonly used antibiotics (16, 24, 26). CA-MRSA causes predominantly skin and soft-tissue infections but can cause serious necrotizing pneumonitis. The increased virulence is due in part to the Panton-Valentine leucocidin (PVL) gene, which is generally present in CA-MRSA isolates. The presence of PVL along with superantigens can result in severe tissue necrosis (9, 25, 35). The CA-MRSA clone in the United States has resulted in several pediatric deaths (16, 23, 25), suggesting that children may have an increased risk of serious MRSA infections compared to adults.

Methicillin resistance in S. aureus is mediated by production of low-affinity penicillin binding protein 2a that is encoded by the mecA gene (3, 19). The gene is located on a mobile element, the staphylococcal chromosomal cassette mec (SCCmec) (2, 28). To date, five different SCCmec elements have been identified in MRSA. The SCCmec typing provides strong evidence for the independent deviation of HA-MRSA and CA-MRSA clones (28). The SCCmec types I, II, and III are predominantly found in HA-MRSA strains, whereas the SCCmec types IV and V are mainly associated with CA-MRSA throughout the world (2, 9, 15, 17).

The aim of this study was to determine the SCCmec types and occurrence of the PVL gene and to correlate these with phenotypic antibiotic susceptibility patterns for MRSA strains isolated from children and adults at Vanderbilt University Medical Center (VUMC) during a 12-month study period. We focused on the differences between children and adults because of the perception that children were having an increased incidence of serious staphylococcal infections (6, 11).

(This study was orally presented in part at the 16th European Congress of Clinical Microbiology and Infectious Diseases, Nice, France, 1 to 4 April 2006.)

Top Abstract Introduction Materials and Methods Results Discussion References

 
Patient demographics. Vanderbilt University Medical Center includes Vanderbilt University Hospital (501 beds) and Vanderbilt Children's Hospital (304 beds). More than 700,000 patient visits occur each year, with approximately 35,000 patients being admitted. The ratio of adult visits/admissions to children's visits/admissions is similar to the ratio of available beds, with 62% adults and 38% children.

Bacterial strains. From 15 November 2004 through 14 November 2005, all clinical MRSA strains isolated in the Clinical Microbiology Laboratory at VUMC were included in the study. To avoid overrepresentation, only the first isolate from each patient during the study period was included. Computerized culture data included the sex, age, and site of isolation of each isolate. The isolates were identified by standard phenotypic procedures and stored at –70°C (36). Children and adults included in the study were defined as <18 and 18 years old, respectively.

Antimicrobial susceptibility testing. In vitro antimicrobial susceptibility testing for amoxicillin-clavulanate, cefazolin, clindamycin, erythromycin, gentamicin, levofloxacin, minocycline, penicillin, rifampin, trimethoprim-sulfamethoxazole (SXT), and vancomycin was determined by a disc diffusion method in accordance with Clinical and Laboratory Standards Institute standards (4). Inducible clindamycin resistance was identified as a D-shaped inhibition zone by the clindamycin-erythromycin double-disk test (34).

SCCmec typing and PVL detection. A loopful of each purified bacterial isolate was placed into 1 ml of distilled water and heated at 95°C for 7 min. The supernatant was used for PCR amplification. A real-time TaqMan PCR was performed on the 7700 ABI Prism Sequence Detector (Applied Biosystems Foster City, CA) to determine the SCCmec types I, II, III, and IV and to detect the PVL gene as described previously (10), with modifications. In brief, 1 µl of the extracted nucleic acid was added to 24 µl of reaction mixture containing 0.8 µM of each primer and 0.4 µM fluorophore probe (final concentration), and the solution was mixed with 25 µl of TaqMan Universal PCR Master Mix (Applied Biosystems). The TaqMan cycling conditions were a 2-min degradation of the preamplified templates at 50°C and then 40 cycles of denaturation at 95°C for 15 s and annealing and extension at 58°C for 60 s (21). The primers and fluorophore TaqMan probes for SCCmec types I, II, III, and IV and the PVL gene were modified from those published previously (10) (SCCmec-I, 5'-TTT GGC ACG TAA TAC TTC CGA TT-3', 5'-AAA ATT CAA CAT TTT GGC GAT GA-3', and 5'-6-carboxyfluorescein [FAM]-TTA CAA TCG TCG AAG AAC-MGB-3'; SCCmec-II, 5'-AAC GAG ACG TGC CCA AGA AG-3', 5'-CAT CAG TTC ATG TTT ACT ATT AGG TAT TTT GTC-3', and 5'-VIC-ATT TGC CGC TGG GCT-minor groove binder [MGB]-3'; SCCmec-III, 5'-GCA GAA CAG ATA ATC GAA CAG GCT AT-3', 5'-GCG ATA ACA ACA TAA TAC GTC ACA TTG-3', and 5'-FAM-AAC GCA TCC AAC AAA-MGB-3'; SCCmec-IV, 5'-GAA CAG ACC TGA GCT CCA ACG T-3', 5'-GGT TTG TYT TGT AKA YCA TAA CAC A-3', and 5'-VIC-AAG ATG CAA AAG AAG GCA ATA-MGB-3'; PVL, 5'-AAA ATG CCA GTG TTA TCC AGA GGT A-3', 5'-TTT GCA GCG TTT TGT TTT CG-3', and 5'-FAM-CTT CAA TCC AGA ATT TAT TGG TGT-MGB-3'; K = G or T; Y = C or T).

Statistical analysis. Statistical comparisons were performed with Epi Info software (version 6; Centers for Disease Control and Prevention, Atlanta, GA). Associations between SCCmec-II and SCCmec-IV MRSA for patient demographics, antibiotic resistance, PVL occurrence, and culture site were analyzed using the ² test or the Student's t test. P 0.05 was considered statistically significant.

Top Abstract Introduction Materials and Methods Results Discussion References

 
A total of 2,740 consecutive Staphylococcus aureus isolates, of which 1,315 (48.6%) were MRSA, were collected for a full year from the Clinical Microbiology Laboratory at VUMC. Among the MRSA isolates, 482 (36.7%) were isolated from children. A total of 448 (34.1%) were SCCmec-II, 847 (64.4%) were SCCmec-IV, 2 (0.2%) were mixed SCCmec-II/IV, and 18 (1.4%) were nontypeable isolates. Fifty (11.2%) SCCmec-II isolates and 424 (50.1%) SCCmec-IV isolates were recovered from children (odds ratio [OR], 0.13; P < 0.000001). Since MRSA isolates from VUMC predominantly carried either SCCmec-IV or SCCmec-II, analysis was focused mainly on these two groups of MRSA isolates. Among the 1,295 isolates, 241 (53.8%) and 399 (47.1%) were from males and carried SCCmec-II and SCCmec-IV, respectively. More SCCmec-II isolates were recovered from an older population (49.3 ± 21.8 years) than the SCCmec-IV isolates (22.4 ± 20.3 years; P < 0.000001). The demographic parameters between the SCCmec-II and SCCmec-IV MRSA strains in child and adult patients are listed in Tables 1 and 2.

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TABLE 1. Characteristics and antibiotic resistance profiles of MRSA strains recovered from adults at Vanderbilt University Medical Center, 15 November 2004 to 14 November 2005

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TABLE 2. Characteristics and antibiotic resistance profiles of MRSA strains recovered from children at Vanderbilt University Medical Center, 15 November 2004 to 14 November 2005

The PVL gene was detected in 93.6% of SCCmec-IV isolates, in contrast to 0.2% in SCCmec-II (Tables 1 and 2). We further studied PVL presence proportions in variable culture sites in CA-MRSA isolates recovered from both children and adults (Table 3). The PVL presence proportion was statistically higher in children (416/424; 98.1%) than in adults (377/423; 89.1%) (OR, 6.34; P < 0.000001). A higher PVL occurrence was detected from SCCmec-IV strains recovered from the bloodstream in children (9/9; 100.0%) than in adults (19/31; 61.3%) (P < 0.028), while PVL occurrence was higher among SCCmec-IV strains recovered from respiratory sites in adults (100.0%) than in children (72.2%) (P < 0.018) (Table 3).

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TABLE 3. PVL-positive proportions in SCCmec-IV isolates recovered from children and adults

SCCmec-II MRSA strains were predominantly recovered from the respiratory tract (40.6%) and from skin, soft tissue, abscesses, and postsurgery wounds (31.0%), while SCCmec-IV strains were predominantly isolated from skin, soft tissue, abscesses, and postsurgery wounds (87.6%) (Tables 1 and 2). A total of 129 MRSA isolates (10.0%) were bloodstream isolates, among which 114 (88.4%) were from adults and 15 (11.6%) were from children. SCCmec-II strains were recovered more frequently from the respiratory tract of children (62.0%) than of adults (37.9%) (OR, 2.67; P = 0.0011) (Tables 1 and 2).

Antibiotic susceptibility for amoxicillin-clavulanate, cefazolin, clindamycin, erythromycin, gentamicin, levofloxacin, minocycline, penicillin, rifampin, trimethoprim-sulfamethoxazole (SXT), and vancomycin was determined, and the resistance rates of the SCCmec-II and SCCmec-IV strains are compared in Tables 1 and 2. MRSA strains recovered from adults were more resistant to clindamycin (SCCmec-II, P < 0.000001; SCCmec-IV, P = 0.0137) and levofloxacin (SCCmec-II, P < 0.00001; SCCmec-IV, P < 0.000001) than those recovered from children, and this trend remained the same in both SCCmec-II and SCCmec-IV strains (Tables 1 and 2). SCCmec-II MRSA strains showed greater resistance than SCCmec-IV strains to clindamycin, erythromycin, levofloxacin, gentamicin, rifampin, minocycline, and SXT. All isolates were resistant to methicillin, amoxicillin-clavulanate, cefazolin, and penicillin. No isolate was resistant to vancomycin (Tables 1 and 2).

Top Abstract Introduction Materials and Methods Results Discussion References

 
This is the first large-scale investigation of antimicrobial susceptibility patterns, PVL occurrence, and SCCmec types in MRSA isolates from middle Tennessee. Among 1,315 MRSA isolates, 34.1% were SCCmec-II and 64.4% were SCCmec-IV. The results of this study demonstrate that the SCCmec-IV MRSA isolates frequently infect children in middle Tennessee and are likely to harbor the PVL gene.

Exploration of age and culture site distribution of these MRSA isolates indicated that the MRSA isolates recovered in middle Tennessee possessed the characteristics reported in previous studies (6, 31, 37). When isolation site distribution of these MRSA isolates was analyzed, there was no significant difference in MRSA isolate numbers between those recovered from children and adults, except for a significantly higher rate of SCCmec-II isolates recovered from the respiratory tract of children (62%) than of adults (38%). Both children and adults were likely to have a staphylococcal bloodstream isolate with SCCmec-II strains. Our data demonstrated that 19.9% of SCCmec-II and 4.7% of SCCmec-IV strains were isolated from the bloodstream, which is consistent with previous findings that MRSA causes 5% to 19% of health care-associated bloodstream infections (7, 12).

There were significant differences regarding isolation sites between SCCmec-II and SCCmec-IV isolates. While SCCmec-IV isolates recovered in middle Tennessee were still mainly from abscess, surgical, and skin and soft-tissue specimens, our study discovered that SCCmec-II strains were recovered more frequently from the respiratory tract of children than adults, indicating that more respiratory-site infections are caused by SCCmec-II strains in children (15). In general, SCCmec-II isolates were mainly recovered from the respiratory tract as well as skin, soft tissue, abscesses, and postsurgery wounds, while SCCmec-IV isolates were recovered dominantly from the latter site(s). These data, especially higher numbers of SCCmec-II isolates recovered from the respiratory tract in children, support recent findings that the nosocomial spread of MRSA happens mainly via the nasal route (5, 20, 26). CA-MRSA has now been introduced from its site of origin in the community into the hospital setting (27, 31). It has been reported that CA-MRSA strains cause skin infections and pneumonia (6, 22).

The PVL gene was present in 93.6% of SCCmec-IV strains, in contrast to 0.2% of SCCmec-II isolates. Within SCCmec-IV strains, a significantly higher incidence of the PVL gene was detected in children than in adults. First discovered in 1932 (29), PVL is a biocomponent synergohymenotropic toxin that is present in the majority of CA-MRSA carrying SCCmec-IV (9, 25). An association between PVL-containing strains of MRSA and virulent necrotizing pneumonia mainly in previously healthy children has been reported (14, 16, 23). Therefore, rapidly determining PVL presence/absence in the early clinical stage may improve patient outcomes and guide proper therapy, such as immunoglobulin administration (13, 32).

In contrast to the multidrug resistance usually seen in HA-MRSA, antibiotic resistance in CA-MRSA strains is often limited to ß-lactams (6). In our study, the SCCmec typing correlated well with major antimicrobial susceptibility patterns. Antimicrobial susceptibility results in MRSA strains included in this study were consistent with previous findings, in that most SCCmec-IV isolates remain susceptible to tetracycline-minocycline, clindamycin, gentamicin, rifampin, and SXT (25). However, in comparison to these antibiotics, 4.2% and 16.8% levofloxacin resistance was noticed in SCCmec-IV strains isolated from children and adults, respectively. SCCmec-II isolates possessed significantly greater resistance than SCCmec-IV isolates to several commonly used antibiotics, especially clindamycin, erythromycin, and levofloxacin. Similar emerging fluoroquinolone resistance has been reported in other parts of the world, such as Australia (27). Considering fluoroquinolone resistance spread rapidly in SCCmec-II isolates in the past, a high rate of fluoroquinolone resistance in SCCmec-IV strains can be predicted in the near future.

Our study did not define these MRSA isolates as hospital acquired or community acquired based on patient history. SCCmec types are considered an independent deviation of HA-MRSA and CA-MRSA clones (28). The term "community-acquired," however, may need to be modified, since MRSA strains carrying SCCmec type IV or V are now being introduced from their community site of origin into the hospital setting with the potential to cause nosocomial spread (27, 30, 33). MRSA isolates carrying SCCmec type I, II, or III can eventually be acquired and spread in communities or vice versa. SCCmec typing is not reliable for determining either HA- or CA-MRSA clonal spread. Other molecular techniques with higher discriminatory power, including pulsed-field gel electrophoresis, spa gene sequencing, and multilocus sequence typing (8, 36) as well as epidemiologic information, should be used to determine the epidemiologic relatedness of a group of MRSA isolates recovered in the hospital and/or community.

 
We thank Susan Sefers, Rosemary Verrall, Joni Williams, Bunny Ambrose, Christine Barberic, Jasper Benton, Donna Brewer, Billie Calloway, Kathy Ewing, Tonia Goodman, Monna Jedd, Sue May, Amy Montgomery, Kim Neville, Carla Nicholson, Jennifer Steinhauer, and Lyndell Weeks for helping collect clinical specimens; Patrice Francois, Jacques Schrenzel, Rodrigo Mendes, and Antonio Pignatari for providing positive control DNA for SCCmec-I, -II, -III, and -IV and PVL; and William Schaffner and Erika D'Agata for critically reviewing the manuscript.

 
* Corresponding author. Mailing address: Molecular Infectious Disease Laboratory, Vanderbilt University Hospital, 4605 TVC, Nashville, TN 37232-5310. Phone: (615) 322-2035. Fax: (615) 343-8420. E-mail: yiwei.tang{at}vanderbilt.edu.

Published ahead of print on 25 October 2006.

Top Abstract Introduction Materials and Methods Results Discussion References

 

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Journal of Clinical Microbiology, December 2006, p. 4436-4440, Vol. 44, No. 12
0095-1137/06/$08.00+0     doi:10.1128/JCM.01546-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

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