Natural history of community-acquired methicillin-resistant Staphylococcus aureus colonization and infection in soldiers

被引:364
作者
Ellis, MW
Hospenthal, DR
Dooley, DP
Gray, PJ
Murray, CK
机构
[1] Brooke Army Med Ctr, Dept Med, Ft Sam Houston, TX 78234 USA
[2] Brooke Army Med Ctr, Dept Prevent Med, Ft Sam Houston, TX 78234 USA
关键词
D O I
10.1086/423965
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Community- acquired methicillin- resistant Staphylococcus aureus ( CA- MRSA) is an emerging pathogen for which the prevalence, risk factors, and natural history are incompletely understood. Methods. In this prospective observational study, we evaluated 812 US Army soldiers to determine the prevalence of and risk factors for CA- MRSA colonization and the changes in colonization rate over time, as well as to determine the clinical significance of CA- MRSA colonization. Demographic data and swab samples from the nares for S. aureus cultures were obtained from participants at the start of their training and 8 - 10 weeks later. Over this time period, participants were observed prospectively to monitor for soft- tissue infections. S. aureus isolates were characterized by in vitro examination of antibiotic susceptibilities, mecA confirmation, pulsed- field gel electrophoresis, and Panton- Valentine leukocidin ( PVL) gene testing. Results. At the initial sampling, 24 of the participants ( 3%) were colonized with CA- MRSA, 9 of whom ( 38%) developed soft- tissue infections during the study period. In contrast, 229 participants ( 28%) were colonized with methicillin- susceptible S. aureus ( MSSA), 8 ( 3%) of whom developed clinical infections during the same period ( relative risk, 10.7; 95% confidence interval, 4.6 - 25.2;). At follow- up culture, the CA- MRSA colonization rate dropped to 1.6% without eradication efforts. Previous antibiotic use was a risk factor for CAMRSA colonization at the initial sampling (P = .03). PVL genes were detected in 66% of 45 recovered CA- MRSA isolates, including all 9 clinical isolates available for analysis. Of subjects hospitalized, 5 of 6 had PVL- positive CA- MRSA infections. Conclusions. CA- MRSA colonization with PVL- positive strains was associated with a significant risk of soft-tissue infection, suggesting that CA- MRSA may be more virulent than MSSA. Previous antibiotic use may play a role in CA- MRSA colonization.
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收藏
页码:971 / 979
页数:9
相关论文
共 48 条
[1]  
[Anonymous], 1999, MMWR-MORBID MORTAL W, V48, P707
[2]   Genome and virulence determinants of high virulence community-acquired MRSA [J].
Baba, T ;
Takeuchi, F ;
Kuroda, M ;
Yuzawa, H ;
Aoki, K ;
Oguchi, A ;
Nagai, Y ;
Iwama, N ;
Asano, K ;
Naimi, T ;
Kuroda, H ;
Cui, L ;
Yamamoto, K ;
Hiramatsu, K .
LANCET, 2002, 359 (9320) :1819-1827
[3]   PULSED-FIELD GEL-ELECTROPHORESIS AS A REPLACEMENT FOR BACTERIOPHAGE-TYPING OF STAPHYLOCOCCUS-AUREUS [J].
BANNERMAN, TL ;
HANCOCK, GA ;
TENOVER, FC ;
MILLER, JM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (03) :551-555
[4]  
BOELAERT JR, 1993, NEPHROL DIAL TRANSPL, V8, P235
[5]   Panton-Valentine leukocidin and staphyloccoccal skin infections in schoolchildren [J].
Boubaker, K ;
Diebold, P ;
Blanc, DS ;
Vandenesch, F ;
Praz, G ;
Dupuis, G ;
Troillet, N .
EMERGING INFECTIOUS DISEASES, 2004, 10 (01) :121-124
[6]   Emergence of methicillin-resistant Staphylococcus aureus as a community pathogen [J].
Bukharie, HA ;
Abdelhadi, MS ;
Saeed, IA ;
Rubaish, AM ;
Larbi, EB .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2001, 40 (1-2) :1-4
[7]  
*CDCP, 2003, MMWR-MORBID MORTAL W, V52, P88
[8]   The changing epidemiology of Staphylococcus aureus? [J].
Chambers, HF .
EMERGING INFECTIOUS DISEASES, 2001, 7 (02) :178-182
[9]   Population-based community prevalence of methicillin-resistant Staphylococcus aureus in the urban poor of San Francisco [J].
Charlebois, ED ;
Bangsberg, DR ;
Moss, NJ ;
Moore, MR ;
Moss, AR ;
Chambers, HF ;
Perdreau-Remington, F .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (04) :425-433
[10]   Methicillin-resistant Staphylococcus aureus in the community:: New battlefronts, or are the battles lost? [J].
Cookson, BD .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2000, 21 (06) :398-403