Abstract
Bacteria that are resistant to antimicrobial agents, which were previously isolated primarily in acute-care hospitals, now cause infection in a wide range of other healthcare settings. Improved detection of new resistant strains — especially by using practical and affordable screening methods and by evaluating mechanisms of resistance — is a priority for tackling this problem effectively. Standardized, effective surveillance systems for evaluating the emergence and prevalence of resistant strains are necessary to assess the success of intervention strategies.
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References
Tenover, F. C. Development and spread of bacterial resistance to antimicrobial agents: an overview. Clin. Infect. Dis. 33, S108–S115 (2001).
Wood, M. J. & Moellering, R. C. Jr. Microbial resistance: bacteria and more. Clin. Infect. Dis. 36, S2–S3 (2003).
Diekema, D. J. et al. Antimicrobial resistance trends and outbreak frequency in United States hospitals. Clin. Infect. Dis. 38, 78–85 (2004).
Mahgoub, S., Ahmed, J. & Glatt, A. E. Completely resistant Acinetobacter baumannii strains. Infect. Control Hosp. Epidemiol. 23, 477–479 (2002).
Livermore, D. M. Multiple mechanisms of antimicrobial resistance in Pseudomonas aeruginosa: our worst nightmare? Clin. Infect. Dis. 34, 634–640 (2002).
Fridkin, S. K. et al. Surveillance of antimicrobial use and antimicrobial resistance in United States hospitals: project ICARE phase 2. Clin. Infect. Dis. 29, 245–252 (1999).
Min, S. S. et al. Multidrug-resistant Enterococcus faecium in a patient with burns. Clin. Infect. Dis. 36, 1210–1211 (2003).
Pournaras, S. et al. Hospital outbreak of multiple clones of Pseudomonas aeruginosa carrying the unrelated metallo-β-lactamase gene variants blaVIM-2 and blaVIM-4. J. Antimicrob. Chemother. 51, 1409–1414 (2003).
Saiman, L. et al. Hospital transmission of community-acquired methicillin-resistant Staphylococcus aureus among postpartum women. Clin. Infect. Dis. 37, 1313–1319 (2003).
Howard, D. H., Scott, R. D., Packard, R. & Jones, D. The global impact of drug resistance. Clin. Infect. Dis. 36, S4–S10 (2003).
Cosgrove, S. E. & Carmeli, Y. The impact of antimicrobial resistance on health and economic outcomes. Clin. Infect. Dis. 36, 1433–1437 (2003).
Engemann, J. J. et al. Adverse clinical and economic outcomes attributable to methicillin resistance among patients with Staphylococcus aureus surgical site infection. Clin. Infect. Dis. 36, 592–598 (2003).
Cosgrove, S. E., Kaye, K. S., Eliopoulous, G. M. & Carmeli, Y. Health and economic outcomes of the emergence of third-generation cephalosporin resistance in Enterobacter species. Arch. Intern. Med. 162, 185–190 (2002).
Fridkin, S. K. et al. Epidemiological and microbiological characterization of infections caused by Staphylococcus aureus with reduced susceptibility to vancomycin, United States, 1997–2001. Clin. Infect. Dis. 36, 429–439 (2003).
Chang, S. et al. Infection with vancomycin-resistant Staphylococcus aureus containing the vanA resistance gene. N. Engl. J. Med. 348, 1342–1347 (2003).
Centers for Disease Control and Prevention. Vancomycin-resistant Staphylococcus aureus — Pennsylvania, 2002. Morb. Mortal. Wkly Rep. 51, 902 (2002).
Raney, P. M., Williams, P. P., McGowan, J. E. & Tenover, F. C. Validation of Vitek version 7. 01 software for testing staphylococci against vancomycin. Diagn. Microbiol. Infect. Dis. 43, 135–140 (2002).
Liu, C. & Chambers, H. F. Staphylococcus aureus with heterogeneous resistance to vancomycin: epidemiology, clinical significance, and critical assessment of diagnostic methods. Antimicrob. Agents Chemother. 47, 3040–3045 (2003).
Tenover, F. C. et al. Characterization of staphylococci with reduced susceptibilities to vancomycin and other glycopeptides. J. Clin. Microbiol. 36, 1020–1027 (1998).
Tenover, F. C. et al. Vancomycin-resistant Staphylococcus aureus isolate from a patient in Pennsylvania. Antimicrob. Agents Chemother. 48, 275–280 (2004).
Hirakata, Y. et al. Clinical and bacteriological characteristics of IMP-type metallo-β-lactamase-producing Pseudomonas aeruginosa. Clin. Infect. Dis. 37, 26–32 (2003).
Urban, C., Segal-Maurer, S. & Rahal, J. J. Considerations in control and treatment of nosocomial infections due to multidrug-resistant Acinetobacter baumannii. Clin. Infect. Dis. 36, 1268–1274 (2003).
Ouderkirk, J. P., Nord, J. A., Turett, G. S. & Kislak, J. W. Polymyxin B nephrotoxicity and efficacy against nosocomial infections caused by multiresistant Gram-negative bacteria. Antimicrob. Agents Chemother. 47, 2659–2662 (2003).
Wang, S. H. et al. Healthcare-associated outbreak due to pan-drug resistant Acinetobacter baumannii in a surgical intensive care unit. J. Hosp. Infect. 53, 97–102 (2003).
Melano, R. et al. Multiple antibiotic-resistance mechanisms including a novel combination of extended-spectrum β-lactamases in a Klebsiella pneumoniae clinical strain isolated in Argentina. J. Antimicrob. Chemother. 52, 36–42 (2003).
Karlowsky, J. A., Jones, M. E., Thornsberry, C., Friedland, I. R. & Sahm, D. F. Trends in antimicrobial susceptibilities among Enterobacteriaceae isolated from hospitalized patients in the United States from 1998 to 2001. Antimicrob. Agents Chemother. 47, 1672–1680 (2003).
Canton, R., Coque, T. M. & Baquero, F. Multi-resistant Gram-negative bacilli: from epidemics to endemics. Curr. Opin. Infect. Dis. 16, 315–325 (2003).
Tenover, F. C. et al. Evaluation of the NCCLS extended-spectrum β-lactamase confirmation methods for Escherichia coli with isolates collected during Project ICARE. J. Clin. Microbiol. 41, 3142–3146 (2003).
Samaha-Kfoury, J. N. & Araj, G. F. Recent developments in β-lactamases and extended spectrum β-lactamases. Br. Med. J. 327, 1209–1213 (2003).
Alvarez, M., Tran, J. H., Chow, N. & Jacoby, G. A. Epidemiology of conjugative plasmid-mediated AmpC β-lactamases in the United States. Antimicrob. Agents Chemother. 48, 533–537 (2004).
Queenan, A. M., Foleno, B., Gownley, C., Wira, E. & Bush, K. Effects of inoculum and β-lactamase activity in AmpC- and extended-spectrum β-lactamase (ESBL)-producing Escherichia coli and Klebsiella pneumoniae clinical isolates tested by using NCCLS ESBL methodology. J. Clin. Microbiol. 42, 269–275 (2004).
Hubert, S. K. et al. Glycopeptide-intermediate Staphylococcus aureus: evaluation of a novel screening method and results of a survey of selected US hospitals. J. Clin. Microbiol. 37, 3590–3593 (1999).
Neuhauser, M. M. et al. Antibiotic resistance among Gram-negative bacilli in US intensive care units: implications for fluoroquinolone use. J. Am. Med. Assoc. 289, 885–888 (2003).
Fridkin, S. K. Vancomycin-intermediate and-resistant Staphylococcus aureus: what the infectious disease specialist needs to know. Clin. Infect. Dis. 32, 108–115 (2001).
Garnacho-Montero, J. et al. Treatment of multidrug-resistant Acinetobacter baumannii ventilator-associated pneumonia (VAP) with intravenous colistin: a comparison with imipenem-susceptible VAP. Clin. Infect. Dis. 36, 1111–1118 (2003).
Jevitt, L. A. et al. In vitro activities of daptomycin, linezolid, and quinupristin-dalfopristin against a challenge panel of staphylococci and enterococci, including vancomycin-intermediate S. aureus and vancomycin–resistant E. faecium. Microb. Drug Resist. 9, 389–393.
Marshall, S. H., Donskey, C. J., Hutton-Thomas, R., Salata, R. A. & Rice, L. B. Gene dosage and linezolid resistance in Enterococcus faecium and Enterococcus faecalis. Antimicrob. Agents Chemother. 46, 3334–3336 (2002).
Pillai, S. K. et al. Linezolid resistance in Staphylococcus aureus: characterization and stability of resistant phenotype. J. Infect. Dis. 186, 1603–1607 (2002).
Cercenado, E., Cercenado, S., Gomez, J. A. & Bouza, E. In vitro activity of tigecycline (GAR-936), a novel glycylcycline, against vancomycin-resistant enterococci and staphylococci with diminished susceptibility to glycopeptides. J. Antimicrob. Chemother. 52, 138–139 (2003).
Centers for Disease Control and Prevention. National nosocomial infections surveillance (NNIS) system report, data summary from January 1990–May 1999, issued June 1999. Am. J. Infect. Control 27, 520–532 (1999).
Fridkin, S. K. et al. Temporal changes in prevalence of antimicrobial resistance in 23 US hospitals. Emerg. Infect. Dis. 8, 697–701 (2002).
Centers for Disease Control and Prevention. National nosocomial infections surveillance (NNIS) system report, data summary from January 1992–June 2002, issued August 2002. Am. J. Infect. Control. 30, 458–475 (2002).
McCarthy, M. Resistant bacteria spread through US communities. 70% of isolates are now resistant to all β-lactam antibiotics. Lancet 362, 1554–1555 (2003).
Okuma, K. et al. Dissemination of new methicillin-resistant Staphylococcus aureus clones in the community. J. Clin. Microbiol. 40, 4289–4294 (2002).
Hunter, P. A. & Reeves, D. S. The current status of surveillance of resistance to antimicrobial agents: report on a meeting. J. Antimicrob. Chemother. 49, 17–23 (2002).
Kahlmeter, G. & Brown, D. F. Resistance surveillance studies — comparability of results and quality assurance of methods. J. Antimicrob. Chemother. 50, 775–777 (2002).
Steward, C. D. et al. Antimicrobial susceptibility testing of carbapenems: multicenter validity testing and accuracy levels of five antimicrobial test methods for detecting resistance in Enterobacteriaceae and Pseudomonas aeruginosa isolates. J. Clin. Microbiol. 41, 351–358 (2003).
Tenover, F. C., Mohammed, M. J., Stelling, J., O'Brien, T. & Williams, R. Ability of laboratories to detect emerging antimicrobial resistance: proficiency testing and quality control results from the World Health Organization's external quality assurance system for antimicrobial susceptibility testing. J. Clin. Microbiol. 39, 241–250 (2001).
Chaitram, J. M., Jevitt, L. A., Lary, S. & Tenover, F. C. The World Health Organization's external quality assurance system proficiency testing program has improved the accuracy of antimicrobial susceptibility testing and reporting among participating laboratories using NCCLS methods. J. Clin. Microbiol. 41, 2372–2377 (2003).
Skov, R. et al. Evaluation of a cefoxitin 30 μg disc on Iso-Sensitest agar for detection of methicillin-resistant Staphylococcus aureus. J. Antimicrob. Chemother. 52, 204–207 (2003).
Felten, A., Grandry, B., Lagrange, P. H. & Casin, I. Evaluation of three techniques for detection of low-level methicillin-resistant Staphylococcus aureus (MRSA): a disk diffusion method with cefoxitin and moxalactam, the Vitek 2 system, and the MRSA-screen latex agglutination test. J. Clin. Microbiol. 40, 2766–2771 (2002).
Gregson, D. B. et al. Evaluation of the IDI-MRSA assay for the rapid detection of methicillin-resistant S. aureus in nasal and rectal swabs (abstract K–1394). Abstracts of the 43rd Annual Interscience Conference on Antimicrobial Agents and Chemotherapy (Chicago, Illinois, 2003).
Francois, P. et al. Rapid detection of methicillin-resistant Staphylococcus aureus directly from sterile or nonsterile clinical samples by a new molecular assay. J. Clin. Microbiol. 41, 254–260 (2003).
Swenson, J. M., Williams, P. P., Killgore, G., O'Hara, C. M. & Tenover, F. C. Performance of eight methods, including two new rapid methods, for detection of oxacillin resistance in a challenge set of Staphylococcus aureus organisms. J. Clin. Microbiol. 39, 3785–3788 (2001).
Rasheed, J. K. & Tenover, F. C. in Manual of Clinical Microbiology 8th edn (eds Murray, P. R., Baron, E. J., Jorgensen, J. H., Pfaller, M. A. & Yolken, R. H.) 1196–1212 (ASM, Washington DC, 2003).
Kahlmeter, G. et al. European harmonization of MIC breakpoints for antimicrobial susceptibility testing of bacteria. J. Antimicrob. Chemother. 52, 145–148 (2003).
Cockerill, F. R. Genetic methods for assessing antimicrobial resistance. Antimicrob. Agents Chemother. 43, 199–212 (1999).
Potera, C. Signature chips could help to identify, classify bacteria. ASM News 69, 485–486 (2003).
Call, D. R., Bakko, M. K., Krug, M. J. & Roberts, M. C. Identifying antimicrobial resistance genes with DNA microarrays. Antimicrob. Agents Chemother. 47, 3290–3295 (2003).
Volokhov, D., Chizhikov, V., Chumakov, K. & Rasooly, A. Microarray analysis of erythromycin resistance determinants. J. Appl. Microbiol. 95, 787–798 (2003).
Holzman, D. Microarray analyses may speed antibiotic resistance testing. ASM News 69, 538–539 (2003).
Swenson, J. M., Hill, B. C. & Thornsberry, C. Problems with the disk diffusion test for detection of vancomycin resistance in enterococci. J. Clin. Microbiol. 27, 2140–2142 (1989).
Schwaber, M. J. et al. Utility of NCCLS guidelines for identifying extended-spectrum β-lactamases in non-Escherichia coli and non-Klebsiella spp. of Enterobacteriaceae. J. Clin. Microbiol. 42, 294–298 (2004).
Stevenson, K. B. et al. Detection of antimicrobial resistance by small rural hospital microbiology laboratories: comparison of survey responses with current NCCLS laboratory standards. Diagn. Microbiol. Infect. Dis. 47, 303–311 (2003).
Wegener, H. C., Aarestrup, F. M., Jensen, L. B., Hammerum, A. M. & Bager, F. Use of antimicrobial growth promoters in food animals and Enterococcus faecium resistance to therapeutic antimicrobial drugs in Europe. Emerg. Infect. Dis. 5, 329–335 (1999).
Gales, A. C., Reis, A. O. & Jones, R. N. Contemporary assessment of antimicrobial susceptibility testing methods for polymyxin B and colistin: review of available interpretative criteria and quality control guidelines. J. Clin. Microbiol. 39, 183–190 (2001).
European Committee on Antimicrobial Susceptibility Testing. EUCAST Definitive Document E.DEF 3.1, June 2000. Determination of minimum inhibitory concentrations (MICs) of antibacterial agents by broth dilution. Clin. Microbiol. Infect. 9, 4–15 (2003).
Hallgren, A. et al. Genetic relatedness among Enterococcus faecalis with transposon-mediated high-level gentamicin resistance in Swedish intensive care units. J. Antimicrob. Chemother. 52, 162–167 (2003).
Flannagan, S. E. et al. Plasmid content of a vancomycin-resistant Enterococcus faecalis isolate from a patient also colonized by Staphylococcus aureus with a VanA phenotype. Antimicrob. Agents Chemother. 47, 3954–3959 (2003).
McGeer, A. & Low, D. E. Is resistance futile? Nature Med. 9, 390–392 (2003).
Miranda, G. et al. Clonal and horizontal dissemination of Klebsiella pneumoniae expressing SHV-5 extended-spectrum β-lactamase in a Mexican pediatric hospital. J. Clin. Microbiol. 42, 30–35 (2004).
Tenover, F. C. & Rasheed, J. K. in Manual of Clinical Microbiology (eds Murray, P. R., Baron, E. J., Jorgensen, J. H., Pfaller, M. A. & Yolken, R. H.) (ASM, Washington DC, 2003).
Bruinsma, N. et al. Hospitalization, a risk factor for antibiotic-resistant Escherichia coli in the community? J. Antimicrob. Chemother. 51, 1029–1032 (2003).
Warren, D. K., Kollef, M. H., Seiler, S. M., Fridkin, S. K. & Fraser, V. J. The epidemiology of vancomycin-resistant Enterococcus colonization in a medical intensive care unit. Infect. Control Hosp. Epidemiol. 24, 257–263 (2003).
Zeana, C. et al. The epidemiology of multidrug-resistant Acinetobacter baumannii: does the community represent a reservoir? Infect. Control Hosp. Epidemiol. 24, 275–279 (2003).
McDougal, L. K. et al. Pulsed-field gel electrophoresis typing of oxacillin-resistant Staphylococcus aureus isolates from the United States: establishing a national database. J. Clin. Microbiol. 41, 5113–5120 (2003).
Barlow, M. & Hall, B. G. Experimental prediction of the natural evolution of antibiotic resistance. Genetics 163, 1237–1241 (2003).
Weigel, L. M. et al. Genetic analysis of a high-level vancomycin-resistant isolate of Staphylococcus aureus. Science 302, 1569–1571 (2003).
Barlow, M. & Hall, B. G. Origin and evolution of the AmpC β-lactamases of Citrobacter freundii. Antimicrob. Agents Chemother. 46, 1190–1198 (2002).
Hall, B. G., Salipante, S. J. & Barlow, M. The metallo-β-lactamases fall into two distinct phylogenetic groups. J. Mol. Evol. 57, 249–254 (2003).
Andreev, D., Kreitman, M., Phillips, T. W., Beeman, R. W. & Ffrench-Constant, R. H. Multiple origins of cyclodiene insecticide resistance in Tribolium castaneum (Coleoptera: Tenebrionidae). J. Mol. Evol. 48, 615–624 (1999).
Salipante, S. J., Barlow, M. & Hall, B. G. GeneHunter, a transposon tool for identification and isolation of cryptic antibiotic resistance genes. Antimicrob. Agents Chemother. 47, 3840–3845 (2003).
Duck, W. M., Steward, C. D., Banerjee, S. N., McGowan, J. E. Jr & Tenover, F. C. Optimization of computer software settings improves accuracy of pulsed-field gel electrophoresis macrorestriction fragment pattern analysis. J. Clin. Microbiol. 41, 3035–3042 (2003).
Finch, R. Antibiotic resistance — from pathogen to disease surveillance. Clin. Microbiol. Infect. 8, 317–320 (2002).
NCCLS. Analysis and Presentation of Cumulative Antimicrobial Susceptibility Test Data; Approved Guideline (M39-A) (NCCLS, Pennsylvania, 2002).
Arias, C. A. et al. Multicentre surveillance of antimicrobial resistance in enterococci and staphylococci from Colombian hospitals, 2001–2002. J. Antimicrob. Chemother. 51, 59–68 (2003).
Watson, J. et al. Comparative analysis of multidrug-resistant, non-multidrug-resistant, and archaic methicillin-resistant Staphylococcus aureus isolates from Central Sydney, Australia. J. Clin. Microbiol. 41, 867–872 (2003).
Karlowsky, J. A. et al. Surveillance for antimicrobial susceptibility among clinical isolates of Pseudomonas aeruginosa and Acinetobacter baumannii from hospitalized patients in the United States, 1998 to 2001. Antimicrob. Agents Chemother. 47, 1681–1688 (2003).
Fritsche, T. R., Sader, H. S. & Jones, R. N. Comparative activity and spectrum of broad-spectrum β-lactams (cefepime, ceftazidime, ceftriaxone, piperacillin/tazobactam) tested against 12,295 staphylococci and streptococci: report from the SENTRY antimicrobial surveillance program. Diagn. Microbiol. Infect. Dis. 47, 435–440 (2003).
Sader, H. S., Biedenbach, D. J. & Jones, R. N. Global patterns of susceptibility for 21 commonly utilized antimicrobial agents tested against 48,440 Enterobacteriaceae in the SENTRY antimicrobial surveillance program (1997–2001). Diagn. Microbiol. Infect. Dis. 47, 361–364 (2003).
Halstead, D. C., Gomez, N. & McCarter, Y. S. Reality of developing a community-wide antibiogram. J. Clin. Microbiol. 42, 1–6 (2004).
McGowan, J. E. Jr et al. Does antimicrobial resistance cluster in individual hospitals? J. Infect. Dis. 186, 1362–1365 (2002).
Hall, R. & Partridge, S. Unambiguous numbering of antibiotic resistance genes. Antimicrob. Agents Chemother. 47, 3998–3999 (2003).
Salgado, C. D., Farr, B. M. & Calfee, D. P. Community-acquired methicillin-resistant Staphylococcus aureus: a meta-analysis of prevalence and risk factors. Clin. Infect. Dis. 36, 131–139 (2003).
Monnet, D. L. Toward multinational antimicrobial resistance surveillance systems in Europe. Int. J. Antimicrob. Agents 15, 91–101 (2000).
Bronzwaer, S. L. et al. A European study on the relationship between antimicrobial use and antimicrobial resistance. Emerg. Infect. Dis. 8, 278–282 (2002).
College of American Pathologists. Commission on Laboratory Accreditation. Microbiology Checklist — Changes for 2003, Guideline MIC. 21946. Vol. 2003 (College of American Pathologists, USA, 2003).
Jones, R. N. & Masterton, R. Determining the value of antimicrobial surveillance programs. Diagn. Microbiol. Infect. Dis. 41, 171–175 (2001).
Choudhry, N. K., Stelfox, H. T. & Detsky, A. S. Relationships between authors of clinical practice guidelines and the pharmaceutical industry. JAMA 287, 612–617 (2002).
DeAngelis, C. D., Fontanarosa, P. B. & Flanagin, A. Reporting financial conflicts of interest and relationships between investigators and research sponsors. JAMA 286, 89–91 (2001).
Ehrle, L. H. Partnerships between universities and industry. JAMA 287, 1398–1399 (2002).
Poupard, J., Brown, J., Gagnon, R., Stanhope, M. J. & Stewart, C. Methods for data mining from large multinational surveillance studies. Antimicrob. Agents Chemother. 46, 2409–2419 (2002).
Acknowledgements
The authors thank D. Shapiro and M. Barlow for helpful discussions.
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Research by Project ICARE is funded by Abbott Laboratories; AstraZeneca; Bayer Corporation, Pharmaceuticals Division; Cubist; Elan Pharmaceuticals; Pfizer, Inc.; and Roche Laboratories.
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Glossary
- ANTIBIOGRAM
-
The results of all susceptibility tests for a given organism considered as an overall group. The term is often used to refer both to such a profile for an individual organism and to cumulative summaries of such profiles for a given period of time.
- ANTIBIOTYPE
-
The subgroup into which a bacterial organism is classified on the basis of a comparison of its antibiogram with those of organisms of the same genus and species. The antibiotype is the result of the application of a typing system on the basis of this phenotypic characterization.
- CLONAL DISSEMINATION
-
The spread of a single strain of a bacterial organism, or of a single resistance determinant, in a given geographical area, or the introduction of such a strain or element from a geographically distant population.
- LOCAL SELECTION
-
The proliferation and spread, usually under the influence of local antimicrobial use, of resistant bacteria that have either accumulated mutations that reduce their susceptibility to antimicrobial agents or have acquired novel resistance genes by direct DNA transfer
- PRINCIPAL-COMPONENT ANALYSIS
-
A means of representing multidimensional data in a reduced-dimension space to obtain an overview of the data.
- ZONE DIAMETER
-
The measurement (in millimetres) of the diameter of the zone of inhibition of organism growth around a disk that contains a standard amount of an antimicrobial agent. Used in one method of standardized susceptibility testing (agar-disk diffusion) to define the activity of the drug against a bacterial organism.
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McGowan, J., Tenover, F. Confronting bacterial resistance in healthcare settings: a crucial role for microbiologists. Nat Rev Microbiol 2, 251–258 (2004). https://doi.org/10.1038/nrmicro845
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DOI: https://doi.org/10.1038/nrmicro845
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