Cited by 2,685Antimicrobial Resistance in StaphylococcusAntibiotic Use and ResistanceBacterial biofilms and quorum sensing

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The role of nasal carriage in Staphylococcus aureus infections

Wertheim, Heiman FL, Melles, Damian C, Vos, Margreet C, van Leeuwen, Willem, van Belkum, Alex, Verbrugh, Henri A, Nouwen, Jan L·2005·The Lancet Infectious Diseases

DOI 10.1016/s1473-3099(05)70295-4

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Abstract

Staphylococcus aureus is a frequent cause of infections in both the community and hospital. Worldwide, the increasing resistance of this pathogen to various antibiotics complicates treatment of S aureus infections. Effective measures to prevent S aureus infections are therefore urgently needed. It has been shown that nasal carriers of S aureus have an increased risk of acquiring an infection with this pathogen. The nose is the main ecological niche where S aureus resides in human beings, but the determinants of the carrier state are incompletely understood. Eradication of S aureus from nasal carriers prevents infection in specific patient categories-eg, haemodialysis and general surgery patients. However, recent randomised clinical trials in orthopaedic and non-surgical patients failed to show the efficacy of eliminating S aureus from the nose to prevent subsequent infection. Thus we must elucidate the mechanisms behind S aureus nasal carriage and infection to be able to develop new preventive strategies. We present an overview of the current knowledge of the determinants (both human and bacterial) and risks of S aureus nasal carriage. Studies on the population dynamics of S aureus are also summarised.

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Staphylococcus aureus Infections
Lowy, F. D. (1998) · New England Journal of Medicine · doi:10.1056/nejm199808203390806 · Cited by 6,018
Nosocomial Bloodstream Infections in US Hospitals: Analysis of 24,179 Cases from a Prospective Nationwide Surveillance Study
Wisplinghoff, H., Bischoff, T., Tallent, S. M., Seifert, H., Wenzel, R. P., & Edmond, M. B. (2004) · Clinical Infectious Diseases · doi:10.1086/421946 · Cited by 4,496
Multilocus Sequence Typing for Characterization of Methicillin-Resistant and Methicillin-Susceptible Clones ofStaphylococcus aureus
Enright, M. C., Day, N., Davies, C. E., Peacock, S. J., & Spratt, B. G. (2000) · Journal of Clinical Microbiology · doi:10.1128/jcm.38.3.1008-1015.2000 · Cited by 3,039
Nasal carriage of Staphylococcus aureus: epidemiology, underlying mechanisms, and associated risks
Kluytmans, J., van Belkum, A., & Verbrugh, H. (1997) · Clinical Microbiology Reviews · doi:10.1128/cmr.10.3.505 · Cited by 2,595
Self-citation
Nasal Carriage as a Source of Staphylococcus aureus Bacteremia
von Eiff, C., Becker, K., Machka, K., Stammer, H., & Peters, G. (2001) · New England Journal of Medicine · doi:10.1056/nejm200101043440102 · Cited by 1,984
Endogenous Antimicrobial Peptides and Skin Infections in Atopic Dermatitis
Ong, P. Y., Ohtake, T., Brandt, C., Strickland, I., Boguniewicz, M., Ganz, T., Gallo, R. L., & Leung, D. Y. M. (2002) · New England Journal of Medicine · doi:10.1056/nejmoa021481 · Cited by 1,960
Whole genome sequencing of meticillin-resistant Staphylococcus aureus
Kuroda, M., Ohta, T., Uchiyama, I., Baba, T., Yuzawa, H., Kobayashi, I., Cui, L., Oguchi, A., Aoki, K.-I., Nagai, Y., et al. (2001) · The Lancet · doi:10.1016/s0140-6736(00)04403-2 · Cited by 1,950
eBURST: Inferring Patterns of Evolutionary Descent among Clusters of Related Bacterial Genotypes from Multilocus Sequence Typing Data
Feil, E. J., Li, B. C., Aanensen, D. M., Hanage, W. P., & Spratt, B. G. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.5.1518-1530.2004 · Cited by 1,861
"Celbenin" - resistant Staphylococci
Jevons, M. P. (1961) · BMJ · doi:10.1136/bmj.1.5219.124-a · Cited by 1,730
Community-Acquired Methicillin-ResistantStaphylococcus aureusCarrying Panton-Valentine Leukocidin Genes: Worldwide Emergence
Vandenesch, F., Naimi, T. S., Enright, M. C., Lina, G., Nimmo, G. R., Heffernan, H., Liassine, N., Bes, M., Greenland, T., Reverdy, M. E., et al. (2003) · Emerging infectious diseases · doi:10.3201/eid0908.030089 · Cited by 1,718

Show all 198 references

Research works printed but not linked: 2

Noble, 1967, Carriage of Staphylococcus aureus in random samples of a normal population, J Hyg (Lond), 65, 567
Wertheim HFL, Kleef M, Vos MC, Ott A, Verbrugh H, Fokkens W. Nosepicking and nasal carriage of Staphylococcus aureus. Infect Control Hosp Epidemiol (in press).

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Authors: Wertheim, H. F., Melles, D. C., Vos, M. C., van Leeuwen, W., van Belkum, A., Verbrugh, H. A., & Nouwen, J. L.
Affiliations: Erasmus MC (NL)
Corresponding author: Wertheim, Heiman FL
ORCID: Wertheim, Heiman FL
Nouwen, Jan L
Venue: The Lancet Infectious Diseases
Publisher: Elsevier BV
Published: 2005-12
Volume: 5
Issue: 12
Pages: 751-762
ISSN: 1473-3099 (ISSN-L)
DOI: 10.1016/s1473-3099(05)70295-4
OpenAlex: W2098533519
Cited by: 2,685
References: 198
Citations by year: 2026: 96 · 2025: 138 · 2024: 175 · 2023: 130 · 2022: 146 · 2021: 181 · 2020: 191 · 2019: 161 · 2018: 173 · 2017: 162 · 2016: 145 · 2015: 155 · 2014: 162 · 2013: 155 · 2012: 127
FWCI: 4.58
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/legal/tdmrep-license (tdm)
Locations: The Lancet Infectious Diseases (publishedVersion)
PubMed (publishedVersion)
EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
Funders: Nierstichting
Topics: Health Sciences › Medicine › Infectious Diseases › Antimicrobial Resistance in Staphylococcus
Health Sciences › Medicine › Infectious Diseases › Antibiotic Use and Resistance
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
Keywords: Staphylococcus aureus, nasal carriage, infection control, antibiotic resistance, hemodialysis patients, orthopedic surgery, population dynamics, community-acquired infections, nosocomial infections
MeSH terms: Adolescent, Adult, Aged, Carrier State, Child, Child, Preschool, Female, Humans, Infant, Male, Middle Aged, Nose, Risk Factors, Staphylococcal Infections, Staphylococcus aureus

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The role of nasal carriage in Staphylococcus aureus infections

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