Patient nostril microbial flora: individual-dependency and diversity precluding prediction of Staphylococcus aureus acquisition

被引:12
作者
Alvarez, A. S. [1 ,2 ,3 ]
Remy, L. [1 ,2 ,3 ]
Allix-Beguec, C. [4 ]
Ligier, C. [5 ,6 ]
Dupont, C. [1 ,5 ,6 ,7 ]
Leminor, O. [1 ,5 ,6 ,7 ]
Lawrence, C. [1 ,2 ,3 ]
Supply, P. [4 ,8 ,9 ,10 ,11 ]
Guillemot, D. [1 ,5 ,6 ,7 ,12 ]
Gaillard, J. L. [1 ,2 ,3 ]
Salomon, J. [5 ,6 ,13 ]
Herrmann, J-L. [1 ,2 ,3 ]
机构
[1] Univ Versailles St Quentin, Yvelines, France
[2] UFR Sci Sante, F-78 Montigny Le Bretonneux, France
[3] Hop Raymond Poincare, AP HP, Microbiol Lab, Garches, France
[4] Inst Pasteur, Genoscreen, F-59019 Lille, France
[5] Inst Pasteur, Pharmacoepidemiol & Infect Dis Unit, Paris, France
[6] INSERM, U657 Unit, Paris, France
[7] UFR Sci Sante, F-78 Montigny Le Bretonneux, France
[8] INSERM, U1019 Lille, F-59045 Lille, France
[9] Inst Pasteur, Ctr Immunol & Biol Parasitaire, CNRS, UMR 8204, F-59019 Lille, France
[10] Inst Pasteur, Ctr Infect & Immun Lille, F-59019 Lille, France
[11] Univ Lille Nord France, Lille, France
[12] Hop Raymond Poincare, AP HP, Unite Sante Publ, Garches, France
[13] Conservatoire Natl Arts & Metiers, Lab Modelisat Epidemiol & Surveillance Risques Sa, Paris, France
关键词
Bacterial interference; carriage; microbial flora; Staphylococcus aureus; NASAL CARRIAGE; COLONIZATION; HAEMOLYTICUS; RESISTANCE; IDENTIFICATION; ASSOCIATION; SECRETIONS; CAVITIES; SPREAD;
D O I
10.1111/1469-0691.12208
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The potential role of a patient's resident microbial flora in the risk of acquiring multiresistant bacteria (MRB) during hospitalization is unclear. We investigated this role by cross-sectional study of 103 patients at risk of acquisition of Staphylococcus aureus (SA), resistant (MRSA) or not (MSSA) to methicillin, recruited in four French hospitals. The flora was analysed by an exhaustive culture-based approach combined with molecular and/or mass-spectrometry-based identification, and SA strain typing. Forty-three of the 53 SA-negative patients at entry were followed for up to 52weeks: 19 (44.2%) remained negative for SA and 24 (55.8%) became positive, including 19 (79%) who acquired an MSSA, four (17%) who acquired an MRSA and one who acquired both (4%). Fifty-one different species were identified among the 103 patients, of which two, Corynebacterium accolens and Staphylococcus haemolyticus (p=0.02-0.01), were more prevalent in the absence of SA. However, the same number of patients carrying or not these two species acquired an MSSA/MRSA during follow-up, regardless of antibiotic treatment received. Clustering analysis showed that the microbial flora was highly specific to each patient, and not predictive for acquisition of MSSA/MRSA or not. Patient-specific microbial resident flora is not predictive of SA acquisition.
引用
收藏
页码:70 / 78
页数:9
相关论文
共 29 条
[1]   Corynebacterium accolens isolated from breast abscess:: Possible association with granulomatous mastitis [J].
Ang, Lei M. N. ;
Brown, Harnish .
JOURNAL OF CLINICAL MICROBIOLOGY, 2007, 45 (05) :1666-1668
[2]   Staphylococcus haemolyticus as an Important Hospital Pathogen and Carrier of Methicillin Resistance Genes [J].
Barros, E. M. ;
Ceotto, H. ;
Bastos, M. C. F. ;
dos Santos, K. R. N. ;
Giambiagi-deMarval, M. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (01) :166-168
[3]   Innate antimicrobial activity of nasal secretions [J].
Cole, AM ;
Dewan, P ;
Ganz, T .
INFECTION AND IMMUNITY, 1999, 67 (07) :3267-3275
[4]   Community-Associated Methicillin-Resistant Staphylococcus aureus: Epidemiology and Clinical Consequences of an Emerging Epidemic [J].
David, Michael Z. ;
Daum, Robert S. .
CLINICAL MICROBIOLOGY REVIEWS, 2010, 23 (03) :616-+
[5]   Identification of clinical coagulase-negative staphylococci, isolated in microbiology laboratories, by matrix-assisted laser desorption/ionization-time of flight mass spectrometry and two automated systems [J].
Dupont, C. ;
Sivadon-Tardy, V. ;
Bille, E. ;
Dauphin, B. ;
Beretti, J. L. ;
Alvarez, A. S. ;
Degand, N. ;
Ferroni, A. ;
Rottman, M. ;
Herrmann, J. L. ;
Nassif, X. ;
Ronco, E. ;
Carbonnelle, E. .
CLINICAL MICROBIOLOGY AND INFECTION, 2010, 16 (07) :998-1004
[6]   The Human Nasal Microbiota and Staphylococcus aureus Carriage [J].
Frank, Daniel N. ;
Feazel, Leah M. ;
Bessesen, Mary T. ;
Price, Connie S. ;
Janoff, Edward N. ;
Pace, Norman R. .
PLOS ONE, 2010, 5 (05)
[7]   Molecular typing of methicillin-resistant Staphylococcus aureus on the basis of protein A gene polymorphism [J].
Frenay, HME ;
Bunschoten, AE ;
Schouls, LM ;
vanLeeuwen, WJ ;
VandenbrouckeGrauls, CMJE ;
Verhoef, J ;
Mooi, FR .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1996, 15 (01) :60-64
[8]   ANTIMICROBIAL RESISTANCE IN NOSOCOMIAL ISOLATES OF STAPHYLOCOCCUS-HAEMOLYTICUS [J].
FROGGATT, JW ;
JOHNSTON, JL ;
GALETTO, DW ;
ARCHER, GL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (04) :460-466
[9]   Strategies to prevent and control the emergence and spread of antimicrobial-resistant microorganisms in hospitals - A challenge to hospital leadership [J].
Goldmann, DA ;
Weinstein, RA ;
Wenzel, RP ;
Tablan, OC ;
Duma, RJ ;
Gaynes, RP ;
Schlosser, J ;
Martone, WJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (03) :234-240
[10]   Vancomycin resistance in Staphylococci [J].
Hiramatsu, K .
DRUG RESISTANCE UPDATES, 1998, 1 (02) :135-150