1. bookVolume 57 (2018): Edition 4 (January 2018)
Détails du magazine
Première parution
01 Mar 1961
4 fois par an
Anglais, Polonais
Accès libre


Publié en ligne: 26 Feb 2022
Volume & Edition: Volume 57 (2018) - Edition 4 (January 2018)
Pages: 348 - 359
Reçu: 01 Mar 2018
Accepté: 01 Aug 2018
Détails du magazine
Première parution
01 Mar 1961
4 fois par an
Anglais, Polonais

Aanensen D.M., Spratt B.G.: The multilocus sequence typing network: mlst.net. Nucleic Acids Res. 1, DOI: 10.1093/nar/gki415 (2005)10.1093/nar/gki415116017615980573Search in Google Scholar

Archer G.L.: Molecular epidemiology of multiresistant Staphylococcus epidermidis. J. Antimicrob. Chemother. 21, 133–138 (1988)Search in Google Scholar

Asaad A.M., Qureshib M.A., Hasanc S.M.: Clinical significance of coagulase-negative staphylococci isolates from nosocomial bloodstream infections. Infect. Dis. 48, 356–360 (2016)Search in Google Scholar

Barbier F., Ruimy R. i wsp.: Methicillin-resistant coagulase-negative staphylococci in the community: high homology of SCCmec IVa between Staphylococcus epidermidis and major clones of methicillin-resistant Staphylococcus aureus. J. Infect. Dis. 15, 270–281 (2010)Search in Google Scholar

Bates D.W., Goldman L., Lee T.H.: Contaminant blood cultures and resource utilization. The true consequences of false-positive results. JAMA, 265, 365–369 (1991)10.1001/jama.1991.03460030071031Search in Google Scholar

Bathoorn E., Hetem D.J., Alphenaar J., Kusters J.G., Bonten M.J. Emergence of high-level mupirocin resistance in coagulase-negative staphylococci associated with increased short-term mupirocin use. J. Clin. Microbiol. 50, 2947–2950 (2012)Search in Google Scholar

Bearman G.M., Wenzel R.P.: Bacteremias: a leading cause of death. Arch. Med. Res. 36, 646–659 (2005)Search in Google Scholar

Becker K., Heilmann C., Peters G.: Coagulase-negative staphylococci. Clin. Microbiol. Rev. 27, 870–926 (2014)Search in Google Scholar

Biavasco, F., Vignaroli, C., Varaldo, P.E.: Glycopeptide resistance in coagulase negative staphylococci. Eur. J. Clin. Microbiol. Infect. Dis. 19, 403–417 (2000)Search in Google Scholar

Boghossian N.S., Higgins R.D. i wsp.: Late-onset sepsis invery low birth weight infants from singleton and multiple-gestation births. J. Pediatr. 162, 1120–1124 (2013)Search in Google Scholar

Cerca N., Jefferson K.K., Oliveira R., Pier G.B., Azeredo J.: Comparative antibody-mediated phagocytosis of Staphylococcus epidermidis cells grown in a biofilm or in the planktonic state. Infect. Immun. 74, 4849–4855 (2006)Search in Google Scholar

Cerca N., Martins S., Cerca F., Jefferson K.K., Pier G.B., Oliveira R., Azeredo J.: Comparative assessment of antibiotic susceptibility of coagulase-negative staphylococci in biofilm versus planktonic culture as assessed by bacterial enumeration or rapid XTT colorimetry. J. Antimicrob. Chemoth. 56, 331–336 (2005)10.1093/jac/dki217131730115980094Search in Google Scholar

Cherifi S., Byl B., Deplano A., Nonhoff C., Denis O., Hallin M.: Comparative epidemiology of Staphylococcus epidermidis isolates from patients with catheter-related bacteremia and from healthy volunteers. J. Clin. Microbiol. 51, 1541–1547 (2013)Search in Google Scholar

Chong J., Quach C., Blanchard A.C., Poliquin P.G., Golding G.R., Laferrière C., Lévesque S.: Molecular epidemiology of a vancomycin-intermediate heteroresistant Staphylococcus epidermidisoutbreak in a neonatal intensive care unit. Antimicrob. Agents Chemother. 60, 5673–5681 (2016)10.1128/AAC.00726-16503829527401579Search in Google Scholar

Chu V.H., Fowler V.G.Jr. i wsp.: Emergence of coagulase-negative staphylococci as a cause of native valve endocarditis. Clin. Infect. Dis. 46, 232–242 (2008)Search in Google Scholar

Conlan S., Segre J.A. i wsp.: Staphylococcus epidermidis pan-genome sequence analysis reveals diversity of skin commensal and hospital infection-associated isolates. Genome Biol. 13, DOI: 10.1186/gb-2012-13-7-r64 (2012)10.1186/gb-2012-13-7-r64405373122830599Search in Google Scholar

Costa S.S., Viveiros M., Pomba C., Couto I.: Active antimicrobial efflux in Staphylococcus epidermidis: building up of resistance to fluoroquinolones and biocides in a major opportunistic pathogen. J. Antimicrob. Chemot. 73, 320–324 (2018)10.1093/jac/dkx40029126275Search in Google Scholar

De N., Godlove M.: Prevalence of S. aureus and S. epidermidisamong patients with indwelling catheters and their antibiogram using some commonly used antibiotics. J. Am. Sci. 6, 515-520 (2010)Search in Google Scholar

Denton C., Pappas E.G., Uricchio J.F., Goldberg H., Likoff W.: Bacterial endocarditis following cardiac surgery. Circulation,15, 525–531 (1957)10.1161/01.CIR.15.4.525Search in Google Scholar

Do G., Jarvis W.R. i wsp.: The emergence of decreased susceptibility to vancomycin in Staphylococcus epidermidis. Infect. Control. Hosp. Epidemiol. 20, 167–170 (1999)Search in Google Scholar

Domingo P., Fontanet A.: Management of complications associated with totally implantable ports in patients with AIDS. AIDS Patient Care STDS, 15: 7–13 (2001)10.1089/10872910146005611177583Search in Google Scholar

Donker T., Wallinga J., Grundmann H.: Dispersal of antibiotic-resistant high risk clones by hospital networks: changing the patient direction can make all the difference. J. Hosp. Infect. 86, 34–41 (2014)10.1016/j.jhin.2013.06.02124075292Search in Google Scholar

Du X., Zhu Y., Song Y., Li T., Luo T., Sun G., Yang C., Cao C., Lu Y., Li M.: Molecular analysis of Staphylococcus epidermidisstrains isolated from community and hospital environments in China. Plos One, 8, e62742 (2013)10.1371/journal.pone.0062742365286823675424Search in Google Scholar

Duah M.: Daptomycin for methicillin-resistant Staphylococcus epidermidis native-valve endocarditis: a case report. Ann. Clin. Microbiol. Antimicrob. 9, DOI: 10.1186/1476-0711-9-9 (2010)10.1186/1476-0711-9-9283627720167084Search in Google Scholar

European Centre for Disease Prevention and Control (ECDC): Point prevalence survey of healthcare associated infections and antimicrobial use in European acute care hospitals 2011-2012. (2013) https://ecdc.europa.eu/en/publications-data/point-pre valence-survey-healthcare-associated-infections-and-antimicro bial-use-0 (26.02.2018)Search in Google Scholar

Farrell D.J., Mendes R.E., Ross J.E., Jones R.N.: Linezolid surveillance program results for 2008 (LEADER Program for 2008). Diagn. Microbiol. Infect. Dis. 65, 392–403 (2009)Search in Google Scholar

Franca A., Carvalhais V., Vilanova M., Pier G.B., Cerca N.: Characterization of an in vitro fed-batch model to obtain cells released from S. epidermidis biofilms. AMB Express,6, DOI: 10.1186/s13568-016-0197-9 (2016)10.1186/s13568-016-0197-9480182327001438Search in Google Scholar

Frebourg N.B., Lefebvre S., Baert S., Lemeland J.F.: PCR-based assay for discrimination between invasive and contaminating Staphylococcus epidermidis strains. J. Clin. Microbiol. 38, 877– 880 (2000)Search in Google Scholar

Galdbart J.O., Allignet J., Tung H.S., Ryde’n C., El Solh N.: Screening for Staphylococcus epidermidis markers discriminating between skin-flora strains and those responsible for infections of joint prostheses. J. Infecti. Dis. 182, 351–355 (2000)Search in Google Scholar

Gatermann S.G., Koschinski T., Friedrich S.: Distribution and expression of macrolide resistance genes in coagulase-negative staphylococci. Clin. Microbiol. Infect. 13, 777–781 (2007)Search in Google Scholar

Ghassemi A., Farhangi H., Badiee Z., Banihashem A., Mosaddegh M.R.: Evaluation of nosocomial infection in patients at hematology-oncology ward of Dr. Sheikh children’s hospital. Iran. J. Ped. Hematol. Oncol. 5, 179–185 (2015)Search in Google Scholar

Gill S.R., Fraser C.M. i wsp.: Insights on evolution of virulence and resistance from the complete genome analysis of an early methicillin-resistant Staphylococcus aureus strain and a biofilm-producing methicillin-resistant Staphylococcus epidermidisstrain. J. Bacteriol. 187, 2426–2438 (2005)Search in Google Scholar

Grice E.A., Segre J.A. i wsp.: Topographical and temporal diversity of the human skin microbiome. Science, 29, 1190–1192 (2009)Search in Google Scholar

Hellmark B., Unemo M., Nilsdotter-Augustinsson A., Söderquist B.: Antibiotic susceptibility among Staphylococcus epidermidis isolated from prosthetic joint infections with special focus on rifampicin and variability of the rpoB gene. Clin. Microbiol. Infect. 15, 238–244 (2009)10.1111/j.1469-0691.2008.02663.x19196261Search in Google Scholar

Hidron A.I., Edwards J.R., Patel J., Horan T.C., Sievert D.M., Pollock D.A., Fridkin S.K.: Antimicrobial-resistant pathogens associated with healthcare-associated infections: annual summary of data reported to the National Healthcare Safety Network at the Centers for Disease Control and Prevention, 2006–2007. Infect. Control Hosp. Epidemiol. 29, 996–1011 (2008)10.1086/59186118947320Search in Google Scholar

Hira V., Sluijter M., Goessens W.H., Ott A., de Groot R., Hermans P.W., Kornelisse R.F.: Coagulase-negative staphylococcal skin carriage among neonatal intensive care unit personnel: from population to infection. J. Clin. Microbiol. 48, 3876–3881 (2010)10.1128/JCM.00967-10302088620826641Search in Google Scholar

Hovelius B., Mardh P.A.: Staphylococcus saprophyticus as a common cause of urinary tract infections. Rev. Infect. Dis. 6, 328-337 (1984)Search in Google Scholar

Hu H., Johani K., Gosbell I.B., Jacombs A.S., Almatroudi A., Whiteley G.S., Deva A.K., Jensen S., Vickery K.: Intensive care unit environmental surfaces are contaminated by multidrug-resistant bacteria in biofilms: combined results of conventional culture, pyrosequencing, scanning electron microscopy, and confocal laser microscopy. J. Hosp. Infect. 91, 35–44 (2015)Search in Google Scholar

Hwang J.H., Choi C.W., Chang Y.S., Choe Y. H., Park W.S., Shin S.M., Lee M., Lee S.I.: The efficacy of clinical strategies to reduce nosocomial sepsis in extremely low birth weight infants. J. Korean Med. Sci. 20, 177–181 (2005)Search in Google Scholar

International Working Group on the Classification of Staphylococcal Cassette Chromosome Elements (IWG-SCC): Classification of staphylococcal cassette chromosome mec (SCCmec): guidelines for reporting novel SCCmec elements. Antimicrob. Agents Chemother. 53, 4961–4967 (2009)10.1128/AAC.00579-09278632019721075Search in Google Scholar

Kelly S., Collins J., Maguire M., Gowing C., Flanagan M., Donnelly M., Murphy P.G.: An outbreak of colonization with linezo- lid-resistant Staphylococcus epidermidis in an intensive therapy unit. J. Antimicrob. Chemother. 61, 901–907 (2008)Search in Google Scholar

Kocianova S., Vuong C., Yao Y., Voyich J.M., Fischer E.R., DeLeo F.R., Otto M.: Key role of poly-gamma-DL-glutamic acid in immune evasion and virulence of Staphylococcus epidermidis. J. Clin. Invest. 115, 688–694 (2005)10.1172/JCI200523523Search in Google Scholar

Kozitskaya S., Cho S.H., Dietrich K., Marre R., Naber K., Ziebuhr W.: The bacterial insertion sequence element IS256occurs preferentially in nosocomial Staphylococcus epidermidisisolates: association with biofilm formation and resistance to aminoglycosides. Infect. Immun. 72, 1210–1215 (2004)Search in Google Scholar

Kübler A., Mayzner-Zawadzka E., Durek G., Gaszyński W., Nestorowicz A., Karpel E.: Prevalence and incidence of severe sepsis in intensive therapy units in Poland. Anest. Int. Ther. 39, 90–94 (2007)Search in Google Scholar

Kurtz S.M., Lau E., Watson H., Schmier J.K., Parvizi J.: Economic burden of periprosthetic joint infection in the United States. J. Arthroplasty, 27, 61–65 (2012)10.1016/j.arth.2012.02.02222554729Search in Google Scholar

Lee J.Y.H., Monk I.R., Pidot S.J., Singh S., Chua K.Y.L., Seemann T., Stinear T.P., Howden B.P.: Functional analysis of the first complete genome sequence of a multidrug resistant sequence type 2 Staphylococcus epidermidis. Microb. Genom. 2(9): e000077 DOI:10.1099/mgen.0.000077 (2016)10.1099/mgen.0.000077553762928785416Search in Google Scholar

Luk A., Kim M.L., Ross H.J., Rao V., David T.E., Butany J: Native and prosthetic valve infective endocarditis: clinicopathologic correlation and review of the literature. Malays. J. Pathol. 36, 71–81 (2014)10.1097/01.PAT.0000443577.12293.bfSearch in Google Scholar

McCann M.T., Gilmore B.F., Gorman S.P.: Staphylococcus epidermidis device-related infections: pathogenesis and clinical management. J Pharm. Pharmacol. 60, 1551–1571 (2008)10.1211/jpp/60.12.000119000360Search in Google Scholar

McTaggart L.A., Rigby R.C., Elliott T.S.: The pathogenesis of urinary tract infections associated with Escherichia coli, Staphylococcus saprophyticus and S. epidermidis. J. Med. Microbiol. 32, 135–141 (1990)Search in Google Scholar

Mendes R.E., Deshpande L.M., Costello A.J., Farrell D.J.: Molecular epidemiology of Staphylococcus epidermidis clinical isolates from U.S. hospitals. Antimicrob. Agents Chemother. 56, 4656–4661 (2012)10.1128/AAC.00279-12342185522687512Search in Google Scholar

Mermel L.A., Allon M., Bouza E., Craven D.E., Flynn P., O’Grady N.P., Raad I.I., Rijnders B.J., Sherertz R.J., Warren D.K.: Clinical practice guidelines for the diagnosis and management of intravascular catheter-related infection: 2009 update by the Infectious Diseases Society of America. Clin. Infect. Dis. 49, 1–45 (2009)Search in Google Scholar

Miller J.J., Scott I.U., Flynn H.W.J., Smiddy W.E., Newton J.: Acute-onset endophthalmitis after cataract surgery (2000– 2004): incidence, clinical settings, and visual acuity outcomes after treatment. Am. J. Ophthalmol. 139, 983–987 (2005)10.1016/j.ajo.2005.01.02515953426Search in Google Scholar

Miragaia M., Carriço J.A., Thomas J.C., Couto I., Enright M.C., de Lencastre H.: Comparison of molecular typing methods for characterization of Staphylococcus epidermidis: proposal for clone definition. J. Clin. Microbiol. 46, 118–129 (2008)10.1128/JCM.01685-07222428917989196Search in Google Scholar

Miragaia M., Thomas J.C., Couto I., Enright M.C., de Lencastre H.: Inferring a population structure for Staphylococcus epidermidis from multilocus sequence typing data. J. Bacteriol. 189, 2540–2552 (2007)10.1128/JB.01484-06189936717220222Search in Google Scholar

Moloney T.P., Park J.: Microbiological isolates and antibiotic sensitivities in culture-proven endophthalmitis: a 15-year review. Br. J. Ophthalmol. 98, 1492–1497 (2014)10.1136/bjophthalmol-2014-30503024939423Search in Google Scholar

Monsen T., Karlsson C., Wiström J.: Spread of clones of multidrug-resistant, coagulase-negative staphylococci within a university hospital. Infect. Control Hosp. Epidemiol. 26, 76–80 (2005)Search in Google Scholar

Montanaro L., Speziale P., Campoccia D., Ravaioli S., Cangini I., Pietrocola G., Giannini S., Arciola C.: Scenery of Staphylococcusimplant infections in orthopedics. Future Microbiol. 6, 1329– 1349 (2011)10.2217/fmb.11.11722082292Search in Google Scholar

Morris S., Gould K., Ferguson L.P.:. The use of daptomycin to treat methicillin-resistant Staphylococcus epidermidis bacteremia in a critically III child with renal failure. J. Pediatr. Pharmacol. Ther. 22, 300–303 (2017)Search in Google Scholar

Najar-Peerayeh S., Moghadas A.J., Behmanesh M.: Antibiotic susceptibility and mecA frequency in Staphylococcus epidermidis, isolated from Intensive Care Unit patients. Jundishapur J. Microbiol. 7, e11188, DOI: 10.5812/jjm.11188 (2014)10.5812/jjm.11188425521225485050Search in Google Scholar

Nikbakht M., Nahaei M.R., Akhi M.T., Asgharzadeh M., Nikvash S.: Molecular fingerprinting of meticillin-resistant Staphylococcus aureus strains isolated from patients and staff of two Iranian hospitals. J. Hosp. Infect. 69, 46–55 (2008)Search in Google Scholar

NPOA – Narodowy Program Ochrony Antybiotyków.: Definicje zakażeń związanych z opieką zdrowotną (HAI) obowiązujące od 1 stycznia 2016 r. wg ECDC. (2016), http://www.antybiotyki. edu.pl/zakazenia-szpitalne.php (26.02.2018)Search in Google Scholar

O’Callaghan R.J.: The pathogenesis of Staphylococcus aureuseye infections. Pathogens, 7, DOI: 10.3390/pathogens7010009 (2018)10.3390/pathogens7010009587473529320451Search in Google Scholar

Otto M.: Staphylococcus epidermidis– the ‘accidental’ pathogen. Nat. Rev. Microbiol. 7, 555–567 (2009)Search in Google Scholar

Parte A.C.: LPSN-list of prokaryotic names with standing in nomenclature. Nucleic Acids Res. 42, DOI: 10.1093/nar/ gkt1111(2014)Search in Google Scholar

Pien B.C., Sundaram P., Raoof N., Costa S.F., Mirrett S., Woods C.W., Reller L.B., Weinstein M.P.: The clinical and prognostic importance of positive blood cultures in adults. Am. J. Med. 123, 819–828 (2010)10.1016/j.amjmed.2010.03.02120800151Search in Google Scholar

Pinheiro L., Brito C.I., Pereira V.C., Oliveira A., Bartolomeu A.R., Camargo C.H.: Susceptibility profile of Staphylococcus epidermidis and Staphylococcus haemolyticus isolated from blood cultures to vancomycin and novel antimicrobial drugs over a period of 12 years. Microb. Drug Resist. 22, 283–293 (2016)10.1089/mdr.2015.006426623676Search in Google Scholar

Pournaras S., Ntokou E., Zarkotou O., Ranellou K., Themeli-Digalaki K., Stathopoulos C., Tsakris A.: Linezolid dependence in Staphylococcus epidermidis bloodstream isolates. Emerg. Infect. Dis. 19, 129–132 (2013)Search in Google Scholar

Qazi S.A., Stoll B.J.: Neonatal sepsis: a major global public health challenge. Pediatr. Infect. Dis. J. 28, DOI: 10.1097/ INF.0b013e31819587a9 (2009)Search in Google Scholar

Relhan N., Albini T., Pathengay A., Flynn H.W.: Bilateral endogenous endophthalmitis caused by vancomycin-resistant Staphylococcus epidermidis in a neonate. J. Ophthalmic Inflamm. Infect. 5,DOI: 10.1186/s12348-015-0039-y (2015)10.1186/s12348-015-0039-y439203925883685Search in Google Scholar

Ribeiro M., Monteiro F.J., Ferraz M.P.: Infection of orthopedic implants with emphasis on bacterial adhesion process and techniques used in studying bacterial-material interactions. Biomatter. 2, 176–194 (2012)10.4161/biom.22905356810423507884Search in Google Scholar

Rolo J., de Lencastre H., Miragaia M.: Strategies of adaptation of Staphylococcus epidermidis to hospital and community: amplification and diversification of SCCmec. J. Antimicrob. Chemother. 67, 1333–1341 (2012)10.1093/jac/dks06822422509Search in Google Scholar

Rosenthal V.D, Graves N. i wsp.: Time-dependent analysis of length of stay and mortality due to urinary tract infections in ten developing countries: INICC findings. J. Infect. 62, 136-141 (2011)Search in Google Scholar

Rotger M., Trampuz A., Piper K.E., Steckelberg J.M., Patel R.: Phenotypic and genotypic mupirocin resistance among staphylococci causing prosthetic joint infection. J. Clin. Microbiol. 43, 4266–4268 (2005)Search in Google Scholar

Rupp M.E., Archer G.L.: Coagulase-negative staphylococci: pathogens associated with medical progress. Clin. Infect. Dis. 19, 231–245 (1994)Search in Google Scholar

Salih. L., Tevell S., Mansson E., Nilsdotter-Augustinsson A., Hellmark B., Soderquist B.: Staphylococcus epidermidis isolates from nares and prosthetic joint infections are mupirocin susceptible. J. Bone Joint Infect. 3, DOI: 10.7150/jbji.22459 (2018)10.7150/jbji.22459574418929291157Search in Google Scholar

Siddiq M., Darouiche R.O.: New strategies to prevent catheter-associated urinary tract infections. Nat. Rev. Urol. 9, 305–314 (2012)Search in Google Scholar

Sieradzki K., Villari P., Tomasz A.: Decreased susceptibilities to teicoplanin and vancomycin among coagulase-negative methicillin resistant clinical isolates of staphylococci. Antimicrob. Agents Chemother. 42, 100–107 (1998)10.1128/AAC.42.1.1001054639449268Search in Google Scholar

Söderquist B., Andersson M., Nilsson M., Nilsdotter-Augustinsson A., Persson L., Friberg O., Jacobsson S.: Staphylococcus epidermidis surface protein I (SesI): a marker of the invasive capacity of S. epidermidis? J. Med. Microbiol. 58, 1395–1397 (2009)10.1099/jmm.0.008771-019556370Search in Google Scholar

Taylor S.D., Palmer M.: The action mechanism of daptomycin. Bioorg. Med. Chem. 15, 6253–6268 (2016)Search in Google Scholar

Thomas J.C., Vargas M.R., Miragaia M., Peacock S.J., Archer G.L., Enright M.C.: Improved multilocus sequence typing scheme for Staphylococcus epidermidis. J. Clin. Microbiol. 45, 616–619 (2007)Search in Google Scholar

Thylefors J.D., Harbarth S., Pittet D.: Increasing bacteremia due to coagulase-negative staphylococci: fiction or reality? Infect. Control. Hosp. Epidemiol. 19, 581–589 (1998)Search in Google Scholar

Tolo I., Thomas J.C., Fischer R.S.B., Brown E.L., Gray B.M., Robinson D.A.: Do Staphylococcus epidermidis genetic clusters predict isolation sources? J. Clin. Microbiol. 54, 1711–1719 (2016)Search in Google Scholar

Trevino M., Martinez-Lamas L., Romero-Jung P.A., Giraldez J.M, Alvarez-Escuder J., Regueir B.J.: Endemic linezolid-resistant Staphylococcus epidermidis in a critical care unit. Eur. J. Clin. Microbiol. Infect. Dis. 28, 527–533 (2009)Search in Google Scholar

Vasudevan R.: Urinary tract infection: an overview of the infection and the associated risk factors. J. Microbiol. Exp. 1, DOI: 10.15406/jmen.2014.01.00008 (2014)10.15406/jmen.2014.01.00008Search in Google Scholar

von Eiff, C.; Reinert, R.R.; Kresken, M.; Brauers, J.; Hafner, D.: Nationwide German multicenter study on prevalence of antibiotic resistance in staphylococcal bloodstream isolates and comparative in vitro activities of quinupristin dalfopristin. J. Clin. Microbiol. 38, 2819–2823 (2000)10.1128/JCM.38.8.2819-2823.20008711910921933Search in Google Scholar

Widerström M., Wiström J., Edebro H., Marklund E., Backman M., Lindqvist P., Monsen T.: Colonization of patients, healthcare workers, and the environment with healthcare-associated Staphylococcus epidermidis genotypes in an intensive care unit: a prospective observational cohort study. BMC Infect. Dis. 16, DOI: 10.1186/s12879-016-2094-x (2016a)10.1186/s12879-016-2094-x514892027938344Search in Google Scholar

Widerström M.: Significance of Staphylococcus epidermidis in health care-associated infections, from contaminant to clinically relevant pathogen: this is a wake-up call!J. Clin. Microbiol. 54, 1679–1681 (2016b)10.1128/JCM.00743-16492207627170016Search in Google Scholar

Widerström M., McCullough C.A., Coombs G.W., Monsen T., Christiansen K.J.: A multidrug-resistant Staphylococcus epidermidis clone (ST2) is an ongoing cause of hospital-acquired infection in a Western Australian Hospital. J. Clin. Microbiol. 50, 2147–2151 (2012a)10.1128/JCM.06456-11337215522442320Search in Google Scholar

Widerström M., Wiström J., Sjöstedt A., Monsen T.: Coagulase-negative staphylococci: update on the molecular epidemiology and clinical presentation, with a focus on Staphylococcus epidermidis and Staphylococcus saprophyticus. Eur. J. Clin. Microbiol. Infect. Dis. 31, 7–20 (2012b)10.1007/s10096-011-1270-621533877Search in Google Scholar

Widerstrom M., Monsen T., Karlsson C., Edebro H., Johansson A., Wistrom J.: Clonality among multidrug-resistant hospital-associated Staphylococcus epidermidis in Northern Europe. Scand. J. Infect. Dis. 41, 642–649 (2009)Search in Google Scholar

Widerstrom M., Monsen T., Karlsson C., Wistrom J.: Molecular epidemiology of meticillin-resistant coagulase-negative staphylococci in a Swedish county hospital: evidence of intra- and interhospital clonal spread. J. Hosp. Infect. 64, 177–183 (2006)10.1016/j.jhin.2006.06.01316911846Search in Google Scholar

Wu H., Moser C., Wang H.Z., Høiby N. Song Z.J.: Strategies for combating bacterial biofilm infections. Int. J. Oral Sci. 7, DOI: 10.1038/ijos.2014.65 (2014)10.1038/ijos.2014.65481753325504208Search in Google Scholar

Yamada M., Yoshida J., Hatou S., Yoshida T., Minagawa Y.: Mutations in the quinolone resistance determining region in Staphylococcus epidermidisrecovered from conjunctiva and their association with susceptibility to various fluoroquinolones. Br. J. Ophthalmol. 92, 848–851 (2008)Search in Google Scholar

Yilmaz C, Colak M, Yilmaz B.C. i wsp.: Bacteriophage therapy in implant-related infections: an experimental study. J. Bone Joint Surg. Am. 95, 117–125 (2013)Search in Google Scholar

Zhang Y.Q., Wen Y.M. i wsp.: Genome-based analysis of virulence genes in a non-biofilm-forming Staphylococcus epidermidis strain (ATCC 12228). Mol. Microbiol. 49, 1577–1593 (2003)Search in Google Scholar

Ziebuhr W., Hennig S., Eckart M., Kranzler H., Batzilla C., Kozitskaya S.: Nosocomial infections by Staphylococcus epidermidis: how a commensal bacterium turns into a pathogen. Int. J. Antimicrob. Ag. 28, 14–20 (2006)Search in Google Scholar

Ziebuhr W., Heilmann C., Götz F., Meyer P., Wilms K., Straube E., Hacker J.: Detection of the intercellular adhesion gene cluster (ica) and phase variation in Staphylococcus epidermidis blood culture strains and mucosal isolates. Infect. Immun. 65, 890–896 (1997)10.1128/iai.65.3.890-896.1997Search in Google Scholar

Articles recommandés par Trend MD

Planifiez votre conférence à distance avec Sciendo