Literature DB >> 17243050

An outbreak in an intensive care unit of a strain of methicillin-resistant Staphylococcus aureus sequence type 239 associated with an increased rate of vascular access device-related bacteremia.

Jonathan D Edgeworth1, Ghasem Yadegarfar, Smriti Pathak, Rahul Batra, Joshua D Cockfield, Duncan Wyncoll, Richard Beale, Jodi A Lindsay.   

Abstract

BACKGROUND: Patients in intensive care units are at high risk of developing methicillin-resistant Staphylococcus aureus (MRSA) bacteremia. We report an epidemiological and bacterial genomic analysis of a 2-year outbreak in an intensive care unit of a variant of MRSA sequence type 239 (hereafter designated TW).
METHODS: A cohort study was conducted to compare risk factors for MRSA bacteremia in patients who acquired TW versus patients who acquired non-TW strains of MRSA. Genetic analysis of TW was performed using multilocus sequence typing and microarray analysis.
RESULTS: Patients who acquired TW were more likely than patients who acquired non-TW strains of MRSA to have MRSA isolated from blood samples (47% vs. 13%; P<.001) and to have MRSA-positive vascular access device-sample cultures (59% vs. 26%; P<.001), but less likely to have MRSA isolated from screening swab samples (30% vs. 71%; P<.001). This increased rate of TW bacteremia was confined to the first week after acquisition of TW infection. Using Cox regression analysis, the adjusted hazard ratio for bacteremia with TW was 4.5 times that of non-TW strains of MRSA (95% confidence interval, 2.25-9.00; P<.001). Microarray analysis revealed that TW had accumulated all detectable mobile genetic elements that were variably expressed by other epidemic strains of MRSA sequence type 239 in the United Kingdom.
CONCLUSIONS: To our knowledge, this is the first report to provide direct evidence that strains of MRSA can differ in their ability to cause bacteremia. Further genetic and in vitro analysis of the TW strain may provide insight into the mechanism of vascular access device-related bacteremia in the intensive care unit environment.

Entities:  

Mesh:

Year:  2007        PMID: 17243050     DOI: 10.1086/511034

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


  44 in total

1.  An association between bacterial genotype combined with a high-vancomycin minimum inhibitory concentration and risk of endocarditis in methicillin-resistant Staphylococcus aureus bloodstream infection.

Authors:  Clare E Miller; Rahul Batra; Ben S Cooper; Amita K Patel; John Klein; Jonathan A Otter; Theodore Kypraios; Gary L French; Olga Tosas; Jonathan D Edgeworth
Journal:  Clin Infect Dis       Date:  2011-12-20       Impact factor: 9.079

2.  Rapid detection of the pandemic methicillin-resistant Staphylococcus aureus clone ST 239, a dominant strain in Asian hospitals.

Authors:  Edward J Feil; Emma K Nickerson; Narisara Chantratita; Vanaporn Wuthiekanun; Pramot Srisomang; Richard Cousins; Wubin Pan; Ge Zhang; Banglao Xu; Nicholas P J Day; Sharon J Peacock
Journal:  J Clin Microbiol       Date:  2008-01-30       Impact factor: 5.948

3.  Genome sequence of a recently emerged, highly transmissible, multi-antibiotic- and antiseptic-resistant variant of methicillin-resistant Staphylococcus aureus, sequence type 239 (TW).

Authors:  Matthew T G Holden; Jodi A Lindsay; Craig Corton; Michael A Quail; Joshua D Cockfield; Smriti Pathak; Rahul Batra; Julian Parkhill; Stephen D Bentley; Jonathan D Edgeworth
Journal:  J Bacteriol       Date:  2009-11-30       Impact factor: 3.490

4.  Spa type distribution in MRSA and MSSA bacteremias and association of spa clonal complexes with the clinical characteristics of bacteremia.

Authors:  Elina Jokinen; Laura Lindholm; Reetta Huttunen; Heini Huhtala; Risto Vuento; Jaana Vuopio; Jaana Syrjänen
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2018-02-10       Impact factor: 3.267

5.  Staphylococcus aureus strains that are hypersusceptible to resistance gene transfer from enterococci.

Authors:  Julia M-L Sung; Jodi A Lindsay
Journal:  Antimicrob Agents Chemother       Date:  2007-03-19       Impact factor: 5.191

6.  The A, B, BI, and Cs of Clostridium difficile.

Authors:  Erik R Dubberke
Journal:  Clin Infect Dis       Date:  2009-10-15       Impact factor: 9.079

7.  Distribution of Staphylococcal cassette chromosome mec Types and correlation with comorbidity and infection type in patients with MRSA bacteremia.

Authors:  Jiun-Ling Wang; Jann-Tay Wang; Shey-Ying Chen; Yee-Chun Chen; Shan-Chwen Chang
Journal:  PLoS One       Date:  2010-03-05       Impact factor: 3.240

8.  Community-associated and healthcare-associated methicillin-resistant Staphylococcus aureus virulence toward Caenorhabditis elegans compared.

Authors:  Shandra R Day; Christopher M Moore; John R Kundzins; Costi D Sifri
Journal:  Virulence       Date:  2012-10-17       Impact factor: 5.882

9.  Evolution of hypervirulence by a MRSA clone through acquisition of a transposable element.

Authors:  Meredith A Benson; Elizabeth A Ohneck; Chanelle Ryan; Francis Alonzo; Hannah Smith; Apurva Narechania; Sergios-Orestis Kolokotronis; Sarah W Satola; Anne-Catrin Uhlemann; Robert Sebra; Gintaras Deikus; Bo Shopsin; Paul J Planet; Victor J Torres
Journal:  Mol Microbiol       Date:  2014-07-16       Impact factor: 3.501

10.  Population structure of a hybrid clonal group of methicillin-resistant Staphylococcus aureus, ST239-MRSA-III.

Authors:  Davida S Smyth; Linda K McDougal; Frode W Gran; Anand Manoharan; Mark C Enright; Jae-Hoon Song; Herminia de Lencastre; D Ashley Robinson
Journal:  PLoS One       Date:  2010-01-05       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.