Increasing incidence of bloodstream infections due to Staphylococcus aureus clonal complex 398 in a French hospital between 2010 and 2017.
Bloodstream infection
Epidemiology
Methicillin-susceptible Staphylococcus aureus
Staphylococcus aureus CC398
Journal
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology
ISSN: 1435-4373
Titre abrégé: Eur J Clin Microbiol Infect Dis
Pays: Germany
ID NLM: 8804297
Informations de publication
Date de publication:
Nov 2019
Nov 2019
Historique:
received:
03
06
2019
accepted:
21
07
2019
pubmed:
3
8
2019
medline:
8
2
2020
entrez:
3
8
2019
Statut:
ppublish
Résumé
The epidemiology of Staphylococcus aureus is changing and several surveillances worldwide have evidenced an increasing incidence of S. aureus bloodstream infections (BSIs). Here, we described the long-term epidemiology of the emergent clonal group CC398 among S. aureus isolated from BSIs in our French university hospital between 2010 and 2017. Each patient with at least one blood culture positive with S. aureus during the study period was included (N = 1455). Cefoxitin susceptibility was determined using the disk diffusion method according to EUCAST recommendations. CC398 isolates were first screened from the whole S. aureus collection with a matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) typing method confirmed by a CC398-specific PCR. In our hospital, the incidence of hospital- and community-acquired BSIs due to S. aureus and MSSA increased in parallel between 2010 and 2017 while that of BSIs with MRSA decreased. The prevalence of CC398 isolates among S. aureus from BSIs increased from 3.6 in 2010 to 20.2% in 2017 (p < 0.05). CC398-MRSA emerged but remains very sparse. Our data suggested that CC398-MSSA disseminates in the community. We showed here the emergence and the diffusion of CC398-MSSA, a subclone associated with invasive infections, in our hospital. The monitoring of this particular human-adapted S. aureus clone is needed and genomic studies will have to identify the determinants of its diffusion.
Identifiants
pubmed: 31372905
doi: 10.1007/s10096-019-03653-5
pii: 10.1007/s10096-019-03653-5
doi:
Substances chimiques
Anti-Bacterial Agents
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2127-2132Références
J Clin Microbiol. 2011 Feb;49(2):732-4
pubmed: 21123532
Clin Microbiol Infect. 2013 May;19(5):465-71
pubmed: 22616816
Clin Microbiol Infect. 2016 May;22(5):451-5
pubmed: 26851655
MBio. 2012 Feb 28;3(2):null
pubmed: 22375071
PLoS One. 2012;7(12):e51172
pubmed: 23272091
Emerg Infect Dis. 2014 Sep;20(9):1511-5
pubmed: 25148514
J Antimicrob Chemother. 2013 Apr;68(4):954-9
pubmed: 23194721
Emerg Infect Dis. 2007 Feb;13(2):255-8
pubmed: 17479888
PLoS One. 2009 Jul 13;4(7):e6216
pubmed: 19593449
Eur J Clin Microbiol Infect Dis. 2018 May;37(5):911-916
pubmed: 29450768
J Microbiol Methods. 2016 Aug;127:20-23
pubmed: 27192668
PLoS One. 2012;7(10):e41855
pubmed: 23094014
J Clin Microbiol. 2013 Jul;51(7):2443-7
pubmed: 23658269
PLoS One. 2018 Oct 9;13(10):e0204977
pubmed: 30300375
J Clin Microbiol. 2014 Feb;52(2):701-2
pubmed: 24478519
Clin Infect Dis. 2013 Sep;57(5):700-3
pubmed: 23728142
J Infect. 2014 Jul;69(1):51-9
pubmed: 24576825
Vector Borne Zoonotic Dis. 2011 Apr;11(4):327-39
pubmed: 20925523
Clin Microbiol Infect. 2013 Sep;19(9):860-8
pubmed: 23039210
PLoS One. 2017 Nov 30;12(11):e0188855
pubmed: 29190721
PLoS One. 2011;6(12):e28369
pubmed: 22163008
Clin Microbiol Infect. 2011 Mar;17(3):451-8
pubmed: 20491834
Antimicrob Resist Infect Control. 2017 Jun 5;6:55
pubmed: 28593043
MBio. 2017 Jan 17;8(1):
pubmed: 28096484