Evolution of community-associated MRSA: a 20-year genomic and epidemiological study in Region Örebro County, Sweden
2024 (English) In: Frontiers in Microbiology, E-ISSN 1664-302X, Vol. 15, article id 1504860Article in journal (Refereed) Published
Abstract [en]
BACKGROUND: Methicillin-resistant Staphylococcus aureus (MRSA) has been an issue in healthcare since the 1960s. It was initially found only in healthcare facilities, but in the late 1990s it began to be seen with no healthcare connexion. The mechanisms of intercontinental and national spread are not fully understood, as sometimes novel outbreaks occur without any identifiable source or connexion to locally dominant clonal clusters.
METHODS: This study investigated the epidemiology and genomics of community-associated MRSA in Region Örebro County, Sweden, through 330 isolates collected between 2000 and 2019.
RESULTS: A shift in the dominant sequence type (ST) from ST80 to ST22 occurred in 2011-2019, along with an increase in the prevalence of STs belonging to clonal complexes CC5 and CC22. Both ST8 and ST80 isolates seemed to give way to emerging ST22 isolates, also indicated by the declining presence of the USA300 clone. The staphylococcal chromosomal cassette mec (SCCmec) type IV Remained dominant.
CONCLUSIONS: The SCCmec type IV characteristic appears to be relatively geographically stable, possibly due to its low fitness cost and transductal capabilities. This warrants further studies of SCCmec type IV variant's survival mechanics as well as the effects of migratory flow on local epidemiology, in preparation for future possible outbreaks.
Place, publisher, year, edition, pages Frontiers Media S.A., 2024. Vol. 15, article id 1504860
Keywords [en]
CA-MRSA, MLST, SCCmec, Staphylococcus aureus, clonal complex, epidemiology
National Category
Microbiology in the medical area
Identifiers URN: urn:nbn:se:oru:diva-118166 DOI: 10.3389/fmicb.2024.1504860 ISI: 001390484300001 PubMedID: 39764449 Scopus ID: 2-s2.0-85214142219 OAI: oai:DiVA.org:oru-118166 DiVA, id: diva2:1925721
2025-01-092025-01-092025-01-20 Bibliographically approved