A tale of two STs: molecular and clinical epidemiology of MRSA t304 in Norway 2008-2016.

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    • Source:
      Publisher: Springer Country of Publication: Germany NLM ID: 8804297 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1435-4373 (Electronic) Linking ISSN: 09349723 NLM ISO Abbreviation: Eur J Clin Microbiol Infect Dis Subsets: MEDLINE
    • Publication Information:
      Publication: Berlin : Springer
      Original Publication: [Wiesbaden, Federal Republic of Germany] : Vieweg, [c1988-
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    • Abstract:
      The purpose of this study was to investigate the epidemiological, molecular, and clinical characteristics of MRSA t304/ST8 and t304/ST6 in Norway from 2008 to 2016. Clinical and epidemiological data were collected for each case included in the study. Strains were characterized by PCR, spa typing, antimicrobial susceptibility testing, and whole genome sequencing. The overall number of cases of MRSA t304 increased from 27 in 2008 to 203 in 2016. Most MRSA t304/ST8 cases were defined as HA-MRSA (89.9%) and diagnosed in persons with Norwegian background, many of them living in nursing homes (62.3%). The number of t304/ST8 cases declined throughout the study period and it has not been reported in Norway since 2014. The increasing MRSA t304/ST6 genotype has mainly been introduced to Norway by immigration from the Middle East, but also from other parts of the world. The t304/ST6 clone is mostly classified as CA-MRSA (75.1%), does not seem to cause serious infections, is not multi-resistant, and has not yet caused outbreaks in Norway. This study provides an example of two MRSA clones with the same spa type found in different epidemiological settings. This is very unusual, but still a reminder that spa typing in some cases may have insufficient discriminatory power for surveillance of MRSA. Our results highlight the importance of active surveillance and characterization of emerging MRSA clones with high potential for spread in the community, which may potentially cause outbreaks in healthcare facilities.
      (© 2021. The Author(s).)
    • References:
      Cassini A, Hogberg LD, Plachouras D, Quattrocchi A, Hoxha A, Simonsen GS, Colomb-Cotinat M, Kretzschmar ME, Devleesschauwer B, Cecchini M, Ouakrim DA, Oliveira TC, Struelens MJ, Suetens C, Monnet DL, Burden of AMRCG, (2019) Attributable deaths and disability-adjusted life-years caused by infections with antibiotic-resistant bacteria in the EU and the European Economic Area in 2015: a population-level modelling analysis. Lancet Infect Dis 19(1):56–66. (PMID: 10.1016/S1473-3099(18)30605-4304096836300481)
      NORM/NORM-VET 2016. Usage of Antimicrobial agents and occurrence of antimicrobial resistance in Norway. Tromsø / Oslo 2017.
      NORM/NORM-VET 2008. Usage of antimicrobial agents and occurrence of antimicrobial resistance in Norway. Tromsø / Oslo 2009.
      Petersen A, Larssen KW, Gran FW, Enger H, Haeggman S, Makitalo B, Haraldsson G, Lindholm L, Vuopio J, Henius AE, Nielsen J, Larsen AR (2021) Increasing incidences and clonal diversity of methicillin-resistant Staphylococcus aureus in the Nordic countries - results from the Nordic MRSA surveillance. Front Microbiol 12:668900. (PMID: 10.3389/fmicb.2021.668900339953338119743)
      Blomfeldt A, Hasan AA, Aamot HV (2016) Can MLVA differentiate among endemic-like MRSA isolates with identical spa-type in a low-prevalence region? PLoS One 11(2):e0148772. (PMID: 10.1371/journal.pone.0148772268597654747572)
      Uhlemann AC, Dumortier C, Hafer C, Taylor BS, Sanchez J, Rodriguez-Taveras C, Leon P, Rojas R, Olive C, Lowy FD (2012) Molecular characterization of Staphylococcus aureus from outpatients in the Caribbean reveals the presence of pandemic clones. Eur J Clin Microbiol Infect Dis 31(4):505–511. (PMID: 10.1007/s10096-011-1339-221789605)
      Bartels MD, Worning P, Andersen LP, Bes M, Enger H, Ås CG, Hansen TA, Holzknecht BJ, Larssen KW, Laurent F, Mäkitalo B, Pichon B, Svartström O, Westh H (2021) Repeated introduction and spread of the MRSA clone t304/ST6 in northern Europe. Clin Microbiol Infect 27(2):284.e1–284.e5.  https://doi.org/10.1016/j.cmi.2020.05.004.
      Udo EE, Al-Lawati BA, Al-Muharmi Z, Thukral SS (2014) Genotyping of methicillin-resistant Staphylococcus aureus in the Sultan Qaboos University Hospital, Oman reveals the dominance of Panton-Valentine leucocidin-negative ST6-IV/t304 clone. New Microbes New Infect 2(4):100–105. (PMID: 10.1002/nmi2.47253563544184578)
      Sonnevend A, Blair I, Alkaabi M, Jumaa P, Al Haj M, Ghazawi A, Akawi N, Jouhar FS, Hamadeh MB, Pal T (2012) Change in meticillin-resistant Staphylococcus aureus clones at a tertiary care hospital in the United Arab Emirates over a 5-year period. J Clin Pathol 65(2):178–182. (PMID: 10.1136/jclinpath-2011-20043622039280)
      Li D, Wu C, Wang Y, Fan R, Schwarz S, Zhang S (2015) Identification of multiresistance gene cfr in methicillin-resistant Staphylococcus aureus from pigs: plasmid location and integration into a staphylococcal cassette chromosome mec complex. Antimicrob Agents Chemother 59(6):3641–3644. (PMID: 10.1128/AAC.00500-15258242344432165)
      Stegger M, Andersen PS, Kearns A, Pichon B, Holmes MA, Edwards G, Laurent F, Teale C, Skov R, Larsen AR (2012) Rapid detection, differentiation and typing of methicillin-resistant Staphylococcus aureus harbouring either mecA or the new mecA homologue mecA(LGA251). Clin Microbiol Infect 18(4):395–400. (PMID: 10.1111/j.1469-0691.2011.03715.x22429460)
      Harmsen D, Claus H, Witte W, Rothganger J, Claus H, Turnwald D, Vogel U (2003) Typing of methicillin-resistant Staphylococcus aureus in a university hospital setting by using novel software for spa repeat determination and database management. J Clin Microbiol 41(12):5442–5448. (PMID: 10.1128/JCM.41.12.5442-5448.200314662923309029)
      Mellmann A, Friedrich AW, Rosenkotter N, Rothganger J, Karch H, Reintjes R, Harmsen D (2006) Automated DNA sequence-based early warning system for the detection of methicillin-resistant Staphylococcus aureus outbreaks. PLoS Med 3(3):e33. (PMID: 10.1371/journal.pmed.0030033163966091325475)
      Ridom spaServer. Ridom GmbH, https://spaserver.ridom.de/ . Accessed 31 Dec 2016.
      Seemann T, Goncalves da Silva A, Bulach DM, Schultz MB, Kwong JC, Howden BP. Nullarbor,  https://github.com/tseemann/nullarbor . Accessed 13 Oct 2019.
      National Database of Antibiotic Resistant Organisms (NDARO). National Center for Biotechnology Information,  https://www.ncbi.nlm.nih.gov/pathogens/antimicrobial-resistance/ . Accessed 19 Apr 2020.
      Chen L, Yang J, Yu J, Yao Z, Sun L, Shen Y, Jin Q (2005) VFDB: a reference database for bacterial virulence factors. Nucleic Acids Res 33(Data issue):D325-328. (PMID: 15608208)
      Kaya H, Hasman H, Larsen J, Stegger M, Johannesen TB, Allesøe RL, Lemvigh CK, Aarestrup FM, Lund O, Larsen AR (2018) SCCmecFinder, a Web-Based Tool for Typing of Staphylococcal Cassette Chromosome mec in Staphylococcus aureus Using Whole-Genome Sequence Data. mSphere 3(1):e00612–e00617.  https://doi.org/10.1128/mSphere.00612-17.
      Page AJ, Cummins CA, Hunt M, Wong VK, Reuter S, Holden MT, Fookes M, Falush D, Keane JA, Parkhill J (2015) Roary: rapid large-scale prokaryote pan genome analysis. Bioinformatics 31(22):3691–3693. (PMID: 10.1093/bioinformatics/btv421261981024817141)
      Price MN, Dehal PS, Arkin AP (2010) FastTree 2–approximately maximum-likelihood trees for large alignments. PLoS One 5(3):e9490. (PMID: 10.1371/journal.pone.0009490202248232835736)
      Kumar S, Stecher G, Li M, Knyaz C, Tamura K (2018) MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol 35(6):1547–1549. (PMID: 10.1093/molbev/msy096297228875967553)
      Letunic I, Bork P (2021) Interactive Tree Of Life (iTOL) v5: an online tool for phylogenetic tree display and annotation. Nucleic Acids Res 49(W1):W293–W296.  https://doi.org/10.1093/nar/gkab301.
      Steen TW, Jorgensen SB, Garder KM, Kollerud Rdel R, Kvalvaag G, Blomfeldt A (2013) Cases of MRSA in nursing homes in Oslo 2005–11. Tidsskr Nor Laegeforen 133(17):1819–1823. (PMID: 10.4045/tidsskr.12.093524042294)
      Tegegne HA, Kolackova I, Florianova M, Gelbicova T, Wattiau P, Boland C, Karpiskova R (2019) Genome sequences of livestock-associated methicillin-resistant Staphylococcus aureus spa type t899 strains Belonging to three different sequence types (ST398, ST9, and ST4034). Microbiol Resour Announc 8 (2).
      Bartels MD, Worning P, Andersen LP, Bes M, Enger H, As CG, Hansen TA, Holzknecht BJ, Larssen KW, Laurent F, Makitalo B, Pichon B, Svartstrom O, Westh H (2021) Repeated introduction and spread of the MRSA clone t304/ST6 in northern Europe. Clin Microbiol Infect 27(2):284 e281-284 e285. (PMID: 10.1016/j.cmi.2020.05.004)
      Kristinsdottir I, Haraldsson A, Thorkelsson T, Haraldsson G, Kristinsson KG, Larsen J, Larsen AR, Thors V (2019) MRSA outbreak in a tertiary neonatal intensive care unit in Iceland. Infect Dis (Lond) 51(11–12):815–823. (PMID: 10.1080/23744235.2019.1662083)
      Brown NM, Reacher M, Rice W, Roddick I, Reeve L, Verlander NQ, Broster S, Ogilvy-Stuart AL, D'Amore A, Ahluwalia J, Robinson S, Thaxter R, Moody C, Kearns A, Greatorex J, Martin H, Török ME, Enoch DA (2019) An outbreak of meticillin-resistant Staphylococcus aureus colonization in a neonatal intensive care unit: use of a case-control study to investigate and control it and lessons learnt. J Hosp Infect 103(1):35–43. https://doi.org/10.1016/j.jhin.2019.05 .009.
    • Contributed Indexing:
      Keywords: Epidemiology; Genotyping; MRSA; Surveillance; t304/ST6; t304/ST8
    • Publication Date:
      Date Created: 20211023 Date Completed: 20220131 Latest Revision: 20220812
    • Publication Date:
      20231215
    • Accession Number:
      PMC8770451
    • Accession Number:
      10.1007/s10096-021-04353-9
    • Accession Number:
      34687359