MRSA outbreak in a tertiary neonatal intensive care unit in Iceland

被引:7
作者
Kristinsdottir, Iris [1 ]
Haraldsson, Asgeir [1 ,2 ]
Thorkelsson, Thordur [1 ,2 ]
Haraldsson, Gunnsteinn [1 ,3 ]
Kristinsson, Karl G. [1 ,3 ]
Larsen, Jesper [4 ]
Larsen, Anders Rhod [4 ]
Thors, Valtyr [1 ,2 ]
机构
[1] Univ Iceland, Fac Med, Reykjavik, Iceland
[2] Landspitali Univ Hosp, Childrens Hosp Iceland, Reykjavik, Iceland
[3] Landspitali Univ Hosp, Dept Clin Microbiol, Reykjavik, Iceland
[4] Statens Serum Inst, Dept Bacteria Parasites & Fungi, Copenhagen, Denmark
关键词
MRSA; MLST; neonates; NICU; whole genome sequencing; decolonization; RESISTANT STAPHYLOCOCCUS-AUREUS; METHICILLIN-RESISTANT; MAXIMUM-LIKELIHOOD; RISK-FACTORS; INFECTION; TRANSMISSION; ALGORITHMS; ALIGNMENT; IDENTIFICATION; DECOLONIZATION;
D O I
10.1080/23744235.2019.1662083
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: Preventing the spread of methicillin-resistant Staphylococcus aureus (MRSA) and understanding the pathophysiology and transmission is essential. This study describes an MRSA outbreak in a neonatal intensive care unit in Reykjavik, Iceland at a time where no screening procedures were active. Materials and methods: After isolating MRSA in the neonatal intensive care unit in 2015, neonates, staff members and parents of positive patients were screened and environmental samples collected. The study period was from 14 April 2015 until 31 August 2015. Antimicrobial susceptibility testing, spa-typing and whole genome sequencing were done on MRSA isolates. Results: During the study period, 96/143 admitted patients were screened for colonization. Non-screened infants had short admissions not including screening days. MRSA was isolated from nine infants and seven parents. All tested staff members were negative. Eight infants and six parents carried MRSA ST30-IVc with spa-type t253 and one infant and its parent carried MRSA CC9-IVa (spa-type t4845) while most environmental samples were MRSA CC9-IVa (spa-type t4845). Whole genome sequencing revealed close relatedness between all ST30-IVc and CC9-IVa isolates, respectively. All colonized infants received decolonization treatment, but 3/9 were still positive when last sampled. Discussion: The main outbreak source was a single MRSA ST30-IVc (spa-type t253), isolated for the first time in Iceland. A new CC9-IVa (spa-type t4845) was also identified, most abundant on environmental surfaces but only in one patient. The reason for the differences in the epidemiology of the two strains is not clear. The study highlights a need for screening procedures in high-risk settings and guidelines for neonatal decolonization.
引用
收藏
页码:815 / 823
页数:9
相关论文
共 36 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]   Prospective evaluation of a multi-factorial prevention strategy on the impact of nosocomial infection in very-low-birthweight infants [J].
Andersen, C ;
Hart, J ;
Vemgal, P ;
Harrison, C .
JOURNAL OF HOSPITAL INFECTION, 2005, 61 (02) :162-167
[3]   Safety of chlorhexidine gluconate used for skin antisepsis in the preterm infant [J].
Chapman, A. K. ;
Aucott, S. W. ;
Milstone, A. M. .
JOURNAL OF PERINATOLOGY, 2012, 32 (01) :4-9
[4]   Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins [J].
Croucher, Nicholas J. ;
Page, Andrew J. ;
Connor, Thomas R. ;
Delaney, Aidan J. ;
Keane, Jacqueline A. ;
Bentley, Stephen D. ;
Parkhill, Julian ;
Harris, Simon R. .
NUCLEIC ACIDS RESEARCH, 2015, 43 (03) :e15
[5]   Fast algorithms for large-scale genome alignment and comparison [J].
Delcher, AL ;
Phillippy, A ;
Carlton, J ;
Salzberg, SL .
NUCLEIC ACIDS RESEARCH, 2002, 30 (11) :2478-2483
[6]   A framework for variation discovery and genotyping using next-generation DNA sequencing data [J].
DePristo, Mark A. ;
Banks, Eric ;
Poplin, Ryan ;
Garimella, Kiran V. ;
Maguire, Jared R. ;
Hartl, Christopher ;
Philippakis, Anthony A. ;
del Angel, Guillermo ;
Rivas, Manuel A. ;
Hanna, Matt ;
McKenna, Aaron ;
Fennell, Tim J. ;
Kernytsky, Andrew M. ;
Sivachenko, Andrey Y. ;
Cibulskis, Kristian ;
Gabriel, Stacey B. ;
Altshuler, David ;
Daly, Mark J. .
NATURE GENETICS, 2011, 43 (05) :491-+
[7]   Multilocus sequence typing for characterization of methicillin-resistant and methicillin-susceptible clones of Staphylococcus aureus [J].
Enright, MC ;
Day, NPJ ;
Davies, CE ;
Peacock, SJ ;
Spratt, BG .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (03) :1008-1015
[8]   Molecular typing of methicillin-resistant Staphylococcus aureus on the basis of protein A gene polymorphism [J].
Frenay, HME ;
Bunschoten, AE ;
Schouls, LM ;
vanLeeuwen, WJ ;
VandenbrouckeGrauls, CMJE ;
Verhoef, J ;
Mooi, FR .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1996, 15 (01) :60-64
[9]   Methicillin-resistant Staphylococcus aureus nasal colonization in a level III neonatal intensive care unit: Incidence and risk factors [J].
Giuffre, Mario ;
Amodio, Emanuele ;
Bonura, Celestino ;
Geraci, Daniela M. ;
Saporito, Laura ;
Ortolano, Rita ;
Corsello, Giovanni ;
Mammina, Caterina .
AMERICAN JOURNAL OF INFECTION CONTROL, 2015, 43 (05) :476-481
[10]   A Network Model of Hand Hygiene: How Good Is Good Enough to Stop the Spread of MRSA? [J].
Goldstein, Neal D. ;
Eppes, Stephen C. ;
Mackley, Amy ;
Tuttle, Deborah ;
Paul, David A. .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2017, 38 (08) :945-952