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Eurosurveillance, Volume 9, Issue 11, 01 November 2004
Surveillance report
Panton-Valentine leukocidin positive MRSA in 2003: the Dutch situation

Citation style for this article: Wannet WJ, Heck ME, Pluister GN, Spalburg E, Van Santen MG, Huijsdans XW, Tiemersma E, de Neeling AJ. Panton-Valentine leukocidin positive MRSA in 2003: the Dutch situation. Euro Surveill. 2004;9(11):pii=484. Available online: http://www.eurosurveillance.org/ViewArticle.aspx?ArticleId=484

 

WJB Wannet, MEOC Heck, GN Pluister, E Spalburg, MG van Santen, XW Huijsdens, E Tiemersma, AJ de Neeling

National Institute of Public Health and the Environment (RIVM), Bilthoven, the Netherlands

 


Analysis of methicillin-resistant Staphylococcus aureus (MRSA) isolates in the Netherlands in 2003 revealed that 8% of the hospital isolates carried the loci for Panton-Valentine leukocidin (PVL). Molecular subtyping showed that most Dutch PVL-MRSA genotypes corresponded to well-documented global epidemic types. The most common PVL-MRSA genotypes were sequence type ST8, ST22, ST30, ST59 and ST80. MRSA with ST8 increased in the Netherlands from 1% in 2002 to 17% in 2003. It is emphasised that PVL-MRSA might not only emerge in the community, but also in the hospital environment.
 
The worldwide emergence of hypervirulent MRSA strains carrying the loci for Panton-Valentine leukocidin (PVL) is not limited to the community, but may also be emerging in the hospital environment. Since 1989, the National Institute of Public Health and the Environment (RIVM) serves as the national reference center for the surveillance of MRSA in Dutch hospitals [1]. In 2003, we reported the first detection of PVL-MRSA in the Netherlands [2]. Since then, all hospital MRSA isolates (1 per patient) from the national surveillance programme are routinely tested by PCR for the presence of the PVL loci. In the period 2000-2002, approximately 10% of all Dutch hospital MRSA isolates carried the PVL loci, and molecular subtyping by multilocus sequence typing (MLST) revealed a predominant sequence type: ST80 [2]. This article summarises the characteristics of PVL-MRSA in the Netherlands in the year 2003.

In 2003, the PVL loci were detected in 8% (123/1601) of the MRSA isolates sent to the RIVM by Dutch hospitals. The national programme is solely based on surveillance of MRSA, so the proportion of PVL-positive methicillin-sensitive S. aureus (MSSA) remains unclear, but deserves attention in the future. Approximately 75% of the PVL-MRSA isolates were obtained from abscesses, furuncles, wounds or blood, the remainder from nose or throat; in non-PVL MRSA isolates the reverse ratio was observed. The male:female ratio was 1:1 and the mean age was 37 years (range 1-88 years). The PVL-MRSA isolates were obtained from clinics (40%), outpatient clinics (35%), and patients visiting general practitioners (25%).

Fifty isolates belonged to epidemic clusters and 73 were sporadic isolates. These 123 isolates belonged to 49 different PFGE types (Dice cut-off 95%, used for local epidemiology). There were 13 outbreaks with PVL-MRSA in the Netherlands in 2003, varying from 2-10 cases per outbreak.

One representative of each of the 49 PFGE types was subjected to MLST, resulting in 11 different STs. The 5 most common STs (found among 78% (38/49) of the PFGE types) were well-documented global epidemic types: ST8 (USA300), ST22 (EMRSA-15), ST30 (related to EMRSA-16), ST59 (Europe and the United States) and ST80 (common 'European' type) [3].

In the period 2000-2002, the predominant PVL-MRSA genotype was ST80 [2]. This was also the case in 2003: 20% (10/49) of all PVL-MRSA isolates was assigned ST80. This PVL-MRSA genotype is predominant in other European countries as well [3-5]. However, another dominant genotype, ST8, emerged in 2003: 16% (8/49) compared to 1% in 2002. PVL-positive S. aureus isolates with this genotype have recently been observed in outbreaks among prisoners and gay men in the United States. [6,7].

Approximately 65% of the PVL-MRSA isolates in 2003 were assigned staphylococcal cassette chromosome mec (SCCmec) type IV [8], followed by SCCmec type III (20%) and type I (15%). Recent data have indicated the presence of SCCmec type IV in community-acquired MRSA [9,10]. Since 40% of the Dutch isolates were obtained from clinics, PVL-MRSA isolates are also present, and presumably spreading, in the hospital environment. The presence of type IV SCCmec MRSA isolates in European hospitals has been reported before [11]. In general, it is assumed that type IV SCCmec can be transferred relatively easily and is present in a wide range of S. aureus backgrounds [12,13]. Because of the low (= 1%) MRSA prevalence in the Netherlands, we are able to study virtually all hospital-acquired MRSA found in the national surveillance programme, which provides an accurate representation of the actual MRSA situation in our country. The data presented here seem to confirm the hypothesis that PVL-MRSA might also be or become a hospital-associated public health threat.
 


References

1. Wannet WJB, Spalburg E, Heck MEOC, Pluister GN, Willems RJL, de Neeling AJ. Widespread dissemination in the Netherlands of the epidemic Berlin methicillin-resistant Staphylococcus aureus clone with low-level resistance to oxacillin. J Clin Microbiol. 2004; 42: 3077-3082.
2. Wannet WJB. Virulent MRSA strains containing the Panton-Valentine leukocidin gene in the Netherlands. Eurosurveillance Weekly. 2003;7 (http://www.eurosurveillance.org/ew/2003/030306.asp).
3. Vandenesch F, Naimi T, Enright MC, Lina G, Nimmo GR, Heffernan H, Liassine N, Bes M, Greenland T, Reverdy M-E and Etienne J. Community-acquired methicillin-resistant Staphylococcus aureus carrying Panton-Valentine leukocidin genes: worldwide emergence. Emerg Infect Dis. 2003; 9: 978-984.
4. Witte W, Cuny C, Strommenger B, Braulke C and Heuck D. Emergence of a new community-acquired MRSA strain in Germany. Euro Surveill. 2004; 9(1):16-8
5. Denis O, Malavoille X, Toteca G, Struelens MJ, Garrino MG, Glupczynski Y and Etienne J. Emergence of Panton-Valentine leukocidin positive community-acquired MRSA infections in Belgium. Eurosurveillance Weekly. 2004; 8 (http://www.eurosurveillance.org/ew/2004/040610.asp).
6. Anonymous. Skin infection spreads among gay men in L.A., posting date 27 January 2003 (http://www.promedmail.org).
7. Pan ES, Diep BA, Carleton HA, Charlebois ED, Sensabaugh GF, Haller BL and Perdreau-Remington F. Increasing prevalence of methicillin-resistant Staphylococcus aureus infection in California jails. Clin Infect Dis. 2003; 37: 1384-1388.
8. Oliveira DC and de Lencastre H. Multiplex PCR strategy for rapid identification of structural types and variants of the mec element in methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 2002; 46: 2155-2161.
9. Eady EA and Cove JH. Staphylococcal resistance revisited: community-acquired methicillin-resistant Staphylococcus aureus - an emerging problem for the management of skin and soft tissue infections. Curr Opin Infect Dis. 2003 Apr;16(2):103-24
10. Ma XX, Ito T, Tiensasitorn C, Jamklang M, Chongtrakool P, Boyle-Vavra S, Daum RS and Hiramatsu K. Novel type of staphylococcal cassette chromosome mec identified in community-acquired methicillin-resistant Staphylococcus aureus strains. Antimicrob Agents Chemother. 2002; 46: 1147-1152.
11. Sa-Leao R, Saches I and Dias D. Detection of an archaic clone of Staphylococcus aureus with low-level resistance to methicillin in a pediatric hospital in Portugal and in international samples: relics of a formerly widely disseminated strain. J Clin Microbiol. 1999; 37: 1913-1920.
12. Enright MC, Ashley Robinson DA, Randle G, Feil EJ, Grundmann H and Spratt BG. The evolutionary history of methicillin-resistant Staphylococcus aureus (MRSA). Proc Natl Acad Sci USA. 2002 May 28;99(11):7687-92.
13. Aires de Sousa M and de Lencastre H. Evolution of sporadic isolates of methicillin-resistant Staphylococcus aureus (MRSA) in hospitals and their similarities to isolates of community-acquired MRSA. J Clin Microbiol. 2003 Aug;41(8):3806-15.

 



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