Isolates of methicillin-resistant Staphylococcus aureus (MRSA) not belonging to the Brazilian epidemic clone
© Martino et al.; licensee BioMed Central. 2015
Received: 26 March 2015
Accepted: 28 April 2015
Published: 2 August 2015
Methicillin-resistant Staphylococcus aureus (MRSA) is an important cause of healthcare-associated infections.
Isolates of MRSA not belonging to the Brazilian Epidemic Clone (BEC) are colonizing and infecting patients at the hospital. These include strains carrying SCCmec type II, not previously described in the city of São Paulo, showing a trend to a MRSA genetic diversity.
KeywordsMRSA SCCmec Genetic diversity Colonization Infection
SCCmec typing revealed that Brazilian clone isolates harbor SCCmec III. We found that is possible a MRSA genetic diversity in Brazil, when strains of MRSA not belonging to the Brazilian Epidemic Clone (BEC) that were isolated in patients at the hospital.
Methicillin-resistant Staphylococcus aureus (MRSA) is involved in increasing number of serious infectious with high risk for morbidity and mortality and it is an important cause of healthcare-associated infections . Although the active surveillance and the impact of MRSA colonization on the occurrence of S. aureus infections are unclear, some studies described that asymptomatic colonization with MRSA is a risk factor for in a subsequent MRSA infection patients [2, 3].
In Brazil, a considerable number of hospital infections have been caused by an unique multi-resistant MRSA clone designated as the Brazilian epidemic clone (BEC) . SCCmec typing revealed that Brazilian clone isolates harbor SCCmec III .
During a study on hand hygiene compliance, samples were obtained by nasal swab every four days from 446 patients admitted patients at two step-down units (SDUs) of a private tertiary care hospital in São Paulo, Brazil. Blood Culture samples were also obtained at an intensive care unit (ICU) of the same hospital, as part of an antimicrobial resistance surveillance project (unpublished data). The study period was from March 20, 2007 to September 20, 2007 . The open model ICU is a 38-bed medical-surgical unit; where approximately 2,200 patients are admitted annually and the SDUs are medical-surgical 20-bed units each. Nasal samples were plated onto chromagar (CHROMagar, MRSA, CHROMagar, Paris, France) and selective staphylococcal media (Mannitol Salt Agar). Blood cultures were performed at BACTEC 9240 instrument (BACTEC 9240, BD Diagnostics, Sparks, MD) and the positive samples were plated onto chocolate and sheep blood agar.
Twenty-one MRSA strains were isolated from nasal carriers (in the SDUs) and two MRSA strains obtained from patients with bloodstream infections (in the ICU). Staphylococcus species were confirmed by an automated (Vitek 2 System,, Hazelwood, MO)) and manual biochemical tests. For the susceptibility profile determination oxacillin agar screening was used with automated system according with Clinical Laboratory Standards Institute (CLSI) recommendations .
SCCmec typing was performed using a polymerase chain reaction (PCR) method . All MRSA isolates from nasal cultures were typed by pulsed-field gel electrophoresis (PFGE). Bacterial cells grown overnight were embedded in agarose, lysed and deproteinated to isolate near intact genomic DNA. The DNA was digested with restriction endonuclease SmaI (3 μl/sample) (new England Biolabs, Ipswich, MA) and the restriction fragments were separated using CHEF DR III (BioRad, Hercules, CA) under the following conditions: 1 % agarose, 0.5 × TBE, 200 v and a switch interval ranging from 5-40 sec over 21 h period. The gel was stained in a 1.5 μl/ml ethidium bromide solution .
PFGE patterns were compared to MRSA Brazilian Epidemic, Pediatric and New York-Japan clones. Tenover’s criteria  were used to PFGE analyses, patterns were designated by a capital letter (e.g. A, B, C) when all bands were shown to match. When a difference in one to six bands occurred, the strains were assigned as a subtype or variant of the major type, and were designated with the same capital letter followed by an Arabic number (Ex.: A1, A2, A3). Cluster analysis was provided by BioNumeric software (Applied Maths, Kortrijk, Belgium).
MRSA remains as an important pathogen in Brazilian hospitals, involved in serious infections. While a study was performed in Brazil with strains isolated from 1995 to 1997 in several private and public hospitals showed all isolates with the same PFGE pattern (BEC), in our sample these represent only 61.9 % .
Recent studies published in Brazil show Type III and even Type IVSCCmec MRSA in hospital isolates [11, 12] indicating that the strains obtained from our blood cultures do not represent a typical pattern and are similar to New York-Japan clone.
In-patient colonization and infection with isolates of MRSA not belonging to the Brazilian Epidemic Clone (BEC) have been observed, and include strains carrying SCCmec type II, not previously described in the city of São Paulo, showing a trend toward MRSA genetic diversity.
- Moreillon P. New and emerging treatment of Staphylococcus aureus infections in the hospital setting. Clin Microbiol Infect. 2008;14:S32–41.View ArticleGoogle Scholar
- Davis KA, Stewart JJ, Crouch HK, Florez CE, Hospenthal DR. Methicillin-resistant Staphylococcus aureus (MRSA) nares colonization at hospital admission and its effect on subsequent MRSA infection. Clin Infect Dis. 2004;39:776–82.View ArticlePubMedGoogle Scholar
- Lucet JC, Paoletti X, Lolom I, Paugam-Burtz C, Trouillet JL, Timsit JF, et al. Successful long-term program for controlling methicillin-resistant Staphylococcus aureus in intensive care units. Intensive Care Med. 2005;31:1051–17.View ArticlePubMedGoogle Scholar
- Da Silva Coimbra MV, Teixeira LA, Ramos RL, Predari SC, Castello L, Famiglietti A, et al. Spread of the Brazilian epidemic clone of a multiresistant MRSA in two cities in Argentina. J Med Microbiol. 2000;49(2):187–92.View ArticlePubMedGoogle Scholar
- Vivoni AM, Diep BA, Santos KR, Riley LW, Sensabaugh GF, Moreira BM. Clonal composition of Staphylococcus aureus isolates at a Brazilian university hospital: identification of international circulating lineages. J Clin Microbiol. 2006;44(5):1686–91.View ArticlePubMedPubMed CentralGoogle Scholar
- Marra AR, D’Arco C, Bravim Bde A, Martino MD, Correa L, Silva CV, et al. Controlled trial measuring the effect of a feedback intervention on hand hygiene compliance in a step-down unit. Infect Control Hosp Epidemiol. 2008;29(8):730–5.View ArticlePubMedGoogle Scholar
- CLINICAL LABORATORY STANDARDS INSTITUTE. Performance standands for antimicrobial susceptibility tests; Approved Standard Ninth Edition. CLSI publication n.M2-A9. Clinical Laboratory Standards Institute: Wayne, PA; 2006.Google Scholar
- Zhang K, McClure JA, Elsayed S, Louie T, Conly JM. Novel multiples PCR assay for characterization and concomitant subtyping of staphylococcal cassette chromosome mec types I to V in methicillin-resistant Staphylococcus aureus. J. Clin. Microbiol. 2005;43(10):5026-5033.
- McDougal LK, Steward CD, Killgore GE, Chailtram JM, McAllister SK, Tenover FC. Pulsed-field gel electrophoresis typing of oxacillin-resistatn Staphylococcus aureus isolates from the United States: establishing a national database. J Clin Microbiol. 2003;41(11):5113–20.View ArticlePubMedPubMed CentralGoogle Scholar
- Oliveira GA, Faria JB, Levy CE, Mamizuka EM. Characterization of the Brazilian endemic clone of methicillin-resistant Staphylococcus aureus (MRSA) from hospitals throughout Brazil. Braz J Infect Dis. 2001;5(4):163–70.View ArticlePubMedGoogle Scholar
- Trindade PA, Pacheco RL, Costa SF, Rossi F, Barone AA, Mamizuka EM, et al. Prevalence of SCCmec type IV in nosocomial bloodstream isolates of methicillin-resistant Staphylococcus aureus. J Clin Microbiol. 2005;43(7):3435–7.View ArticlePubMed CentralGoogle Scholar
- Perez LRR, D’Azevedo PA. Clonal types and antimicrobial resistance profiles of mehticillin-resistant Staphylococcus aureus isolates from hospitals in south Brazil. Rev Inst Med Trop. 2008;50:135–7.View ArticleGoogle Scholar
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.