期刊论文详细信息
BMC Infectious Diseases
Molecular typing and characterization of nasal carriage and community-onset infection methicillin-susceptible Staphylococcus aureus isolates in two Taiwan medical centers
Po-Liang Lu3  Chen-Her Wang2  Jung-Chung Lin1  Leung-Kei Kristopher Siu4  Feng-Jui Chen2 
[1] Department of Internal Medicine, Division of Infectious Diseases and Tropical Medicine, Tri-Service General Hospital, Taipei, Taiwan;Division of Infectious Diseases, National Health Research Institutes, Zhunan, Taiwan;School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan;Graduate Institute of Basic Medical Science, China Medical University, Taichung, Taiwan
关键词: Spa typing;    Multi-locus sequence typing;    Pulsed-field gel electrophoresis;    Lineage;    Staphylococcus aureus;    MSSA;    Infection;    Community onset;    Nasal carriage;   
Others  :  1158728
DOI  :  10.1186/1471-2334-12-343
 received in 2012-06-08, accepted in 2012-12-03,  发布年份 2012
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【 摘 要 】

Background

Compared to methicillin-resistant Staphylococcus aureus (MRSA), characteristics of nasal carriage and community-onset infection methicillin-susceptible S. aureus (MSSA) are less well known. No characteristics of MSSA in Taiwan have been reported previously.

Methods

We analyzed 100 nasal carriage and 34 community-onset infection MSSA isolates by pulsed-field gel electrophoresis (PFGE), spa typing, multi-locus sequence typing, agr typing, virulence gene detection, growth rate measurement, and antimicrobial susceptibility.

Results

In PFGE analysis, most (68%) infection isolates could be grouped in one major cluster using a 70% similarity cutoff. In contrast, only 17% of nasal carriage isolates belonged to this cluster. A similar classification was obtained using Based Upon Repeat Pattern analysis of spa types. The MSSA infection isolates cluster was closely related to the virulent clones of clonal complex 1 (CC1), which includes strains MW2 (USA400) and MSSA476. ST188 of CC1 was the predominant clone detected for community-onset MSSA infections. The only common ST type for MSSA and MRSA in Taiwan was ST59, the community-associated MRSA clone. It is likely, therefore, that MRSA originated from MSSA clones through SCCmec transfer. Compared to nasal carriage isolates, infection isolates less frequently possessed egc, tst and hlg genes, were more commonly susceptible to erythromycin (91% vs. 54%), and had shorter mean doubling times (38 min vs. 55 min).

Conclusions

The clonal lineages of MSSA nasal carriage and infection isolates differed in our sample of Taiwan isolates. Most community-onset MSSA infections resulted from relatively few clonal lineages. Nasal carriage isolates more frequently possessed the egc, tst and hlg genes, were more resistant to erythromycin, and grew more slowly.

【 授权许可】

   
2012 Chen et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Lowy FD: Staphylococcus aureus infections. N Engl J Med 1998, 339(8):520-532.
  • [2]Enright MC, Robinson DA, Randle G, Feil EJ, Grundmann H, Spratt BG: The evolutionary history of methicillin-resistant Staphylococcus aureus (MRSA). Proc Natl Acad Sci USA 2002, 99(11):7687-7692.
  • [3]von Eiff C, Becker K, Machka K, Stammer H, Peters G: Nasal carriage as a source of Staphylococcus aureus bacteremia. N Engl J Med 2001, 344(1):11-16.
  • [4]Wertheim HF, Melles DC, Vos MC, van Leeuwen W, van Belkum A, Verbrugh HA, Nouwen JL: The role of nasal carriage in Staphylococcus aureus infections. Lancet Infect Dis 2005, 5(12):751-762.
  • [5]Peacock SJ, Moore CE, Justice A, Kantzanou M, Story L, Mackie K, O'Neill G, Day NP: Virulent combinations of adhesin and toxin genes in natural populations of Staphylococcus aureus. Infect Immun 2002, 70(9):4987-4996.
  • [6]Lu PL, Chin LC, Peng CF, Chiang YH, Chen TP, Ma L, Siu LK: Risk factors and molecular analysis of community methicillin-resistant Staphylococcus aureus carriage. J Clin Microbiol 2005, 43(1):132-139.
  • [7]Klevens RM, Morrison MA, Nadle J, Petit S, Gershman K, Ray S, Harrison LH, Lynfield R, Dumyati G, Townes JM, et al.: Invasive methicillin-resistant Staphylococcus aureus infections in the United States. JAMA 2007, 298(15):1763-1771.
  • [8]McDougal LK, Steward CD, Killgore GE, Chaitram JM, McAllister SK, Tenover FC: Pulsed-field gel electrophoresis typing of oxacillin-resistant Staphylococcus aureus isolates from the United States: establishing a national database. J Clin Microbiol 2003, 41(11):5113-5120.
  • [9]Tenover FC, Arbeit RD, Goering RV, Mickelsen PA, Murray BE, Persing DH, Swaminathan B: Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol 1995, 33(9):2233-2239.
  • [10]Harmsen D, Claus H, Witte W, Rothganger J, Claus H, Turnwald D, Vogel U: 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 2003, 41(12):5442-5448.
  • [11]Mellmann A, Weniger T, Berssenbrugge C, Rothganger J, Sammeth M, Stoye J, Harmsen D: Based Upon Repeat Pattern (BURP): an algorithm to characterize the long-term evolution of Staphylococcus aureus populations based on spa polymorphisms. BMC Microbiol 2007, 7(1):98. BioMed Central Full Text
  • [12]Strommenger B, Braulke C, Heuck D, Schmidt C, Pasemann B, Nubel U, Witte W: spa typing of Staphylococcus aureus as a frontline tool in epidemiological typing. J Clin Microbiol 2008, 46(2):574-581.
  • [13]Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S: MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 2011, 28(10):2731-2739.
  • [14]Enright MC, Day NP, Davies CE, Peacock SJ, Spratt BG: Multilocus sequence typing for characterization of methicillin-resistant and methicillin-susceptible clones of Staphylococcus aureus. J Clin Microbiol 2000, 38(3):1008-1015.
  • [15]Lina G, Boutite F, Tristan A, Bes M, Etienne J, Vandenesch F: Bacterial competition for human nasal cavity colonization: role of Staphylococcal agr alleles. Appl Environ Microbiol 2003, 69(1):18-23.
  • [16]Chen FJ, Hiramatsu K, Huang IW, Wang CH, Lauderdale TL: Panton-Valentine leukocidin (PVL)-positive methicillin-susceptible and resistant Staphylococcus aureus in Taiwan: identification of oxacillin-susceptible mecA-positive methicillin-resistant S. aureus. Diagn Microbiol Infect Dis 2009, 65(4):351-357.
  • [17]Jarraud S, Mougel C, Thioulouse J, Lina G, Meugnier H, Forey F, Nesme X, Etienne J, Vandenesch F: Relationships between Staphylococcus aureus genetic background, virulence factors, agr groups (alleles), and human disease. Infect Immun 2002, 70(2):631-641.
  • [18]Ma XX, Galiana A, Pedreira W, Mowszowicz M, Christophersen I, Machiavello S, Lope L, Benaderet S, Buela F, Vincentino W, et al.: Community-acquired methicillin-resistant Staphylococcus aureus, Uruguay. Emerg Infect Dis 2005, 11(6):973-976.
  • [19]Kuda T, Shimizu K, Yano T: Comparison of rapid and simple colorimetric microplate assays as an index of bacterial count. Food Control 2004, 15(6):421-425.
  • [20]Shiloh MU, Ruan J, Nathan C: Evaluation of bacterial survival and phagocyte function with a fluorescence-based microplate assay. Infect Immun 1997, 65(8):3193-3198.
  • [21]Clinical and Laboratory Standards Institute: Performance standards for antimicrobial susceptibility testing; 20th informational supplement. Wayne, PA, USA: CLSI document M100-S20, CLSI; 2010.
  • [22]Chen FJ, Lauderdale TL, Huang IW, Lo HJ, Lai JF, Wang HY, Shiau YR, Chen PC, Ito T, Hiramatsu K: Methicillin-resistant Staphylococcus aureus in Taiwan. Emerg Infect Dis 2005, 11(11):1761-1763.
  • [23]Wang WY, Chiueh TS, Sun JR, Tsao SM, Lu JJ: Molecular typing and phenotype characterization of methicillin-resistant Staphylococcus aureus isolates from blood in Taiwan. PLoS One 2012, 7(1):e30394.
  • [24]Goering RV, Shawar RM, Scangarella NE, O'Hara FP, Amrine-Madsen H, West JM, Dalessandro M, Becker JA, Walsh SL, Miller LA, et al.: Molecular epidemiology of methicillin-resistant and methicillin-susceptible Staphylococcus aureus isolates from global clinical trials. J Clin Microbiol 2008, 46(9):2842-2847.
  • [25]Huang TW, Chen FJ, Miu WC, Liao TL, Lin AC, Huang IW, Wu KM, Tsai SF, Chen YT, Lauderdale TL: Complete genome sequence of Staphylococcus aureus M013, a pvl-positive, ST59-SCCmec type V strain isolated in Taiwan. J Bacteriol 2012, 194(5):1256-1257.
  • [26]Deurenberg RH, Stobberingh EE: The evolution of Staphylococcus aureus. Infect Genet Evolution 2008, 8(6):747-763.
  • [27]Feil EJ, Cooper JE, Grundmann H, Robinson DA, Enright MC, Berendt T, Peacock SJ, Smith JM, Murphy M, Spratt BG, et al.: How clonal is Staphylococcus aureus? J Bacteriol 2003, 185(11):3307-3316.
  • [28]Hallin M, Deplano A, Denis O, De Mendonca R, De Ryck R, Struelens MJ: Validation of pulsed-field gel electrophoresis and spa typing for long-term, nationwide epidemiological surveillance studies of Staphylococcus aureus infections. J Clin Microbiol 2007, 45(1):127-133.
  • [29]Baba T, Takeuchi F, Kuroda M, Yuzawa H, Aoki K, Oguchi A, Nagai Y, Iwama N, Asano K, Naimi T, et al.: Genome and virulence determinants of high virulence community-acquired MRSA. Lancet 2002, 359(9320):1819-1827.
  • [30]Balzli CL, Bartell J, Dajcs JJ, McCormick CC, Caballero AR, Stroman D, O'Callaghan RJ: A highly virulent Staphylococcus aureus: rabbit anterior chamber infection, characterization, and genetic analysis. Invest Ophthalmol Vis Sci 2010, 51(10):5114-5120.
  • [31]Holden MTG, Feil EJ, Lindsay JA, Peacock SJ, Day NPJ, Enright MC, Foster TJ, Moore CE, Hurst L, Atkin R, et al.: Complete genomes of two clinical Staphylococcus aureus strains: evidence for the rapid evolution of virulence and drug resistance. Proc Natl Acad Sci USA 2004, 101(26):9786-9791.
  • [32]Voyich JM, Otto M, Mathema B, Braughton KR, Whitney AR, Welty D, Long RD, Dorward DW, Gardner DJ, Lina G, et al.: Is Panton‐Valentine leukocidin the major virulence determinant in community‐associated methicillin‐resistant Staphylococcus aureus disease? J Infect Dis 2006, 194(12):1761-1770.
  • [33]Ferry T, Thomas D, Genestier A-L, Bes M, Lina G, Vandenesch F, Etienne J: Comparative prevalence of superantigen genes in Staphylococcus aureus isolates causing sepsis with and without septic shock. Clin Infect Dis 2005, 41(6):771-777.
  • [34]Grumann D, Scharf SS, Holtfreter S, Kohler C, Steil L, Engelmann S, Hecker M, Völker U, Bröker BM: Immune cell activation by enterotoxin gene cluster (egc)-encoded and non-egc superantigens from Staphylococcus aureus. J Immunol 2008, 181(7):5054-5061.
  • [35]Omoe K, Ishikawa M, Shimoda Y, Hu D-L, Ueda S, Shinagawa K: Detection of seg, seh, and sei genes in Staphylococcus aureus isolates and determination of the enterotoxin productivities of S. aureus isolates harboring seg, seh, or sei genes. J Clin Microbiol 2002, 40(3):857-862.
  • [36]van Belkum A, Melles DC, Snijders SV, van Leeuwen WB, Wertheim HFL, Nouwen JL, Verbrugh HA, Etienne J: Clonal distribution and differential occurrence of the enterotoxin gene cluster, egc, in carriage- versus bacteremia-associated isolates of Staphylococcus aureus. J Clin Microbiol 2006, 44(4):1555-1557.
  • [37]Vandenesch F, Naimi T, Enright MC, Lina G, Nimmo GR, Heffernan H, Liassine N, Bes M, Greenland T, Reverdy ME, et al.: Community-acquired methicillin-resistant Staphylococcus aureus carrying Panton-Valentine leukocidin genes: worldwide emergence. Emerg Infect Dis 2003, 9(8):978-984.
  • [38]van Leeuwen W, van Nieuwenhuizen W, Gijzen C, Verbrugh H, van Belkum A: Population studies of methicillin-resistant and -sensitive Staphylococcus aureus strains reveal a lack of variability in the agrD gene, encoding a staphylococcal autoinducer peptide. J Bacteriol 2000, 182(20):5721-5729.
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