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Methicillin-resistantStaphylococcus aureus disease in a portuguese hospital: Characterization of clonal types by a combination of DNA typing methods

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Abstract

Fifteen pediatric patients as well as the five nursing staff of the Burn Unit of the Hospital D. Estefania in Lisbon, Portugal, were assayed at weekly intervals over a five-month period in order to identify the nature and number of methicillin-resistantStaphylococcus aureus (MRSA) clones associated with colonization and wound infection. Methicillin resistance was confirmed by amec-specific DNA probe. MRSA isolates were classified into chromosomal types (clones) on the basis of a variety of techniques: (i) ribotyping; (ii) restriction digestion by the endonucleaseClaI followed by Southern hybridization with themecA-specific DNA probe and (iii) by hybridization with Tn554; and (iv) pulsed-field electrophoresis (PFE) ofSmaI digests followed by (v) Southern hybridization with themecA DNA probe. A sixth, physiological technique (population analysis) was used to define the mode of phenotypic expression of methicillin resistance in each isolate. All isolates carried a single, common polymorph (ClaI type III) of themecA gene. Hybridization with Tn554 resolved these isolates to two novel patterns (alpha and beta), of which one (Tn554 alpha) was predominant (90 %). This pattern could be further resolved to four closely related PFE types (A through D). In contrast, all isolates with the Tn554 beta pattern belonged to an additional, grossly different PFE type E. The Tn554 beta class was also unique in that these bacteria carried themecA gene in aSmaI fragment smaller (about 170 kb) than that found in the alpha type strains (194 kb). Most isolates (83 %) showed a single heterogeneous (population analysis Class 3) mode of resistance expression. The data demonstrate the full capacity of the globally rare (ClaI type III) MRSA clone for colonization and virulence. The results also document the stability of the complex heterogeneous resistance phenotype as well as the stability of the chromosomal types under conditions of in vivo carriage over a period of several months. In a few isolates the samemecA polymorph was present in several, grossly different genetic backgrounds, suggesting horizontal transfer of themecA gene.

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References

  1. Matsuhashi M, Song MD, Ishino F, Wachi M, Doi M, Inoue M, Ubukata K, Yamashita N, Konno M Molecular cloning of the gene of a penicillin binding protein supposed to cause high resistance to beta-lactam antibiotics inStaphylococcus aureus. Journal of Bacteriology 1986, 167: 975–980.

    PubMed  CAS  Google Scholar 

  2. Ryffel C, Tesch W, Birch-Machin I, Reynolds PE, Barberis-Maino L, Kayser FH, Berger-Bachi B Sequence comparison ofmecA genes isolated from methicillin-resistantStaphylococcus aureus andStaphylococcus epidermidis. Gene 1990, 94: 137–138.

    Article  PubMed  CAS  Google Scholar 

  3. Wu CYE, Hoskins J, Blaszczak LC, Preston DA, Skatrud PL Construction of a water-soluble form of penicillin-binding protein 2a from a methicillin-resistantStaphylococcus aureus isolate. Antimicrobial Agents and Chemotherapy 1992, 36: 533–539.

    PubMed  CAS  Google Scholar 

  4. Lacey RW, Grinsted J Genetic analysis of methicillin-resistant strains ofStaphylococcus aureus; evidence for their evolution from a single clone. Journal of Medical Microbiology 1973, 6: 511–526.

    Article  PubMed  CAS  Google Scholar 

  5. Pattee PA, Lee H-C, Bannantine JP Genetic and physical mapping of the chromosome ofStaphylococcus aureus. In: Novick R, Skurray RA (ed): Molecular biology of the staphylococci. VCH Publishers, New York, 1990, p. 41–58.

    Google Scholar 

  6. Kreiswirth B, Kornblum J, Arbeit RD, Eisner W, Maslow JN, McGeer A, Low DE, Novick RP Evidence for a clonal origin of methicillin resistance inStaphylococcus aureus. Science 1993, 259: 227–230.

    PubMed  CAS  Google Scholar 

  7. Musser JM, Selander RK Genetic analysis of natural populations ofStaphylococcus aureus. In: Novick R, Skurray RA (ed): Molecular biology of the staphylococci. VCH Publishers, New York, 1990, p. 59–67.

    Google Scholar 

  8. Barber M Methicillin-resistant staphylococci. Journal of Clinical Pathology 1961, 14: 385–393.

    PubMed  CAS  Google Scholar 

  9. Gaisford C, Reynolds PE Methicillin resistance inStaphylococcus epidermidis. Relationship between the additional penicillin-binding protein and an attachment transpeptidase. European Journal of Biochemistry 1989, 185: 211–218.

    Article  PubMed  CAS  Google Scholar 

  10. Ubukata K, Nonoguchi R, Song MD, Matsuhashi M, Konno M Homology ofmecA gene in methicillin-resistantStaphylococcus haemolyticus andStaphylococcus simulans to that ofStaphylococcus aureus. Antimicrobial Agents and Chemotherapy 1990, 34: 170–172.

    PubMed  CAS  Google Scholar 

  11. Pierre J, Williamson R, Bornet M, Gutmann L Presence of an additional penicillin-binding protein in methicillin-resistantStaphylococcus epidermidis, Staphyococcus haemolyticus, Staphylococcus hominis, andStaphylococcus simulans with a low affinity for methicillin, cephalothin, and cefamandole. Antimicrobial Agents and Chemotherapy 1990, 34: 1691–1694.

    PubMed  CAS  Google Scholar 

  12. Stratton CW, Gelfand MS, Gerberding JL, Chambers HF Characterization of mechanisms of resistance to beta-lactam antibiotics in methicillin-resistant strains ofStaphylococcus saprophyticus. Antimicrobial Agents and Chemotherapy 1990, 34: 1780–1782.

    PubMed  CAS  Google Scholar 

  13. Suzuki E, Hiramatsu K, Yokota T Survey of methicillin-resistant clinical strains of coagulase-negative staphylococci formecA gene distribution. Antimicrobial Agents and Chemotherapy 1992, 36: 429–434.

    PubMed  CAS  Google Scholar 

  14. De Buyser M-L, Morvan A, Grimont F, El Solh N Characterization ofStaphylococcus species by ribosomal RNA gene restriction patterns. Journal of General Microbiology 1989, 135: 989–999.

    PubMed  Google Scholar 

  15. Goering RV, Duensing TD Rapid field inversion gel electrophoresis in combination with an rRNA gene probe in the epidemiological evaluation of staphylococci. Journal of Clinical Microbiology 1990, 28: 426–429.

    PubMed  CAS  Google Scholar 

  16. Goering RV, Winters MA Rapid method for epidemiological evaluation of gram-positive cocci by field inversion gel electrophoresis. Journal of Clinical Microbiology 1992, 30: 577–580.

    PubMed  CAS  Google Scholar 

  17. El-Adhami W, Roberts L, Vickery A, Inglis B, Gibbs A, Stewart PR Epidemiological analysis of a methicillin-resistantStaphylococcus aureus outbreak using restriction fragment length polymorphisms of genomic DNA. Journal of General Microbiology 1991, 137: 2713–2720.

    PubMed  CAS  Google Scholar 

  18. Musser JM, Kapur V Clonal analysis of methicillin-resistantStaphylococcus aureus strains from intercontinental sources: association of themec gene with divergent phylogenetic lineages implies dissemination by horizontal transfer and recombination. Journal of Clinical Microbiology 1992, 30: 2058–2063.

    PubMed  CAS  Google Scholar 

  19. Tomasz A, Nachman S, Leaf H Stable classes of phenotypic expression in methicillin-resistant clinical isolates of staphylococci. Antimicrobial Agents and Chemotherapy 1991, 35: 124–129.

    PubMed  CAS  Google Scholar 

  20. Melo-Cristino JAG, Torres Pereira A Methicillin-resistantStaphylococcus aureus: a 6-month survey in a Lisbon paediatric hospital. Journal of Hygiene (Cambridge) 1986, 97: 265–272.

    CAS  Google Scholar 

  21. Sambrook J, Fritsch EF, Maniatis T Molecular cloning, a laboratory manual. Second edition. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1989.

    Google Scholar 

  22. De Lencastre H, Figueiredo AMS, Urban C, Rahal J, Tomasz A Multiple mechanisms of methicillin resistance and improved methods for detection in clinical isolates ofStaphylococcus aureus. Antimicrobial Agents and Chemotherapy 1991, 35: 632–639.

    PubMed  Google Scholar 

  23. Matthews P, Tomasz A Insertional inactivation of themec gene in a transposon mutant of a methicillin-resistant clinical isolate ofStaphylococcus aureus. Antimicrobial Agents and Chemotherapy 1990, 34: 1777–1779.

    PubMed  CAS  Google Scholar 

  24. Iglesias A, Ceglowski P, Trautner TA Plasmid transformation inBacillus subtilis. Effects of the insertion ofBacillus subtilis rRNA genes into plasmids. Molecular and General Genetics 1983, 192: 149–155.

    Article  PubMed  CAS  Google Scholar 

  25. Archer GL, Pennell E Detection of methicillin resistance in staphylococci by using a DNA probe. Antimicrobial Agents and Chemotherapy 1990, 34: 1720–1724.

    PubMed  CAS  Google Scholar 

  26. Kreiswirth BN, McGeer A, Kornblum J, Simor AE, Elsner W, Poon R, Righter J, Campbell I, Low DE The use of variable gene probes to investigate a multihospital outbreak of MRSA. In: Novick R, Skurray RA (ed): Molecular biology of the staphylococci. VCH Publishers, New York, 1990, p. 521–530.

    Google Scholar 

  27. De Lencastre H, Figueiredo AMS, Tomasz A Genetic control of population structure in heterogeneous strains of methicillin resistantStaphylococcus aureus. European Journal of Clinical Microbiology and Infectious Diseases 1993, 12, Supplement 1: 13–18.

    Google Scholar 

  28. Schlichting C, Branger C, Fournier J-M, Witte W, Boutonnier A, Wolz C, Goullet P, Doring G Typing ofStaphylococcus aureus by pulsed-field gel electrophoresis, zymotyping, capsular typing, and phage typing: resolution of clonal relationships. Journal of Clinical Microbiology 1993, 31: 227–232.

    PubMed  CAS  Google Scholar 

  29. Berger-Bachi B, Barberis-Maino L, Strassle A, Kayser FH FemA, a host-mediated factor essential for methicillin resistance inStaphylococcus aureus: molecular cloning and characterization. Molecular and General Genetics 1989, 219: 263–269.

    PubMed  CAS  Google Scholar 

  30. Kornblum J, Hartman BJ, Novick RP, Tomasz A Conversion of a homogeneously methicillin-resistant strain ofStaphylococcus aureus to heterogeneous resistance by Tn551-mediated insertional inactivation. European Journal of Clinical Microbiology 1986, 5: 714–718.

    Article  PubMed  CAS  Google Scholar 

  31. Murakami K, Tomasz A Involvement of multiple genetic determinants in high-level methicillin resistance inStaphylococcus aureus. Journal of Bacteriology 1989, 171: 874–879.

    PubMed  CAS  Google Scholar 

  32. Berger-Bachi B, Strassle A, Gustafson JE, Kayser FH Mapping and characterization of multiple chromosomal factors involved in methicillin resistance inStaphylococcus aureus. Antimicrobial Agents and Chemotherapy 1992, 36: 1367–1373.

    PubMed  CAS  Google Scholar 

  33. De Jonge BLM, de Lencastre H, Tomasz A Suppression of autolysis and cell wall turnover in heterogeneous Tn551 mutants of a methicillin-resistantStaphylococcus aureus strain. Journal of Bacteriology 1991, 173: 1105–1110.

    PubMed  Google Scholar 

  34. De Jonge BLM, Chang Y-S, Gage D, Tomasz A Peptidoglycan composition in heterogeneous Tn551 mutants of a methicillin-resistantStaphylococcus aureus strain. Journal of Biological Chemistry 1992, 267: 11255–11259.

    PubMed  Google Scholar 

  35. Maidhof H, Reinicke B, Blumel P, Berger-Bachi B, Labischinski H FemA, which encodes a factor essential for expression of methicillin resistance, affects glycine content of peptidoglycan in methicillin-resistant and methicillin-susceptibleStaphylococcus aureus strains. Journal of Bacteriology 1991, 173: 3507–3513.

    PubMed  CAS  Google Scholar 

  36. Figueiredo AMS, Ha E, Kreiswirth BN, de Lencastre H, Noel BJ, Senterfit L, Tomasz A In vivo stability of heterogeneous expression classes in clinical isolates of methicillin-resistant staphylococci. Journal of Infectious Diseases 1991, 164: 883–887.

    PubMed  CAS  Google Scholar 

  37. Inglis B, Matthews PR, Stewart PR Induced deletions within a cluster of resistance genes in themec region of the chromosome ofStaphylococcus aureus. Journal of General Microbiology 1990, 136: 2231–2239.

    PubMed  CAS  Google Scholar 

  38. Preheim L, Pitcher D, Owen R, Cookson B Typing of methicillin resistant and susceptibleStaphylococcus aureus strains by ribosomal RNA gene restriction patterns using a biotinylated probe. European Journal of Clinical Microbiology and Infectious Diseases 1991, 10: 428–436.

    Article  CAS  Google Scholar 

  39. Thomson-Carter FM, Carter PE, Pennington TH Differentiation of staphylococcal species and strains by ribosomal RNA gene restriction patterns. Journal of General Microbiology 1989, 135: 2093–2097.

    PubMed  CAS  Google Scholar 

  40. Costas M, Cookson BD, Talsania HG, Owen RJ Numerical analysis of electrophoretic protein patterns of methicillin-resistant strains ofStaphylococcus aureus. Journal of Clinical Microbiology 1989, 27: 2574–2581.

    PubMed  CAS  Google Scholar 

  41. Goh S-H, Byrne SK, Zhang JL, Chow AW Molecular typing ofStaphylococcus aureus on the basis of coagulase gene polymorphisms. Journal of Clinical Microbiology 1992, 30: 1642–1645.

    PubMed  CAS  Google Scholar 

  42. Grimont F, Grimont PAD Ribosomal ribonucleic acid gene restriction patterns as potential taxonomic tools. Annales de l'Institut Pasteur (Microbiologie) 1986, 137B: 165–175.

    CAS  Google Scholar 

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de Lencastre, H., Couto, I., Santos, I. et al. Methicillin-resistantStaphylococcus aureus disease in a portuguese hospital: Characterization of clonal types by a combination of DNA typing methods. Eur. J. Clin. Microbiol. Infect. Dis. 13, 64–73 (1994). https://doi.org/10.1007/BF02026129

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