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Isoenzyme genotyping and phylogenetic analysis of oxacillin-resistance Staphylococcus aureus isolates
Boriollo, Marcelo Fabiano Gomes; Rodrigues Netto, Manoel Francisco; Silva, Jeferson Júnior da; Silva, Thaísla Andrielle da; Castro, Maysa Eduarda de; Elias, Júlio César; Höfling, José Francisco.
  • Boriollo, Marcelo Fabiano Gomes; Universidade Estadual de Campinas. Faculdade de Odontologia de Piracicaba. Departamento de Diagnóstico Oral. Piracicaba. BR
  • Rodrigues Netto, Manoel Francisco; Universidade Estadual de Campinas. Faculdade de Odontologia de Piracicaba. Departamento de Diagnóstico Oral. Piracicaba. BR
  • Silva, Jeferson Júnior da; Universidade Estadual de Campinas. Faculdade de Odontologia de Piracicaba. Departamento de Diagnóstico Oral. Piracicaba. BR
  • Silva, Thaísla Andrielle da; Universidade José do Rosário Vellano. Faculdade de Medicina. Departamento de Patologia e Farmacologia Animal. Alfenas. BR
  • Castro, Maysa Eduarda de; Universidade José do Rosário Vellano. Faculdade de Medicina. Departamento de Patologia e Farmacologia Animal. Alfenas. BR
  • Elias, Júlio César; Universidade José do Rosário Vellano. Faculdade de Medicina. Departamento de Patologia e Farmacologia Animal. Alfenas. BR
  • Höfling, José Francisco; Universidade Estadual de Campinas. Faculdade de Odontologia de Piracicaba. Departamento de Diagnóstico Oral. Piracicaba. BR
Braz. j. oral sci ; 16: e17052, jan.-dez. 2017. tab
Article in English | LILACS, BBO | ID: biblio-884032
ABSTRACT

Aim:

The propagation of S. aureus in hospital and dental environments is considered an important public health problem since resistant strains can cause serious infections in humans. The genetic variability of 99 oxacillin-resistant S. aureus isolates (ORSA) from the dental patients (oral cavity) and environments (air) was studied by isoenzyme genotyping.

Methods:

S. aureus isolates were studied using isoenzyme markers (alcohol dehydrogenase, sorbitol dehydrogenase, mannitol-1-phosphate dehydrogenase, malate dehydrogenase, glucose dehydrogenase, D-galactose dehydrogenase, glucose-6-phosphate dehydrogenase, catalase and α/ß-esterase) and genetic (Nei's statistics) and cluster analysis (UPGMA algorithm).

Results:

A highly frequent polyclonal pattern was observed in this population of ORSA isolates, suggesting various sources of contamination or microbial dispersion. Genetic relationship analysis showed a high degree of polymorphism between the strains, and it revealed three taxa (A, B and C) distantly genetically related (0.653≤dij≤1.432) and fifteen clusters (I to XV) moderately related (0.282≤dij<0.653). These clusters harbored two or more highly related strains (0≤dij<0.282), and the existence of microevolutionary processes in the population of ORSA.

Conclusion:

This research reinforces the hypothesis of the existence of several sources of contamination and/or dispersal of ORSA of clinical and epidemiologically importance, which could be associated with carriers (patients) and dental environmental (air) (AU)
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Oxacillin / Staphylococcus aureus / Dental Offices / Air / Isoenzymes / Mouth Language: English Journal: Braz. j. oral sci Journal subject: Dentistry Year: 2017 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Estadual de Campinas/BR / Universidade José do Rosário Vellano/BR

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Full text: Available Index: LILACS (Americas) Main subject: Oxacillin / Staphylococcus aureus / Dental Offices / Air / Isoenzymes / Mouth Language: English Journal: Braz. j. oral sci Journal subject: Dentistry Year: 2017 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Estadual de Campinas/BR / Universidade José do Rosário Vellano/BR