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Quantitation of biofilm and planktonic life forms of coexisting periodontal species.
Karched, Maribasappa; Bhardwaj, Radhika G; Inbamani, Anandavalli; Asikainen, Sirkka.
Afiliação
  • Karched M; Oral Microbiology, General Facility Laboratory, Faculty of Dentistry, Kuwait University, Kuwait.
  • Bhardwaj RG; Oral Microbiology, General Facility Laboratory, Faculty of Dentistry, Kuwait University, Kuwait.
  • Inbamani A; Oral Microbiology, General Facility Laboratory, Faculty of Dentistry, Kuwait University, Kuwait.
  • Asikainen S; Oral Microbiology, General Facility Laboratory, Faculty of Dentistry, Kuwait University, Kuwait. Electronic address: sirkka.asikainen@hsc.edu.kw.
Anaerobe ; 35(Pt A): 13-20, 2015 Oct.
Article em En | MEDLINE | ID: mdl-25926392
ABSTRACT

BACKGROUND:

Complexity of oral polymicrobial communities has prompted a need for developing in vitro models to study behavior of coexisting bacteria. Little knowledge is available of in vitro co-growth of several periodontitis-associated species without early colonizers of dental plaque. THE

AIM:

was to determine temporal changes in the quantities of six periodontal species in an in vitro biofilm model in comparison with parallel planktonic cultures. MATERIAL AND

METHODS:

Porphyromonas gingivalis, Aggregatibacter actinomycetemcomitans, Prevotella intermedia, Parvimonas micra, Campylobacter rectus and Fusobacterium nucleatum were anaerobically grown as multispecies and monospecies biofilms and parallel planktonic cultures using cell culture plates and microfuge tubes, respectively. After incubating 2, 4, 6, 8 days, biofilms and planktonic cultures were harvested, DNA extracted and the target species quantified using qPCR with species-specific 16S rDNA primers. Biofilm growth as monocultures was visualized at day 2 and 8 with confocal microscopy and crystal violet staining.

RESULTS:

The six species were found throughout the test period in all culture conditions, except that P. gingivalis and F. nucleatum were not detected in multispecies planktonic cultures at day 8. In multispecies biofilm, P. gingivalis qPCR counts (cells/ml) increased (P<0.05) from day 2-8 and were then higher (P<0.05) than those of A. actinomycetemcomitans and C. rectus, whereas in monospecies biofilm, P. gingivalis counts were lower (P<0.05) than those of the other species, except A. actinomycetemcomitans. When multi- and monospecies biofilm cultures were compared, P. gingivalis counts were higher (P<0.05) but those of the other species, except P. intermedia, lower (P<0.05) in multispecies biofilm. Comparison between planktonic and biofilm cultures showed that A. actinomycetemcomitans, P. micra and C. rectus had higher (P<0.05) counts in planktonic cultures no matter whether grown in mono- or multispecies environment.

CONCLUSIONS:

Six periodontal species were able to form multispecies biofilm up to 8 days in vitro without pioneer plaque bacteria. P. gingivalis seemed to prefer multispecies biofilm environment whereas P. micra and A. actinomycetemcomitans planktonic culture.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plâncton / Periodonto / Biofilmes / Placa Dentária Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plâncton / Periodonto / Biofilmes / Placa Dentária Idioma: En Ano de publicação: 2015 Tipo de documento: Article