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The ultrastructure of subgingival dental plaque, revealed by high-resolution field emission scanning electron microscopy

The ultrastructure of subgingival dental plaque, revealed by high-resolution field emission scanning electron microscopy

 

 

Richard Holliday, Philip M Preshaw, Leon Bowen & Nicholas S Jakubovics

 

 

 

Abstract Abstract • Introduction • Materials and Methods • Results • Discussion • Conclusions • References • Acknowledgements • Author information

Objectives/Aims:

To explore the ultrastructure of subgingival dental plaque using high-resolution field emission scanning electron microscopy (FE-SEM) and to investigate whether extracellular DNA (eDNA) could be visualised in ex vivo samples.

 

Materials and Methods:

Ten patients were recruited who fulfilled the inclusion criteria (teeth requiring extraction with radiographic horizontal bone loss of over 50% and grade II/III mobility). In total, 12 teeth were extracted using a minimally traumatic technique. Roots were sectioned using a dental air turbine handpiece, under water cooling to produce 21 samples. Standard fixation and dehydration protocols were followed. For some samples, gold-labelled anti-DNA antibodies were applied before visualising biofilms by FE-SEM.

Results:

High-resolution FE-SEMs of subgingival biofilm were obtained in 90% of the samples. The sectioning technique left dental plaque biofilms undisturbed. Copious amounts of extracellular material were observed in the plaque, which may have been eDNA as they had a similar appearance to labelled eDNA from in vitro studies. There was also evidence of membrane vesicles and open-ended tubular structures. Efforts to label eDNA with immune-gold antibodies were unsuccessful and eDNA was not clearly labelled.

Conclusions:

High-resolution FE-SEM images were obtained of undisturbed subgingival ex vivo dental plaque biofilms. Important structural features were observed including extracellular polymeric material, vesicles and unusual open tubule structures that may be remnants of lysed cells. The application of an eDNA immune-gold-labelling technique, previously used successfully in in vitro samples, did not clearly identify eDNA in ex vivo samples. Further studies are needed to characterise the molecular composition of the observed extracellular matrix material.

 

 

 Δείτε το πλήρες άρθρο [ΔΩΡΕΑΝ] στον ακόλουθο σύνδεσμο:

http://www.nature.com/articles/bdjopen20153

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