Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 154 (2008), 1927-1938; DOI  10.1099/mic.0.2008/016576-0
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Google Scholar
Right arrow Articles by Chávez de Paz, L. E.
Right arrow Articles by Svensäter, G.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chávez de Paz, L. E.
Right arrow Articles by Svensäter, G.
Agricola
Right arrow Articles by Chávez de Paz, L. E.
Right arrow Articles by Svensäter, G.
Microbiology 154 (2008), 1927-1938; DOI  10.1099/mic.0.2008/016576-0
© 2008 Society for General Microbiology

Oral bacteria in biofilms exhibit slow reactivation from nutrient deprivation

Luis E. Chávez de Paz1, Ian R. Hamilton2 and Gunnel Svensäter1

1 Department of Oral Biology, Faculty of Odontology, Malmö University, Malmö 20506, Sweden
2 Department of Oral Biology, Faculty of Dentistry, University of Manitoba, Winnipeg, MB, Canada

Correspondence
Luis Chávez de Paz
luis.chavez.de.paz{at}od.mah.se

The ability of oral bacteria to enter a non-growing state is believed to be an important mechanism for survival in the starved micro-environments of the oral cavity. In this study, we examined the reactivation of nutrient-deprived cells of two oral bacteria in biofilms, Streptococcus anginosus and Lactobacillus salivarius. Non-growing cells were generated by incubation in 10 mM potassium phosphate buffer for 24 h and the results were compared to those of planktonic cultures. When both types of cells were shifted from a rich, peptone–yeast extract–glucose (PYG) medium to buffer for 24 h, dehydrogenase and esterase activity measured by the fluorescent dyes 5-cyano-2,3-ditolyl-tetrazolium chloride (CTC) and fluorescein diacetate (FDA), respectively, was absent in both species. However, the membranes of the vast majority of nutrient-deprived cells remained intact as assessed by LIVE/DEAD staining. Metabolic reactivation of the nutrient-deprived biofilm cells was not observed for at least 48 h following addition of fresh PYG medium, whereas the non-growing planktonic cultures of the same two strains were in rapid growth in less than 2 h. At 72 h, the S. anginosus biofilm cells had recovered 78 % of the dehydrogenase activity and 61 % of the esterase activity and the biomass mm–2 had increased by 30–35 %. With L. salivarius at 72 h, the biofilms had recovered 56 % and 75 % of dehydrogenase and esterase activity, respectively. Reactivation of both species in biofilms was enhanced by removal of glucose from PYG, and S. anginosus cells were particularly responsive to yeast extract (YE) medium. The data suggest that the low reactivity of non-growing biofilm cells to the introduction of fresh nutrients may be a survival strategy employed by micro-organisms in the oral cavity.


Abbreviations: CSLM, confocal scanning laser microscopy; CTC, 5-cyano-2,3-ditolyl tetrazolium chloride; EB, ethidium bromide; FDA, fluorescein diacetate; PY; peptone-yeast extract; PYG, peptone-yeast extract-glucose; YE, yeast extract







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2008 Society for General Microbiology.