Single-Cell Analysis of Growth and Cell Division of the Anaerobe Desulfovibrio vulgaris Hildenborough
Recent years have seen significant progress in understanding basic bacterial cell cycle properties such as cell growth and cell division. While characterization and regulation of bacterial cell cycle is quite well-documented in the case of fast growing aerobic model organisms, no data has been so fa...
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Published in | Frontiers in microbiology Vol. 6; p. 1378 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media
08.12.2015
Frontiers Media S.A |
Subjects | |
Online Access | Get full text |
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Summary: | Recent years have seen significant progress in understanding basic bacterial cell cycle properties such as cell growth and cell division. While characterization and regulation of bacterial cell cycle is quite well-documented in the case of fast growing aerobic model organisms, no data has been so far reported for anaerobic bacteria. This lack of information in anaerobic microorganisms can mainly be explained by the absence of molecular and cellular tools such as single cell microscopy and fluorescent probes usable for anaerobes and essential to study cellular events and/or subcellular localization of the actors involved in cell cycle. In this study, single-cell microscopy has been adapted to study for the first time, in real time, the cell cycle of a bacterial anaerobe, Desulfovibrio vulgaris Hildenborough (DvH). This single-cell analysis provides mechanistic insights into the cell division cycle of DvH, which seems to be governed by the recently discussed so-called incremental model that generates remarkably homogeneous cell sizes. Furthermore, cell division was reversibly blocked during oxygen exposure. This may constitute a strategy for anaerobic cells to cope with transient exposure to oxygen that they may encounter in their natural environment, thereby contributing to their aerotolerance. This study lays the foundation for the first molecular, single-cell assay that will address factors that cannot otherwise be resolved in bulk assays and that will allow visualization of a wide range of molecular mechanisms within living anaerobic cells. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Frank Schreiber, Eawag-Swiss Federal Institute of Aquatic Science and Technology, Switzerland Present Address: Adrien Ducret, Department of Biology, Indiana University, Bloomington, IN, USA This article was submitted to Microbial Physiology and Metabolism, a section of the journal Frontiers in Microbiology Reviewed by: Marc Bramkamp, Ludwig-Maximilians-University Munich, Germany; Manuel Loic Campos, Yale and Howard Hughes Medical Institute, USA These authors have contributed equally to this work. |
ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2015.01378 |