Bacterial growth dynamics in a rhythmic symbiosis
- Editor:
- Goley, Erin
Abstract
The symbiotic relationship between the bioluminescent bacterium Vibrio fischeri and the bobtail squid Euprymna scolopes serves as a valuable system to investigate bacterial growth and peptidoglycan (PG) synthesis within animal tissues. To better understand the growth dynamics of V. fischeri in the crypts of the light-emitting organ of its juvenile host, we showed that, after the daily dawn-triggered expulsion of most of the population, the remaining symbionts rapidly proliferate for ∼6 h. At that point the population enters a period of extremely slow growth that continues throughout the night until the next dawn. Further, we found that PG synthesis by the symbionts decreases as they enter the slow-growing stage. Surprisingly, in contrast to the most mature crypts (i.e., Crypt 1) of juvenile animals, most of the symbiont cells in the least mature crypts (i.e., Crypt 3) were not expelled and, instead, remained in the slow-growing state throughout the day, with almost no cell division. Consistent with this observation, the expression of the gene encoding the PG-remodeling enzyme, L,D-transpeptidase (LdtA), was greatest during the slowly growing stage of Crypt 1 but, in contrast, remained continuously high in Crypt 3. Finally, deletion of the ldtA gene resulted in a symbiont that grew and survived normally in culture, but was increasingly defective in competing against its parent strain in the crypts. This result suggests that remodeling of the PG to generate additional 3–3 linkages contributes to the bacterium’s fitness in the symbiosis, possibly in response to stresses encountered during the very slow-growing stage.
Copyright and License
© 2024 Yang et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 4.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/4.0).
Acknowledgement
The authors would like to thank the Ruby and McFall-Ngai laboratories for helpful discussions, and especially Joani Viliunas for extracting symbiont RNA, Vera Beilinson for analyzing the NanoString data, and Vanya Tepavcevic and Eve Otjacques for proofreading. We would also like to thank the Caltech Biological Imaging Center, where we performed much of the microscopy imaging. This work was supported by National Institutes of Health grants R37 AI50661 (to M.M.-N. and E.R.), and R01 OD11024 and R01 GM135254 (to E.R. and M.M.-N.), as well as R35 GM148385 (to M.J.M.).
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Additional details
- ISSN
- 1939-4586
- National Institutes of Health
- R37 AI50661
- National Institutes of Health
- R01 OD11024
- National Institutes of Health
- R01 GM135254
- National Institutes of Health
- R35 GM148385
- Caltech groups
- Division of Biology and Biological Engineering