Structural remodeling of Coxiella burnetii during its biphasic developmental cycle revealed by cryo-electron tomography
Abstract
Coxiella burnetii is an obligate zoonotic bacterium that targets macrophages to cause a disease known as Q fever. It has a biphasic developmental lifecycle where the extracellular and metabolically inactive small cell variant (SCV) transforms, under host acidic environment, into the vegetative large cell variant (LCV). However, the details about the morphological and structural changes that accompany this biphasic cycle are still lacking. Here, we used cryo-electron tomography to image the different cell variants of C. burnetii grown either under axenic conditions in different pH or purified directly from host cells revealing the major developmental, morphological and structural transitions. We show that SCVs are characterized by equidistant stacks of inner membrane that presumably allow a smooth transition to LCV, a transition coupled with the expression of the Dot/Icm type IVB secretion system (T4BSS). A class of T4BSS particles were associated with extracellular densities including a tubular structure possibly involved in host interaction or effector delivery. Also, SCVs and cells in the transition state contained spherical multilayered membrane structures of different sizes and locations suggesting that they are not related to a sporulation process as once assumed.
Additional Information
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. This project was funded by the National Institutes of Health (grant R01 AI127401 to G.J.J), an NHMRC grant (APP1196924 to DG), and the Intramural Research Program of the National Institutes of Health, National Institute of Allergy and Infectious Diseases (Grant number AI000931-20 to R.A.H. and C.L.L.). DCS is supported by the Melbourne Research Scholarship. We are grateful to Prof. Hayley Newton for critically reading the manuscript, Prof. Elitza Tocheva for insightful discussions, and Somavally Dalvi for her help with figure preparation. The authors have declared no competing interest.Attached Files
Submitted - 2022.08.23.505044v1.full.pdf
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Additional details
- Eprint ID
- 120354
- Resolver ID
- CaltechAUTHORS:20230322-368470000.41
- NIH
- R01 AI127401
- National Medical Research Council (Australia)
- APP1196924
- NIH
- AI000931-20
- University of Melbourne
- Created
-
2023-03-25Created from EPrint's datestamp field
- Updated
-
2023-03-25Created from EPrint's last_modified field
- Caltech groups
- Division of Biology and Biological Engineering (BBE)