Coxiella burnetii encodes an LvgA-related protein important for intracellular replication
- PMID: 33774901
- DOI: 10.1111/cmi.13331
Coxiella burnetii encodes an LvgA-related protein important for intracellular replication
Abstract
Coxiella burnetii is a bacterial pathogen that replicates in a specialised lysosome-derived organelle called the Coxiella-containing vacuole (CCV). Establishment of the CCV requires the Dot/Icm type IVB secretion system. A previous transposon mutagenesis screen identified the gene cbu1754 as being important for the intracellular replication of C. burnetii. To understand the function of the protein encoded by cbu1754, CCV maturation and intracellular replication phenotypes of a cbu1754 mutant were analysed. In contrast to vacuoles containing wild-type C. burnetii Nine Mile phase II, vacuoles containing the isogenic cbu1754 mutant were smaller and did not display detectible amounts of the autophagy protein LC3, which indicated a CCV biogenesis defect. The Cbu1754 protein was not efficiently delivered into the host cell cytosol during infection, which indicated this protein is not a Dot/Icm-translocated effector protein. Secondary structure predictions suggested that Cbu1754 could be similar to the Legionella pneumophila LvgA protein, which is a component of the Dot/Icm apparatus. Consistent with this hypothesis, production of Cbu1754 in an L. pneumophila ∆lvgA mutant restored LvgA-dependent activities. The L. pneumophila proteins LvgA, IcmS and IcmW are interacting partners that comprise a subassembly of the coupling protein complex that mediates Dot/Icm-dependent effector translocation. Similarly, the Cbu1754 protein was found to be a component of the chaperone complex containing the C. burnetii proteins IcmS and IcmW. Thus, the Cbu1754 protein is an LvgA-related protein important for Dot/Icm function and intracellular replication of C. burnetii.
Keywords: Coxiella burnetii; Dot/Icm type IVB secretion system; T4SS; infection; intracellular replication.
© 2021 John Wiley & Sons Ltd.
References
REFERENCES
-
- Bardill, J. P., Miller, J. L., & Vogel, J. P. (2005). IcmS-dependent translocation of SdeA into macrophages by the Legionella pneumophila type IV secretion system. Molecular Microbiology, 56(1), 90-103. https://doi.org/10.1111/j.1365-2958.2005.04539.x
-
- Beare, P. A., Gilk, S. D., Larson, C. L., Hill, J., Stead, C. M., Omsland, A., … Heinzen, R. A. (2011). Dot/Icm type IVB secretion system requirements for Coxiella burnetii growth in human macrophages. mBio, 2(4), e00175-e00111. https://doi.org/10.1128/mBio.00175-11
-
- Berger, K. H., & Isberg, R. R. (1993). Two distinct defects in intracellular growth complemented by a single genetic locus in Legionella pneumophila. Molecular Microbiology, 7(1), 7-19. https://doi.org/10.1111/j.1365-2958.1993.tb01092.x
-
- Berón, W., Gutierrez, M. G., Rabinovitch, M., & Colombo, M. I. (2002). Coxiella burnetii localizes in a Rab7-labeled compartment with autophagic characteristics. Infection and Immunity, 70(10), 5816-5821. https://doi.org/10.1128/IAI.70.10.5816-5821.2002
-
- Bitew, M. A., Khoo, C. A., Neha, N., De Souza, D. P., Tull, D., Wawegama, N. K., … Sansom, F. M. (2018). De novo NAD synthesis is required for intracellular replication of Coxiella burnetii, the causative agent of the neglected zoonotic disease Q fever. The Journal of Biological Chemistry, 293(48), 18636-18645. https://doi.org/10.1074/jbc.RA118.005190
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
