Cox, J. V., Y. M. AbdelRahman, J. Peters, N. Naher, and R. J. Belland, "Chlamydia trachomatis utilizes the mammalian CLA1 lipid transporter to acquire host phosphatidylcholine essential for growth.", Cellular microbiology, vol. 18, issue 3, pp. 305-18, 2016 Mar. Abstractcox_et_al-2016-cellular_microbiology.pdf

Phosphatidylcholine is a constituent of Chlamydia trachomatis membranes that must be acquired from its mammalian host to support bacterial proliferation. The CLA1 (SR-B1) receptor is a bi-directional phosphatidylcholine/cholesterol transporter that is recruited to the inclusion of Chlamydia-infected cells along with ABCA1. C. trachomatis growth was inhibited in a dose-dependent manner by BLT-1, a selective inhibitor of CLA1 function. Expression of a BLT-1-insensitive CLA1(C384S) mutant ameliorated the effect of the drug on chlamydial growth. CLA1 knockdown using shRNAs corroborated an important role for CLA1 in the growth of C. trachomatis. Trafficking of a fluorescent phosphatidylcholine analogue to Chlamydia was blocked by the inhibition of CLA1 or ABCA1 function, indicating a critical role for these transporters in phosphatidylcholine acquisition by this organism. Our analyses using a dual-labelled fluorescent phosphatidylcholine analogue and mass spectrometry showed that the phosphatidylcholine associated with isolated Chlamydia was unmodified host phosphatidylcholine. These results indicate that C. trachomatis co-opts host phospholipid transporters normally used to assemble lipoproteins to acquire host phosphatidylcholine essential for growth.

Abdelrahman, Y., S. P. Ouellette, R. J. Belland, and J. V. Cox, "Polarized Cell Division of Chlamydia trachomatis.", PLoS pathogens, vol. 12, issue 8, pp. 1-20, 2016 Aug. Abstractjournal.ppat_.1005822.pdf

Bacterial cell division predominantly occurs by a highly conserved process, termed binary fission, that requires the bacterial homologue of tubulin, FtsZ. Other mechanisms of bacterial cell division that are independent of FtsZ are rare. Although the obligate intracellular human pathogen Chlamydia trachomatis, the leading bacterial cause of sexually transmitted infections and trachoma, lacks FtsZ, it has been assumed to divide by binary fission. We show here that Chlamydia divides by a polarized cell division process similar to the budding process of a subset of the Planctomycetes that also lack FtsZ. Prior to cell division, the major outer-membrane protein of Chlamydia is restricted to one pole of the cell, and the nascent daughter cell emerges from this pole by an asymmetric expansion of the membrane. Components of the chlamydial cell division machinery accumulate at the site of polar growth prior to the initiation of asymmetric membrane expansion and inhibitors that disrupt the polarity of C. trachomatis prevent cell division. The polarized cell division of C. trachomatis is the result of the unipolar growth and FtsZ-independent fission of this coccoid organism. This mechanism of cell division has not been documented in other human bacterial pathogens suggesting the potential for developing Chlamydia-specific therapeutic treatments.

Ouellette, S. P., K. J. Rueden, Y. M. AbdelRahman, J. V. Cox, and R. J. Belland, "Identification and Partial Characterization of Potential FtsL and FtsQ Homologs of Chlamydia.", Frontiers in Microbiology, vol. 6, issue 1264, pp. 1-12, 2015.
Bruhn, D. F., S. L. Waidyarachchi, D. B. Madhura, D. Shcherbakov, Z. Zheng, J. Liu, Y. M. AbdelRahman, A. P. Singh, S. Duscha, C. Rathi, et al., "Aminomethyl spectinomycins as therapeutics for drug-resistant respiratory tract and sexually transmitted bacterial infections", Science Translational Medicine, vol. 7, issue 288, pp. 1-12, 2015. bruhn_et_al.pdf
Lewis, M. E., R. J. Belland, Y. M. AbdelRahman, W. L. Beatty, A. A. Aiyar, A. H. Zea, S. J. Greene, L. Marrero, L. R. Buckner, D. J. Tate, et al., "Morphologic and molecular evaluation of Chlamydia trachomatis growth in human endocervix reveals distinct growth patterns", Frontiers in Cellular and Infection Microbiology, vol. 4, issue 71, pp. 1-12, 2014. fcimb-04-00071.pdf
Yao, J., Y. M. AbdelRahman, R. M. Robertson, J. V. Cox, R. J. Belland, S. W. White, and C. O. Rock, "Type II fatty acid synthesis is essential for the replication of Chlamydia trachomatis", Journal od Biological Chemistry, vol. 289, issue 32, pp. 22365–22376, 2014. j._biol._chem.-2014-yao-22365-76.pdf
Ouellette, S. P., T. P. Hatch, Y. M. AbdelRahman, L. A. Rose, R. J. Belland, and G. I. Byrne, "Global transcriptional upregulation in the absence of increased translation in Chlamydia during IFN$\gamma$-mediated host cell tryptophan starvation", Molecular microbiology, vol. 62, no. 5: Wiley Online Library, pp. 1387–1401, 2006. Abstractouellette_sp_et_al.pdf

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Ouellette, S. P., Y. M. AbdelRahman, R. J. Belland, and G. I. Byrne, "The Chlamydia pneumoniae type III secretion-related lcrH gene clusters are developmentally expressed operons", Journal of bacteriology, vol. 187, no. 22: Am Soc Microbiol, pp. 7853–7856, 2005. Abstractouellette_sp_et_al2.pdf

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AbdelRahman, Y. M., and R. J. Belland, "The chlamydial developmental cycle", FEMS microbiology reviews, vol. 29, no. 5: Wiley Online Library, pp. 949–959, 2005. Abstractthe_chlamydial_developmental_cycle.pdf

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O'Connell, C. M., Y. M. AbdelRahman, E. Green, H. K. Darville, K. Saira, B. Smith, T. Darville, A. M. Scurlock, C. R. Meyer, and R. J. Belland, "Toll-like receptor 2 activation by Chlamydia trachomatis is plasmid dependent, and plasmid-responsive chromosomal loci are coordinately regulated in response to glucose limitation by C. trachomatis but not by C. muridarum", Infection and immunity, vol. 79, no. 3: Am Soc Microbiol, pp. 1044–1056, 2011. Abstractoconnell_cm_et_al.pdf

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