Exploitation of host lipids by bacteria

Mycobacterial persistence requires the utilization of host cholesterol

Pandey, A. K., & Sassetti, C. M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711159105 · Cited by 1,064 · see citing works

Microbiota Regulate Intestinal Absorption and Metabolism of Fatty Acids in the Zebrafish

Semova, I., Carten, J. D., Stombaugh, J., Mackey, L. C., Knight, R. D., Farber, S. A., & Rawls, J. F. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.08.003 · Cited by 881 · see citing works

Mycobacterium tuberculosis Uses Host Triacylglycerol to Accumulate Lipid Droplets and Acquires a Dormancy-Like Phenotype in Lipid-Loaded Macrophages

Daniel, J., Maamar, H., Deb, C., Sirakova, T., & Kolattukudy, P. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002093 · Cited by 595 · see citing works

Tnf dually mediates resistance and susceptibility to mycobacteria via mitochondrial reactive oxygen species

Roca, F. J., & Ramakrishnan, L. (2013) · Cell · doi:10.1016/j.cell.2013.03.022 · Cited by 592 · see citing works

Phagosomal Rupture by Mycobacterium tuberculosis Results in Toxicity and Host Cell Death

Simeone, R., Bobard, A., Lippmann, J., Bitter, W., Majlessi, L., Brosch, R., & Enninga, J. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002507 · Cited by 561 · see citing works

Bacterial lipids: Metabolism and membrane homeostasis

Parsons, J. B., & Rock, C. O. (2013) · Progress in Lipid Research · doi:10.1016/j.plipres.2013.02.002 · Cited by 524 · see citing works

SopB, a protein required for virulence of Salmonella dublin , is an inositol phosphate phosphatase

Norris, F. A., Wilson, M. P., Wallis, T. S., Galyov, E. E., & Majerus, P. W. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.24.14057 · Cited by 439 · see citing works

Intracellular Mycobacterium tuberculosis Exploits Host-derived Fatty Acids to Limit Metabolic Stress

Lee, W., VanderVen, B. C., Fahey, R. J., & Russell, D. G. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.445056 · Cited by 424 · see citing works

Diverse type VI secretion phospholipases are functionally plastic antibacterial effectors

Russell, A. B., LeRoux, M., Hathazi, K., Agnello, D. M., Ishikawa, T., Wiggins, P. A., Wai, S. N., & Mougous, J. D. (2013) · Nature · doi:10.1038/nature12074 · Cited by 415 · see citing works

Chlamydia trachomatis interrupts an exocytic pathway to acquire endogenously synthesized sphingomyelin in transit from the Golgi apparatus to the plasma membrane.

Hackstadt, T., Rockey, D. D., Heinzen, R. A., & Scidmore, M. A. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00433.x · Cited by 390 · see citing works

Lipid metabolism in Chlamydia trachomatis-infected cells: directed trafficking of Golgi-derived sphingolipids to the chlamydial inclusion.

Hackstadt, T., Scidmore, M. A., & Rockey, D. D. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.11.4877 · Cited by 355 · see citing works

Cytoplasmic lipid droplets are translocated into the lumen of the Chlamydia trachomatis parasitophorous vacuole

Cocchiaro, J. L., Kumar, Y., Fischer, E. R., Hackstadt, T., & Valdivia, R. H. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712241105 · Cited by 298 · see citing works

Mycobacterium tuberculosis-Driven Targeted Recalibration of Macrophage Lipid Homeostasis Promotes the Foamy Phenotype

Singh, V., Jamwal, S., Jain, R., Verma, P., Gokhale, R., & Rao, K. V. S. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.09.012 · Cited by 295 · see citing works

Legionella pneumophila Exploits PI(4)P to Anchor Secreted Effector Proteins to the Replicative Vacuole

Weber, S. S., Ragaz, C., Reus, K., Nyfeler, Y., & Hilbi, H. (2006) · PLoS Pathogens · doi:10.1371/journal.ppat.0020046 · Cited by 292 · see citing works

Cholesterol glucosylation promotes immune evasion by Helicobacter pylori

Wunder, C., Churin, Y., Winau, F., Warnecke, D. C., Vieth, M. W., Lindner, B., Zähringer, U., Mollenkopf, H., Heinz, E., & Meyer, T. F. (2006) · Nature Medicine · doi:10.1038/nm1480 · Cited by 291 · see citing works

Cyclic β-1,2-glucan is a brucella virulence factor required for intracellular survival

Arellano-Reynoso, B., Lapaque, N., Salcedo, S. P., Briones, G., Ciocchini, A. E., Ugalde, R. A., Moreno, E., Moriyón, I., & Gorvel, J. (2005) · Nature Immunology · doi:10.1038/ni1202 · Cited by 288 · see citing works

The Lipid Transfer Protein CERT Interacts with the Chlamydia Inclusion Protein IncD and Participates to ER-Chlamydia Inclusion Membrane Contact Sites

Derré, I., Swiss, R. L., & Agaisse, H. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002092 · Cited by 287 · see citing works

In Vivo Evidence of Pseudomonas aeruginosa Nutrient Acquisition and Pathogenesis in the Lungs of Cystic Fibrosis Patients

Son, M. S., Matthews, W. J., Kang, Y., Nguyen, D. T., & Hoang, T. T. (2007) · Infection and Immunity · doi:10.1128/iai.01807-06 · Cited by 280 · see citing works

Ehrlichia chaffeensis and Anaplasma phagocytophilum Lack Genes for Lipid A Biosynthesis and Incorporate Cholesterol for Their Survival

Lin, M., & Rikihisa, Y. (2003) · Infection and Immunity · doi:10.1128/iai.71.9.5324-5331.2003 · Cited by 272 · see citing works

Golgi-dependent transport of cholesterol to the Chlamydia trachomatis inclusion

Carabeo, R. A., Mead, D. J., & Hackstadt, T. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1131289100 · Cited by 264 · see citing works

Chlamydia trachomatis Co-opts GBF1 and CERT to Acquire Host Sphingomyelin for Distinct Roles during Intracellular Development

Elwell, C. A., Jiang, S., Kim, J. H., Lee, A., Wittmann, T., Hanada, K., Melançon, P., & Engel, J. N. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002198 · Cited by 231 · see citing works

Emerging Roles for Lipid Droplets in Immunity and Host-Pathogen Interactions

Saka, H. A., & Valdivia, R. H. (2011) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-153958 · Cited by 221 · see citing works

SopB promotes phosphatidylinositol 3-phosphate formation on Salmonella vacuoles by recruiting Rab5 and Vps34

Mallo, G. V., Espina, M., Smith, A. C., Terebiznik, M. R., Alemán, A., Finlay, B. B., Rameh, L. E., Grinstein, S., & Brumell, J. H. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200804131 · Cited by 218 · see citing works

A Comparative Lipidomics Platform for Chemotaxonomic Analysis of Mycobacterium tuberculosis

Layre, E., Sweet, L., Hong, S., Madigan, C. A., Desjardins, D., Young, D. C., Cheng, T., Annand, J. W., Kim, K., Shamputa, I. C., et al. (2011) · Chemistry & Biology · doi:10.1016/j.chembiol.2011.10.013 · Cited by 201 · see citing works

The protein SdhA maintains the integrity of the Legionella -containing vacuole

Creasey, E. A., & Isberg, R. R. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1121286109 · Cited by 198 · see citing works

Host cell phospholipids are trafficked to and then modified by Chlamydia trachomatis

Wylie, J., Hatch, G. M., & McClarty, G. A. (1997) · Journal of Bacteriology · doi:10.1128/jb.179.23.7233-7242.1997 · Cited by 197 · see citing works

Leishmania donovani Targets Dicer1 to Downregulate miR-122, Lower Serum Cholesterol, and Facilitate Murine Liver Infection

Ghosh, J., Bose, M., Roy, S., & Bhattacharyya, S. N. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.02.005 · Cited by 191 · see citing works

Salmonella Transforms Follicle-Associated Epithelial Cells into M Cells to Promote Intestinal Invasion

Tahoun, A. A. E., Mahajan, S. M., Paxton, E. A., Malterer, G., Donaldson, D. S., Wang, D., Tan, A., Gillespie, T., O’Shea, M. F., Roe, A. J., et al. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.10.009 · Cited by 181 · see citing works

Proteolytic elimination of N-myristoyl modifications by the Shigella virulence factor IpaJ

Burnaevskiy, N., Fox, T. G., Plymire, D. A., Ertelt, J. M., Weigele, B. A., Selyunin, A. S., Way, S. S., Patrie, S. M., & Alto, N. M. (2013) · Nature · doi:10.1038/nature12004 · Cited by 160 · see citing works

Lipids in host–pathogen interactions: Pathogens exploit the complexity of the host cell lipidome

van der Meer-Janssen, Y. P. M., van Galen, J., Batenburg, J. J., & Helms, J. B. (2009) · Progress in Lipid Research · doi:10.1016/j.plipres.2009.07.003 · Cited by 159 · see citing works

Specific chlamydial inclusion membrane proteins associate with active Src family kinases in microdomains that interact with the host microtubule network

Mital, J., Miller, N. J., Fischer, E. R., & Hackstadt, T. (2010) · Cellular Microbiology · doi:10.1111/j.1462-5822.2010.01465.x · Cited by 139 · see citing works

Lipid Body–Phagosome Interaction in Macrophages during Infectious Diseases: Host Defense or Pathogen Survival Strategy?

Melo, R. C. N., & Dvorak, A. M. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002729 · Cited by 139 · see citing works

Lipid Exchange between Borrelia burgdorferi and Host Cells

Crowley, J. T., Toledo, A. M., LaRocca, T. J., Coleman, J. L., London, E., & Benach, J. L. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003109 · Cited by 129 · see citing works

Effects of Clostridium perfringens Alpha-Toxin (PLC) and Perfringolysin O (PFO) on Cytotoxicity to Macrophages, on Escape from the Phagosomes of Macrophages, and on Persistence of C. perfringens in Host Tissues

O'Brien, D. K., & Melville, S. B. (2004) · Infection and Immunity · doi:10.1128/iai.72.9.5204-5215.2004 · Cited by 129 · see citing works

Coxiella burnetii inhabits a cholesterol-rich vacuole and influences cellular cholesterol metabolism

Howe, D., & Heinzen, R. A. (2005) · Cellular Microbiology · doi:10.1111/j.1462-5822.2005.00641.x · Cited by 125 · see citing works

Lipid acquisition by intracellular Chlamydiae

Elwell, C. A., & Engel, J. N. (2012) · Cellular Microbiology · doi:10.1111/j.1462-5822.2012.01794.x · Cited by 118 · see citing works

Cholesterol depletion in Mycobacterium avium-infected macrophages overcomes the block in phagosome maturation and leads to the reversible sequestration of viable mycobacteria in phagolysosome-derived autophagic vacuoles

de Chastellier, C., & Thilo, L. (2006) · Cellular Microbiology · doi:10.1111/j.1462-5822.2005.00617.x · Cited by 118 · see citing works

Proving Lipid Rafts Exist: Membrane Domains in the Prokaryote Borrelia burgdorferi Have the Same Properties as Eukaryotic Lipid Rafts

LaRocca, T. J., Pathak, P., Chiantia, S., Toledo, A. M., Silvius, J. R., Benach, J. L., & London, E. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003353 · Cited by 118 · see citing works

Structural basis for substrate recognition by a unique Legionella phosphoinositide phosphatase

Hsu, F., Zhu, W., Brennan, L. D., Tao, L., Luo, Z., & Mao, Y. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1207903109 · Cited by 117 · see citing works

Salmonella enterica Serovar Typhimurium Requires Nonsterol Precursors of the Cholesterol Biosynthetic Pathway for Intracellular Proliferation

Catron, D. M., Lange, Y., Borensztajn, J., Sylvester, M. D., Jones, B. D., & Haldar, K. (2004) · Infection and Immunity · doi:10.1128/iai.72.2.1036-1042.2004 · Cited by 111 · see citing works

Lipid profile of Helicobacter spp.: presence of cholesteryl glucoside as a characteristic feature

Haque, M., Hirai, Y., Yokota, K., Mori, N., Jahan, I., Ito, H., Hotta, H., Yano, I., Kanemasa, Y., & Oguma, K. (1996) · Journal of Bacteriology · doi:10.1128/jb.178.7.2065-2070.1996 · Cited by 108 · see citing works

The Salmonella-containing vacuole is a major site of intracellular cholesterol accumulation and recruits the GPI-anchored protein CD55

Catron, D. M., Sylvester, M. D., Lange, Y., Kadekoppala, M., Jones, B. D., Monack, D. M., Falkow, S., & Haldar, K. (2002) · Cellular Microbiology · doi:10.1046/j.1462-5822.2002.00198.x · Cited by 107 · see citing works

Secreted bacterial phospholipase A2 enzymes: better living through phospholipolysis

Sitkiewicz, I., Stockbauer, K. E., & Musser, J. M. (2006) · Trends in Microbiology · doi:10.1016/j.tim.2006.12.003 · Cited by 104 · see citing works

Helicobacter pylori Growth and Urease Detection in the Chemically Defined Medium Ham's F-12 Nutrient Mixture

Testerman, T. L., McGee, D. J., & Mobley, H. L. T. (2001) · Journal of Clinical Microbiology · doi:10.1128/jcm.39.11.3842-3850.2001 · Cited by 95 · see citing works

Subversion of membrane transport pathways by vacuolar pathogens

Alix, E., Mukherjee, S., & Roy, C. R. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201105019 · Cited by 93 · see citing works

Lipid metabolism of Borrelia hermsi

Livermore, B. P., Bey, R., & Johnson, R. C. (1978) · Infection and Immunity · doi:10.1128/iai.20.1.215-220.1978 · Cited by 84 · see citing works

Acylated Cholesteryl Galactoside as a Novel Immunogenic Motif in Borrelia burgdorferi Sensu Stricto

Schröder, N. W. J., Schombel, U., Heine, H., Göbel, U. B., Zähringer, U., & Schumann, R. R. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m305799200 · Cited by 83 · see citing works

Helicobacter pylori cholesteryl glucosides interfere with host membrane phase and affect type IV secretion system function during infection in AGS cells

Wang, H., Cheng, W., Cheng, H., Lai, C., & Wang, W. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07910.x · Cited by 73 · see citing works

Bacterial Colonization of Host Cells in the Absence of Cholesterol

Gilk, S. D., Cockrell, D. C., Luterbach, C., Hansen, B. T., Knodler, L. A., Ibarra, J. A., Steele‐Mortimer, O., & Heinzen, R. A. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003107 · Cited by 72 · see citing works

Phospholipid Composition of PurifiedChlamydia trachomatisMimics That of the Eucaryotic Host Cell

Hatch, G. M., & McClarty, G. A. (1998) · Infection and Immunity · doi:10.1128/iai.66.8.3727-3735.1998 · Cited by 72 · see citing works

Shigella Effector IpaB-Induced Cholesterol Relocation Disrupts the Golgi Complex and Recycling Network to Inhibit Host Cell Secretion

Mounier, J., Boncompain, G., Šenerović, L., Lagache, T., Chrétien, F. C., Perez, F., Kolbe, M., Olivo‐Marín, J., Sansonetti, P. J., & Sauvonnet, N. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.07.010 · Cited by 67 · see citing works

Identification of Two Legionella pneumophila Effectors that Manipulate Host Phospholipids Biosynthesis

Viner, R., Chetrit, D., Ehrlich, M., & Segal, G. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002988 · Cited by 61 · see citing works

Phosphoproteomic Analysis of Salmonella -Infected Cells Identifies Key Kinase Regulators and SopB-Dependent Host Phosphorylation Events

Rogers, L. D., Brown, N. F., Yuan, F., Pelech, S., & Foster, L. J. (2011) · Science Signaling · doi:10.1126/scisignal.2001668 · Cited by 60 · see citing works

Host HDL biogenesis machinery is recruited to the inclusion ofChlamydia trachomatis-infected cells and regulates chlamydial growth

Cox, J. V., Naher, N., AbdelRahman, Y. M., & Belland, R. J. (2012) · Cellular Microbiology · doi:10.1111/j.1462-5822.2012.01823.x · Cited by 46 · see citing works

The cell membrane of Mycoplasma penetrans: lipid composition and phospholipase A1 activity

Salman, M., & Rottem, S. (1995) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(95)80026-c · Cited by 42 · see citing works

The Outer Surface Lipoprotein VolA Mediates Utilization of Exogenous Lipids by Vibrio cholerae

Pride, A. C., Herrera, C. M., Guan, Z., Giles, D. K., & Trent, M. S. (2013) · mBio · doi:10.1128/mbio.00305-13 · Cited by 40 · see citing works

Phosphatidylserine found in intestinal mucus serves as a sole source of carbon and nitrogen for salmonellae and Escherichia coli

Krivan, H. C., Franklin, D. P., Wang, W., Laux, D. C., & Cohen, P. S. (1992) · Infection and Immunity · doi:10.1128/iai.60.9.3943-3946.1992 · Cited by 40 · see citing works

Preferential invasion of mitotic cells by Salmonella reveals that cell surface cholesterol is maximal during metaphase

Santos, A. J. M., Meinecke, M., Fessler, M. B., Holden, D. W., & Boucrot, E. (2013) · Journal of Cell Science · doi:10.1242/jcs.115253 · Cited by 38 · see citing works

Subversion of NPC1 pathway of cholesterol transport by Anaplasma phagocytophilum

Xiong, Q., & Rikihisa, Y. (2011) · Cellular Microbiology · doi:10.1111/j.1462-5822.2011.01742.x · Cited by 36 · see citing works

Lipidomic profiling of model organisms and the world's major pathogens

Layre, E., & Moody, D. B. (2012) · Biochimie · doi:10.1016/j.biochi.2012.08.012 · Cited by 36 · see citing works

Involvement of lipid rafts in the budding-like exit of Orientia tsutsugamushi

Kim, M., Kim, M.-K., & Kang, J. (2013) · Microbial Pathogenesis · doi:10.1016/j.micpath.2013.06.002 · Cited by 33 · see citing works

Changes in phospholipid fatty acid composition and triacylglycerol content in mouse tissues after infection with bacille Calmette-Guérin.

Jackson, S. K., Stark, J. M., Taylor, S., & Harwood, J. L. (1989) · PubMed Central · Cited by 20 · see citing works

Mycoplasma penetransunder nutritional stress: influence on lipid and lipoprotein profiles and on the binding to and invasion of HeLa cells

Zeiman, E., Tarshis, M. A., & Rottem, S. (2008) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2008.01322.x · Cited by 10 · see citing works

Macrophage defense mechanisms against intracellular bacteria

Weiss, G., & Schaible, U. E. (2015) · Immunological Reviews · doi:10.1111/imr.12266 · Cited by 989 · see citing works

Control of Phagocytosis by Microbial Pathogens

Uribe‐Querol, E., & Rosales, C. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01368 · Cited by 310 · see citing works

Toll-Like Receptors Induce Signal-Specific Reprogramming of the Macrophage Lipidome

Hsieh, W.-Y., Zhou, Q., York, A. G., Williams, K. J., Scumpia, P. O., Kronenberger, E. B., Hoi, X. P., Su, B., Chi, X., Bui, V. L., et al. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.05.003 · Cited by 160 · see citing works

Molecular basis of mycobacterial survival in macrophages

Awuh, J. A., & Flo, T. H. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2422-8 · Cited by 155 · see citing works

PPAR-α Activation Mediates Innate Host Defense through Induction of TFEB and Lipid Catabolism

Kim, Y. S., Lee, H. M., Kim, J. K., Yang, C., Kim, T. S., Jung, M., Jin, H. S., Kim, S., Jang, J., Oh, G. T., et al. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601920 · Cited by 151 · see citing works

Lipid metabolism and its implication in mycobacteria–host interaction

Gago, G., Diacovich, L., & Gramajo, H. C. (2017) · Current Opinion in Microbiology · doi:10.1016/j.mib.2017.11.020 · Cited by 96 · see citing works

Foliar Spraying of Chlorpyrifos Triggers Plant Production of Linolenic Acid Recruiting Rhizosphere Bacterial Sphingomonas sp.

Li, Y., Feng, F., Mu, Q., Li, M., Ma, L., Wan, Q., Jousset, A., Liu, C., & Yu, X. (2023) · Environmental Science & Technology · doi:10.1021/acs.est.3c04593 · Cited by 67 · see citing works

Cardiovascular disease and type 2 diabetes in evolutionary perspective: A critical role for helminths?

Gurven, M., Trumble, B. C., Stieglitz, J., Blackwell, A. D., Michalik, D. E., Finch, C. E., & Kaplan, H. S. (2016) · Evolution Medicine and Public Health · doi:10.1093/emph/eow028 · Cited by 67 · see citing works

Glycerophospholipid synthesis and functions in Pseudomonas

Kondakova, T., D’Heygere, F., Feuilloley, M. G. J., Orange, N., Heipieper, H. J., & Poc, C. D. (2015) · Chemistry and Physics of Lipids · doi:10.1016/j.chemphyslip.2015.06.006 · Cited by 61 · see citing works

Chlamydia trachomatis Relies on Autonomous Phospholipid Synthesis for Membrane Biogenesis

Yao, J., Cherian, P., Frank, M. W., & Rock, C. O. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.657148 · Cited by 51 · see citing works

Mycobacteria Modify Their Cell Size Control under Sub-Optimal Carbon Sources

Priestman, M., Thomas, P., Robertson, B. D., & Shahrezaei, V. (2017) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2017.00064 · Cited by 50 · see citing works

Redox (phospho)lipidomics of signaling in inflammation and programmed cell death

Tyurina, Y. Y., Croix, C. M. S., Watkins, S. C., Watson, A. M., Epperly, M. W., Anthonymuthu, T. S., Kisin, E. R., Vlasova, I. I., Krysko, O., Krysko, D. V., et al. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.3mir0119-004rr · Cited by 43 · see citing works

Cholesterol plays a larger role during Mycobacterium tuberculosis in vitro dormancy and reactivation than previously suspected

Soto-Ramírez, M. D., Aguilar-Ayala, D. A., García-Morales, L., Rodriguez-Peredo, S. M., Badillo-López, C., Rios-Muñiz, D. E., Meza-Segura, M., Rivera-Morales, G. Y., León-Solís, L. E., Cerna-Cortés, J. F., et al. (2016) · Tuberculosis · doi:10.1016/j.tube.2016.12.004 · Cited by 38 · see citing works

Anaplasma phagocytophilumRab10-dependent parasitism of thetrans-Golgi network is critical for completion of the infection cycle

Truchan, H. K., VieBrock, L., Cockburn, C. L., Ojogun, N., Griffin, B. P., Wijesinghe, D. S., Chalfant, C. E., & Carlyon, J. A. (2015) · Cellular Microbiology · doi:10.1111/cmi.12500 · Cited by 37 · see citing works

Revolutionizing control strategies against Mycobacterium tuberculosis infection through selected targeting of lipid metabolism

Kim, H., & Shin, S. J. (2023) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-04914-5 · Cited by 34 · see citing works

Identification and Characterization of Lipase Activity and Immunogenicity of LipL from Mycobacterium tuberculosis

Cao, J. P., Dang, G., Li, H., Li, T., Yue, Z., Li, N., Liu, Y., Liu, S., & Chen, L. (2015) · PLoS ONE · doi:10.1371/journal.pone.0138151 · Cited by 31 · see citing works

The crystal structure of monoacylglycerol lipase from M. tuberculosis reveals the basis for specific inhibition

Aschauer, P., Zimmermann, R., Breinbauer, R., Pavkov‐Keller, T., & Oberer, M. (2018) · Scientific Reports · doi:10.1038/s41598-018-27051-7 · Cited by 28 · see citing works

Lipids in infectious diseases – The case of AIDS and tuberculosis

Dumas, F., & Haanappel, E. (2017) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2017.05.007 · Cited by 27 · see citing works

Bacterial-induced cell reprogramming to stem cell-like cells: new premise in host–pathogen interactions

Hess, S., & Rambukkana, A. (2014) · Current Opinion in Microbiology · doi:10.1016/j.mib.2014.11.021 · Cited by 26 · see citing works

Cell lipid biology in infections: an overview

Prado, L. G., Câmara, N. O. S., & Barbosa, A. S. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1148383 · Cited by 24 · see citing works

Outer membrane vesicles from a mosquito commensal mediate targeted killing of Plasmodium parasites via the phosphatidylcholine scavenging pathway

Gao, H., Jiang, Y., Wang, L., Wang, G., Hu, W., Dong, L., & Wang, S. (2023) · Nature Communications · doi:10.1038/s41467-023-40887-6 · Cited by 23 · see citing works

The DUF582 Proteins of Chlamydia trachomatis Bind to Components of the ESCRT Machinery, Which Is Dispensable for Bacterial Growth In vitro

Vromman, F., Perrinet, S., Gehre, L., & Subtil, A. (2016) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2016.00123 · Cited by 22 · see citing works

Rv1075c of Mycobacterium tuberculosis is a GDSL-Like Esterase and Is Important for Intracellular Survival

Yang, D., He, X., Li, S., Liu, J., Stabenow, J. M., Zalduondo, L., White, S. W., & Kong, Y. (2019) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiz169 · Cited by 21 · see citing works

Nutritional Interactions between Bacterial Species Colonising the Human Nasal Cavity: Current Knowledge and Future Prospects

Adolf, L. A., & Heilbronner, S. (2022) · Metabolites · doi:10.3390/metabo12060489 · Cited by 23 · see citing works

Regulation of the Mitochondrion-Fatty Acid Axis for the Metabolic Reprogramming of Chlamydia trachomatis during Treatment with β-Lactam Antimicrobials

Shima, K., Kaufhold, I., Eder, T., Käding, N., Schmidt, N., Ogunsulire, I. M., Deenen, R., Köhrer, K., Friedrich, D., Isay, S. E., et al. (2021) · mBio · doi:10.1128/mbio.00023-21 · Cited by 17 · see citing works

Targeting of the Hydrophobic Metabolome by Pathogens

Helms, J. B., Kaloyanova, D. V., Strating, J. R. P. M., van Hellemond, J. J., van der Schaar, H. M., Tielens, A. G. M., van Kuppeveld, F. J. M., & Brouwers, J. F. H. M. (2015) · Traffic · doi:10.1111/tra.12280 · Cited by 17 · see citing works

Rv0518, a nutritive stress inducible GDSL lipase of Mycobacterium tuberculosis, enhanced intracellular survival of bacteria by cell wall modulation

Kaur, J., & Kaur, J. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.05.121 · Cited by 17 · see citing works

Clinical strains of Mycobacterium tuberculosis exhibit differential lipid metabolism-associated transcriptome changes in in vitro cholesterol and infection models

Moopanar, K. R., Nyide, A. N. G., Senzani, S., & Mvubu, N. E. (2022) · Pathogens and Disease · doi:10.1093/femspd/ftac046 · Cited by 16 · see citing works

A Sympoietic View of Life: Gaia as a Holobiont CommunityPreprint

Gilbert, S. F. (2023) · Preprints.org · doi:10.20944/preprints202309.1072.v1 · Cited by 14 · see citing works

Is Mycobacterium tuberculosis carcinogenic to humans?

Roy, D., Ehtesham, N. Z., & Hasnain, S. E. (2021) · The FASEB Journal · doi:10.1096/fj.202001581rr · Cited by 14 · see citing works

Macrophage sphingolipids are essential for the entry of mycobacteria

Viswanathan, G., Jafurulla, M., Kumar, G. A., Raghunand, T. R., & Chattopadhyay, A. (2018) · Chemistry and Physics of Lipids · doi:10.1016/j.chemphyslip.2018.03.004 · Cited by 13 · see citing works

Roles of the Mevalonate Pathway and Cholesterol Trafficking in Pulmonary Host Defense

Gabor, K. A., & Fessler, M. B. (2016) · Current Molecular Pharmacology · doi:10.2174/1874467209666160112123603 · Cited by 13 · see citing works

Genotypic and phenotypic diversity of Mycobacterium tuberculosis complex genotypes prevalent in West Africa

Osei-Wusu, S., Otchere, I. D., Morgan, P. A., Musah, A. B., Siam, I. M., Asandem, D. A., Afum, T., Asare, P. P. A., Asante-Poku, A., Kusi, K. A., et al. (2021) · PLoS ONE · doi:10.1371/journal.pone.0255433 · Cited by 12 · see citing works

Rv3091, An Extracellular Patatin-Like Phospholipase in Mycobacterium tuberculosis, Prolongs Intracellular Survival of Recombinant Mycolicibacterium smegmatis by Mediating Phagosomal Escape

Cui, Z., Dang, G., Song, N., Cui, Y., Li, Z., Zang, X., Liu, H., Wang, Z., & Liu, S. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.532371 · Cited by 11 · see citing works

G2A AttenuatesPropionibacterium acnesInduction of Inflammatory Cytokines in Human Monocytes

Park, A. J., Agak, G. W., Qin, M., Hisaw, L. D., Pirouz, A., Kao, S., Marinelli, L. J., Garbán, H., Thiboutot, D. M., Liu, P. T., et al. (2017) · Annals of Dermatology · doi:10.5021/ad.2017.29.6.688 · Cited by 7 · see citing works

FasR Regulates Fatty Acid Biosynthesis and Is Essential for Virulence of Mycobacterium tuberculosis

Mondino, S., Vázquez, C. L., Cabruja, M., Sala, C., Cazenave‐Gassiot, A., Blanco, F. C., Wenk, M. R., Bigi, F., Cole, S. T., Gramajo, H. C., et al. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.586285 · Cited by 4 · see citing works

Incorporation of fluorophore–cholesterol conjugates into liposomal and mycobacterial membranes

Wercholuk, A. N., Thuman, J. M., Stanley, J. L., Sargent, A. L., Anderson, E. S., & Allen, W. E. (2016) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2016.01.030 · Cited by 3 · see citing works

HPTLC-MALDI TOF MS Imaging Analysis of Phospholipids

Kondakova, T., Machour, N., & Poc, C. D. (2017) · Neuromethods · doi:10.1007/978-1-4939-6946-3_12 · Cited by 3 · see citing works

Differential metabolic host response to pathogens associated with community-acquired pneumonia

den Hartog, I., Karu, N., Zwep, L. B., Voorn, G. P., van de Garde, E. M. W., Hankemeier, T., & van Hasselt, J. G. C. (2023) · Metabolism Open · doi:10.1016/j.metop.2023.100239 · Cited by 3 · see citing works

Draft Genome Sequences of Micrococcus luteus MFP06 and MFP07, Isolated from the Skin of Healthy Volunteers

Souak, D., Boukerb, A. M., Barreau, M., Poc, C. D., & Feuilloley, M. G. J. (2020) · Microbiology Resource Announcements · doi:10.1128/mra.00545-20 · Cited by 3 · see citing works

Altered host pyruvate metabolism fuels and regulates fungal asexual reproductionPreprint

Lee, M. Y., Jaenisch, J., McRae, A. G., Hirai-Adachi, C., Louie, K., Silva, L. P., Bowen, B. P., Northen, T. R., & Wildermuth, M. C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.22.609210 · Cited by 3 · see citing works

FabT, régulateur transcriptionnel de la voie de biosynthèse des acides gras, impliqué dans la virulence de Streptococcus pyogenes

Lambert, C. (2022) · doi:10.70675/0a672633zd25bz421ez97c3z330032546087

Host Lipid Manipulation by Intracellular Bacteria: Moonlighting for Immune Evasion

Challagundla, N., Phadnis, D., Gupta, A., & Agrawal-Rajput, R. (2023) · The Journal of Membrane Biology · doi:10.1007/s00232-023-00296-8 · Cited by 6 · see citing works

Hijacking and Use of Host Lipids by Intracellular Pathogens

Toledo, A. M., & Benach, J. L. (2015) · Microbiology Spectrum · doi:10.1128/microbiolspec.vmbf-0001-2014 · Cited by 58 · see citing works

Lipid larceny: channelizing host lipids for establishing successful pathogenesis by bacteria

Chatterjee, R., Chowdhury, A. R., Mukherjee, D., & Chakravortty, D. (2020) · Virulence · doi:10.1080/21505594.2020.1869441 · Cited by 20 · see citing works

Modulation of Host Lipid Pathways by Pathogenic Intracellular Bacteria

Allen, P. E., & Martinez, J. J. (2020) · Pathogens · doi:10.3390/pathogens9080614 · Cited by 38 · see citing works

Abstract 3068 Control of host lipids, a critical determinant of infection outcomes

O’Connor, T. J. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.109453