Mazmanian, Sarkis

Article from CaltechAUTHORS

• Griffiths, Jessica A. and Yoo, Bryan B., et el. (2024) Peripheral neuronal activation shapes the microbiome and alters gut physiology; Cell Reports; Vol. 43; No. 4; 113953; PMCID PMC11132177; 10.1016/j.celrep.2024.113953
• Nemet, Ina and Funabashi, Masanori, et el. (2023) Microbe-derived uremic solutes enhance thrombosis potential in the host; mBio; Vol. 14; No. 6; e01331-23; 10.7907/ha07h-ryw11
• Morton, James T. and Jin, Dong-Min, et el. (2023) Multi-level analysis of the gut–brain axis shows autism spectrum disorder-associated molecular and microbial profiles; Nature Neuroscience; Vol. 26; No. 7; 1208-1217; PMCID PMC10322709; 10.1038/s41593-023-01361-0
• Boktor, Joseph C. and Sharon, Gil, et el. (2023) Integrated Multi‐Cohort Analysis of the Parkinson's Disease Gut Metagenome; Movement Disorders; Vol. 38; No. 3; 399-409; 10.1002/mds.29300
• Ousey, James and Boktor, Joseph C., et el. (2023) Gut microbiota suppress feeding induced by palatable foods; Current Biology; Vol. 33; No. 1; 147-157.e7; PMCID PMC9839363; 10.1016/j.cub.2022.10.066
• Boktor, Joseph C. and Adame, Mark D., et el. (2022) Global metabolic profiles in a non-human primate model of maternal immune activation: implications for neurodevelopmental disorders; Molecular Psychiatry; Vol. 27; No. 12; 4959-4973; PMCID PMC9772216; 10.1038/s41380-022-01752-y
• Abdel-Haq, Reem and Schlachetzki, Johannes C. M., et el. (2022) A prebiotic diet modulates microglial states and motor deficits in α-synuclein overexpressing mice; eLife; Vol. 11; Art. No. e81453; PMCID PMC9668333; 10.7554/elife.81453
• Chen, Xinhong and Ravindra Kumar, Sripriya, et el. (2022) Engineered AAVs for non-invasive gene delivery to rodent and non-human primate nervous systems; Neuron; Vol. 110; No. 14; 2242-2257; PMCID PMC9308721; 10.1016/j.neuron.2022.05.003
• Bostick, John W. and Schonhoff, Aubrey M., et el. (2022) Gut microbiome-mediated regulation of neuroinflammation; Current Opinion in Immunology; Vol. 76; Art. No. 102177; PMCID PMC9167715; 10.1016/j.coi.2022.102177
• Cryan, John F. and Mazmanian, Sarkis K. (2022) Microbiota–brain axis: Context and causality; Science; Vol. 376; No. 6596; 938-939; 10.1126/science.abo4442
• Schonhoff, Aubrey M. and Mazmanian, Sarkis K. (2022) Lung microbes mediate spinal-cord autoimmunity; Nature; Vol. 603; No. 7899; 38-40; 10.1038/d41586-022-00468-x
• Stewart Campbell, A. and Needham, Brittany D., et el. (2022) Safety and target engagement of an oral small-molecule sequestrant in adolescents with autism spectrum disorder: an open-label phase 1b/2a trial; Nature Medicine; Vol. 28; No. 3; 528-534; 10.1038/s41591-022-01683-9
• Bostick, John W. and Mazmanian, Sarkis K. (2022) Impaired gut barrier affects microglia health; Nature Neuroscience; Vol. 25; No. 3; 268-270; 10.1038/s41593-022-01028-2
• Needham, Brittany D. and Funabashi, Masanori, et el. (2022) A gut-derived metabolite alters brain activity and anxiety behaviour in mice; Nature; Vol. 602; No. 7899; 647-653; PMCID PMC9170029; 10.1038/s41586-022-04396-8
• Wu, Wei-Li and Adame, Mark D., et el. (2021) Microbiota regulate social behaviour via stress response neurons in the brain; Nature; Vol. 595; No. 7867; 409-414; PMCID PMC8346519; 10.1038/s41586-021-03669-y
• Morais, Livia H. and Schreiber, Henry L., IV, et el. (2021) The gut microbiota–brain axis in behaviour and brain disorders; Nature Reviews Microbiology; Vol. 19; No. 4; 241-255; 10.1038/s41579-020-00460-0
• Needham, Brittany D. and Adame, Mark D., et el. (2021) Plasma and Fecal Metabolite Profiles in Autism Spectrum Disorder; Biological Psychiatry; Vol. 89; No. 5; 451-462; PMCID PMC7867605; 10.1016/j.biopsych.2020.09.025
• LaPelusa, Michael and Donoviel, Dorit, et el. (2021) Microbiome for Mars: surveying microbiome connections to healthcare with implications for long-duration human spaceflight, virtual workshop, July 13, 2020; Microbiome; Vol. 9; Art. No. 2; PMCID PMC7781430; 10.1186/s40168-020-00951-5
• Needham, Brittany D. and Kaddurah-Daouk, Rima, et el. (2020) Gut microbial molecules in behavioural and neurodegenerative conditions; Nature Reviews Neuroscience; Vol. 21; No. 12; 717-731; 10.1038/s41583-020-00381-0
• Schattgen, Stefan A. and Crawford, Jeremy C., et el. (2020) Intestinal intraepithelial lymphocyte repertoires are imprinted clonal structures selected for MHC reactivity; Journal of Immunology; Vol. 204; No. S1; Art. No. 84.4
• Donaldson, Gregory P. and Chou, Wen-Chi, et el. (2020) Spatially distinct physiology of Bacteroides fragilis within the proximal colon of gnotobiotic mice; Nature Microbiology; Vol. 5; No. 5; 746-756; 10.1038/s41564-020-0683-3
• Quinn, Robert A. and Melnik, Alexey V., et el. (2020) Global chemical effects of the microbiome include new bile-acid conjugations; Nature; Vol. 579; No. 7797; 123-129; 10.1038/s41586-020-2047-9
• Challis, Collin and Hori, Acacia, et el. (2020) Gut-seeded α-synuclein fibrils promote gut dysfunction and brain pathology specifically in aged mice; Nature Neuroscience; Vol. 23; No. 3; 327-336; PMCID PMC7065967; 10.1038/s41593-020-0589-7
• Sampson, Timothy R. and Challis, Collin, et el. (2020) A gut bacterial amyloid promotes α-synuclein aggregation and motor impairment in mice; eLife; Vol. 9; Art. No. e53111; PMCID PMC7012599; 10.7554/elife.53111
• Pizarro, Theresa T. and Stappenbeck, Thaddeus S., et el. (2019) Challenges in IBD Research: Preclinical Human IBD Mechanisms; Inflammatory Bowel Diseases; Vol. 25; No. S2; S5-S12; 10.1093/ibd/izz075
• Sharon, Gil and Cruz, Nikki Jamie, et el. (2019) Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice; Cell; Vol. 177; No. 6; 1600-1618; PMCID PMC6993574; 10.1016/j.cell.2019.05.004
• Ramakrishna, Chandran and Kujawski, Maciej, et el. (2019) Bacteroides fragilis polysaccharide A induces IL-10 secreting B and T cells that prevent viral encephalitis; Nature Communications; Vol. 10; Art. No. 2153; PMCID PMC6517419; 10.1038/s41467-019-09884-6
• Abdel-Haq, Reem and Schlachetzki, Johannes C. M., et el. (2019) Microbiome–microglia connections via the gut–brain axis; Journal of Experimental Medicine; Vol. 216; No. 1; 41-59; PMCID PMC6314531; 10.1084/jem.20180794
• Griffiths, Jessica A. and Mazmanian, Sarkis K. (2018) Emerging evidence linking the gut microbiome to neurologic disorders; Genome Medicine; Vol. 10; Art. No. 98; PMCID PMC6302417; 10.1186/s13073-018-0609-3
• Schretter, Catherine E. and Vielmetter, Jost, et el. (2018) A gut microbial factor modulates locomotor behavior in Drosophila; Nature; Vol. 563; No. 7731; 402-406; PMCID PMC6237646; 10.1038/s41586-018-0634-9
• Lee, Yun Kyung and Mehrabian, Parpi, et el. (2018) The Protective Role of Bacteroides fragilis in a Murine Model of Colitis-Associated Colorectal Cancer; mSphere; Vol. 3; No. 6; Art. No. e00587-18; PMCID PMC6236802; 10.1128/msphere.00587-18
• Cekanaviciute, Egle and Pröbstel, Anne-Katrin, et el. (2018) Multiple sclerosis-associated changes in the composition and immune functions of spore-forming bacteria; mSystems; Vol. 3; No. 6; Art. No. e00083-18; PMCID PMC5690666; 10.1128/mSystems.00083-18
• Donaldson, G. P. and Ladinsky, M. S., et el. (2018) Gut microbiota utilize immunoglobulin A for mucosal colonization; Science; Vol. 360; No. 6390; 795-800; PMCID PMC5973787; 10.1126/science.aaq0926
• Schretter, Catherine E. and Mazmanian, Sarkis K. (2018) Cultivating a Relationship with Gut Bacteria; Cell Metabolism; Vol. 27; No. 2; 267-268; 10.1016/j.cmet.2018.01.010
• Cekanaviciute, Egle and Yoo, Bryan B., et el. (2017) Gut bacteria from multiple sclerosis patients modulate human T cells and exacerbate symptoms in mouse models; Proceedings of the National Academy of Sciences of the United States of America; Vol. 114; No. 40; 10713-10718; PMCID PMC5635915; 10.1073/pnas.1711235114
• Edelblum, Karen L. and Sharon, Gil, et el. (2017) The microbiome activates CD4 T-cell-mediated immunity to compensate for increased intestinal permeability; Cellular and Molecular Gastroenterology and Hepatology; Vol. 4; No. 2; 285-297; PMCID PMC5540699; 10.1016/j.jcmgh.2017.06.001
• Chan, Ken Y. and Jang, Min J., et el. (2017) Engineered AAVs for efficient noninvasive gene delivery to the central and peripheral nervous systems; Nature Neuroscience; Vol. 20; No. 8; 1172-1179; PMCID PMC5529245; 10.1038/nn.4593
• Yoo, Bryan B. and Mazmanian, Sarkis K. (2017) The Enteric Network: Interactions between the Immune and Nervous Systems of the Gut; Immunity; Vol. 46; No. 6; 910-926; PMCID PMC5551410; 10.1016/j.immuni.2017.05.011
• Wu, Wei-Li and Hsiao, Elaine Y., et el. (2017) The Placental Interleukin-6 Signaling Controls Fetal Brain Development and Behavior; Brain, Behavior, and Immunity; Vol. 62; 11-23; PMCID PMC5373986; 10.1016/j.bbi.2016.11.007
• Kollmann, Tobias R. and Kampmann, Beate, et el. (2017) Protecting the Newborn and Young Infant from Infectious Diseases: Lessons from Immune Ontogeny; Immunity; Vol. 46; No. 3; 350-363; 10.1016/j.immuni.2017.03.009
• Baranzini, Sergio E. and Cekanaviciute, Egle, et el. (2017) The MS-Associated Gut Microbiome; Multiple Sclerosis Journal; Vol. 23; No. Suppl. 1; 100; 10.1177/1352458517693714
• Meisel, Marlies and Mayassi, Toufic, et el. (2017) Interleukin-15 promotes intestinal dysbiosis with butyrate deficiency associated with increased susceptibility to colitis; ISME Journal; Vol. 11; No. 1; 15-30; PMCID PMC5315477; 10.1038/ismej.2016.114
• Lee, Cho-Rong and Kwak, Yewon, et el. (2016) Myeloid-Derived Suppressor Cells Are Controlled by Regulatory T Cells via TGF-β during Murine Colitis; Cell Reports; Vol. 17; No. 12; 3219-3232; 10.1016/j.celrep.2016.11.062
• Mazmanian, Sarkis K. and Sampson, Timothy R., et el. (2016) Gut Microbiota Regulate Motor Deficits and Neuroinflammation in a Model of Parkinson's Disease; Cell; Vol. 167; No. 6; 1469-1480; PMCID PMC5718049; 10.1016/j.cell.2016.11.018
• Sharon, Gil and Sampson, Timothy R., et el. (2016) The Central Nervous System and the Gut Microbiome; Cell; Vol. 167; No. 4; 915-932; PMCID PMC5127403; 10.1016/j.cell.2016.10.027
• Neff, C. Preston and Rhodes, Matthew E., et el. (2016) Diverse Intestinal Bacteria Contain Putative Zwitterionic Capsular Polysaccharides with Anti-inflammatory Properties; Cell Host & Microbe; Vol. 20; No. 4; 535-547; PMCID PMC5113727; 10.1016/j.chom.2016.09.002
• Choi, Harry M. T. and Calvert, Colby R., et el. (2016) Mapping a multiplexed zoo of mRNA expression; Development; Vol. 143; No. 19; 3632-3637; PMCID PMC5087610; 10.1242/dev.140137
• Casaccia, P. and Zhu, Y., et el. (2016) Effect of oral versus injectable disease-modifying therapies on the epigenome-wide DNA methylation and gut microbiota in multiple sclerosis patients; Multiple Sclerosis Journal; Vol. 22; No. S3; 598
• Cekanaviciute, E. and Debelius, J. W., et el. (2016) Gut dysbiosis is a feature of MS and it is characterized by bacteria able to regulate lymphocyte differentiation in vitro; Multiple Sclerosis Journal; Vol. 22; No. S3; 58-59
• Chu, Huitung and Khosravi, Arya, et el. (2016) Gene-microbiota interactions contribute to the pathogenesis of inflammatory bowel disease; Science; Vol. 352; No. 6289; 1116-1120; PMCID PMC4996125; 10.1126/science.aad9948
• Chandran, Ramakrishna and Liu, Hiutung, et el. (2016) Immunomodulation of Host Immunity by Bacteriodes fragillis Polysaccharide A (PSA) Prevents Viral Encephalitis; Journal of Immunology; Vol. 196; No. S1; Art. No. 217.11
• Donaldson, Gregory P. and Lee, S. Melanie, et el. (2016) Gut biogeography of the bacterial microbiota; Nature Reviews Microbiology; Vol. 14; No. 1; 20-32; PMCID PMC4837114; 10.1038/nrmicro3552
• Chu, Hiutung and Mazmanian, Sarkis K. (2015) Winning the Microbial Battle, but Not the War; Cell; Vol. 163; No. 2; 271-272; 10.1016/j.cell.2015.09.050
• Yang, Yang and Wang, Chunlin, et el. (2015) Distinct mechanisms define murine B cell lineage immunoglobulin heavy chain (IgH) repertoires; eLife; Vol. 4; Art. No. 09083; PMCID PMC4714975; 10.7554/eLife.09083
• Cekanaviciute, E. and Runia, T. F., et el. (2015) The influence of microbiota on the adaptive immune response in MS; Multiple Sclerosis Journal; Vol. 21; 454
• Sampson, Timothy R. and Mazmanian, Sarkis K. (2015) Control of Brain Development, Function and Behavior by the Microbiome; Cell Host & Microbe; Vol. 17; No. 5; 565-576; PMCID PMC4442490; 10.1016/j.chom.2015.04.011
• Yano, Jessica M. and Yu, Kristie, et el. (2015) Indigenous Bacteria from the Gut Microbiota Regulate Host Serotonin Biosynthesis; Cell; Vol. 161; No. 2; 264-276; PMCID PMC4393509; 10.1016/j.cell.2015.02.047
• Wu, Wei-Li and Hsiao, Elaine Y., et el. (2015) Maternal Immune Activation Perturbs Fetal Brain Development and Adult Behaviors Through Placental Trophoblast IL-6 Activation; Schizophrenia Bulletin; Vol. 41; No. S1; Art. No. S216
• Mayer, Emeran A. and Knight, Rob, et el. (2014) Gut Microbes and the Brain: Paradigm Shift in Neuroscience; Journal of Neuroscience; Vol. 34; No. 46; 15490-15496; PMCID PMC4228144; 10.1523/JNEUROSCI.3299-14.2014
• Sharon, Gil and Garg, Neha, et el. (2014) Specialized Metabolites from the Microbiome in Health and Disease; Cell Metabolism; Vol. 20; No. 5; 719-730; PMCID PMC4337795; 10.1016/j.cmet.2014.10.016
• Stefka, Andrew T. and Feehley, Taylor, et el. (2014) Commensal bacteria protect against food allergen sensitization; Proceedings of the National Academy of Sciences of the United States of America; Vol. 111; No. 36; 13145-13150; PMCID PMC4246970; 10.1073/pnas.1412008111
• Baranzini, S. E. and Katz-Sand, I., et el. (2014) The MS Microbiome Consortium (MSMC): an academic multi-disciplinary collaborative effort to elucidate the role of the gut microbiota in MS; Multiple Sclerosis Journal; Vol. 20; No. S1; 339; 10.1177/1352458514547105
• Ravel, Jacques and Mazmanian, Sarkis K. (2014) Human microbiome science: vision for the future, Bethesda, MD, July 24 to 26, 2013; Microbiome; Vol. 2; Art. No. 16; PMCID PMC4102747; 10.1186/2049-2618-2-16
• Dorrestein, Pieter C. and Mazmanian, Sarkis K., et el. (2014) Finding the Missing Links among Metabolites, Microbes, and the Host; Immunity; Vol. 40; No. 6; 824-832; PMCID PMC4503329; 10.1016/j.immuni.2014.05.015
• Lee, Yun Kyung and Mazmanian, Sarkis K. (2014) Microbial Learning Lessons: SFB Educate the Immune System; Immunity; Vol. 40; No. 4; 457-459; 10.1016/j.immuni.2014.04.002
• Khosravi, Arya and Yáñez, Alberto, et el. (2014) Gut Microbiota Promote Hematopoiesis to Control Bacterial Infection; Cell Host & Microbe; Vol. 15; No. 3; 374-381; PMCID PMC4144825; 10.1016/j.chom.2014.02.006
• Mahdavi, Alborz and Szychowski, Janek, et el. (2014) Identification of secreted bacterial proteins by noncanonical amino acid tagging; Proceedings of the National Academy of Sciences of the United States of America; Vol. 111; No. 1; 433-438; PMCID PMC3890788; 10.1073/pnas.1301740111
• Hsiao, Elaine Y. and McBride, Sara W., et el. (2013) Microbiota Modulate Behavioral and Physiological Abnormalities Associated with Neurodevelopmental Disorders; Cell; Vol. 155; No. 7; 1451-1463; PMCID PMC3897394; 10.1016/j.cell.2013.11.024
• Lee, S. Melanie and Donaldson, Gregory P., et el. (2013) Bacterial colonization factors control specificity and stability of the gut microbiota; Nature; Vol. 501; No. 7467; 426-429; PMCID PMC3893107; 10.1038/nature12447
• Chu, Hiutung and Mazmanian, Sarkis K. (2013) Innate immune recognition of the microbiota promotes host-microbial symbiosis; Nature Immunology; Vol. 14; No. 7; 668-675; PMCID PMC4109969; 10.1038/ni.2635
• Feehley, Taylor and Stefka, Andrew, et el. (2013) Commensal bacteria induce a barrier protective response to prevent sensitization to food allergens; Journal of Immunology; Vol. 190; 120.19
• Khosravi, Arya and Mazmanian, Sarkis K. (2013) Disruption of the gut microbiome as a risk factor for microbial infections; Current Opinion in Microbiology; Vol. 16; No. 2; 221-227; PMCID PMC5695238; 10.1016/j.mib.2013.03.009
• McFall-Ngai, Margaret and Hadfield, Michael G., et el. (2013) Animals in a bacterial world, a new imperative for the life sciences; Proceedings of the National Academy of Sciences of the United States of America; Vol. 110; No. 9; 3229-3236; PMCID PMC3587249; 10.1073/pnas.1218525110
• Rivas, Magali Noval and Burton, Oliver T., et el. (2013) A microbiota signature associated with experimental food allergy promotes allergic sensitization and anaphylaxis; Journal of Allergy and Clinical Inmunology; Vol. 131; No. 1; 201-212; PMCID PMC3860814; 10.1016/j.jaci.2012.10.026
• Hsiao, Elaine Y. and McBride, Sara W., et el. (2012) Gastrointestinal symptoms and probiotic treatment in a mouse model of an autism risk factor; Journal of Neuroimmunology; Vol. 253; No. 1-2; 47-48; 10.1016/j.jneuroim.2012.10.001
• Hsiao, Elaine Y. and McBride, Sara W., et el. (2012) Neuroimmune changes in a mouse model of the maternal infection risk factor for schizophrenia and autism; Journal of Neuroimmunology; Vol. 253; No. 1-2; 48; 10.1016/j.jneuroim.2012.10.001
• Shen, Yue and Torchia, Maria Letizia Giardino, et el. (2012) Outer Membrane Vesicles of a Human Commensal Mediate Immune Regulation and Disease Protection; Cell Host & Microbe; Vol. 12; No. 4; 509-520; PMCID PMC3895402; 10.1016/j.chom.2012.08.004
• Mahdavi, Alborz and Mazmanian, Sarkis, et el. (2012) Identifying Secreted Proteins by Non-canonical Amino Acid Tagging; Protein Science; Vol. 21; No. S1; 151; 10.1002/pro.2113
• Wingender, Gerhard and Stepniak, Dariusz, et el. (2012) Intestinal Microbes Affect Phenotypes and Functions of Invariant Natural Killer T Cells in Mice; Gastroenterology; Vol. 143; No. 2; 418-428; PMCID PMC3404247; 10.1053/j.gastro.2012.04.017
• Hsiao, Elaine Y. and McBride, Sara W., et el. (2012) Modeling an autism risk factor in mice leads to permanent immune dysregulation; Proceedings of the National Academy of Sciences of the United States of America; Vol. 109; No. 31; 12776-12781; PMCID PMC3411999; 10.1073/pnas.1202556109
• Khosravi, Arya and Mazmanian, Sarkis K. (2012) Breathe easy: microbes protect from allergies; Nature Medicine; Vol. 18; No. 4; 492-494; PMCID PMC4122662; 10.1038/nm.2723
• Chow, Janet and Tang, Haiqing, et el. (2011) Pathobionts of the gastrointestinal microbiota and inflammatory disease; Current Opinion in Immunology; Vol. 23; No. 4; 473-480; PMCID PMC3426444; 10.1016/j.coi.2011.07.010
• Huang, Julie Y. and Lee, S. Melanie, et el. (2011) The human commensal Bacteroides fragilis binds intestinal mucin; Anaerobe; Vol. 17; No. 4; 137-141; PMCID PMC3163789; 10.1016/j.anaerobe.2011.05.017
• Round, June L. and Lee, S. Melanie, et el. (2011) The Toll-Like Receptor 2 Pathway Establishes Colonization by a Commensal of the Human Microbiota; Science; Vol. 332; No. 6032; 974-977; PMCID PMC3164325; 10.1126/science.1206095
• Lee, Yun Kyung and Menezes, Juscilene S., et el. (2011) Proinflammatory T-cell responses to gut microbiota promote experimental autoimmune encephalomyelitis; Proceedings of the National Academy of Sciences of the United States of America; Vol. 108; No. Supplement; 4615-4622; PMCID PMC3063590; 10.1073/pnas.1000082107
• Lee, Yun Kyung and Mazmanian, Sarkis K. (2010) Has the Microbiota Played a Critical Role in the Evolution of the Adaptive Immune System?; Science; Vol. 330; No. 6012; 1768-1773; PMCID PMC3159383; 10.1126/science.1195568
• Round, June L. and Mazmanian, Sarkis K. (2010) Inducible Foxp3^+ regulatory T-cell development by a commensal bacterium of the intestinal microbiota; Proceedings of the National Academy of Sciences of the United States of America; Vol. 107; No. 27; 12204-12209; PMCID PMC2901479; 10.1073/pnas.0909122107
• Round, June L. and O'Connell, Ryan M., et el. (2010) Coordination of tolerogenic immune responses by the commensal microbiota; Journal of Autoimmunity; Vol. 34; No. 3; J220-J225; PMCID PMC3155383; 10.1016/j.jaut.2009.11.007
• Chow, Janet and Mazmanian, Sarkis K. (2010) A Pathobiont of the Microbiota Balances Host Colonization and Intestinal Inflammation; Cell Host & Microbe; Vol. 7; No. 4; 265-276; PMCID PMC2859213; 10.1016/j.chom.2010.03.004
• Mazmanian, Sarkis K. (2009) Gut Immune Balance Is as Easy as S-F-B; Immunity; Vol. 31; No. 4; 536-538; 10.1016/j.immuni.2009.09.005
• Mazmanian, Sarkis and McBride, Sarah (2009) The Microbial Health Factor; The Scientist; Vol. 23; No. 8; 34-38
• Round, June L. and Mazmanian, Sarkis K. (2009) The gut microbiota shapes intestinal immune responses during health and disease; Nature Reviews. Immunology; Vol. 9; No. 5; 313-323; PMCID PMC4095778; 10.1038/nri2515
• Chow, Janet and Mazmanian, Sarkis K. (2009) Getting the bugs out of the immune system: do bacterial microbiota "fix" intestinal T cell responses?; Cell Host & Microbe; Vol. 5; No. 1; 8-12; 10.1016/j.chom.2008.12.006
• Mazmanian, Sarkis K. and Round, June L., et el. (2008) A microbial symbiosis factor prevents intestinal inflammatory disease; Nature; Vol. 453; No. 7195; 620-5; 10.1038/nature07008
• Mazmanian, Sarkis K. (2008) Capsular polysaccharides of symbiotic bacteria modulate immune responses during experimental colitis; Journal of Pediatric Gastroenterology and Nutrition; Vol. 46; No. S1; E11-E12; 10.1097/01.mpg.0000313824.70971.a7
• Liu, Cui Hua and Lee, S. Melanie, et el. (2008) Regulation of surface architecture by symbiotic bacteria mediates host colonization; Proceedings of the National Academy of Sciences of the United States of America; Vol. 105; No. 10; 3951-3956; PMCID PMC2268772; 10.1073/pnas.0709266105
• Garrett, Wendy S. and Lord, Graham M., et el. (2007) Communicable Ulcerative Colitis Induced by T-bet Deficiency in the Innate Immune System; Cell; Vol. 131; No. 1; 33-45; PMCID PMC2169385; 10.1016/j.cell.2007.08.017
• Mazmanian, Sarkis K. and Kasper, Dennis L. (2006) The love–hate relationship between bacterial polysaccharides and the host immune system; Nature Reviews. Immunology; Vol. 6; No. 11; 849-858; 10.1038/nri1956
• Mazmanian, Sarkis K. and Liu, Cui Hua, et el. (2005) An Immunomodulatory Molecule of Symbiotic Bacteria Directs Maturation of the Host Immune System; Cell; Vol. 122; No. 1; 107-118; 10.1016/j.cell.2005.05.007
• Zhang, Rongguang and Wu, Ruiying, et el. (2004) Structures of Sortase B from Staphylococcus aureus and Bacillus anthracis Reveal Catalytic Amino Acid Triad in the Active Site; Structure; Vol. 12; No. 7; 1147-1156; PMCID PMC2792001; 10.1016/j.str.2004.06.001
• Zong, Yinong and Mazmanian, Sarkis K., et el. (2004) The Structure of Sortase B, a Cysteine Transpeptidase that Tethers Surface Protein to the Staphylococcus aureus Cell Wall; Structure; Vol. 12; No. 1; 105-112; 10.1016/j.str.2003.11.021
• Jonsson, Ing-Marie and Mazmanian, Sarkis K., et el. (2003) The role of Staphylococcus aureus sortase A and sortase B in murine arthritis; Microbes and Infection; Vol. 5; No. 9; 775-780; 10.1016/s1286-4579(03)00143-6
• Mazmanian, Sarkis K. and Skaar, Eric P., et el. (2003) Passage of Heme-Iron Across the Envelope of Staphylococcus aureus; Science; Vol. 299; No. 5608; 906-909; 10.1126/science.1081147
• Jonsson, Ing-Marie and Mazmanian, Sarkis K., et el. (2002) On the role of Staphylococcus aureus sortase and sortase-catalyzed surface protein anchoring in murine septic arthritis; Journal of Infectious Diseases; Vol. 185; No. 10; 1417-1424; 10.1086/340503
• Perry, Adrienne M. and Ton-That, Hung, et el. (2002) Anchoring of Surface Proteins to the Cell Wall of Staphylococcus aureus. III. Lipid II is an in vivo peptidoglycan substrate for sortase-catalyzed surface protein anchoring; Journal of Biological Chemistry; Vol. 277; No. 18; 16241-16248; 10.1074/jbc.M109194200
• Ton-That, Hung and Mazmanian, Sarkis K., et el. (2002) Anchoring of Surface Proteins to the Cell Wall of Staphylococcus aureus: cysteine 184 and histidine 120 of sortase form a thiolate-imidazolium ion pair for catalysis; Journal of Biological Chemistry; Vol. 277; No. 9; 7447-7452; 10.1074/jbc.M109945200
• Mazmanian, Sarkis K. and Ton-That, Hung, et el. (2002) An iron-regulated sortase anchors a class of surface protein during Staphylococcus aureus pathogenesis; Proceedings of the National Academy of Sciences of the United States of America; Vol. 99; No. 4; 2293-2298; PMCID PMC122358; 10.1073/pnas.032523999
• Bierne, Hélène and Mazmanian, Sarkis K., et el. (2002) Inactivation of the srtA gene in Listeria monocytogenes inhibits anchoring of surface proteins and affects virulence; Molecular Microbiology; Vol. 43; No. 4; 869-881; 10.1046/j.1365-2958.2002.02798.x
• Lee, Vincent T. and Mazmanian, Sarkis K., et el. (2001) A Program of Yersinia enterocolitica Type III Secretion Reactions Is Activated by Specific Signals; Journal of Bacteriology; Vol. 183; No. 17; 4970-4978; PMCID PMC95371; 10.1128/JB.183.17.4970-4978.2001
• Mazmanian, Sarkis K. and Ton-That, Hung, et el. (2001) Sortase-catalysed anchoring of surface proteins to the cell wall of Staphylococcus aureus; Molecular Microbiology; Vol. 40; No. 5; 1049-1057; 10.1046/j.1365-2958.2001.02411.x
• Mazmanian, Sarkis K. and Liu, Gwen, et el. (2000) Staphylococcus aureus sortase mutants defective in the display of surface proteins and in the pathogenesis of animal infections; Proceedings of the National Academy of Sciences of the United States of America; Vol. 97; No. 10; 5510-5515; PMCID PMC25859; 10.1073/pnas.080520697
• Ton-That, Hung and Mazmanian, Sarkis K., et el. (2000) Anchoring of Surface Proteins to the Cell Wall of Staphylococcus aureus: sortase catalyzed in vitro transpeptidation reaction using LPXTG peptide and NH2-Gly3 substrates; Journal of Bacteriology; Vol. 275; No. 13; 9876-9881; 10.1074/jbc.275.13.9876
• Ton-That, Hung and Liu, Gwen, et el. (1999) Purification and characterization of sortase, the transpeptidase that cleaves surface proteins of Staphylococcus aureus at the LPXTG motif; Proceedings of the National Academy of Sciences of the United States of America; Vol. 96; No. 22; 12424-12429; PMCID PMC22937; 10.1073/pnas.96.22.12424
• Mazmanian, Sarkis K. and Liu, Gwen, et el. (1999) Staphylococcus aureus Sortase, an Enzyme that Anchors Surface Proteins to the Cell Wall; Science; Vol. 285; No. 5428; 760-763; 10.1126/science.285.5428.760