Uropathogenic Escherichia coli subverts mitochondrial metabolism to enable intracellular bacterial pathogenesis in urinary tract infection
Year: 2022
Type: article
Source: Nature Microbiology
Institutions: Vanderbilt University, Vanderbilt University Medical Center
Language: English
Subfield: Endocrinology
Domain: Life Sciences
Open Access status: green
Funders: Howard Hughes Medical Institute, U.S. Department of Health and Human Services, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, National Institute of Mental Health, National Eye Institute, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Allergy and Infectious Diseases, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Neurological Disorders and Stroke, National Center for Research Resources
Awards: G1097110356, High-Performance Computer Cluster for Biomedical Research, G113219404, G1344704808, G1714318908, G1779004922, G1967979126, G2019238319, The impact of mitochondrial and peroxisomal fission dynamics on metabolic signaling during corticogenesis., G2206197203, G2883034075, Modeling developmental gradients and supportive tissue signaling networks using iPSC-derived forebrain organoids embedded in fluidic hydrogels, G3217217337, G3472967045, Medical Scientist Training Program, Neisseria gonorrhoeae metal transporters that subvert nutritional, Two-component system interactions as uropathogenic Escherichia coli drug targets, G4201875207, G4383762441, G5333329530, The effect of cancer-associated missense mutations in XPA on nucleotide excision repair activity and platinum-based chemotherapy response, The Vanderbilt Institute for Clinical and Translational Research (VICTR) UL1, G725763919, VANTAGE:Consolidation to create the Vanderbilt Technologies for Advanced Genomics, G805864436, G8284380279, G8286558993, G8330851724, G8740516457, The Vanderbilt Urologic Infection Repository, a Resource for Personalized Clinical Discovery, G8948605914, Exploiting metabolic vulnerabilities of CD4 T cell subsets to control inflammatory disease, Clinical Pharmacology Training Program, The impact of mitochondrial and peroxisomal fission dynamics on metabolic signaling during corticogenesis., Vanderbilt Diabetes Research Center, Core Grant in Vision Research, Molecular Principles Governing Mitochondrial and Peroxisomal Remodeling as Drivers of Cell Fate and Identity, Host-mediated zinc sequestration during Acinetobacter baumannii infection, G949362299
OpenAlex ID: W4292641149