Daniel E. Voth
Department Chairperson
faculty
Department Chairs, College of Medicine
Research Areas
Links
Biography and Research Information
OverviewAI-generated summary
Daniel E. Voth's research program focuses on understanding host-pathogen interactions, particularly concerning intracellular bacterial pathogens like *Coxiella burnetii*, the causative agent of Q fever. His work investigates the mechanisms by which these bacteria subvert host cellular processes, such as antioxidant signaling pathways, to establish infection. Voth also explores strategies for combating these infections, including the evaluation of host-directed drugs that can target bacterial growth within human cells. His laboratory employs a range of infection models, including in vitro cell cultures, in vivo animal models, and ex vivo lung tissue models, to gain comprehensive insights into pathogen invasion and host defense.
Metrics
- h-index: 30
- Publications: 77
- Citations: 21,647
Selected Publications
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Late-Stage Functionalization of the Rifamycin Core via Click Chemistry Toward New Antibacterial Derivatives (2026)
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<i>Coxiella burnetii</i> Nine Mile II Δ <i>cbu0533</i> as a suitable laboratory replacement strain (2025)
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β-glucan-induced monocyte-derived alveolar macrophages confer protection against Mycobacterium tuberculosis 4395 (2025)
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Control of human Q fever by vaccination: the journey to Q-VAX and beyond (2025)
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Coxiella burnetii Strains Elicit Distinct Inflammatory Responses in Human Macrophages (2025)
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The intracellular agent of Q fever, <i>Coxiella burnetii</i> , alters human alveolar macrophage metabolism and mitochondrial physiology (2025)
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<i>Coxiella burnetii</i> strains elicit distinct inflammatory responses in human macrophages (2025)
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Guanylate-Binding Proteins Promote Host Defense Against <i>Leishmania major</i> by Balancing iNOS/Arg-1 in Myeloid Cells (2025)
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Embracing multiple infection models to tackle Q fever: A review of in vitro, in vivo, and lung ex vivo models (2024)
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Development and validation of systems for genetic manipulation of the Old World tick-borne relapsing fever spirochete, Borrelia duttonii (2024)
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MicroRNAs Contribute to Host Response to <i>Coxiella burnetii</i> (2022)
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Editorial: Obligate intracellular bacteria: Evasion and adaptative tactics shaping the host-pathogen interface (2022)
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Breathe In, Breathe Out: Metabolic Regulation of Lung Macrophages in Host Defense Against Bacterial Infection (2022)
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MicroRNAs contribute to the host response to <i>Coxiella burnetii</i> (2022)
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Neurotransmitter System-Targeting Drugs Antagonize Growth of the Q Fever Agent, Coxiella burnetii, in Human Cells (2021)
Federal Grants 4 $8,412,384 total
Defining the impact of host-directed drugs on Coxiella burnetii growth in macrophages
Coxiella burnetii Subversion of Host Nrf2 Antioxidant Signaling- Resubmission
Glycan Expression Analysis using an Odyssey CLx Infrared Imaging System
Grants & Funding
- Coxiella burnetii Regulation of Macrophage cAMP/PKA Signaling NIH Principal Investigator
- Defining the impact of host-directed drugs on Coxiella burnetii growth in macrophages UAMS Internal Research Awards Principal Investigator
- Bacterial cell wall synthesis, shape and septation NIH Principal Investigator
- Role of the Coxiella burnetii Cryptic Plasmid in Host Cell Parasitism NIH Principal Investigator
- Manipulation of host signaling by the Q fever agent, Coxiella burnetii American Heart Association (South Central Affiliate) Principal Investigator
- Coxiella burnetii Subversion of Host Nrf2 Antioxidant Signaling- Resubmission NIH Principal Investigator
- A Novel Human Lung Infection Platform to Define Staphylococcus aureus Virulence Determinants NIH Principal Investigator
- Defining Coxiella burnetii Infection of Primary Human Cardiac Cells NIH/Nat. Inst. of Allergy & Infectious Diseases Principal Investigator
Collaboration Network
Top Collaborators
- MicroRNAs Contribute to Host Response to <i>Coxiella burnetii</i>
- MicroRNAs contribute to the host response to <i>Coxiella burnetii</i>
- <i>Coxiella burnetii</i> strains elicit distinct inflammatory responses in human macrophages
- Coxiella burnetii Strains Elicit Distinct Inflammatory Responses in Human Macrophages
- MicroRNAs Contribute to Host Response to <i>Coxiella burnetii</i>
- MicroRNAs contribute to the host response to <i>Coxiella burnetii</i>
- <i>Coxiella burnetii</i> strains elicit distinct inflammatory responses in human macrophages
- Coxiella burnetii Strains Elicit Distinct Inflammatory Responses in Human Macrophages
- Neurotransmitter System-Targeting Drugs Antagonize Growth of the Q Fever Agent, Coxiella burnetii, in Human Cells
- MicroRNAs Contribute to Host Response to <i>Coxiella burnetii</i>
- Development and validation of systems for genetic manipulation of the Old World tick-borne relapsing fever spirochete, Borrelia duttonii
- Neurotransmitter System-Targeting Drugs Antagonize Growth of the Q Fever Agent, Coxiella burnetii, in Human Cells
- MicroRNAs Contribute to Host Response to <i>Coxiella burnetii</i>
- MicroRNAs contribute to the host response to <i>Coxiella burnetii</i>
- Breathe In, Breathe Out: Metabolic Regulation of Lung Macrophages in Host Defense Against Bacterial Infection
- The intracellular agent of Q fever, <i>Coxiella burnetii</i> , alters human alveolar macrophage metabolism and mitochondrial physiology
- β-glucan-induced monocyte-derived alveolar macrophages confer protection against Mycobacterium tuberculosis 4395
- The intracellular agent of Q fever, <i>Coxiella burnetii</i> , alters human alveolar macrophage metabolism and mitochondrial physiology
- Control of human Q fever by vaccination: the journey to Q-VAX and beyond
- <i>Coxiella burnetii</i> Nine Mile II Δ <i>cbu0533</i> as a suitable laboratory replacement strain
- Take my breath away: studying pathogen invasion of the human lung using primary tissue models
- Neurotransmitter System-Targeting Drugs Antagonize Growth of the Q Fever Agent, Coxiella burnetii, in Human Cells
- Breathe In, Breathe Out: Metabolic Regulation of Lung Macrophages in Host Defense Against Bacterial Infection
- β-glucan-induced monocyte-derived alveolar macrophages confer protection against Mycobacterium tuberculosis 4395
- Guanylate-Binding Proteins Promote Host Defense Against <i>Leishmania major</i> by Balancing iNOS/Arg-1 in Myeloid Cells
- <i>Coxiella burnetii</i> strains elicit distinct inflammatory responses in human macrophages
- <i>Coxiella burnetii</i> strains elicit distinct inflammatory responses in human macrophages
- Coxiella burnetii Strains Elicit Distinct Inflammatory Responses in Human Macrophages
- The intracellular agent of Q fever, <i>Coxiella burnetii</i> , alters human alveolar macrophage metabolism and mitochondrial physiology
- Coxiella burnetii Strains Elicit Distinct Inflammatory Responses in Human Macrophages
- Control of human Q fever by vaccination: the journey to Q-VAX and beyond
- <i>Coxiella burnetii</i> Nine Mile II Δ <i>cbu0533</i> as a suitable laboratory replacement strain
- Neurotransmitter System-Targeting Drugs Antagonize Growth of the Q Fever Agent, Coxiella burnetii, in Human Cells
- Neurotransmitter System-Targeting Drugs Antagonize Growth of the Q Fever Agent, Coxiella burnetii, in Human Cells
- Breathe In, Breathe Out: Metabolic Regulation of Lung Macrophages in Host Defense Against Bacterial Infection
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