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One or more keywords matched the following properties of Guentzel, M. Neal
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overview Dr. Guentzel’s research expertise is in microbial pathogenesis and immunology. Initially, he worked with cholera (Vibrio cholerae) and was the first to show motility as a virulence factor for any bacterial pathogen and extensively characterized an animal model for studies of cholera pathogenesis and putative vaccines for cholera. Motility has since been shown to be important in pathogenesis of a variety of microbes and the model is a mainstay for cholera studies. He also studied pathogenesis of the major fungal pathogen Candida albicans, developed a new animal model for candidiasis, and demonstrated systemic spread from the GI tract as a consequence of different treatments used in human patients. Current studies have focused on pathogenesis and putative vaccines for Chlamydia trachomatis, the world’s leading cause of bacterial STD, which is often asymptomatic but if left untreated can induce ascending infection in the uterus and fallopian tubes, causing pelvic inflammatory disease (PID) and complications such as ectopic pregnancy and infertility in women, and infant pneumonia in children with serious respiratory sequelae later in life. The lab's studies on the select agent Francisella tularensis have helped to define the virulence determinants of this pathogen and characterized the immune response and protection afforded by putative attenuated vaccine stains. Acinetobacter baumannii is a multi-drug resistant, important wound, nosocomial (hospital acquired), and pulmonary pathogen with a high mortality, which is being studied for mechanisms of colonization, pathogenesis and control.
One or more keywords matched the following items that are connected to Guentzel, M. Neal
Item TypeName
Academic Article Francisella tularensis T-cell antigen identification using humanized HLA-DR4 transgenic mice.
Academic Article The Fischer 344 rat reflects human susceptibility to francisella pulmonary challenge and provides a new platform for virulence and protection studies.
Academic Article Mast cell/IL-4 control of Francisella tularensis replication and host cell death is associated with increased ATP production and phagosomal acidification.
Academic Article Non-FceR bearing mast cells secrete sufficient interleukin-4 to control Francisella tularensis replication within macrophages.
Academic Article Comparison of bone marrow-derived and mucosal mast cells in controlling intramacrophage Francisella tularensis replication.
Academic Article Perforin- and granzyme-mediated cytotoxic effector functions are essential for protection against Francisella tularensis following vaccination by the defined F. tularensis subsp. novicida ?fopC vaccine strain.
Academic Article Mast cell TLR2 signaling is crucial for effective killing of Francisella tularensis.
Academic Article Mucosal immunization with live attenuated Francisella novicida U112?iglB protects against pulmonary F. tularensis SCHU S4 in the Fischer 344 rat model.
Academic Article Enhancement of vaccine efficacy by expression of a TLR5 ligand in the defined live attenuated Francisella tularensis subsp. novicida strain U112?iglB::fljB.
Academic Article Contribution of Fc?RI-associated vesicles to mast cell-macrophage communication following Francisella tularensis infection.
Academic Article M-Cells Contribute to the Entry of an Oral Vaccine but Are Not Essential for the Subsequent Induction of Protective Immunity against Francisella tularensis.
Academic Article Mast cells inhibit intramacrophage Francisella tularensis replication via contact and secreted products including IL-4.
Academic Article Oral live vaccine strain-induced protective immunity against pulmonary Francisella tularensis challenge is mediated by CD4+ T cells and antibodies, including immunoglobulin A.
Academic Article Vaccination with a defined Francisella tularensis subsp. novicida pathogenicity island mutant (DeltaiglB) induces protective immunity against homotypic and heterotypic challenge.
Academic Article The presence of infectious extracellular Francisella tularensis subsp. novicida in murine plasma after pulmonary challenge.
Academic Article CD4+ T cells are required during priming but not the effector phase of antibody-mediated IFN-gamma-dependent protective immunity against pulmonary Francisella novicida infection.
Concept Francisella tularensis
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  • Francisella tularensis
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