First name,Last name,Preferred title,Overview,Position,Department,Individual
John,Edwards,Professor,,Professor,Veterinary Pathobiology,https://scholars.library.tamu.edu/vivo/display/n09bbd732
Dominique,Wiener,Clinical Assistant Professor,"I am an anatomic veterinary pathologist from Bern, Switzerland with broad experience in macroscopical and histological evaluation of tissues from various animal species. I am specialized in Dermatopathology and I provide diagnostic service in the Dermatopathology Speciality Service as well as diagnostic service to the Veterinary Medical Teaching Hospital at TAMU. My research focuses on understanding the pathogenesis of non-inflammatory alopecia in dogs. I am investigating the molecular pathways involved in the activation of follicular stem cells and the regulation of the hair cycle. Our research group in Bern could establish a method to investigate the colony forming capacity of canine follicular stem cells and transit amplifying cells. In Utrecht, The Netherlands, I established the culturing of canine skin organoids (derived from interfollicular epidermis and hair follicles). This model system recapitulates in vitro skin stratification more faithfully than currently used 2D lines. These organoid lines provide the basis to explore epidermal function, to investigate culture conditions necessary for the development of organoids with a HF signature and to address cutaneous disorders in dogs and potentially human patients.",Clinical Assistant Professor,Veterinary Pathobiology,https://scholars.library.tamu.edu/vivo/display/n1c67c8f3
Sara,Lawhon,Professor,"My research group studies zoonotic bacterial pathogens and focuses primarily on salmonellosis and staphylococcal infections with emphasis on molecular host-pathogen interactions and antimicrobial resistance. We are particularly interested in how bacteria sense environmental signals, communicate with each other (quorum sensing), cause disease, and resist antimicrobial therapy. These fundamental processes are common to the organisms in which we work. We use basic, applied, and clinical science approaches in our studies. Salmonella, Staphylococcus, and Campylobacter infect a broad range of animal host species as well as humans thus making our work relevant to both human and animal health. In addition to this work, we conduct clinical research projects to support the mission of our veterinary teaching hospital and we provide support to other researchers who need microbiology expertise or access resources for their work. Our work has been funded by the FDA, CDC, and several foundations focused on diseases in veterinary species.",Professor,Veterinary Pathobiology,https://scholars.library.tamu.edu/vivo/display/n370f31f1
Leslie,Adams,Senior Professor,"My research is focused on the: 1) investigation of the comparative molecular pathogenesis of zoonotic intracellular bacterial pathogens in natural animal models, particularly brucellosis, salmonellosis, and mycobacterial diseases; 2) development of vaccines and host gene expression-based diagnostics for zoonotic and select agent caused diseases, and especially 3) development of in silico host:pathogen interactome predictive models based upon bi-directional in vivo host (bovine/murine) and Brucella spp., Mycobacterium spp.and Salmonella enterica Typhimurium interactions. We developed an in silico computational infection biology model based on actuall temporal in vivo bovine model microarray-based transcriptomic and proteomic profiling of the acute infectious process. We developed a systems biology analysis of both host and pathogen comprehensive transcriptomic and proteomic datasets derived from our in vivo biological model. We computationally fused the datasets based on actual Salmonella, Brucella and Mycobacterium data and computationally predicted bovine host structural proteins to identify maximum likelihoods of host and pathogen protein:protein interactions as the basis for our preliminary in silico interactome model to predict mechanistic genes and linked perturbed cellular pathways.",Senior Professor,Veterinary Pathobiology,https://scholars.library.tamu.edu/vivo/display/n75fee121
Tracy,Vemulapalli,Dr.,,Clinical Professor||Clinical Professor,Small Animal Clinical Sciences||Veterinary Pathobiology,https://scholars.library.tamu.edu/vivo/display/nc82bc997
Angela,Arenas-Gamboa,Assistant Professor,My laboratory is interested in the development of vaccines against select agents focusing onBrucella spp. We incorporate the microencapsulation technology to increase safety and efficacy of vaccines for human and animal use. These studies are principally targeted on the understanding of the response to infection by the host and elucidating the correlates of protective immunity elicited by the encapsulated and non-encapsulated vaccines.,Assistant Professor,Veterinary Pathobiology,https://scholars.library.tamu.edu/vivo/display/ncc8f35b9
Sargurunathan,Subashchandrabose,Assistant Professor,I have a long-standing interest in elucidating the molecular and cellular effectors at the host-pathogen interface to identify therapeutic targets against infectious diseases.,Assistant Professor,Veterinary Pathobiology,https://scholars.library.tamu.edu/vivo/display/nd12152ed
Julian,Leibowitz,Professor,We have two projects in my lab. The first project is focused on identifying evolutionarily conserved RNA secondary structures in the coronavirus RNA genome and functionally examining their role in viral replication through reverse genetic and biochemical approaches. We have previously done this for a number of RNA secondary structures contained within the 5? and 3? regions of the genome and shown that they function as cis-acting elements in replication. Studies in my laboratory have identified a structurally dynamic region of the 5'UTR that interacts with the 3'UTR to facilitate transcription.
A second project in my laboratory has been to develop a reverse genetic system for MHV-1. In collaboration with investigators in Toronto and Pennsylvania my laboratory has demonstrated that MHV-1 infection of susceptible mice provides a safe and convenient rodent model for severe coronavirus infections such as SARS and MERS. The development of a reverse genetic system will allow us to investigate the contributions of individual viral genes to the pathogenesis of the severe pulmonary disease caused by this virus.,Professor||Professor,Microbial Pathogenesis and Immunology||Veterinary Pathobiology,https://scholars.library.tamu.edu/vivo/display/ne2185aa0
Albert,Mulenga,"Professor and Interim head, Veterinary Pathobiology","For generations ticks and tick borne diseases have had significant impact of animal health and livestock productivity around the world. In public health the effect of ticks and tick borne diseases is also tremendous. Since the 1980s when the causative agent of Lyme disease was described, numerous human tick borne diseases have been reported. In absence of effective vaccines against major tick borne diseases, prevention of animal and human tick borne disease infections relies on the use chemicals (acaricides) to kill ticks. Although acaricide based tick control methods are effective in the short-term, they do not offer a permanent solution because of serious limitations such as ticks developing resistance and contamination of the environment and the food chain. Immunization of animals against is a validated alternative tick control method. The attraction is that tick vaccines will be effective against both acaricide resistant and susceptible tick populations. The major limiting factor is the availability of effective tick vaccine targets. The tick cannot cause damage to host or transmit disease agents without successful feeding. Thus, our plan is to understand molecular mechanisms of how ticks accomplish feeding. In this way we will find targets that will be used for development of effective tick vaccines. We are currently studying the feeding physiology of the blacklegged tick (Ixodes scapularis) and the Lone Star tick (Amblyomma americanum). According to the US Centers for Disease Control, these two medically important tick species transmit a combined nine of the 14 human tick borne disease agents in the United States. Major work is on discovery and characterization of proteins that the Lone Star and the Blacklegged tick into animals every 24h through out feeding. The area of particular emphasis is to understanding roles of serine protease inhibitors (serpins) the blacklegged tick and the Lone Star tick inject into animals during feeding. We have identified serpins",Professor and associate head||Professor & Interim Head,School of Veterinary Medicine and Biomedical Sciences||Veterinary Pathobiology,https://scholars.library.tamu.edu/vivo/display/ne8f0c620
Roger,Smith,Professor,Application of flow cytometry to study of animal disease and clinical veterinary medicine; core flow cytometry laboratory.,Professor,Veterinary Pathobiology,https://scholars.library.tamu.edu/vivo/display/nefd6ee54