Mary B. Brown
Department of Infectious Diseases and Pathology
PO Box 110880
2015 SW 16th AV
Gainesville, FL 32611-0880
- PhD, Biology, University of Alabama at Birmingham, 1984
Honors and Awards
- 1990-92, Membership Secretary, International Organization for Mycoplasmology
- 1992, Division G. Councilor, American Society for Microbiology
- 1992-96, Treasurer, International Organization for Mycoplasmology Member, working teams on bovine, wildlife and zoological mycoplasmas, International Research Program on Comparative Mycoplasmology (IRPCM)
- 1990-96, Board of Directors, International Organization for Mycoplasmology
- 1992 Division G Councilor, American Society for Microbiology Fellow, Morris Animal Foundation
- 1992-1996 Treasurer, International Organization for Mycoplasmology
- 1998-99 Chair, Division G, American Society for Microbiology
- 1998-2002, Program Committee, 13th & 14th Congresses of the IOM
- 2001 Division G Lecturer, American Society for Microbiology Annual Meeting
My laboratory is involved in defining the pathogenic mechanisms by which mycoplasmas cause both respiratory and urogenital infections. We work with a number of host species, including rodents, food and fiber animals, reptiles, and humans.
Emerging mycoplasmal infections in reptiles
Recently we have been involved in the elucidation of the etiologic agent, characterization of clinical disease, and diagnosis of respiratory mycoplasmosis in two environmentally threatened species of tortoise and in American alligators. In experimental transmission studies designed to fulfill Koch’s postulates, we demonstrated that Mycoplasma agassizii was the etiologic agent of upper respiratory tract disease (URTD in both gopher and desert tortoises and that Mycoplasma alligatoris caused a septic. Lethal infection in alligators. We have developed serological diagnostic tests (ELISA) as well as a PCR based diagnostic tests to allow epidemiological surveys of large natural populations. We have ongoing investigations into mechanisms of transmission and pathogenesis of these infections.
Recurrent urinary tract infection in women
Urinary tract infections (UTI) represent a significant medical problem for women. The major infectious agents associated with UTI are Gram negative aerobic rods (primarily Escherichia coli) and Staphylococcus saprophyticus. However, as many as one third of women seen with clinical signs of UTI (dysuria, frequency, and urgency) are considered to have UTI which is “abacterial” in origin. Although the evidence for involvement of Ureaplasma urealyticum in nongonococcal urethritis and prostatitis in men is compelling, few studies have addressed the role of this microorganism in UTI in women. This prospective study will follow women from the onset of a clinical episode of UTI over a minimum one year period including periods of quiescence as well as any subsequent UTI. The overall objective of this project is determine the role of U. urealyticum both as an etiologic agent of UTI in women and as a potential risk factor for establishment of susceptibility to recurrent and chronic urinary tract infection.
Models of Intrauterine Infection
Microbial infections of the chorioamnion and amniotic fluid have devastating effects on pregnancy outcome. Genital mycoplasmosis is a naturally occurring disease of rats that makes it ideally suited as a model to study the adverse effects of infectious agents in pregnancy as well as the immunomodulatory effects of infectious agents and their impact on reproductive function. We have demonstrated that M. pulmonis causes an ascending infection in Sprague Dawley rats which is characterized by placentitis and chorioamnionitis and results in significant fetal wastage and decreased birth weight. It is our hypothesis that an infectious agent could trigger host responses which have deleterious effects on pregnancy maintenance by altering the normal cytokine levels secreted for pregnancy regulation.
Mycoplasmosis in food and fiber animals
Our laboratory is studying the role of an extracellular protease produced by Mycoplasma mycoides in virulence of mycoplasmal infections of goats. In addition, we have ongoing studies to elucidate the pathogenic mechanisms of M. bovis infections of dairy calves.
- Immune profiling of BALB/C and C57BL/6 mice reveals a correlation between Ureaplasma parvum-Induced fetal inflammatory response syndrome-like pathology and increased placental expression of TLR2 and CD14.
Additional publications here