The main objective of this program is to perform epidemiological, clinical, immunological and genetic studies to expand our knowledge of the pathogenesis and control of visceral, cutaneous and mucosal leishmaniasis. The UFBA, UFRN, FIOCRUZ, Tropical Medicine Research Center consortium was formed in 1996 and has now built a highly synergistic and productive collaboration among researchers from the major academic centers in Northeast Brazil where these diseases are endemic. The overall pragmatic theme is to determine the role of host (immunological response, genetics), pathogens (genetical and phenotypic markers) and environment (sand fly) factors in disease expression and adverse outcome. These studies will contribute to the identification of new forms of interventions to control and ameliorate disease outcomes due to these common endemic diseases. Project """"""""Host and Parasite Factors in Mucosal Leishmaniasis"""""""", will determine the roles played by the host immune response and genetics, as well as parasite polymorphism, in driving the clinical outcome to mucosal leishmaniasis. Project """"""""Human Immunological Responses to Phlebotomine Saliva"""""""", will evaluate how the effect of phlebotomine's salivary products in the initial host immune response to Leishmania and how the established host immune response to these products influence disease outcome. Project """"""""Determinants of Disease in Visceral Leishmaniasis"""""""", will attempt to identify specific host genetic and environmental determinants of infection and disease progression in a family cohort followed prospectively in an area endemic for L chagasi. Host immunological response plays an important role in the control of leishmaniasis. This project will explore a new area in the parasite host interaction by evaluating how immunological response to salivary gland products correlate with clinical outcome of L. chagasi infection. Emphasis will be placed on the understanding of the pathogenesis of mucosal leishmaniasis, which eventually will contribute to new source of therapy and prophylactic measures to decrease the burden of this leishmaniasis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Specialized Center (P50)
Project #
5P50AI030639-12
Application #
6661954
Study Section
Special Emphasis Panel (ZAI1-GLM-M (J2))
Program Officer
Rao, Malla R
Project Start
1991-03-01
Project End
2007-06-30
Budget Start
2003-07-01
Budget End
2004-06-30
Support Year
12
Fiscal Year
2003
Total Cost
$641,714
Indirect Cost
Name
Federal University of Bahia
Department
Type
DUNS #
900845397
City
Salvador
State
Country
Brazil
Zip Code
40110-160
Sousa, Rosana; Andrade, Viviane M; Bair, Thomas et al. (2018) Early Suppression of Macrophage Gene Expression by Leishmania braziliensis. Front Microbiol 9:2464
Silva, Silvana C; Guimarães, Luiz Henrique; Silva, Juliana A et al. (2018) Molecular epidemiology and in vitro evidence suggest that Leishmania braziliensis strain helps determine antimony response among American tegumenary leishmaniasis patients. Acta Trop 178:34-39
Teixeira, D G; Monteiro, G R G; Martins, D R A et al. (2017) Comparative analyses of whole genome sequences of Leishmania infantum isolates from humans and dogs in northeastern Brazil. Int J Parasitol 47:655-665
Lima, Josivan Gomes; Nobrega, Lucia Helena C; Lima, Natalia Nobrega et al. (2017) Normal bone density and trabecular bone score, but high serum sclerostin in congenital generalized lipodystrophy. Bone 101:21-25
Lima, Ádila L M; de Lima, Iraci D; Coutinho, José F V et al. (2017) Changing epidemiology of visceral leishmaniasis in northeastern Brazil: a 25-year follow-up of an urban outbreak. Trans R Soc Trop Med Hyg 111:440-447
Kelly, Patrick H; Bahr, Sarah M; Serafim, Tiago D et al. (2017) The Gut Microbiome of the Vector Lutzomyia longipalpis Is Essential for Survival of Leishmania infantum. MBio 8:
Gimblet, Ciara; Meisel, Jacquelyn S; Loesche, Michael A et al. (2017) Cutaneous Leishmaniasis Induces a Transmissible Dysbiotic Skin Microbiota that Promotes Skin Inflammation. Cell Host Microbe 22:13-24.e4
Almeida, Lucas; Silva, Juliana A; Andrade, Viviane M et al. (2017) Analysis of expression of FLI1 and MMP1 in American cutaneous leishmaniasis caused by Leishmania braziliensis infection. Infect Genet Evol 49:212-220
Weirather, Jason L; Duggal, Priya; Nascimento, Eliana L et al. (2017) Comprehensive candidate gene analysis for symptomatic or asymptomatic outcomes of Leishmania infantum infection in Brazil. Ann Hum Genet 81:41-48
Novais, Fernanda O; Carvalho, Augusto M; Clark, Megan L et al. (2017) CD8+ T cell cytotoxicity mediates pathology in the skin by inflammasome activation and IL-1? production. PLoS Pathog 13:e1006196

Showing the most recent 10 out of 85 publications