E-GEOD-10777 - Sm29 is a protective surface protein from the tegument of lung-stage Schistosoma mansoni

Status
Submitted on 11 March 2008, released on 15 May 2010, last updated on 1 May 2014
Organism
Schistosoma mansoni
Samples (16)
Array (1)
Protocols (6)
Description
Schistosomiasis continues to be a significant public health problem1. Although vaccine development against this disease has experienced more failures than successes, encouraging results have recently been obtained using membrane-spanning protein antigens from the tegument of S. mansoni. Our group recently identified Sm29, an antigen that is predominantly recognized by IgG1 and IgG3 antibodies of resistant patients2. In the present study, we show that Sm29 is located on the surface of adult worms and lung-stage schistosomula. Immunization of mice with recombinant (r) Sm29 engendered 51% reduction in adult worm burdens, 60% reduction in intestinal eggs and 55% reduction in liver granulomas. Protective immunity in mice was associated with high titers of specific IgG1 and IgG2a and elevated production of IFN-γ, TNF-α and IL-12. Further, cellular responses of infected schistosomiasis patients to rSm29 consisted of elevated IFN-γ and an absence of IL-5. Gene expression analysis of worms recovered from rSm29 vaccinated mice relative to control mice revealed a significant (q< 0.01) down-regulation of 498 genes, while no up-regulation was detected. Among down-regulated genes, many of them encode surface antigens and proteins associated with immune signals suggesting that under immune attack schistosomes reduce the expression of critical surface proteins. This study demonstrates that the membrane-bound Sm29 protein is a new molecule that has great potential as a vaccine candidate against schistosomiasis. Keywords: Schistosoma mansoni gene expression in vaccinated mice Two biological samples were used in the study, each used in two arrays (technical replicates with dye swap) and each array containing two replicates of each spot. Overall, there are eight data points data points for each spot. Only cases with more than 4 of 8 points are valid ratios were considered. Value and its respective dye swap value [after changing the log(ratio) signal] were averaged, reducing the data point to four. The average values were than used in the significance testing using SAM (Tusher et al., 2001). The samples were used to get average values using the following combination: 3000139790L with 3000139792L; 3000139790R with 3000139792R; 3000139791L with 3000139795L; 3000139791R with 3000139795R The normalized, averaged dyeswap values are provided in a supplementary file at the foot of the record.
Experiment type
transcription profiling by array 
Contacts
Thiago Motta Venancio <thiago.venancio@gmail.com>, Alan L Melo, Elisandra Gava, Fernanda C Cardoso, Gilson C Macedo, Giulliana T Almeida, Gregory T Kitten, Luciana S Cardoso, Marcelo V Caliari, Sergio C Oliveira, Sergio Verjovski-Almeida, Thiago M Venancio, Vitor L Mati
Citation
Schistosoma mansoni tegument protein Sm29 is able to induce a Th1-type of immune response and protection against parasite infection. Cardoso FC, Macedo GC, Gava E, Kitten GT, Mati VL, de Melo AL, Caliari MV, Almeida GT, Venancio TM, Verjovski-Almeida S, Oliveira SC.
MIAME
PlatformsProtocolsFactorsProcessedRaw
Files
Investigation descriptionE-GEOD-10777.idf.txt
Sample and data relationshipE-GEOD-10777.sdrf.txt
Raw data (1)E-GEOD-10777.raw.1.zip
Processed data (1)E-GEOD-10777.processed.1.zip
Experiment designE-GEOD-10777.biosamples.png, E-GEOD-10777.biosamples.svg
Array designA-GEOD-3929.adf.txt
Links