Literature DB >> 18262165

Proteome analysis of the cardiac and pericardial tissue of Biomphalaria tenagophila populations susceptible and resistant to Schistosoma mansoni infection.

Liana K Jannotti-Passos1, Hélida M Andrade, Roberta L Caldeira, Alvaro J Romanha, Silvane M F Murta, Donat A Chapeaurouge, Jonas Perales, Paulo Marcos Z Coelho, Omar S Carvalho.   

Abstract

For a better comprehension of the parasite-host interaction, proteins expressed by the cardiac and pericardial tissues were compared between susceptible (Cabo Frio) and resistant (Taim) Biomphalaria tenagophila populations, challenged (c) and non-challenged (nc) with Schistosoma mansoni. Proteins were separated by two-dimensional gel electrophoresis (2DE) and stained with Coomassie blue. A total of 146 and 135 spots were observed in Cabo Frio (CFnc) and in Taim (Tnc) non-challenged populations, respectively, whereas 153 spots were detected in both Cabo Frio (CFc) and Taim (Tc) challenged populations. Regarding comparisons between CFnc and CFc, the numbers of exclusive spots obtained were one and nine, respectively, whereas Tnc yielded 17 and Tc eight exclusive spots. By comparing the total of spots in CF (nc+c) with T (nc+c) populations, we obtained: four exclusive spots for CFc; zero for CFnc; four for Tc and; one for Tnc. A quantitative comparison (reason>2.5) of the total spots of CF (nc+c) with T (nc+c) populations allowed us to distinguish five more intense spots for Tc, 14 for Tnc, 15 for CFnc and 11 for CFc. In the CFnc population, two proteins were identified: actin and ATP synthase alpha chain; in the CFc population, four proteins: actin, calmodulin, HSP70, and dehydrogenase; in the Tnc population, five proteins: matrilin, HSP70, actin, ATP synthase alpha chain and intermediate filament of the protein; and in the Tc population, three proteins: actin, alpha-S1 casein and ATP synthase alpha chain. Out of a total of 79 spots, only nine proteins were identified due to the low number of available nucleotide sequences in the GenBank. Nevertheless, knowing proteins regarded as differentially expressed is indispensable for hitherto unidentified genes implicated in B. tenagophila resistance and or susceptibility to S. mansoni infection.

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Year:  2007        PMID: 18262165     DOI: 10.1016/j.actatropica.2007.12.003

Source DB:  PubMed          Journal:  Acta Trop        ISSN: 0001-706X            Impact factor:   3.112


  4 in total

1.  Identification of protein components of egg masses indicates parental investment in immunoprotection of offspring by Biomphalaria glabrata (gastropoda, mollusca).

Authors:  Jennifer J M Hathaway; Coen M Adema; Barbara A Stout; Charlotte D Mobarak; Eric S Loker
Journal:  Dev Comp Immunol       Date:  2009-12-16       Impact factor: 3.636

2.  Pathogen-associated molecular patterns activate expression of genes involved in cell proliferation, immunity and detoxification in the amebocyte-producing organ of the snail Biomphalaria glabrata.

Authors:  Si-Ming Zhang; Eric S Loker; John T Sullivan
Journal:  Dev Comp Immunol       Date:  2015-11-22       Impact factor: 3.636

3.  Identification and expression of differentially expressed genes in the hard clam, Mercenaria mercenaria, in response to quahog parasite unknown (QPX).

Authors:  Mickael Perrigault; Arnaud Tanguy; Bassem Allam
Journal:  BMC Genomics       Date:  2009-08-14       Impact factor: 3.969

4.  Diminished adherence of Biomphalaria glabrata embryonic cell line to sporocysts of Schistosoma mansoni following programmed knockout of the allograft inflammatory factor.

Authors:  Fernanda Sales Coelho; Rutchanee Rodpai; André Miller; Shannon E Karinshak; Victoria H Mann; Omar Dos Santos Carvalho; Roberta Lima Caldeira; Marina de Moraes Mourão; Paul J Brindley; Wannaporn Ittiprasert
Journal:  Parasit Vectors       Date:  2020-10-13       Impact factor: 3.876

  4 in total

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