Browsing by Author "Casiano-Rivera, Félix M."

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    Analysis of Polysaccharide and Biofilm Production of the Emerging Cystic Fibrosis Pathogen Stenotrophomonas maltophilia
    (Office of the Vice Chancellor for Research, 2016-04-08) Casiano-Rivera, Félix M.; Anderson, Gregory G.
    Stenotrophomonas maltophilia is an emerging Cystic Fibrosis (CF) lung pathogen, which displays high intrinsic resistance to a number of different antibiotics. Additionally, S. maltophilia is thought to increase antibiotic resistance by forming biofilms during infection. Biofilm disruption could promote clearance of the microorganism from CF-infected lungs. However, the genetic, biochemical and immunological mechanisms underlying S. maltophilia biofilm formation are not well understood. Secreted polysaccharides have been proven to form a vital component of the matrix that surrounds and protects biofilm bacteria. Hundreds of S. maltophilia mutants were generated by transposon mutagenesis and screened for strains with reduced polysaccharide secretion.. These strains were screened through the use of agar plates containing the polysaccharide-binding dye, Congo red. Experimental controls included a S. maltophilia wild-type strain (positive control) and a confirmed polysaccharide deficient mutant (negative control). A Congo red liquid binding assay was utilized to identify the amount of Congo red bound in the samples, which confirmed the amount of polysaccharide present in them. A total of 1,728 mutants were screened with 61 mutants showing reduced polysaccharide production. The mutants were further narrowed down to 8 samples showing the most consistent phenotype. Arbitrary-primed polymerase chain reactions (AP-PCR), followed by sequencing, will be performed on the selected samples in an effort to identify the genes mutated in polysaccharide deficient strains. We will also perform immunological assays in an effort to understand underlying immune responses to S. maltophilia. In order to determine the effects of the deletion of gpmA in S. maltophilia, we will be performing an in-vitro co-culture assay using the wild-type strain and the gpmA mutant strain. These studies will yield evidence to the molecular process involved in polysaccharide production, which could lead to mechanisms to disrupt biofilm formation in CF patients.
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    Mechanisms of Gene Regulation by Soy Peptide Lunasin in Innate Immune Cells
    (Office of the Vice Chancellor for Research, 2015-04-17) Casiano-Rivera, Félix M.; Tung, Chun-Yu; Chang, Hua-Chen
    Lunasin is a seed peptide containing 43 amino acids, originally isolated from soybeans. Recently, a novel function of lunasin was discovered, as it acts as an immune modulating agent regulating gene expression of various innate immune cells. Lunasin strongly activated the expression of genes encoding for type I interferon and inflammatory cytokines. Nonetheless, the molecular mechanisms of lunasin’s gene regulation are relatively unknown. Our current hypothesis states that lunasin is able to induce activation of various transcription factors, resulting in gene expression in immune cells. Human dendritic cells (DCs) or monocytes were purified from peripheral blood mononuclear cells (PBMCs) in order to determine the activation of transcription factors. Phosphorylation of STAT1 and NF-ĸB (p65) were evident in cells treated with lunasin using flow cytometry and Western blotting. The results will ultimately lead to the signaling pathways involved in gene expression regulated by lunasin in innate immune cells. By defining the signaling pathway of lunasin, we can have a better understanding of its application in immune modulation.