Charaterization of the Genes Related to Invasivity and Intrecellular Survival of P. Salmonis: an in Vitro Study of New Virulence Markers in Chilean Isolates of the Causal Agent of Srs

Objetivo general

Establish whether or not genes clpB, dnaK, bipA, groEL, acnA and icmE, or other candidate genes of P. salmonis, are expressed differentially in different national strains cultured in vitro in SHK-1 salmon cell lines and correlate this with invasivity and survival of bacteria and the expression of Toll-like receptors.

Objetivos específicos

1.- Identify genes within the genomes of different strains of P. salmonis related to invasivity and intracellular resistance, via comparative genomic analyses. 2.- Analyze the expression via RT-qPCR of the genes previously identified in the genome of different strains of P. salmonis cultured in the SHK-1 cell line and in liquid medium. 3.- Analyze the specific expression in tissues of adult salmon via RT-qPCR and Western blot of Toll-like receptors of Atlantic salmon (TLR1, TLR5, TLR2, TLR22, TLR3, TLR6). 4.- Identifying genes of antibiotic resistance in strains of P. salmonis and genes related to virulence and pathogenicity through in vitro analysis in liquid medium and cell culture respectively. 5.- Analyze and compare the protein expression of P. salmonis with polyclonal antibodies against previously identified proteins of interest, which have displayed differential expression via RT-qPCR between bacterial cultures in cell lines and in liquid medium.

Descripción

Clasificaciones

Código: 1130069

Base fuente: Base Nacional de Proyectos

199242000

199242000

0

Fecha inicio: 15/03/2013

Fecha término: 15/03/2017

1461

122

4

Tipo instrumento: Proyecto (PYT)

Año: 2013

Ejecutor: Universidad Austral de Chile

Coordinador principal: Figueroa Valdeverde, Jaime Eugenio

Asociado(s): Centro de Investigaciones Bioquímica - CIB

Región(es): Los Ríos

Temas: Biotecnología - Sanidad animal

Sector-Subsector-Rubro: Acuícola / Peces / Peces de agua de mar

Especie(s): Salmón

Estado: Terminado

Fuente de financiamiento: ANID (ex CONICYT) / FONDECYT

Otra Información de Interés: URL