2010
DOI: 10.1051/vetres/2010031
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Physiology, pathogenicity and immunogenicity oflonand/orcpxRdeleted mutants ofSalmonellaGallinarum as vaccine candidates for fowl typhoid

Abstract: To construct a novel live vaccine candidate for fowl typhoid (FT) caused by Salmonella Gallinarum (SG), the lon and cpxR genes that are related to host-pathogen interaction were deleted from a wild type SG using the allelic exchange method. The mutants were grown normally, as was the wild type. The biochemical properties of the mutants remained very similar to those of the wild-type, while JOL914 (Δlon) and JOL916 (ΔlonΔcpxR) were mucoid. Extracellular polysaccharide increased 30.6-, 1.3-, and 46.2-fold in JOL… Show more

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Cited by 50 publications
(31 citation statements)
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“…This pathogen enters the small intestine and is carried to various organs, including the spleen and liver (46)(47)(48). Expression of chicken IL-17 transcript increases in the cecum during Salmonella enterica serovar Enteritidis infection (20,49).…”
Section: Discussionmentioning
confidence: 99%
“…This pathogen enters the small intestine and is carried to various organs, including the spleen and liver (46)(47)(48). Expression of chicken IL-17 transcript increases in the cecum during Salmonella enterica serovar Enteritidis infection (20,49).…”
Section: Discussionmentioning
confidence: 99%
“…Titers of S. Enteritidis antigen-specific immunoglobulin G (IgG) and secretory immunoglobulin A (sIgA) antibodies, in addition to LTB-specific IgG titers, were determined by indirect ELISA following immunization. Plasma samples were obtained by centrifuging heparinized blood samples collected from the wing vein, whereas intestinal wash samples were collected using the pilocarpine-based intestinal lavage procedure, as previously described (20). To quantify S. Enteritidis-specific plasma IgG and intestinal sIgA titers, outer membrane protein (OMP) (extracted from S. Enteritidis strain JOL860 cells) was used as the coating antigen.…”
Section: Methodsmentioning
confidence: 99%
“…Macrophage uptake of SM and reference strains was assessed as described earlier40 with minor modifications. The experiment was performed by infecting chicken primary intraperitoneal macrophages with a multiplicity of infection (MOI) of 10:1.…”
Section: Methodsmentioning
confidence: 99%