2011
DOI: 10.1016/j.vetimm.2011.08.015
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Immunogenicity of a Salmonella Enteritidis mutant as vaccine candidate and its protective efficacy against salmonellosis in chickens

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Cited by 41 publications
(28 citation statements)
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“…Bacterial growth is a prerequisite for gene E lysis, because the tunnel structure is formed only in the growing regions of the cell, such as the central division zone or the pole zone (22). Strains carrying a conventional ghost cassette system are generally able to survive at 28°C (15,41), whereas the ghost strain used in the present study was grown at 37°C, which is the optimum temperature for normal growth of Salmonella (24,31). As suboptimal growth temperatures reduce the rate of bacterial multiplication, they slow the production process of BGs.…”
Section: Discussionmentioning
confidence: 99%
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“…Bacterial growth is a prerequisite for gene E lysis, because the tunnel structure is formed only in the growing regions of the cell, such as the central division zone or the pole zone (22). Strains carrying a conventional ghost cassette system are generally able to survive at 28°C (15,41), whereas the ghost strain used in the present study was grown at 37°C, which is the optimum temperature for normal growth of Salmonella (24,31). As suboptimal growth temperatures reduce the rate of bacterial multiplication, they slow the production process of BGs.…”
Section: Discussionmentioning
confidence: 99%
“…A gross lesion score of 0, 1, 2, or 3 was given based on the number of necrotic foci on the organ and the extent of organ enlargement. A score of 0 indicated no lesion, a score of 1 was assigned to necrotic foci, a score of 2 indicated enlarged and necrotic organs, and a score of 3 was associated with more debilitated, necrotic, and distorted organs (31). Aseptically collected tissue samples were homogenized and preenriched in 3 ml buffered peptone water (BPW) (Becton Dickinson and Company), and 100 l of homogenates was plated on brilliant green agar (BGA) (Becton Dickinson and Company) for determination of the bacterial count on direct culture.…”
Section: Methodsmentioning
confidence: 99%
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“…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. The titers of anti-OMP plasma IgG and intestinal sIgA antibodies were determined by using a chicken IgG and IgA ELISA quantitation kit (Bethyl Laboratories, Montgomery, TX, USA), as previously described (21). To determine LTB-specific plasma IgG titers, purified LTB was used as the coating antigen.…”
Section: Methodsmentioning
confidence: 99%
“…The OMP mixture was extracted from JOL401, as described previously (Kang et al 2002). The indirect enzyme linked immunosorbent assay (ELISA) was carried out for detection of S. Typhimurium OMP-specific IgG and sIgA using a chicken IgG and IgA ELISA quantitation kit (Bethyl Laboratories, Montgomery, TX, USA), as previously described (Nandre et al 2011). The wells of a Microlon Ò ELISA plate were coated with 100 mL OMP at a concentration of 0.2 mg/mL.…”
Section: Sample Collection and Antibody Response Of Vaccinated Chickensmentioning
confidence: 99%