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Original Articles

The feathering gene is linked to degranulation and oxidative burst not cytokine/chemokine mRNA expression levels or Salmonella enteritidis organ invasion in broilers

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Pages 465-470 | Received 20 Jun 2006, Published online: 24 Jul 2007

Figures & data

Figure 1. Degranulation of heterophils isolated from 2-day-old chickens was compared to determine their ability to release toxic granules when stimulated with opsonized S. enteritidis. Data are pooled and presented as the mean±standard error of the mean of the µM β-d glucuronidase released from triplicate assays from three separate experiments (n = 450 chickens). All statistical differences are for comparisons between females (FF vs SF) or between males (FM vs SM) (*P < 0.05).

Figure 1.  Degranulation of heterophils isolated from 2-day-old chickens was compared to determine their ability to release toxic granules when stimulated with opsonized S. enteritidis. Data are pooled and presented as the mean±standard error of the mean of the µM β-d glucuronidase released from triplicate assays from three separate experiments (n = 450 chickens). All statistical differences are for comparisons between females (FF vs SF) or between males (FM vs SM) (*P < 0.05).

Figure 2. Heterophils isolated from FF, SF, FM, and SM 2-day-old chickens were compared to determine their ability to generate an oxidative burst response following stimulation with the inflammatory agonist phorbol A-myristate 13-acetate. Data are pooled and presented as the mean±standard error of the mean of the RFU of triplicate assays from three separate experiments (n = 450 chickens). All statistical differences are for comparisons between females (FF vs SF) or between males (FM vs SM) (*P < 0.05).

Figure 2.  Heterophils isolated from FF, SF, FM, and SM 2-day-old chickens were compared to determine their ability to generate an oxidative burst response following stimulation with the inflammatory agonist phorbol A-myristate 13-acetate. Data are pooled and presented as the mean±standard error of the mean of the RFU of triplicate assays from three separate experiments (n = 450 chickens). All statistical differences are for comparisons between females (FF vs SF) or between males (FM vs SM) (*P < 0.05).

Table 1.  Control, S. enteritidis-treated, and fold change of IL-6, CXCLi2, and IFN-α mRNA expression levels in heterophils isolated from F1 cross C and D chickens separated by sexa

Figure 3. Two-day-old chickens were challenged orally with S. enteritidis (5×106 CFU/chicken) and liver/spleen organ invasion was determined using standard microbiological techniques. Data are pooled from 90 chickens and presented as the mean±standard error of the mean of triplicate organ invasion experiments. Data shown are the percentages obtained from the number of S. enteritidis-positive chickens/90. All comparisons are between females (FF vs SF) or between males (FM vs SM) (*P < 0.05).

Figure 3.  Two-day-old chickens were challenged orally with S. enteritidis (5×106 CFU/chicken) and liver/spleen organ invasion was determined using standard microbiological techniques. Data are pooled from 90 chickens and presented as the mean±standard error of the mean of triplicate organ invasion experiments. Data shown are the percentages obtained from the number of S. enteritidis-positive chickens/90. All comparisons are between females (FF vs SF) or between males (FM vs SM) (*P < 0.05).

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