|Genovese, Kenneth - Ken|
Submitted to: Current Microbiology
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: 8/24/2012
Publication Date: 12/31/2012
Citation: Nisbet, D.J., Edrington, T.S., Farrow, R.L., Genovese, K.J., Callaway, T.R., Anderson, R.C., Krueger, N.A. 2012. Lack of effect of feeding lactoferrin on intestinal populations and fecal shedding of Salmonella typhimurium in experimentally infected weaned pigs. Current Microbiology. 2(4):280-290.
Interpretive Summary: Pigs are naturally infected with Salmonella, a bacterium that causes food sickness in humans. Lactoferrin is a compound that may be beneficial in reducing the populations of Salmonella in young pigs. We investigated the ability of lactoferrin to reduce Salmonella in experimentally infected pigs in two experiments. Results showed that feeding lactoferrin was not effective in reducing the prevalence of Salmonella in the feces or in reducing the populations within various segments of the digestive tract. These findings do not support the use of lactoferrin as a tool to reduce Salmonella in young pigs under the experimental conditions tested.
Technical Abstract: Two experiments were conducted to evaluate the effect of the iron-binding molecule lactoferrin on reducing gut populations and fecal shedding of Salmonella typhimurium in experimentally infected weaned pigs. For each experiment, crossbred barrows and gilts were purchased locally and transported to our laboratory facilities. All pigs were fed a ground starter diet available for ad libitum consumption and randomly assigned to pen (2 pigs/pen) and treatment (10 pigs/treatment; 5 pens/treatment): Control [1.25 g whey protein concentrate (WPC)/kg BW/d]; 1X lactoferrin [0.25 g lactoferrin (LF) + 1.0 g WPC/kg BW/d]; and 5X LF (1.25 g LF/kg BW/d). Experimental treatments were fed prior to inoculation via oral gavage with Salmonella typhimurium. Rectal swabs were collected daily for 4 days for quantification of the challenge Salmonella strain and scour and activity scores, and body temperatures were recorded daily following inoculation. Five days post-challenge, pigs were euthanized and tissue and luminal content samples were aseptically collected from the stomach, ileum, cecum, spiral colon, and rectum. Additional tissue samples were collected from the ileo-cecal lymph nodes, spleen, tonsil, and liver. Quantitative and qualitative bacterial culture was conducted for the challenge strain of Salmonella. No treatment differences (P > 0.10) were observed for daily fecal shedding or luminal concentrations of Salmonella in either experiment. The percentage of tissue samples Salmonella positive was not significantly different among treatments with the exception of liver tissue in Experiment I, which was lower (P < 0.05) in the 1X and 5X treatments compared to control pigs. Body weights and BW change were not affected (P > 0.10) by treatment. Following inoculation, body temperatures, scour, and activity scores were not different when examined by day or when data was combined across days. The lack of treatment effect in this experiment may be explained by the high challenge dose utilized in these experiments that may have overwhelmed any protective effect exerted by the lactoferrin. Future research should evaluate increasing the duration of feeding and/or the levels of lactoferrin fed in conjunction with a more subtle Salmonella challenge.