Impact of in-feed sodium butyrate or sodium heptanoate protected with medium-chain fatty acids on gut health in weaned piglets challenged with Escherichia coli F4+

2020 ◽  
Vol 74 (4) ◽  
pp. 271-295
Author(s):  
Paola López-Colom ◽  
Lorena Castillejos ◽  
Agustina Rodríguez-Sorrento ◽  
Mónica Puyalto ◽  
Juan José Mallo ◽  
...  
2020 ◽  
Author(s):  
Roger A. Cochrane ◽  
Raghavendra G. Amachawadi ◽  
Sarah E. Remfry ◽  
Annie B. Lerner ◽  
Tiruvoor G. Nagaraja ◽  
...  

Abstract Research has demonstrated that medium chain fatty acids (MCFA) can serve as reduction strategies for bacterial and viral pathogens in animal feed and ingredients. However, it is unknown how the type or level of MCFA impact bacteria growth. This can be tested through a minimum inhibitory concentration (MIC) benchtop assay, which identifies the lowest concentration of a chemical that prevents visible growth of a bacterium. The objective of this study was to 1) determine the MCFA MIC of C6:0, C8:0, C10:0, and C12:0 for generic Escherichia coli, Enterotoxigenic Escherichia coli, Salmonella Typhimurium, Campylobacter coli, and Clostridium perfringens; 2) determine the MIC of commercial based MCFA products against the same bacteria; and 3) determine the effect of 2 commercial based MCFA products on the quantification of Enterotoxigenic Escherichia coli. For Exp. 1 and 2, MIC were determined by modified microbroth dilution method using a 96 well microtiter plate with a concentration of 105 CFU/mL for each bacterial strain. For Exp. 3, the two products selected for quantification were mixed with a complete swine diet and inoculated with two concentrations (106 or 102 CFU/g of feed) of a NalR strain of Enterotoxigenic Escherichia coli (ETEC) for bacterial enumeration. From Exp. 1, the MIC of MCFA varied among bacteria species. The lowest MIC of the MCFA was 0.43% of a 1:1:1 blend of C6:0, C8:0, and C10:0 for Campylobacter coli, 0.25% C12:0 for Clostridium perfringens, 0.60% 1:1:1 blend for generic Escherichia coli, 0.53% C6:0 for ETEC, and 0.40% C6:0 for Salmonella Typhimurium. In Exp. 2, products containing high concentrations of C6:0 or C8:0 had lower MIC in gram negative bacteria. In Exp. 3, feed containing either of the commercial based MCFA products reduced (linear, P < 0.05) quantifiable ETEC. Overall, the inhibitory efficacy of MCFA varies among bacteria species. This suggests that MCFA mixtures may provide a wider spectrum of bacterial control. As commercial products containing MCFA become available for livestock, it is important to consider the interaction between MCFA chain length and concentration on the potential to effectively mitigate various feed-based bacteria.


2019 ◽  
Vol 97 (Supplement_3) ◽  
pp. 325-326
Author(s):  
Junmin Zhang ◽  
Chaohua Tang ◽  
Yunsheng Han

Abstract This study was conducted to determine the effects of organic and medium chain fatty acids (OMCFA) as antibiotic substitutes on growth performance, immune function, intestinal morphology, and ileum microbiota of weaned piglets challenged with Escherichia coli K88. Over 28 days, 150 weaned piglets (28-day old, 8.80 ± 0.19 kg) were allocated to five treatments (with five replicates of six piglets each): negative basal diet (NBD), positive basal diet (PBD), antibiotic growth promoters diet (AGPD, BD+0.04 g/kg zinc bacitracin, 0.03 g/kg chlortetracycline, and 0.05 g/kg kitasamycin), OMCFA 1 diet (BD+0.2% OMCFA, OMCFA is a synergistic blend of a phenolic compound, slow release C12, target release butyrates, formic, acetic, lactic, propionic, citric, sorbic acid), and OMCFA 2 diet (Day 1 to 14: BD+0.8% OMCFA, Day 15 to 28: BD+0.6% OMCFA). On the 15th day, piglets in the PBD, AGPD, OMCFA 1, and OMCFA 2 treatment groups were orally challenged with 20 mL Escherichia coli K88 (108 CFU/mL). Body weight on day 14 and average daily gain from 1st to 14th day of the subjects in the AGPD and OMCFA 1 groups were higher than those in the NBD and PBD groups (P &lt; 0.05). Diarrhea rate after challenge was lower in the AGPD group than PBD one, and there was no significant difference between the AGPD and OMCFA 1 group. OMCFA decreased total leukocytes and the percentage of neutrophils (P &lt; 0.05), increased the percentage of lymphocytes (P &lt; 0.05), on day 14, and increased villus height and villus height/crypt depth ratio in the duodenum, jejunum, and ileum, compared with PBD group. 16S rDNA sequencing showed that OMCFA might stabilize the ileum microbiota caused by E. coli K88 challenge. These results indicated that OMCFA could be used as potential alternatives to AGPs in weaned piglets.


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