ORIGINAL PAPER
Effect of lactic acid bacterial probiotic
on piglet performance and serum biochemical parameters
in Xiangcun Black lactating sows
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1
Hengyang Normal University, College of Life Sciences, College of Nanyue, Hunan Provincial Key Laboratory of Biological
Resources Protection and Utilization in NanYue Mountain Area, Hengyang, Hunan, 421008, China
2
Hunan Vocational Technical College of Environment and Biology, College of Bioengineering, Hengyang, Hunan, 421005, China
3
Hunan Xiangjia Animal Husbandry Co., Ltd, Changde, Hunan, 415300, China
4
Xiangcun High-Technology Agricultural Co. Ltd, Loudi, Hunan, 417000, China
These authors had equal contribution to this work
Publication date: 2025-01-16
Corresponding author
C. Yang
Hengyang Normal University, College of Life Sciences, College of Nanyue, Hunan Provincial Key Laboratory of Biological
Resources Protection and Utilization in NanYue Mountain Area, Hengyang, Hunan, 421008, China
J. Anim. Feed Sci. 2025;34(1):61-70
KEYWORDS
TOPICS
ABSTRACT
The present study was conducted to evaluate the effect of lactic
acid bacterial probiotic (LABP) supplementation on piglet performance and
serum biochemical parameter. Gestating Xiangcun Black sows (n = 50, day 7
ante partum) were randomly divided into 5 groups: C, L50, L100, L200, L300.
These groups were administered daily 0, 50, 100, 200, and 300 ml of LABP
(live Lactobacillus plantarum CCFM8610 ≥ 1 × 109 CFU/ml), respectively.
The results showed that litter weight at weaning (P < 0.01) increased linearly
with raising dietary LABP levels. Sows that received LABP from day 107 of
gestation (G107) until weaning (L21) had the highest piglet survival rate over
the three week period compared to the control group (P < 0.05). Serum alkaline
phosphatase (P < 0.01) activity and total cholesterol (P < 0.05) level decreased
but triglyceride concentration increased linearly with the increasing dietary
LABP levels. Furthermore, serum sarcosine and carnosine concentrations were
significantly higher in the L200 group compared to the C, L100, and L300 groups
(P < 0.05). Sows in the L50 group had the highest serum levels of leucine, lysine,
valine, and arginine compared to the other groups (P < 0.05). In conclusion,
our findings demonstrated that increasing dietary LABP levels in Xiangcun
Black sows enhanced litter weight at weaning and reduced piglet mortality by
influencing lipid and amino acid metabolism.
FUNDING
This research was supported by key projects of the Hunan provincial department of education (22A0504); the key research and development programme of the Hunan science and technology department (2022WK2020); the research foundation for education of Hunan province (21C1122); general project of the Hunan Science and Technology Department (2021JJ30061).
CONFLICT OF INTEREST
The Authors declare that there is no conflict of interest.
REFERENCES (29)
1.
Ajouz H., Mukherji D., Shamseddine A., 2014. Secondary bile acids: an underrecognized cause of colon cancer. World J. Surg. Oncol. 12, 164,
https://doi.org/10.1186/1477-7....
2.
Alakomi H.L., Skyttä E., Saarela M., Mattila-Sandholm T., Latva-Kala K., Helander I.M., 2000. Lactic acid permeabilizes gram-negative bacteria by disrupting the outer membrane. Appl. Environ. Microbiol. 66, 2001–2005,
https://doi.org/10.1128/AEM.66....
3.
Andersson E., Frossling J., Westin R., Algers B., Gunnarsson S., 2020. Associations between litter size and medical treatment of sows during farrowing and lactation. Acta Agr. Scand. - A Anim. Sci. 69, 176–182,
https://doi.org/10.1080/090647....
4.
Hamaya R., Mora S., Lawler P.R., Cook N.R., Ridker P.M., Buring J.E., Lee I.M., Manson J.E., Tobias D.K., 2021. Association of plasma branched-chain amino acid with biomarkers of inflammation and lipid metabolism in women. Circ. Genom. Precis. Med. 14, e003330,
https://doi.org/10.1161/CIRCGE....
5.
Hattab J., Marruchella G., Pallavicini A., Gionechetti F., Mosca F., Trachtman A.R., Lanci L., Gabrielli L., Tiscar P.G., 2021. Insights into the oral bacterial microbiota of sows. Microorganisms 9, 2314,
https://doi.org/10.3390/microo....
6.
Hruby Weston A., Teixeira I., Yoder P.S., Pilonero T., and Hanigan M.D., 2024. Valine and nonessential amino acids affect bidirectional transport rates of leucine and isoleucine in bovine mammary epithelial cells. J. Dairy Sci. 107, 2026–2046,
https://doi.org/10.3168/jds.20....
7.
Huang X., Gao J., Zhao Y. et al., 2019. Dramatic remodeling of the gut microbiome around parturition and its relationship with host serum metabolic changes in sows. Front. Microbiol. 10, 2123,
https://doi.org/10.3389/fmicb.....
8.
Lan R., Kim I., 2020. Enterococcus faecium supplementation in sows during gestation and lactation improves the performance of sucking piglets. Vet. Med. Sci. 6, 92–99,
https://doi.org/10.1002/vms3.2....
10.
Martín R., Delgado S., Maldonado A., Jiménez E., Olivares M., Fernández L., Sobrino O.J., Rodríguez J.M., 2009. Isolation of lactobacilli from sow milk and evaluation of their probiotic potential. J. Dairy Res. 76, 418–425,
https://doi.org/10.1017/S00220....
11.
O’Shea E.F., Cotter P.D., Stanton C., Ross R.P., Hill C., 2012. Production of bioactive substances by intestinal bacteria as a basis for explaining probiotic mechanisms: bacteriocins and conjugated linoleic acid. Int. J. Food Microbiol. 152, 189–205,
https://doi.org/10.1016/j.ijfo....
12.
Oh J.K., Kim Y.R., Lee B., Choi Y.M., Kim S.H., 2021. Prevention of cholesterol gallstone formation by Lactobacillus acidophilus ATCC 43121 and Lactobacillus fermentum MF27 in lithogenic diet-induced mice. Food Sci. Anim. Resour. 41, 343–352,
https://doi.org/10.5851/kosfa.....
13.
Pajarillo E.A.B., Chae J.P., Balolong M.P., Kim H.B., Seo K.S., Kang D.K., 2014. Pyrosequencing-based analysis of fecal microbial communities in three purebred pig lines. J. Microbiol. 52, 646–651,
https://doi.org/10.1007/s12275....
14.
Patil Y., Gooneratne R., Ju X.H., 2020. Interactions between host and gut microbiota in domestic pigs: a review. Gut Microbes 11, 310–334,
https://doi.org/10.1080/194909....
15.
Perez P.F., Doré J., Leclerc M., Levenez F., Benyacoub J., Serrant P., Segura-Roggero I., Schiffrin E.J., Donnet-Hughes A., 2007. Bacterial imprinting of the neonatal immune system: lessons from maternal cells? Pediatrics 119, e724–e732,
https://doi.org/10.1542/peds.2....
16.
Reverter M., Lundh T., Gonda H.L., Lindberg J.E., 2000. Portal net appearance of amino acids in growing pigs fed a barley-based diet with inclusion of three different forage meals. Brit. J. Nutr. 84, 483–494,
https://doi.org/10.1017/S00071....
17.
Shimomura Y., Obayashi M., Murakami T., Harris R.A., 2001. Regulation of branched-chain amino acid catabolism: nutritional and hormonal regulation of activity and expression of the branched-chain alpha-keto acid dehydrogenase kinase. Curr. Opin. Clin. Nutr. Metab. Care 4, 419–423,
https://doi.org/10.1097/000751....
18.
Štšepetova J., Rätsep M., Gerulis O., Jõesaar A., Mikelsaar M., Songisepp E., 2023. Impact of Lactiplantibacillus plantarum inducia on metabolic and antioxidative response in cholesterol and BMI variable indices: randomised, double-blind, placebo-controlled trials. Beneficial microbes. 14, 1–15,
https://doi.org/10.3920/BM2022....
19.
Trottier N.L., Guan X., Ku P.K., Bequette B.J., Calder G., Ames K.N., 2002. Amino acid availability affects amino acid flux and protein metabolism in the porcine mammary gland. J. Nutr. 132, 1224–1234,
https://doi.org/10.1093/jn/132....
20.
Wang C., Wei S., Liu B., Wang F., Lu Z., Jin M., Wang Y., 2022a. Maternal consumption of a fermented diet protects offspring against intestinal inflammation by regulating the gut microbiota. Gut Microbes 14, 2057779,
https://doi.org/10.1080/194909....
21.
Wang C., Wei S., Xu B., Hao L., Su W., Jin M., Wang Y., 2021a. Bacillus subtilis and Enterococcus faecium co-fermented feed regulates lactating sow’s performance, immune status and gut microbiota. Microb. Biotechnol. 14, 614–627,
https://doi.org/10.1111/1751-7....
22.
Wang J., Ji H.F., Hou C.L., Wang S.X., Zhang D.Y., Liu H., Shan D.C., Wang Y.M., 2014. Effects of lactobacillus johnsonii XS4 supplementation on reproductive performance, gut environment, and blood biochemical and immunological index in lactating sows. Livest. Sci. 164, 96-101,
https://doi.org/10.1016/j.livs....
23.
Wang W., Ma H., Zhu Y., Ni K., Qin G., Tan Z., Wang Y., Wang L., Pang H., 2021b. Screening of lactic acid bacteria with inhibitory activity against ETEC K88 as feed additive and the effects on sows and piglets. Animals 11, 1719,
https://doi.org/10.3390/ani110....
24.
Wang X., Lu H., Li Q., Zhou Y., Zhou J., 2022b. Comparative genome and transcriptome of Rhodococcus pyridinivorans GF3 for analyzing the detoxification mechanism of anthraquinone compounds. Ecotoxicol. Environ. Saf. 237, 113545,
https://doi.org/10.1016/j.ecoe....
25.
Yang H., Xiao Y., Wang J., Xiang Y., Gong Y., Wen X., Li D., 2018. Core gut microbiota in Jinhua pigs and its correlation with strain, farm and weaning age. J. Microbiol. 56, 346–355,
https://doi.org/10.1007/s12275....
26.
Zhang C., Wang G., Zheng Z., Maddipati K.R., Zhang X., Dyson G., Williams P., Duncan S.A., Kaufman R.J., Zhang K., 2012. Endoplasmic reticulum-tethered transcription factor cAMP responsive element-binding protein, hepatocyte specific, regulates hepatic lipogenesis, fatty acid oxidation, and lipolysis upon metabolic stress in mice. Hepatology 55, 1070–1082,
https://doi.org/10.1002/hep.24....
27.
Zhang J., Liu M., Ke S., Huang X., Fang S., He M., Fu H., Chen C., Huang L., 2021. Gut and vagina microbiota associated with estrus return of weaning sows and its correlation with the changes in serum metabolites. Front. Microbiol. 12, 690091,
https://doi.org/10.3389/fmicb.....
28.
Zheng D., Wang X., Ju N. et al., 2021. Immune responses in pregnant sows induced by recombinant Lactobacillus johnsonii expressing the COE protein of porcine epidemic diarrhea virus provide protection for piglets against PEDV infection. Viruses 14, 7,
https://doi.org/10.3390/v14010....
29.
Zhou H., Chen Y., Zhuo Y. et al., 2017. Effects of 25-hydroxycholecalciferol supplementation in maternal diets on milk quality and serum bone status markers of sows and bone quality of piglets. Anim. Sci. J. 88, 476–483,
https://doi.org/10.1111/asj.12....