Acknowledgement
This study was supported by 2023 the RDA Fellowship Program of the National Institute of Animal Science, Rural Development Administration, Korea.
References
- Bikker P, Dirkzwager A, Fledderus J, Trevisi P, Le Huerou-Luron I, Lallès JP, et al. The effect of dietary protein and fermentable carbohydrates levels on growth performance and intestinal characteristics in newly weaned piglets. J Anim Sci. 2006;84:3337-45. https://doi.org/10.2527/jas.2006-076
- Koh A, De Vadder F, Kovatcheva-Datchary P, Backhed F. From dietary fiber to host physiology: short-chain fatty acids as key bacterial metabolites. Cell. 2016;165:1332-45. https://doi.org/10.1016/j.cell.2016.05.041
- Burrough ER, Arruda BL, Patience JF, Plummer PJ. Alterations in the colonic microbiota of pigs associated with feeding distillers dried grains with solubles. PLOS ONE. 2015;10:e0141337. https://doi.org/10.1371/journal.pone.0141337
- Cao KF, Zhang HH, Han HH, Song Y, Bai XL, Sun H. Effect of dietary protein sources on the small intestine microbiome of weaned piglets based on high-throughput sequencing. Lett Appl Microbiol. 2016;62:392-8. https://doi.org/10.1111/lam.12559
- Yoon SA, Kang SI, Shin HS, Ko HC, Kim SJ. Anti-diabetic potential of a Sasa quelpaertensis Nakai extract in L6 skeletal muscle cells. Food Sci Biotechnol. 2014;23:1335-9. https://doi.org/10.1007/s10068-014-0183-4
- Kim SJ, Hwang JH, Shin HS, Jang MG, Ko HC, Kang SI. Antioxidant and anti-inflammatory activities of Sasa quelpaertensis leaf extracts. In: Venketeshwer Rao, editor. Phytochemicals as nutraceuticals - global approaches to their role in nutrition and health. Rijeka: IntechOpen; 2012.
- Kang H, Lee C. Sasa quelpaertensis Nakai extract suppresses porcine reproductive and respiratory syndrome virus replication and modulates virus-induced cytokine production. Arch Virol. 2015;160:1977-88. https://doi.org/10.1007/s00705-015-2469-0
- Lee S, Baek YC, Lee M, Jeon S, Bang HT, Seo S. Evaluating feed value of native Jeju bamboo (Sasa quelpaertensis Nakai) for beef cattle. Anim Biosci. 2023;36:238-47. https://doi.org/10.5713/ab.22.0160
- Yoon SH, Ha SM, Kwon S, Lim J, Kim Y, Seo H, et al. Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies. Int J Syst Evol Microbiol. 2017;67:1613-7. https://doi.org/10.1099/ijsem.0.001755
- Segata N, Izard J, Waldron L, Gevers D, Miropolsky L, Garrett WS, et al. Metagenomic biomarker discovery and explanation. Genome Biol. 2011;12:R60. https://doi.org/10.1186/gb2011-12-6-r60
- Turnbaugh PJ, Hamady M, Yatsunenko T, Cantarel BL, Duncan A, Ley RE, et al. A core gut microbiome in obese and lean twins. Nature. 2009;457:480-4. https://doi.org/10.1038/nature07540
- Guo X, Xia X, Tang R, Wang K. Real-time PCR quantification of the predominant bacterial divisions in the distal gut of Meishan and Landrace pigs. Anaerobe. 2008;14:224-8. https://doi.org/10.1016/j.anaerobe.2008.04.001
- Hampson DJ, Ahmed N. Spirochaetes as intestinal pathogens: lessons from a Brachyspira genome. Gut Pathog. 2009;1:10. https://doi.org/10.1186/1757-4749-1-10
- Kim KM, Kim YS, Lim JY, Min SJ, Ko HC, Kim SJ, et al. Intestinal anti-inflammatory activity of Sasa quelpaertensis leaf extract by suppressing lipopolysaccharide-stimulated inflammatory mediators in intestinal epithelial Caco-2 cells co-cultured with RAW 264.7 macrophage cells. Nutr Res Pract. 2015;9:3-10. https://doi.org/10.4162/nrp.2015.9.1.3
- Ko YS, Tark D, Moon SH, Kim DM, Lee TG, Bae DY, et al. Alteration of the gut microbiota in pigs infected with African swine fever virus. Vet Sci. 2023;10:360. https://doi.org/10.3390/vetsci10050360
- Binda C, Lopetuso LR, Rizzatti G, Gibiino G, Cennamo V, Gasbarrini A. Actinobacteria: a relevant minority for the maintenance of gut homeostasis. Dig Liver Dis. 2018;50:421-8. https://doi.org/10.1016/j.dld.2018.02.012
- Yang F, Hou C, Zeng X, Qiao S. The use of lactic acid bacteria as a probiotic in swine diets. Pathogens. 2015;4:34-45. https://doi.org/10.3390/pathogens4010034
- Cao Y, Wang F, Wang H, Wu S, Bao W. Exploring a possible link between the fecal microbiota and the production performance of pigs. Vet Sci. 2022;9:527. https://doi.org/10.3390/vetsci9100527
- Song W, Song C, Li L, Wang T, Hu J, Zhu L, et al. Lactobacillus alleviated obesity induced by high-fat diet in mice. J Food Sci. 2021;86:5439-51. https://doi.org/10.1111/1750-3841.15971
- Chen C, Fang S, Wei H, He M, Fu H, Xiong X, et al. Prevotella copri increases fat accumulation in pigs fed with formula diets. Microbiome. 2021;9:175. https://doi.org/10.1186/s40168-021-01110-0
- Kang SI, Shin HS, Kim HM, Hong YS, Yoon SA, Kang SW, et al. Anti-obesity properties of a Sasa quelpaertensis extract in high-fat diet-induced obese mice. Biosci Biotechnol Biochem. 2012;76:755-61. https://doi.org/10.1271/bbb.110868
- Park JY, Jang MG, Oh JM, Ko HC, Hur SP, Kim JW, et al. Sasa quelpaertensis leaf extract ameliorates dyslipidemia, insulin resistance, and hepatic lipid accumulation in high-fructose-diet-fed rats. Nutrients. 2020;12:3762. https://doi.org/10.3390/nu12123762