Enhanced biodiversity of gut flora and feed efficiency in pond cultured tilapia under reduced frequency feeding strategies
pmc-PMC7377384.pdf · Phiên bản 1 · 23 trang
47. Tengjaroenkul B, Smith BJ, Caceci T, Smith SA. Distribution of intestinal enzyme activities along the intestinal tract of cultured Nile tilapia, Oreochromis niloticus L. Aquaculture. 2000; 182: 317–327. 48. Costa J, Reis-Henriques MA, Castro LFC, Ferreira M. Gene expression analysis of ABC efflux trans- porters, CYP1A and GSTα in Nile tilapia after exposure to benzo(a)pyrene. Comp Biochem Physiol C. 2012; 155: 469–482. 49. Verri T, Kottra G, Romano A, Tiso N, Peric M, Maffia M, et al. Molecular and functional characterisation of the zebrafish (Danio rerio) PEPT1-type peptide transporter. FEBS Lett. 2003; 549: 115–122. https:// doi.org/10.1016/s0014-5793(03)00759-2 PMID: 12914936 50. Ferraris RP, Diamond J. Regulation of intestinal sugar transport. Physiol Rev. 1997; 77(1): 257–302. https://doi.org/10.1152/physrev.1997.77.1.257 PMID: 9016304 51. Mueckler M, Thorens B. The SLC2 (GLUT) family of membrane transporters. Mol Aspects Med. 2013; 34: 121–138. https://doi.org/10.1016/j.mam.2012.07.001 PMID: 23506862 52. Barone S, Fussell SL, Singh AK, Lucas F, Xu J, Kim C, et al. Slc2a5 (Glut5) is essential for the absorp- tion of fructose in the intestine and generation of fructose-induced hypertension. J Biol Chem. 2009; 284: 5056–5066. https://doi.org/10.1074/jbc.M808128200 PMID: 19091748 53. Ferraris RP. Dietary and developmental regulation of intestinal sugar transport. Biochem J. 2001; 360: 265–276. https://doi.org/10.1042/0264-6021:3600265 PMID: 11716754 54. Jiang L, David ES, Espina N, Ferraris RP. GLUT-5 expression in neonatal rats: crypt-villus location and
age-dependent regulation. Am J Physiol Gastrointest Liver Physiol. 2001; 281: G666–G674. https:// doi.org/10.1152/ajpgi.2001.281.3.G666 PMID: 11518678 55. Woting A, Pfeiffer N, Loh G, Klaus S, Blaut M. Clostridium ramosum promotes high-fat diet-induced obesity in gnotobiotic mouse models. mBio. 2014; 5: e01530–14. https://doi.org/10.1128/mBio.01530- 14 PMID: 25271283 56. Yu H, You X, Li J, Liu H, Meng Z, Xiao L, et al. Genome-wide mapping of growth-related quantitative trait loci in orange-spotted grouper (Epinephelus coioides) using double digest restriction-site associ- ated DNA sequencing (ddRADseq). Int J Mol Sci. 2016; 17: 501. https://doi.org/10.3390/ijms17040501 PMID: 27058532 57. Franchi-Gazzola R, Gaccioli F, Bevilacqua E, Visigalli R, Dall’Asta V, Sala R, et al. The synthesis of SNAT2 transporters is required for the hypertonic stimulation of system A transport activity. Biochimica et Biophysica Acta. 2004; 1667: 157–166. https://doi.org/10.1016/j.bbamem.2004.09.012 PMID: 15581851 58. Franchi-Gazzola R, Dall’Asta V, Sala R, Visigalli R, Bevilacqua E, Gaccioli F, et al. The role of the neu- tral amino acid transporter SNAT2 in cell volume regulation. Acta Physiologica. 2006; 187: 273–283. https://doi.org/10.1111/j.1748-1716.2006.01552.x PMID: 16734764 59. Gaccioli F, Huang CC, Wang C, Bevilacqua E, Franchi-Gazzola R, Gazzola GC, et al. Amino acid star- vation induces the SNAT2 neutral amino acid transporter by a mechanism that involves Eukaryotic Initi- ation Factor 2α phosphorylation and cap-independent translation. J Biol Chem. 2006; 281:17929–
17940. https://doi.org/10.1074/jbc.M600341200 PMID: 16621798 60. Nardi F, Hoffmann TM, Stretton C, Cwiklinski E, Taylor PM, Hundal HS. Proteasomal modulation of cel- lular SNAT2 (SLC38A2) Abundance and function by unsaturated fatty acid availability. J Biol Chem. 2015; 290: 8173–8184. https://doi.org/10.1074/jbc.M114.625137 PMID: 25653282 61. Schio¨ th HB, Roshanbin S, Ha¨gglund MGA, Fredriksson R. Evolutionary origin of amino acid transporter families SLC32, SLC36 and SLC38 and physiological, pathological and therapeutic aspects. Mol Aspects Med. 2013; 34: 571–585. https://doi.org/10.1016/j.mam.2012.07.012 PMID: 23506890 62. Taylor PM. Role of amino acid transporters in amino acid sensing. Am J Clin Nutr. 2014; 99: 223S– 230S. https://doi.org/10.3945/ajcn.113.070086 PMID: 24284439 63. Peng Y, Gubin J, Harper E, Vavich MG, Kemmerer AR. Food intake regulation: amino acid toxicity and changes in rat brain and plasma amino acids. J Nutr. 1973; 103(4): 608–617. https://doi.org/10.1093/jn/ 103.4.608 PMID: 4693672 64. Jumpertz R, Le DS, Turnbaugh PJ, Trinidad C, Bogardus C, Gordon JI, et al. Energy-balance studies reveal associations between gut microbes, caloric load, and nutrient absorption in humans. Am. J. Clin. Nutr. 2011; 94: 58–65. https://doi.org/10.3945/ajcn.110.010132 PMID: 21543530 65. Ley RE, Turnbaugh PJ, Klein S, Gordon JI. Microbial ecology: human gut microbes associated with obesity. Nature. 2006; 444: 1022–1023. https://doi.org/10.1038/4441022a PMID: 17183309
66. 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: 480–484. https://doi.org/10.1038/nature07540 PMID: 19043404 67. Olsen I. The Family Fusobacteriaceae. In: Rosenberg E, DeLong EF, Loy S, Stackebrandt E, Thomp- son F, editors. The Prokaryotes, Fourth Edition: Firmicutes and Tenericutes. New York, NY: Springer- Verlag New York; 2014. pp. 109–132. PLOS ONE Enhanced biodiversity of gut flora and feed efficiency in pond cultured tilapia PLOS ONE | https://doi.org/10.1371/journal.pone.0236100 July 23, 2020 22 / 23