Consumption of Lamb Meat or Basa Fish Shapes the Gut Microbiota and Aggravates Pulmonary Inflammation in Asthmatic Mice

References

• World Health Organization. The global asthma report. Available from: http://www.globalasthmareport.org. Accessed 923, 2020.
   Google Scholar
• Bateman ED, Hurd SS, Barnes PJ, et al. Global strategy for asthma management and prevention: GINA executive summary. Eur Respir J. 2008;31(1):143–178. doi:10.1183/09031936.0013870718166595
   PubMed Web of Science ®Google Scholar
• Willett W. Diet and health: what should we eat. Science. 1994;264(5158):532–537. doi:10.1126/science.81600118160011
   PubMed Web of Science ®Google Scholar
• Guilleminault L, Williams EJ, Scott HA, Berthon BS, Jensen M, Wood LG. Diet and asthma: is it time to adapt our message. Nutrients. 2017;9(11):1227. doi:10.3390/nu9111227
   Web of Science ®Google Scholar
• Deversux G, Seaton A. Diet as a risk factor for atopy and asthma. J Allergy Clin Immunol. 2005;115(6):1109–1117. doi:10.1016/j.jaci.2004.12.113915940119
   PubMed Web of Science ®Google Scholar
• Huang D. A literature study on “stimulating foods” in Chinese medicine dietary taboos. [dissertation]. China: Beijing University of Chinese Medicine; 2009.
   Google Scholar
• Zhu F, Xie G. Discussion on Chinese medicine diet taboo-fawu. Chin J Tradit Chin Med Pharm. 2018;7.
   Google Scholar
• Hill CS DJ, Hosking FM, De Benedictis AP, et al. Confirmation of the association between high levels of immunoglobulin E food sensitization and eczema in infancy: an international study. Clin Exp Allergy. 2008;8(1):61–68. doi:10.1111/j.1365-2222.2007.02861.x
   Web of Science ®Google Scholar
• Mckenzie C, Tan J, Macia L, Mackay CR. The nutrition-gut microbiome-physiology axis and allergic diseases. Immunol Rev. 2017;278(1):277–295. doi:10.1111/imr.1255628658542
   PubMed Web of Science ®Google Scholar
• Hecke TV, Vrieze JD, Boon N, Vos WHK, Vossen E, Smet SD. Combined consumption of beef-based cooked mince and sucrose stimulates oxidative stress, cardiac hypertrophy, and colonic outgrowth of desulfovibrionaceae in rats. Mol Nutr Food Res. 2019;63(2):e1800962. doi:10.1002/mnfr.20180096230379400
   PubMed Web of Science ®Google Scholar
• Ge Y, Lin S, Li B, et al. Oxidized pork induces oxidative stress and inflammation by altering gut microbiota in mice. Mol Nutr Food Res. 2020;64(2):e1901012. doi:10.1002/mnfr.20190101231845486
   PubMed Web of Science ®Google Scholar
• Li N, Wu X, Zhuang W, et al. Fish consumption and multiple health outcomes: umbrella review. Trends Food Sci Technol. 2020;99:273–283. doi:10.1016/j.tifs.2020.02.033
   Web of Science ®Google Scholar
• Earl CS, An S, Ryan RP. The changing face of asthma and its relation with microbes. Trends Microbiol. 2015;23(7):408–418. doi:10.1016/j.tim.2015.03.00525840766
   PubMed Web of Science ®Google Scholar
• Abrahamsson TR, Jakobsson HE, Andersson AF, Björkstén B, Engstrand L, Jenmalm MC. Low gut microbiota diversity in early infancy precedes asthma at school age. Clin Exp Allergy. 2014;44(6):842–850. doi:10.1111/cea.1225324330256
   PubMed Web of Science ®Google Scholar
• Russell SL, Gold MJ, Willing BP, Thorson L, McNagny KM, Finlay BB. Perinatal antibiotic treatment affects murine microbiota, immune responses and allergic asthma. Gut Microbes. 2013;4(2):158–164. doi:10.4161/gmic.2356723333861
   PubMed Web of Science ®Google Scholar
• Akay HK, Bahar Tokman H, Hatipoglu N, et al. The relationship between Bifidobacteria and allergic asthma and/or allergic dermatitis: A prospective study of 0–3 years-old children in Turkey. Anaerobe. 2014;28:98–103. doi:10.1016/j.anaerobe.2014.05.00624878320
   PubMed Web of Science ®Google Scholar
• Wang W, Luo X, Zhang Q, He X, Zhang Z, Wang X. Bifidobacterium infantis relieves allergic asthma in mice by regulating Th1/Th2. Med Sci Monit. 2020;26:e920583-1–e920583-11. doi:10.12659/MSM.920583
   Web of Science ®Google Scholar
• Wu CT, Chen PJ, Lee YT, Ko JL, Lue KH. Effects of immunomodulatory supplementation with Lactobacillus rhamnosus on airway inflammation in a mouse asthma model. J Microbiol Immunol Infect. 2014;49(5):625–635. doi:10.1016/j.jmii.2014.08.00125440975
   PubMedGoogle Scholar
• Lloyd CM. Regulatory T cells in asthma. Immunity. 2009;31(3):438–449. doi:10.1016/j.immuni.2009.08.00719766086
   PubMed Web of Science ®Google Scholar
• Bettelli E, Carrier Y, Gao W, Korn T, Strom TB, Oukka M. Reciprocal developmental pathways for the generation of pathogenic effector TH 17 and regulatory T cells. Nature. 2006;441(7090):235–238. doi:10.1038/nature0475316648838
   PubMed Web of Science ®Google Scholar
• Morita H, Moro K, Koyasu S. Innate lymphoid cells in allergic and nonallergic inflammation. J Allergy Clin Immunol. 2016;138(5):1253–1264. doi:10.1016/j.jaci.2016.09.01127817797
   PubMed Web of Science ®Google Scholar
• Wolterink RGJK, Kleinjan A, Nimwegen M, Bergen I, Bruijn M, Levani Y. Pulmonary innate lymphoid cells are major producers of IL‐5 and IL‐13 in murine models of allergic asthma. Eur J Immunol. 2012;42(5):1106–1116. doi:10.1002/eji.20114201822539286
   PubMed Web of Science ®Google Scholar
• Haung Y, Guo L, Qiu J, et al. IL-25-responsive, lineage-negative KLRG1hi cells are multipotential ‘inflammatory’ type 2 innate lymphoid cells. Nature. 2015;16(2):161–169. doi:10.1038/ni.3078
   Web of Science ®Google Scholar
• Huang Y, Mao K, Chen X, et al. S1P-dependent interorgan trafficking of group 2 innate lymphoid cells supports host defense. Science. 2018;359(6371):114–119. doi:10.1126/science.aam580929302015
   PubMed Web of Science ®Google Scholar
• Mao K, Baptista AP, Tamoutounour S, et al. Innate and adaptive lymphocytes sequentially shape the gut microbiota and lipid metabolism. Nature. 2018;554(7691):255–259. doi:10.1038/nature2543729364878
   PubMed Web of Science ®Google Scholar
• Ding Y, Xu J, Bromberg JS. Regulatory T cell migration during an immune response. Trends Immunol. 2012;33(4):174–180. doi:10.1016/j.it.2012.01.00222305714
   PubMed Web of Science ®Google Scholar
• Atarashi K, Honda K. Microbiota in autoimmunity and tolerance. Curr Opin Immunol. 2011;23(6):761–768. doi:10.1016/j.coi.2011.11.00222115876
   PubMed Web of Science ®Google Scholar
• Hu Y, Li T, Chen X, Zhang H, Yu A, Wang G. Effects of stimulating food on allergic contact dermatitis in BALB/c mice. J Nanjing Univ Tradit Chin Med. 2013;6.
   Google Scholar
• Xu W, Hu M, Zhang Q, Yu J, Su W. Effects of anthraquinones from Cassia occidentalis L. on ovalbumin-induced airways inflammation in a mouse model of allergic asthma. J Ethnopharmacol. 2018;221:1–9. doi:10.1016/j.jep.2018.04.01229649507
   PubMed Web of Science ®Google Scholar
• Li Q, Li DL, Zhang X, Zhang W, Zheng M. The E3 ligase VHL promotes group 2 innate lymphoid cell maturation and function via inhibition of glycolysis and induction of interleukin 33 receptor. Immunity. 2018;48(2):258–270. doi:10.1016/j.immuni.2017.12.01329452935
   PubMed Web of Science ®Google Scholar
• Andrianasolo RM, Hercberg S, Touvier M, et al. Association between processed meat intake and asthma symptoms in the french nutrinet-santé cohort. Eur J Nutr. 2020;59(4):1153–1162. doi:10.1007/s00394-019-02011-7
   Web of Science ®Google Scholar
• Takemura Y, Sakurai Y, Honjo S, et al. The relationship between fish intake and the prevalence of asthma: the Tokorozawa childhood asthma and pollinosis study. Prev Med. 2002;34(2):221–225. doi:10.1006/pmed.2001.097811817918
   PubMed Web of Science ®Google Scholar
• US department of agriculture. FoodData central. Available from: https://fdc.nal.usda.gov/. Accessed 923, 2020.
   Google Scholar
• Antonio Ortenzi PP, Vincenzetti S, Beghelli D. Dietary properties of lamb meat and human health. Mediterr J Nutr Metab. 2011;4(1):53–56. doi:10.1007/s12349-010-0032-9
   Google Scholar
• Nagel G, Linseisen J. Dietary intake of fatty acids, antioxidants and selected food groups and asthma in adults. Eur J Nutr. 2005;59(1):8–15. doi:10.1038/sj.ejcn.1602025
   Web of Science ®Google Scholar
• Kim EK, Ju SY. Asthma and dietary intake of fish, seaweeds, and fatty acids in korean adults. Nutrients. 2019;11(9):2187. doi:10.3390/nu11092187
   Web of Science ®Google Scholar
• Broadfield EC, McKeever TM, Whitehurst A, et al. A case–control study of dietary and erythrocyte membrane fatty acids in asthma. Clin Exp Allergy. 2004;34(8):1232–1236. doi:10.1111/j.1365-2222.2004.02032.x15298563
   PubMed Web of Science ®Google Scholar
• Cani PD, Amar J, Iglesias MA, et al. Metabolic endotoxemia initiates obesity and insulin resistance. Diabetes. 2007;56(7):1761–1772. doi:10.2337/db06-149117456850
   PubMed Web of Science ®Google Scholar
• Fritsche KL. The science of fatty acids and inflammation. Adv Nutr. 2015;6(3):293S301S. doi:10.3945/an.114.006940
   Web of Science ®Google Scholar
• Mueller K, Ash C, Pennisi E, Smith O. The gut microbiota. Science. 2012;336(6086):1245. doi:10.1126/science.336.6086.124522674336
   PubMed Web of Science ®Google Scholar
• Legatzki A, Rösler B, Mutius EV. Microbiome diversity and asthma and allergy risk. Curr Allergy Asthma Rep. 2014;14(10):466. doi:10.1007/s11882-014-0466-025149168
   PubMed Web of Science ®Google Scholar
• Gerner RR, Moschen AR, Wang J, et al. Lipocalin2 deficiency results in colitis exacerbation and tumor development in IL-10 mice by Alistipes overgrowth. Z Gastroenterol. 2016;54(05). doi:10.1055/s-0036-1583976
   Google Scholar
• Yan F, Li N, Shi J, et al. Lactobacillus acidophilus alleviates type 2 diabetes by regulating hepatic glucose and lipid metabolism and gut microbiota in mice. Food Funct. 2019;10(9):5804–5815. doi:10.1039/c9fo01062a31461095
   PubMed Web of Science ®Google Scholar
• Biddle A, Stewart LC, Susan Leschine JB. Untangling the genetic basis of fibrolytic specialization by lachnospiraceae and ruminococcaceae in diverse gut communities. Diversity. 2013;5(3):627–640. doi:10.3390/d5030627
   Google Scholar
• Zhang J, Song L, Wang Y, et al. Beneficial effect of butyrate-producing Lachnospiraceae on stress-induced visceral hypersensitivity in rats. J Gastroenterol Hepatol. 2019;34(8):1368–1376. doi:10.1111/jgh.1453630402954
   PubMed Web of Science ®Google Scholar
• Costello ME, Ciccia F, Willner D, et al. Brief report: intestinal dysbiosis in ankylosing spondylitis. Arthritis Rheumatol. 2015;67(3):686–691. doi:10.1002/art.3896725417597
   PubMed Web of Science ®Google Scholar
• Wu G, Chen J, Hoffmann C, et al. Linking long-term dietary patterns with gut microbial enterotypes. Science. 2011;334(6052):105–108. doi:10.1126/science21885731
   PubMed Web of Science ®Google Scholar
• Bando JK, Gilfillan S, Di Luccia B, et al. ILC2s are the predominant source of intestinal ILC-derived IL-10. J Exp Med. 2020;217(2):e20191520. doi:10.1084/jem.2019152031699824
   PubMed Web of Science ®Google Scholar
• Rigas D, Lewis G, Aron JL, et al. Type 2 innate lymphoid cell suppression by regulatory T cells attenuates airway hyperreactivity and requires inducible T-cell costimulator-inducible T-cell costimulator ligand interaction. J Allergy Clin Immunol. 2017;139(5):1468–1477. doi:10.1016/j.jaci.2016.08.03427717665
   PubMed Web of Science ®Google Scholar