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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Current Pharmaceutical Biotechnology</journal-id><journal-title-group><journal-title xml:lang="en">Current Pharmaceutical Biotechnology</journal-title><trans-title-group xml:lang="ru"><trans-title>Current Pharmaceutical Biotechnology</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1389-2010</issn><issn publication-format="electronic">1873-4316</issn><publisher><publisher-name xml:lang="en">Bentham Science</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">644799</article-id><article-id pub-id-type="doi">10.2174/1389201025666230915103052</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Biotechnology</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Akkermansia muciniphila - A Potential Next-generation Probiotic for Non-alcoholic Fatty Liver Disease</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Banerjee</surname><given-names>Goutam</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Papri</surname><given-names>Suraya</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Satapathy</surname><given-names>Sanjaya</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Banerjee</surname><given-names>Pratik</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff id="aff1"><institution>Department of Food Science and Human Nutrition, University of Illinois at Urbana-Champaign</institution></aff><aff id="aff2"><institution>Department of Medicine, Northwell Health Center for Liver Disease &amp; Transplantation, North Shore University Hospital/Northwell Health</institution></aff><pub-date date-type="pub" iso-8601-date="2024-02-15" publication-format="electronic"><day>15</day><month>02</month><year>2024</year></pub-date><volume>25</volume><issue>4</issue><issue-title xml:lang="ru"/><fpage>426</fpage><lpage>433</lpage><history><date date-type="received" iso-8601-date="2025-01-07"><day>07</day><month>01</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Bentham Science Publishers</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Bentham Science Publishers</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://journals.eco-vector.com/1389-2010/article/view/644799">https://journals.eco-vector.com/1389-2010/article/view/644799</self-uri><abstract xml:lang="en"><p id="idm46041443555952">Nonalcoholic fatty liver disease (NAFLD) is a spectrum of liver conditions, and its growing prevalence is a serious concern worldwide, especially in Western countries. Researchers have pointed out several genetic mutations associated with NAFLD; however, the imbalance of the gut microbial community also plays a critical role in the progression of NAFLD. Due to the lack of approved medicine, probiotics gain special attention in controlling metabolic disorders like NAFLD. Among these probiotics, Akkermansia muciniphila (a member of natural gut microflora) is considered one of the most efficient and important in maintaining gut health, energy homeostasis, and lipid metabolism. In this perspective, we discussed the probable molecular mechanism of A. muciniphila in controlling the progression of NAFLD and restoring liver health. The therapeutic potential of A. muciniphila in NAFLD has been tested primarily on animal models, and thus, more randomized human trials should be conducted to prove its efficacy.</p></abstract><kwd-group xml:lang="en"><kwd>Nonalcoholic fatty liver disease</kwd><kwd>gut microbiota</kwd><kwd>probiotics</kwd><kwd>Akkermansia muciniphila</kwd><kwd>energy homeostasis</kwd><kwd>gut health.</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Eslam, M.; Sanyal, A.J.; George, J.; Sanyal, A.; Neuschwander-Tetri, B.; Tiribelli, C. MAFLD: A consensus-driven proposed nomenclature for metabolic associated fatty liver disease. Gastroenterology, 2020, 158(7), 1999-2014. doi: 10.1053/j.gastro.2019.11.312</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Satapathy, S.K.; Banerjee, P.; Pierre, J.F.; Higgins, D.; Dutta, S.; Heda, R.; Khan, S.D.; Mupparaju, V.K.; Mas, V.; Nair, S.; Eason, J.D.; Kleiner, D.E.; Maluf, D.G. Characterization of gut microbiome in liver transplant recipients with nonalcoholic steatohepatitis. Transplant. Direct, 2020, 6(12), e625. doi: 10.1097/TXD.0000000000001033 PMID: 33204823</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Neuschwander-Tetri, B.A. Non-alcoholic fatty liver disease. BMC Med., 2017, 15(1), 45. doi: 10.1186/s12916-017-0806-8 PMID: 28241825</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Hazlehurst, J.M.; Woods, C.; Marjot, T.; Cobbold, J.F.; Tomlinson, J.W. Non-alcoholic fatty liver disease and diabetes. Metabolism, 2016, 65(8), 1096-1108. doi: 10.1016/j.metabol.2016.01.001 PMID: 26856933</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Asgharpour, A.; Cazanave, S.C.; Pacana, T.; Seneshaw, M.; Vincent, R.; Banini, B.A.; Kumar, D.P.; Daita, K.; Min, H.K.; Mirshahi, F.; Bedossa, P.; Sun, X.; Hoshida, Y.; Koduru, S.V.; Contaifer, D., Jr; Warncke, U.O.; Wijesinghe, D.S.; Sanyal, A.J. A diet-induced animal model of non-alcoholic fatty liver disease and hepatocellular cancer. J. Hepatol., 2016, 65(3), 579-588. doi: 10.1016/j.jhep.2016.05.005 PMID: 27261415</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Miele, L.; Valenza, V.; La Torre, G.; Montalto, M.; Cammarota, G.; Ricci, R.; Mascianà, R.; Forgione, A.; Gabrieli, M.L.; Perotti, G.; Vecchio, F.M.; Rapaccini, G.; Gasbarrini, G.; Day, C.P.; Grieco, A. Increased intestinal permeability and tight junction alterations in nonalcoholic fatty liver disease. Hepatology, 2009, 49(6), 1877-1887. doi: 10.1002/hep.22848 PMID: 19291785</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>De Munck, T.J.I.; Xu, P.; Verwijs, H.J.A.; Masclee, A.A.M.; Jonkers, D.; Verbeek, J.; Koek, G.H. Intestinal permeability in human nonalcoholic fatty liver disease: A systematic review and meta-analysis. Liver Int., 2020, 40(12), 2906-2916. doi: 10.1111/liv.14696 PMID: 33037768</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Kim, S-K.; Guevarra, R.B.; Kim, Y-T.; Kwon, J.; Kim, H.; Cho, J.H. Role of probiotics in human gut microbiome-associated diseases. J. Microbiol. Biotechnol., 2019, 29(9), 1335-1340. doi: 10.4014/jmb.1906.06064</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Huang, Z.; Liu, K.; Ma, W.; Li, D.; Mo, T.; Liu, Q. The gut microbiome in human health and diseaseWhere are we and where are we going? A bibliometric analysis. Front. Microbiol., 2022, 13, 1018594. doi: 10.3389/fmicb.2022.1018594 PMID: 36590421</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Albhaisi, S.A.M.; Bajaj, J.S. The influence of the microbiome on NAFLD and NASH. Clin. Liver Dis., 2021, 17(1), 15-18. doi: 10.1002/cld.1010 PMID: 33552480</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Imajo, K.; Fujita, K.; Yoneda, M.; Nozaki, Y.; Ogawa, Y.; Shinohara, Y.; Kato, S.; Mawatari, H.; Shibata, W.; Kitani, H.; Ikejima, K.; Kirikoshi, H.; Nakajima, N.; Saito, S.; Maeyama, S.; Watanabe, S.; Wada, K.; Nakajima, A. Hyperresponsivity to low-dose endotoxin during progression to nonalcoholic steatohepatitis is regulated by leptin-mediated signaling. Cell Metab., 2012, 16(1), 44-54. doi: 10.1016/j.cmet.2012.05.012 PMID: 22768838</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Zhu, L.; Baker, S.S.; Gill, C.; Liu, W.; Alkhouri, R.; Baker, R.D.; Gill, S.R. Characterization of gut microbiomes in nonalcoholic steatohepatitis (NASH) patients: A connection between endogenous alcohol and NASH. Hepatology, 2013, 57(2), 601-609. doi: 10.1002/hep.26093 PMID: 23055155</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Wong, V.W.S.; Tse, C.H.; Lam, T.T.Y.; Wong, G.L.H.; Chim, A.M.L.; Chu, W.C.W.; Yeung, D.K.W.; Law, P.T.W.; Kwan, H.S.; Yu, J.; Sung, J.J.Y.; Chan, H.L.Y. Molecular characterization of the fecal microbiota in patients with nonalcoholic steatohepatitis--a longitudinal study. PLoS One, 2013, 8(4), e62885. doi: 10.1371/journal.pone.0062885 PMID: 23638162</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Mouzaki, M.; Comelli, E.M.; Arendt, B.M.; Bonengel, J.; Fung, S.K.; Fischer, S.E.; McGilvray, I.D.; Allard, J.P. Intestinal microbiota in patients with nonalcoholic fatty liver disease. Hepatology, 2013, 58(1), 120-127. doi: 10.1002/hep.26319 PMID: 23401313</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Umirah, F.; Neoh, C.F.; Ramasamy, K.; Lim, S.M. Differential gut microbiota composition between type 2 diabetes mellitus patients and healthy controls: A systematic review. Diabetes Res. Clin. Pract., 2021, 173, 108689. doi: 10.1016/j.diabres.2021.108689 PMID: 33549678</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Hassouneh, R.; Kim, C.; Behary, J.; Zekry, A.; Bajaj, J. Microbiota and liver disease.: year in review. Microb. Health Dis., 2021, 3, e584. doi: 10.26355/mhd_20219_584</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Palmas, V.; Pisanu, S.; Madau, V.; Casula, E.; Deledda, A.; Cusano, R.; Uva, P.; Vascellari, S.; Loviselli, A.; Manzin, A.; Velluzzi, F. Gut microbiota markers associated with obesity and overweight in Italian adults. Sci. Rep., 2021, 11(1), 5532. doi: 10.1038/s41598-021-84928-w PMID: 33750881</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Ruuskanen, M.O.; Åberg, F.; Männistö, V.; Havulinna, A.S.; Méric, G.; Liu, Y.; Loomba, R.; Vázquez-Baeza, Y.; Tripathi, A.; Valsta, L.M.; Inouye, M.; Jousilahti, P.; Salomaa, V.; Jain, M.; Knight, R.; Lahti, L.; Niiranen, T.J. Links between gut microbiome composition and fatty liver disease in a large population sample. Gut Microbes, 2021, 13(1), 1888673. doi: 10.1080/19490976.2021.1888673 PMID: 33651661</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Ferguson, D.; Finck, B.N. Emerging therapeutic approaches for the treatment of NAFLD and type 2 diabetes mellitus. Nat. Rev. Endocrinol., 2021, 17(8), 484-495. doi: 10.1038/s41574-021-00507-z PMID: 34131333</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Astbury, S.; Atallah, E.; Vijay, A.; Aithal, G.P.; Grove, J.I.; Valdes, A.M. Lower gut microbiome diversity and higher abundance of proinflammatory genus Collinsella are associated with biopsy-proven nonalcoholic steatohepatitis. Gut Microbes, 2020, 11(3), 569-580. doi: 10.1080/19490976.2019.1681861 PMID: 31696774</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Loomba, R.; Seguritan, V.; Li, W.; Long, T.; Klitgord, N.; Bhatt, A. Gut microbiome-based metagenomic signature for non-invasive detection of advanced fibrosis in human nonalcoholic fatty liver disease. Cell Metab., 2017, 25(5), 1054-1062. doi: 10.1016/j.cmet.2017.04.001</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Rinella, M.E.; Neuschwander-Tetri, B.A.; Siddiqui, M.S.; Abdelmalek, M.F.; Caldwell, S.; Barb, D.; Kleiner, D.E.; Loomba, R. AASLD practice guidance on the clinical assessment and management of nonalcoholic fatty liver disease. Hepatology, 2023, 77(5), 1797-1835. doi: 10.1097/HEP.0000000000000323 PMID: 36727674</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Abenavoli, L.; Scarpellini, E.; Rouabhia, S.; Balsano, C.; Luzza, F. Probiotics in non-alcoholic fatty liver disease: Which and when. Ann. Hepatol., 2013, 12(3), 357-363. doi: 10.1016/S1665-2681(19)30997-4 PMID: 23619251</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Depommier, C.; Everard, A.; Druart, C.; Plovier, H.; Van Hul, M.; Vieira-Silva, S.; Falony, G.; Raes, J.; Maiter, D.; Delzenne, N.M.; de Barsy, M.; Loumaye, A.; Hermans, M.P.; Thissen, J.P.; de Vos, W.M.; Cani, P.D. Supplementation with Akkermansia muciniphila in overweight and obese human volunteers: A proof-of-concept exploratory study. Nat. Med., 2019, 25(7), 1096-1103. doi: 10.1038/s41591-019-0495-2 PMID: 31263284</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Roshanravan, N.; Bastani, S.; Tutunchi, H.; Kafil, B.; Nikpayam, O.; Mesri Alamdari, N. A comprehensive systematic review of the effectiveness of Akkermansia muciniphila, a member of the gut microbiome, for the management of obesity and associated metabolic disorders. Arch. Physiol. Biochem., 2023, 129(3), 741-751. doi: 10.3390/microorganisms9051098 PMID: 33449810</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Derrien, M.; Vaughan, E.E.; Plugge, C.M.; de Vos, W.M. Akkermansia muciniphila gen. nov., sp. nov., a human intestinal mucin-degrading bacterium. Int. J. Syst. Evol. Microbiol., 2004, 54(5), 1469-1476. doi: 10.1099/ijs.0.02873-0 PMID: 15388697</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Zhang, T.; Ji, X.; Lu, G.; Zhang, F. The potential of akkermansia muciniphila in inflammatory bowel disease. Appl. Microbiol. Biotechnol., 2021, 105(14-15), 5785-5794. doi: 10.1007/s00253-021-11453-1 PMID: 34312713</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Shi, Z.; Lei, H.; Chen, G.; Yuan, P.; Cao, Z.; Ser, H.L.; Zhu, X.; Wu, F.; Liu, C.; Dong, M.; Song, Y.; Guo, Y.; Chen, C.; Hu, K.; Zhu, Y.; Zeng, X.; Zhou, J.; Lu, Y.; Patterson, A.D.; Zhang, L. Impaired intestinal Akkermansia muciniphila and aryl hydrocarbon receptor ligands contribute to nonalcoholic fatty liver disease in mice. mSystems, 2021, 6(1), e00985-e20. doi: 10.1128/mSystems.00985-20 PMID: 33622853</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Sanjiwani, M.I.D.; Aryadi, I.P.H.; Semadi, I.M.S. Review of literature on Akkermansia muciniphila and its possible role in the etiopathogenesis and therapy of type 2 diabetes mellitus. J. ASEAN Fed. Endocr. Soc., 2022, 37(1), 69-74. doi: 10.15605/jafes.037.01.13 PMID: 35800592</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Nistal, E.; Saenz de Miera, L.E.; Ballesteros Pomar, M.; Sánchez-Campos, S.; García-Mediavilla, M.V.; Álvarez-Cuenllas, B. An altered fecal microbiota profile in patients with non-alcoholic fatty liver disease (NAFLD) associated with obesity. Rev. Esp. Enferm. Dig., 2019, 111(4), 275-282. doi: 10.17235/reed.2019.6068/2018</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Perraudeau, F.; McMurdie, P.; Bullard, J.; Cheng, A.; Cutcliffe, C.; Deo, A.; Eid, J.; Gines, J.; Iyer, M.; Justice, N.; Loo, W.T.; Nemchek, M.; Schicklberger, M.; Souza, M.; Stoneburner, B.; Tyagi, S.; Kolterman, O. Improvements to postprandial glucose control in subjects with type 2 diabetes: A multicenter, double blind, randomized placebo-controlled trial of a novel probiotic formulation. BMJ Open Diabetes Res. Care, 2020, 8(1), e001319. doi: 10.1136/bmjdrc-2020-001319 PMID: 32675291</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Rao, Y.; Kuang, Z.; Li, C.; Guo, S.; Xu, Y.; Zhao, D.; Hu, Y.; Song, B.; Jiang, Z.; Ge, Z.; Liu, X.; Li, C.; Chen, S.; Ye, J.; Huang, Z.; Lu, Y. Gut Akkermansia muciniphila ameliorates metabolic dysfunction-associated fatty liver disease by regulating the metabolism of L-aspartate via gut-liver axis. Gut Microbes, 2021, 13(1), 1927633. doi: 10.1080/19490976.2021.1927633 PMID: 34030573</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Zhou, J.; Zhang, Q.; Zhao, Y.; Zou, Y.; Chen, M.; Zhou, S.; Wang, Z. The relationship of megamonas species with nonalcoholic fatty liver disease in children and adolescents revealed by metagenomics of gut microbiota. Sci. Rep., 2022, 12(1), 22001. doi: 10.1038/s41598-022-25140-2 PMID: 36539432</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Liang, T.; Li, D.; Zunong, J.; Li, M.; Amaerjiang, N.; Xiao, H.; Khattab, N.; Vermund, S.; Hu, Y. Interplay of lymphocytes with the intestinal microbiota in children with nonalcoholic fatty liver disease. Nutrients, 2022, 14(21), 4641. doi: 10.3390/nu14214641 PMID: 36364902</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Jinato, T.; Chayanupatkul, M.; Dissayabutra, T.; Chutaputti, A.; Tangkijvanich, P.; Chuaypen, N. Litchi-derived polyphenol alleviates liver steatosis and gut dysbiosis in patients with non-alcoholic fatty liver disease: A randomized double-blinded, placebo-controlled study. Nutrients, 2022, 14(14), 2921. doi: 10.3390/nu14142921 PMID: 35889878</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Pan, X.; Kaminga, A.C.; Liu, A.; Wen, S.W.; Luo, M.; Luo, J. Gut microbiota, glucose, lipid, and water-electrolyte metabolism in children with nonalcoholic fatty liver disease. Front. Cell. Infect. Microbiol., 2021, 11, 683743. doi: 10.3389/fcimb.2021.683743 PMID: 34778099</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Schwimmer, J.B.; Johnson, J.S.; Angeles, J.E.; Behling, C.; Belt, P.H.; Borecki, I.; Bross, C.; Durelle, J.; Goyal, N.P.; Hamilton, G.; Holtz, M.L.; Lavine, J.E.; Mitreva, M.; Newton, K.P.; Pan, A.; Simpson, P.M.; Sirlin, C.B.; Sodergren, E.; Tyagi, R.; Yates, K.P.; Weinstock, G.M.; Salzman, N.H. Microbiome signatures associated with steatohepatitis and moderate to severe fibrosis in children with nonalcoholic fatty liver disease. Gastroenterology, 2019, 157(4), 1109-1122. doi: 10.1053/j.gastro.2019.06.028 PMID: 31255652</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Iacono, A.; Raso, G.M.; Canani, R.B.; Calignano, A.; Meli, R. Probiotics as an emerging therapeutic strategy to treat NAFLD: Focus on molecular and biochemical mechanisms. J. Nutr. Biochem., 2011, 22(8), 699-711. doi: 10.1016/j.jnutbio.2010.10.002 PMID: 21292470</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Khan, A.; Ding, Z.; Ishaq, M.; Bacha, A.S.; Khan, I.; Hanif, A.; Li, W.; Guo, X. Understanding the effects of gut microbiota dysbiosis on nonalcoholic fatty liver disease and the possible probiotics role: Recent updates. Int. J. Biol. Sci., 2021, 17(3), 818-833. doi: 10.7150/ijbs.56214 PMID: 33767591</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Ritze, Y.; Bárdos, G.; Claus, A.; Ehrmann, V.; Bergheim, I.; Schwiertz, A.; Bischoff, S.C. Lactobacillus rhamnosus GG protects against non-alcoholic fatty liver disease in mice. PLoS One, 2014, 9(1), e80169. doi: 10.1371/journal.pone.0080169 PMID: 24475018</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Yan, Y.; Liu, C.; Zhao, S.; Wang, X.; Wang, J.; Zhang, H.; Wang, Y.; Zhao, G. Probiotic Bifidobacterium lactis V9 attenuates hepatic steatosis and inflammation in rats with non-alcoholic fatty liver disease. AMB Express, 2020, 10(1), 101. doi: 10.1186/s13568-020-01038-y PMID: 32472368</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Si, J.; Kang, H.; You, H.J.; Ko, G. Revisiting the role of Akkermansia muciniphila as a therapeutic bacterium. Gut Microbes, 2022, 14(1), 2078619. doi: 10.1080/19490976.2022.2078619 PMID: 35613313</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Cao, F.; Ding, Q.; Zhuge, H.; Lai, S.; Chang, K.; Le, C.; Yang, G.; Valencak, T.G.; Li, S.; Ren, D. Lactobacillus plantarum ZJUIDS14 alleviates non-alcoholic fatty liver disease in mice in association with modulation in the gut microbiota. Front. Nutr., 2023, 9, 1071284. doi: 10.3389/fnut.2022.1071284 PMID: 36698477</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Depommier, C.; Vitale, R.M.; Iannotti, F.A.; Silvestri, C.; Flamand, N.; Druart, C.; Everard, A.; Pelicaen, R.; Maiter, D.; Thissen, J.P.; Loumaye, A.; Hermans, M.P.; Delzenne, N.M.; de Vos, W.M.; Di Marzo, V.; Cani, P.D. Beneficial effects of Akkermansia muciniphila are not associated with major changes in the circulating Endocannabinoidome but linked to higher Mono-Palmitoyl-Glycerol levels as new PPARα agonists. Cells, 2021, 10(1), 185. doi: 10.3390/cells10010185 PMID: 33477821</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Rau, M.; Rehman, A.; Dittrich, M.; Groen, A.K.; Hermanns, H.M.; Seyfried, F.; Beyersdorf, N.; Dandekar, T.; Rosenstiel, P.; Geier, A. Fecal SCFAs and SCFA-producing bacteria in gut microbiome of human NAFLD as a putative link to systemic T-cell activation and advanced disease. United European Gastroenterol. J., 2018, 6(10), 1496-1507. doi: 10.1177/2050640618804444 PMID: 30574320</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Yoon, S.J.; Yu, J.S.; Min, B.H.; Gupta, H.; Won, S.M.; Park, H.J.; Han, S.H.; Kim, B.Y.; Kim, K.H.; Kim, B.K.; Joung, H.C.; Park, T.S.; Ham, Y.L.; Lee, D.Y.; Suk, K.T. Bifidobacterium-derived short-chain fatty acids and indole compounds attenuate nonalcoholic fatty liver disease by modulating gut-liver axis. Front. Microbiol., 2023, 14, 1129904. doi: 10.3389/fmicb.2023.1129904 PMID: 36937300</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>LeBlanc, J.G.; Chain, F.; Martín, R.; Bermúdez-Humarán, L.G.; Courau, S.; Langella, P. Beneficial effects on host energy metabolism of short-chain fatty acids and vitamins produced by commensal and probiotic bacteria. Microb. Cell Fact., 2017, 16(1), 79. doi: 10.1186/s12934-017-0691-z PMID: 28482838</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Gou, H.Z.; Zhang, Y.L.; Ren, L.F.; Li, Z.J.; Zhang, L. How do intestinal probiotics restore the intestinal barrier? Front. Microbiol., 2022, 13, 929346. doi: 10.3389/fmicb.2022.929346 PMID: 35910620</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Nian, F.; Wu, L.; Xia, Q.; Tian, P.; Ding, C.; Lu, X. Akkermansia muciniphila and Bifidobacterium bifidum prevent NAFLD by regulating FXR expression and gut microbiota. J. Clin. Transl. Hepatol., 2023, 11, 763-776. doi: 10.14218/JCTH.2022.00415</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Kim, S.; Lee, Y.; Kim, Y.; Seo, Y.; Lee, H.; Ha, J.; Lee, J.; Choi, Y.; Oh, H.; Yoon, Y. Akkermansia muciniphila prevents fatty liver disease, decreases serum triglycerides, and maintains gut homeostasis. Appl. Environ. Microbiol., 2020, 86(7), e03004-e03019. doi: 10.1128/AEM.03004-19 PMID: 31953338</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Cao, C.; Shou, D.; Xu, H.; Huang, H.; Xia, Y.; Mei, Q.; Quan, Y.; Chen, H.; Zhao, C.; Tang, W.; Chen, H.; Zhau, Y. IDDF2021-ABS-0205 Akkermansia viable bacteria improves liver steatosis induced by high-fat diet relating to the regulation of gut microbiota in C57BL/6J MICE. Gut, 2021, 70, A8-A9. doi: 10.1136/gutjnl-2021-IDDF.11</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Gu, C.; Zhou, Z.; Yu, Z.; He, M.; He, L.; Luo, Z.; Xiao, W.; Yang, Q.; Zhao, F.; Li, W.; Shen, L.; Han, J.; Cao, S.; Zuo, Z.; Deng, J.; Yan, Q.; Ren, Z.; Zhao, M.; Yu, S. The microbiota and its correlation with metabolites in the gut of mice with nonalcoholic fatty liver disease. Front. Cell. Infect. Microbiol., 2022, 12, 870785. doi: 10.3389/fcimb.2022.870785 PMID: 35694542</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Kersten, S. Integrated physiology and systems biology of PPARα. Mol. Metab., 2014, 3(4), 354-371. doi: 10.1016/j.molmet.2014.02.002 PMID: 24944896</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Hasan, A.; Rahman, A.; Kobori, H. Interactions between host PPARs and gut microbiota in health and disease. Int. J. Mol. Sci., 2019, 20(2), 387. doi: 10.3390/ijms20020387 PMID: 30658440</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Plovier, H.; Everard, A.; Druart, C.; Depommier, C.; Van Hul, M.; Geurts, L.; Chilloux, J.; Ottman, N.; Duparc, T.; Lichtenstein, L.; Myridakis, A.; Delzenne, N.M.; Klievink, J.; Bhattacharjee, A.; van der Ark, K.C.H.; Aalvink, S.; Martinez, L.O.; Dumas, M.E.; Maiter, D.; Loumaye, A.; Hermans, M.P.; Thissen, J.P.; Belzer, C.; de Vos, W.M.; Cani, P.D. A purified membrane protein from Akkermansia muciniphila or the pasteurized bacterium improves metabolism in obese and diabetic mice. Nat. Med., 2017, 23(1), 107-113. doi: 10.1038/nm.4236 PMID: 27892954</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Yan, J.; Pan, Y.; Shao, W.; Wang, C.; Wang, R.; He, Y.; Zhang, M.; Wang, Y.; Li, T.; Wang, Z.; Liu, W.; Wang, Z.; Sun, X.; Dong, S. Beneficial effect of the short-chain fatty acid propionate on vascular calcification through intestinal microbiota remodelling. Microbiome, 2022, 10(1), 195. doi: 10.1186/s40168-022-01390-0 PMID: 36380385</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Xiong, J.; Chen, X.; Zhao, Z.; Liao, Y.; Zhou, T.; Xiang, Q. A potential link between plasma short chain fatty acids, TNF-α level and disease progression in non alcoholic fatty liver disease: A retrospective study. Exp. Ther. Med., 2022, 24(3), 598. doi: 10.3892/etm.2022.11536 PMID: 35949337</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Raftar, S.K.A.; Ashrafian, F.; Abdollahiyan, S.; Yadegar, A.; Moradi, H.R.; Masoumi, M.; Vaziri, F.; Moshiri, A.; Siadat, S.D.; Zali, M.R. The anti-inflammatory effects of Akkermansia muciniphila and its derivates in HFD/CCL4-induced murine model of liver injury. Sci. Rep., 2022, 12(1), 2453. doi: 10.1038/s41598-022-06414-1 PMID: 35165344</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Martin-Gallausiaux, C.; Garcia-Weber, D.; Lashermes, A.; Larraufie, P.; Marinelli, L.; Teixeira, V.; Rolland, A.; Béguet-Crespel, F.; Brochard, V.; Quatremare, T.; Jamet, A.; Doré, J.; Gray-Owen, S.D.; Blottière, H.M.; Arrieumerlou, C.; Lapaque, N. Akkermansia muciniphila upregulates genes involved in maintaining the intestinal barrier function via ADP-heptose-dependent activation of the ALPK1/TIFA pathway. Gut Microbes, 2022, 14(1), 2110639. doi: 10.1080/19490976.2022.2110639 PMID: 36036242</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Han, Y.; Li, L.; Wang, B. Role of Akkermansia muciniphila in the development of nonalcoholic fatty liver disease: Current knowledge and perspectives. Front. Med., 2022, 16(5), 667-685. doi: 10.1007/s11684-022-0960-z PMID: 36318353</mixed-citation></ref></ref-list></back></article>
