دورية أكاديمية

The Intestinal Commensal, Bacteroides fragilis, Modulates Host Responses to Viral Infection and Therapy: Lessons for Exploration during Mycobacterium tuberculosis Infection.

التفاصيل البيبلوغرافية
العنوان: The Intestinal Commensal, Bacteroides fragilis, Modulates Host Responses to Viral Infection and Therapy: Lessons for Exploration during Mycobacterium tuberculosis Infection.
المؤلفون: Eribo OA; DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa., du Plessis N; DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa., Chegou NN; DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
المصدر: Infection and immunity [Infect Immun] 2022 Jan 25; Vol. 90 (1), pp. e0032121. Date of Electronic Publication: 2021 Oct 04.
نوع المنشور: Journal Article; Review
اللغة: English
بيانات الدورية: Publisher: American Society For Microbiology Country of Publication: United States NLM ID: 0246127 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-5522 (Electronic) Linking ISSN: 00199567 NLM ISO Abbreviation: Infect Immun Subsets: MEDLINE
أسماء مطبوعة: Publication: Washington, DC : American Society For Microbiology
Original Publication: [Bethesda, Md.] American Society for Microbiology.
مواضيع طبية MeSH: Gastrointestinal Microbiome* , Host-Pathogen Interactions*/immunology , Microbial Interactions*, Bacteroides fragilis/*physiology , Virus Diseases/*etiology , Virus Diseases/*therapy, Antibiosis ; Cytokines/metabolism ; Disease Management ; Disease Resistance/immunology ; Disease Susceptibility ; Humans ; Immunomodulation ; Inflammation Mediators/metabolism ; Interferons/metabolism ; Organ Specificity ; Polysaccharides, Bacterial/immunology ; Probiotics ; Symbiosis ; Tuberculosis/etiology ; Virus Diseases/metabolism
مستخلص: The gut microbiota has emerged as a critical player in host health. Bacteroides fragilis is a prominent member of the gut microbiota within the phyla Bacteroidetes. This commensal bacterium produces unique capsular polysaccharides processed by antigen-presenting cells and activates CD4 + T cells to secrete inflammatory cytokines. Indeed, due to their immunomodulatory functions, B. fragilis and its capsular polysaccharide-A (PSA) are arguably the most explored single commensal microbiota/symbiotic factor. B. fragilis / PSA has been shown to protect against colitis, encephalomyelitis, colorectal cancer, pulmonary inflammation, and asthma. Here, we review recent data on the immunomodulatory role of B. fragilis/PSA during viral infections and therapy, B. fragilis PSA's dual ability to mediate pro-and anti-inflammatory processes, and the potential for exploring this unique characteristic during intracellular bacterial infections such as with Mycobacterium tuberculosis. We also discuss the protective roles of single commensal-derived probiotic species, including B. fragilis in lung inflammation and respiratory infections that may provide essential cues for possible exploration of microbiota based/augmented therapies in tuberculosis (TB). Available data on the relationship between B. fragilis / PSA, the immune system, and disease suggest clinical relevance for developing B. fragilis into a next-generation probiotic or, possibly, the engineering of PSA into a potent carbohydrate-based vaccine.
References: Mucosal Immunol. 2010 Sep;3(5):487-95. (PMID: 20531465)
Glycobiology. 2011 Apr;21(4):401-9. (PMID: 21030538)
Curr Opin Virol. 2011 Dec;1(6):519-25. (PMID: 22328912)
Glycobiology. 2018 Dec 1;28(1):50-58. (PMID: 29087497)
J Pathol. 2015 Jan;235(2):266-76. (PMID: 25302625)
World J Microbiol Biotechnol. 2019 Jun 3;35(6):91. (PMID: 31161259)
Mucosal Immunol. 2019 May;12(3):772-783. (PMID: 30783183)
Eur J Cancer. 2020 Jun;132:168-175. (PMID: 32375103)
Front Biosci (Landmark Ed). 2010 Jan 01;15:25-34. (PMID: 20036803)
Sci Rep. 2014 Apr 10;4:4638. (PMID: 24717726)
Biosci Biotechnol Biochem. 2010;74(5):939-45. (PMID: 20460726)
Future Virol. 2013 Mar 1;8(3):259-272. (PMID: 23956785)
Immunity. 2012 Jul 27;37(1):171-86. (PMID: 22749822)
Cell. 2020 May 28;181(5):1080-1096.e19. (PMID: 32380006)
Cell Res. 2020 Jun;30(6):492-506. (PMID: 32433595)
Eur J Immunol. 1995 Sep;25(9):2718-21. (PMID: 7589152)
Cancer Immunol Immunother. 2012 Apr;61(4):581-5. (PMID: 22297566)
J Immunol. 2012 Jun 15;188(12):6205-15. (PMID: 22566567)
Proc Natl Acad Sci U S A. 2008 Apr 1;105(13):5183-8. (PMID: 18381820)
Virology. 2012 Apr 10;425(2):71-81. (PMID: 22305621)
Front Microbiol. 2015 Oct 07;6:1085. (PMID: 26500629)
J Microbiol Immunol Infect. 2016 Feb;49(1):16-23. (PMID: 25304268)
Nature. 2001 Nov 29;414(6863):555-8. (PMID: 11734857)
Int J Environ Res Public Health. 2014 May 05;11(5):4745-67. (PMID: 24859749)
Nat Commun. 2017 Nov 15;8(1):1512. (PMID: 29142211)
Glycobiology. 2016 Oct;26(10):1029-1040. (PMID: 27236197)
Nature. 2010 Aug 19;466(7309):973-7. (PMID: 20725040)
PLoS Pathog. 2018 Jan 19;14(1):e1006822. (PMID: 29352287)
Tissue Barriers. 2017 Oct 2;5(4):e1373208. (PMID: 28956703)
Proc Natl Acad Sci U S A. 2011 Mar 29;108(13):5354-9. (PMID: 21402903)
Immunology. 2009 May;127(1):73-82. (PMID: 18778282)
Cancer Res. 2013 Dec 15;73(24):7199-210. (PMID: 24165160)
Microorganisms. 2019 Jan 10;7(1):. (PMID: 30634578)
Cell. 2004 May 28;117(5):677-87. (PMID: 15163414)
J Immunol. 1998 May 15;160(10):5000-6. (PMID: 9590249)
Nature. 2008 Oct 23;455(7216):1109-13. (PMID: 18806780)
Clin Infect Dis. 2015 Sep 1;61(5):683-91. (PMID: 25956891)
Glycobiology. 2011 Oct;21(10):1266-76. (PMID: 21321054)
Cell. 2014 Mar 27;157(1):121-41. (PMID: 24679531)
PLoS One. 2012;7(9):e45839. (PMID: 23029268)
J Virol. 2012 Dec;86(24):13445-55. (PMID: 23015724)
Front Immunol. 2020 Oct 26;11:556813. (PMID: 33193325)
J Biol Chem. 2015 Feb 20;290(8):5007-5014. (PMID: 25540199)
Proc Natl Acad Sci U S A. 2019 Nov 26;116(48):24285-24295. (PMID: 31712445)
J Immunol. 2010 Oct 1;185(7):4101-8. (PMID: 20817872)
Front Immunol. 2018 Nov 14;9:2656. (PMID: 30487801)
J Virol. 2008 Jul;82(14):7078-88. (PMID: 18480436)
Immunity. 2012 Jul 27;37(1):158-70. (PMID: 22705104)
PLoS Pathog. 2017 Nov 16;13(11):e1006687. (PMID: 29145483)
Chemotherapy. 2001 Jan-Feb;47(1):43-9. (PMID: 11125232)
EBioMedicine. 2020 Jan;51:102590. (PMID: 31901868)
Cell Mol Life Sci. 2019 Oct;76(20):3917-3937. (PMID: 31250035)
J Immunol. 2002 Dec 1;169(11):6149-53. (PMID: 12444118)
Nature. 2008 May 29;453(7195):620-5. (PMID: 18509436)
Proc Natl Acad Sci U S A. 2010 Jul 27;107(30):13402-7. (PMID: 20624978)
Immunopharmacol Immunotoxicol. 2019 Apr;41(2):207-213. (PMID: 30706742)
J Innate Immun. 2018;10(3):163-171. (PMID: 29131106)
Glycobiology. 2015 Apr;25(4):368-75. (PMID: 25347992)
Pharmacol Res. 2011 May;63(5):366-76. (PMID: 21349334)
PLoS Pathog. 2016 May 31;12(5):e1005667. (PMID: 27244558)
Cell Mol Life Sci. 2020 Apr;77(8):1497-1509. (PMID: 31729564)
J Biol Chem. 1992 Sep 5;267(25):18230-5. (PMID: 1517250)
Curr Infect Dis Rep. 2017 Mar;19(3):13. (PMID: 28251511)
Eur J Immunol. 2017 May;47(5):765-779. (PMID: 28393361)
Nat Immunol. 2012 Sep;13(9):832-42. (PMID: 22842346)
Immunity. 2006 Sep;25(3):373-81. (PMID: 16979569)
Nat Rev Immunol. 2014 Jan;14(1):36-49. (PMID: 24362405)
Nat Rev Immunol. 2011 May;11(5):343-54. (PMID: 21475309)
Trans Assoc Am Physicians. 1991;104:285-95. (PMID: 1845153)
Mucosal Immunol. 2021 Mar;14(2):296-304. (PMID: 33500564)
J Neurol Neurosurg Psychiatry. 1997 Sep;63(3):321-6. (PMID: 9328248)
Front Immunol. 2016 Nov 28;7:529. (PMID: 27965663)
Nat Commun. 2019 May 14;10(1):2153. (PMID: 31089128)
Nature. 2011 May 12;473(7346):174-80. (PMID: 21508958)
Antivir Chem Chemother. 2012 Sep 25;23(1):13-8. (PMID: 23018202)
Tuberculosis (Edinb). 2016 Dec;101:146-150. (PMID: 27865385)
J Clin Microbiol. 1993 Jul;31(7):1850-5. (PMID: 8349763)
Sci Rep. 2019 Mar 18;9(1):4812. (PMID: 30886158)
J Virol. 2014 Dec;88(24):14222-31. (PMID: 25275129)
Front Microbiol. 2021 Jan 21;11:512581. (PMID: 33552001)
Open Forum Infect Dis. 2020 Apr 09;7(5):ofaa126. (PMID: 32391404)
Lancet. 2016 Jun 4;387(10035):2312-2322. (PMID: 27017310)
Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4162-70. (PMID: 17724202)
Cell. 2020 Nov 25;183(5):1312-1324.e10. (PMID: 33212011)
Eur J Immunol. 2020 Dec;50(12):1976-1987. (PMID: 32673409)
Rev Immunogenet. 1999;1(1):60-74. (PMID: 11256573)
Cell. 2005 Jul 15;122(1):107-18. (PMID: 16009137)
Cell Host Microbe. 2014 Mar 12;15(3):382-392. (PMID: 24629344)
Ann N Y Acad Sci. 2018 Apr;1417(1):116-129. (PMID: 29528123)
Infect Immun. 1991 Jun;59(6):2075-82. (PMID: 2037368)
Sci Rep. 2016 Dec 07;6:38362. (PMID: 27924827)
Clin Microbiol Rev. 2007 Oct;20(4):593-621. (PMID: 17934076)
Gut. 2016 Apr;65(4):575-83. (PMID: 26511795)
Curr Opin Immunol. 2012 Apr;24(2):207-12. (PMID: 22236695)
mSphere. 2018 Nov 14;3(6):. (PMID: 30429227)
J Exp Med. 2006 Dec 25;203(13):2853-63. (PMID: 17178920)
معلومات مُعتمدة: National Research Foundation (NRF)
فهرسة مساهمة: Keywords: Bacteroides fragilis; Gut microbiota; Mycobacterium tuberculosis; polysaccharide A; probiotics; tuberculosis; viral infection
المشرفين على المادة: 0 (Cytokines)
0 (Inflammation Mediators)
0 (Polysaccharides, Bacterial)
9008-11-1 (Interferons)
تواريخ الأحداث: Date Created: 20211004 Date Completed: 20220221 Latest Revision: 20220726
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC8788684
DOI: 10.1128/IAI.00321-21
PMID: 34606367
قاعدة البيانات: MEDLINE
الوصف
تدمد:1098-5522
DOI:10.1128/IAI.00321-21