Alterations in the relative abundance of Faecalibacterium prausnitzii correlate with changes in fecal calprotectin in patients with ileal Crohn's disease: a longitudinal study

被引:16
作者
Bjorkqvist, Olle [1 ]
Repsilber, Dirk [1 ]
Seifert, Maike [2 ]
Brislawn, Colin [3 ]
Jansson, Janet [3 ]
Engstrand, Lars [2 ]
Rangel, Ignacio [1 ]
Halfvarson, Jonas [4 ]
机构
[1] Orebro Univ, Sch Med Sci, Orebro, Sweden
[2] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, Stockholm, Sweden
[3] Pacific Northwest Natl Lab, Earth & Biol Sci Directorate, Richland, WA 99352 USA
[4] Orebro Univ, Dept Gastroenterol, Fac Med & Hlth, SE-70182 Orebro, Sweden
关键词
Faecalibacterium prausnitzii; Crohn's disease; calprotectin; butyrate; dysbiosis; BUTYRATE-PRODUCING BACTERIA; ULCERATIVE-COLITIS; MICROBIAL ECOLOGY; QUANTITATIVE PCR; PATHOGENESIS; INFLAMMATION; METABOLISM; TWIN;
D O I
10.1080/00365521.2019.1599417
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives: Crohn's disease is characterized by a gut dysbiosis with decreased abundance of butyrate producers such as Faecalibacterium prausnitzii. Although F. prausnitzii secretes anti-inflammatory molecules, few studies have addressed the importance of F. prausnitzii in a longitudinal setting. We aimed to examine the relationship between temporal profiles of F. prausnitzii, the C. leptum group, overall butyrate production, and inflammatory activity. Material and methods: Fecal samples (n = 59) were collected every third month from nine patients with ileal Crohn's disease. The abundance of F. prausnitzii and C. leptum was quantified relative to the total amount of bacteria using quantitative-PCR. To assess butyrate production of gut microbiota, gene copy numbers of the butyryl-CoA:acetate-CoA transferase (BCoAT) gene were quantified by qPCR. The inflammatory activity was defined by fecal (f)-calprotectin. Results: No correlation between the relative abundance of F. prausnitzii, the C. leptum group, or copy numbers of the BCoAT gene, and f-calprotectin was observed in the total sample set. By analyzing alterations between consecutive samples, a negative correlation between changes in the relative abundance of F. prausnitzii and f-calprotectin was observed (R = -0.39; p = .009). Changes in C. leptum (R = -0.18, p = .23) and number of copies of the BCoAT gene (R = -0.12; p = .42) did not correlate with f-calprotectin. Conclusions: There was an inverse correlation between temporal changes in the relative abundance of F. prausnitzii, but not overall butyrate producing capacity, and changes in inflammatory activity in ileal Crohn's disease. These findings indicate that F. prausnitzii may play a role in gut homeostasis, even though causality is still to be demonstrated.
引用
收藏
页码:577 / 585
页数:9
相关论文
共 42 条
  • [1] Enteric salmonellosis disrupts the microbial ecology of the murine gastrointestinal tract
    Barman, Melissa
    Unold, David
    Shifley, Kathleen
    Amir, Elad
    Hung, Kueichun
    Bos, Nicolaas
    Salzman, Nita
    [J]. INFECTION AND IMMUNITY, 2008, 76 (03) : 907 - 915
  • [2] Universality of human microbial dynamics
    Bashan, Amir
    Gibson, Travis E.
    Friedman, Jonathan
    Carey, Vincent J.
    Weiss, Scott T.
    Hohmann, Elizabeth L.
    Liu, Yang-Yu
    [J]. NATURE, 2016, 534 (7606) : 259 - +
  • [3] Canani RB, 2011, WORLD J GASTROENTERO, V17, P1519, DOI [10.3748/wjg.v17.i12.1519, 10.3748/wjg.v17.i12. 1519]
  • [4] Impaired butyrate oxidation in ulcerative colitis is due to decreased butyrate uptake and a defect in the oxidation pathway
    De Preter, Vicky
    Arijs, Ingrid
    Windey, Karen
    Vanhove, Wiebe
    Vermeire, Severine
    Schuit, Frans
    Rutgeerts, Paul
    Verbeke, Kristin
    [J]. INFLAMMATORY BOWEL DISEASES, 2012, 18 (06) : 1127 - 1136
  • [5] Mucosal metabolism in ulcerative colitis and Crohn's disease
    Duffy, MM
    Regan, MC
    Ravichandran, P
    O'Keane, C
    Harrington, MG
    Fitzpatrick, JM
    O'Connell, PR
    [J]. DISEASES OF THE COLON & RECTUM, 1998, 41 (11) : 1399 - 1405
  • [6] The Treatment-Naive Microbiome in New-Onset Crohn's Disease
    Gevers, Dirk
    Kugathasan, Subra
    Denson, Lee A.
    Vazquez-Baeza, Yoshiki
    Van Treuren, Will
    Ren, Boyu
    Schwager, Emma
    Knights, Dan
    Song, Se Jin
    Yassour, Moran
    Morgan, Xochitl C.
    Kostic, Aleksandar D.
    Luo, Chengwei
    Gonzalez, Antonio
    McDonald, Daniel
    Haberman, Yael
    Walters, Thomas
    Baker, Susan
    Rosh, Joel
    Stephens, Michael
    Heyman, Melvin
    Markowitz, James
    Baldassano, Robert
    Griffiths, Anne
    Sylvester, Francisco
    Mack, David
    Kim, Sandra
    Crandall, Wallace
    Hyams, Jeffrey
    Huttenhower, Curtis
    Knight, Rob
    Xavier, Ramnik J.
    [J]. CELL HOST & MICROBE, 2014, 15 (03) : 382 - 392
  • [7] HALFVARSON J, 2017, NAT MICROBIOL, V2, DOI DOI 10.1038/NMICROBIOL.2017.4
  • [8] ROLE OF THE FECAL STREAM IN THE MAINTENANCE OF CROHNS COLITIS
    HARPER, PH
    LEE, ECG
    KETTLEWELL, MGW
    BENNETT, MK
    JEWELL, DP
    [J]. GUT, 1985, 26 (03) : 279 - 284
  • [9] The gut microbiota of siblings offers insights into microbial pathogenesis of inflammatory bowel disease
    Hedin, Charlotte R.
    van der Gast, Christopher J.
    Stagg, Andrew J.
    Lindsay, James O.
    Whelan, Kevin
    [J]. GUT MICROBES, 2017, 8 (04) : 359 - 365
  • [10] Dysbiosis of the faecal microbiota in patients with Crohn's disease and their unaffected relatives
    Joossens, Marie
    Huys, Geert
    Cnockaert, Margo
    De Preter, Vicky
    Verbeke, Kristin
    Rutgeerts, Paul
    Vandamme, Peter
    Vermeire, Severine
    [J]. GUT, 2011, 60 (05) : 631 - 637