General | Carbohydrate O/F | Substrate utilisation | Enzymes | Metabolites | Antibiotics

Overview


  • Akkermansia muciniphila is a Gram-negative, non-spore-forming, strictly anaerobic, non-motile, oval-shaped bacterium. It has been detected in at least 26 gut microbiome compilation studies or metastudies. The DNA G+C content is 55.8%. Akkermansia muciniphila is often a widespread coloniser of gut. (Derrien2004; Derrien2010aBergey; Terekhov2018)



  • This organism has been recovered from human faeces. The risk classification (www.baua.de) for this organism is 1, i.e., low risk of infection and spread. Pathogenicity status unknown, or very unlikely to be pathogenic. A known mutualist. Robust growth can have positive consequences for gut health.

  • QUIRKS
  • This organism might not be picked up in all microbiome surveys as the conventional probes used often don't bind well to its DNA. Found in human breast milk (Jeurink2013).

  • GENERAL CHARACTERISTICS (Derrien2004); (Derrien2010aBergey);
    Character Response
  • Substrates hydrolysed or digested:
  • mucin;
  • pH
  • Acidity tolerance:
  • tolerates pH 5.5; tolerates pH 8; doesn't tolerate pH >8; Grows optimally at pH 6.5.
  • 🌡
  • Temperature tolerance:
  • doesn't grow at 15℃; grows at 20℃; grows at 40℃; doesn't grow at 41℃; Grows optimally at 37℃.
  • H+
  • Acid from carbohydrates usually produced:
  • glucose;
  • Substrates assimilated or utilised:
  • mucin;
  • Active enzymes:
  • N-Ac β-glucosaminidase; β-galactosidase;

  • SPECIAL FEATURES (Derrien2004); (Derrien2010aBergey);
    Character Response
  • Metabolites produced:
  • acetate; propionate; ethanol;
  • Metabolites not produced:
  • H₂S; indole;
  • Nitrate:
  • not reduced
  • Sulfate:
  • not reduced
  • Thiosulfate:
  • not reduced

  • RESPONSE TO ANTIBIOTICS
    Class Active Resistant
  • Penicillins:
  • amoxicillin; ampicillin; azlocillin; benzylpenicillin; cloxacillin; dicloxacillin; imipenem; meropenem; oxacillin; piperacillin; ticarcillin;
  • aztreonam; bacampicillin;
  • Cephalosporins:
  • cefazolin; cefdinir; cefepime; cefoperazone; cefotaxime; cefuroxime;
  • cefaclor; cefadroxil; cefixime; cefmetazole; cefotetan; cefotiam; cefoxitin; ceftazidime; cephalothin; moxalactam;
  • Macrolides:
  • azithromycin; clarithromycin; erythromycin; josamycin; roxithromycin; spiramycin;
  • Tetracyclines:
  • chlortetracycline; doxycycline; meclocycline; methacycline; minocycline; oxytetracycline; tetracycline;
  • Quinolines:
  • ciprofloxacin; clavulanic-acid; clinafloxacin; enoxacin; gatifloxacin; moxifloxacin; nalidixic-acid; norfloxacin; ofloxacin; pefloxacin; pipemidic-acid; sarafloxacin; sparfloxacin;
  • Aminoglycosides:
  • amikacin; dihydrostreptomycin; gentamicin; kanamycin; neomycin; sisomicin; spectinomycin; streptomycin; tobramycin;
  • Polypep/ketides:
  • rifabutin; rifampicin; rifapentine;
  • bacitracin;
  • Heterocycles:
  • chloramphenicol; metronidazole; trimethoprim;
  • fusidic-acid; isoniazid; nitrofurantoin; sulfadiazine; sulfadimethoxine; sulfamethoxazole; sulfanilamide;
  • Vancomycins:
  • vancomycin;
  • Miscellaneous antibiotics:
  • clindamycin; lincomycin; linezolid; colistin;

  • NOTES

    This species is associated with a healthy metabolic status and it is being investigated as a probiotic to treat obesity, diabetes and other related metabolic disorders.

    Fuel sources used:
    It lives in the mucus layer of the intestine and uses the mucus as it main energy source. Mucus turnover is a normal part of our gut function and this species plays an important role in regulating mucus turnover so the right amount occurs.

    Metabolites produced:
    Our genomic analysis indicates that most members of this species can produce the following metabolites: acetate, BCAAs, GABA, hydrogen sulphide, lactate, propionate, succinate, folate, biotin, riboflavin.

    Metabolites consumed:
    In addition, our genomic analysis indicates that most members of this species do not consume any reported metabolites.

    Disease associations:
    Although this bacterium appears to have mostly beneficial effects, studies have shown it is elevated in patients with multiple sclerosis and Parkinson's disease.

    Emerging research:
    By living in the mucus layer, A. muciniphila prevents potentially harmful bacteria from colonising this space through competition. Studies have observed low levels of A. muciniphila in patients with irritable bowel syndrome, appendicitis, type II diabetes, obesity and high fat diets, indicating it plays a beneficial role in metabolism.

    Research has also indicated this species can improve the efficacy of a common immunotherapy drug used in cancer patients called PD-1 inhibitors.

    Levels of this bacterium tend to decrease with age.

  • Isolated from the human intestinal tract based on its capacity to efficiently use mucus as a carbon and nitrogen source. This anaerobic resident is associated with the protective mucus lining of the intestines. [PMID: 21390229]

  • GutFeeling KnowledgeBase COMMENTS [Website]

    Akkermansia muciniphila strain ATCC BAA-835 (the type strain) was isolated as a novel, strictly anaerobic, mucin-degrading bacterium from a healthy human fecal sample in anaerobic medium containing gastric mucin as the sole carbon and nitrogen source. Cells are oval-shaped, showing a different size depending on the medium, in mucin medium being 640 nm in diameter and 690 nm in length and rich medium being 830 nm in diameter and 1 um in length. Cells stained Gram-negative, while flagella were not seen on negatively stained electron micrograph preparations. Formation of spores by the strain was never observed. In mucin medium, the organism produced a capsule and could grow as single cells or in pairs, rarely in chains and often formed aggregates. It counts for 1-3% of cells in the human feces and is a normal component of the intestinal tract. [UP000001031]

    Present knowledge suggests that A. muciniphila is important in maintaining a healthy mucus layer in the human gut. In previous researches, A. muciniphila has been proposed to be a contributor to the maintenance of gut health. In mouse studies, A. muciniphila played a causative role in lowering the body fat index, decreasing adipose tissue inflammation, improving glucose homeostasis, decreasing metabolic endotoxaemia, increasing the number of goblet cells, and increasing gut mucin integrity. Tests in humans have shown A. muciniphila is more abundant in the normal glucose tolerance group than in the prediabetes group which suggests that it may be a marker of type-2 diabetes (T2DM). Other research has shown that, in the process of degrading mucin, A. muciniphila produces acetate and propionate. It is also linked to a protective or anti-inflammatory role. As a probiotic reckoned to have health-promoting effects in humans, the activity of A. muciniphilaat the surface of mucosa can help to maintain the mucus layer. [PMID: 26666632] Akkermansia muciniphila, a mucin-degrading bacteria, is a member of the Verrucomicrobia phylum. [PMID: 26666632] Akkermansia muciniphila, an anaerobic Gram-negative bacterium, plays an important role in maintaining a healthy mucus layer in the human gut, and it may represent 3-5% of the microbial composition in the healthy human intestinal tract. [PMID: 31399846] UP000092519 is redundant to UP000235992

  • Derrien, M., Vaughan, E. E., Plugge, C. M., & de Vos, W. M. (2004). Akkermansia muciniphila gen. nov., sp. nov., a human intestinal mucin-degrading bacterium. International Journal of Systematic and Evolutionary Microbiology, 54(Pt 5), 1469–1476.


  • Details


    GENERAL
    Lineage Physiology General Growth Tolerances Hydrol./digest./degr.
    Phylum:  Verrucomicrobia Class:  Verrucomicrobiae Order:  Verrucomicrobiales Family:  Akkermansiaceae Genus:  Akkermansia Gram stain:  neg O2 Relation.:  strictly anaerobic Spore:  No spore Motility:  Sessile Morphology:  Oval-shaped
    Health:   Positive
    Source:  human faeces
    DNA G+C(%):  55.8
    Opt. T:  37℃
    Low T(℃):  15(neg)
    Lower T(℃):  20(+)
    Mid T(℃):  40(+)
    High T(℃):  41(neg)
    Opt. pH:  6.5
    pH 4.2-5.9:  5.5(+)
    pH 6.0-8.0:  8(+)
    pH >8:  >8(neg)
    Aesculin:  neg Urea:  neg Gelatin:  neg

    CARBOHYDRATE ACID FORMATION
    Monosaccharide O/F Oligosaccharide O/F Polysaccharide O/F Polyol O/F Other O/F
    Arabinose:  neg Glucose:  + Mannose:  neg Rhamnose:  neg Xylose:  neg Cellubiose:  neg Lactose:  neg Maltose:  neg Melezitose:  neg Sucrose:  neg Trehalose:  neg Glycerol:  neg Mannitol:  neg Sorbitol:  neg Salicin:  neg

    SUBSTRATE ASSIMILATION & UTILISATION
    Monosaccharide util/assim Oligosaccharide util/assim Other carboh. util/assim Amino acid util/assim Organic acid util/assim
    Fucose:  neg Galactose:  neg Glucose:  w Rhamnose:  neg Xylose:  neg Cellubiose:  neg Lactose:  neg Maltose:  neg N_Acetyl_glucosamine:  w Asp:  neg Glu:  neg Gly:  neg Pro:  neg Ser:  neg Thr:  neg Acetate:  neg Butyrate:  neg Fumarate:  neg Lactate:  neg Succinate:  neg

    ENZYME ACTIVITY
    Enzymes: General Enzymes: Carbohydrate Enzymes: Protein Enzymes: Arylamidases Enzymes: Esters/fats
    Urease:  neg Ac-β-glcamnd:  + α-Fucosidase:  neg α-Galactosidase:  vr β-Galactosidase:  + α-Glucosidase:  neg β-Glucosidase:  neg β-Glucuronidase:  neg ArgDH:  neg GluDC:  vr AlanineAA:  neg GluGluAA:  neg GlyAA:  neg LeuAA:  neg LeuGlyAA:  neg PyrrolidAA:  neg AlkalineP:  neg

    METABOLITES - PRODUCTION & USE
    Fuel Usable Metabolites Metabolites Released Special Products Compounds Produced

    Mucus

    None/Unknown

    Branched-Chain AA, Cobalamin, Biotin, Riboflavin, Acetate, Lactate, Propionate, Succinate, GABA, Hydrogen Sulfide

    Acetate:  + Propionate:  + Ethanol:  + H2S:  neg Indole:  neg

    ANTIBIOTICS ℞
    Penicillins & Penems (μg/mL) Cephalosporins (μg/mL) Aminoglycosides (μg/mL) Macrolides (μg/mL) Quinolones (μg/mL)
    amoxicillin:  Sens
    ampicillin:  Sens
    azlocillin:  Sens
    aztreonam:  Res
    bacampicillin:  Res
    benzyl-pen:  Sens
    cloxacillin:  Sens
    dicloxacillin:  Sens
    oxacillin:  Sens
    piperacillin:  Sens
    ticarcillin:  Sens
    imipenem:  Sens
    meropenem:  Sens
    cefaclor:  Res
    cefadroxil:  Res
    cefazolin:  Sens
    cefdinir:  Sens
    cefepime:  Sens
    cefixime:  Res
    cefmetazole:  Res
    cefoperazone:  Sens
    cefotaxime:  Sens
    cefotetan:  Res
    cefotiam:  Res
    cefoxitin:  Res
    ceftazidime:  Res
    cefuroxime:  Sens
    cephalothin:  Res
    moxalactam:  Res
    amikacin:  Res
    dihydrostrept:  Res
    gentamicin:  Res
    kanamycin:  Res
    neomycin:  Res
    sisomicin:  Res
    spectinomycin:  Res
    streptomycin:  Res
    tobramycin:  Res
    azithromycin:  Sens
    erythromycin:  Sens
    clarithromycin:  Sens
    roxithromycin:  Sens
    spiramycin:  Sens
    josamycin:  Sens
    linezolid:  Sens
    ciprofloxacin:  Res
    clavulanate:  Res
    clinafloxacin:  Res
    enoxacin:  Res
    gatifloxacin:  Res
    moxifloxacin:  Res
    nalidixic-acid:  Res
    norfloxacin:  Res
    ofloxacin:  Res
    pefloxacin:  Res
    pipemidic_acid:  Res
    sarafloxacin:  Res
    sparfloxacin:  Res
    Tetracyclines (μg/mL) Vancomycin Class (μg/mL) Polypep/ketides (μg/mL) Heterocycles (μg/mL) Other (μg/mL)
    doxycycline:  Sens
    chlortetracycline:  Sens
    meclocycline:  Sens
    methacycline:  Sens
    minocycline:  Sens
    oxytetracycline:  Sens
    tetracycline:  Sens
    vancomycin:  Res
    bacitracin:  Res
    rifabutin:  Sens
    rifampicin:  Sens
    rifapentine:  Sens
    chloramphenicol:  Sens
    isoniazid:  Res
    metronidazole:  Sens
    nitrofurantoin:  Res
    sulfadiazine:  Res
    sulfadimethoxine:  Res
    sulfamethoxazole:  Res
    sulfanilamide:  Res
    trimethoprim:  Sens
    clindamycin:  Sens
    lincomycin:  Sens
    colistin:  Sens
    fusidic-acid:  Res

    References


    SPECIFIC REFERENCES FOR AKKERMANSIA MUCINIPHILA
  • Derrien2004 - Akkermansia muciniphila gen. nov., sp. nov., a human intestinal mucin-degrading bacterium.
  • Derrien2010aBergey - Bergey's manual of systematic bacteriology. Vol. 4, The Verrucomicrobia. Family Akkermansiaceae, Genus I. Akkermansia
  • Terekhov2018 - Ultrahigh-throughput functional profiling of microbiota communities.
  • Gao2020 - Functional Microbiomics Reveals Alterations of the Gut Microbiome and Host Co-Metabolism in Patients With Alcoholic Hepatitis
  • Allin2018 - Aberrant intestinal microbiota in individuals with prediabetes
  • Bajer2017 - Distinct gut microbiota profiles in patients with primary sclerosing cholangitis and ulcerative colitis
  • Bedarf2017 - Functional implications of microbial and viral gut metagenome changes in early stage L-DOPA-naïve Parkinson's disease patients
  • Candela2012 - Unbalance of intestinal microbiota in atopic children
  • Cekanaviciute2018 - Multiple Sclerosis-Associated Changes in the Composition and Immune Functions of Spore-Forming Bacteria
  • DeAngelis2013 - Fecal microbiota and metabolome of children with autism and pervasive developmental disorder not otherwise specified
  • Demirci2019 - Reduced Akkermansia muciniphila and Faecalibacterium prausnitzii levels in the gut microbiota of children with allergic asthma
  • Fassatoui2019 - Gut microbiota imbalances in Tunisian participants with type 1 and type 2 diabetes mellitus
  • Fischer2015 - Altered microbiota in microscopic colitis
  • Gargari2018 - Evidence of dysbiosis in the intestinal microbial ecosystem of children and adolescents with primary hyperlipidemia and the potential role of regular hazelnut intake
  • Gryp2020 - Isolation and Quantification of Uremic Toxin Precursor-Generating Gut Bacteria in Chronic Kidney Disease Patients
  • Hayden2020 - Fecal dysbiosis in infants with cystic fibrosis is associated with early linear growth failure
  • Hoffman2014 - Escherichia coli dysbiosis correlates with gastrointestinal dysfunction in children with cystic fibrosis
  • Hu2019 - The Gut Microbiome Signatures Discriminate Healthy From Pulmonary Tuberculosis Patients
  • Huang2019 - Analysis of microbiota in elderly patients with Acute Cerebral Infarction
  • Jackson2016 - Signatures of early frailty in the gut microbiota
  • Kim2020a - Altered Gut Microbiome Profile in Patients With Pulmonary Arterial Hypertension
  • Malham2019 - The microbiome reflects diagnosis and predicts disease severity in paediatric onset inflammatory bowel disease
  • Marvasti2020 - The First Report of Differences in Gut Microbiota Composition between Obese and Normal Weight Iranian Subjects
  • Opstelten2016 - Gut Microbial Diversity Is Reduced in Smokers with Crohn's Disease
  • Qin2012 - Metagenome-wide association study of gut microbiota in type 2 diabetes
  • Tan2018 - The Akkermansia muciniphila is a gut microbiota signature in psoriasis
  • Unger2016 - Short chain fatty acids and gut microbiota differ between patients with Parkinson's disease and age-matched controls
  • Vakili2020 - Characterization of Gut Microbiota in Hospitalized Patients with Clostridioides difficile Infection
  • Wan2019 - Alterations of the Gut Microbiota in Multiple System Atrophy Patients
  • Wang2019 - Differential composition of gut microbiota among healthy volunteers, morbidly obese patients and post-bariatric surgery patients
  • Weir2013 - Stool microbiome and metabolome differences between colorectal cancer patients and healthy adults
  • Xu2019 - Altered gut microbiota and mucosal immunity in patients with schizophrenia
  • Ying2020 - Gut microbiota and Chinese medicine syndrome: altered fecal microbiotas in spleen (Pi)-deficient patients
  • Zhong2019 - Distinct gut metagenomics and metaproteomics signatures in prediabetics and treatment-naïve type 2 diabetics
  • Zhu2020 - Metagenome-wide association of gut microbiome features for schizophrenia
  • Laue2020 - Prospective associations of the infant gut microbiome and microbial function with social behaviors related to autism at age 3 years
  • LopezSiles2018 - Alterations in the Abundance and Co-occurrence of Akkermansia muciniphila and Faecalibacterium prausnitzii in the Colonic Mucosa of Inflammatory Bowel Disease Subjects.
  • Luna2016 - Distinct Microbiome-Neuroimmune Signatures Correlate With Functional Abdominal Pain in Children With Autism Spectrum Disorder.
  • Png2010 - Mucolytic bacteria with increased prevalence in IBD mucosa augment in vitro utilization of mucin by other bacteria.
  • Karcher2021 - Genomic diversity and ecology of human-associated Akkermansia species in the gut microbiome revealed by extensive metagenomic assembly.
  • Cani2018 - Human gut microbiome: hopes, threats and promises.
  • ...............................
  • GUT MICROBIOME COMPILATIONS AND METASTUDIES FOR AKKERMANSIA MUCINIPHILA
  • Byrd2020 - Stability and dynamics of the human gut microbiome and its association with systemic immune traits.
  • Chen2020 - Structural and Functional Characterization of the Gut Microbiota in Elderly Women With Migraine
  • Chen2020a - Featured Gut Microbiomes Associated With the Progression of Chronic Hepatitis B Disease
  • De2020 - Metagenomic analysis of gut microbiome and resistome of diarrheal fecal samples from Kolkata, India, reveals the core and variable microbiota including signatures of microbial dark matter.
  • Dubinkina2017 - Links of gut microbiota composition with alcohol dependence syndrome and alcoholic liver disease
  • Hu2019 - The Gut Microbiome Signatures Discriminate Healthy From Pulmonary Tuberculosis Patients
  • Jeong2021 - The effect of taxonomic classification by full-length 16S rRNA sequencing with a synthetic long-read technology
  • Jie2017 - The gut microbiome in atherosclerotic cardiovascular disease
  • Karlsson2013 - Gut metagenome in European women with normal, impaired and diabetic glucose control
  • King2019 - Baseline human gut microbiota profile in healthy people and standard reporting template.
  • Lagier2016 - Culture of previously uncultured members of the human gut microbiota by culturomics.
  • Li2019b - Disordered intestinal microbes are associated with the activity of Systemic Lupus Erythematosus
  • Minerbi2019 - Altered microbiome composition in individuals with fibromyalgia
  • New2022 - Collective effects of human genomic variation on microbiome function.
  • Nielsen2014 - MetaHIT Consortium. Identification and assembly of genomes and genetic elements in complex metagenomic samples without using reference genomes.
  • PerezBrocal2015 - Metagenomic Analysis of Crohn's Disease Patients Identifies Changes in the Virome and Microbiome Related to Disease Status and Therapy, and Detects Potential Interactions and Biomarkers
  • Qin2012 - Metagenome-wide association study of gut microbiota in type 2 diabetes
  • RajilicStojanovic2014 - The first 1000 cultured species of the human gastrointestinal microbiota.
  • Rothschild2018 - Environment dominates over host genetics in shaping human gut microbiota.
  • Tyakht2013 - Human gut microbiota community structures in urban and rural populations in Russia.
  • Walker2011 - High-throughput clone library analysis of the mucosa-associated microbiota reveals dysbiosis and differences between inflamed and non-inflamed regions of the intestine in inflammatory bowel disease.
  • Wang2018 - A metagenome-wide association study of gut microbiota in asthma in UK adults
  • Wang2018a - Morphine induces changes in the gut microbiome and metabolome in a morphine dependence model.
  • Wang2020a - Aberrant gut microbiota alters host metabolome and impacts renal failure in humans and rodents
  • Zeller2014 - Potential of fecal microbiota for early-stage detection of colorectal cancer
  • Zou2019 - 1,520 reference genomes from cultivated human gut bacteria enable functional microbiome analyses.
  • Zupancic2012 - Analysis of the Gut Microbiota in the Old Order Amish and Its Relation to the Metabolic Syndrome.
  • ...............................
  • GENERAL REFERENCES FOR AKKERMANSIA MUCINIPHILA
  • CCUG - Culture Collection University of Gothenburg - Entire Collection
  • Derrien2010Bergey - Bergey's manual of systematic bacteriology. Vol. 4, The Lentisphaerae. Family Victivallaceae, Genus I. Victivallis
  • Derrien2010aBergey - Bergey's manual of systematic bacteriology. Vol. 4, The Verrucomicrobia. Family Akkermansiaceae, Genus I. Akkermansia
  • Derrien2010 - Mucin-bacterial interactions in the human oral cavity and digestive tract.