Method of diagnosing a dysbiosis
The present disclosure relates to methods of diagnosing a dysbiosis in a subject, methods of determining a suitable treatment, and methods of treating a dysbiosis. In some aspects, the present disclosure relates to diagnosing or determining a subtype of irritable bowel syndrome (IBS).
1. A method of diagnosing and treating a dysbiosis in a human subject, comprising measuring an abundance of at least 5 species of bacteria in a sample from the subject and at least 5 species of bacteria in a sample derived from a reference population, wherein the at least 5 species of bacteria include Corynebacterium minutissimum, Prevotella oulora, Fusobacterium naviforme, Prevotella ruminicola , and Bifidobacterium thermacidophilum , and wherein a diagnosis of is made when the abundance of one or more species of bacteria differs in abundance between the sample from the human subject and the sample derived from the reference population; and treating the subject for dysbiosis by administering to the subject a composition to the subject which increases and/or decreases the abundance of the one or more species of bacteria that differs in abundance between the sample from the human subject and the sample derived from the reference population.
2. The method of claim 1 , wherein the dysbiosis is IBS.
3. The method of claim 1 , wherein the composition is a nutraceutical.
4. The method of claim 1 , wherein the composition is a probiotic.
5. The method of claim 1 , wherein the composition is a faecal microbiota transplant.
6. The method of claim 1 , wherein the subject has previously been administered a chemotherapy or an antibiotic.
7. The method of claim 1 , wherein the sample is a faecal sample.
8. The method of claim 1 , further comprising measuring the abundance of at least one species of bacteria selected from Dysgonomonas wimpennyi, Propionibacterium acnes, Corynebacterium tuberculostearicum, Brevibacterium casei, Lachnobacterium bovis, Prevotella dentasini, Prevotella albensis, Veillonella atypica, Kytococcus schroeteri, Prevotella copri, Bacteroides barnesiae, Prevotella conceptionensis, Anaerofustis stercorihominis, Bifidobacterium thermophilum, Prevotella brevis, Roseburia intestinalis, Clostridium symbiosum, Barnesiella intestinihominis, Bacteroides fragilis, Anaerostipes rhamnosus, Collinsella aerofaciens, Clostridium bolteae, Arthrobacter creatinolyticus, Atopobium fossor, Prevotella paludivivens , and Pelotomaculum isophthalicicum.
9. A method of diagnosing and treating a dysbiosis in a human subject, comprising measuring an abundance of at least one species of each of 5 genera of bacteria in a sample from the subject and at least one species of each of 5 genera of bacteria in a sample derived from a reference population, wherein the at least 5 genera of bacteria include Corynebacterium, Lachnobacterium, Propionibacterium, Kytococcus , and Fusobacterium , and wherein a diagnosis of dysbiosis is made when the abundance of one or more genera of bacteria differs in abundance between the sample from the human subject and the sample derived from the reference population; and treating the subject for dysbiosis by administering to the subject a composition which increases and/or decreases the abundance of the at least one species of the one or more genera of bacteria in the subject, thereby treating the subject.
10. The method of claim 9 , wherein the dysbiosis is IBS.
11. The method of claim 9 , further comprising measuring the abundance of at least one species of at least one genus of bacteria selected from Veillonella, Prevotella, Anaerofustis, Arthrobacter, Dysgonomonas, Calothrix, Atopobium, Brevibacterium, Micrococcus, Burkholderia, Veillonella, Pelotomaculum, Acidaminococcus, Mitsuokella, Allisonella, Odoribacter, Bacteroides, Coprobacter, Alistipes, Ruminococcus, Ferrimonas, Alkaliphilus , and Lautropia.
12. A method of determining a subtype of IBS in a human subject with IBS and treating the subject, comprising a) measuring an abundance of at least 5 species of bacteria in a sample from the subject, wherein the at least 5 species of bacteria include Christensenella minuta, Soleaferrea massiliensis, Papillibacter cinnamivorans, Oscillibacter valericigenes , and Ruminococcus bromii and comparing the abundance of the at least 5 species of bacteria in the sample from the human subject to the abundance of the at least 5 species of bacteria in a sample derived from a reference population thereby determining a subtype of IBS; and b) administering a composition to the subject which increases and/or decreases the abundance of one or more species of bacteria in the subject, thereby treating the subject.
13. The method of claim 12 , further comprising measuring the abundance of at least one species of bacteria selected from Gemmiger formicilis, Desulfitobacterium frappieri, Alistipes obesi, Anaerofilum pentosovorans, Akkermansia muciniphila, Alkaliphilus crotonatoxidans, Eubacterium sulci, Bdellovibrio exovorus, Curtobacterium pusillum, Flavonifractor plautii, Ruminococcus lactaris, Mogibacterium neglectum, Roseburia inulinivorans, Butyricimonas virosa, Intestinimonas butyriciproducens, Butyrivibrio crossotus, Barnesiella intestinihominis, Flavobacterium resistens, Flavobacterium cauense, Clostridium glycyrrhizinilyticum, Anaerostipes hadrus, Prevotella ruminicola, Blautia wexlerae , and Anaerostipes coli.