Protection of the Human Gut Microbiome From Antibiotics

From BugSigDB
incomplete
Citation
PMID PubMed identifier for scientific articles.
DOI Digital object identifier for electronic documents.
URI
Authors
de Gunzburg J, Ghozlane A, Ducher A, Le Chatelier E, Duval X, Ruppé E, Armand-Lefevre L, Sablier-Gallis F, Burdet C, Alavoine L, Chachaty E, Augustin V, Varastet M, Levenez F, Kennedy S, Pons N, Mentré F, Andremont A
Journal
The Journal of infectious diseases
Year
2018
Keywords:
Clostridium difficile, antibiotics, fluoroquinolones, microbiome
Background: Antibiotics are life-saving drugs but severely affect the gut microbiome with short-term consequences including diarrhea and selection of antibiotic-resistant bacteria. Long-term links to allergy and obesity are also suggested. We devised a product, DAV132, and previously showed its ability to deliver a powerful adsorbent, activated charcoal, in the late ileum of human volunteers. Methods: We performed a randomized controlled trial in 28 human volunteers treated with a 5-day clinical regimen of the fluoroquinolone antibiotic moxifloxacin in 2 parallel groups, with or without DAV132 coadministration. Two control goups of 8 volunteers each receiving DAV132 alone, or a nonactive substitute, were added. Results: The coadministration of DAV132 decreased free moxifloxacin fecal concentrations by 99%, while plasmatic levels were unaffected. Shotgun quantitative metagenomics showed that the richness and composition of the intestinal microbiota were largely preserved in subjects co-treated with DAV132 in addition to moxifloxacin. No adverse effect was observed. In addition, DAV132 efficiently adsorbed a wide range of clinically relevant antibiotics ex vivo. Conclusions: DAV132 was highly effective to protect the gut microbiome of moxifloxacin-treated healthy volunteers and may constitute a clinical breakthrough by preventing adverse health consequences of a wide range of antibiotic treatments. Clinical Trials Registration: NCT02176005.

Experiment 1


Reviewed Marked as Reviewed by ChiomaBlessing on 2024-1-11

Curated date: 2021/01/10

Curator: WikiWorks

Revision editor(s): WikiWorks, ChiomaBlessing

Subjects

Location of subjects
France
Host species Species from which microbiome was sampled. Contact us to have more species added.
Homo sapiens
Body site Anatomical site where microbial samples were extracted from according to the Uber Anatomy Ontology
Feces Cow dung,Cow pat,Droppings,Dung,Excrement,Excreta,Faeces,Fecal material,Fecal matter,Fewmet,Frass,Guano,Matières fécales@fr,Merde@fr,Ordure,Partie de la merde@fr,Piece of shit,Porción de mierda@es,Portion of dung,Portion of excrement,Portion of faeces,Portion of fecal material,Portion of fecal matter,Portion of feces,Portion of guano,Portion of scat,Portionem cacas,Scat,Spoor,Spraint,Stool,Teil der fäkalien@de,Feces,feces
Condition The experimental condition / phenotype studied according to the Experimental Factor Ontology
Antimicrobial agent antibiotic,antibiotics,Antibiotika,Antibiotikum,antibiotique,antimicrobial,antimicrobial agents,microbicide,microbicides,Antimicrobial agent,antimicrobial agent
Group 0 name Corresponds to the control (unexposed) group for case-control studies
Negative control group (CLT)
Group 1 name Corresponds to the case (exposed) group for case-control studies
moxifloxacin treated group (MXF)
Group 1 definition Diagnostic criteria applied to define the specific condition / phenotype represented in the case (exposed) group
healthy male and female volunteers aged >18 years
Group 0 sample size Number of subjects in the control (unexposed) group
8
Group 1 sample size Number of subjects in the case (exposed) group
14
Antibiotics exclusion Number of days without antibiotics usage (if applicable) and other antibiotics-related criteria used to exclude participants (if any)
3 months

Lab analysis

Sequencing type
WMS
16S variable region One or more hypervariable region(s) of the bacterial 16S gene
Not specified
Sequencing platform Manufacturer and experimental platform used for quantifying microbial abundance
Mass spectrometry

Statistical Analysis

Data transformation Data transformation applied to microbial abundance measurements prior to differential abundance testing (if any).
relative abundances
Statistical test
Mann-Whitney (Wilcoxon)
Significance threshold p-value or FDR threshold used for differential abundance testing (if any)
0.05
MHT correction Have statistical tests be corrected for multiple hypothesis testing (MHT)?
Yes

Alpha Diversity

Richness Number of species
decreased

Signature 1

Needs review

Curated date: 2021/01/10

Curator: Mst Afroza Parvin

Revision editor(s): WikiWorks

Source: Supplementary table 3, Supplementary figure 1

Description: A detailed analysis of the MGSs that differed significantly between treatment groups

Abundance in Group 1: increased abundance in moxifloxacin treated group (MXF)

NCBI Quality ControlLinks
Archaea
Blautia

Revision editor(s): WikiWorks

Signature 2

Needs review

Curated date: 2021/01/10

Curator: Mst Afroza Parvin

Revision editor(s): Lwaldron, WikiWorks

Source: Supplementary table 3, Supplementary figure 1

Description: A detailed analysis of the MGSs that differed significantly between treatment groups

Abundance in Group 1: decreased abundance in moxifloxacin treated group (MXF)

NCBI Quality ControlLinks
Alistipes
Alistipes finegoldii
Alistipes onderdonkii
Alistipes putredinis
Alistipes shahii
Bacteroidales
Barnesiella intestinihominis
Bifidobacterium adolescentis
Bifidobacterium pseudocatenulatum
Bilophila wadsworthia
Blautia
Blautia sp.
Butyricimonas
Butyricimonas virosa
Catenibacterium
Cloacibacterium sp.
Clostridium
Clostridium sp.
Coprobacillus
Dorea formicigenerans
Eubacteriales
Eubacterium
Faecalibacterium
Faecalibacterium prausnitzii
Bacillota
Haemophilus parainfluenzae
Intestinibacter bartlettii
Lachnospira eligens
Lachnospiraceae
Odoribacter splanchnicus
Oscillibacter
Oscillibacter sp.
Oscillospiraceae
Parabacteroides distasonis
Parasutterella excrementihominis
Roseburia inulinivorans
Ruminococcus callidus
Streptococcus parasanguinis

Revision editor(s): Lwaldron, WikiWorks

Experiment 2


Needs review

Curated date: 2021/01/10

Curator: WikiWorks

Revision editor(s): WikiWorks

Differences from previous experiment shown

Subjects

Group 0 name Corresponds to the control (unexposed) group for case-control studies
moxifloxacin treated group (MXF)
Group 1 name Corresponds to the case (exposed) group for case-control studies
DAV132+moxifloxacin treated group (MXF+DAV132)
Group 0 sample size Number of subjects in the control (unexposed) group
14

Lab analysis

Statistical Analysis

Data transformation Data transformation applied to microbial abundance measurements prior to differential abundance testing (if any).
Not specified

Alpha Diversity

Richness Number of species
increased

Signature 1

Needs review

Curated date: 2021/01/10

Curator: Mst Afroza Parvin

Revision editor(s): WikiWorks

Source: Supplementary table 3, Supplementary figure 1

Description: A detailed analysis of the MGSs that differed significantly between treatment groups

Abundance in Group 1: increased abundance in DAV132+moxifloxacin treated group (MXF+DAV132)

NCBI Quality ControlLinks
Parabacteroides distasonis
Bilophila wadsworthia
Roseburia inulinivorans
Odoribacter splanchnicus
Lachnospiraceae
Blautia sp.
Clostridium sp.
Bacillota
Faecalibacterium prausnitzii
Ruminococcus callidus
Alistipes shahii
Alistipes
Faecalibacterium
Parasutterella excrementihominis
Cloacibacterium sp.
Bifidobacterium adolescentis
Alistipes onderdonkii
Blautia
Oscillibacter
Oscillibacter sp.
Coprobacillus
Alistipes finegoldii
Butyricimonas virosa
Oscillospiraceae
Eubacteriales
Eubacterium
Alistipes putredinis
Butyricimonas
Barnesiella intestinihominis
Lachnospira eligens
Catenibacterium
Dorea formicigenerans
Haemophilus parainfluenzae
Alistipes senegalensis

Revision editor(s): WikiWorks

Signature 2

Needs review

Curated date: 2021/01/10

Curator: Mst Afroza Parvin

Revision editor(s): WikiWorks

Source: Supplementary table 3, Supplementary figure 1

Description: A detailed analysis of the MGSs that differed significantly between treatment groups

Abundance in Group 1: decreased abundance in DAV132+moxifloxacin treated group (MXF+DAV132)

NCBI Quality ControlLinks
Blautia

Revision editor(s): WikiWorks

Experiment 3


Needs review

Curated date: 2021/01/10

Curator: WikiWorks

Revision editor(s): WikiWorks

Differences from previous experiment shown

Subjects

Group 0 name Corresponds to the control (unexposed) group for case-control studies
Negative control group (CLT)
Group 0 sample size Number of subjects in the control (unexposed) group
8

Lab analysis

Statistical Analysis

Alpha Diversity

Richness Number of species
unchanged

Signature 1

Needs review

Curated date: 2021/01/10

Curator: Mst Afroza Parvin

Revision editor(s): WikiWorks

Source: Supplementary table 3, Supplementary figure 1

Description: A detailed analysis of the MGSs that differed significantly between treatment groups

Abundance in Group 1: increased abundance in DAV132+moxifloxacin treated group (MXF+DAV132)

NCBI Quality ControlLinks
Bacillota
Lachnospiraceae

Revision editor(s): WikiWorks

Signature 2

Needs review

Curated date: 2021/01/10

Curator: Mst Afroza Parvin

Revision editor(s): WikiWorks

Source: Supplementary table 3, Supplementary figure 1

Description: A detailed analysis of the MGSs that differed significantly between treatment groups

Abundance in Group 1: decreased abundance in DAV132+moxifloxacin treated group (MXF+DAV132)

NCBI Quality ControlLinks
Bilophila wadsworthia
Bifidobacterium adolescentis
Intestinibacter bartlettii
Bifidobacterium pseudocatenulatum
Catenibacterium
Flavonifractor plautii

Revision editor(s): WikiWorks