Faecal microbiota and cytokine profiles of rural Cambodian infants linked to diet and diarrhoeal episodes

From BugSigDB
Needs review
Citation
PMID PubMed identifier for scientific articles.
DOI Digital object identifier for electronic documents.
URI
Authors
Dalby MJ, Kiu R, Serghiou IR, Miyazaki A, Acford-Palmer H, Tung R, Caim S, Phillips S, Kujawska M, Matsui M, Iwamoto A, Taking B, Cox SE, Hall LJ
Journal
NPJ biofilms and microbiomes
Year
2024
The gut microbiota of infants in low- to middle-income countries is underrepresented in microbiome research. This study explored the faecal microbiota composition and faecal cytokine profiles in a cohort of infants in a rural province of Cambodia and investigated the impact of sample storage conditions and infant environment on microbiota composition. Faecal samples collected at three time points from 32 infants were analysed for microbiota composition using 16S rRNA amplicon sequencing and concentrations of faecal cytokines. Faecal bacterial isolates were subjected to whole genome sequencing and genomic analysis. We compared the effects of two sample collection methods due to the challenges of faecal sample collection in a rural location. Storage of faecal samples in a DNA preservation solution preserved Bacteroides abundance. Microbiota analysis of preserved samples showed that Bifidobacterium was the most abundant genus with Bifidobacterium longum the most abundant species, with higher abundance in breast-fed infants. Most infants had detectable pathogenic taxa, with Shigella and Klebsiella more abundant in infants with recent diarrhoeal illness. Neither antibiotics nor infant growth were associated with gut microbiota composition. Genomic analysis of isolates showed gene clusters encoding the ability to digest human milk oligosaccharides in B. longum and B. breve isolates. Antibiotic-resistant genes were present in both potentially pathogenic species and in Bifidobacterium. Faecal concentrations of Interlukin-1alpha and vascular endothelial growth factor were higher in breast-fed infants. This study provides insights into an underrepresented population of rural Cambodian infants, showing pathogen exposure and breastfeeding impact gut microbiota composition and faecal immune profiles.

Experiment 1


Needs review

Curated date: 2024/10/16

Curator: Aishat

Revision editor(s): Aishat

Subjects

Location of subjects
Cambodia
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
Diarrhea , Diarrhea, Infantile , Malnutrition Diarrhea,Diarrhoea,Watery stool,diarrhea,Diarrhea, Infantile,diarrhea, Infantile,Lack of food,Malnutrition,malnutrition
Group 0 name Corresponds to the control (unexposed) group for case-control studies
Infants who are not breast-fed
Group 1 name Corresponds to the case (exposed) group for case-control studies
Infants who are breast-fed
Group 1 definition Diagnostic criteria applied to define the specific condition / phenotype represented in the case (exposed) group
Infants that are being breastfed at the time of the research/sample collection
Group 0 sample size Number of subjects in the control (unexposed) group
9
Group 1 sample size Number of subjects in the case (exposed) group
23

Lab analysis

Sequencing type
16S
16S variable region One or more hypervariable region(s) of the bacterial 16S gene
V9
Sequencing platform Manufacturer and experimental platform used for quantifying microbial abundance
Illumina

Statistical Analysis

Statistical test
PERMANOVA
MaAsLin2
Pearson Correlation
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
Confounders controlled for Confounding factors that have been accounted for by stratification or model adjustment
time

Alpha Diversity

Pielou Quantifies how equal the community is numerically
decreased
Richness Number of species
decreased

Signature 1

Needs review

Curated date: 2024/10/16

Curator: Aishat

Revision editor(s): Aishat

Source: Figure 2C

Description: Bacterial genera differentially abundant between breastfed infants and infants who were not breastfed.

Abundance in Group 1: increased abundance in Infants who are breast-fed

NCBI Quality ControlLinks
Bifidobacterium
Streptococcus

Revision editor(s): Aishat

Signature 2

Needs review

Curated date: 2024/10/16

Curator: Aishat

Revision editor(s): Aishat

Source: Figure 3c

Description: Bacterial species differentially abundant between breastfed infants and infants who were not breastfed.

Abundance in Group 1: increased abundance in Infants who are breast-fed

NCBI Quality ControlLinks
Bifidobacterium longum

Revision editor(s): Aishat

Signature 3

Needs review

Curated date: 2024/10/17

Curator: Aishat

Revision editor(s): Aishat

Source: Figure 3c

Description: Bacterial species difference between breastfed infants and infants who were not breastfed

Abundance in Group 1: decreased abundance in Infants who are breast-fed

NCBI Quality ControlLinks
Klebsiella pneumoniae

Revision editor(s): Aishat

Experiment 2


Needs review

Curated date: 2024/10/16

Curator: Aishat

Revision editor(s): Aishat

Differences from previous experiment shown

Subjects

Group 0 name Corresponds to the control (unexposed) group for case-control studies
Infants without diarrhea
Group 1 name Corresponds to the case (exposed) group for case-control studies
Infants with diarrhea
Group 1 definition Diagnostic criteria applied to define the specific condition / phenotype represented in the case (exposed) group
Infants who experienced diarrhea within the 7 days prior to sample collection.
Group 0 sample size Number of subjects in the control (unexposed) group
26
Group 1 sample size Number of subjects in the case (exposed) group
6

Lab analysis

16S variable region One or more hypervariable region(s) of the bacterial 16S gene
Not specified

Statistical Analysis

Statistical test
MaAsLin2
Significance threshold p-value or FDR threshold used for differential abundance testing (if any)
0.25


Signature 1

Needs review

Curated date: 2024/10/16

Curator: Aishat

Revision editor(s): Aishat

Source: Figure 2c

Description: Bacterial genera differentially abundant between infants with diarrheal illness and infants without diarrheal illness

Abundance in Group 1: increased abundance in Infants with diarrhea

NCBI Quality ControlLinks
Clostridium
Shigella
Klebsiella

Revision editor(s): Aishat

Signature 2

Needs review

Curated date: 2024/10/16

Curator: Aishat

Revision editor(s): Aishat

Source: Figure 2c

Description: Bacterial genera differentially abundant between infants with diarrheal illness and infants without diarrheal illness.

Abundance in Group 1: decreased abundance in Infants with diarrhea

NCBI Quality ControlLinks
Bacteroides

Revision editor(s): Aishat

Signature 3

Needs review

Curated date: 2024/10/16

Curator: Aishat

Revision editor(s): Aishat

Source: Figure 3c

Description: Bacterial species difference between infants with diarrheal illness and infants without diarrheal illness

Abundance in Group 1: increased abundance in Infants with diarrhea

NCBI Quality ControlLinks
Shigella flexneri
Clostridium perfringens

Revision editor(s): Aishat

Signature 4

Needs review

Curated date: 2024/10/16

Curator: Aishat

Revision editor(s): Aishat

Source: Figure 3c

Description: Bacterial species differentially abundant between infants with diarrheal illness and infants without diarrheal illness.

Abundance in Group 1: increased abundance in Infants with diarrhea

NCBI Quality ControlLinks
Shigella flexneri
Clostridium perfringens

Revision editor(s): Aishat