Microbial gut evaluation in an angolan paediatric population with sickle cell disease

From BugSigDB
Needs review
study design
Citation
PMID PubMed identifier for scientific articles.
DOI Digital object identifier for electronic documents.
Authors
Delgadinho M, Ginete C, Santos B, Mendes J, Miranda A, Vasconcelos J, Brito M
Journal
Journal of cellular and molecular medicine
Year
2022
Keywords:
16S rRNA, foetal haemoglobin, microbiome, sickle cell disease
Sickle cell disease (SCD) is one of the most common genetic conditions worldwide. It can contribute up to 90% of under-5 mortality in sub-Saharan Africa. Clinical manifestations are very heterogeneous, and the intestinal microbiome appears to be crucial in the modulation of inflammation, cell adhesion and induction of aged neutrophils, the main interveners of recurrent vaso-occlusive crisis. Enterocyte injury, increased permeability, altered microbial composition and bacterial overgrowth have all been documented as microbial and pathophysiologic changes in the gut microbiome of SCD patients in recent studies. Our aim was to sequence the bacterial 16S rRNA gene in order to characterize the gut microbiome of Angolan children with SCA and healthy siblings as a control. A total of 72 stool samples were obtained from children between 3 and 14 years old. Our data showed that the two groups exhibit some notable differences in microbiota relative abundance at different classification levels. Children with SCA have a higher number of the phylum Actinobacteria. As for the genus level, Clostridium cluster XI bacteria was more prevalent in the SCA children, whereas the siblings had a higher abundance of Blautia, Aestuariispira, Campylobacter, Helicobacter, Polaribacter and Anaerorhabdus. In this study, we have presented the first microbiota analysis in an Angolan paediatric population with SCD and provided a detailed view of the microbial differences between patients and healthy controls. There is still much to learn before fully relying on the therapeutic approaches for gut modulation, which is why more research in this field is crucial to making this a reality.

Experiment 1


Needs review

Curated date: 2024/10/22

Curator: Aleru Divine

Revision editor(s): Aleru Divine

Subjects

Location of subjects
Angola
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
Sickle cell anemia drepanocytosis,Hb SC disease,Hb-S/Hb-C disease,Hb-SS disease without crisis,HbS disease,Hemoglobin S disease,Hemoglobin S disease without crisis,hemoglobin SC disease,sickle cell anemia,Sickle cell disease,sickle cell disease,sickle-cell/Hb-C disease without crisis,sickling disorder due to Hemoglobin S,Sickle cell anemia
Group 0 name Corresponds to the control (unexposed) group for case-control studies
Healthy Siblings
Group 1 name Corresponds to the case (exposed) group for case-control studies
Sickle Cell Anaemia cases
Group 1 definition Diagnostic criteria applied to define the specific condition / phenotype represented in the case (exposed) group
Angolan children between 3 and 14 years with Sickle Cell Anemia
Group 0 sample size Number of subjects in the control (unexposed) group
36
Group 1 sample size Number of subjects in the case (exposed) group
36
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
16S
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
Illumina

Statistical Analysis

Data transformation Data transformation applied to microbial abundance measurements prior to differential abundance testing (if any).
relative abundances
Statistical test
Welch's T-Test
Significance threshold p-value or FDR threshold used for differential abundance testing (if any)
0.05


Signature 1

Needs review

Curated date: 2024/10/23

Curator: Aleru Divine

Revision editor(s): Aleru Divine

Source: Figure 4

Description: Differential abundance in the microbiota of sickle cell anaemia (SCA) children compared to their siblings(controls).

Abundance in Group 1: increased abundance in Sickle Cell Anaemia cases

NCBI Quality ControlLinks
Actinomycetota
Coriobacteriales
Peptostreptococcaceae
Acidimicrobiia
Coriobacteriaceae
Bacteroides clarus
Bifidobacterium bohemicum
Collinsella bouchesdurhonensis
Sutterella massiliensis

Revision editor(s): Aleru Divine

Signature 2

Needs review

Curated date: 2024/10/23

Curator: Aleru Divine

Revision editor(s): Aleru Divine

Source: Figure 4

Description: Differential abundance in the microbiota of sickle cell anaemia (SCA) children compared to their siblings(controls).

Abundance in Group 1: decreased abundance in Sickle Cell Anaemia cases

NCBI Quality ControlLinks
Campylobacterales
Rhodospirillales
Polaribacter
Aestuariispira
Helicobacter
Anaerorhabdus
Campylobacter
Epsilonproteobacteria
Rhodospirillaceae
Alloprevotella rava
Anaerorhabdus furcosa
Caproiciproducens galactitolivorans
Prevotella histicola
Segatella oris
Segatella oulorum
Leyella stercorea
Prevotella veroralis
Rhodospirillaceae bacterium
Ruminococcus flavefaciens
Campylobacteraceae

Revision editor(s): Aleru Divine

Experiment 2


Needs review

Curated date: 2024/10/23

Curator: Aleru Divine

Revision editor(s): Aleru Divine

Differences from previous experiment shown

Subjects

Condition The experimental condition / phenotype studied according to the Experimental Factor Ontology
Sickle cell disease associated with an other hemoglobin anomaly Double heterozygotes sickling disorder,sickle cell disease associated with an other hemoglobin anomaly,Sickle cell disease associated with an other hemoglobin anomaly
Group 0 name Corresponds to the control (unexposed) group for case-control studies
Foetal haemoglobin level < 5%
Group 1 name Corresponds to the case (exposed) group for case-control studies
Foetal haemoglobin level > 5%
Group 1 definition Diagnostic criteria applied to define the specific condition / phenotype represented in the case (exposed) group
Sickle Cell Anemia(SCA) children with Foetal haemoglobin level > 5%
Group 0 sample size Number of subjects in the control (unexposed) group
27
Group 1 sample size Number of subjects in the case (exposed) group
9

Lab analysis

Statistical Analysis

Alpha Diversity

Shannon Estimator of species richness and species evenness: more weight on species richness
unchanged

Signature 1

Needs review

Curated date: 2024/10/23

Curator: Aleru Divine

Revision editor(s): Aleru Divine

Source: Figure 7B

Description: Differential abundance in the microbiota of sickle cell anaemia (SCA) children with < 5% of HbF compared SCA children with < 5% of HbF.

Abundance in Group 1: increased abundance in Foetal haemoglobin level > 5%

NCBI Quality ControlLinks
Ruminococcus

Revision editor(s): Aleru Divine

Signature 2

Needs review

Curated date: 2024/10/23

Curator: Aleru Divine

Revision editor(s): Aleru Divine

Source: Figure 7B

Description: Differential abundance in the microbiota of sickle cell anaemia (SCA) children with < 5% of HbF compared SCA children with < 5% of HbF.

Abundance in Group 1: decreased abundance in Foetal haemoglobin level > 5%

NCBI Quality ControlLinks
Kandleria

Revision editor(s): Aleru Divine