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

Mariana Delgadinho1, Catarina Ginete1, Brígida Santos2,3

  • 1H&TRC- Health & Technology Research Center, ESTeSL- Escola Superior de Tecnologia da Saúde, Instituto Politécnico de Lisboa, Lisbon, Portugal.

Insights

Sickle cell disease (SCD) in Angolan children alters the gut microbiome, with SCA patients showing higher Actinobacteria and Clostridium cluster XI. This highlights differences from healthy siblings, impacting potential therapies.

Area of Science:

  • Microbiology
  • Genetics
  • Pediatrics

Background:

  • Sickle cell disease (SCD) is a prevalent genetic disorder globally, causing significant under-5 mortality in sub-Saharan Africa.
  • The gut microbiome plays a role in SCD's inflammation and vaso-occlusive crises.
  • Previous studies indicate gut dysbiosis, including enterocyte injury and increased permeability, in SCD patients.

Purpose of the Study:

  • To characterize the gut microbiome of Angolan children with SCD using 16S rRNA gene sequencing.
  • To compare the gut microbiota composition between children with SCD and their healthy siblings.

Main Methods:

  • Collected 72 stool samples from children aged 3-14 years.
  • Sequenced the bacterial 16S rRNA gene to analyze microbiota composition.
  • Compared microbial relative abundance at phylum and genus levels between SCD patients and controls.

Main Results:

  • Significant differences in gut microbiota were observed between children with SCD and healthy siblings.
  • Children with SCD exhibited a higher abundance of the phylum Actinobacteria.
  • The genus Clostridium cluster XI was more prevalent in SCA children, while healthy siblings showed higher levels of Blautia, Aestuariispira, Campylobacter, Helicobacter, Polaribacter, and Anaerorhabdus.

Conclusions:

  • This study presents the first microbiota analysis in Angolan pediatric SCD patients.
  • Distinct microbial differences exist between SCD patients and healthy controls in this population.
  • Further research is needed to understand gut modulation therapies for SCD.

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