AI Article Synopsis

  • This study sequenced sputum samples from 120 TB patients in Uganda to explore how microbiota changes with treatment and HIV status.
  • Major bacterial groups found were Bacteroidetes, Firmicutes, and Proteobacteria, with specific genera changing in abundance at different treatment follow-ups (months 2 and 5).
  • The research revealed a decrease in microbial diversity linked to HIV status and TB treatment, suggesting that microbiota analysis could be useful for monitoring treatment responses.

Article Abstract

Information on microbiota dynamics in pulmonary tuberculosis (TB) in Africa is scarce. Here, we sequenced sputa from 120 treatment-naïve TB patients in Uganda, and investigated changes in microbiota of 30 patients with treatment-response follow-up samples. Overall, HIV-status and anti-TB treatment were associated with microbial structural and abundance changes. The predominant phyla were Bacteroidetes, Firmicutes, Proteobacteria, Fusobacteria and Actinobacteria, accounting for nearly 95% of the sputum microbiota composition; the predominant genera across time were Prevotella, Streptococcus, Veillonella, Haemophilus, Neisseria, Alloprevotella, Porphyromonas, Fusobacterium, Gemella, and Rothia. Treatment-response follow-up at month 2 was characterized by a reduction in abundance of Mycobacterium and Fretibacterium, and an increase in Ruminococcus and Peptococcus; month 5 was characterized by a reduction in Tannerella and Fusobacterium, and an increase in members of the family Neisseriaceae. The microbiota core comprised of 44 genera that were stable during treatment. Hierarchical clustering of this core's abundance distinctly separated baseline (month 0) samples from treatment follow-up samples (months 2/5). We also observed a reduction in microbial diversity with 9.1% (CI 6-14%) of the structural variation attributed to HIV-status and anti-TB treatment. Our findings show discernible microbiota signals associated with treatment with potential to inform anti-TB treatment response monitoring.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8716532PMC
http://dx.doi.org/10.1038/s41598-021-04271-yDOI Listing

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