TY - JOUR
T1 - Ecology and Machine Learning-Based Classification Models of Gut Microbiota and Inflammatory Markers May Evaluate the Effects of Probiotic Supplementation in Patients Recently Recovered from COVID-19
AU - Laterza, Lucrezia
AU - Putignani, Lorenza
AU - Settanni, Carlo Romano
AU - Petito, Valentina
AU - Varca, Simone
AU - De Maio, Flavio
AU - Macari, Gabriele
AU - Guarrasi, Valerio
AU - Gremese, Elisa
AU - Tolusso, Barbara
AU - Wlderk, Giulia
AU - Pirro, Maria Antonia
AU - Fanali, Caterina
AU - Scaldaferri, Franco
AU - Turchini, Laura
AU - Amatucci, Valeria
AU - Sanguinetti, Maurizio
AU - Gasbarrini, Antonio
PY - 2023
Y1 - 2023
N2 - Gut microbiota (GM) modulation can be investigated as possible solution to enhance recovery after COVID-19. An open-label, single-center, single-arm, pilot, interventional study was performed by enrolling twenty patients recently recovered from COVID-19 to investigate the role of a mixed probiotic, containing Lactobacilli, Bifidobacteria and Streptococcus thermophilus, on gastrointestinal symptoms, local and systemic inflammation, intestinal barrier integrity and GM profile. Gastrointestinal Symptom Rating Scale, cytokines, inflammatory, gut permeability, and integrity markers were evaluated before (T-0) and after 8 weeks (T-1) of probiotic supplementation. GM profiling was based on 16S-rRNA targeted-metagenomics and QIIME 2.0, LEfSe and PICRUSt computational algorithms. Multiple machine learning (ML) models were trained to classify GM at T-0 and T-1. A statistically significant reduction of IL-6 (p < 0.001), TNF-a (p < 0.001) and IL-12RA (p < 0.02), citrulline (p value < 0.001) was reported at T-1. GM global distribution and microbial biomarkers strictly reflected probiotic composition, with a general increase in Bifidobacteria at T-1. Twelve unique KEGG orthologs were associated only to T-0, including tetracycline resistance cassettes. ML classified the GM at T-1 with 100% score at phylum level. Bifidobacteriaceae and Bifidobacterium spp. inversely correlated to reduction of citrulline and inflammatory cytokines. Probiotic supplementation during post-COVID-19 may trigger anti-inflammatory effects though Bifidobacteria and related-metabolism enhancement.
AB - Gut microbiota (GM) modulation can be investigated as possible solution to enhance recovery after COVID-19. An open-label, single-center, single-arm, pilot, interventional study was performed by enrolling twenty patients recently recovered from COVID-19 to investigate the role of a mixed probiotic, containing Lactobacilli, Bifidobacteria and Streptococcus thermophilus, on gastrointestinal symptoms, local and systemic inflammation, intestinal barrier integrity and GM profile. Gastrointestinal Symptom Rating Scale, cytokines, inflammatory, gut permeability, and integrity markers were evaluated before (T-0) and after 8 weeks (T-1) of probiotic supplementation. GM profiling was based on 16S-rRNA targeted-metagenomics and QIIME 2.0, LEfSe and PICRUSt computational algorithms. Multiple machine learning (ML) models were trained to classify GM at T-0 and T-1. A statistically significant reduction of IL-6 (p < 0.001), TNF-a (p < 0.001) and IL-12RA (p < 0.02), citrulline (p value < 0.001) was reported at T-1. GM global distribution and microbial biomarkers strictly reflected probiotic composition, with a general increase in Bifidobacteria at T-1. Twelve unique KEGG orthologs were associated only to T-0, including tetracycline resistance cassettes. ML classified the GM at T-1 with 100% score at phylum level. Bifidobacteriaceae and Bifidobacterium spp. inversely correlated to reduction of citrulline and inflammatory cytokines. Probiotic supplementation during post-COVID-19 may trigger anti-inflammatory effects though Bifidobacteria and related-metabolism enhancement.
KW - gut microbiota
KW - probiotic supplementation
KW - post-COVID-19
KW - gut microbiota
KW - probiotic supplementation
KW - post-COVID-19
UR - http://hdl.handle.net/10807/240235
U2 - 10.3390/ijms24076623
DO - 10.3390/ijms24076623
M3 - Article
SN - 1422-0067
VL - 24
SP - 6623-N/A
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
ER -