Quantitative characterization of Clostridioides difficile population in the gut microbiome of patients with C. difficile infection and their association with clinical factors
Objective was to analyse bacterial composition and abundance of Clostridioides difficile in gut microbiome of patients with C. difficile infection (CDI) in association with clinical characteristics. Whole metagenome sequencing of gut microbiome of 26 CDI patients was performed, and the relative abun...
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Veröffentlicht in: | Scientific reports 2020-10, Vol.10 (1), p.17608-17608, Article 17608 |
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Zusammenfassung: | Objective was to analyse bacterial composition and abundance of
Clostridioides difficile
in gut microbiome of patients with
C. difficile
infection (CDI) in association with clinical characteristics. Whole metagenome sequencing of gut microbiome of 26 CDI patients was performed, and the relative abundance of
C. difficile
and its toxin genes was measured. Clinical characteristics of the patients were obtained through medical records. A strong correlation between the abundance of
C. difficile
and
tcdB
genes in CDI patients was found. The relative abundance of
C. difficile
in the gut microbiome ranged from undetectable to 2.8% (median 0.089)
.
Patients with fever exhibited low abundance of
C. difficile
in their gut, and patients with fewer
C. difficile
organisms required long-term anti-CDI treatment. Abundance of
Bifidobacterium
and
Bacteroides
negatively correlated with that of
C. difficile
at the genus level. CDI patients were clustered using the bacterial composition of the gut: one with high population of
Enterococcus
(cluster 1, n = 12) and another of
Bacteroides
or
Lactobacillus
(cluster 2, n = 14). Cluster1 showed significantly lower bacterial diversity and clinical cure at the end of treatment. Additionally, patients with CDI exhibited increased ARGs; notably,
bla
TEM
, bla
SHV
and
bla
CTX-M
were enriched.
C. difficile
existed in variable proportion of the gut microbiome in CDI patients. CDI patients with
Enterococcus
-rich microbiome in the gut had lower bacterial diversity and poorer clinical cure. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-020-74090-0 |