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Microbial interactions impact the growth response of Clostridioides difficile to antibiotics
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ABSTRACT
In the human gut, the growth of
Clostridioides difficile
is impacted by a complex web of inter-species interactions with members of human gut microbiota. We investigate the contribution of inter-species interactions on the antibiotic response of
C. difficile
to clinically relevant antibiotics using bottom-up assembly of human gut communities. We discover two classes of microbial interactions that alter
C.
difficile’s antibiotic susceptibility: infrequent increases in tolerance at high antibiotic concentrations and frequent growth enhancements at low antibiotic concentrations. Based on genome-wide transcriptional profiling data, we demonstrate that metal sequestration due to hydrogen sulfide production by the prevalent gut species
Desulfovibrio piger
increases metronidazole tolerance of
C. difficile
. Competition with species that display higher sensitivity to the antibiotic than
C. difficile
leads to enhanced growth of
C. difficile
at low antibiotic concentrations. A dynamic computational model identifies the ecological design principles driving this effect. Our results provide a deeper understanding of ecological and molecular principles shaping
C. difficile
’s response to antibiotics, which could inform therapeutic interventions.
Title: Microbial interactions impact the growth response of
Clostridioides difficile
to antibiotics
Description:
ABSTRACT
In the human gut, the growth of
Clostridioides difficile
is impacted by a complex web of inter-species interactions with members of human gut microbiota.
We investigate the contribution of inter-species interactions on the antibiotic response of
C.
difficile
to clinically relevant antibiotics using bottom-up assembly of human gut communities.
We discover two classes of microbial interactions that alter
C.
difficile’s antibiotic susceptibility: infrequent increases in tolerance at high antibiotic concentrations and frequent growth enhancements at low antibiotic concentrations.
Based on genome-wide transcriptional profiling data, we demonstrate that metal sequestration due to hydrogen sulfide production by the prevalent gut species
Desulfovibrio piger
increases metronidazole tolerance of
C.
difficile
.
Competition with species that display higher sensitivity to the antibiotic than
C.
difficile
leads to enhanced growth of
C.
difficile
at low antibiotic concentrations.
A dynamic computational model identifies the ecological design principles driving this effect.
Our results provide a deeper understanding of ecological and molecular principles shaping
C.
difficile
’s response to antibiotics, which could inform therapeutic interventions.
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