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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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