Publication | Open Access
Antibiotic Treatment of <i>Clostridium difficile</i> Carrier Mice Triggers a Supershedder State, Spore-Mediated Transmission, and Severe Disease in Immunocompromised Hosts
352
Citations
48
References
2009
Year
DysbiosisMicrobial PathogensImmunologyBacterial PathogensHost ResponseMedical MicrobiologyInfection CyclePathogen TransmissionSevere DiseaseInfectious SporesInfection ControlIntestinal MicrobiotaAntimicrobial ResistanceHost-pathogen InteractionsSpore-mediated TransmissionSupershedder StateHost-microbe InteractionMicrobiomeClinical MicrobiologyAntibiotic TreatmentPathogenicityMicrobial DiseaseMucosal ImmunologyAntibioticsPathogenesisMicrobiologyGut BarrierMedicine
Clostridium difficile persists in hospitals by exploiting an infection cycle that depends on humans shedding highly resistant, infectious spores. The study aims to use mice as a surrogate model to investigate stages of the C. difficile infection cycle, spore‑mediated transmission, and host–microbiota interactions to inform infection control.
Clostridium difficile persists in hospitals by exploiting an infection cycle that is dependent on humans shedding highly resistant and infectious spores. Here we show that human virulent C. difficile can asymptomatically colonize the intestines of immunocompetent mice, establishing a carrier state that persists for many months. C. difficile carrier mice consistently shed low levels of spores but, surprisingly, do not transmit infection to cohabiting mice. However, antibiotic treatment of carriers triggers a highly contagious supershedder state, characterized by a dramatic reduction in the intestinal microbiota species diversity, C. difficile overgrowth, and excretion of high levels of spores. Stopping antibiotic treatment normally leads to recovery of the intestinal microbiota species diversity and suppresses C. difficile levels, although some mice persist in the supershedding state for extended periods. Spore-mediated transmission to immunocompetent mice treated with antibiotics results in self-limiting mucosal inflammation of the large intestine. In contrast, transmission to mice whose innate immune responses are compromised (Myd88(-/-)) leads to a severe intestinal disease that is often fatal. Thus, mice can be used to investigate distinct stages of the C. difficile infection cycle and can serve as a valuable surrogate for studying the spore-mediated transmission and interactions between C. difficile and the host and its microbiota, and the results obtained should guide infection control measures.
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