Effect of Antimicrobial Prophylaxis on Corynebacterium bovis Infection and the Skin Microbiome of Immunodeficient Mice

Author:

Manuel Christopher A1,Johnson Linda K2,Pugazhenthi Uma3,Fong Derek L4,Fink Michaelk5,Habenicht Lauren M4,Leszczynski Jori K4,Diana IR6,Charles E Robertson 6,Schurr Michael J7,Frank Daniel N6

Affiliation:

1. Office of Laboratory Animal Resources, University of Colorado Cancer Center, Aurora, CO; Department of Pathology, University of Colorado Cancer Center, Aurora, CO; University of Colorado Cancer Center, Aurora, CO;, Email: chris.manuel@cuanschutz.edu

2. Department of Pathology, University of Colorado Cancer Center, Aurora, CO; Deceased

3. Division of Endocrinology, Metabolism, and Diabetes, University of Colorado Anschutz Medical Campus, Aurora, CO

4. Office of Laboratory Animal Resources, University of Colorado Cancer Center, Aurora, CO; Department of Pathology, University of Colorado Cancer Center, Aurora, CO

5. Office of Laboratory Animal Resources, University of Colorado Cancer Center, Aurora, CO; Department of Pathology; University of Colorado Cancer Center, Aurora, CO

6. Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO

7. Department of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO

Abstract

Corynebacterium bovis is an opportunistic pathogen of the skin of immunodeficient mice and is sensitive to oral antibiotics that reach therapeutic blood concentrations. However, prophylactic antibiotics are considered to be ineffective at preventing C. bovis infection. In addition, the effect of C. bovis on the skin microbiome (SM) of common immunodeficient mouse strains has yet to be characterized. Consequently, we evaluated whether oral prophylactic antibiotics prevent C. bovis infection after inoculation. An infectious dose of C. bovis was applied to the skin of Hsd:Athymic Nude (nude) and NOD. Cg-Prkdcscid Il2rgtm1Wjl/SzJ (NSG) mice. Mice were then housed individually and assigned randomly to receive either untreated drinking water (Cb+Abx–group) or prophylactic amoxicillin-clavulanic acid in the drinking water (0.375 mg/mL) for 14 d (Cb+Abx+group). A third treatment group of each mouse strain was uninoculated and untreated (Cb–Abx–group). Mice from all groups were serially sampled by using dermal swabs to monitor C. bovis infection via quantitative real-time PCR and the SM via 16S rRNA sequence analysis. Fourteen days of prophylactic antibiotics prevented the perpetuation of C. bovis skin infection in both strains. Only the combination of C. bovis inoculation and oral antibiotics (Cb+Abx+) significantly affected the SM of NSG mice at day 14; this effect resolved by the end of the study (day 70). In mice that did not receive antibiotics, C. bovis significantly altered the SM of nude mice but not NSG mice at days 14 and 70. These findings demonstrate the potential benefit of prophylactic antibiotics for prevention of C. bovis infection. However, indirect effect of antibiotics on commensal bacteria and potential effects on xenograft models must be considered.

Publisher

American Association for Laboratory Animal Science

Subject

General Veterinary,General Biochemistry, Genetics and Molecular Biology

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