Abstract
In late 2020, the mouse barrier facility at Stanford University experienced an outbreak of diarrhea in adult mice and sudden deaths in mid-lactation females. Affected strains were immunodeficient, carrying either the Prkdcscid or Ragnull mutations and the Il2rγnull mutation, predominantly NOD.Cg-Prkdcscid Il2rγtm1Wjl/SzJ (NSG) mice. The diarrhea was transmissible to naïve NSG mice by co-housing or gavage of intestinal homogenates from diarrheic mice, suggesting the involvement of an infectious agent and thus was given the name “infectious diarrhea.” Conventional testing failed to identify an etiology. Strain-resolved metagenomic analyses using DNA from diarrheic and control fecal samples yielded the genome sequence of an enterotoxin-encoding Clostridium cuniculi strain, a candidate factor underlying the diarrhea outbreak. We hypothesized that the presence of C. cuniculi and its enterotoxin in fecal samples could serve as biomarkers. Quantitative real-time PCR (qPCR) assays using specific primers for C. cuniculi and its enterotoxin were generated and validated. We analyzed fecal samples from 111 NSG or NSG-related mice that were healthy, 37 that had clinical signs of infectious diarrhea, and 28 that had diarrhea attributable to known causes. Positive qPCR results for C. cuniculi and its enterotoxin only occurred in feces from mice with infectious diarrhea. All positive samples contained both C. cuniculi and its enterotoxin. Our data suggest that infectious diarrhea in these cases is mediated, at least in part, by the transmission of C. cuniculi and its enterotoxin. Our novel qPCR assays for C. cuniculi and its enterotoxin are effective tools for the detection of infectious diarrhea in NSG mice.
Get full access to this article
View all access options for this article.
References
Supplementary Material
Please find the following supplemental material available below.
For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.
For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.
