Maternal antibodies or nonproductive infections confound the need for rederivation

Claude M Nagamine1, Lei Chen, Wen Qi Ho

  • 1Department of Comparative Medicine, Stanford University School of Medicine, Stanford, CA, USA. cnagamin@stanford.edu

Insights

Mouse parvovirus (MPV) seropositivity in rederived pups may not indicate infection. Further transmissibility testing is crucial before repeating rederivation procedures to ensure MPV eradication.

Area of Science:

  • Veterinary Virology
  • Laboratory Animal Science
  • Immunology

Background:

  • Mouse parvovirus (MPV) is a significant pathogen in research mouse colonies, necessitating effective rederivation strategies.
  • MPV contamination was identified in a transgenic mouse strain, prompting rederivation using a surrogate dam.
  • Standard protocols for rederivation include serological and PCR testing of surrogate dams and rederived offspring.

Observation:

  • A surrogate dam and three rederived pups tested positive for MPV-1 via serology.
  • Despite seropositivity, fecal PCR and sentinel contact tests for the pups were negative.
  • One surviving rederived male mouse successfully bred, with no evidence of MPV transmission to its progeny or mates.

Findings:

  • The rederived male mouse remained serologically and PCR-negative for MPV at 14.5 months of age.
  • Post-mortem examination of the rederived male's tissues also yielded negative MPV results.
  • The initial seropositivity in rederived pups is hypothesized to be due to passive maternal antibody transfer or a non-productive infection.

Implications:

  • Routine serological screening of surrogate mothers and pups is valuable but requires confirmation.
  • Positive serological results for MPV in rederived animals necessitate further investigation using transmissibility assays (fecal PCR, sentinel testing).
  • Accurate diagnosis is critical to prevent the reintroduction of MPV into cleared mouse colonies and ensure research integrity.

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