Murine chapparvovirus (MuCPV)/mouse kidney parvovirus (MKPV) eradication by cross foster rederivation

Ibrahim Faseeh1,2, Vatthana Vongphakham3, Patrick Sharp1,3,4

  • 1Animal Resources Centre, Murdoch, Western Australia, Australia.

Laboratory Animals
|February 4, 2025
PubMed

Insights

Mouse kidney parvovirus (MKPV) was eradicated from a specific-pathogen-free (SPF) barrier using cross-foster (XF) rederivation. This method, combined with disinfection, offers a solution for controlling persistent viral agents in research settings.

Area of Science:

  • Veterinary Virology
  • Laboratory Animal Science
  • Infectious Disease Control

Background:

  • Mouse kidney parvovirus (MKPV), also known as murine chapparvovirus (MuCPV), is a novel viral agent.
  • MKPV was detected in the specific-pathogen-free (SPF) barrier area of an animal research facility, primarily in imported mice from non-approved vendors.

Purpose of the Study:

  • To determine the prevalence of MKPV in a research facility.
  • To eradicate MKPV from the SPF barrier area.
  • To evaluate the efficacy of different eradication methods.

Main Methods:

  • Facility-wide screening for MKPV using diagnostic tests.
  • Implementation of a multi-modal eradication approach including testing, cage separation, and cross-foster (XF) rederivation.
  • Monitoring of rederived mice for MKPV negativity over a 20-week period.

Main Results:

  • MKPV was exclusively found in the SPF barrier area, linked to imported mice.
  • A test-and-separate strategy proved ineffective due to MKPV's environmental stability and high infectivity.
  • Cross-foster (XF) rederivation successfully produced 11 MKPV-negative litters from 16 attempts.

Conclusions:

  • Cross-foster (XF) rederivation is an effective method for eradicating MKPV from research animal colonies.
  • XF rederivation, alongside stringent disinfection, can be applied to control other persistent and highly infectious viral agents.
  • This study highlights the importance of import controls and effective rederivation techniques in maintaining pathogen-free research animal populations.

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