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Detection and elimination of contaminating microorganisms in transplantable tumors and cell lines

N Nakai1, C Kawaguchi, K Nawa

  • 1Developmental Research Laboratory, Nippon Shinyaku Co., Ltd., Kyoto, Japan.

Experimental Animals
|December 8, 2000
PubMed

Insights

Microbiological contamination, including lactic dehydrogenase elevating virus (LDV), mycoplasmas, and Pasteurella pneumotropica, is a significant risk in transplantable tumors. Effective elimination strategies exist, highlighting the need for stringent quality control in biological material quarantine.

Area of Science:

  • Microbiology
  • Cell Biology
  • Animal Models

Background:

  • Transplantable tumors and cell lines are crucial research tools.
  • Microbiological contamination poses a significant threat to experimental validity.
  • Existing quarantine protocols require rigorous microbiological assessment.

Purpose of the Study:

  • To assess the microbial contamination status of 96 transplantable tumors and cell lines.
  • To identify common contaminants and compare contamination rates between in vivo and in vitro propagated tumors.
  • To evaluate the efficacy of different methods for eliminating detected contaminants.

Main Methods:

  • Mouse antibody production (MAP) test.
  • Enzymatic assays.
  • Microbiological cultures.
  • In vitro subculture and subpassage in nude rats or mice.
  • Mycoplasma removal agents.

Main Results:

  • Contamination with lactic dehydrogenase elevating virus (LDV), mycoplasmas, and Pasteurella pneumotropica was detected in tested samples.
  • A notable difference in contamination rates was observed between tumors propagated in vivo versus in vitro.
  • LDV was eliminated by in vitro subculture and subpassage in nude rats.
  • Mycoplasmas were eradicated using a mycoplasma-removal agent.
  • Pasteurella pneumotropica was eliminated through subpassage in mice.

Conclusions:

  • Transplantable tumors carry a substantial risk of microbial contamination.
  • Adequate microbiological quality control is essential for biological material quarantine.
  • Specific methods can effectively eliminate common contaminants like LDV, mycoplasmas, and P. pneumotropica.

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