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A new cecal slurry preparation protocol with improved long-term reproducibility for animal models of sepsis

Producción científica: Articlerevisión exhaustiva

156 Citas (Scopus)

Resumen

Sepsis, a life-threatening systemic inflammatory response syndrome induced by infection, is widely studied using laboratory animal models. While cecal-ligation and puncture (CLP) is considered the gold standard model for sepsis research, it may not be preferable for experiments comparing animals of different size or under different dietary regimens. By comparing cecum size, shape, and cecal content characteristics in mice under different experimental conditions (aging, diabetes, pancreatitis), we show that cecum variability could be problematic for some CLP experiments. The cecal slurry (CS) injection model, in which the cecal contents of a laboratory animal are injected intraperitoneally to other animals, is an alternative method for inducing polymicrobial sepsis; however, the CS must be freshly prepared under conventional protocols, which is a major disadvantage with respect to reproducibility and convenience. The objective of this study was to develop an improved CS preparation protocol that allows for long-term storage of CS with reproducible results. Using our new CS preparation protocol we found that bacterial viability is maintained for at least 6 months when the CS is prepared in 15% glycerol-PBS and stored at -80°C. To test sepsis-inducing efficacy of stored CS stocks, various amounts of CS were injected to young (4-6 months old), middleaged (12-14 months old), and aged (24-26 months old) male C57BL/6 mice. Doseand age-dependent mortality was observed with high reproducibility. Circulating bacteria levels strongly correlated with mortality suggesting an infection-mediated death. Further, injection with heat-inactivated CS resulted in acute hypothermia without mortality, indicating that CS-mediated death is not due to endotoxic shock. This new CS preparation protocol results in CS stocks which are durable for.

Idioma originalEnglish
Número de artículoe115705
PublicaciónPLoS ONE
Volumen9
N.º12
DOI
EstadoPublished - dic 22 2014

Nota bibliográfica

Publisher Copyright:
© 2014 Starr et al.

Financiación

This research was supported by the National Institutes of Health grants (R01 AG039732). The authors would like to thank Ms. Donna Gilbreath of the Markey Cancer Center Research Communications Office for illustrative assistance.

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)R01 AG03973
National Institutes of Health (NIH)
National Institute on AgingR01AG039732
National Institute on Aging

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