Chronic wound microbiome colonization on mouse model following cryogenic preservation

• Published in: PloS one 2019-08, Vol.14 (8), p.e0221565-e0221565
• Main Authors: Tipton, Craig D, Sanford, Nicholas E, Everett, Jake A, Gabrilska, Rebecca A, Wolcott, Randall D, Rumbaugh, Kendra P, Phillips, Caleb D
• Format: Article
• Language: English
• Subjects: Animal models; Animals; Archives & records; Bacterial Load; Biofilms; Biology and Life Sciences; Cell Survival; Chronic Disease; Chronic infection; Colonization; Communities; Community composition; Community structure; Complementation; Criminal investigation; Cryopreservation; Disease Models, Animal; Ecology and Environmental Sciences; Female; Freezing; Genes; Glycerol; Health sciences; Humans; Infection; Infections; Inoculation; Laboratory animals; Liquid nitrogen; Medicine and Health Sciences; Mice; Microbial activity; Microbiomes; Microbiota; Microbiota (Symbiotic organisms); Microorganisms; Nitrogen; Physical Sciences; Physiological aspects; Polymerase chain reaction; Refrigeration; Relative abundance; Research and Analysis Methods; RNA; rRNA 16S; Studies; Surgery; Surgical wound infections; Testing laboratories; Transplantation; Viability; Wetlands; Wound healing; Wounds; Wounds and Injuries - microbiology
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0221565

Chronic wound infections are increasingly recognized to be dynamic and polymicrobial in nature, necessitating the development of wound models which reflect the complexities of infection in a non-healing wound. Wound slough isolated from human chronic wounds and transferred to mice was recently shown to create polymicrobial infection in mice, and there is potential this tool may be improved by cryogenic preservation. The purpose of this study was to investigate the application of cryogenic preservation to transferring polymicrobial communities, specifically by quantifying the effects of cryopreservation and wound microbiome transplantation. Slough from an established murine polymicrobial surgical excision model and five patients were subjected to three preservation strategies: refrigeration until infection, freezing in liquid nitrogen, or freezing in liquid nitrogen with glycerol solution prior to infection in individual mice. Four days following inoculation onto mice, wound microbiota were quantified using either culture isolation or by 16s rRNA gene community profiling and quantitative PCR. Cryogenic preservation did not significantly reduce bacterial viability. Reestablished microbial communities were significantly associated with patient of origin as well as host context (i.e., originally preserved from a patient versus mouse infection). Whereas preservation treatment did not significantly shape community composition, the transfers of microbiomes from human to mouse were characterized by reduced diversity and compositional changes. These findings indicated that changes should be expected to occur to community structure after colonization, and that compositional change is likely due to the rapid change in infection context as opposed to preservation strategy. Furthermore, species that were present in higher relative abundance in wound inoculate were more likely to colonize subsequent wounds, and wound inoculate with higher bacterial load established wound communities that were more compositionally similar. Results inform expectations for the complementation of chronic wound in vivo modeling with cryogenic preservation archives.