Temperature Influences Commensal-Pathogen Dynamics in a Nasal Epithelial Cell Co-culture Model

Abstract

ABSTRACTChronic rhinosinusitis (CRS) is an inflammatory disease of the paranasal sinuses, and microbial dysbiosis associated with CRS is thought to be a key driver of host inflammation that contributes to disease progression.Staphylococcus aureusis a common upper respiratory tract (URT) pathobiont that is associated with higher carriage rates in CRS populations, whereS. aureussecreted toxins can be identified in CRS tissue samples. Although many genera of bacteria colonize the URT, relatively few account for the majority of sequencing reads. These includeS. aureus, as well as several species belonging to the genusCorynebacterium, includingCorynebacterium propinquumandCorynebacterium pseudodiphtheriticum, which are observed at high relative abundance in the URT of healthy individuals. Studies have examined the bacterial interactions between the major microbionts of the URT andS. aureus, but few have done so in the context of a healthy versus diseased URT environment. Here, we examine the role of temperature in commensal, pathogen, and epithelial dynamics using an air-liquid interface cell culture model mimicking the nasal epithelial environment. The healthy URT temperature changes from the nares to the nasopharynx and is altered during disease. Temperatures representative of the healthy URT increase persistence and aggregate formation of commensalC. propinquum and C. pseudodiphtheriticum, reduceS. aureusgrowth, and lower epithelial cytotoxicity compared to higher temperatures correlating with the diseased CRS sinus. Dual-species colonization revealed species-specific interactions between commensalCorynebacteriumspecies andS. aureusdependent on temperature. Our findings suggest that URT mucosal temperature plays a significant role in mediating polymicrobial and host-bacterial interactions that may exacerbate microbial dysbiosis found in chronic URT disease.IMPORTANCEChronic rhinosinusitis is a complex inflammatory disease with a significant healthcare burden. Although presence ofS. aureusand microbial dysbiosis are considered mediators of inflammation in CRS, no studies have examined the influence of temperature onS. aureusinteractions with the nasal epithelium and the dominant genus of the healthy URT,Corynebacterium. Interactions betweenCorynebacterium speciesandS. aureushave been documented in several studies, but none to date have examined how environmental changes in the URT may alter their interactions with the epithelium or each other. This study utilizes a polarized epithelial cell culture model at air-liquid interface to study the colonization and spatial dynamics ofS. aureusand clinical isolates ofCorynebacteriumfrom people with CRS to characterize the role temperature has in single-and dual-species dynamics on the nasal epithelium.