Microbial community structure and composition is associated with host species and sex in Sigmodon cotton rats.
Britton A Strickland, Mira C Patel, Meghan H Shilts, Helen H Boone, Arash Kamali, Wei Zhang, Daniel Stylos, Marina S Boukhvalova, Christian Rosas-Salazar, Shibu Yooseph, Seesandra V Rajagopala, Jorge C G Blanco, Suman R Das
Author Information
Britton A Strickland: Pathology Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Mira C Patel: Sigmovir Biosystems Inc., 9610 Medical Center Drive, Suite 100, Rockville, MD, 20850, USA.
Meghan H Shilts: Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Helen H Boone: Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Arash Kamali: Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Wei Zhang: Sigmovir Biosystems Inc., 9610 Medical Center Drive, Suite 100, Rockville, MD, 20850, USA.
Daniel Stylos: Sigmovir Biosystems Inc., 9610 Medical Center Drive, Suite 100, Rockville, MD, 20850, USA.
Marina S Boukhvalova: Sigmovir Biosystems Inc., 9610 Medical Center Drive, Suite 100, Rockville, MD, 20850, USA.
Christian Rosas-Salazar: Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Shibu Yooseph: Department of Computer Science, Genomics and Bioinformatics Cluster, University of Central Florida, Orlando, FL, USA.
Seesandra V Rajagopala: Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Jorge C G Blanco: Sigmovir Biosystems Inc., 9610 Medical Center Drive, Suite 100, Rockville, MD, 20850, USA. j.blanco@sigmovir.com.
Suman R Das: Pathology Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA. suman.r.das@vanderbilt.edu. ORCID
BACKGROUND: The cotton rat (genus Sigmodon) is an essential small animal model for the study of human infectious disease and viral therapeutic development. However, the impact of the host microbiome on infection outcomes has not been explored in this model, partly due to the lack of a comprehensive characterization of microbial communities across different cotton rat species. Understanding the dynamics of their microbiome could significantly help to better understand its role when modeling viral infections in this animal model. RESULTS: We examined the bacterial communities of the gut and three external sites (skin, ear, and nose) of two inbred species of cotton rats commonly used in research (S. hispidus and S. fulviventer) by using 16S rRNA gene sequencing, constituting the first comprehensive characterization of the cotton rat microbiome. We showed that S. fulviventer maintained higher alpha diversity and richness than S. hispidus at external sites (skin, ear, nose), but there were no differentially abundant genera. However, S. fulviventer and S. hispidus had distinct fecal microbiomes composed of several significantly differentially abundant genera. Whole metagenomic shotgun sequencing of fecal samples identified species-level differences between S. hispidus and S. fulviventer, as well as different metabolic pathway functions as a result of differential host microbiome contributions. Furthermore, the microbiome composition of the external sites showed significant sex-based differences while fecal communities were not largely different. CONCLUSIONS: Our study shows that host genetic background potentially exerts homeostatic pressures, resulting in distinct microbiomes for two different inbred cotton rat species. Because of the numerous studies that have uncovered strong relationships between host microbiome, viral infection outcomes, and immune responses, our findings represent a strong contribution for understanding the impact of different microbial communities on viral pathogenesis. Furthermore, we provide novel cotton rat microbiome data as a springboard to uncover the full therapeutic potential of the microbiome against viral infections.
