Intestinal microbiota profiles of captive-bred cynomolgus macaques reveal influence of biogeography and age
Abstract Background Age-associated changes to the intestinal microbiome may be linked to inflammageing and the development of age-related chronic diseases. Cynomolgus macaques, a common animal model in biomedical research, have strong genetic physiological similarities to humans and may serve as ben...
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BMC
2025-05-01
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| Series: | Animal Microbiome |
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| Online Access: | https://doi.org/10.1186/s42523-025-00409-9 |
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| author | C. Purse A. Parker S. A. James D. J. Baker C. J. Moss R. Evans J. Durham S. G. P. Funnell S. R. Carding |
| author_facet | C. Purse A. Parker S. A. James D. J. Baker C. J. Moss R. Evans J. Durham S. G. P. Funnell S. R. Carding |
| author_sort | C. Purse |
| collection | DOAJ |
| description | Abstract Background Age-associated changes to the intestinal microbiome may be linked to inflammageing and the development of age-related chronic diseases. Cynomolgus macaques, a common animal model in biomedical research, have strong genetic physiological similarities to humans and may serve as beneficial models for the effect of age on the human microbiome. However, age-associated changes to their intestinal microbiome have previously only been investigated in faecal samples. Here, we have characterised and investigated the effects of age in the cynomolgus macaque intestinal tract in luminal samples from both the small and large intestine. Results Whole metagenomic shotgun sequencing was used to analyse the microbial communities in intestinal content obtained from six different intestinal regions, covering the duodenum to distal colon, of 24 healthy, captive-bred cynomolgus macaques, ranging in age from 4 to 20 years. Both reference-based and assembly-based computational profiling approaches were used to analyse changes to intestinal microbiota composition and metabolic potential associated with intestinal biogeography and age. Reference-based computational profiling revealed a significant and progressive increase in both species richness and evenness along the intestinal tract. The microbial community composition also significantly differed between the small intestine, caecum, and colon. Notably, no significant changes in the taxonomic abundance of individual taxa with age were found except when sex was included as a covariate. Additionally, using an assembly-based computational profiling approach, 156 putative novel bacterial and archaeal species were identified. Conclusions We observed limited effects of age on the composition of the luminal microbiota in the profiled regions of the intestinal tract except when sex was included as a covariate. The enteric microbial communities of the small and the large intestine were, however, distinct, highlighting the limitations of frequently used faecal microbial profiling as a proxy for the intestinal microbiota. The identification of a number of putative novel microbial taxa contributes to knowledge of the full diversity of the cynomolgus macaque intestinal microbiome. |
| format | Article |
| id | doaj-art-5e1efc2143d54fb9aefe169fcafacbd1 |
| institution | Kabale University |
| issn | 2524-4671 |
| language | English |
| publishDate | 2025-05-01 |
| publisher | BMC |
| record_format | Article |
| series | Animal Microbiome |
| spelling | doaj-art-5e1efc2143d54fb9aefe169fcafacbd12025-08-20T03:48:06ZengBMCAnimal Microbiome2524-46712025-05-017112110.1186/s42523-025-00409-9Intestinal microbiota profiles of captive-bred cynomolgus macaques reveal influence of biogeography and ageC. Purse0A. Parker1S. A. James2D. J. Baker3C. J. Moss4R. Evans5J. Durham6S. G. P. Funnell7S. R. Carding8Food, Microbiome and Health, Quadram Institute Bioscience, Norwich Research ParkFood, Microbiome and Health, Quadram Institute Bioscience, Norwich Research ParkFood, Microbiome and Health, Quadram Institute Bioscience, Norwich Research ParkFood, Microbiome and Health, Quadram Institute Bioscience, Norwich Research ParkFood, Microbiome and Health, Quadram Institute Bioscience, Norwich Research ParkFood, Microbiome and Health, Quadram Institute Bioscience, Norwich Research ParkUK Health Security AgencyFood, Microbiome and Health, Quadram Institute Bioscience, Norwich Research ParkFood, Microbiome and Health, Quadram Institute Bioscience, Norwich Research ParkAbstract Background Age-associated changes to the intestinal microbiome may be linked to inflammageing and the development of age-related chronic diseases. Cynomolgus macaques, a common animal model in biomedical research, have strong genetic physiological similarities to humans and may serve as beneficial models for the effect of age on the human microbiome. However, age-associated changes to their intestinal microbiome have previously only been investigated in faecal samples. Here, we have characterised and investigated the effects of age in the cynomolgus macaque intestinal tract in luminal samples from both the small and large intestine. Results Whole metagenomic shotgun sequencing was used to analyse the microbial communities in intestinal content obtained from six different intestinal regions, covering the duodenum to distal colon, of 24 healthy, captive-bred cynomolgus macaques, ranging in age from 4 to 20 years. Both reference-based and assembly-based computational profiling approaches were used to analyse changes to intestinal microbiota composition and metabolic potential associated with intestinal biogeography and age. Reference-based computational profiling revealed a significant and progressive increase in both species richness and evenness along the intestinal tract. The microbial community composition also significantly differed between the small intestine, caecum, and colon. Notably, no significant changes in the taxonomic abundance of individual taxa with age were found except when sex was included as a covariate. Additionally, using an assembly-based computational profiling approach, 156 putative novel bacterial and archaeal species were identified. Conclusions We observed limited effects of age on the composition of the luminal microbiota in the profiled regions of the intestinal tract except when sex was included as a covariate. The enteric microbial communities of the small and the large intestine were, however, distinct, highlighting the limitations of frequently used faecal microbial profiling as a proxy for the intestinal microbiota. The identification of a number of putative novel microbial taxa contributes to knowledge of the full diversity of the cynomolgus macaque intestinal microbiome.https://doi.org/10.1186/s42523-025-00409-9Non-human primateCynomolgus macaqueMicrobiomeAgeingIntestinal biogeographyMetagenomics |
| spellingShingle | C. Purse A. Parker S. A. James D. J. Baker C. J. Moss R. Evans J. Durham S. G. P. Funnell S. R. Carding Intestinal microbiota profiles of captive-bred cynomolgus macaques reveal influence of biogeography and age Animal Microbiome Non-human primate Cynomolgus macaque Microbiome Ageing Intestinal biogeography Metagenomics |
| title | Intestinal microbiota profiles of captive-bred cynomolgus macaques reveal influence of biogeography and age |
| title_full | Intestinal microbiota profiles of captive-bred cynomolgus macaques reveal influence of biogeography and age |
| title_fullStr | Intestinal microbiota profiles of captive-bred cynomolgus macaques reveal influence of biogeography and age |
| title_full_unstemmed | Intestinal microbiota profiles of captive-bred cynomolgus macaques reveal influence of biogeography and age |
| title_short | Intestinal microbiota profiles of captive-bred cynomolgus macaques reveal influence of biogeography and age |
| title_sort | intestinal microbiota profiles of captive bred cynomolgus macaques reveal influence of biogeography and age |
| topic | Non-human primate Cynomolgus macaque Microbiome Ageing Intestinal biogeography Metagenomics |
| url | https://doi.org/10.1186/s42523-025-00409-9 |
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