Mounting evidence suggests that the cyclic interaction between host cells and the gut microbiota orchestrates metabolic and immunological homeostasis throughout the day. Yet, examples of gut microbial rhythms in natural populations are scarce, limiting our understanding of their downstream consequences for host health, particularly in mammals that demonstrate strong co-evolutionary links with their microbiota. Furthermore, disregarding diurnal microbial variation restricts our ability to account and control for them in future studies. Here, we re-analyzed gut microbiota data from a 23-year longitudinal field study of 12 wild adult female spotted hyenas (Crocuta crocuta) in the Masai Mara National Reserve in Kenya to examine whether time of day was correlated with variation in gut microbial composition in this crepuscular–nocturnal carnivore. Overall, we found that gut microbial composition and structure, but not alpha diversity, slightly changed over the course of the day. Differences in microbiota composition between morning and afternoon became particularly apparent when restricting the analysis to the core microbiota (i.e., bacterial genera present in more than 85% of samples). Among the core microbiota, 11 genera—composed largely of the bacterial class Clostridia—varied in abundance with time of day, making this the second study to document gut microbial rhythms in a longitudinally sampled wildlife population. In contrast with the diurnal gut microbial oscillations of wild meerkats, those of hyenas are subtle, yet both species exhibit shifts specifically in the bacterial class Clostridia. This pattern implies that diurnal fluctuations are likely a characteristic of specific, common host-associated bacteria and their amplitude may be a product of host ecology. While our study detected diurnal trends, we encourage studies to employ a temporally denser sampling scheme. In this way, one can overlay short-term oscillations of the microbiome with information on host ecology and clarify consequences for the circadian phenotype of the host.
- Award ID(s):
- 1853934
- PAR ID:
- 10132920
- Date Published:
- Journal Name:
- FEMS Microbiology Ecology
- Volume:
- 96
- Issue:
- 2
- ISSN:
- 0168-6496
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract -
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Abstract How social development in early‐life affects fitness remains poorly understood.
Though there is growing evidence that early‐life relationships can affect fitness, little research has investigated how social positions develop or whether there are particularly important periods for social position development in an animal's life history. In long‐lived species in particular, understanding the lasting consequences of early‐life social environments requires detailed, long‐term datasets.
Here we used a 25‐year dataset to test whether social positions held during early development predicted adult fitness. Specifically, we quantified social position using three social network metrics: degree, strength and betweenness. We determined the social position of each individual in three types of networks during each of three stages of ontogeny to test whether they predict annual reproductive success (ARS) or longevity among adult female spotted hyenas
Crocuta crocuta .The social positions occupied by juvenile hyenas did predict their fitness, but the effects of social position on fitness measures differed between stages of early development. Network metrics when individuals were young adults better predicted ARS, but network metrics for younger animals, particularly when youngsters were confined to the communal den, better predicted longevity than did metrics assessed during other stages of development.
Our study shows how multiple types of social bonds formed during multiple stages of social development predict lifetime fitness outcomes. We suggest that social bonds formed during specific phases of development may be more important than others when considering fitness outcomes.