Bananas may be on grocery shelves year-round, but wild animals live differently. They eat what grows seasonally. This seasonal rhythm creates a challenge, especially in temperate regions with strong variations, such as Japan. Animals must adapt as food sources shift with the climate, and their guts play a key role in coping with these changes.
Among primates, Japanese macaques live farther north than any other. Their home is colder, and food choices are limited. These “snow monkeys” prefer fruits and seeds, but in winter they must chew bark and leaves. How such dietary changes shape their survival has fascinated ecologists for decades.
Many studies show that gut microbes shift with diet and environment. The microbiome helps animals digest food, but the precise impact on efficiency remains unclear. This question drove a Kyoto University research team to investigate Japanese macaques on Yakushima Island.
The researchers combined fieldwork and laboratory analysis. They observed macaques, documenting what and how much they ate. They also collected fresh fecal samples, extracting gut microbes for study.
Using 16S rRNA gene analysis, they examined microbial composition. They then tested fermentation ability through in vitro assays, seeing how microbes processed real foods from the monkeys’ diet.
“This study was challenging because I often had to wake up in the middle of the night to monitor fermentation and then continue following monkeys the next day,” said corresponding author Wanyi Lee. “But it was worth it to see the in vitro fermentation assay reveal the hidden power of gut microbes.”
The findings revealed flexible shifts. Gut microbial composition and fermentative power both changed with the seasons. Fermentative ability increased sharply during winter, when macaques ate mature leaves.
Fruits and seeds, in contrast, posed little challenge and were digested easily across seasons by many gut microbes.
The study showed that it wasn’t fiber alone driving fermentative shifts. Instead, mature leaf consumption itself boosted microbial efficiency.
This suggests that microbes were adapting to handle not only fiber but also plant secondary compounds. Such compounds often act as chemical defenses, making leaves difficult to eat without specialized microbial help.
Leaf fermentation remained stable across months, while fermentation of easy foods like monkey chow showed greater variability. This points to a dual strategy: stability for hard-to-digest leaves and flexibility for more accessible foods. Such balance may be crucial for survival in a habitat where diet swings sharply with season.
The analysis revealed core microbes that were consistently active across conditions. Genera like Streptococcus, Ligilactobacillus, Lactobacillus, Faecalibacterium, and Bifidobacterium played central roles. These microbes produce short-chain fatty acids (SCFAs) that directly fuel the host.
The presence of these microbes suggests that snow monkeys maintain a functional core microbiome while adjusting around it with seasonal shifts.
Comparisons with more leaf-eating macaque groups show even stronger microbial adaptation. Populations relying heavily on leaves exhibit higher fermentative efficiency and microbial activity than frugivorous groups. This highlights how ecological pressures shape microbial evolution within the same species.
Comparing Japanese macaques with tropical primates highlights key differences. Howler monkeys, for example, increase microbial fermentation when fruit is scarce.
Macaques, by contrast, show reduced SCFA levels when eating mature leaves, reflecting different ecological pressures. These contrasts emphasize how gut microbiomes adapt to specific habitats.
Even with microbial help, limits remain. Fermentation time in macaques is shorter than in gorillas or orangutans. This means leaves may not be fully digested before passing through the gut. As a result, microbial efficiency cannot completely erase the energetic challenges of low-quality foods.
Other mammals show similar reliance on microbes. Woodrats consuming toxin-rich plants harbor gut microbes that help detoxify harmful compounds. When treated with antibiotics, these rodents lose this ability and suffer weight loss.
Pandas also demonstrate seasonal microbial shifts. Their microbiome adapts to bamboo shoots, boosting fat storage during that season, but leaves provide fewer microbial benefits. These examples reveal a universal theme: gut microbes are critical partners for survival during dietary shifts.
“By linking both microbial composition and function, our study provides a comprehensive perspective that can be applied not only to other primates but also to a wide range of wild animals,” said Lee.
As climate change and deforestation alter habitats, these microbial strategies may prove vital. The resilience of wildlife could depend on the hidden adaptability of their gut microbes. Understanding this flexibility will help predict survival under future environmental stress.
The study is published in the journal Ecology and Evolution.
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