The Awkward Adolescence of Microbiome Science

And how stool DNA tests may ultimately teach us what matters 😉

Stool DNA and the Gut Microbiome

Quick Takes

📋 Species lists aren't the point. What your gut microbiome does matters more than which bacteria are in it — the metabolites produced, the barriers maintained, the functions performed. But there’s more:

💃 Redundancy is the real measure of a healthy gut. A resilient microbiome isn't just one that "has" key functions — it's one where multiple species can perform the same job if another falters.

🐠 Your gut is like a coral reef, not a gladiator arena. Bacteria constantly cooperate, share resources, and cross-feed each other. Competition exists, but thriving depends just as much on flexible collaboration.

❓️ We've been asking the wrong questions. Instead of "do I have enough of the good bugs?", the better question is: "how well can my gut community adapt when things go wrong?”

🤲🏼 Push back on the idea that competition is the only useful arrangement: the same was initially said about evolution, but instead we find that mutually beneficial relationships are critical.

Favorite Finds

  • My colleague Dr. Lovina Chahal who sent me the Science article in the first place. Thank you!

  • Nirvanabiome offers stool DNA testing that includes some functions along with the species list. I hope they continue to improve over time.

  • Tiny Health is a very similar stool DNA testing company. This company has guidelines for what may be normal or healthy for children as well as adults.

  • Finding the Mother Tree (2021) is a memoir by Canadian forest ecologist Suzanne Simard, whose groundbreaking research revealed that trees communicate and share resources through underground mycorrhizal fungal networks — a phenomenon she coined the "wood wide web." Equal parts science and story, the book uncovers the tender, surprising relationships that animate forest life, while tracing Simard's personal struggle to convince a scientific establishment long wedded to competitive, "survival of the fittest" thinking.

  • The Science paper that inspired this is

    Corral LĂłpez R, Bonachela JA, Dominguez-Bello MG, Manhart M, Levin SA, Blaser MJ, MuĂąoz MA. Imbalance in gut microbial interactions as a marker of health and disease. Science. 2026

Deep Dive

How To Use Ecology to Understand the Gut Microbiome and Our World

We are in an awkward adolescence with microbiome science.

On one hand, the tools are dazzling: we can now sequence stool DNA and get long lists of bacterial species and genes in a matter of days. On the other hand, we’re still tempted to interpret those lists with a 19th‑century lens—ranking species as “good” or “bad,” imagining heroic individual strains, and importing our cultural stories about competition and “survival of the fittest” into an ecosystem that is just as likely to show interdependence and collaboration.

A recent paper in Science on gut microbial interaction networks drives home how much our thinking needs to change. It suggests a path away from single‑species and single‑function thinking, toward something closer to true ecology: functions, redundancy, and the quality of relationships in the gut community.

Step 1: From species lists to microbial functions

Most stool DNA tests still give us a census: who is there, and in what relative abundance.

That’s a start, but it’s also a very limited way of seeing things:

  • The same species can behave very differently in different communities and diets.

  • Different species can perform the same biochemical job (e.g., butyrate production, bile acid transformation, vitamin synthesis).

  • Health outcomes usually track what the community does—the metabolites produced, the barriers maintained, the signals sent—not which Latin names appear on the report.

The first major shift we need is to move from:

> “Do you have Faecalibacterium prausnitzii?”

to:

> “Is butyrate production capacity robust here? Are mucin degraders balanced? Do we have active pathways for fiber fermentation, bile acid detoxification, and vitamin synthesis?”

That’s a functional view. It asks about the state of the system performing the core services that keep the gut lining intact, the immune system regulated, and the metabolic environment hospitable.

Step 2: From single functions to redundancy and cross‑feeding

But even that functional step is not enough.

You can imagine two very different communities that both appear to “perform” a function:

  • Community A: two interdependent fragile species doing almost all of the butyrate production, with no backup.

  • Community B: several unrelated species, each capable of making butyrate under slightly different dietary and environmental conditions, sharing intermediates via flexible cross‑feeding networks.

On a basic functional readout, these communities might look similar. Ecologically, they are not.

Robust ecosystems don’t just have key functions present; they have redundant, overlapping ways to perform those functions. Multiple players can step in if one partner is lost. Paths are flexible, not bottlenecked through single points of failure.

In gut terms, that means looking at:

  • Redundancy: how many different taxa can perform a given function? Is there backup?

  • Cross‑feeding: how metabolites flow from one organism to another—who is sharing what, and are those networks open and flexible or narrow and brittle?

  • Balance: whether positive (cooperative) interactions and negative (competitive) interactions coexist in ways that support diversity and resilience.

When a community becomes dysbiotic, it doesn’t just “lose good bugs.” It often loses redundancy and falls back onto a few rigid, obligate cross‑feeding cliques that depend heavily on one another. The network becomes less like a healthy forest and more like a plantation of one or two tightly interdependent crops. That system can be efficient in one context but fragile, inflexible, and easier to push into collapse.

So the real question isn’t just: “Is function X present?”

It’s: “How many ways can this community achieve function X, and how flexible are the relationships that support it?”

How our frameworks bias what we see in nature

There’s another layer here: how our human stories shape what we notice in biology.

For over a century, “survival of the fittest” has been misinterpreted to mean endless competition, as if nature were a corporate ladder with tooth and claw. Under that lens, we look at an ecosystem and see mainly:

  • Competition for scarce resources

  • Winners and losers

  • Dominance and exclusion

And then, in a neat psychological loop, we turn around and use those same stories to justify our social and economic systems. Nature, we say, is a “zero-sum war of all against all” — so therefore, so must we be.

But ecology has repeatedly complicated that picture:

  • Mutualisms and symbioses are ubiquitous—from plant–fungus relationships to corals and their algae.

  • Altruism and cooperation are fundamental for bacteria, insects, birds, mammals, and humans.

  • Many systems persist not because the “strongest” outcompete all others, but because cooperation, niche sharing, and redundancy buffer the community against shocks.

❝

The gut microbiome is much closer to a coral reef than a gladiator arena.

Yes, there is competition for nutrients and space. Yes, some species inhibit others. But at the same time, there is extraordinary collaboration: one species breaking down complex plant fibers, another cross‑feeding on the intermediate products, yet another converting those into butyrate or propionate that feed colonocytes and shape immune tone. Waste products for one become food for another. Signals and metabolites constantly negotiate peace, defense, and repair.

If you approach that system with a competition‑first mindset, you will tend to spotlight the inhibitory edges and describe them as stabilizing, while treating cooperative edges as suspicious or “dysbiotic.” If you approach it with an ecological mindset, you see something different:

Resilience comes from diverse, flexible, overlapping cooperation, where no single relationship is a brittle point of failure and many species can take on essential roles under changing conditions.

Ecology as the better metaphor for the gut

Ecology offers us a more accurate—and more generative—metaphor for the microbiome:

  • There will always be competition; resources are finite.

  • Thriving, however, depends on how well cooperation, redundancy, and niche sharing are cultivated on top of that competitive base.

  • Health is less about which individual species “win” and more about whether the entire network can adapt to stress, dietary shifts, infections, and insults without collapsing.

For clinical practice and self‑care, that suggests a different emphasis:

  • Instead of chasing or eradicating individual organisms, we support ecosystem properties: diversity, redundancy of key functions, and healthy cross‑feeding networks.

  • Instead of asking “How do I boost this one ‘good’ strain?”, we ask “How do I feed the web?”—with fiber variety, polyphenols, fermented foods (when appropriate), and lifestyle factors that support a resilient community.

  • Instead of reading interaction data as proof that “competition is good and cooperation is bad,” we look for signs of flexible, non‑exclusive cooperation layered on top of healthy competitive checks.

Bringing it back to how we live

Clearly the first lesson is about diversity of inputs: 

  • 30 different plant sources each week (fruits and vegetables, nuts, legumes, herbs and spices)

  • Layering on other positive influences: exercise, stress reduction, sleep, community and connection, purpose and integrity.

  • And, who knows, also a life that makes space for collaboration and interdependence?

There is an irony here.

We study the gut and see that communities thrive when they have:

  • Shared resources.

  • Overlapping skills and functions.

  • Flexible, non‑exclusive cooperation.

  • A balance of competition and collaboration.

Then we return to our human systems — and too often forget all of this. Ecology has already learned that restoration means rebuilding relationships and processes, not just removing enemies. That insight has traveled down to the scale of bacterial communities. Whether we let it travel upward, into how we structure our societies, may be the question that makes the rest much more likely to succeed.

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I know the world offers too much information, I hope to suggest new ways of thinking and being healthy.

Simple Science was created so I could share the multiple tips and insights I have discovered from 39 years of medical practice, and that I continue to gain through reading the science literature and collaborating with colleagues.

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