Bacillota (formerly Firmicutes): the 'fat bacteria' that aren't
Bacillota is the bacterial phylum (a top-level branch of the bacterial family tree) formerly called Firmicutes, renamed in 2021 when phylum names were formally standardized. It is one of the two dominant groups in the human colon and includes both the butyrate producers that feed the gut lining and pathogens such as Clostridioides difficile. The popular 'Firmicutes-to-Bacteroidetes ratio' is not a reliable obesity marker.
If you have ever had a stool test come back with a bar chart, the biggest bar was probably labelled Firmicutes. The report may have told you it means you are "wired for weight gain." Here is what the actual studies say about that bar, and about the phylum that now goes by a new name.
What Bacillota is
Bacillota is a phylum of bacteria: a top-level branch of the bacterial family tree, the same rank at which "chordates" sits among animals. Most of its members have a thick, single-layer cell wall (they stain Gram-positive) — the Negativicutes, which stain Gram-negative, are the standing exception — and a genome relatively poor in the DNA letters G and C, which is why older textbooks call them "low G+C Gram-positives."
The name is new. For decades the phylum was Firmicutes, from the Latin for "tough skin." In 2021 1 the International Committee on Systematics of Prokaryotes brought the rank of phylum under its naming code, and Oren and Garrity validly published standardized names for 42 phyla 1, each built on a type genus. Firmicutes became Bacillota, the new name built on the type genus Bacillus. Nothing about the organisms changed; only the label did. You will still meet the old name on almost every consumer test and in every paper written before the switch, so this entry uses both.
Where it lives in you
Mostly in the large intestine. When Eckburg and colleagues at Stanford sequenced 13,355 2 ribosomal gene sequences from the colon lining and stool of healthy adults in 2005 2, the two dominant phyla were the Firmicutes and the Bacteroidetes, and most of the sequences belonged to species no one had ever grown in a lab 2. That picture has held. The Human Microbiome Project, sampling healthy adults across many body sites, found that even healthy people differ remarkably in which microbes they carry, with strong niche specialization from one site to the next 3. The MetaHIT catalogue put numbers on the scale: 3.3 million 4 non-redundant microbial genes in the stool of 124 4 Europeans, roughly 150 times 4 the human gene count, and at least 160 4 prevalent bacterial species in every single person.
Bacillota do not stop at the gut. Lactobacilli, which belong to this phylum, dominated four of the five 8 community types Ravel and colleagues found when they sequenced the vaginal microbiome of 396 8 asymptomatic women. And Staphylococcus aureus, another member, lives chiefly in the nose: Wertheim's review in The Lancet Infectious Diseases calls the nose its main ecological niche in humans 13.
What it does for us
Start with the mechanism, because the benefit follows from it. Fibre and resistant starch reach the colon undigested. Gut bacteria ferment them into short-chain fatty acids, and two of those, butyrate and propionate, are the ones Louis and Flint's review credits with a range of health-promoting functions, butyrate being the preferred fuel of the cells lining the colon 5. The major butyrate producers they describe, Faecalibacterium prausnitzii, Eubacterium rectale and the Roseburia group, are all Bacillota, and they depend on cross-feeding: one species' lactate or succinate becomes another's raw material 5.
The best-studied of those producers has its own evidence. Sokol and colleagues followed Crohn's disease patients after surgical resection and found that a lower share of F. prausnitzii on the gut lining predicted recurrence 6 months 6 later. In the lab, the bacterium made human blood cells produce significantly less IL-12 and IFN-gamma and more IL-10, and its culture supernatant blocked NF-kappaB activation, a central inflammation switch 6. The caveat, said out loud: the treatment arm of that study was mice with chemically induced colitis, not people. It shows a plausible mechanism, not a proven therapy.
There is also a survival trick. Browne and colleagues at the Sanger Institute managed to culture 137 7 species from healthy human stool that had been written off as unculturable, and their genomes suggested that at least 50–60 % 7 of gut bacterial genera make resilient spores. Most of those spore-formers are Bacillota. Spores let oxygen-hating gut bacteria survive the trip between one person and the next, which is likely how much of this community is shared in the first place 7.
What it does against us
The same phylum holds some of the most serious pathogens we carry. Clostridioides difficile is a spore-forming Bacillota member that takes over the colon after antibiotics clear its competitors. In active surveillance across 10 12 US regions, Lessa and colleagues estimated 453,000 12 infections and about 29,000 12 deaths in 2011 12 alone; 65.8 % 12 of cases were healthcare-associated, and people 65 12 or older had a rate ratio of 8.65 12 compared with younger adults. Staphylococcus aureus is the other everyday example: the Wertheim review notes that nasal carriers have a higher risk of going on to infection with their own strain, and that the pathogen's rising antibiotic resistance complicates treatment worldwide 13.
Note what these two have in common with the helpful members above: the spore, the thick wall, the persistence. The traits that make Bacillota resilient allies also make its pathogens hard to clear.
The obesity ratio, honestly
Now the bar chart. In 2006 9 Ley, Turnbaugh, Klein and Gordon reported in Nature that 12 9 obese volunteers carried a lower share of Bacteroidetes than lean people, and that the share rose as they lost weight on two 9 low-calorie diets. The companion mouse study found that an "obese" microbiome extracted more energy from food and that the trait transferred to germ-free mice 10. From those papers the Firmicutes/Bacteroidetes ratio entered popular culture as a fat-versus-thin dial.
The evidence since has not cooperated. Magne and colleagues reviewed the literature in 2020 11 and found the results across studies contradictory, with differences explained as easily by sample handling, sequencing method and poorly described lifestyle as by body weight. Their conclusion, in their own terms: it is currently difficult to associate the ratio with a determined health status, and more specifically to consider it a hallmark of obesity 11. So a high Bacillota bar on a test report is not a diagnosis. It is a snapshot of a phylum that contains both the butyrate producers your colon lining runs on and the pathogens your hospital worries about, and the bar cannot tell you which ones you have.
Key facts
- Bacillota is the valid name for the phylum formerly called Firmicutes; the name was validly published together with 41 other phylum names in 2021.1
- In the first large sequencing survey of the human colon and stool (13,355 ribosomal gene sequences), the Firmicutes and Bacteroidetes were the two dominant phyla and most sequences belonged to species never grown in a lab.2
- The MetaHIT catalogue found 3.3 million non-redundant microbial genes in the stool of 124 Europeans, about 150 times the human gene count, with each person carrying at least 160 prevalent bacterial species.4
- Butyrate and propionate, the short-chain fatty acids most tied to gut-lining health, are made mainly by gut bacteria that ferment fibre we cannot digest; the main butyrate producers belong to Bacillota.5
- Faecalibacterium prausnitzii, a major Bacillota member, lowered pro-inflammatory IL-12 and IFN-gamma and raised IL-10 in human blood cells, and its loss predicted Crohn's recurrence 6 months after surgery.6
- At least 50–60 % of bacterial genera in a healthy gut make resilient spores built for passing between people; the study isolated 137 gut species that had been called 'unculturable'.7
- Clostridioides difficile, a Bacillota member, caused an estimated 453,000 infections and about 29,000 deaths in the United States in 2011.12
- A 2020 review of the Firmicutes/Bacteroidetes ratio concluded that the contradictory published results make it currently difficult to associate the ratio with a determined health status, and more specifically to consider it a hallmark of obesity.11
Questions people ask
Is Bacillota the same thing as Firmicutes?
Yes. Firmicutes is the older name for the same phylum. In 2021, after the International Committee on Systematics of Prokaryotes voted to bring the rank of phylum under the naming code, Oren and Garrity validly published standardized names for 42 phyla, and Firmicutes became Bacillota. Older papers and most consumer test reports still say Firmicutes; the organisms did not change, only the label.
Is a high Firmicutes-to-Bacteroidetes ratio a sign I am gaining weight?
The idea came from a 2006 Nature study of 12 obese people whose Bacteroidetes share rose as they lost weight. A 2020 review of the literature found the results across studies contradictory and concluded that it is currently difficult to associate the ratio with a determined health status, let alone treat it as a hallmark of obesity. A single ratio on a test report tells you very little.
Are Bacillota bacteria good or bad for me?
Both, depending on the member. The phylum holds the main butyrate producers that feed the colon lining, the lactobacilli that dominate a healthy vaginal microbiome, and also Clostridioides difficile and Staphylococcus aureus. Judging a phylum as a whole is like judging 'mammals' as good or bad.
Where in my body do Bacillota live?
Mainly in the large intestine, where they are one of the two dominant phyla. Lactobacilli, which belong to this phylum, dominate the vaginal microbiome of most women, and Staphylococcus aureus, another member, lives chiefly in the nose.
Can I raise my 'good' Bacillota with diet?
The main butyrate producers grow on fibre and resistant starch that reach the colon undigested, and they cross-feed on each other's by-products. That is the mechanism the Louis and Flint review lays out. How much your own numbers move is individual, and no test on this page can predict it.
Sources
- Oren A, Garrity GM. Valid publication of the names of forty-two phyla of prokaryotes. Int J Syst Evol Microbiol, 2021 — doi:10.1099/ijsem.0.005056
- Eckburg PB et al. Diversity of the human intestinal microbial flora. Science, 2005 — doi:10.1126/science.1110591
- Human Microbiome Project Consortium. Structure, function and diversity of the healthy human microbiome. Nature, 2012 — doi:10.1038/nature11234
- Qin J et al. A human gut microbial gene catalogue established by metagenomic sequencing. Nature, 2010 — doi:10.1038/nature08821
- Louis P, Flint HJ. Formation of propionate and butyrate by the human colonic microbiota. Environ Microbiol, 2017 — doi:10.1111/1462-2920.13589
- Sokol H et al. Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients. PNAS, 2008 — doi:10.1073/pnas.0804812105
- Browne HP et al. Culturing of 'unculturable' human microbiota reveals novel taxa and extensive sporulation. Nature, 2016 — doi:10.1038/nature17645
- Ravel J et al. Vaginal microbiome of reproductive-age women. PNAS, 2011 — doi:10.1073/pnas.1002611107
- Ley RE, Turnbaugh PJ, Klein S, Gordon JI. Microbial ecology: human gut microbes associated with obesity. Nature, 2006 — doi:10.1038/4441022a
- Turnbaugh PJ et al. An obesity-associated gut microbiome with increased capacity for energy harvest. Nature, 2006 — doi:10.1038/nature05414
- Magne F et al. The Firmicutes/Bacteroidetes ratio: a relevant marker of gut dysbiosis in obese patients? Nutrients, 2020 — doi:10.3390/nu12051474
- Lessa FC et al. Burden of Clostridium difficile infection in the United States. N Engl J Med, 2015 — doi:10.1056/NEJMoa1408913
- Wertheim HFL et al. The role of nasal carriage in Staphylococcus aureus infections. Lancet Infect Dis, 2005 — doi:10.1016/S1473-3099(05)70295-4
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