The genus Coprococcus

Members of the bacterial genus Coprococcus were first isolated and identified in human faeces (Holdeman and Moore, Reference Holdeman and Moore1974). C. eutactus, C. catus, and C. comes are recognised as Gram-positive, obligate anaerobic cocci that produce butyric and acetic acids by fermentation of carbohydrates, and are classified in the phylum Firmicutes, class Clostridia, order Eubacteriales, and family Peptococcaceae (Holdeman and Moore, Reference Holdeman and Moore1974). Bacterial taxonomy was previously based on similarities in morphology and functional features; however, the use of 16S ribosomal RNA (16S rRNA) gene sequencing techniques showed different clustering, resulting in the reclassification of the Coprococcus genus in the family Lachnospiraceae (Ezaki et al., Reference Ezaki, Li, Hashimoto, Miura and Yamamoto1994; Ludwig et al., Reference Ludwig, Schleifer, Whitman, De Vos, Garrity, Jones, Krieg, Ludwig, Rainey, Schleifer and Whitman2009; Ezaki, Reference Ezaki and Whitman2015). Although grouped into a single family, Coprococcus spp. show large phylogenetic distances within their genus members (Vacca et al., Reference Vacca, Celano, Calabrese, Portincasa, Gobbetti and De Angelis2020; Figure 1A). A potential new genus member, Coprococcus phoceensis, which clustered closely with C. comes, was recently isolated from the colon of a patient with Crohn’s disease (Bonnet et al., Reference Bonnet, Ricaboni, Mailhe, Vitton, Benezech, Delerce, Raoult, Cassir, Lascola and Khelaifia2019). A 2021 study indicated five potential new Coprococcus species members based on 16S rRNA gene sequencing of faecal samples combined with symmetric pairwise average nucleotide identity values (ANI) and metabolic pathway network analyses (Nogal et al., Reference Nogal, Louca, Zhang, Wells, Steves, Spector, Falchi, Valdes and Menni2021). Three of the proposed novel species clustered closely with C. eutactus and shared several metabolic features. However, these newly identified species have not yet been officially characterised. It should be noted that the frequently used approach to define bacterial species based on genotypic and phenotypic properties is controversial, as it leads to an underestimation of true bacterial diversity (Dykhuizen, Reference Dykhuizen1998; Staley, Reference Staley2006). In particular, taxonomic assignment using 16S rRNA gene sequencing is limited because genetically distinct bacteria can share similar or even identical 16S rRNA sequences (Jaspers and Overmann, Reference Jaspers and Overmann2004). The use of novel techniques with a higher resolution, such as multilocus sequence analysis and whole genome sequencing, can help gain a broader insight into the diversity of the Coprococcus genus and the speciation process.

Figure 1. Phylogenetic tree and microscopic characteristics of Coprococcus. (A) Evolutionary relationships of Coprococcus species and their closest human gut bacteria relatives. Bootstrap values are shown at branches. Image retrieved from Alessi et al. (Reference Alessi, Gray, Farquharson, Flores-López, Shaw, Stead, Wegmann, Shearman, Gasson, Collie-Duguid, Flint and Louis2020). (B) Gram-stained photomicrograph depicting a number of chains of Gram-positive, anaerobic, coccoid Coprococcus eutactus bacteria. Image retrieved from the Public Health Image Library (1976). (C) Transmission electron microscopy image of cultured C. eutactus cells. Arrows indicate spore ultrastructures. Image retrieved from Browne et al. (Reference Browne, Forster, Anonye, Kumar, Neville, Stares, Goulding and Lawley2016).

Cell morphology

Holdeman and Moore (Reference Holdeman and Moore1974) first described Coprococcus spp. as nonmotile, Gram-positive cocci, with C. eutactus ranging from 0.7 to 1.3 μm in diameter usually observed in pairs, although long strings of C. eutactus have since also been found (Figure 1B). C. catus showed a slightly elongated morphology, with an average cell size of 1.1 by 1.7 μm, presented in pairs forming long chains (Holdeman and Moore, Reference Holdeman and Moore1974). C. comes was found to be an elongated coccus with tapered ends, with an average cell size of 1.6 by 2.3 μm, although the size range showed quite some variability. Cells occurred either singly, in duplets, or in chains of 4–20 elements. The cell wall peptidoglycan of Coprococcus spp. contains meso-diaminopimelic acid at position three with no interpeptides (Ezaki et al., Reference Ezaki, Li, Hashimoto, Miura and Yamamoto1994). Although coccoid morphology is the simplest bacterial form to generate, the ancestral bacterial morphology is that of a rod, not a sphere, and several lines of evidence suggest that environmental selective pressure is the driving force behind this shape change (Yang et al., Reference Yang, Blair and Salama2016). Size minimisation and coccoid morphology of Coprococcus spp. could have improved their ability to colonise the mucosal surface of the gut and reduce their susceptibility to host defences.

Genome

Type strains of Coprococcus were isolated from human faeces and registered in the American Type Culture Collection (ATCC) database. The type strain of C. eutactus (ATCC 27759) carries a genome of 3.11 Mb containing 2,654 genes and 1,380 hypothetical proteins (ATCC, 2020; Benton et al., Reference Benton, King, Greenfield, Puthuveetil, Reese, Duncan, Marlow, Tabron, Pierola, Yarmosh, Combs, Riojas, Bagnoli and Jacobs2021). Its G+C content is considered relatively low at 43.1% (Ezaki et al., Reference Ezaki, Li, Hashimoto, Miura and Yamamoto1994). The genome of C. comes (ATCC 27758) is somewhat larger with 3.38 Mb, 3,177 genes, and 1,616 hypothetical proteins (ATCC, 2021). The G+C content was determined to 42.52%. Finally, the genome of C. catus (ATCC 27761) contains 3.66 Mb, 3,346 genes and 1,726 hypothetical proteins, with a G+C content of 43.01% (ATCC, 2022). Coprococcus spp. are considered part of the core microbiome with carbohydrate-fermenting properties in the healthy human gut (King et al., Reference King, Desai, Sylvetsky, LoTempio, Ayanyan, Carrie, Crandall, Fochtman, Gasparyan, Gulzar, Howell, Issa, Krampis, Mishra, Morizono, Pisegna, Rao, Ren, Simonyan, Smith, VedBrat, Yao and Mazumder2019), and genes for SCFA synthesis pathways have been found in different Coprococcus species (see section “Production and synthesis pathways”). Additionally, glycoside hydrolase (GH) genes for cellulose breakdown (see section “Oxygen sensitivity and cultivation”) have been specifically identified in the genome of C. eutactus (Alessi et al., Reference Alessi, Gray, Farquharson, Flores-López, Shaw, Stead, Wegmann, Shearman, Gasson, Collie-Duguid, Flint and Louis2020). Sporulation genes are described in the following section.

Life cycle and growth requirements

Coprococcus spp. reside in the human colon as obligate anaerobic bacteria and have been isolated from oral samples of 45% of healthy adult subjects (Segata et al., Reference Segata, Haake, Mannon, Lemon, Waldron, Gevers, Huttenhower and Izard2012). Once shed through faeces, intestinal bacteria temporarily encounter environmental stress before being transmitted to a new host. Rapid colonisation by direct human-to-human contact, modulation of metabolism, and high activity of repair pathways are strategies to counteract environmental challenges. The classes Clostridia and Bacilli within the Firmicutes phylum are known to produce spores and metabolically dormant structures to withstand atmospheric oxygen during environmental exposure (Browne et al., Reference Browne, Neville, Forster and Lawley2017). C. eutactus and its members have long been assumed to be non-sporulating bacteria (Collins et al., Reference Collins, Lawson, Willems, Cordoba, Fernandez-Garayzabal, Garcia, Cai, Hippe and Farrow1994); however, this has been disputed by Browne et al. (Reference Browne, Forster, Anonye, Kumar, Neville, Stares, Goulding and Lawley2016), who combined the culture-independent approach of metagenomic sequencing with bacterial culturing and estimated that 60% of the intestinal microbiota genera, representing approximately 30% of the total intestinal microbial abundance, produces spores. Selection of bacterial spore-forming species by treating faecal samples with ethanol resulted in the isolation of 66 ethanol-resistant species, including members of the genus Coprococcus; Coprococcus spp. contain 53% of the known sporulation genes, and transmission electron microscopy revealed typical spore structures in cultured C. eutactus (Browne et al., Reference Browne, Forster, Anonye, Kumar, Neville, Stares, Goulding and Lawley2016; Figure 1C).

Analysis of the distribution of the main sporulation-associated gene families cot, spo, sps, and ssp within the genomes of Lachnospiraceae revealed that 27 out of 84 sporulation genes of the spore-forming bacterium Bacillus subtilis had no known homologues in the sequenced genomes of Lachnospiraceae (Meehan and Beiko, Reference Meehan and Beiko2014). Interestingly, 29 of the remaining 57 genes were present in the majority of gut-associated Lachnospiraceae, including C. eutactus and C. comes, but were completely absent from the rumen and oral-associated family members of Lachnospiraceae, suggesting that the acquisition of sporulation genes is a specific ecological adaptation to the gut environment; representatives of all the main sporulation-associated gene families, including cot (2 genes), spo (31 genes), sps (5 genes), and ssp (4 genes), were identified in the genomes of C. eutactus and C. comes (Meehan and Beiko, Reference Meehan and Beiko2014). Once excreted from the body in faeces, Coprococcus spp. should be able to tolerate the local environment and colonise a new host. Dormant bacterial spores are extremely resistant and can cope with the toxic effects of atmospheric oxygen, ultraviolet radiation, lack of nutrients, adverse temperatures, and desiccation (Browne et al., Reference Browne, Neville, Forster and Lawley2017). Bacterial spores have great application potential as probiotic food supplements, as they offer the benefit of higher survival rates during passage through the acidic stomach and better stability during processing and storage than the widely used lactic acid bacteria (Bader et al., Reference Bader, Albin and Stahl2012).

Common bile acids (taurocholate, glycocholate, and cholate) were evaluated for their stimulatory effects on spore germination in the gut. In particular, taurocholate proved to be a potent germinant for all sporeformers, increasing the culturability of spores from commensal bacteria by up to 70,000-fold. Bile acids did not affect the culturability of non-spore-forming bacteria. Browne et al. (Reference Browne, Neville, Forster and Lawley2017) proposed a bile acid-triggered “germination cue” to initiate colonisation by intestinal spore-forming bacteria. Spore formation ensures environmental survival and human-to-human transmission, whereas germination ensures bacterial persistence in the human host.

Coprococcus spp. are obligatory anaerobic bacteria. In a systematic investigation of the effects of atmospheric oxygen exposure on human intestinal microorganisms, 200 anaerobic bacterial strains were isolated (Brusa et al., Reference Brusa, Canzi, Pacini, Zanchi and Ferrari1989). Of this subset, 30 strains showed high O₂-intolerance, including Coprococcus species. Similar to other highly O₂-sensitive strains, C. comes cells showed only 50% survival after 4–5 min of oxygen exposure and 100% mortality after 100–120 min. The growth of highly O₂-intolerant species needs to occur under strict anoxic conditions, making the cultivation of Coprococcus spp. tedious. Moreover, C. eutactus, C. catus, and C. comes have different preferences for nutrients and conditions. Holdeman and Moore (Reference Holdeman and Moore1974) reported the growth of these three species under anoxic conditions in rumen fluid-glucose-cellobiose agar roll tubes. C. eutactus showed poor or no growth in peptone yeast (PY) broth without fermentable carbohydrates, while PY-glucose cultures had the most abundant growth. Growth resulted in the production of formic, butyric, lactic, and acetic acids, with abundant hydrogen release. When the medium was enriched with pyruvate, formate, and acetate were formed. Growth occurred equally well at 37 C and 45 C but was poor to moderate at 25 C and 30 C. The researchers noted in their paper that C. eutactus was easily recognizable by its production of formate, lactate, and butyrate from glucose, and its uniform fermentation of these substrates.

Coprococcus catus displayed a different growth behaviour. Substrate utilisation was restricted, and slight to moderate growth was observed in PY broth. In contrast to glucose, fructose led to abundant growth. This resulted in the production of large amounts of butyric and propionic acids with hydrogen formation. There was usually no growth at 30 C, whereas the best growth occurred between 37 C and 45 C. The third species, C. comes, showed moderate growth in PY broth without carbohydrates. PY-glucose cultures showed abundant growth, resulting in the production of lactate, butyrate, and acetate. Interestingly, the metabolic pathways used did not result in hydrogen release. Additionally, cultures grown on PY-pyruvate and C. comes could use a range of carbohydrates as substrates. The temperature for optimal growth was 37 C; most strains grew well at 45 C, but not at 30 C. According to Holdeman and Moore (Reference Holdeman and Moore1974), the fermentation of arabinose and xylose helps to differentiate it from the other two species in the genus.

The ability to use lactate for growth also differs among species. Reichardt et al. (Reference Reichardt, Duncan, Young, Belenguer, McWilliam Leitch, Scott, Flint and Louis2014) confirmed that both C. eutactus ATCC 27759 and C. comes ATCC 27758 could not grow on lactate, but C. catus GD/7 was able to grow with 25 mM lactate on YCFA medium containing 30 mM acetate. Lactate utilisation also occurred in the presence of 10 mM fructose, and propionate was the main product in all lactose-supplemented cultures. A different metabolic pathway was used during growth on fructose in the absence of lactate, resulting in butyrate production and the net consumption of acetate. In a recent study, Alessi et al. (Reference Alessi, Gray, Farquharson, Flores-López, Shaw, Stead, Wegmann, Shearman, Gasson, Collie-Duguid, Flint and Louis2020) examined the ability of Coprococcus spp. to utilise carbohydrate substrates by measuring the optical density and acidification. GH is associated with cellulose breakdown, with two GH9-encoding and four GH5-encoding genes in C. eutactus ART55/1 and a related strain, Coprococcus sp. L2-50. However, both strains failed to utilise cellulose. In other Coprococcus species, no GH genes were present, apart from a single GH5 gene, in one of the examined C. comes strains. As reported by Holdeman and Moore (Reference Holdeman and Moore1974), C. eutactus displayed the highest promiscuousness for carbohydrate utilisation among Coprococcus members. Coprococcus L2-50 exhibited growth on glucose, cellobiose, β-glucan, and lichenan but limited growth on potato starch. C. eutactus ART55/1 and C. eutactus ATCC 27759 were also able to grow on glucomannan, galactomannan, galactan and potato starch, and weak fermentation of mannan was detected. C. comes and C. catus showed more restricted carbohydrate utilisation; C. comes strains only grew well on glucose, while C. catus GD/7 showed limited growth on potato starch. The known substrate utilisation of Coprococcus spp. is listed in Supplementary Table S1.

The impact of Coprococcus on gut homeostasis

In the gut, 90% of resident microbes are obligate anaerobes, constituting the main SCFA producers, and their presence is associated with homeostasis. Coprococcus spp. produce butyrate (Vital et al., Reference Vital, Howe and Tiedje2014) together with other fermenters from the bacterial class of anaerobic Clostridia. C. eutactus significantly contributes to the pool of intestinal butyrate, listed at the fourth position in butyrate producers in the microbiota community, regarding the dominant metabolic butyrate pathway, the acetyl-CoA pathway (Vital et al., Reference Vital, Howe and Tiedje2014). Faecalibacterium prausnitzii, Ruminococcaceae, and Eubacterium rectale were positioned at numbers 1, 2, and 3, respectively, whereas C. comes only at position 10 and C. catus at position 18. However, the exact ordering of species needs to be treated with caution, since analyses were only based on stool samples from only 15 individuals.

Microbiota-produced butyrate is oxidised to carbon dioxide by mature colonocytes for energy (ATP) generation, which is necessary for the transport of sodium (Na⁺) enabling water absorption. Butyrate metabolism requires colonocytes to consume high levels of oxygen, creating a hypoxic epithelial surface (Rivera-Chávez et al., Reference Rivera-Chávez, Lopez and Bäumler2017). Disruption of this hypoxic surface has pathophysiological consequences: antibiotic treatment with streptomycin preferentially depletes the Clostridia class, thereby reducing butyrate production and increasing partial oxygen pressure, leading to diffusion of oxygen into the intestinal lumen. This creates a window of opportunity for oxygen-tolerant microbes and is associated with the uncontrolled expansion of facultative anaerobic bacteria such as Enterobacteriaceae, including pathogenic Escherichia coli or Salmonella enterica species (Rivera-Chávez et al., Reference Rivera-Chávez, Zhang, Faber, Lopez, Byndloss, Olsan, Xu, Velazquez, Lebrilla, Winter and Bäumler2016; Rivera-Chávez et al., Reference Rivera-Chávez, Lopez and Bäumler2017). Oxidative stress is known to have pathogenic effects through the generation of reactive oxygen species (ROS) and reactive nitrogen species (RNS). Million and Raoult (Reference Million and Raoult2018) investigated the link between faecal redox potential and human gut microbiome. A significant positive correlation was found between faecal redox potential and the predominance of aerotolerant species. Healthy subjects showed a lower redox potential than diseased subjects due to different forms of malnutrition.

Homeostasis and redox balance in the intestine are achieved by cross-feeding mechanisms. To understand the interdependency of the different microbial clades in the gut and the role of Coprococcus spp., the fermentation process must be considered in more detail. Fermentation, similar to aerobic respiration, involves the breakdown of nutrients by redox reactions (the oxidation of one molecule coupled to the reduction of another) to generate ATP. Hydrogen (H₂), carbon dioxide (CO₂), and methane (CH₄) are produced by colonic microbes that ferment dietary components while producing SCFAs (Carbonero et al., Reference Carbonero, Benefiel and Gaskins2012). In aerobic respiration, oxygen serves as the terminal electron, and nutrients are fully oxidised. However, during fermentation, nutrients are incompletely oxidised and the reduced fermentation products function as terminal electron acceptors. To maintain the redox balance, the reduced pyridine (NADH) and flavin (FADH) nucleotides must be reoxidised. This reaction is the primary source of hydrogen gas in the colon. Hydrogen production by hydrogenogenic microbes ensures the efficiency of fermentation, but hydrogen accumulation inhibits further fermentation owing to thermodynamic restrictions. Therefore, the simultaneous oxidation of hydrogen by hydrogenotrophic (H₂-utilising) microbes that generate energy through anaerobic respiration forms a crucial companionship for SCFA-producing colonic microbes, such as Coprococcus species. The hydrogen-consuming clades consist of reductive acetogens, methanogenic archaea, and sulphate-reducing bacteria. Notably, a disturbed hydrogen economy has been associated with IBD (King et al., Reference King, Elia and Hunter1998; Carbonero et al., Reference Carbonero, Benefiel and Gaskins2012).

In summary, under homeostatic conditions, the colonic epithelium is hypoxic because of the metabolism of SCFAs by mature colonocytes. With the loss of butyrate-producing microbes, such as Coprococcus spp., oxygen diffuses into the lumen and supports the expansion of pathogenic oxygen-tolerant microbes. The production of SCFAs by obligate anaerobes results in the release of H₂ into the gut. The co-occurrence of hydrogen-producing and hydrogen-utilising microbes is crucial for ensuring continued SCFA production. When the balance of this companionship is disturbed, butyrate production is diminished, and oxygen levels in the gut rise, leading to reduced epithelial barrier function and opportunity for colonisation of pathogenic clades.

Acquirement, prevalence, and abundance of the Coprococcus genus in the gut

An individual’s core microbiome shapes itself from birth and displays characteristic patterns according to age and changes in diet (Yao et al., Reference Yao, Cai, Ye, Wang, Chen and Zheng2021; see Textbox). Colonisation by the Coprococcus genus in the early life stages has been demonstrated in at least 87% of 3–4 months’ old Canadian infants (n = 24), with a low abundance of approximately 0.8% (Azad et al., Reference Azad, Konya, Maughan, Guttman, Field, Chari, Sears, Becker, Scott and Kozyrskyj2013). It should be noted that differential abundance analysis is controversial throughout microbiome research, neglecting total microbial load, or absolute number of microorganisms (Morton et al., Reference Morton, Marotz, Washburne, Silverman, Zaramela, Edlund, Zengler and Knight2019), and core species are not necessary the most abundant ones. Many highly significant synergistic interactions have been identified among low-abundance species forming a connected network (Claussen et al., Reference Claussen, Skiecevičienė, Wang, Rausch, Karlsen, Lieb, Baines, Franke and Hütt2017). However, the prevalence and abundance of Coprococcus spp. increased over time as both were positively correlated with age. For example, Coprococcus spp. could be detected in the faecal samples of 78.2% of Chinese children at the age of 3 (n = 729) with a mean abundance of 0.21% (Niu et al., Reference Niu, Xu, Qian, Sun, Yu, Huang, Zhou, Wang, Zhang, Ren, Li, Yu and Gao2020). In contrast, Kostick et al. (Reference Kostic, Gevers, Siljander, Vatanen, Hyötyläinen, Hämäläinen, Peet, Tillmann, Pöhö, Mattila, Lähdesmäki, Franzosa, Vaarala, de Goffau, Harmsen, Ilonen, Virtanen, Clish, Orešič, Huttenhower, Knip and Xavier2015) demonstrated large fluctuations with a rise and drop below the baseline of C. eutactus in children up to 3 years from Finland and Estonia (n = 33). The children were selected based on type I DM susceptibility (HLA DR-DQ alleles conferring risk of T1DM), which could explain the different findings compared with the Chinese cohort. Geographical factors should also be considered, since the intestinal microbiota of infants from different countries exhibit different types of microbe-dominant compositions (Kuang et al., Reference Kuang, Li, Guo, Lu, He, Luo, Jiang, Shen, Papasian, Pang, Xia, Deng and Qiu2016). These consist of the P-, A-, and F-types, referring to abundances in Proteobacteria, Actinobacteria, and Firmicutes, respectively. Most Chinese infants are P-type, whereas children from Western countries are predominantly A-type, which could impact the initial colonisation of Coprococcus species. The P-type was also determined in a cohort of Ugandan children (n = 139), and similar to the observations in the Chinese cohort, the prevalence of C. eutactus increased with age; C. eutactus prevalence increased from 24 to 36 months from 62 to 81% (Kort et al., Reference Kort, Schlösser, Vazquez, Atukunda, Muhoozi, Wacoo, Sybesma, Westerberg, Iversen and Schoen2021).

Odamaki et al. (Reference Odamaki, Kato, Sugahara, Hashikura, Takahashi, Xiao, Abe and Osawa2016) analysed faecal samples from 367 healthy Japanese individuals between the ages of 0 and 104 years and found a distinct, adult-associated co-abundance group (CAG) of bacterial species that were increased compared to the infant and elderly microbiome compositions. The adult-like CAG included Lachnospiraceae, Blautia, Roseburia, Faecalibacterium, Lachnospira, and Coprococcus. These findings have also been observed in other large cohort studies. Coprococcus spp. were identified as part of the 20 adult core genera in the Belgian Flemish Gut Flora (FGFP) cohort (n = 1106), and they were listed in the 14 core genera (prevalence of 95% or higher) from the combined Western and non-Western cohorts (n ≈ 4,300; Falony et al., Reference Falony, Joossens, Vieira-Silva, Wang, Darzi, Faust, Kurilshikov, Bonder, Valles-Colomer, Vandeputte, Tito, Chaffron, Rymenans, Verspecht, de Sutter, Lima-Mendez, D’hoe, Jonckheere, Homola, Garcia, Tigchelaar, Eeckhaudt, Fu, Henckaerts, Zhernakova, Wijmenga and Raes2016). Coprococcus was present in 99.73% of the samples in the FGFP cohort, whereas the coverage for the non-Western cohort was lower (84.09%). King et al. (Reference King, Desai, Sylvetsky, LoTempio, Ayanyan, Carrie, Crandall, Fochtman, Gasparyan, Gulzar, Howell, Issa, Krampis, Mishra, Morizono, Pisegna, Rao, Ren, Simonyan, Smith, VedBrat, Yao and Mazumder2019) constituted a healthy human reference microbiome list (based on faecal and metagenomic faecal samples of approximately 100 adults) with 157 organisms. Scoring both a prevalence of 100%, C. eutactus ART55/1 and C. catus were included in this list of the healthy core microbiome, with a mean relative abundance of 0.68 and 0.37%, respectively. Coprococcus spp. were also included in the top 33 most abundant taxa in the FGFP cohort, ranking ninth place when scaled by the rarefied abundance data (Falony et al., Reference Falony, Joossens, Vieira-Silva, Wang, Darzi, Faust, Kurilshikov, Bonder, Valles-Colomer, Vandeputte, Tito, Chaffron, Rymenans, Verspecht, de Sutter, Lima-Mendez, D’hoe, Jonckheere, Homola, Garcia, Tigchelaar, Eeckhaudt, Fu, Henckaerts, Zhernakova, Wijmenga and Raes2016). However, the abundance of Coprococcus differs largely per person, as Coprococcus spp. were listed in the top 10 contributors of interindividual variation in microbiota composition, resting on changes in the relative abundance of the core taxa. Shetty et al. (Reference Shetty, Hugenholtz, Lahti, Smidt and de Vos2017) specifically identified C. eutactus as a member of the core microbiota in adult subjects across mainland Europe, UK/Ireland, and the USA (n = 401), with a prevalence of 100%. Moreover, C. eutactus was ranked fifth in relative abundance, while the other Coprococcus members were absent from the list of 80 core bacterial species.

Later in life, new shifts in microbiota configuration occur (Odamaki et al., Reference Odamaki, Kato, Sugahara, Hashikura, Takahashi, Xiao, Abe and Osawa2016), where seven genera, including Coprococcus, are negatively correlated with age and are found to be significantly lower in centenarians than in elderly people aged 80–99 years (Fang et al., Reference Fang, Ting, Guohong, Da, Xiaolin, Haiyan, Zhenjun, Danlei, Yang, Peihong, Ruifeng, Lian and Mouming2015). In summary, Coprococcus spp. are acquired by age and can occur in the early months of life. The mechanism of colonisation is unclear, but may be facilitated through spore-mediated horizontal transmission. C. eutactus is part of the healthy Western adult core microbiome (Shetty et al., Reference Shetty, Hugenholtz, Lahti, Smidt and de Vos2017), but with advanced age, the abundance of the genus Coprococcus decreases again (Fang et al., Reference Fang, Ting, Guohong, Da, Xiaolin, Haiyan, Zhenjun, Danlei, Yang, Peihong, Ruifeng, Lian and Mouming2015).

Association between host genetics and Coprococcus abundance in the gut microbiome

A number of studies have shown evidence for associations between the abundance of Coprococcus in the gut microbiome and host genotypes, particularly with respect to IBD pathogenesis. A genetic association study performed by Rausch et al. (Reference Rausch, Rehman, Künzel, Häsler, Ott, Schreiber, Rosenstiel, Franke and Baines2011) in Caucasian populations, including healthy subjects and patients with Crohn’s disease (n = 47), indicated an association between the human FUT2 gene located on chromosome 19 and the abundance of Coprococcus, Alistipes, and unclassified Lachnospiraceae in the human gut (Rausch et al., Reference Rausch, Rehman, Künzel, Häsler, Ott, Schreiber, Rosenstiel, Franke and Baines2011). More specifically, through a host genotyping and 16S V1–V2 rRNA taxonomic profiling approach, the authors detected associations between the three OTUs and individuals with Crohn’s disease (CD) that were homozygous for the loss-of-function allele “A” at position rs601338. An association between the abundance of Coprococcus and genetic variation in a risk locus linked to CD was also observed Li et al. (Reference Li, Achkar, Haritunians, Jacobs, Hui, D’Amato, Brand, Radford-Smith, Halfvarson, Niess, Kugathasan, Büning, Schumm, Klei, Ananthakrishnan, Aumais, Baidoo, Dubinsky, Fiocchi, Glas, Milgrom, Proctor, Regueiro, Simms, Stempak, Targan, Törkvist, Sharma, Devlin, Borneman, Hakonarson, Xavier, Daly, Brant, Rioux, Silverberg, Cho, Braun, McGovern and Duerr2016), who performed a genotyping analysis of large cohorts (n = 16,249) of IBD patients and healthy subjects. They found that a well-known pleotropic missense variant in the SLC39A8 gene (rs13107325) was correlated with the abundance of five genera in the microbiome (Anaerostipes, Coprococcus, Roseburia, Lachnospira, and SMB53) in individuals with CD and healthy controls. Missense variants have also been strongly associated with an increased risk of schizophrenia (Schizophrenia Working Group of the Psychiatric Genomics Consortium, 2014).

Although the aforementioned studies did not directly investigate the influence of host genetics on the microbiome in mental health-related diseases, there is increasing evidence linking the gut–brain axis to the development of both gastrointestinal and neurological diseases (Günther et al., Reference Günther, Rothhammer, Karow, Neurath and Winner2021). The rationale behind this connection is that the metabolites produced by gut microbes and molecules released by the mucosal immune system in response to inflammation or infection (such as cytokines) both affect the integrity of the blood–brain barrier (BBB) and epithelial barrier, and thus influence CNS functions. This suggests that indirect mechanisms may exist through which gut bacteria modulate neurological diseases. Significant associations have been found between IBD and neurodegenerative and neuroinflammatory diseases. For example, a recent study by Villumsen et al. (Reference Villumsen, Aznar, Pakkenberg, Jess and Brudek2019) on a large Danish cohort n = 7,548,259), showed that IBD patients had a 22% increased risk of developing Parkinson’s disease (PD). Kosmidou et al. (Reference Kosmidou, Katsanos, Katsanos, Kyritsis, Tsivgoulis, Christodoulou and Giannopoulos2017) performed a large meta-analysis (total n = 1,086,430) indicating that both IBD and MS patients have more than 50% increased risk to have concomitant MS and IBD, respectively. In conclusion, recent studies have shown that indirect mechanisms through which gut bacteria modulate neurological diseases may exist. However, future research is needed to elucidate the interaction between the abundance of specific Coprococcus species, such as C. eutactus, and the host genome and how this impacts the direct or indirect development of mental disorders.

Coprococcus species and general health associations

In a recent analysis of a large microbiome population cohort (FGFP, n = 1,054), both Faecalibacterium and Coprococcus bacteria were consistently associated with higher quality of life (QoL) indicators, addressed by mental and physical scoring indicators (Valles-Colomer et al., Reference Valles-Colomer, Falony, Darzi, Tigchelaar, Wang, Tito, Schiweck, Kurilshikov, Joossens, Wijmenga, Claes, Van Oudenhove, Zhernakova, Vieira-Silva and Raes2019). Indeed, Coprococcus spp. have been implicated as beneficial health factors in previous studies; microbiome alpha-diversity was found to be positively correlated with circulating acetate levels in a cohort of 948 women from TwinsUK, while four bacterial genera, including Coprococcus, were linked to higher serum acetate levels (Nogal et al., Reference Nogal, Louca, Zhang, Wells, Steves, Spector, Falchi, Valdes and Menni2021). The latter study also identified a negative correlation between visceral fat and serum acetate level. Similarly, in 1,018 middle-aged women from the TwinsUK cohort, microbiome alpha diversity was positively correlated with serum IPA levels, a metabolite produced by intestinal microbes from dietary tryptophan (Menni et al., Reference Menni, Hernandez, Vital, Mohney, Spector and Valdes2019). IPA regulates the gastrointestinal barrier function (Venkatesh et al., Reference Venkatesh, Mukherjee, Wang, Li, Sun, Benechet, Qiu, Maher, Redinbo, Phillips, Fleet, Kortagere, Mukherjee, Fasano, Le Ven, Nicholson, Dumas, Khanna and Mani2014) and is associated with a reduced risk of type II DM (de Mello et al., Reference de Mello, Paananen, Lindström, Lankinen, Shi, Kuusisto, Pihlajamäki, Auriola, Lehtonen, Rolandsson, Bergdahl, Nordin, Ilanne-Parikka, Keinänen-Kiukaanniemi, Landberg, Eriksson, Tuomilehto, Hanhineva and Uusitupa2017). Along with F. prausnitzii, Mollicutes (phylum Tenericutes), Ruminococcaceae (mostly butyrate-producing bacteria), and C. eutactus and its members were positively correlated with IPA serum levels (Menni et al., Reference Menni, Hernandez, Vital, Mohney, Spector and Valdes2019).

Preeclampsia (PE) is a pregnancy-specific hypertensive disorder that impairs maternal and foetal health, but it also shares similarities in clinical features and pathogenic mechanisms with metabolic diseases such as DM (Valdés et al., Reference Valdés, Sepúlveda-Martínez, Manukián and Parra-Cordero2014; Liu et al., Reference Liu, Yang, Yin, Jiang, Zhong, Qiu, Zhu and Li2017). In studies investigating faecal samples from South-Chinese (n = 100) and Australian (n = 213) pregnant women, Coprococcus spp. were negatively correlated with the PE status (Liu et al., Reference Liu, Yang, Yin, Jiang, Zhong, Qiu, Zhu and Li2017; Altemani et al., Reference Altemani, Barrett, Gomez-Arango, Josh, David McIntyre, Callaway, Morrison, Tyson and Dekker Nitert2021). However, in a Chinese study, C. catus was specifically decreased, whereas an association was found for the pooled Coprococcus genus in Australian women. The authors of the first study suggested the ability of C. catus to produce propionic acid with its inhibiting effect on cholesterol synthesis as a mode of mechanism, while the Australian group demonstrated additional evidence for butyrate-related mechanisms; Coprococcus abundance significantly and positively correlated with the abundance of genes encoding bacterial butyrate formation. In addition, circulating butyrate levels were lower in PE women prior to the development of symptoms.

A Finnish study investigated the intestinal microbiota composition of 6-month-old infants in relation to eczema and found that the severity of symptoms correlated inversely with microbiota diversity and the abundance of butyrate producers (Nylund et al., Reference Nylund, Nermes, Isolauri, Salminen, de Vos and Satokari2015). Early infants received a 3-month dietary intervention with hydrolysed casein formula with or without Lactobacillus rhamnosus GG supplementation. Clinical symptoms (assessed by SCORAD values) were alleviated in all infants, which coincided with increased microbiota diversity. Moreover, decreased SCORAD values correlated with an increased abundance of eight butyrate-producing bacterial species, with the highest effect size observed for the increased abundance of C. eutactus. Similarly, in a small cohort of children (1–6 years old) with atopic dermatitis, alterations were found in the gut microbiota compared to controls, characterised by lower microbiota diversity and increased abundances of Faecalibacterium, Oscillospira, Bacteroides, Parabacteroides, and Sutterella (Reddel et al., Reference Reddel, Del Chierico, Quagliariello, Giancristoforo, Vernocchi, Russo, Fiocchi, Rossi, Putignani and El Hachem2019). In line with a previous study, a reduced abundance of SCFA-producing bacteria was observed, including Coprococcus. Lastly, the Coprococcus genus has been negatively associated with ileal CD, whereas the ileitis mucosa was enriched in sequences for the facultative anaerobic bacterium E. coli (Baumgart et al., Reference Baumgart, Dogan, Rishniw, Weitzman, Bosworth, Yantiss, Orsi, Wiedmann, McDonough, Kim, Berg, Schukken, Scherl and Simpson2007).

Production and synthesis pathways

The beneficial health effects of the gut microbiota are mostly attributed to the production of SCFAs. SCFAs are found in high concentrations in dairy products and can thus be directly taken up through food or indirectly as the fermentation products of our intestinal microbiota (O’Riordan et al., Reference O’Riordan, Collins, Moloney, Knox, Aburto, Fülling, Morley, Clarke, Schellekens and Cryan2022). All Coprococcus species produce SCFAs acetate and butyrate, but differ in the metabolic pathways and substrates used, as well as the amounts and ratios of the produced SCFAs (Holdeman and Moore, Reference Holdeman and Moore1974). Only C. catus is characterised by its large production of propionate (Holdeman and Moore, Reference Holdeman and Moore1974; Reichardt et al., Reference Reichardt, Duncan, Young, Belenguer, McWilliam Leitch, Scott, Flint and Louis2014).

As the main products of anaerobic fermentation of indigestible polysaccharides by microbiota, SCFAs are small carboxylic acids containing an aliphatic tail with a maximum chain length of six carbon atoms (Parada Venegas et al., Reference Parada Venegas, De la Fuente, Landskron, González, Quera, Dijkstra, Harmsen, Faber and Hermoso2019). Acetate (C2), propionate (C3), and butyrate (C4) are the most abundant SCFAs found in the large intestine (McNeil et al., Reference McNeil, Cummings and James1978; Cummings et al., Reference Cummings, Pomare, Branch, Naylor and Macfarlane1987; Rios-Covian et al., Reference Rios-Covian, González, Nogacka, Arboleya, Salazar, Gueimonde and los Reyes-Gavilán2020), and the substrates for bacterial SCFA production include resistant starch (i.e., starch and products of starch degradation not absorbed in the small intestine), oat and wheat bran, cellulose, and pectin (Parada Venegas et al., Reference Parada Venegas, De la Fuente, Landskron, González, Quera, Dijkstra, Harmsen, Faber and Hermoso2019). Figure 2 provides an overview of the major routes for SCFA formation. Notably, resistant starch forms an important source for butyrate synthesis (Champ, Reference Champ2004). Members of Bacteroidetes are responsible for the production of bulk acetate and propionate, whereas Firmicutes are the main butyrate producers in the human gut (Louis and Flint, Reference Louis and Flint2017).

Figure 2. Degradation pathways for carbohydrates into short-chain fatty acids (SCFAs). Overview of carbohydrate break-down into SCFAs. Image reproduced from Parada Venegas et al. (Reference Parada Venegas, De la Fuente, Landskron, González, Quera, Dijkstra, Harmsen, Faber and Hermoso2019).

The microbial synthesis pathways of SCFAs were first described by Miller and Wolin (Reference Miller and Wolin1996), and additional pathways have since been discovered. Butyrate formation predominantly occurs from carbohydrate hydrolysis and subsequent glycolysis; however, butyrate can also be synthesised from organic acids and amino acids (Louis and Flint, Reference Louis and Flint2017). Butyrate production occurs via either the acetyl-CoA, glutarate, 4-aminobutyrate, or lysine pathways (Vital et al., Reference Vital, Howe and Tiedje2014; Figure 3). The acetyl-CoA pathway accounts for the bulk of bacterial butyrate formation and related genes are found in the majority of butyrate producers (Vital et al., Reference Vital, Howe and Tiedje2014). Genes for the lysine pathway are also present in many phyla, whereas the 4-aminobutyrate- and glutarate-based pathways are the least abundant. Several isolates have been reported to carry genes for multiple butyrate pathways, indicating that butyrate synthesis plays a prominent role in energy conservation.

Figure 3. The butyrate synthesis pathways. The four bacterial butyrate synthesis pathways were retrieved from a study by Vital et al. (Reference Vital, Howe and Tiedje2014). Major enzymes are indicated and terminal genes are highlighted in red. Bcd, butyryl-CoA dehydrogenase (including electron transfer protein α and β subunits); Ptb, phosphate butyryltransferase; 4Hbt, butyryl-CoA:4-hydroxy-butyrate CoA transferase; But, butyryl-CoA:acetate CoA transferase; Ato, butyryl-CoA:acetoacetate CoA transferase; Buk, butyrate kinase.

These pathways merge at a central step, where crotonyl-CoA is transformed to butyryl-CoA, thereby creating a proton motive force to conserve energy in ATP for the bacterium. Thus, butyrate production not only restores the redox balance by regeneration of NAD⁺ from NADH + H⁺ produced upstream in the carbohydrate breakdown for ATP conversion, but also results in additional ATP production (Louis and Flint, Reference Louis and Flint2009; Vital et al., Reference Vital, Howe and Tiedje2014). The final conversion to butyrate is performed by various butyryl-CoA transferases such as butyryl-CoA:acetate CoA transferase (But). The latter requires external acetate as a co-factor, donated through cross-feeding mechanisms (Duncan et al., Reference Duncan, Barcenilla, Stewart, Pryde and Flint2002, Reference Duncan, Holtrop, Lobley, Calder, Stewart and Flint2004). Alternatively, butyryl-CoA is phosphorylated and transformed into butyrate via butyrate kinase (Buk), resulting in additional ATP synthesis (Miller and Wolin, Reference Miller and Wolin1996; Vital et al., Reference Vital, Howe and Tiedje2014; Louis and Flint, Reference Louis and Flint2017).

As mentioned earlier, the majority of intestinal butyrate producers belong to the Firmicutes phylum, particularly Clostridia clusters IV and XIVa, the latter of which includes the Coprococcus genus (Rivière et al., Reference Rivière, Selak, Lantin, Leroy and De Vuyst2016). These clusters contain Gram-positive, highly oxygen-sensitive, and strictly anaerobic saccharolytic bacteria. Considering their relatively high abundance in the human colon, Faecalibacterium prausnitzii (Clostridium cluster IV) and Eubacterium rectale (Clostridium cluster XIVa) are expected to contribute more significantly to intestinal butyrate production than Coprococcus spp. However, specific synthesis pathways and substrates place Coprococcus spp. in a unique position. All Coprococcus spp. are butyrate producers, with C. catus containing only the But and C. comes only the Buk genes; Coprococcus eutactus contains both the But and Buk genes (Vital et al., Reference Vital, Howe and Tiedje2014), allowing butyrate production under less restricted conditions and substrate availability, and potentially higher energy conservation by utilisation of the butyrate-kinase pathway. Importantly, only a few other human gut-associated taxa (Clostridium sp. L2–50, Ruminococcaceae bacterium D16, and Acidaminococcus sp. D21) are known to encode both But and Buk genes (Vital et al., Reference Vital, Howe and Tiedje2014). In addition, Vital et al. (Reference Vital, Howe and Tiedje2014) listed C. eutactus as the fourth bacterial contributor to the dominant butyrate pathway, the acetyl-CoA pathway, highlighting its role in colonic butyrate formation.

Three distinct pathways for propionate production have been described: succinate, acrylate, and propanediol pathways, using polysaccharides, organic acids, lactate, and amino acids as substrates (Reichardt et al., Reference Reichardt, Duncan, Young, Belenguer, McWilliam Leitch, Scott, Flint and Louis2014). Since the succinate pathway is present in the abundant phylum Bacteroidetes, as well as in certain Negativicutes bacteria, it is assumed to be the most dominant route for propionate production (Reichardt et al., Reference Reichardt, Duncan, Young, Belenguer, McWilliam Leitch, Scott, Flint and Louis2014). In the succinate pathway, the decarboxylation of methylmalonyl-CoA to propionyl-CoA is coupled with sodium transport across the membrane, driving ATP generation via sodium-translocating ATPase. In the acrylate pathway, the lactoyl-CoA dehydratase gene serves as a marker, which was identified in C. catus (Reichardt et al., Reference Reichardt, Duncan, Young, Belenguer, McWilliam Leitch, Scott, Flint and Louis2014). Through isotype-labelling experiments, C. catus was found to convert virtually all lactate to propionate via the acrylate pathway. Interestingly, colonic bacteria seem to encode genes for either butyrate synthesis or propionate synthesis, whereas only two bacterial species are known to produce both butyrate and propionate as end products of carbohydrate fermentation; C. catus produces butyrate when grown on fructose and shifts to propionate production when grown on lactate. Similarly, Roseburia inulinivorans generates butyrate from glucose, but converts fucose into propionate. Among the other Coprococcus members, C. comes and C. eutactus lack propionate synthesis genes, are not able to grow on lactate, and instead produce butyrate from sugar fermentation.

As acetate is the most produced SCFA in the gut, anaerobic fermentation of carbohydrates often entails the breakdown of monosaccharides into acetyl coenzyme A (acetyl-CoA) and subsequent acetate production, generating ATP by substrate-level phosphorylation (Zhang et al., Reference Zhang, Lingga, Bowman and Hackmann2021). Five pathways have been reported, all for which acetyl-CoA serves as a precursor (Figure 2), although acetyl phosphate may alternatively function as a high-energy substrate in one pathway. In their investigation of microbiota-produced acetate, Nogal et al. (Reference Nogal, Louca, Zhang, Wells, Steves, Spector, Falchi, Valdes and Menni2021) assigned three acetate pathways to both C. eutactus and C. comes, and two to C. catus, but the authors did not refer to specific metabolic pathways. Therefore, genomic data analysis is required to resolve the pathways for acetate biosynthesis by Coprococcus species.

Coprococcus associations with neurophysiological states and mental disorders

In addition to general health-associated factors, studies have linked the Coprococcus genus to multiple neurological and psychological disorders (Table 1; search methodology specified in the Supplementary File S2), where C. eutactus is specifically associated with Parkinson’s disease (PD; Petrov et al., Reference Petrov, Saltykova, Zhukova, Alifirova, Zhukova, Dorofeeva, Tyakht, Kovarsky, Alekseev, Kostryukova, Mironova, Izhboldina, Nikitina, Perevozchikova, Fait, Babenko, Vakhitova, Govorun and Sazonov2017) and language development in children (Kort et al., Reference Kort, Schlösser, Vazquez, Atukunda, Muhoozi, Wacoo, Sybesma, Westerberg, Iversen and Schoen2021). The association between reduced relative abundance of Coprococcus spp. in the gut and PD was found 2 years earlier in a smaller American cohort (Keshavarzian et al., Reference Keshavarzian, Green, Engen, Voigt, Naqib, Forsyth, Mutlu and Shannon2015). Both studies indicated a reduced abundance of butyrate-producing bacteria Blautia, Coprococcus, and Roseburia in patients with PD, whereas putative pro-inflammatory bacteria, such as Oscillospira, were increased. Moreover, the American team showed a negative correlation between PD duration and the abundance of Lachnospiraceae, a bacterial family comprising many anti-inflammatory butyrate-producers, including Coprococcus. Additionally, they performed predictive metagenomics of the faecal microbiome community functionality and found that genes for lipopolysaccharide biosynthesis and type III bacterial secretion systems were higher in PD patients. These results support the theory that intestinal dysbiosis could trigger leakage of the intestinal barrier, subsequent inflammatory response, and oxidative stress, leading to alpha-synuclein (α-Syn) aggregation. Indeed, α-Syn deposits in the colon of patients with PD have been demonstrated already 2–5 years before the onset of PD symptoms. The mechanism of consequent neuroinflammation and α-Syn deposition in the brain is still highly speculative, but may involve direct pathways via the mesenteric nerve system, reduced anti-inflammatory responses in the CNS due to a shortage of microbiota-produced SCFAs, or even a prion-like spreading of the α-Syn aggregates to the brain.

Table 1. Summary of studies with significant correlation of Coprococcus genus and neurological disorders.

Abbreviations: LEfSe, linear discriminant analysis effect size; SAS, self-rating anxiety scale.

SCFA synthesis and hydrogen formation are inherently linked (see section “The impact of Coprococcus on gut homeostasis” ), and intestinal microbiota from PD patients have been demonstrated to produce 2.2-fold less hydrogen compared to controls (Suzuki et al., Reference Suzuki, Ito, Hamaguchi, Mori, Takeda, Baba, Watanabe, Kurokawa, Asakawa, Hirayama and Ohno2018). Despite a promising pilot study (Yoritaka et al., Reference Yoritaka, Takanashi, Hirayama, Nakahara, Ohta and Hattori2013), the administration of exogenous hydrogen (by hydrogen water) to patients with PD has been proven unsuccessful in a larger-scale investigation (Yoritaka et al., Reference Yoritaka, Ohtsuka, Maeda, Hirayama, Abe, Watanabe, Saiki, Oyama, Fukae, Shimo, Hatano, Kawajiri, Okuma, Machida, Miwa, Suzuki, Kazama, Tomiyama, Kihara, Hirasawa, Shimura, Oda, Ito, Ohno and Hattori2018). Suzuki et al. (Reference Suzuki, Ito, Hamaguchi, Mori, Takeda, Baba, Watanabe, Kurokawa, Asakawa, Hirayama and Ohno2018) claimed that the imbalance in the hydrogen economy in patients with PD may be dependent on many classes of SCFA producers and cross-feeders, and does not only depend on butyrate production. As the authors mentioned, a large proportion of hydrogen was also produced by the reduction of formate. Microbiome metabolism in the gut accounts for approximately 50% of the formate pool in human serum (Pietzke et al., Reference Pietzke, Meiser and Vazquez2020). Formate is involved in many physiological processes including purine synthesis, sterol and tryptophan metabolism, and methylation. Interestingly, circulating urate levels are reduced in PD patients (Ascherio et al., Reference Ascherio, LeWitt, Xu, Eberly, Watts, Matson, Marras, Kieburtz, Rudolph, Bogdanov, Schwid, Tennis, Tanner, Beal, Lang, Oakes, Fahn, Shoulson and Schwarzschild2009). Notably, formate acts as a precursor for purine synthesis, and urate as a product of purine catabolism (Pietzke et al., Reference Pietzke, Meiser and Vazquez2020). Indeed, in early onset PD, mitochondrial formate production is impaired and serum urate levels increase. Although further studies are warranted, we speculate that SCFAs other than butyrate play important roles in the aetiology of PD. Apart from butyrate, C. eutactus produces large amounts of formate, possibly contributing to the association between Coprococcus spp. and PD pathology.

Eight studies demonstrated lower relative abundance of Coprococcus spp. in individuals suffering from depression or depression-like symptoms (Liu et al., Reference Liu, Zhang, Wang, Wang, Zhang, Jiang, Wang, Wang, Liu, Xia, Xu, Nie, Lv, Wu, Zhu and Duan2016; Huang et al., Reference Huang, Shi, Li, Shen, Shi, Wang, Li, Yuan, Wang, Zhang, Zhao, Zhang, Kang and Liang2018; Hu et al., Reference Hu, Li, Huang, Lai, Li, Sublette, Lu, Lu, du, Hu, Ng, Zhang, Lu, Mou, Lu, Wang, Duan, Hu, Huang, Wei, Zhou, Ruan, Li and Xu2019; Valles-Colomer et al., Reference Valles-Colomer, Falony, Darzi, Tigchelaar, Wang, Tito, Schiweck, Kurilshikov, Joossens, Wijmenga, Claes, Van Oudenhove, Zhernakova, Vieira-Silva and Raes2019; Chen et al., Reference Chen, Xue, Yu, Li, Liu, Jia, Yan, Tan, Wang and Peng2021; Leyrolle et al., Reference Leyrolle, Cserjesi, D.G.H. Mulders, Zamariola, Hiel, Gianfrancesco, Portheault, Amadieu, Bindels, Leclercq, Rodriguez, Neyrinck, Cani, Lanthier, Trefois, Bindelle, Paquot, Cnop, Thissen, Klein, Luminet and Delzenne2021; Li et al., Reference Li, Jing, Lu, Li and Zhang2022; Radjabzadeh et al., Reference Radjabzadeh, Bosch, Uitterlinden, Zwinderman, Ikram, van Meurs, Luik, Nieuwdorp, Lok, van Duijn, Kraaij and Amin2022), establishing a link between the Coprococcus genus and the gut–brain axis. The large Flemish and Dutch cohorts showed a significant negative correlation between Coprococcus spp. and depression when findings were corrected for antidepressant medication (Valles-Colomer et al., Reference Valles-Colomer, Falony, Darzi, Tigchelaar, Wang, Tito, Schiweck, Kurilshikov, Joossens, Wijmenga, Claes, Van Oudenhove, Zhernakova, Vieira-Silva and Raes2019), which was recently replicated in two other large Dutch cohorts (Radjabzadeh et al., Reference Radjabzadeh, Bosch, Uitterlinden, Zwinderman, Ikram, van Meurs, Luik, Nieuwdorp, Lok, van Duijn, Kraaij and Amin2022). However, in the latter study, Ruminococcaceae UCG005 was the main predictor of depressive symptoms, whereas the Coprococcus genus was not listed as an important predictor (Radjabzadeh et al., Reference Radjabzadeh, Bosch, Uitterlinden, Zwinderman, Ikram, van Meurs, Luik, Nieuwdorp, Lok, van Duijn, Kraaij and Amin2022). Interestingly, using Mendelian randomisation, the group identified a causal link between Eggerthella and depression. Another interesting finding has been reported by Liu et al. (Reference Liu, Zhang, Wang, Wang, Zhang, Jiang, Wang, Wang, Liu, Xia, Xu, Nie, Lv, Wu, Zhu and Duan2016) found a reduced abundance of Coprococcus spp. in patient groups, but also found high similarities between the intestinal microbiome composition of patients with inflammatory bowel syndrome (IBS) and depressed individuals. Together with the high observed comorbidity rate of IBS and depression, these results may indicate a common dysbiosis-related pathogenesis; intestinal inflammation could disturb the communication between the enteric nervous system and the CNS. Similarly, obesity and depression often coincide, and Leyrolle et al. (Reference Leyrolle, Cserjesi, D.G.H. Mulders, Zamariola, Hiel, Gianfrancesco, Portheault, Amadieu, Bindels, Leclercq, Rodriguez, Neyrinck, Cani, Lanthier, Trefois, Bindelle, Paquot, Cnop, Thissen, Klein, Luminet and Delzenne2021) stratified a cohort of obese adults in high and low intestinal abundance of Coprococcus. High-baseline Coprococcus predicted better mood improvement after a 3-month prebiotic inulin intervention compared to the placebo group and low-baseline group. However, the relative contribution of Coprococcus is difficult to estimate since the positive response was also correlated with an increased inflammatory profile, insulin resistance, and adiposity at baseline. Reininghaus et al. (Reference Reininghaus, Platzer, Kohlhammer-Dohr, Hamm, Mörkl, Bengesser, Fellendorf, Lahousen-Luxenberger, Leitner-Afschar, Schöggl, Amberger-Otti, Wurm, Queissner, Birner, Falzberger, Painold, Fitz, Brunnmayr, Rieger, Wagner-Skacel, Maget, Unterweger, Schwalsberger, Reininghaus, Lenger, Bastiaanssen and Dalkner2020) performed a 4-week multistrain probiotic plus biotin intervention in an inpatient setting for depressed individuals. Ruminococcus gauvreauii, Coprococcus, and β-diversity increased in the probiotic group after 28 days. Moreover, KEGG analysis showed elevated anti-inflammatory and metabolic pathways, including vitamin B1 and B6/7 metabolism. Beneficial effects on clinical parameters were observed, but were similar in the biotin and placebo groups. Four weeks may be insufficient to observe any differences in clinical outcome measures, but the study shows that appropriate probiotic treatment can elevate Coprococcus levels in the short term and simultaneously upregulate inflammation-regulating responses.

These studies share the finding that butyrate-producing bacteria, mostly from the Firmicutes phylum, are reduced in individuals with depression. Although all three Coprococcus spp. produce butyrate, C. eutactus may add more to the microbiota-produced butyrate pool owing to its availability of multiple butyrate-synthesis pathways and higher general abundance, and consequently confer a higher protective effect on the development of depression. However, a study in Polish females investigated the link between faecal SCFA levels and depression and found that acetate and propionate were negatively correlated with clinical parameters of depression (Skonieczna-Żydecka et al., Reference Skonieczna-Żydecka, Grochans, Maciejewska, Szkup, Schneider-Matyka, Jurczak, Łoniewski, Kaczmarczyk, Marlicz, Czerwińska-Rogowska, Pełka-Wysiecka, Dec and Stachowska2018). Differences in absorption rates of individual SCFAs by colonocytes cannot be excluded, although they may explain inconsistencies in findings between faecal microbiome and faecal SCFA analysis. Other possible mechanisms, besides butyrate production, underlying the microbiome association with reduced susceptibility to depression, were proposed by Valles-Colomer et al. (Reference Valles-Colomer, Falony, Darzi, Tigchelaar, Wang, Tito, Schiweck, Kurilshikov, Joossens, Wijmenga, Claes, Van Oudenhove, Zhernakova, Vieira-Silva and Raes2019). The authors analysed the association between microbiome features and the diagnosis of depression and QoL using two large population cohorts (Table 1). First, the authors assessed the neuroactive potential of the gut microbiota. More specifically, through a thorough literature search, they defined 56 gut–brain modules (GBMs), corresponding to distinct microbial pathways by which a neuroactive compound (a chemical that interacts with the human nervous system) is either synthesised or degraded. From a subsequent search in 532 microbial reference genomes of the human gastrointestinal tract, 15 GBMs could be detected within one or more Coprococcus spp. genomes included in the dataset (C. eutactus ATCC 27759, C. comes ATC 27758, C. catus GD/7, and C. sp. ART55/1). A summary of these results is presented in Table 2. Out of the 13 GBMs found in the C. eutactus strain, two GMBs for tryptophan synthesis and acetate degradation were not detected in the C. comes and C. catus strains. Instead, one GMB for isovaleric acid synthesis II was shown to be present in both the C. comes and C. catus strains, but not in the C. eutactus strain. Notably, the three GBMs for p-cresol synthesis, 17-beta-estradiol degradation, and isovaleric acid synthesis II were found in at least one of the available Coprococcus spp. genomes, although their corresponding functions have not yet been experimentally observed and described in the literature. In the microbiome-wide association study, Valles-Colomer et al. (Reference Valles-Colomer, Falony, Darzi, Tigchelaar, Wang, Tito, Schiweck, Kurilshikov, Joossens, Wijmenga, Claes, Van Oudenhove, Zhernakova, Vieira-Silva and Raes2019) found significant covariation of 3,4-dihydroxyphenylacetic acid (DOPAC) synthesis potential with mental QoL scores in both the Flemish and Dutch cohorts. DOPAC is the metabolic end-product of dopamine conversion, and reduced DOPAC levels in cerebrospinal fluid have been observed in patients with PD. Interestingly, DOPAC synthesis potential was strongly associated with the relative abundance of Coprococcus. Although the Coprococcus spp. do not seem to synthesise DOPAC, one of the metabolic steps in the DOPAC synthesis pathway, the second step in the GBM, which converts 3,4-dihydroxyphenylacetaldehyde to DOPAC, is encoded in the genomes of C. comes and C. catus.

Table 2. Summary of the detected gut–brain modules (GBMs) in the genomes of Coprococcus spp. retrieved from Valles-Colomer et al. (Reference Valles-Colomer, Falony, Darzi, Tigchelaar, Wang, Tito, Schiweck, Kurilshikov, Joossens, Wijmenga, Claes, Van Oudenhove, Zhernakova, Vieira-Silva and Raes2019).

Note: For the GBMs indicated in grey, the corresponding functions have not yet been experimentally confirmed in the literature. The finding of only one butyrate-synthesis GBM for Coprococcus eutactus is in contrast with the findings from the study by Vital et al. (Reference Vital, Howe and Tiedje2014) showing that the same strain (ATCC 27759) contains two butyrate synthesis pathways, mediated by the But and Buk genes.

Kang et al. (Reference Kang, Park, Ilhan, Wallstrom, Labaer, Adams and Krajmalnik-Brown2013) published findings on the reduced intestinal abundance of Coprococcus spp. and other fermenters in autistic children, paving the way for new insights into the pathogenesis of neurological disorders. This is in contrast with a recent study showing an increased abundance of Coprococcus spp. in autistic children compared to controls in a cohort of autistic children from Ecuador (Zurita et al., Reference Zurita, Cárdenas, Sandoval, Peña, Fornasini, Flores, Monaco, Berding, Donovan, Kuntz, Gilbert and Baldeón2020). However, the effect size seemed low and Supplementary Material was not included in the analysis. A meta-analysis conducted by Iglesias-Vázquez et al. (Reference Iglesias-Vázquez, Van Ginkel Riba, Arija and Canals2020) on gut microbiome composition included several small studies and indicated a cumulative, significant reduction in Coprococcus spp. in autistic children. Similarly, single studies on generalised anxiety disorder (GAD; Chen et al., Reference Chen, Bai, Wu, Yu, Qiang, Bai, Wang and Peng2019), schizophrenia (Shen et al., Reference Shen, Xu, Li, Huang, Yuan, Wang, Zhang, Hu and Liang2018), and obsessive–compulsory disorder (OCD; Domènech et al., Reference Domènech, Willis, Alemany-Navarro, Morell, Real, Escaramís, Bertolín, Sánchez Chinchilla, Balcells, Segalàs, Estivill, Menchón, Gabaldón, Alonso and Rabionet2022) have shown a reduced relative abundance of Coprococcus spp. in faecal samples of patients. The authors observed a general trend of increased taxa associated with oxidative stress and the reduction of SCFA-producing bacteria. In the OCD study, the authors also considered a DOPAC-mediated mechanism to explain the reduced abundance of Coprococcus spp. in patients, as dopaminergic transmission may be involved in the neurobiology of OCD (Domènech et al., Reference Domènech, Willis, Alemany-Navarro, Morell, Real, Escaramís, Bertolín, Sánchez Chinchilla, Balcells, Segalàs, Estivill, Menchón, Gabaldón, Alonso and Rabionet2022).

Peng et al. (Reference Peng, Qiu, Lai, Li, Zhang, Zhu, He, Duan and Chen2018) found alterations in gut microbiome composition between drug-resistant epileptic patients, drug-sensitive patients, and healthy controls. There was an increased relative abundance of Coprococcus spp. in drug-resistant patients, but while other studies confirmed increased Firmicutes relative to Bacteroides in refractory epileptic individuals, the associated taxa differ per study and findings on increased Coprococcus spp. abundance have not been replicated (Lum et al., Reference Lum, Olson and Hsiao2020). Coprococcus and cognitive capacities have been linked in a recent study on language development in young Ugandan children. The presence of C. eutactus in faeces at 24 months could predict language development at 36 months (Kort et al., Reference Kort, Schlösser, Vazquez, Atukunda, Muhoozi, Wacoo, Sybesma, Westerberg, Iversen and Schoen2021). Comparing their findings to the PD microbiome-related studies, the authors hint at increased butyrate-production as an explanatory mechanism. However, additional studies demonstrating a reduced abundance of Coprococcus spp. and other neurodegenerative/neurocognitive disorders, such as Alzheimer’s disease, are lacking. The only exception may be a study on mindful awareness training in elderly patients diagnosed with mild cognitive impairment; cognitive impairment improved, and Coprococcus spp. were positively correlated with Colour Trails Test 2, Digit Span Backward and Block Design tests (Khine et al., Reference Khine, Voong, Ng, Feng, Rane, Kumar, Kua, Mahendran, Mahendran and Lee2020). Unfortunately, possible explanations for the mechanisms of such bidirectional brain–gut interactions have not been provided.

Neuromyelitis optica spectrum disorders (NMOSDs) are categorised as a group of autoimmune demyelinating diseases of the CNS that lead to visual loss and severe motor impairment. Shi et al. (Reference Shi, Qiu, Wang, Fang, Zhang, Chen, Du, Zhao, Yan, Yang and Zhou2020) discovered significant differences in microbiota composition between patients and controls, and could distinguish patients by increased abundance of the pathogenic genera Flavonifractor and Streptococcus, and decreased abundance of commensal bacteria, including Coprococcus species. KEGG analysis showed that the observed gut microbiome alterations were related to the downregulation of pathways for photosynthesis, and thiamine (vitamin B1) metabolism. The authors hypothesised that thiamine deficiency may exert negative effects on Th1 and Th17 cell subpopulations and reduce the persistence of commensals by interfering with vitamin B1 metabolism, thereby contributing to the loss of intestinal barrier function. Additionally, lower levels of photosynthetic activity could partly explain the observation that patients with NMOSD display low levels of circulating vitamin D. Vitamin D deficiency may increase intestinal permeability even further, thereby enhancing the release of endotoxins in the circulatory system to promote the development of neuroinflammation.

In conclusion, a lower relative abundance of Coprococcus spp. is associated with mental and neurophysiological disorders, although a higher relative abundance has also been demonstrated in patients with autism and refractory epilepsy. Coprococcus-associated disorders cover a broad range of neurological syndromes or states, as recognised in a meta-analysis of gut microbiota composition and psychiatric disorders (Nikolova et al., Reference Nikolova, Smith, Hall, Cleare, Stone and Young2021). Here, the authors could find “a transdiagnostic pattern of microbiota signatures” where “depleted levels of Faecalibacterium and Coprococcus and enriched levels of Eggerthella were consistently shared” between the analysed studies on psychiatric disorders. The combined findings suggest that the disorders are characterised by a reduction in anti-inflammatory butyrate-producing bacteria and an observed enrichment of pro-inflammatory genera. In this review, we analysed Coprococcus in association with cognitive and mental disorders, while excluding psychiatric disorders directly involving diet and nutritional habits (e.g., anorexia nervosa and bulimia). In addition, this review aimed to determine whether C. eutactus is specifically associated with certain mental health disorders. Only two studies specifically indicated an association of C. eutactus with PD or language development, whereas the other studies either did not specify the Coprococcus genus members or found associations with all three Coprococcus species. Without a clear distinction between the Coprococcus species in these studies, such an analysis is difficult to perform. This is further complicated because members of the genus Coprococcus may be poorly characterised in general (Nogal et al., Reference Nogal, Louca, Zhang, Wells, Steves, Spector, Falchi, Valdes and Menni2021), and future studies may first endeavour to unravel the different phylogenetic branches within the genus and possibly categorise the genus into more individual species.

Short-chain fatty acids and the gut–brain axis

As indicated in the previous section, the derived associations between the Coprococcus genus and neuropsychological disorders point towards SCFA-mediated mechanisms. To understand the various ways SCFAs may interact with the gut–brain axis, knowledge of receptors on host cells for SCFA uptake and signalling is crucial. Colonocytes use passive diffusion for SCFA uptake and facilitate SCFA diffusion to co-absorb SCFAs with Na⁺ or K⁺ cations (O’Riordan et al., Reference O’Riordan, Collins, Moloney, Knox, Aburto, Fülling, Morley, Clarke, Schellekens and Cryan2022). The most important transporters are sodium-coupled monocarboxylate transporter (SMCT1) and proton-coupled monocarboxylate transporter (MCT) 1 and 4. MCT1 functions as the primary transporter for butyrate uptake in colonocytes and is upregulated by butyrate and fermentable carbohydrates (Parada Venegas et al., Reference Parada Venegas, De la Fuente, Landskron, González, Quera, Dijkstra, Harmsen, Faber and Hermoso2019). In humans, the proximal colon and ileum contain low expression of SCFA transporters, but MCT1 and MCT4 increase along the colon, reaching their highest number in the distal colon.

Even before SCFAs enter the systemic circulation, where they may exert effects on the brain, SCFAs can activate anti-inflammatory signalling cascades. SCFAs serve as ligands for various G-protein coupled receptors (GPCRs) and hydroxycarboxylic acid receptor 2 (GPR109a/HCAR2) in colonocytes (Parada Venegas et al., Reference Parada Venegas, De la Fuente, Landskron, González, Quera, Dijkstra, Harmsen, Faber and Hermoso2019; O’Riordan et al., Reference O’Riordan, Collins, Moloney, Knox, Aburto, Fülling, Morley, Clarke, Schellekens and Cryan2022). The best characterised GPCRs are GPR43 and GPR41, commonly referred to as free fatty acid receptor 2 (FFAR2) and FFAR3, respectively. FFAR2 has a high affinity for acetate and propionate, whereas FFAR3 prefers longer fatty acid structures such as butyrate. FFAR2 and FFAR3 are not specifically expressed in intestinal epithelial cells, but are found in tissues such as the vasculature and kidneys, as well as in various immune cells (e.g., neutrophils, monocytes, and lymphocytes). Direct activation of the vagus nerve and enteric nervous system by SCFAs may be possible, since FFAR3 is expressed in the periportal afferent neural system, as well as in the enteric neural plexus and autonomic and sensory ganglia.

The proposed roles of SCFAs in brain physiology were described by O’Riordan et al. (Reference O’Riordan, Collins, Moloney, Knox, Aburto, Fülling, Morley, Clarke, Schellekens and Cryan2022). In summary, SCFAs may regulate microglial gene expression, maturation, morphology, and abundance. Acetate may alter (metabolites for) the neurotransmitters glutamate, glutamine, and γ-aminobutyric acid (GABA) as well as anorexigenic neuropeptide expression in the hypothalamus. Microbiota-derived butyrate may improve the integrity of the BBB by inducing higher levels of the tight junction protein occludin. Butyrate may also induce epigenetic changes by increasing histone acetylation and histone crotonylation in the brain. Additionally, butyrate epigenetically regulates microglial responses through the downregulation of pro-inflammatory mediators, while upregulating the expression of anti-inflammatory mediators. Propionate has been associated with reduced experimental autoimmune encephalomyelitis (EAE) and axonal damage through increased T _reg differentiation. The combination of propionate and butyrate regulates tryptophan hydroxylase expression and modulates intracellular potassium levels in the CNS.

Endothelial cells abundantly express MCT, which is the likely mode of transport for SCFAs to cross the BBB (Silva et al., Reference Silva, Bernardi and Frozza2020). FFAR3 has also been found in brain endothelial cells, suggesting a signalling-mediated pathway in which butyrate is involved in BBB protection (O’Riordan et al., Reference O’Riordan, Collins, Moloney, Knox, Aburto, Fülling, Morley, Clarke, Schellekens and Cryan2022). Upon binding of SCFAs to FFAR2 and FFAR3, enteroendocrine colonocytes begin to secrete the anorexigenic hormone peptide YY (PYY) and glucagon-like peptide-1 (GLP-1), which are then transported to the brain via vagal afferents or circulating blood (O’Riordan et al., Reference O’Riordan, Collins, Moloney, Knox, Aburto, Fülling, Morley, Clarke, Schellekens and Cryan2022). PYY and GLP-1 can influence appetite and food intake in the CNS. Notably, acetate increases hypothalamic neuropeptide expression, thereby reducing appetite. In a PYY and GLP-1 independent fashion, propionate has also been associated with reduced appetite and lower energy intake. PYY and GLP-1 have been shown to mediate cognitive processes in the reward centres of the brain, have anti-anxiety and anti-depressant properties, and enhance memory and neuroplasticity. However, the contributions of intestinal PYY and GLP-1 to these processes remain unclear. Furthermore, SCFAs may induce changes in the hormones insulin and leptin, and indirectly reduce ghrelin, an appetite-driving hormone. In addition to their metabolic influence, these hormones have been demonstrated to influence brain function, suggesting an extended repertoire of SCFA-mediated roles in cognitive processes.

In conclusion, the SCFAs butyrate, acetate, and propionate fulfil their roles in neurological function. These roles are mediated through the metabolism of neurotransmitters, epigenetic changes, and BBB integrity, as well as anti-inflammatory effects on microglia, microglial development, and influence on reward centres in the brain. More research is needed to clarify whether the supposed effects are derived from intestinal-derived SCFAs and whether these are directly taken up from the circulation or mediate indirect effects via the vagus nerve or peripheral immune system. In addition, connections between the neurological roles of SCFAs and neurophysiological or neuropsychological clinical outcomes should be further investigated.