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Diet, host gene composition, and alterations in the intestinal microbiota can contribute to obesity. In microbe-induced obesity, metabolic changes stem from primary perturbation of the microbiota, consequent to modern changes in human biology. Microbiota disruption during early development can result in syndromes of metabolic dysfunction. We focus on the pathways involved in these interactions, particularly related to energy extraction and the role of inflammation in the metabolic phenotypes. Model physiologic systems and perturbations including gastric bypass surgery, pregnancy, and hibernation provide insight into the respective roles of the critical participants.
Obesity has markedly increased in the US in the late 20th century (Flegal et al., 2012), as well as worldwide (Haslam and James, 2005). Much focus on the origins of obesity has centered on dietary excesses [diet-induced obesity (DIO)] or on host genes [gene-induced obesity (GIO)] (Hollopeter et al., 1998) (Figure 1). However, in addition to increased calories or alterations in host metabolism, the composition of the intestinal microbiota can contribute to the progression of obesity (Bäckhed et al., 2004; Turnbaugh et al., 2008; Turnbaugh et al., 2006), thus DIO and GIO have both microbe-independent and microbe-dependent mechanisms. Alternately, metabolic changes can stem from a primary perturbation of the microbiota (Cho et al., 2012), consequent to modern changes in human biology (Blaser and Falkow, 2009; Dominguez-Bello et al., 2011) in which the initiating factors lack microbe-independent effects [microbe-induced obesity (MIO)]. Epidemiological studies in humans have shown that antibiotic treatment during the first six months of life (Trasande et al., 2013), or disrupted colonization from Caesarian section delivery (Blustein et al., 2013; Huh et al., 2012) can increase the risk of being overweight later in life. These two interventions have no direct contribution to host caloric intake or metabolism (Coates et al., 1963) but have large effects on the microbiome (Dethlefsen et al., 2008; Dominguez-Bello et al., 2010).
The microbes that colonize humans substantially out-number human cells (Savage, 1977) and the collective unique microbial genes outnumber human genes by more than a factor of 100 (Arumugam et al., 2011; HMPConsortium, 2012; Qin et al., 2010). These co-evolved microbes have a complex role in maintaining health (HMPConsortium, 2012), but can also contribute to disease (Cho and Blaser, 2012; Holmes et al., 2012). Model systems have been used to examine the effects of microbiome change in the context of different diets or on early life development. In this Perspective, we examine mechanistic pathways in which the disrupted microbiome can contribute to obesity through altering energy extraction from food or altering inflammation and immunity (Figure 2). The microbiome is dynamic and resilient, but subject to perturbations that can impact metabolism. We explore major recovery strategies in the microbiome in response to host metabolic perturbations (Figure 3), and discuss metabolic adaptations that aid particular classes of microbiota during recovery in the competitive environments of well-established ecosystems (Figure 4).
The diet provides nutrients to both the host and microbial consortium, which have co-evolved to derive and impart benefits to each other across a wide array of vertebrate lineages (Ley et al., 2008a; Ley et al., 2008b). The microbiota improve the fitness of the host by increasing resistance to pathogens, providing essential vitamins, and increasing caloric extraction from food. The very presence of microbiota influences weight gain and fat storage as germ-free mice have significantly lower weight and body fat percent, despite eating more calories than conventionalized mice (Bäckhed et al., 2004).
Current technologies have allowed more efficient production of food; consequently, the caloric intake has increased in both men and women in the last 30 years (Wright et al., 2004). Increased caloric intake for the host translates to increased energy availability for the microbiota, altering the environment they inhabit (Kau et al., 2011). In addition, readily available processed foods commonly substitute complex carbohydrates for simple refined sugars and contain food preservatives, which affect the composition and diversity of the microbiota (Bernbom et al., 2006; Kau et al., 2011; Payne et al., 2012). In obesity, both reduced microbial diversity and interconnectivity have been observed (Greenblum et al., 2012; Turnbaugh et al., 2009), consistent with our a priori notions of the importance of microbiota diversity to health.
An increase in caloric intake, whether from a high fat diet (DIO) (Turnbaugh et al., 2008), or from overeating normal chow driven by the absence of the satiety hormone leptin in ob/ob mice (GIO) (Turnbaugh et al., 2006), selects for obesogenic microbiota. This was demonstrated by transferring the obesity phenotype to germ-free recipient mice via microbiome transplantation, providing evidence that the microbiota can contribute to obesity in addition to increased caloric consumption (Figure 1). Both DIO and ob/ob GIO caused phylum-level shifts in the intestinal microbiota, increasing Firmicutes and decreasing Bacteroidetes (Ley et al., 2005; Ley et al., 2006; Turnbaugh et al., 2008). That these broad phylum level changes have not been found consistently (Ley, 2010; Ravussin et al., 2012), may indicate that the important events involve lower taxonomic levels within these phyla.
Dietary composition can alter the microbiota, independent of the calories consumed. In a comparison of ad-libitum fed or caloric-restricted mice receiving either a DIO diet or normal chow, the dietary composition had a greater influence on shaping the microbiota than caloric intake or host obese status (Ravussin et al., 2012). However, whether the metabolic phenotype was transferrable to germ-free recipients was not assessed, so it could not be determined whether the dietary composition or the increased calories select for an obesogenic microbiota. That excessive caloric intake in ob/ob mice receiving a normal chow and in mice fed ad-libitum on a DIO diet selects for an obesogenic microbiota argues that the increased caloric intake, not dietary composition, is the driving force.
In the large intestine, complex nutrients that have not been absorbed by the host are fermented to short-chain fatty acids (SCFA), which contribute a small but significant number of calories to the host (Macfarlane and Macfarlane, 2012), estimated to account for up to 10% of caloric intake in humans (Bergman, 1990) (Figure 2). The total production of SCFA, and thus calories contributed by microbiota, depend on both dietary and microbiota composition. The majority of SCFA are produced from carbohydrates, but a smaller fraction can be produced from protein degradation, which yields SCFA plus other metabolic end-products, such as amines, phenols, thiols, and hydrogen sulfide (Macfarlane and Macfarlane, 2012). Leptin-deficient ob/ob mice harbor a microbiota that produce more SCFA than wild type mice (wt) and extract more calories from the diet (Turnbaugh et al., 2006). A similar increase in microbial energy harvest was observed in lean humans switched from consuming 2,400 to 3,400 calories/day (Jumpertz et al., 2011). These findings show that in a GIO murine model and a DIO human simulation, the intestinal microbiota can adapt to an enriched diet and contribute additional calories to the host (Figure 1).
Metabolic disturbances can occur that are not caused by either abnormal host gene status or dietary changes, but instead are driven by an aberrant microbiota (microbe-induced obesity, MIO). For example, the microbiota may become altered as a result of an abnormal founding population, as occurs with Caesarian section (Biasucci et al., 2010; Dominguez-Bello et al., 2010; Huurre et al., 2008; Pandey et al., 2012). Epidemiologic studies indicate an association of C-section with the development of childhood obesity (Blustein et al., 2013; Huh et al., 2012; Li et al., 2013). Similarly, the microbiota can be altered by antibiotic exposure (Antonopoulos et al., 2009; Dethlefsen et al., 2008; Ubeda and Pamer, 2012). In particular, antibiotic exposure in early life, just when host adipocyte populations are developing (Greenwood and Hirsch, 1974), has been associated with the development of adiposity in humans (Ajslev et al., 2011; Trasande et al., 2013). In a murine model of MIO, early life sub-therapeutic antibiotic treatment (STAT) changed microbiome composition and increased fat mass (Cho et al., 2012). STAT increased the abundance of microbial genes involved in SCFA production, as well as increased acetate, butyrate, and propionate concentrations in the intestine. Thus, if SCFA are markers of increased energy extraction, one driving force behind MIO has been identified.
SCFAs also provide important microbial signals to the host, in part via the G protein-coupled receptors GPR41 and GPR43 (FFAR2 and FFAR1, respectively). The GPR41 receptor on enteroendocrine cells sense SCFAs and induce secretion of peptide YY (Ichimura et al., 2009), which both slows intestinal transit time and increases satiety. GPR41-deficient mice are leaner than their wt counterparts (Table 1), due to decreased PYY and increased intestinal transit rate (Samuel et al., 2008). However, germ-free GPR41 −/− mice exhibited no weight differences from germ-free wt mice, indicating that the effects are dependent on the microbiota. Absorbed SCFA also provide metabolic signals to distant tissues. SCFA bind GPR41 on adipocytes, increasing adipogenesis, inhibiting lipolysis, and inducing leptin secretion (Ichimura et al., 2009). The major product of microbial fermentation, acetate, is a substrate for hepatic cholesterol and triglyceride synthesis (Wong et al., 2006). Early life STAT increased intestinal acetate, as well as the downstream (via the portal circulation) hepatic expression of genes involved in fatty acid metabolism and lipogenesis (Cho et al., 2012).
The extent of total energy extracted from the diet depends on the structure of the intestinal tract, the composition of the microbiota, and the composition of the diet. The dynamic metabolic relationships can be understood through considering continuous flow fermentation systems, in which the population of microbes is maintained by balancing nutrient infusion and waste removal. The evolution of a conserved and stable microbial consortium requires overcoming a considerable set of challenges. These concepts were first compiled by Hungate in his classic work: The Rumen and Its Microbes (Hungate, 1966). Because of the constant downward movement of intestinal contents, a stable microbiota can only be achieved if the net microbial growth equals the flow rate of the system. Over-nutrition can disrupt the microbial ecosystem and can have severe consequences for both host and microbiota. When a ruminant (i.e. cow or sheep) is rapidly switched from a grass-based diet to a grain-based diet, the sudden influx of starch in the digestive tract leads to an overgrowth of lactate-producing Streptococcus bovis (Hungate et al., 1952). Lactic acid accumulates in the rumen faster than can be utilized by other ruminant microbes (Nagaraja and Titgemeyer, 2007). The excess lactate decreases the pH of the rumen below 5, resulting in acute systemic acidosis, which can lead to death within 24 hours. This is an extreme example, since ruminants are substantially different from mice and humans in the fundamental digestive tract organization. Ruminants are foregut fermenters, while humans and mice are hindgut fermenters, which may have evolved as an adaptation enabling wider variations in diet. For mice and humans, most of the microbiota only receive nutrients after the host has extracted many of the simple molecules, and thus hindgut fermenters are not vulnerable to fatal indigestion from nutrient excess.
Major anatomical rearrangements of the gastrointestinal tract of mice and humans produce large effects on energy extraction and on the intestinal microbiota, in part due to changing factors related to nutrient flux and pH (Aron-Wisnewsky et al., 2012). In obese subjects undergoing Roux-en-Y gastric bypass (RYGB) surgery, metabolic improvements can be observed in the first week after the surgery, preceding significant weight loss (Ahn et al., 2011; Rubino et al., 2004). These weight-independent metabolic improvements may be mediated by rapid changes in microbiota composition since major reconstruction of the gastrointestinal tract as part of gastric bypass significantly alters the microbiota shortly after the surgery (Graessler et al., 2012; Li et al., 2011). In a recent study by Liou et. al., RYGB had a more substantial effect on the microbiome than sham surgery or caloric restriction, even though mice receiving caloric restriction also were significantly leaner than the sham-surgery mice (Liou et al., 2013), demonstrating that gut structure had greater impact on the microbiota than obesity status. RYBG was associated with increased populations of Proteobacteria (Escherichia) and Verrucomicrobia (Akkermansia), and a reduction in Firmicutes compared to sham-surgery and weight-restriction. Mice that underwent gastric bypass extracted significantly less energy from the diet than mice that underwent sham-surgery or caloric restricted mice, which may have been mediated by a combination of gut restructuring and changes in the intestinal microbiota. Germ-free mice colonized with microbiota from RYGB mice weighed significantly less than mice colonized with microbiota from sham surgery mice, showing that the RYGB-altered microbiota play an active role in weight loss and metabolic status. Both the RYGB cecal donors and their recipient mice had decreased total SCFA compared to sham donors and recipients, with major reductions in acetate levels and a relative increase in propionate levels, providing further evidence that SCFAs influence obesity.
The interaction between diet, genes, and the intestinal microbiota in the context of obesity is complex (Parks et al., 2013), since each of these factors has the potential to modulate inflammation and immunity (Kau et al., 2011). Obesity is a low-grade inflammatory disorder and the role of the microbiota via specific immune pathways has been studied with the aid of experiments involving germ-free and knockout mice (Table 1).
High fat diet can increase absorption of lipopolysaccharide (LPS), a component of gram-negative bacterial cell walls, either by incorporation into chylomicrons or by increasing intestinal permeability (Cani et al., 2007; Cani et al., 2008). LPS is a potent inflammatory mediator that signals in a CD14/TLR4-dependent manner, and infusion of LPS alone can increase weight gain, adiposity, insulin resistance, and liver triglycerides similar to a high fat diet. High dose antibiotic treatment or deletion of CD14 reduces inflammatory cytokine expression and ameliorates weight gain on HFD, demonstrating the important interaction of microbiota and inflammatory signaling cascades. Prebiotic fibers fermented to SCFA by the intestinal microbiota can block LPS-mediated metabolic consequences by increasing colonic expression of tight junction proteins zona occludens 1 and claudin 3, improving gut barrier function and reducing systemic LPS (Neyrinck et al., 2012) (Figure 2).
Akkermansia muciniphila, a microbial specialist that can derive its carbon and energy sources from mucus lining the intestinal tract, increases with prebiotic treatment (Everard et al., 2011). In addition to the metabolic and inflammatory changes previously discussed, HFD reduces A. muciniphila levels and thins the mucus layer (Everard et al., 2013). Introduction of A. muciniphila by daily oral gavage to mice fed HFD restores the mucus layer, decreases circulating LPS levels, decreases fat mass gain, and increases glucose tolerance compared to mice gavaged with PBS. These changes in metabolism and inflammation were not produced by killed A. muciniphila or by the “probiotic” strain Lactobacillus plantarum, indicating that live A. muciniphila has specialist actions that improve the gut barrier and reduce the effects of DIO.
Deletion of the innate immunity receptor TLR5, which senses bacterial flagellin, induces inflammation, which if mild, causes a metabolic syndrome including hyperphagia-dependent weight gain, insulin resistance, and increased adiposity, blood pressure, and cholesterolemia (Vijay-Kumar et al., 2010). These changes were linked with increased adipocyte pro-inflammatory cytokines IL-1β and INF-γ. An antibiotic regimen that reduced microbial density 100-fold abrogated the metabolic syndrome in TLR5 −/− mice, and conversely, germ-free mice that were colonized with TLR5 −/− microbiota showed many of the disease phenotypes. Together these results indicate the sufficiency of the altered microbiota to yield the pathologies that accompany TLR5 deficiency. However, some TLR5 −/− mice have an opposing phenotype of severe colitis leading to weight loss, not gain (Vijay-Kumar et al., 2007). In a separate study, TLR5 −/− mice housed at two different animal facilities did not show an obesity phenotype or increased basal intestinal inflammation (Letran et al., 2011). The circulating microbes in separate facilities can lead to animals with differential microbiota colonization, altering host immune phenotypes (Ivanov et al., 2009). Since the genetic background was the same for the TLR5 −/− mice, the local microbiota in each animal facility most likely accounted for differences in the immune and metabolic phenotypes. Thus, in this model, the colonizing microbiota characteristics might determine inflammation extent and which pathway dominates.
Lymphotoxin, secreted by Th1 lymphocytes, and implicated in obesity by GWAS, is involved in the control of mucosal intestinal microbiota (Upadhyay et al., 2012). Lymphotoxin-receptor-deficient (ltbr −/−) mice have reduced colonic IL-22 and RegIII antimicrobial peptide expression, and elevated levels of segmented filamentous bacteria (SFB), consistent with diminished immune control at the mucosal surface (Upadhyay et al., 2012). Addition of HFD further shifts both immune responses and metabolism, including increasing colonic IL-23 expression and increasing in weight and adiposity. When any of the components in the axis are eliminated, including HFD, lymphotoxin α or β subunits, lymphotoxin receptor (ltbr −/−), IL-23, or RORγt (Th17) cells, mice become DIO-resistant (Figure 2, inset). The dietary changes and the differences in ltbr status account for 52% and 18% of the variation in the microbiome, respectively. Several expected microbiome shifts associated with introduction of a high fat diet, such as an increase in Firmicutes and a loss in diversity, were only observed in ltbr +/− mice, but not in ltbr −/− mice. GF wt mice conventionalized with microbiota from HFD-fed ltbr −/− mice transiently resist DIO, but the phenotype gradually reverts, due to their (wt) immune development. When HFD-fed ltbr −/− mice are co-housed with DIO-susceptible ltbr +/− mice, the ltbr −/− mice gain more weight, indicating the dominance of the transferred microbiota selected by HFD in the presence of a functional lymphotoxin pathway.
Multi-protein complexes that sense pathogen-associated molecular patterns (PAMPs), known as inflammasomes, aid in mucosal defenses by activating inflammatory cytokine precursors pro-IL-1β and pro-IL-18. Inflammasomes have been implicated in the progression from non-alcoholic fatty liver disease to non-alcoholic steatohepatitis (NASH) (Henao-Mejia et al., 2012). Apoptosis-associated speck-like protein containing a CARD (Asc) is a key adaptor protein of the inflammasome complex. Asc-deficient mice show higher levels of TLR4 and TLR9 agonists in the portal circulation and higher hepatic TNFα expression than wt mice, indicating that microbial products translocate to the liver and induce inflammation. When given a methionine-choline deficient diet known to induce NASH, mice lacking Asc or other components of the inflammasome complex (caspase 1, NLRP3) or downstream signaling (IL-18 −/−) develop NASH at a higher incidence than wt mice. The enhanced NASH phenotype in asc −/− mice was ablated with deletion of either TLR4, TLR9, MyD88:Trif, or TNFα, demonstrating the importance of innate immune pathways. However, the presence of the intestinal microbiota is also necessary because high dose broad-spectrum antibiotics in asc −/− mice reduces NASH incidence. When wt mice were co-housed with asc −/− mice, wt mice developed NASH more frequently, which was associated with increased Prevotellaceae, showing the importance of the altered microbiome in disease risk.
All told, these models of DIO and GIO illustrate the importance of immune control of intestinal microbiota, whose relaxation or activation can result in pathologic metabolic consequences.
There are long-standing immunologic and metabolic relationships between the host and microbiota, and there can be consequences following natural and artificial perturbations. Microbial diversity and stability are important when considering the complex intra-community interactions that lead to emergent properties of the system. Well-evolved ecosystems often have functional redundancy in which several species can perform the same task. This concept explains how the taxa that constitute the mammalian gut microbiome often are highly diverse and variable from person to person, yet share high degree functional capacity (HMPConsortium, 2012; Kurokawa et al., 2007; Turnbaugh et al., 2009). However, ecosystems can be disrupted. In the case of forests, it might be fires, landslides, or droughts (Paine et al., 1998). For human microbiota, it might be famine, or surfeit, antibiotic treatments, or even parturition. Each of these events has the potential to change the energy flow in tightly regulated systems and consequences, including loss in diversity, vary according to the system’s status and the extent of functional redundancy. As diversity declines, loss of function may not be immediately apparent until the last redundant member able to perform a function is gone, however, communities with lower diversity are less resilient when subject to further perturbations (Kau et al., 2011). For perturbations of host-associated microbiota, timing is important, because the effects and their consequences may differ according to stage of life.
Despite the obvious differences in geography, diet, and lifestyle, there are strong similarities in the age-specific features of the microbial composition in persons living in the United States, Malawi, and Venezuela (Yatsunenko et al., 2012). Regardless of origin, babies begin life with low diversity, which progressively increases over the first years of life, and for all, the outline of the adult microbiome is essentially established by the age of three. Not surprising considering the long-standing differences in diet reflected in the three populations, the biochemical pathways represented in the metagenomes varied substantially. The study subjects differed substantially in the overall diversity in adulthood; the average adult in the US had from 225 to 400 fewer operational taxonomic units (OTUs) (or approximately 15 to 25 percent fewer) than did the Malawians or Venezuelan Amerindians. This observation is consistent with our earlier hypothesis of a ‘disappearing microbiota’ due to the changes represented by modernity (Blaser and Falkow, 2009), and may be the harbinger of functional losses as well.
Parturition is a major biological perturbation, yet a critical event in the animal life cycle. The energetics are complex since the needs of the mother and her offspring must be balanced, and in mammals, the mother’s role extends far beyond birth. Nature’s challenge is to provide a sufficient endowment to the next generation while safeguarding the mother’s own health, for the essential tasks ahead. Multiple adaptations in the maternal immune system allow tolerance of the growing fetus (Erlebacher, 2013; Thellin and Heinen, 2003). The GI microbiota composition shifts remarkably over the course of pregnancy and continuing beyond (Koren et al., 2012). Its progressive nature implies that an optimum exists, timed to the events of parturition, and consistent with a model of balanced outcome.
There are temporal shifts in both the diversity within a single microbial community, known as α-diversity, which can be measured by phylogenetic diversity, species richness, and Shannon’s index, and in the diversity shared among different communities, known as β-diversity, which, for example, can be measured by UniFrac distances, changes in microbial abundance, and the Jaccard index, (Lozupone and Knight, 2008). The microbiota in late pregnancy has reduced α-diversity, but higher β-diversity compared to non-pregnant women or early pregnancy (Koren et al., 2012). In the 3rd trimester, there is greater representation of lactic acid bacteria (Lactobacillus, Streptococcus, and Enterococcus), which are highly prevalent in the infant gut, whereas butyrate-producing bacteria (Faecalibacterium, Blautia, and Ruminococcus), which dominate the gut in adulthood, are enriched in early pregnancy. Since mammals have evolved to provide a portion of their microbes to their offspring, shifts occurring during pregnancy may reflect selection that increases the probability of offspring survival. The greater representation of lactic acid bacteria may be seen as an adaptation to prepare the mother for transfer of these organisms in the birth and peri-natal period to her offspring to take maximum advantage of the main energy source for the child, lactose in its mother’s milk. The increased beta-diversity reflects the variation in the different pathways by which nature accomplishes its goals of intergenerational transfer.
When germ-free mice were conventionalized with fecal microbiota from women in their first (T1) or third (T3) trimester of pregnancy, those receiving the T3 microbiota had increased intestinal cytokines, gained more weight, and were more glucose-intolerant than those receiving the T1 microbiota. This result implies that the T3 microbiota induces an alternative metabolic state in its host, associated with greater energy storage. The findings in mice mimic those in pregnant women who also gain weight and develop insulin-resistance, but vary in the degree of these phenotypes. The trimester-specific differences provide evidence for a microbiota-driven energy optimum to maximize maternal fitness and caloric transfer to the next generation. This concept is consistent with the notion of a co-evolved microbiota that optimizes host survival through effects on its progeny.
Perturbation, an important constraint in biological systems, may be random, episodic, or programed, like pregnancy (see above) or hibernation (see below). Well-evolved ecosystems have long histories of perturbation, in part documented by and captured within their existing population structure (Paine et al., 1998). Ecosystem stability reflects both its resistance to change and its resilience following perturbation (Costello et al., 2012; Shade et al., 2012). Changes in diet in omnivorous hosts substantially perturb the gut microbiome (e.g. adding high fat (Turnbaugh et al., 2008), fiber (Cox et al., 2013), and protein (Faith et al., 2011)), and changes in the mode of birth delivery are associated with alterations in the patterns established for vertical microbiome transmission, comparing vaginal and Caesarian sections (Dominguez-Bello et al., 2010). Direct exposure to anti-bacterial agents has the greatest potential for perturbation, and occurs frequently in the US. Based on recent CDC data (Hicks et al., 2013), more than 250 million courses of antibiotics were prescribed in the US in 2010, which represents 880 courses of antibiotics per 1000 population. Short antibiotic courses in adults cause profound but incompletely understood changes in community structure, with variable resilience (Dethlefsen et al., 2008). Perturbation during early life, when the gut community structure is emerging (Yatsunenko et al., 2012), may be most important, since it is occurring during a developmentally sensitive host window (Cho et al., 2012). The CDC data indicate that the average child in the US is receiving about 3 antibiotic courses in first 2 years of life and nearly 11 by age 10 (Hicks et al., 2013). To understand the impact of these perturbations, ecological theory can guide us through the ground-rules governing ecosystem responses.
Within ecosystems, there are r- or K-selected species, which have evolved alternate strategies to cope with environmental disruption (Reznick et al., 2002). r-selected species evolved to have a rapid growth rate to monopolize resources when competition is low following a large ecological disruption, whereas K-selected species have evolved for efficiency to persist when the carrying capacity of the environment is low (Figure 3). In the intestine, large perturbations can result from antibiotic exposure, extreme changes in diet, surgical interventions, and acute gastrointestinal illnesses. Carrying capacity can be limited by availability of nutrients, electron acceptors (e.g. oxygen), or even physical niches. A weed is an example of an r-selected species with high proliferative potential. Weeds often are normal members of the ecosystem that live at the fringe in microhabitats, since competitors lock up the necessary resources for its expansion, but after a large perturbation, weeds can grow out of control. Whether native or introduced, the r-selected weeds are usually considered as invaders because of their unbalanced residency in the environment. Members of the phylum Proteobacteria or Verrucomicrobia usually represent a minor population within the intestinal microbiome, but can dominate following antibiotic therapy (Dubourg et al., 2013; Ubeda and Pamer, 2012), gastric bypass (Graessler et al., 2012; Liou et al., 2013), or dietary shifts (Parks et al., 2013), and thus may be examples of r-selected species dominating an environment following a perturbation. The gradual shift from facultative anaerobic bacteria (Proteobacteria and Bacilli) to strict anaerobes (Bacteroidia, Clostridia, and Erysipelotrichi) in the developing infant gut (Pantoja-Feliciano et al., 2013) may be driven by a competitive advantage of the K-species strict anaerobes to maintain populations when oxygen is limited.
After an ecosystem is perturbed, exogenous organisms are more likely to successfully invade. Recovery from perturbation requires a full complement of species or of functional groups. In the gut, there appears to be enormous functional redundancy (HMPConsortium, 2012; Turnbaugh et al., 2009). However, there could be keystone species, defined as those that have disproportional influence on the behavior of the system as a whole, that when lost or gained has a profound influence on health. For example, on the plains, wolves have a very small population footprint, but their predatory presence affects much larger communities of grazers, and even larger populations of plants that the grazers eat. An important consequence of perturbations is loss of keystone species, in which small populations can oscillate down to zero, and thus are lost.
Very successful organisms, whether they are r- or K-selected, often have bi-stable states. Bi-stability is an ancient adaptation to long-term niches that are subject to significant and frequent perturbations. Unpredictable food supplies, which constrain most animal populations, are an example of a typical perturbation. The alternative forms in bi-stable states allow optimization in changing milieus. When conditions change, rapid growers like Clostridium species, can form spores to transmit to the next susceptible host. At the cost of not adding to the population of proliferating cells that stably colonize a given host, exchanging metabolic signals with the host and/or other microbiota, Clostridium sp. diverts its metabolism to the spore form that is most likely to survive transmission. There is fitness cost in diverting energy to formation of the seeds that spores represent, but there also is great fitness value, since host life span is finite. Such dynamics affect the partitioning of energy in the gut lumen, with downstream effects on both microbiota and host. Unlike their animal hosts, bacteria have the ability to bloom on a very short time-scale with logarithmic expansion of their share of the energy pie, ultimately affecting transmission at critical junctures. This characteristic is a factor, intrinsic to any well-evolved ecology, subject to competition by other organisms operating with parallel strategies, and to host constraints, which are obligatorily obeyed.
Throughout the biosphere, there is vigorous competition for energy. In well-evolved mature stable ecosystems, carbon metabolism is tightly regulated (Mackelprang et al., 2011), implying that checks exist against one species gaining a disproportionate share of the available nutrients. Hibernation is a massive physiological shift that is programmed that affects both central metabolism and the immune system (Bouma et al., 2010; Carey et al., 2003; Humphries et al., 2003). That energy storage and utilization is central to hibernation physiology provides an excellent model system to examine microbial characteristics associated with an annual perturbation cycle. Some colonizers of the mammalian colon have the ability to obtain their energy, not from the food substrate passing through the intestine, but rather from digesting host-derived molecules (Berry et al., 2013). One important example is Akkermansia muciniphila, a member of the Verrucomicrobia phylum, which can use mucin as its sole carbon and nitrogen source (Derrien et al., 2004). That Akkermansia utilizes mucins for energy, which are virtually unlimited in supply in the vertebrate gut, represents an apparent paradox. With a readily available and apparently inexhaustible relatively exclusive food supply, why are Verrucomicrobia not always the dominant organism in the gut ecosystem? Similarly, what are the consequences to the host of an organism that has the ability to deplete its mucus, an important component of its barrier against potentially pathogenic microbiota and their toxic products?
Verrucomicrobia abundance is not constant in the intestinal microbiota; proportions increase with disruption and dysbiosis, e.g. antibiotic treatment (Dubourg et al., 2013), or increase with an influx of fermentable fiber (Tachon et al., 2012). The change in microbiota in hibernating ground squirrels provides an excellent paradigm (Carey et al., 2013) with broad implications. Squirrels store energy in the summer, and hibernate in the winter. In the late winter, essentially all of the energy available to the microbiota is host-derived. Hibernation, rather than specific host, diet, or age, is the major determinant of the gut microbial community composition. During the seasons of feeding, Firmicutes, which are specialists in dietary carbohydrates (Flint et al., 2012), dominate, but after several months of fasting, their representation falls, replaced by Verrucomicrobia, as well as by Bacteroidetes, which can switch their expression of genes related to diet or host-related energy sources (Martens et al., 2008; Salyers et al., 1977).
This programmed seasonal restructuring in relation to hibernation and its consequent dietary limitation is useful to model the energy relationships between the major gut microbiota taxa classes and the effects on host pathophysiology (Figure 4). In a steady-state in most mammals (and in times of feeding for hibernators), the populations of (r-selected) organisms that utilize host-derived substrates are held in check by competing organisms that use the plentiful dietary food sources. Change in the mucus layer is minimized. Dietary utilizers also break down complex macronutrients into small monomers or ferment them to SCFA, which are required nutrients for other microbial consortia. Use of SCFA by these transactional species is a benefit to dietary utilizers because it is removing a waste product that could detrimentally lower pH. However, in perturbed states (and in times of fasting for hibernators), the organisms that use dietary sources are disrupted and fail to check the growth of the host substrate-users and fail provide cross-feeding metabolites. The resulting overgrowth of organisms that utilize host substrates depletes the mucus layer and diminishes its barrier function. Similarly, butyrate, produced by fermentation of dietary carbohydrates, and known to enhance tight junctions (Wong et al., 2006), is reduced during fasting. These changes are manifested as an increase in the cellularity of the lamina propria and a reduction in villus length (Kurtz and Carey, 2007). To the pathologist, this would be ‘colitis,’ except that in the hibernator, it is the physiologic consequence of its lifestyle. The digestion of mucus and the loss of butyrate resulting from perturbations that affect the microbes requiring dietary energy sources are examples of secondary effects on the interface between the microbiota and the host. These can result in differential signaling to epithelial and immune cells, with both immune and metabolic consequences (Canani, 2011).
The dynamics of the interactions suggest that there are boundary conditions that govern the microbial population structure in each gut locality. However, in total, the conserved nature of the relationships of the major phyla to one another, and their fluctuation with perturbation suggests the operation of a Nash equilibrium (Blaser and Kirschner, 2007), a game theory construct in which good behavior by players is rewarded, and ‘cheaters’ achieve inferior results (Nash, 1951). Within the boundary conditions of the gut, with competing organisms, and alternative energy substrates that affect host viability, the development of a Nash equilibrium can explain the conserved dynamic changes observed between the microbe phyla and the host. The overall conservation of the mammalian colonic microbial community structure is an important observation that indicates shared solutions between hosts and their resident microbes that have persisted for > 50 million years of evolution (Ley et al., 2008a). This time-scale implies that important boundary conditions have selected against marked divergence from a common ancestry. In contrast, the presence of alternative macro-level population structures in mammals (Arumugam et al., 2011) could be a condition inconsistent with a conserved Nash equilibrium.
Host phenotypes in obesity are dependent on the interactions between the diet, the resident microbiota, and host immunity. Evolutionary and ecological theories ultimately govern, but the principal actors include the differential microbial energetics and the host cells that monitor the microbial denizens. We are just beginning to explore a complex and ultimately crucial biological system, all the more important, because it appears to be changing out of proportion to evolutionary time.
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