{"id":12362,"date":"2024-10-20T17:24:34","date_gmt":"2024-10-20T15:24:34","guid":{"rendered":"https:\/\/glutenlight.eu\/?p=12362"},"modified":"2024-10-20T17:42:19","modified_gmt":"2024-10-20T15:42:19","slug":"the-gut-microbiota-and-in%ef%ac%82ammation-an-overview","status":"publish","type":"post","link":"https:\/\/glutenlight.eu\/?p=12362&lang=en","title":{"rendered":"The Gut Microbiota and In\ufb02ammation: An Overview"},"content":{"rendered":"

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\u201cRole of the Gut Microbiota in Immunity and In\ufb02ammation<\/strong>
\nMicrobes possess a variety of functions that in\ufb02uence their ability to grow and colonise, whilst bringing about downstream e\ufb00ects for the host that may be bene\ufb01cial or otherwise [61]. Humans are not capable of digesting some components of dietary \ufb01bre due to the lack of the required enzymes to break down and harness the energy of these carbohydrates [62]. Certain species of microbes produce speci\ufb01c enzymes that enable fermentation of nutrients into absorbable forms, including that of indigestible carbohydrates into short-chain fatty acids (SCFAs) [62,63]. These SCFAs may have anti-in\ufb02ammatory and immunomodulatory e\ufb00ects [63]. SCFAs are only a small part of the bigger picture as, in addition to enzymes and other metabolites produced, components of the bacteria themselves, including lipopolysaccharides, cell capsule carbohydrates and other endotoxins, may also be released and result in secondary e\ufb00ects to the host. These e\ufb00ects include maintenance of gut epithelium (and thereby integrity of the gut wall), production of vitamins, and interactions with several key immune system signalling molecules and cells, activating and inhibiting speci\ufb01c responses [1]. In addition to nutrient metabolism, gut microorganisms a\ufb00ect aspects of pharmacokinetics as they carry out drug metabolism [64]. They provide a natural defence against pathogenic species through competition and maintenance of the mucosa. It is through their contact with the immune system that the microorganisms occupying the gut can elicit or prevent in\ufb02ammation. They may be associated with anti-in\ufb02ammatory mechanisms, stimulating regulatory cells of the immune system to inhibit in\ufb02ammation [65]. On the other hand, as bacteria regulate the permeability of the intestines, certain species can promote a \u201cleaky gut\u201d, where metabolites associated with the microbes leave the gut and enter the bloodstream. In response, the body produces cytokines and other mediators, e\ufb00ectively launching an in\ufb02ammatory response [66]. Similarly, cells within the epithelial tissue of the gut deliver bacterial metabolites to immune cells, promoting in\ufb02ammation on both a local and systemic scale. The persistence of this condition may lead to subacute or chronic in\ufb02ammation, which may subsequently drive the development of diseases such as in\ufb02ammatory bowel disease, diabetes or cardiovascular disease [65].\u201d<\/span><\/strong><\/p>\n

<\/p>\n

The study<\/p>\n

\u201cAbstract: The gut microbiota encompasses a diverse community of bacteria that carry out various functions in\ufb02uencing the overall health of the host. These comprise nutrient metabolism, immune system regulation and natural defence against infection. The presence of certain bacteria is associated with in\ufb02ammatory molecules that may bring about in\ufb02ammation in various body tissues. In\ufb02ammation underlies many chronic multisystem conditions including obesity, atherosclerosis, type 2 diabetes mellitus and in\ufb02ammatory bowel disease. In\ufb02ammation may be triggered by structural components of the bacteria which can result in a cascade of in\ufb02ammatory pathways involving interleukins and other cytokines. Similarly, by-products of metabolic processes in bacteria, including some short-chain fatty acids, can play a role in inhibiting in\ufb02ammatory processes. In this review, we aimed to provide an overview of the relationship between the gut microbiota and in\ufb02ammatory molecules and to highlight relevant knowledge gaps in this \ufb01eld. Based on the current literature, it appears that as the gut microbiota composition di\ufb00ers between individuals and is contingent on a variety of factors like diet and genetics, some individuals may possess bacteria associated with pro-in\ufb02ammatory e\ufb00ects whilst others may harbour those with anti-in\ufb02ammatory e\ufb00ects. Recent technological advancements have allowed for better methods of characterising the gut microbiota. Further research to continually improve our understanding of the in\ufb02ammatory pathways that interact with bacteria may elucidate reasons behind varying presentations of the same disease and varied responses to the same treatment in di\ufb00erent individuals. Furthermore, it can inform clinical practice as anti-in\ufb02ammatory microbes can be employed in probiotic therapies or used to identify suitable prebiotic therapies.<\/p>\n

1. Introduction
\nThe understanding of the symbiotic relationship between the human gut bacteria and the overall functioning of the body has significantly deepened and broadened, with acceleration in research output concerning this area. While initial research generally examined the microbiota composition and its relation to disease presentation, there has recently been a more prominent shift towards the understanding of the mechanisms by which variation of the microbiota can lead to disease manifestation [ 1]. Clarifying these mechanisms can inform the development of novel therapies and optimise clinical practice. Moreover, discerning the structure and function of the microbiota becomes increasingly important in the era of precision medicine as this allows for personalised treatment to improve clinical outcomes [ 2 ]. This review presents a brief introduction to the gut microbiota, influential factors on microbiota, analysis techniques of the microbiome and interpretation of results.
\nThese are followed by a review of the recent literature on the interplay between the gut microbiota, metabolic diseases and in\ufb02ammation. We explore potential underlying pathophysiologies and the intermediate biomarkers associated with gut bacteria and in\ufb02ammatory diseases. Finally, limitations of microbiome studies are discussed, with recommendations for future research directions.<\/p>\n

2. What Is the Gut Microbiota?
\nThe gut microbiota refers to the microorganisms inhabiting the human gastro-intestinal tract. This dynamic community predominately encompasses species from the prokaryotic domain (comprising bacteria and other unicellular microbes lacking specialised organelles) and, to a lesser extent, fungi, parasites and archaea. Viruses are also constituents of this environment. The genetic and functional pro\ufb01le of microbial species is termed the gut microbiome [3]. On a broader level, humans can be classi\ufb01ed according to their enterotypes, which are distinctly similar gut microbial compositions that can be observed in certain populations [4]. In a single individual, the inhabiting gut microbial species collectively have been shown to contain 3.3 million genes which, when compared to the human genome\u2019s ~23,000 genes, demonstrates the sheer magnitude and potential e\ufb00ect of these species on human health [5]. Moreover, the human body contains almost as many bacterial cells as human cells [6].<\/p>\n

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Figure 1. The taxonomic classi\ufb01cation system and the classi\ufb01cation of humans and Lactobacillus delbrueckii as an example [8]. Organisms are classi\ufb01ed by this hierarchical system, where the most general and inclusive group is at the domain level. Organisms within the same species are most genetically similar.
\n3. Methods for Studying the Gut Microbiota
\nResearchers study the gut microbiota through various approaches, and it is the combination of these di\ufb00erent methods that enables a comprehensive construction of knowledge revolving around gut microbiota and health. In human studies, the most established method of characterising the gut microbiome is stool sampling as it is readily available, non-invasive and densely populated by microbes representative of the luminal intestinal gut microbiota [9,10]. Following collection, faecal samples are frozen and stored immediately, generally at \u221280 \u25e6C [11]. DNA is extracted from the faeces with two major steps. First, the sample is puri\ufb01ed through the use of multiple reagents and centrifugation, allowing for the microbes to be stripped of other components of the faeces. The subsequent step involves lysing bacterial cells by incubating the samples with lysis bu\ufb00er with agitation, such as vigorous shaking with or without beads, and carrying out further centrifugation [12]. Following this, the resulting DNA is ampli\ufb01ed using approaches such as multiple displacement ampli\ufb01cation [11]. A 16S rRNA primer is selected and used for gene sequencing. The sequence data obtained undergo \ufb01ltering to ensure the thresholds of quality are met. Subsequently, the sequence count is normalised prior to operational taxonomic units (OTU) analysis; the method by which related bacteria are grouped together.<\/p>\n

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Figure 2. Steps generally undertaken in stool microbiome analysis.
\nMicrobial diversity is assessed according to two parameters; alpha and beta diversity. Alpha diversity refers to the variation within a single sample, whilst beta diversity refers to that between samples [13]. These are generally determined in increasing order of relatedness, from phylum to genus, although some studies also employ species-level analysis [14]. Platforms facilitating these analyses include QIIME, a free software tool that evaluates 16S rRNA sequences [13]. However, using this lower rank classi\ufb01cation could yield unreliable \ufb01ndings; most studies typically only assess one portion of the 16S rRNA gene as opposed to examining the full-length of the gene [15]. Doing so compromises the reliability of species-level classi\ufb01cation as a small portion of the gene can have a highly variable ability to detect species [15]. As reagents used in these steps may introduce contaminants, it is important to test for contamination with 16S rRNA gene ampli\ufb01cation, and computationally erase the contaminant species\u2019 sequences from the overall sequences obtained [11]. A more representative snapshot of the gut microbiota can be obtained through mucosal tissue sampling of the distal gastro-intestinal tract; however, this method comes with various limitations and is, therefore, less commonly used in research [16]. One such limitation is that compared to stool sampling, where human cell contamination is minimal, analysis of mucosal tissue biopsy samples must take into consideration the presence of human cells and genetic material as these may interfere with \ufb01ndings [10]. Other methods less routinely used include lavage and swab sampling, however, these have not been extensively evaluated in terms of protocol consistency and how representative the \ufb01ndings are of the gut microbial community [17]. Studies utilising animal models are key and frequent in this area of research as they enable a more comprehensive understanding of some aspects of the role of the gut microbiota in health. Confounders can be controlled more strongly in animal models, including rodents, \ufb01sh and insects, to better understand experimental variables and their e\ufb00ects, and host\u2013microbiota interactions [10,18]. This is particularly relevant in studies that seek to examine factors that a\ufb00ect the gut microbiota, or the e\ufb00ects of gut microbes on tissues or systems. Germ-free animal models have been utilised to assess microbiota-independent functioning in comparison to normal animal models [19]. Furthermore, gnotobiotic models are used in this \ufb01eld of study, where animals, typically rodents, are prepared with speci\ufb01c known strains or combinations of bacteria and are often genetically altered to determine the downstream e\ufb00ects of certain bacterial products or associated products [20\u201324]. Nevertheless, the results of studies on gnotobiotic models need to be interpreted with caution since the immune system of these animals is altered from early in development. Cell culture systems are also important here as they can be used to further examine controlled interactions between gut microbes and other variables. These techniques may involve the cultivation of native-to-human-gut microbes, human tissue, or arti\ufb01cial tissue [10].
\n4. Factors Associated with Microbiota Composition
\nThe gut microbiota in the gastro-intestinal (GI) tract develops during infancy. The process of microbial colonisation is contingent on a variety of host factors, described in more detail below. Additionally, di\ufb00erent regions of the GI tract have di\ufb00erent chemical environments that allow certain microbes to thrive more than others. Diversity and stability continually increase throughout early development, reaching a certain composition with age [25]. This composition may be modulated by various factors and life events, that may synergise to bring about greater diversity [1]. It is important to note that here, greater diversity is generally associated with better health outcomes, although there have been some reports of increased diversity in certain disease states [26,27]. Factors that in\ufb02uence the gut environment will in turn contribute to the characteristic gut microbial ecosystem thus giving rise to the inter-individual variation we observe.
\n4.1. Mode of Delivery (the manner in which the Products are delivered to End Users, either digitally or tangibly) and Feeding
\nSpecies that partake in the initial colonisation of the GI tract di\ufb00er depending on the mode by which a neonate is born [28]. Both caesarean section and vaginal modes involve exposures to microbes, however, di\ufb00erences come about regarding the source of these microbes. In vaginal delivery births, the neonate is exposed to maternal vaginal bacteria and therefore, their initial microbiota compositions tend to re\ufb02ect this region [29]. More speci\ufb01cally, these bacteria are part of the Lactobacillus, Prevotella and Sneathia genera. In contrast, those delivered by caesarean section are strongly in\ufb02uenced by their maternal skin \ufb02ora and tend to have less diverse microbiotas [29,30]. As such, they have a higher portion of skin dwelling microbes including Staphylococcus, Corynebacterium and Propionibacterium species [29]. Additionally, intrapartum antibiotic use during casesarian section is shown to a\ufb00ect the neonatal gut microbiota [31]. Overall, a greater degree of similarity in gut microbiota has been observed between newborns delivered vaginally and their mothers, compared to babies delivered by C-section [32]. The role of the microbiota is critical in the development of the immune system, therefore di\ufb00erences in gut microbiota may explain why the latter category have a greater risk of developing infections or allergies [33,34]. In addition to the mode of delivery, the type of milk consumed early in life also a\ufb00ects the gut microbiota. Breast milk di\ufb00ers from formula milk as it contains its own bacteria and di\ufb00erent bioactive compounds and nutrients. Speci\ufb01c species of bacteria may be better adapted for guts rich with their preferential nutrient, for example, dietary \ufb01bre, as they are able to extract their energy from these [35]. Because of this, Bi\ufb01dobacterium species predominate in the microbiota of breastfed individuals, whereas Enterobacteriaceae species are more frequent in formula-fed infants [30]. Further, formula-fed babies have more diverse microbiota than their breastfed counterparts, suggesting that the bene\ufb01ts of breast-milk may be due to factors unrelated to the gut microbiota [32]. It is important to note that the gut microbial community undergoes many changes during the initial stage of development of a newborn, and that the e\ufb00ects of intrinsic and extrinsic factors may only lead to temporary and ephemeral structural changes [36].<\/p>\n

4.2. Diet
\nDietary behaviour can result in some strains dominating the gut more than others, and therefore speci\ufb01c downstream phenotypic characteristics in the host. Modi\ufb01cations to the diet will make di\ufb00erent nutrients more readily available, consequently changing which strains dominate, contributing to the dynamic nature of the microbiota [37]. It has been revealed that individuals consuming more meat in their diets have signi\ufb01cantly di\ufb00erent gut microbiomes to those with plant dominant diets, due to certain bacteria \ufb02ourishing in the abundance of protein [38,39]. For instance, Bacteroides species tend to dominate in the GI tract of those consuming animal protein, and Prevotella species are associated with plant-based diets [40]. Moreover, the e\ufb00ect of diet on gut microbiota can be seen in ethnography studies, where culture a\ufb00ects the general kinds of food consumed, and hence collective enterotypes [41]. This can be observed within Asian populations that have a high consumption of starch-rich foods like rice; the enterotypes of these populations are characterised by a notably high abundance of Bi\ufb01dobacterium, a genus known to produce large quantities of starch-metabolising enzymes [4]. The Western diet, rich in saturated fats but low in unsaturated fats, has been studied extensively and found to be positively associated with anaerobic microorganisms and speci\ufb01c genera including Bacteroides and Bilophila [42]. In addition to the e\ufb00ects of speci\ufb01c macro and micronutrients in human diets on the gut microbiota, some animal studies have noted that additives commonly found in the Western diet have associations with altered microbiota composition and its in\ufb02ammatory potential [43].
\n4.3. Age, Sex and Body Mass Index
\nDi\ufb00erences in the composition of microbiota have been noted with respect to age. In a cross-sectional study of 367 healthy participants in Japan, similar phyla were observed in the gut microbiome across age groups ranging from 0\u2013104 years, although in di\ufb00erent proportions [44]. One trend reported was an association between age and abundance of Actinobacteria, where an increase in age was associated with a decrease in abundance. Microorganisms of the phylum Firmicutes became abundant in the microbiotas of individuals post-weaning stage, particularly past the age of 4, whilst the inverse was seen with the Actinobacteria population. Bacteroidetes maintained a stable level of abundance across di\ufb00erent age groups, although individuals above the age of 70 had higher levels of these microbes [44]. The patterns found in this study may be attributed to the various events that occur over the life course, including varied environmental exposures to microorganisms, occurrence of disease, hormonal changes and immune system functioning, thus complicating the in\ufb02uence of age on the gut microbiota [44,45]. Although studied far less than other factors, sex di\ufb00erences have been noted to in\ufb02uence microbiota composition [46]. Di\ufb00erences become more apparent when investigating the microbes on a genus or species level. In an experimental study by Baars et al. [47], sex-related di\ufb00erences were found in how the gut microbiota interacts with the host. Using mice, they determined that compositional and transcriptional dissimilarities were apparent. In turn, these in\ufb02uenced the di\ufb00erences in lipid metabolism observed between male and female mice. Haro et al. [48] found that Bacteroides caccae were more abundant in females than in males, whilst the inverse was observed for the species Bacterioides plebeius. Interestingly, these sex di\ufb00erences interrelate with body mass index (BMI). In the same study by Haro et al. [48], sex variation became more prominent when BMI increased. For instance, males exceeding a BMI of 33 had lower Firmicutes abundance than those of lower BMI, however, this trend was not observed in females. Rather, Firmicutes abundance remained high irrespective of BMI in female participants [48]. These observations are hypothesised to be due to hormonal di\ufb00erences, however, more research must be conducted to understand the exact mechanisms [49]. In general, an association with BMI and gut bacterial diversity has been reported, with a pattern demonstrating that an increase in BMI strongly correlates with decreased diversity [50]. Further, there is a reduced proportion of members of the phylum Bacteroidetes compared to Firmicutes in obesity, and upon weight loss, this ratio reverts to normal [51].
\n4.4. Host Genotype
\nSpeci\ufb01c host genotypes are associated with di\ufb00erences in gut microbial diversity, as well as speci\ufb01c community structures [52]. As genes a\ufb00ect immune system functioning and susceptibility to disease, certain alleles are associated with certain compositions. For example, individuals with the rs651821 variant of the gene APOA5 are more likely to have members of the Lactobacillus, Sutterella and Methanobrevibacter genera in their microbiota, which subsequently correlates with a greater risk of metabolic disorders [52]. Speci\ufb01c variants of microbiome-associated genes have been shown to be associated with conditions including obesity, shizophrenia, type 2 diabetes, amyotrophic lateral sclerosis and in\ufb02ammatory bowel disease, in a number of studies [53]. One such example is the SLIT3 gene; this gene appears to play a role in microbe product-induced in\ufb02ammation, and in a genome-wide association study, variants of the gene were found associated with BMI, suggesting a likely relationship between the gene, its molecular product, the human microbiome and obesity [53]. One polymorphic aspect of human genetics associated with predisposition to autoimmune disorders is the human leukocyte antigen (HLA), which are cell-surface proteins that are encoded by a cluster of genes. The variation in HLA structure and underlying genetics has been shown to correlate with distinct changes in the gut microbiota [54]. For instance, the relationship between the variant HLA-B27 and the in\ufb02ammatory condition ankylosing spondylitis has been well documented in the literature [55]. One study examining individuals with this particular genotype found that there is a distinct gut microbial pro\ufb01le associated with HLA-B27, suggesting that ankylosing spondylitis may be driven in part by a genetic predisposition to speci\ufb01c immunological processes, mediated by the gut microbiota [56]. It should also be noted that existing \ufb01ndings lend to the idea that the composition of the human gut microbiota is in\ufb02uenced mainly by non-genetic factors [57]. Nonetheless, this area of study is still in its infancy and further studies in larger cohorts are underway to better understand how the gut microbiota and human genome interrelate.<\/p>\n

4.5. Antibiotic Use
\nWhen exposed to antibiotics, the host microbiota can undergo quick alterations in its structure, depending on the type and regularity of use. A common outcome is a state known as gut microbiota dysbiosis, whereby there is an imbalance within the micro\ufb02ora, consequently impairing its functioning [58]. Other factors, including diet, infection and existing disorders, may also cause dysbiosis. An individual with dysbiosis will face an increased risk of a plethora of morbidities, namely infection, as a healthy, balanced microbiota serves as a hindrance to potential pathogenic strains, competing for resources and preventing the growth of invading microbes [59]. Other outcomes associated with dysbiosis pertain to immune system and metabolic deregulation. Findings from a large international cross-sectional study of 74,946 individuals exemplify the e\ufb00ects of antibiotic-induced dysbiosis; it was found that the use of antibiotics within the \ufb01rst year of life in male subjects contributed to metabolic dysregulation and therefore an increase in BMI in later stages of childhood, but not in females [60].<\/p>\n

5. Role of the Gut Microbiota in Immunity and In\ufb02ammation
\nMicrobes possess a variety of functions that in\ufb02uence their ability to grow and colonise, whilst bringing about downstream e\ufb00ects for the host that may be bene\ufb01cial or otherwise [61]. Humans are not capable of digesting some components of dietary \ufb01bre due to the lack of the required enzymes to break down and harness the energy of these carbohydrates [62]. Certain species of microbes produce speci\ufb01c enzymes that enable fermentation of nutrients into absorbable forms, including that of indigestible carbohydrates into short-chain fatty acids (SCFAs) [62,63]. These SCFAs may have anti-in\ufb02ammatory and immunomodulatory e\ufb00ects [63]. SCFAs are only a small part of the bigger picture as, in addition to enzymes and other metabolites produced, components of the bacteria themselves, including lipopolysaccharides, cell capsule carbohydrates and other endotoxins, may also be released and result in secondary e\ufb00ects to the host. These e\ufb00ects include maintenance of gut epithelium (and thereby integrity of the gut wall), production of vitamins, and interactions with several key immune system signalling molecules and cells, activating and inhibiting speci\ufb01c responses [1]. In addition to nutrient metabolism, gut microorganisms a\ufb00ect aspects of pharmacokinetics as they carry out drug metabolism [64]. They provide a natural defence against pathogenic species through competition and maintenance of the mucosa. It is through their contact with the immune system that the microorganisms occupying the gut can elicit or prevent in\ufb02ammation. They may be associated with anti-in\ufb02ammatory mechanisms, stimulating regulatory cells of the immune system to inhibit in\ufb02ammation [65]. On the other hand, as bacteria regulate the permeability of the intestines, certain species can promote a \u201cleaky gut\u201d, where metabolites associated with the microbes leave the gut and enter the bloodstream. In response, the body produces cytokines and other mediators, e\ufb00ectively launching an in\ufb02ammatory response [66]. Similarly, cells within the epithelial tissue of the gut deliver bacterial metabolites to immune cells, promoting in\ufb02ammation on both a local and systemic scale. The persistence of this condition may lead to subacute or chronic in\ufb02ammation, which may subsequently drive the development of diseases such as in\ufb02ammatory bowel disease, diabetes or cardiovascular disease [65].<\/p>\n

6. Proposed Mechanisms and Relationships between the Gut Microbiota and Inflammatory Markers<\/p>\n

6.1. Lipopolysaccharides
\nLipopolysaccharides (LPS), also known as endotoxin, form the key cell wall component of Gram-negative bacteria. Increased levels of LPS are observed in obesity and other metabolic disorders as well as adipose tissue in\ufb02ammation and pancreatic beta-cell dysfunction [23,67\u201369]. Under normal conditions, the gut barrier including intestinal epithelial and mucosal layers, minimises movement of LPS from the bowels into the systemic circulation [70]. Disruption of this barrier by factors such as diet or pathogenic bacteria, may lead to LPS dislocation and movement between the junctions of the intestinal barrier into the circulation [70]. This leakiness and dysregulated permeability of the gut means macrophages can in\ufb01ltrate the region, produce and activate in\ufb02ammatory cytokines, leading to local in\ufb02ammation [70]. Moreover, LPS binds to toll-like receptor 4 (TLR-4) found on immune cells, and in doing so can activate pro-in\ufb02ammatory cascades both local to the intestine and in distant sites [67]. In a study by Cani et al. [71], mice fed a high-fat diet were found to have a high amount of LPS circulating in their bloodstreams, exhibiting endotoxaemia, however when administered antibiotics, this elevated level of LPS was not found. This demonstrates that gut microbiota induced by high fat diets release LPS, and when targeted by antibiotics, downstream e\ufb00ects of LPS would be prevented. Here, it is presumed that the antibiotics eliminate most of the microbiota, including LPS-secreting bacteria in locations other than the GI tract. Upon injecting healthy human participants with LPS, Mehta et al. [72] found increased insulin resistance as insulin receptors in adipose tissue became suppressed, although pancreatic beta-cell function was not compromised. Furthermore, a study by Tian et al. [73] reported that probiotic therapy with Lactobacillus paracasei reduced and reversed the e\ufb00ects of LPS-associated pathology in rodents, speci\ufb01cally reducing type 2 diabetes-associated mechanisms such as beta-cell dysfunction. However, it is worth noting that not all members of the Lactobacillus genus have anti-diabetic properties, as in a human study it was found that Lactobacillus gasseri was elevated in those with type 2 diabetes [74].<\/p>\n

6.2. Short-Chain Fatty Acids
\nAs stated above, gut bacteria possess the capability of metabolising complex carbohydrates, otherwise undigested by the host, into SCFAs. SCFAs play a critical role in the interplay between diet, the gut microbiota and downstream activation or inhibition of in\ufb02ammatory cascades. Additionally, they contribute to the homeostatic control of energy and appetite regulation through their e\ufb00ects on metabolic pathways [75]. Depending on the type and concentration of SCFA, their e\ufb00ects on in\ufb02ammation di\ufb00er, and SCFA levels may vary in obese and lean phenotypes [76]. In many animal studies, SCFA butyrate has been associated with a variety of roles that oppose the onset of metabolic disorders [40]. Through epigenetic interactions, butyrate promotes lipolysis and mitochondrial functioning in adipocytes, thus enabling a greater energy expenditure and preventing the onset or maintenance of obesity [77,78]. Butyrate is an anti-in\ufb02ammatory metabolite that is known to inhibit the pathways that lead to the production of pro-in\ufb02ammatory cytokines [79,80]. In a clinical study of 13 patients with Crohn\u2019s disease, oral administration of butyrate was found to alleviate in\ufb02ammation in nine patients [81]. Additionally, butyrate minimises the risk of development of insulin resistance as it improves insulin signalling [82]. Butyrate has also been shown to minimise LPS translocation in the intestines, thus reducing LPS-associated e\ufb00ects [40]. Faecalibacterium prausnitzii has been identi\ufb01ed as a butyrate-producing bacterium with an inverse relationship with di\ufb00erent pro-in\ufb02ammatory markers [83]. In obese individuals, F. prausnitzii abundance is reduced compared to individuals with healthy body weight [84]. Acetate, another SCFA, is an important molecule for the processes of lipogenesis and gluconeogenesis. Acetate can serve as a substrate for cholesterol synthesis, thus contributing to elevated serum cholesterol levels [85]. In a study of rats, contrasting with butyrate, acetate was found to correlate with greater insulin resistance and an increase in ghrelin secretion as a result of its activation of the parasympathetic nervous system [86]. As ghrelin is an appetite-stimulating hormone associated with greater food intake, acetate may consequently be linked with weight gain [86]. Although there is some consensus on SCFAs and their metabolic properties, \ufb01ndings have been inconsistent [87]. Regarding the potential role of acetate in obesity, a study conducted by Frost et al. [88] suggested that acetate is associated with appetite inhibition and therefore a lower risk of obesity. However, Perry et al. [86] reported that acetate was linked with an increased risk of obesity. Variation in the research participants, the employed research methods and analytical techniques may account for these observed di\ufb00erences. Nevertheless, there is a clear need for further research to elucidate the exact mechanisms by which SCFAs relate to changes in in\ufb02ammation, microbiota composition and the subsequent development of metabolic disorders.<\/p>\n

6.3. Bile Acids
\nBile acids have a range of roles in the body, from enabling emulsi\ufb01cation of lipids to allow their absorption by the body, to functioning as signalling ligands [67]. The conversion of primary bile acids to secondary bile acids is carried out by gut bacteria. Changes in the gut microbiota in\ufb02uence the types of secondary bile acids that are synthesised, which in turn, may a\ufb00ect the secretion of appetite hormones from the gut, resulting in di\ufb00erent appetite inclinations [89]. Of particular relevance to this review is that bile acids, via activating the farnesoid X receptor (FXR) signalling pathway in enterocytes and adipocytes, cause in\ufb02ammation [90]. Pars\u00e9us et al. [20] found that mice lacking functional FXRs did not accumulate adipose tissue in the same way as mice with the receptor, suggesting that the gut microbiota may promote the onset of obesity through secondary bile acid formation.<\/p>\n

6.4. C-Reactive Protein
\nC-reactive protein (CRP) is an acute-phase reactant associated with cardiovascular disease, type 2 diabetes and obesity [21]. When macrophages and T cells secrete interleukin (IL)-6, this molecule is subsequently released at high levels into the circulation [91]. In a study conducted by Xu and Song [21], the proportion of Akkermansia muciniphila declined in obese mice with elevated plasma levels of CRP. However, this does not explain whether CRP modulates the gut microbiota, or whether the gut microorganisms contribute to its elevation. The abundance of members of genus Phascolarctobacterium has been associated with lower levels of CRP [92]. This relationship could potentially clarify why a decline in the proportion of this genus is associated with colonic in\ufb02ammation [93]: Phascolarctobacterium are producers of propionate, an SCFA that inhibits pro-in\ufb02ammatory cascades by suppressing the activity of pro-in\ufb02ammatory regulator nuclear factor kappa-B (NF\u03baB) (see Section 6.5) [94,95]. Similarly, the abundance of Faecalibacterium is inversely correlated with levels of CRP [81,96]. Thus, CRP is a downstream in\ufb02ammatory marker that can be down-regulated through the e\ufb00ects of anti-in\ufb02ammatory metabolic products of speci\ufb01c gut microbes. the evaluation of baseline serum and microbiota data of healthy subjects with BMI over 25 showed that those with higher CRP levels had a signi\ufb01cantly lower abundance of bacteria from the genera Lactobacillus and Bi\ufb01dobacterium, but a higher abundance of Escherichia and Bacteroides [97].<\/p>\n

6.5. Cytokines
\nCytokines are signalling molecules secreted by immune cells that a\ufb00ect numerous processes within the body, including immunomodulation [98]. Many transcription factors regulate the production of cytokines, however, the focus of this review will be on NF\u03baB, a regulator deemed prototypical and involved in the activation of various in\ufb02ammation-related genes [99]. Cytokines are generally classi\ufb01ed as either pro-in\ufb02ammatory or anti-in\ufb02ammatory in their downstream e\ufb00ects, although this binary classi\ufb01cation is simplistic and does not account for the fact that speci\ufb01c cytokines can play opposing roles in multiple processes, and are context-dependent [100]. A detailed description of evidence related to all cytokines and the gut microbiota is beyond the scope of this review. In the following sections, we present some of the established correlations between the gut microbiota and TNF alpha and interleukin-6, the two cytokines that have been more commonly studied.<\/p>\n

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Table 1 highlights the general tendencies of various cytokines, as reported in previous studies.<\/p>\n

Zahraa Al Bander, Marloes Dekker Niter t et al.<\/strong><\/em>
\nReceived: 10 September 2020; Accepted: 15 October 2020; Published: 19 October 2020<\/strong><\/em>
\nInternation Journal of Environmental Research and Public Health.<\/strong><\/em><\/p>\n","protected":false},"excerpt":{"rendered":"

Highlighted \u201cRole of the Gut Microbiota in Immunity and In\ufb02ammation Microbes possess a variety of functions that in\ufb02uence their ability to grow and colonise, whilst bringing about downstream e\ufb00ects for the host that may be bene\ufb01cial or otherwise [61]. Humans are not capable of digesting some components of dietary \ufb01bre due to the lack of […]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[73],"tags":[1891,1889,1887],"class_list":["post-12362","post","type-post","status-publish","format-standard","hentry","category-article","tag-gut-inammation","tag-gut-microbiota","tag-gut-permeability"],"yoast_head":"\nThe Gut Microbiota and In\ufb02ammation: An Overview - Glutenlight<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/glutenlight.eu\/?p=12362&lang=en\" \/>\n<meta property=\"og:locale\" content=\"it_IT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"The Gut Microbiota and In\ufb02ammation: An Overview - Glutenlight\" \/>\n<meta property=\"og:description\" content=\"Highlighted \u201cRole of the Gut Microbiota in Immunity and In\ufb02ammation Microbes possess a variety of functions that in\ufb02uence their ability to grow and colonise, whilst bringing about downstream e\ufb00ects for the host that may be bene\ufb01cial or otherwise [61]. 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