Effects of Metabolites Derived From Gut Microbiota and Hosts on Pathogens
Zhendong Li1 
Guomei Quan1 Xinyi Jiang1 Yang Yang1 Xueyan Ding1 Dong Zhang1 Xiuqing Wang1 Philip R. Hardwidge2 
Wenkai Ren3* 
Guoqiang Zhu1*- 1Joint International Research Laboratory of Agriculture and Agri-Product Safety of Ministry of Education of China, Jiangsu Co-innovation Center for Important Animal Infectious Diseases and Zoonoses, College of Veterinary Medicine, Yangzhou University, Yangzhou, China
- 2College of Veterinary Medicine, Kansas State University, Manhattan, KS, United States
- 3Guangdong Provincial Key Laboratory of Animal Nutrition Control, Subtropical Institute of Animal Nutrition and Feed, College of Animal Science, South China Agricultural University, Guangzhou, Guangdong, China
Intestinal metabolites participate in various physiological processes, including energy metabolism, cell-to-cell communication, and host immunity. These metabolites mainly originate from gut microbiota and hosts. Although many host metabolites are dominant in intestines, such as free fatty acids, amino acids and vitamins, the metabolites derived from gut microbiota are also essential for intestinal homeostasis. In addition, some metabolites are only generated and released by gut microbiota, such as bacteriocins, short-chain fatty acids, and quorum-sensing autoinducers. In this review, we summarize recent studies regarding the crosstalk between pathogens and metabolites from different sources, including the influence on bacterial development and the activation/inhibition of immune responses of hosts. All of these functions would affect the colonization of and infection by pathogens. This review provides clear ideas and directions for further exploring the regulatory mechanisms and effects of metabolites on pathogens.
Introduction
A growing number of studies suggest that intestinal microbiota play an important role at the interface of health and disease of hosts, due to a crosstalk of small molecules between the intestinal mucosal surfaces and the microbiota. Examples include food digestion, oxidation and reduction of molecules, and the synthesis of essential amino acids. Some of these molecules are metabolites derived from hosts and microbiota (Donia and Fischbach, 2015). Many studies have reported that the intestinal metabolites regulate pathogen infection in intestines, through genome-based analysis of bacteria and high-throughput metabolomics (Browne et al., 2017; Hirata and Kunisawa, 2017).
Metabolites can affect the invasion of pathogens through different pathways. Some metabolites, such as nisin, and several lantibiotics directly kill pathogens by disrupting bacterial cell structures. Nisin inhibits peptidoglycan synthesis by targeting lipid II, which is a key intermediate in the peptidoglycan biosynthesis machinery within the bacterial cell envelope. Lantibiotics dock with lipid II to promote the formation of pores in the cell membrane, resulting in a loss of membrane and subsequent cell death. In addition, bacteriocins can kill bacterial cells by interfering with bacterial DNA, RNA, and protein metabolism (Cotter et al., 2013). Resource competition between commensal bacteria and pathogens caused by metabolites is also an indirect pathway. Competition in the use of monosaccharides can limit the colonization of Citrobacter rodentium in wild-type mice (Kamada et al., 2012). Another example is iron that is crucial in host–pathogen interaction, in which both opponents compete for iron. Pathogens have specific iron requirements due to the metal's function in metabolism and proliferation (Nairz et al., 2010). Several metabolites also affect cell adhesion and biofilm formation. For example, D-amino acids produced by Bacillus subtilis prevent biofilm formation and reduce existing biofilms (Mühlen and Dersch, 2016). Quorum-sensing autoinducers also affect the adhesion of flagellum, biofilm formation, and production of toxins (Yang et al., 2013). Recent studies have uncovered a major role of metabolites in the regulation of the immune system (especially the microbial metabolites). Intestinal metabolites activate innate immunity through numerous microbial sensors called pattern recognition receptors (PRRs) in intestinal epithelial cells after infection by pathogens. In addition, several microbial metabolites are involved in the regulation of adaptive immune cell development, in particular T lymphocytes (Levy et al., 2017). Furthermore, some of these identified metabolites, including short-chain fatty acids (SCFAs) and vitamins, have been shown to have a protective effect, whereas others, such as quorum-sensing autoinducers, have been shown to directly promote the infection by pathogens.
This review summarizes the findings from past studies on the effects and brief regulatory mechanisms of metabolites from different sources on pathogens in intestines. The growing understanding of the role of intestinal metabolites in bacterial virulence provides new opportunities to interfere with important pathogens or pathogenesis.
The Effects of Metabolites from Gut Microbiota on Pathogens
Gut microbiota is mainly metabolized via absorbing energy and sources from the host and the diet to support their growth and releasing metabolites produced through fermentation. These metabolites in turn influence the host metabolome and the formation of gut microbiota (Flint et al., 2015). Here, we describe the sources of several intestinal microbial metabolites (Table 1), explain in detail how these microbial metabolites regulate pathogens and their effects, and provide a future research direction. (Table 2).
Table 1. The evidence of metabolites from gut microbiota.
Table 2. The pathogens are regulated by gut microbiota-derived metabolites and their mechanisms and effects.
Bacteriocins
Bacteriocins were first identified in Escherichia coli. Fredericq discovered that bacteriocins are proteins and can be active against a limited range of bacteria, but have a specific immunity mechanism for their producers (Fredericq, 1946). Bacteriocins have been found in all major lineages of bacteria and some members of the archaeal community (Riley and Wertz, 2002; Nes et al., 2007; Blum, 2008). In particular, 90% of environmental and clinical isolates of Pseudomonas aeruginosa can produce bacteriocins. The bacteriocins of gram-positive bacteria are plentiful and even more diverse than those generated in gram-negative bacteria. The most typical bacteriocin-producing gram-positive bacteria are lactic acid bacteria (LAB) (Gillor et al., 2008).
The interactions of bacteriocins with target bacteria have been studied in many respects (Figure 1). Since the cell wall is highly conserved among pathogens and does not exist in mammalian cells, it is considered to be a perfect target for inhibiting pathogen infection. A suitable antibacterial substance can inhibit the formation of the cell wall or destroy its integrity (Mazzotta and Montville, 2010; Nayar et al., 2015). For example, nisin A, produced by Lactococcus lactis, is a typical poreforming bacteriocin which binds peptidoglycan precursor lipid II to prevent it from combining with penicillin. This combination induces pore formation by nisin molecules arranged as pore-forming “units” and then rapidly kills cells Lages et al., 2013). The synergistic effects of the Lactobacillus acidophilus surface layer and nisin A inhibit the growth of pathogenic gram-negative Salmonella enterica and potential pathogenic gram-positive bacteria, Staphylococcus aureus and Bacillus cereus. The effect suggests that the synergistic action between bacteriocins and beneficial bacteria can inhibit harmful bacteria. If this mechanism is ubiquitous in other intestinal commensal bacteria, exogenous bacteriocins can enhance the antibacterial capacity of commensal bacteria, and quickly clear the pathogens (Prado-Acosta et al., 2010). In addition, the genetic materials within pathogen cells are targets of bacteriocins. For example, the MccB17 and MccJ25 microcins are toxic peptides secreted by enterobacteria (mostly E. coli), with molecular masses below 10 kDa. Microcins are produced and secreted under conditions of limited essential nutrients and are activated against related species. MccB17 and MccJ25 microcins internalize into the target bacterial cell respectively across the outer-membrane protein OmpF and the outer-membrane receptor FhuA-dependent TonB pathway. The inner-membrane protein SbmA then transports both of the microcins across the inner membrane to the cytoplasmic face. Finally, inside the cell, MccJ25 inhibits the bacterial RNA polymerase and MccB17 acts as a DNA gyrase inhibitor (Mathavan and Beis, 2012). MccB17 exhibits potent bactericidal activity against a wide range of bacteria including Escherichia, Klebsiella, Shigella, Salmonella, and Pseudomonas (Baquero and Moreno, 1984). Besides, bacteriocins can inhibit the synthesis of key proteins in pathogens. The colicin family proteins by E. coli exhibits 16S rRNase activity. They bind the BtuB/Tol translocation machinery for the purpose of crossing the outer membrane and split the 16S rRNA at the 3-end of the coding sequence, inhibiting RNA translation (Toba et al., 1988; Lancaster et al., 2010; Ng et al., 2010).
Figure 1. The gut microbiota release bacteriocins. First, they bind Lipid 2 of the cell wall of the pathogen, inhibiting the synthesis of peptidoglycan. Some bacteriocins enter the cytoplasm of pathogens and bind 16s rRNA to inhibit protein synthesis. Bacteria also inhibit RNA polymerase and DNA gyrase. Ultimately, cell growth is blocked or cells die.
Importantly, in animal models, bacteria have been found to produce bacteriocins and inhibit the growth of pathogens. For example, E. coli strain H22 inhibited many Enterobacteriaceae members in vitro, whereas in vivo, 6 days after simultaneous oral inoculation in germ-free mice, E. coli H22 decreased the fecal population of Shigella flexneri 4 to undetectable levels. Further studies have revealed that E. coli H22 produces a variety of bacteriocins to prevent pathogens, including microcin C7, colicin E1, and colicin Ib (Cursino et al., 2010).
Currently, most studies focus on the discovery of novel bacteriocins produced by bacteria and their functions in vitro. Isolating bacteriocins from the intestine and mimicking the intestinal environment to explore the types of bacteriocin production and the regulatory mechanisms for pathogens could be a useful research direction to better understand the interactions between gut microbiota, bacteriocins, and pathogens. More importantly, to address the problem of antibiotic resistance, using the synergy of bacteriocins and antibiotics is a new approach in the treatment of infectious diseases (Sass and Brötz-Oesterhelt, 2013).
Microbiota-Derived Short-Chain Fatty Acids
Short-chain fatty acids (SCFAs), the metabolites of microbial fermentation, consist of acetic acid, butyric acid, and propionic acid. Acetic acid and propionic acid are mainly produced by Bacteroidetes fermentation, whereas butyric acid is the main metabolite of Firmicutes (Macfarlane and Macfarlane, 2003). SCFAs are mainly observed in the cecum and the ascending colon, but less in the small intestine (Cummings et al., 1987). When nondigestible carbohydrates such as fiber reach the colon, they are hydrolyzed into oligosaccharides by anaerobic bacteria. Oligosaccharides are then converted to phosphoenolpyruvate (PEP) via two major bacterial metabolic pathways, the Embden–Meyerhof–Parnas pathway and the pentose phosphate pathway. Finally, PEP is transformed into an organic acid or alcohol (Fischbach and Sonnenburg, 2011).
SCFAs indirectly affect pathogen infection by maintaining the integrity of the gut barrier and activating intestinal immunity (Figure 2). For example, high concentrations of butyrate protect Caco-2 cells from Campylobacter jejuni invasion and translocation by inducing cell differentiation (Van Deun et al., 2008). Butyrate also increases the intestinal barrier by activating AMP-activated protein kinase (AMPK) in Caco-2 cell monolayers (Peng et al., 2009). AMPK plays a critical role in cellular energy homeostasis and performs cytoprotection under stress (Hardie et al., 2000). SCFAs (propionic acids) decrease the internalization of S. aureus into bovine mammary epithelial cells (bMEC), more importantly, governing the expression of antimicrobial peptide mRNA. However, the explicit relationship between membrane protein activation and cell differentiation is not clear (Alva-Murillo et al., 2012).
Figure 2. SCFAs promote the differentiation of intestinal epithelial cells by activating AMPK to adapt to environmental changes caused by pathogens. They also induce intestinal cells to synthesize antimicrobial peptides. High concentrations of SCFAs affect the osmotic pressure of pathogens and cause cell lysis. However, low concentration of SCFAs induce the expression of pathogen virulence genes.
Direct antibacterial mechanisms of SCFAs show toxic effects on enteric bacteria and present more conspicuously at high concentrations (Van Immerseel et al., 2004). The nonionized forms of SCFAs with a circumneutral pH enter and dissociate in the bacterial cytoplasm, causing the release of SCFA anions (Lambert and Stratford, 1999). These SCFA anions affect the osmotic balance in a high concentration (Roe et al., 1998). However, low concentrations of butyrate promote the expression of the virulence determinants of enterohemorrhagic E. coli (EHEC) strain Sakai. The butyrate is combined with the transcriptional regulator Lrp's ligand-binding domain in response to the expression of the virulence gene (Nakanishi et al., 2009). Different spatial gradients of SCFAs act as a cue, permitting C. jejuni to locate the lower intestine and regulate the expression of virulence and commensalism genes (Luethy et al., 2017).
Consequently, SCFAs enhance the integrity of intestinal epithelial cells and destruct the cellular structure by influencing the osmotic pressure to affect pathogen infection. Appropriate levels of SCFAs contribute to the integrity of epithelial cells and activate the immune system, while high concentrations are toxic (Argenzio and Meuten, 1991). Therefore, the effects of SCFAs on pathogens is concentration-dependent. In the physiological range, whether SCFAs have a specific regulatory effect on epithelial homeostasis, such as affecting epithelial turnover, differentiation, or the barrier function, has not been convincingly demonstrated in humans and animals. Future studies should determine the normal physiological range of the SCFAs in the intestine and the optimal level in animal models (Gill et al., 2018).
Microbial Amino Acids
Most of the amino acids in intestines originate from the metabolism of dietary proteins and tissue proteins of host or the conversion of other nitrogenous substances, while a small proportion of amino acids are synthesized de novo by the gut microbiota (Metges, 2000). For example, a study revealed that approximately 2–20% of circulating lysine in the body's plasma, urine, and body proteins originates from the gut microbiota, by using isotope tracers in humans, pigs, and rats (Metges et al., 2003). A few bacteria can make all 20 of the standard amino acids, which contribute to host amino acid homeostasis (Peng and Harper, 1970; Lin et al., 2017).
Bacteria synthesize a largely different set of D-amino acids (D-aa) that are released as free D-aa. A recent work has demonstrated that intestinal microbiota in mice can produce abundant free D-aas in vivo. Scientists quantified the D- and L-forms of all proteinogenic amino acids by two-dimensional HPLC8 in cecal contents of specific pathogen-free (SPF) mice and germ-free (GF) mice. SPF mice contained D-Ala, D-Asp, D-Glu, and D-Pro (~200–500 nmol/g) while low levels of D-Asp were only detected in GF mice. This result suggests that gut microbiota plays a vital role in producing D-aas (Sasabe et al., 2016). D-aas are involved in the composition of bacterial cell walls, and D-Ala and D-Glu are the basic constituents of bacterial peptidoglycans (Caparrós et al., 1992). However, excess D-aas (such as D-Met, D-Trp, or D-Phe) replace the D-Ala within the short peptide of peptidoglycan and cause the accumulation of two major new muropeptides, which affect the metabolism and hinder cross-linking of peptidoglycan (Caparrós et al., 1992). This means that exogenous D-aas can modulate pathogens by affecting the structure of peptidoglycan and the formation of cell walls. Moreover, D-aas also affect biofilm formation and degradation. D-Tyr (3 μM), D-Met (2 mM), D-Trp (5 mM), and D-Leu (8.5 mM) were effective in inhibiting biofilm formation of B. subtilis, and the synergies of all four D-amino acids were particularly potent (~10 nM). Other D-aas were inert in this experiment (Kolodkin-Gal et al., 2010). Another study observed that only D-Tyr, D-Pro, and D-Phe can inhibit the formation of S. aureus biofilms (Hochbaum et al., 2011). Although their action mechanism is partially associated with the replacement of D-Ala in the peptide side chain, we do not know why only a part of D-aas has the ability to regulate biofilms and why inhibiting different pathogens' biofilms require different D-aas.
In addition, D-aas are employed against gut pathogens through another pathway. D-amino acid oxidase (DAO) exists in the intestinal epithelium of mice and in human goblet cells and is secreted into the intestine lumen. The amount of DAO in SPF mice is higher than that in GE mice, indicating that gut microbiota induce the production of intestinal DAO. DAO can deaminate neutral D-aas to release the antimicrobial product H2O2. Treating some enteric pathogens (Vibrio cholera, P. aeruginosa, S. aureus, and enterohemorrhagic E. coli) with DAO and D-aas can inhibit their growth (Ridler, 2016). Besides, D-Ser activates the SOS response and inhibits the expression of the type III secretion system that is essential for EHEC adhering to host cells (Connolly et al., 2016). Finding commensal bacteria that produce a large amount of D-aas in gut microbiota and then examining their ability and mechanisms against pathogens in vivo are probably good directions (Aliashkevich et al., 2018).
Intestinal Microbial Vitamins
Vitamins are essential micronutrients that maintain the normal development and health of the body. They are abundant in the human body and can be obtained through food intake or transformation and synthesis of other substances. They can also be supplied by intestinal bacteria. For example, the human intestinal bacteria LAB and Bifidobacteria can synthesize most of the water-soluble B vitamins and vitamin K2 from scratch (Hill, 1997). Vitamins produced by microorganisms are mainly absorbed in the colon, whereas vitamins derived from diets and hosts are taken up in the proximal small intestine (Ichihashi et al., 1992; Said and Mohammed, 2011).
E. coli, LAB, and Bacteroides species are major producers of VK2 (menaquinone) in the human body. The potential pathogenic bacteria S. aureus and Salmonella also produce VK2 (Conly and Stein, 1992; Conly et al., 1994). VK2 play an indispensable role in the virulence and survival of some pathogens. For example, S. aureus acquires iron through the high-affinity heme uptake system during invasion into hosts, but excessive heme is highly toxic. Membrane-based quinone molecules and heme form a redox cycle that continuously releases semiquinones and reduces heme (Wakeman et al., 2012). In addition, VK2 have been reported to affect the phenotype expression of pathogens. Different concentrations of VK2 enhance the biofilm formation of S. aureus, and the response to exogenous VK2 signals appears to be under the regulation of sarA in S. aureus (Kirby et al., 2014). In these processes, VK2 play a vital role in maintaining the survival strategies of pathogens. However, the analogs of VK2, such as menadione, 1, 4-naphthoquinone, and coenzymes Q1 to Q3, broadly inhibit the growth of pathogens and reduce the amount of exotoxin generated by gram-positive organisms. Moreover, VK2 not only is a part of the electron transport chain in S. aureus, but also a precursor of menaquinone (Schlievert et al., 2013).
The B vitamins [VB2(riboflavin), VB6(pyridoxine) and VB9(folacin)] are all synthesized by bacteria in the gut (LeBlanc et al., 2013). VB2 is a precursor of the coenzyme flavomononucleotide (FMN) and flavin adenine dinucleotides (FAD), and it participates in cell metabolism. LAB, E. coli, and B. subtilis combine guanosine triphosphate (GTP) and D-ribulose 5-phosphate to synthesize riboflavin (Bacher et al., 2000; Sonenshein et al., 2002). In vivo, an intramuscular injection of VB2 (6.25 mg/kg−100 mg/kg) can enhance the nonspecific resistance of mice to various pathogens. The effect was induced by the stimulation of the proliferation of neutrophils, monocytes, and activated macrophages. This provides evidence that VB2 indirectly regulates immune responses to affect pathogens (Araki et al., 2008). Deficient mice have impaired VB2-dependent NADPH oxidase 2(Nox2) activation and ultimately reduced defense against L. monocytogenes (Schramm et al., 2014). However, VB2 has different effects on pathogens in vitro. It has been reported that VB2 is toxic and can enhance the degree of pathogen infection at high concentrations (Flieger et al., 2016). The reasons for the diverse effects of VB2 on pathogens are still unclear, but concentration seems to be an important factor because VB2 concentration and application conditions were different in these experiments. In addition, a recent study revealed that if worms' diets contain live bacteria, they develop normally until adults. If only killed bacteria were fed, the worms stop eating and growing. Supplementing extra VB2 leads to a return to normal consumption, suggesting that intestinal microbiota plays an important role in supplying micronutrients such as VB2 (Qi et al., 2017).
Most of the members of the vitamin B family mainly induce the immune system to prevent pathogen infection. For example, VB9 is mainly produced by the fermentation of probiotics such as bifidobacteria and lactobacilli in the human body. VB9 deficiency reduces lymphocyte proliferation and natural killer cell activity, and it plays a pivotal role in the survival of regulatory T (Treg) cells (Courtemanche et al., 2004; Troen et al., 2006; Kunisawa et al., 2012). Bacillus, E. coli, P. aeruginosa, and Serratia marcescens can produce VB6 (Dempsey, 1967). The deficiency of VB6 impairs both cellular and humoral immunity in humans and animals. Supplementation with Bacteroides and VB6 can enhance the clearance of pathogens during Salmonella typhimurium infection. We noticed that VB6 can clear pathogens by promoting the growth of Bacteroides, regulating the host immune system, or interfering with the growth or the virulence expression of S. typhimurium. (Talbott et al., 1987; Rall and Meydani, 1993; Sperandio, 2017).
In summary, vitamins produced by gut microbiota play an important role in activating intestinal immune response and defending against the infection by external pathogens. However, the mechanism of direct interaction between microbial vitamins and pathogens remains unclear.
Quorum-Sensing Autoinducers (AI)
With the gradual increase and accumulation of bacterial density in a certain space, the bacteria show some physiological or biochemical changes, facilitating quorum sensing (QS) (Waters and Bassler, 2005). Since the concept was proposed by Fuqua a large number of studies have found and revealed the primary mechanism and fractional functions of QS. In a QS system, one or more signaling molecules produced by bacteria are released into the cytoplasm to sense the bacterial concentration. The signaling molecules bind to QS receptors on the surface of bacteria or other regulated bacteria when the bacterial concentrations reach a certain threshold. Then, the receptors bind the corresponding binding domain of genes to change the bacterial behavior (Papenfort and Bassler, 2016).
In the gut, E. coli is regulated by at least three QS signaling molecules (Walters and Sperandio, 2006). One of them is E. coli-generated autoinducer-2 (AI-2), which is composed of 4,5-dihydroxy-2,3-pentanedione, a metabolite of S-adenosylmethionine (Pereira et al., 2013). AI-2 is encoded by the luxS gene and has diverse effects on different bacteria. For example, the luxS deletion mutant of E. coli reduced the adhesion of flagellum, expression of Stx2e toxin, and production of bacterial surface outer membrane proteins (Yang et al., 2014). However, a recent work demonstrated that the inactivation of the luxS gene of S. aureus increased biofilm formation and higher polysaccharide intercellular adhesion (PIA) production (Ma et al., 2017). Another signaling molecule is acylated homoserine lactone (AHL), mainly found in gram-negative bacteria. Although E. coli cannot synthesize AHLs due to the lack of the luxS gene, it has the AHL receptor protein LuxR. The AHLs produced by P. aeruginosa isolated from the bovine intestine and produced by Clostridium perfringens in the porcine intestine modulate the expression of flagella, a virulence factor of F18 E. coli (Yang et al., 2013). Currently, other autoinducers have also been discovered and most of them affect themselves and other pathogens. For example, 2-heptyl-3-hydroxy-4(1H)-quinolone (PQS) is a QS signaling molecule present in P. aeruginosa. PQS modulates various target genes including those coding for rhamnolipid, elastase, the PA-IL lectin, and pyocyanin as well as influencing biofilm formation and cellular fitness (Diggle et al., 2006). Most of the studies on QS have focused on the effects and mechanisms of pathogen virulence and the discovery of new inhibitors of QS. However, the vast majority of gut microbes are beneficial to the body. Whether QS can be used to enhance the survival ability of these probiotics and to resist pathogen invasion is still an unexplored topic in this field.
The Effects of Metabolites from Hosts on Pathogens
Host-derived metabolites are predominant in the body. They are mainly synthesized by the host and provided by the diets. Here, we briefly summarize some of the most common host-derived metabolites' regulatory mechanisms and effects on pathogens and discuss the problems that exist. (Table 3).
Table 3. The pathogens are regulated by host-derived metabolites and their mechanisms and effects.
Host-Derived Free Fatty Acids
Fatty acids released from host lipids by enzyme action become free fatty acids (FFAs), which play unique roles in host defenses against potential pathogenic microorganisms.
It is unclear how FFAs exert their antibacterial effects, but we know that the central target seems to be the bacterial cell membrane and the diverse essential processes that occur within and at the membrane (Desbois and Smith, 2010). For example, unsaturated FFAs probably bind to the carriers of the electron transport chain directly or insert into the inner membrane when they cross the cell wall or outer membrane of bacteria, leading to the electron carriers moving apart or being displaced from the membrane. These processes suggest that FFAs can affect the energy metabolism of bacteria by destroying the electron transfer chain. More importantly, the insertion of FFAs into the cell membrane increases the permeability of the cell membrane, resulting in the leakage of some cytoplasmic contents and eventually cell death (Galbraith and Miller, 1973; Peters and Chin, 2003; Desbois and Smith, 2010). In addition, FFAs suppress the activity of cell membrane enzymes and the nutrients absorption of bacteria (Galbraith and Miller, 1973; Shibasaki, 1978; Kurihara et al., 1999; Zheng et al., 2005; Sado-Kamdem et al., 2009). However, the type VII secretion system (T7SS) of S. aureus can be triggered by host-specific cis-fatty acids (Lopez et al., 2017). T7SS is a major secretory pathway for S. aureus to produce virulence factors during host infection, contributing to long-term persistence of staphylococcal survival and the formation of abscesses (Kneuper et al., 2014). A lipidomics analysis showed that the host-specific cis-unsaturated fatty acids were linoleic acid (LA) and arachidonic acid. S. aureus use fatty acid kinase (FAK) to integrate the fatty acids into their own phospholipids and lipoproteins, thereby activating EsxA expression, one of the virulence proteins of T7SS (Burts et al., 2005; Parsons et al., 2014; Lopez et al., 2017). We do not know why FFAs have different effects on the same pathogens. We assume that FFAs may be required in the process of pathogen growth and infection. When bacterial growth reaches a critical value, pathogens will switch to a state where a large amount of FFAs in the body is highly toxic for pathogens.
Immune responses induced by FFAs is another important regulatory mechanism. Conjugated linoleic acid (CLA) is a generic term for the position and geometric isomers of linoleic acid with conjugated double bonds at the 6-8 to 13-15 carbon positions (Bergamo et al., 2014). The cis-9, trans-11 isomer (c9, t11-CLA) of CLA inhibits nuclear factor-κB (NF-κB) activation and IL-12 production in dendritic cells through ERK-mediated IL-10 induction, suggesting that CLA affects the occurrence of infectious inflammation in the body by modulating the immune responses (Loscher et al., 2005). Arachidonic acid also simultaneously enhances immune responses (both cellular and humoral immunity). It can modulate macrophages to increase the free radicals that are critical for antimicrobial or tumor-killing effect. Macrophages and T cells in the gut can deliver arachidonic acid to target organs to eliminate pathogen infection and suppress inflammation (Das, 2018).
It is evident that FFAs can influence pathogen infection through different pathways. Therefore, they have potential value as an antimicrobial agent. FFAs are able to selectively improve the growth of beneficial bacteria and possibly prevent the proliferation of harmful microbiota; furthermore, dietary supplementation does not lead to any deleterious effect on gut microbiota (Das, 2018).
Host-Derived Amino Acids
Host-derived amino acids are one of the most common metabolites in the gut and the main oxidative fuel in the intestinal mucosa, as well as the structures that synthesize tissue proteins, nitrogen sources, enzymes, and other biological products. Recent studies have shown that specific amino acids (glutamine, glutamic acid, arginine, glycine, lysine, threonine, and sulfur-containing amino acids) can be used to prevent and treat gut-related diseases in humans and mammals (Wang et al., 2009; Ridler, 2016). For example, L-glutamine is a conditionally essential amino acid in mammalian plasma and an important donor of biosynthetic nucleic acids and other amino acids. It plays a major role in promoting the repair of a damaged gut, preventing pathogen infection, and maintaining the local immune function (Souba et al., 1990; Scheppach et al., 1996). L-glutamine is predominantly present in the small intestine whose intestinal epithelial barrier can protect the internal environment from the invasion of pathogens (Ménard et al., 2010; Veldhoen and Brucklacher-Waldert, 2012). The normal intestinal barrier against pathogen infection primarily depends on the specific IgA antibodies secreted by the gut-associated lymphoid tissue (GALT), which includes lymph nodes, plasma cells, and mucosal intraepithelial lymphocytes (Ruth and Field, 2013). In normal physiological conditions, IgAs are released into the intestine and can be employed as an inhibitor of bacterial adhesion. However, an abnormal regulation of secretory IgA (s-IgA) production leads to bacterial translocation and defective barrier integrity through the weakening the mucosal immune system (Mestecky et al., 1986; Artis, 2008). The addition of L-glutamine reduces the production of s-IgA, helping the intestinal immune system to resist pathogen adhesion and colonization (Alverdy, 1990; Wang et al., 2009). Besides, L-glutamine can activate NF-κB signaling pathway when pathogens invade into the host. This pathway is an essential transcription factors family in the intestinal cells and produces a variety of cytokines to regulate the immune response (Haynes et al., 2009; Pasparakis, 2009; Mondello et al., 2010).
However, amino acids act as a double-edged sword for gut health that not only contribute to disease prevention but also induce the expression of pathogenic virulence genes. L-glutamine can serve as an indicator of environmental change and expression of virulence genes in L. monocytogenes. The intestinal exogenous L-glutamine crosses the bacterial membrane through ABC transporters and accumulates in the cytoplasm when L. monocytogenes invade into hosts, then, the bacteria would know that they have successfully entered host environments by sensing the concentration of exogenous L-glutamine and ultimatly release the endogenous virulence (Haber et al., 2017). Similarly, glutathione, which consists of glutamic acid, glycine, and cysteine, also acts as a signaling molecule to activate the expression of the virulence regulator PrfA in L. monocytogenes (Reniere et al., 2015).
Host-Derived Vitamins
Host-derived vitamins are the main source of most vitamins in the intestines, hence their roles in the body are more pronounced. Vitamin A is obtained directly from the diets or in the form of retinyl esters and carotenoids. According to studies in animal models, it can be considered as an anti-infective vitamin owing to its important role in the immune system, such as for regulating lymphocyte proliferation, cytokine expression, and antibody production. The role of vitamin A is mainly associated with intestinal epithelial cells (Semba, 1999). A lack of vitamin A impairs the integrity of the intestinal mucosal barrier, changing the gut microbiota and mucus protein expression and components, reducing the immunity, increasing the risk of susceptibility to pathogens, and spontaneously inducing the death of thymocytes and mature T cells. In addition, all-trans retinoic acid, a metabolite of vitamin A in the intestinal mucosal dendritic cells, shapes the intestinal immune responses and establishes the tolerance of intestinal immunity, thereby affecting the body's specific immune function (Amit-Romach et al., 2009; Litwack and Litwack, 2011; Cassani et al., 2012). Clinical trials have also shown that supplementation of vitamin A increase the cure rate of infectious diseases (Green and Mellanby, 1928; Semba, 1999). For example, diarrhea is a common disease caused by pathogens in the intestine. Vitamin supplementation reduces the incidence and mortality of diarrheal diseases in children. Though the detailed mechanism of action is not entirely clear, it is certain that the regulation of vitamin A for the mucosal immune system may depend on the type of enteric pathogens (Long et al., 2006). Another reason perhaps is that the diversity of intestinal microbiota will decrease in the absence of vitamins. For example, there is a significant reduction in butyric acid-producing bacteria in children's gut microbiota when vitamin A is deficient, whereas the proportion of Enterococcus is significantly increased (including Clostridium and Clostridium butyricum). An appropriate level of vitamin A inhibits the overgrowth of pathogens and strengthens the defense barrier of the intestine. Enterococci increase the expression of inflammatory cells and destroy the mucosa of the gastrointestinal tract (Lv et al., 2016; Wang et al., 2016).
Vitamin C is a major dietary nutrient that can kill or inhibit the growth of pathogens. For example, 5 mM vitamin C completely inhibits the growth of S. aureus (Kallio et al., 2012; Vilchèze et al., 2013). Recently, one of the antibacterial mechanisms of vitamin C revealed that the bacterial biofilm formation was effectively destructed by inhibiting the production of extracellular polymeric substances (EPS). Vitamin C inhibits QS and other stationary phase control mechanisms that support biofilm development and specifically lead to inhibition of polysaccharide biosynthesis (Pandit et al., 2017).
Other vitamins, such as vitamin E and vitamin D, are also linked to the homeostasis of the intestinal environments. For example, in the absence of vitamin E, the pathogenicity of Citrobacter in the intestinal tract of mice is enhanced (Smith et al., 2011). Vitamin D deficiency reduces the number of defensins that are necessary antimicrobial molecules required to maintain the intestinal microbiota in the body (Su et al., 2016). In summary, vitamin deficiency can affect the structure of the gut microbiota. The mechanism of the action of vitamins on pathogens is no different from that of other metabolites that have been described above, mainly inhibiting the developments of pathogens and activating the immune system.
Conclusion and Direction
Intestinal microbiota and their metabolites, as a whole, are now considered an important and versatile “organ” that maintains the body's physiological homeostasis. Application of the metabonomics technology, isotope tracer method, and fluorescent probe technology has led to numerous evidences suggesting that metabolites play a vital role in regulating the infection of pathogens. On the one hand, these metabolites prevent the invasion of pathogens by killing the pathogens directly, resisting the colonization and internalization, and inducing the immune responses indirectly. On the other hand, metabolites are also involved in the process that contributes to the pathogen infection. Some metabolites serve as signaling molecules to activate bacterial quorum sensing that allows bacteria to produce toxins and form biofilms, and to promote the invasion of pathogens by activating the expression of virulence factors. More importantly, we found that these mechanisms also share common characteristics. The interaction between metabolites and the membrane of pathogens is of great significance. Secondly, metabolites also activate a large number of immune factors to defend against pathogens. These two common characteristics may provide ideas for further exploring the regulation of metabolites on pathogens. Moreover, we also found some problems in these studies. The reasons for the diverse effects of some metabolites on pathogens are still unclear, and we speculate that this is related to the different growth stages of pathogens.
Therefore, we provide some possible directions for future research. First, we should further explore the regulation mechanisms of various metabolites on pathogens, especially the interaction with bacterial membranes and the induced immune response in the intestines. Changes in the levels of genes involved in regulation of pathogens by metabolites should also be noted (Qin et al., 2018). Second, metabolomics should be used to quantitatively analyze the amounts of various metabolites in animal models, while developing novel specific fluorescent probes for different metabolites to track and localize metabolites from different sources in the gut. Finally, we hope that we will relieve or eliminate pathogens by inducing specific metabolites from specific gut bacteria and hosts in the future.
Author Contributions
GZ, WR, and ZL designed the review article, and ZL wrote the review article. GQ, XD, and PH revised the review article. XJ, DZ, and XW helped with good discussions and comments and provided relevant literature. YY conducted a detailed examination of the content, structure and citation of the article.
Funding
This study was supported by Grant Nos. 2017YFD0500105, 2016YFD0500905 from the National Key Research and Development Program of China, grants from the Chinese National Science Foundation Grant (Nos. 31672579, 30571374, 30771603, 31072136, 31270171), and a project founded by the Priority Academic Program of Development Jiangsu High Education Institution. It also grants from the Yangzhou Science and Technology Bureau International Cooperation Project (YZ2018154).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
Aliashkevich, A., Alvarez, L., and Cava, F. (2018). New insights into the mechanisms and biological roles of D- complex eco-systems. Front. Microbiol. 9:683. doi: 10.3389/fmicb.2018.00683
Alva-Murillo, N., Ochoa-Zarzosa, A., and López-Meza, J. E. (2012). Short chain fatty acids (propionic and hexanoic) decrease Staphylococcus aureus internalization into bovine mammary epithelial cells and modulate antimicrobial peptide expression. Vet. Microbiol. 155:324. doi: 10.1016/j.vetmic.2011.08.025
Alverdy, J. C. (1990). Effects of glutamine-supplemented diets on immunology of the gut. JPEN J. Parenter. Enteral Nutr. 14, 109S−113S. doi: 10.1177/014860719001400415
Amit-Romach, E., Uni, Z., Cheled, S., Berkovich, Z., and Reifen, R. (2009). Bacterial population and innate immunity-related genes in rat gastrointestinal tract are altered by vitamin A-deficient diet. J. Nutr. Biochem. 20, 50–77. doi: 10.1016/j.jnutbio.2008.01.002
Araki, S., Suzuki, M., Fujimoto, M., and Kimura, M. (2008). Enhancement of resistance to bacterial infection in mice by vitamin B2. J. Veter. Med. Sci. 57, 599–602. doi: 10.1292/jvms.57.599
Argenzio, R. A., and Meuten, D. J. (1991). Short-chain fatty acids induce reversible injury of porcine colon. Digest. Dis. Sci. 36, 5459–1468. doi: 10.1007/BF01296816
Artis, D. (2008). Epithelial-cell recognition of commensal bacteria and maintenance of immune homeostasis in the gut. Nature Rev. Immunol. 8, 511–420. doi: 10.1038/nri2316
Bacher, A., Eberhardt, S., Fischer, M., Kis, K., and Richter, G. (2000). Biosynthesis of vitamin B2 (Riboflavin). Annu. Rev. Nutr. 20:553. doi: 10.1146/annurev.nutr.20.1.153
Baquero, F., and Moreno, F. (1984). The microcins. Fems Microbiol. Lett. 23, 117–124. doi: 10.1111/j.1574-6968.1984.tb01046.x
Bayro, M. J., Mukhopadhyay, J., Swapna, G. V., Huang, J. Y., Ma, L. C., Sineva, E., et al. (2003). Structure of antibacterial peptide microcin J25: a 21-residue lariat protoknot. J. Am. Chem. Soc. 125, 52382–12383. doi: 10.1021/ja036677e
Bergamo, P., Luongo, D., Miyamoto, J., Cocca, E., Kishino, S., Ogawa, J., et al. (2014). Immunomodulatory activity of a gut microbial metabolite of dietary linoleic acid, 10-hydroxy-cis-12-octadecenoic acid, associated with improved antioxidant/detoxifying defences. J. Funct. Foods 11, 192–202. doi: 10.1016/j.jff.2014.10.007
Browne, H. P., Neville, B. A., Forster, S. C., and Lawley, T. D. (2017). Transmission of the gut microbiota: spreading of health. Nature Rev. Microbiol. 15, 531–543. doi: 10.1038/nrmicro.2017.50
Burts, M. L., Williams, W. A., DeBord, K., and Missiakas, D. M. (2005). EsxA and EsxB are secreted by an ESAT-6-like system that is required for the pathogenesis of Staphylococcus aureus infections. Proc. Natl. Acad. Sci. U.S.A. 102, 5169–1174. doi: 10.1073/pnas.0405620102
Caparrós, M., Pisabarro, A. G., and de Pedro, M. A. (1992). Effect of D-amino acids on structure and synthesis of peptidoglycan in Escherichia coli. J. Bacteriol. 174, 5549–5559. doi: 10.1128/jb.174.17.5549-5559.1992
Cascales, E., Buchanan, S. K., Duch,é, D., Kleanthous, C., Lloubès, R., Postle, K., et al. (2007). Colicin biology. Microbiol. Mol. Biol. Rev. 71, 558–229. doi: 10.1128/MMBR.00036-06
Cassani, B., Villablanca, E. J., De Calisto, J. D., Wang, S., and Mora, J. R. (2012). Vitamin A and immune regulation: role of retinoic acid in gut-associated dendritic cell education, immune protection and tolerance. Mol. Aspects Med. 33, 53–76. doi: 10.1016/j.mam.2011.11.001
Conly, J. M., and Stein, K. (1992). Quantitative and qualitative measurements of K vitamins in human intestinal contents. Am. J. Gastroenterol. 87:511.
Conly, J. M., Stein, K., Worobetz, L., and Rutledge-Harding, S. (1994). The contribution of vitamin K2 (menaquinones) produced by the intestinal microflora to human nutritional requirements for vitamin K. Am. J. Gastroenterol. 89, 515–923.
Connolly, J. P., Gabrielsen, M., Goldstone, R. J., Grinter, R., Wang, D., Cogdell, R. J., et al. (2016). A highly conserved bacterial D-Serine uptake system links host metabolism and virulence. PLoS Pathog. 12:e1005359. doi: 10.1371/journal.ppat.1005359
Cotter, P. D., Ross, R. P., and Hill, C. (2013). Bacteriocins - a viable alternative to antibiotics? Nature Rev. Microbiol. 11, 55–105. doi: 10.1038/nrmicro2937
Courtemanche, C., Elson-Schwab, I., Mashiyama, S. T., Kerry, N., and Ames, B. N. (2004). Folate deficiency inhibits the proliferation of primary human CD8+ T lymphocytes in vitro. J. Immunol. 173, 5186–3192. doi: 10.4049/jimmunol.173.5.3186
Cummings, J. H., Pomare, E. W., Branch, W. J., Naylor, C. P., and Macfarlane, G. T. (1987). Short chain fatty acids in human large intestine, portal, hepatic and venous blood. Gut 28, 5221–1227. doi: 10.1136/gut.28.10.1221
Cursino, L., Smajs, D., Smarda, J., Nardi, R. M., Nicoli, J. R., Chartonesouza, E., et al. (2010). Exoproducts of the Escherichia coli strain H22 inhibiting some enteric pathogens both in vitro and in vivo. J. Appl. Microbiol. 100, 521–829. doi: 10.1111/j.1365-2672.2006.02834.x
Das, U. N. (2018). Arachidonic acid and other unsaturated fatty acids and some of their metabolites function as endogenous antimicrobial molecules. J. Adv. Res. 11, 57–66. doi: 10.1016/j.jare.2018.01.001
Desbois, A. P., and Smith, V. J. (2010). Antibacterial free fatty acids: activities, mechanisms of action and biotechnological potential. Appl. Microbiol. Biotechnol. 85, 5629–1642. doi: 10.1007/s00253-009-2355-3
Diggle, S. P., Cornelis, P., Williams, P., and Cámara, M. (2006). 4-Quinolone signalling in Pseudomonas aeruginosa: Old molecules, new perspectives. Int. J. Medical Microbiol. 296, 83–91. doi: 10.1016/j.ijmm.2006.01.038
Donia, M. S., and Fischbach, M. A. (2015). HUMAN MICROBIOTA. Small molecules from the human microbiota. Science 349:5254766. doi: 10.1126/science.1254766
Fischbach, M. A., and Sonnenburg, J. L. (2011). Eating for two: how metabolism establishes interspecies interactions in the gut. Cell Host Microbe 10, 536–347. doi: 10.1016/j.chom.2011.10.002
Flieger, M., Bandouchova, H., Cerny, J., Chudícková, M., Kolarik, M., Kovacova, V., et al. (2016). Vitamin B2 as a virulence factor in Pseudogymnoascus destructansskin infection. Sci. Rep. 6.
Flint, H. J., Duncan, S. H., Scott, K. P., and Louis, P. (2015). Links between diet, gut microbiota composition and gut metabolism. Proc. Nutr. Soc. 74, 53–22. doi: 10.1017/S0029665114001463
Fredericq, P. (1946). Sur la spécificité des actions antibiotiques. Pathobiology 9, 585–390. doi: 10.1159/000159549
Galbraith, H., and Miller, T. B. (1973). Effect of long chain fatty acids on bacterial respiration and amino acid uptake. J. Appl. Microbiol. 36:559. doi: 10.1111/j.1365-2672.1973.tb04151.x
Gill, P. A., van Zelm, M. C., Muir, J. G., and Gibson, P. R. (2018). Review article: short chain fatty acids as potential therapeutic agents in human gastrointestinal and inflammatory disorders. Aliment. Pharmacol. Ther. 48, 15–34. doi: 10.1111/apt.14689
Gillor, O., Etzion, A., and Riley, M. A. (2008). The dual role of bacteriocins as anti- and probiotics. Appl. Microbiol. Biotechnol. 81, 591–606. doi: 10.1007/s00253-008-1726-5
Green, H. N., and Mellanby, E. (1928). Vitamin A As An Anti-Infective Agent. Br. Med. J. 2, 591. doi: 10.1136/bmj.2.3537.691
Haber, A., Friedman, S., Lobel, L., Burg-Golani, T., Sigal, N., Rose, J., et al. (2017). L-glutamine Induces Expression of Listeria monocytogenes Virulence Genes. PLoS Pathog. 13:e1006161. doi: 10.1371/journal.ppat.1006161
Hardie, D. G., Salt, I. P., and Davies, S. P. (2000). Analysis of the role of the AMP-activated protein kinase in the response to cellular stress. Methods Mol. Biol. 99, 53–74. doi: 10.1385/1-59259-054-3:63
Haynes, T. E., Li, P., Li, X. L., Shimotori, K., Sato, H., Flynn, N. E., et al. (2009). L-glutamine or L-alanyl-L-glutamine prevents oxidant- or endotoxin-induced death of neonatal enterocytes. Amino Acids 37, 531–142. doi: 10.1007/s00726-009-0243-x
Hill, M. J. (1997). Intestinal flora and endogenous vitamin synthesis. Eur. J. Cancer Prevent. 6:S43. doi: 10.1097/00008469-199703001-00009
Hirata, S. I., and Kunisawa, J. (2017). Gut microbiome, metabolome, and allergic diseases. Allergol. Int. 66, 523–528. doi: 10.1016/j.alit.2017.06.008
Hochbaum, A. I., Kolodkingal, I., Foulston, L., Kolter, R., Aizenberg, J., and Losick, R. (2011). inhibitory effects of d-Amino Acids on Staphylococcus aureus biofilm development. J. Bacteriol. 193:5616. doi: 10.1128/JB.05534-11
Ichihashi, T., Takagishi, Y., Uchida, K., and Yamada, H. (1992). Colonic absorption of menaquinone-4 and menaquinone-9 in rats. J. Nutr. 122, 506–512. doi: 10.1093/jn/122.3.506
Kallio, J., Jaakkola, M., Mäki, M., Kilpeläinen, P., and Virtanen, V. (2012). Vitamin C inhibits Staphylococcus aureus growth and enhances the inhibitory effect of quercetin on growth of Escherichia coli in vitro. Planta Med. 78, 5824–1830. doi: 10.1055/s-0032-1315388
Kamada, N., Kim, Y. G., Sham, H. P., Vallance, B. A., Puente, J. L., Martens, E. C., et al. (2012). Regulated virulence controls the ability of a pathogen to compete with the Gut Microbiota. Science 336, 5325–1329. doi: 10.1126/science.1222195
Kirby, D. T., Savage, J. M., and Plotkin, B. J. (2014). Menaquinone (Vitamin K2) Enhancement of Staphylococcus aureus Biofilm Formation. J. Biosci. Med. 02, 56–32. doi: 10.4236/jbm.2014.21004
Kneuper, H., Cao, Z. P., Twomey, K. B., Zoltner, M., Jäger, F., Cargill, J. S., et al. (2014). Heterogeneity in ess transcriptional organization and variable contribution of the Ess/Type VII protein secretion system to virulence across closely related Staphylocccus aureus strains. Mol. Microbiol. 93, 528–943. doi: 10.1111/mmi.12707
Kolodkin-Gal, I., Romero, D., Cao, S., Clardy, J., Kolter, R., and Losick, R. (2010). D-Amino acids trigger biofilm disassembly. Science 328, 527–629. doi: 10.1126/science.1188628
Kunisawa, J., Hashimoto, E., Ishikawa, I., and Kiyono, H. (2012). A pivotal role of Vitamin B9 in the maintenance of regulatory T cells in vitro and in vivo. PLoS ONE 7:e32094. doi: 10.1371/journal.pone.0032094
Kurihara, H., Goto, Y., Aida, M., Hosokawa, M., and Takahashi, K. (1999). Antibacterial activity against cariogenic bacteria and inhibition of insoluble glucan production by free fatty acids obtained from dried Gloiopeltis furcata. Fish. Sci. 65, 529–132. doi: 10.2331/fishsci.65.129
Lages, M. C., Beilharz, K., Morales Angeles, D., Veening, J. W., and Scheffers, D. J. (2013). The localization of key Bacillus subtilis penicillin binding proteins during cell growth is determined by substrate availability. Environ. Microbiol. 15, 5272–3281. doi: 10.1111/1462-2920.12206
Lambert, R. J., and Stratford, M. (1999). Weak-acid preservatives: modelling microbial inhibition and response. J. Appl. Microbiol. 86, 557–164. doi: 10.1046/j.1365-2672.1999.00646.x
Lancaster, L. E., Savelsbergh, A., Kleanthous, C., Wintermeyer, W., and Rodnina, M. V. (2010). Colicin E3 cleavage of 16S rRNA impairs decoding and accelerates tRNA translocation on Escherichia coli ribosomes. Mol. Microbiol. 69, 590–401. doi: 10.1111/j.1365-2958.2008.06283.x
LeBlanc, J. G., Milani, C., de Giori, G. S., Sesma, F., van Sinderen, D., and Ventura, M. (2013). Bacteria as vitamin suppliers to their host: a gut microbiota perspective. Curr. Opin. Biotechnol. 24, 560–168. doi: 10.1016/j.copbio.2012.08.005
Levy, M., Blacher, E., and Elinav, E. (2017). Microbiome, metabolites and host immunity. Curr. Opin. Microbiol. 35, 8–15. doi: 10.1016/j.mib.2016.10.003
Li, Y. M., Milne, J. C., Madison, L. L., Kolter, R., and Walsh, C. T. (1996). From peptide precursors to oxazole and thiazole-containing peptide antibiotics: microcin B17 synthase. Science 274, 5188–1193. doi: 10.1126/science.274.5290.1188
Lin, R., Liu, W., Piao, M., and Zhu, H. (2017). A review of the relationship between the gut microbiota and amino acid metabolism. Amino Acids 49, 5083–2090. doi: 10.1007/s00726-017-2493-3
Litwack, G., and Litwack, G. (2011). Vitamins and the immune system. Elsevier Ltd Oxford 17, 555–456.
Long, K. Z., Estrada-Garcia, T., Rosado, J. L., Ignacio, S. J., Haas, M., Firestone, M., et al. (2006). The effect of vitamin A supplementation on the intestinal immune response in Mexican children is modified by pathogen infections and diarrhea. J. Nutr. 136:5365. doi: 10.1093/jn/136.5.1365
Lopez, M. S., Tan, I. S., Yan, D., Kang, J., McCreary, M., Modrusan, Z., et al. (2017). Host-derived fatty acids activate type VII secretion in Staphylococcus aureus. Proc. Natl. Acad. Sci. U.S.A. 114:51223. doi: 10.1073/pnas.1700627114
Loscher, C. E., Draper, E., Leavy, O., Kelleher, D., Mills, K. H., and Roche, H. M. (2005). Conjugated linoleic acid suppresses NF-kappa B activation and IL-12 production in dendritic cells through ERK-mediated IL-10 induction. J. Immunol. 175, 5990–4998. doi: 10.4049/jimmunol.175.8.4990
Luethy, P. M., Huynh, S., Ribardo, D. A., Winter, S. E., Parker, C. T., and Hendrixson, D. R. (2017). Microbiota-derived short-chain fatty acids modulate expression of Campylobacter jejuni determinants required for Commensalism and Virulence. MBio 8, e00407–00417. doi: 10.1128/mBio.00407-17
Lv, Z., Wang, Y., Yang, T., Xue, Z., Li, Z., Hu, H., et al. (2016). Vitamin A deficiency impacts the structural segregation of gut microbiota in children with persistent diarrhea. J. Clin. Biochem. Nutr. 59, 513–121. doi: 10.3164/jcbn.15-148
Ma, R., Qiu, S., Jiang, Q., Sun, H., Xue, T., Cai, G., et al. (2017). AI-2 quorum sensing negatively regulates rbf expression and biofilm formation in Staphylococcus aureus. Int. J. Med. Microbiol. 307, 257–267. doi: 10.1016/j.ijmm.2017.03.003
Macfarlane, S., and Macfarlane, G. T. (2003). Regulation of short-chain fatty acid production. Proc. Nutr. Soc. 62, 57–72. doi: 10.1079/PNS2002207
Mathavan, I., and Beis, K. (2012). The role of bacterial membrane proteins in the internalization of microcin MccJ25 and MccB17. Biochem. Soc. Trans. 40, 5539. doi: 10.1042/BST20120176
Mazzotta, A. S., and Montville, T. J. (2010). Nisin induces changes in membrane fatty acid composition of Listeria monocytogenes nisin-resistant strains at 10 degrees C and 30 degrees C. J. Appl. Microbiol. 82, 52–38.
Ménard, S., Cerfbensussan, N., and Heyman, M. (2010). Multiple facets of intestinal permeability and epithelial handling of dietary antigens. Mucosal Immunol. 3, 547. doi: 10.1038/mi.2010.5
Mestecky, J., Russell, M. W., Jackson, S., and Brown, T. A. (1986). The human IgA system: a reassessment?. Clin. Immunol. Immunopathol. 40, 505–114. doi: 10.1016/0090-1229(86)90073-5
Metges, C. C. (2000). Contribution of microbial amino acids to amino acid homeostasis of the host. J. Nutr. 130:5857S. doi: 10.1093/jn/130.7.1857S
Metges, C. C., Loh, G., Souffrant, W. B., and Metges, C. C. (2003). “Intestinal microbial amino acid synthesis and its importance for the amino acid homeostasis of the monogastric host,” in Progress in Research on Energy and Protein Metabolism. International Symposium (Rostock-Warnemünde).
Mondello, S., Galuppo, M., Mazzon, E., Domenico, I., Mondello, P., Carmela, A., et al. (2010). Glutamine treatment attenuates the development of ischaemia/reperfusion injury of the gut. Eur. J. Pharmacol. 643, 504–315. doi: 10.1016/j.ejphar.2010.06.044
Mühlen, S., and Dersch, P. (2016). Anti-virulence strategies to target bacterial infections. Curr. Top. Microbiol. Immunol. 398:147. doi: 10.1007/82_2015_490
Nairz, M., Schroll, A., Sonnweber, T., and Weiss, G. (2010). The struggle for iron - a metal at the host-pathogen interface. Cell. Microbiol. 12, 5691–1702. doi: 10.1111/j.1462-5822.2010.01529.x
Nakanishi, N., Tashiro, K., Kuhara, S., Hayashi, T., Sugimoto, N., and Tobe, T. (2009). Regulation of virulence by butyrate sensing in enterohaemorrhagic Escherichia coli. Microbiology 155 (Pt 2), 521. doi: 10.1099/mic.0.023499-0
Nayar, A. S., Dougherty, T. J., Ferguson, K. E., Granger, B. A., Mcwilliams, L., Stacey, C., et al. (2015). Novel antibacterial targets and compounds revealed by a high-throughput cell wall reporter assay. J. Bacteriol. 197, 5726. doi: 10.1128/JB.02552-14
Nes, I. F., Diep, D. B., and Holo, H. (2007). Bacteriocin diversity in Streptococcus and Enterococcus. J. Bacteriol. 189, 5189. doi: 10.1128/JB.01254-06
Ng, C., Lang, K., Meenan, N., Sharma, A., Kelley, A., Kleanthous, C., et al. (2010). Structural basis for 16S ribosomal RNA cleavage by the cytotoxic domain of colicin E3. Nat. Struct. Mol. Biol. 17:5241. doi: 10.1038/nsmb.1896
Pandit, S., Ravikumar, V., Abdelhaleem, A. M., Derouiche, A., Mokkapati, V., Sihlbom, C., et al. (2017). Low concentrations of Vitamin C reduce the synthesis of extracellular polymers and destabilize bacterial biofilms. Front. Microbiol. 8:2599. doi: 10.3389/fmicb.2017.02599
Papenfort, K., and Bassler, B. L. (2016). Quorum sensing signal-response systems in Gram-negative bacteria. Nature Rev. Microbiol. 14:576. doi: 10.1038/nrmicro.2016.89
Parsons, J. B., Broussard, T. C., Bose, J. L., Rosch, J. W., Jackson, P., Subramanian, C., et al. (2014). Identification of a two-component fatty acid kinase responsible for host fatty acid incorporation by Staphylococcus aureus. Proc. Natl. Acad. Sci. U.S.A. 111, 50532–10537. doi: 10.1073/pnas.1408797111
Pasparakis, M. (2009). Regulation of tissue homeostasis by NF-|[kappa]|B signalling: implications for inflammatory diseases. Nat. Rev. Immunol. 9:578. doi: 10.1038/nri2655
Peng, L. Y., ZhongRong, L., Green, R. S., Holzman, I. R., and Lin, J. (2009). Butyrate enhances the intestinal barrier by facilitating tight junction assembly via activation of AMP-activated protein kinase in Caco-2 cell monolayers. J. Nutr. 139:5619. doi: 10.3945/jn.109.104638
Peng, Y., and Harper, A. E. (1970). Amino acid balance and food intake: effect of different dietary amino acid patterns on the plasma amino acid pattern of rats. J. Nutr. 100, 529–437. doi: 10.1093/jn/100.4.429
Pereira, C. S., Thompson, J. A., and Xavier, K. B. (2013). AI-2-mediated signalling in bacteria. FEMS Microbiol. Rev. 37, 556–181. doi: 10.1111/j.1574-6976.2012.00345.x
Peters, J., and Chin, C. K. (2003). Inhibition of photosynthetic electron transport by palmitoleic acid is partially correlated to loss of thylakoid membrane proteins. Plant Physiol. Biochem. 41, 517–124. doi: 10.1016/S0981-9428(02)00014-1
Prado-Acosta, M., Ruzal, S. M., Allievi, M. C., Palomino, M. M., and Sanchez, R. C. (2010). Synergistic effects of the Lactobacillus acidophilus surface layer and nisin on bacterial growth. Appl. Environ. Microbiol. 76, 574–977. doi: 10.1128/AEM.01427-09
Qi, B., Kniazeva, M., and Min, H. (2017). A vitamin-B2-sensing mechanism that regulates gut protease activity to impact animal's food behavior and growth. eLife 6:e26243. doi: 10.7554/eLife.26243
Qin, Y., Roberts, J. D., Grimm, S. A., Lih, F. B., Deterding, L. J., Li, R., et al. (2018). An obesity-associated gut microbiome reprograms the intestinal epigenome and leads to altered colonic gene expression. Genome Biol. 19:5. doi: 10.1186/s13059-018-1389-1
Rall, L. C., and Meydani, S. N. (1993). Vitamin B6 and Immune Competence. Nutr. Rev. 51, 517–225. doi: 10.1111/j.1753-4887.1993.tb03109.x
Reniere, M. L., Whiteley, A. T., Hamilton, K. L., John, S. M., Lauer, P., Brennan, R. G., et al. (2015). Glutathione activates virulence gene expression of an intracellular pathogen. Nature 517, 570–173. doi: 10.1038/nature14029
Ridler, C. (2016). Gut microbiota: D-amino acids employed against gut pathogens. Nature Rev. Gastroenterol. Hepatol. 13:499. doi: 10.1038/nrgastro.2016.131
Riley, M. A., and Wertz, J. E. (2002). Bacteriocin diversity: ecological and evolutionary perspectives. Biochimie 84, 557–364. doi: 10.1016/S0300-9084(02)01421-9
Roe, A. J., Mclaggan, D., Davidson, I., O'Byrne, C., and Booth, I. R. (1998). Perturbation of anion balance during inhibition of growth of Escherichia coli by weak acids. J. Bacteriol. 180, 567–772.
Ruth, M. R., and Field, C. J. (2013). The immune modifying effects of amino acids on gut-associated lymphoid tissue. J. Ani. Sci. Biotechnol. (?????????(??? ) 4:57. doi: 10.1186/2049-1891-4-27
Sado-Kamdem, S. L., Vannini, L., and Guerzoni, M. E. (2009). Effect of alpha-linolenic, capric and lauric acid on the fatty acid biosynthesis in Staphylococcus aureus. Int. J. Food Microbiol. 129, 588–294. doi: 10.1016/j.ijfoodmicro.2008.12.010
Said, H. M., and Mohammed, Z. M. (2011). Intestinal absorption of water-soluble vitamins: an update. Biochem. J. 437, 557–372. doi: 10.1042/BJ20110326
Sasabe, J., Miyoshi, Y., Rakoff-Nahoum, S., Zhang, T., Mita, M., Davis, B. M., et al. (2016). Interplay between microbial d-amino acids and host d-amino acid oxidase modifies murine mucosal defence and gut microbiota. Nature Microbiol. 1:56125. doi: 10.1038/nmicrobiol.2016.125
Sass, P., and Brötz-Oesterhelt, H. (2013). Bacterial cell division as a target for new antibiotics. Curr. Opin. Microbiol. 16, 522–530. doi: 10.1016/j.mib.2013.07.006
Scheppach, W., Dusel, G., Kuhn, T., Loges, C., Karch, H., Bartram, H. P., et al. (1996). Effect of L-glutamine and n-butyrate on the restitution of rat colonic mucosa after acid induced injury. Gut 38:578. doi: 10.1136/gut.38.6.878
Schlievert, P. M., Merriman, J. A., Salgadopabón, W., Mueller, E. A., Spaulding, A. R., Vu, B. G., et al. (2013). Menaquinone analogs inhibit growth of bacterial pathogens. Antimicrob. Agents Chemother. 57, 5432–5437. doi: 10.1128/AAC.01279-13
Schramm, M., Wiegmann, K., Schramm, S., Gluschko, A., Herb, M., Utermöhlen, O., et al. (2014). Riboflavin (vitamin B 2) deficiency impairs NADPH oxidase 2 (Nox2) priming and defense against Listeria monocytogenes. Eur. J. Immunol. 44, 528–741. doi: 10.1002/eji.201343940
Semba, R. D. (1999). Vitamin A and immunity to viral, bacterial and protozoan infections. Proc. Nutr. Soc. 58, 719–727. doi: 10.1017/S0029665199000944
Shibasaki, I. (1978). In Combined effects on antibacterial activity of fatty acids and their esters against gram-negative bacteria. J. Am. Oil Chem. Soc. 55, A235.
Smith, A. D., Botero, S., Sheadonohue, T., and Urban, , J. F. (2011). The pathogenicity of an enteric citrobacter rodentium infection is enhanced by deficiencies in the antioxidants selenium and vitamin E. Infect. Immun. 79, 5471–1478. doi: 10.1128/IAI.01017-10
Sonenshein, A. L., Hoch, J. A., and Losick, R. (2002). Bacillus subtilis and its closest relatives: from genes to cells. Nature 415, 563–264. doi: 10.1128/9781555817992
Souba, W. W., Klimberg, V. S., Plumley, D. A., Salloum, R. M., Flynn, T. C., Bland, K. I., et al. (1990). The role of glutamine in maintaining a healthy gut and supporting the metabolic response to injury and infection. J. Surg. Res. 48, 583–391. doi: 10.1016/0022-4804(90)90080-L
Sperandio, V. (2017). Take your pick: vitamins and microbiota facilitate pathogen clearance. Cell Host Microbe 21:530. doi: 10.1016/j.chom.2017.01.013
Su, D., Nie, Y., Zhu, A., Chen, Z., Wu, P., Zhang, L., et al. (2016). Vitamin D signaling through induction of paneth cell defensins maintains gut microbiota and improves metabolic disorders and hepatic steatosis in animal models. Front. Physiol. 7:498. doi: 10.3389/fphys.2016.00498
Talbott, M. C., Miller, L. T., and Kerkvliet, N. I. (1987). Pyridoxine supplementation: effect on lymphocyte responses in elderly persons. Am. J. Clin. Nutr. 46, 559–664. doi: 10.1093/ajcn/46.4.659
Toba, M., Masaki, H., and Ohta, T. (1988). Colicin E8, a DNase which indicates an evolutionary relationship between colicins E2 and E3. J. Bacteriol. 170, 5237–3242. doi: 10.1128/jb.170.7.3237-3242.1988
Troen, A. M., Mitchell, B., Sorensen, B., Wener, M. H., Johnston, A., Wood, B., et al. (2006). Unmetabolized folic acid in plasma is associated with reduced natural killer cell cytotoxicity among postmenopausal women. J. Nutr. 136:589. doi: 10.1093/jn/136.1.189
Van Deun, K., Pasmans, F., Van Immerseel, F., Ducatelle, R., and Haesebrouck, F. (2008). Butyrate protects Caco-2 cells from Campylobacter jejuni invasion and translocation. Br. J. Nutr. 100:580. doi: 10.1017/S0007114508921693
Van Immerseel, F., De Buck, J., De Smet, I., Pasmans, F., Haesebrouck, F., and Ducatelle, R. (2004). Interactions of Butyric Acid– and acetic acid–treated salmonella with chicken primary cecal epithelial cells in vitro. Avian Dis. 48:584. doi: 10.1637/7094
Veldhoen, M., and Brucklacher-Waldert, V. (2012). Dietary influences on intestinal immunity. Nature Rev. Immunol. 12, 596–708. doi: 10.1038/nri3299
Vilchèze, C., Hartman, T., Weinrick, B., and Jacobs, W. R. Jr (2013). Mycobacterium tuberculosis is extraordinarily sensitive to killing by a vitamin C-induced Fenton reaction. Nat. Commun. 4:5881. doi: 10.1038/ncomms2898
Wakeman, C. A., Hammer, N. D., Stauff, D. L., Attia, A. S., Anzaldi, L. L., Dikalov, S. I., et al. (2012). Menaquinone biosynthesis potentiates haem toxicity in Staphylococcus aureus. Mol. Microbiol. 86, 5376–1392. doi: 10.1111/mmi.12063
Walters, M., and Sperandio, V. (2006). Quorum sensing in Escherichia coli and Salmonella. Int. J. Med. Microbiol. Ijmm 296:125. doi: 10.1016/j.ijmm.2006.01.041
Wang, W. W., Qiao, S. Y., and Li, D. F. (2009). Amino acids and gut function. Amino Acids 37, 505–110. doi: 10.1007/s00726-008-0152-4
Wang, Y., Gao, Y., Liu, Q., Zhan, X., Li, Z., Hu, H., et al. (2016). Effect of vitamin A and Zn supplementation on indices of vitamin A status, haemoglobin level and defecation of children with persistent diarrhea. J. Clin. Biochem. Nutr. 59, 58–64. doi: 10.3164/jcbn.15-68
Waters, C. M., and Bassler, B. L. (2005). Quorum sensing: cell-to-cell communication in bacteria. Annu. Rev. Cell Dev. Biol. 21, 519–346. doi: 10.1146/annurev.cellbio.21.012704.131001
Yang, Y., Yao, F., Zhou, M., Zhu, J., Zhang, X., Bao, W., et al. (2013). F18ab Escherichia coli flagella expression is regulated by acyl-homoserine lactone and contributes to bacterial virulence. Veterin. Microbiol. 165, 378–383. doi: 10.1016/j.vetmic.2013.04.020
Yang, Y., Zhou, M., Hou, H., Zhu, J., Yao, F., Zhang, X., et al. (2014). Quorum-sensing gene luxS regulates flagella expression and Shiga-like toxin production in F18ab Escherichia coli. Can. J. Microbiol. 60, 555–361. doi: 10.1139/cjm-2014-0178
Keywords: metabolites, pathogen infection, gut microbiota, dietary nutrients, regulatory effects
Citation: Li Z, Quan G, Jiang X, Yang Y, Ding X, Zhang D, Wang X, Hardwidge PR, Ren W and Zhu G (2018) Effects of Metabolites Derived From Gut Microbiota and Hosts on Pathogens. Front. Cell. Infect. Microbiol. 8:314. doi: 10.3389/fcimb.2018.00314
Received: 07 May 2018; Accepted: 16 August 2018;
Published: 14 September 2018.
Edited by:
Yongqun He, University of Michigan Health System, United StatesReviewed by:
Mauricio J. Farfan, Universidad de Chile, ChileMin Dong, Boston Children's Hospital and Harvard University, United States
Copyright © 2018 Li, Quan, Jiang, Yang, Ding, Zhang, Wang, Hardwidge, Ren and Zhu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Wenkai Ren, renwenkai19@126.com
Guoqiang Zhu, yzgqzhu@yzu.edu.cn