Entamoeba histolytica and the Microbiome

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This entry is adapted from the peer-reviewed paper 10.3390/microorganisms9030581

In the gut, E. histolytica feeds on bacteria. Increasing evidences support the role of the gut microbiota in the development of the disease.

gut microbiota entamoeba histolytica resistance to oxidative stress

1. Introduction

Amebiasis is caused by the protozoan parasite Entamoeba histolytica. This disease is a significant hazard in underdeveloped countries with reduced socioeconomic and poor sanitation. It is assessed that amebiasis accounted for 55,500 deaths and 2.237 million disability-adjusted life years (the sum of years of life lost and years lived with disability) in 2010 ^[1]. Amebiasis has also been diagnosed in tourists from developed countries who return from vacation in endemic regions. Inflammation of the large intestine and liver abscess represent the main clinical manifestations of amebiasis. Amebiasis is caused by the ingestion of food contaminated with cysts, the infective form of the parasite. Following excystation, the trophozoites migrates to the large intestine resulting in either asymptomatic colonization (90% of all infections) or causing bloody diarrhea. For unknown reasons, the trophozoites can become virulent and invasive, cause amebic dysentery, and migrate to the liver via the portal veins, where they cause hepatocellular damage. No vaccine against amebiasis currently exists; the drug of choice for treating amebiasis is metronidazole, which may have severe side effects. Additionally, some clinical strains of E. histolytica are less sensitive to metronidazole, suggesting the emergence of metronidazole-resistant strains ^[2]. E. histolytica trophozoites proliferate in the intestinal lumen and phagocytose the resident gut flora with a preference for some species like Lactobacillus ruminus ^[3]. At first glance, the interaction between E. histolytica and the gut microbiota can be perceived as a simple interaction between a predator and its prey.

2. Change Occurring in the Large Intestine Microbiota Following Infection with E. histolytica

Over the last few decades, it has become evident that E. histolytica’s pathogenicity is directly linked to the parasite’s interaction with the gut microbiota ^[4]. This interaction is very selective as only those bacteria with the appropriate recognition molecules are ingested by the parasite ^[5]. It has been reported that association with specific intestinal bacteria changes the E. histolytica cell surface architecture ^[6]^[7] and that phagocytosis of pathogenic bacteria boosts E. histolytica cytopathogenicity, increases the expression of Gal/GalNAc lectin on the cell surface, and boosts cysteine proteinase activity and resistance to oxidative stress (OS) when E. histolytica trophozoites are co-cultured with the enteropathogenic E.coli (EPEC) O55 ^[8] or Shigella dysenteriae ^[9]. Finally, bacteria-induced augmentation of E. histolytica virulence seems to occur only when the trophozoites phagocytose intact live cells ^[5]. The gut flora of patients suffering from amebiasis shows a significant decrease in the population of Bacteroides, Clostridium coccoides, Clostridium leptum, Lactobacillus, and Campylobacter and an increase in Bifidobacterium, while there is no change in Ruminococcus compared to healthy patients ^[10]. Interestingly, the fecal microbiota composition can be used as a predictive tool of Entamoeba colonization with an accuracy of 79% ^[11]. Some of the taxa, like Clostridiales Ruminococcaceae or Prevotella copri, which were central for the identification of patients infected with Entamoeba, have been associated with inflammatory bowel disease ^[12]^[13]. It is still not clear how a specific gut microbiota becomes associated with patients infected by Entamoeba. It is possible that the colonization of the gut by Entamoeba is predisposed by the gut microbiota of the host. Certain species of bacteria may also prevent the development of Entamoeba as it has been suggested for the commensal Clostridia, segmented filamentous bacteria ^[14]. Alternatively, E. histolytica feeds preferentially on certain species of bacteria ^[3] which may allow other species to proliferate.

3. Response of E. histolytica to OS

ROS play a key role in eliciting OS response in cells. They are capable of damaging essential biomolecules in the cell such as DNA, proteins, lipids, and they primarily inhibit cellular functions. Once formed, ROS leads to the oxidative damage of proteins thereby affecting their structure and functional properties ^[15]^[16]. In the large intestine, the invading E. histolytica trophozoites encounter OS. The sources of these stresses are fluctuations in oxygen tension in the intestinal lumen and the generation of ROS by cells of the immune system. Anti-amebic drugs like metronidazole and auranofin also induce oxidative damage of proteins by inhibiting thioredoxin reductase, a central enzyme in the protection of the parasite against OS ^[17]. Hydrogen peroxide (H2O2) is capable of damaging proteins by its interaction with thiol groups, which are present in the cysteine side chains as well as with metal cofactors. E. histolytica lacks antioxidant enzymes, such as catalase, glutathione reductase, and γ-glutamyl transpeptidase ^[18]. Thus, proteins such as the 29-kDa peroxiredoxin ^[19] and iron-containing peroxide dismutase ^[20] aid in OS resistance. It has been showed that E. histolytica strains sustain the exposure to OS better than avirulent strains, due to the presence of peroxiredoxin ^[21]^[22]. OS resistance contributes to the pathogenic potential of E. histolytica ^[23]. Additionally, OS leads to the oxidation of hundreds of proteins in the parasite including proteins involved in redox homeostasis, lipid metabolism, small molecule metabolism, carbohydrate derivative metabolism, and organonitrogen compound biosynthesis ^[24]^[25]. Oxidation of these proteins often lead to their inhibition as reported for glycolytic enzymes ^[26], virulence factors like the Galactose/N-acetylgalactosamine lectin which is essential for the binding of the parasite to host cells ^[25], and arginase, an enzyme that catalyzes the conversion of l-arginine to l-ornithine ^[25], a precursor of polyamine synthesis ^[27]. Polyamines and their biosynthetic enzymes are considered essential for growth and survival of unicellular parasites including Trypanosoma, Leishmania, and Plasmodium ^[27]. One of these polyamines, putrescine, has been linked to OS resistance and one of the proposed mechanism of OS resistance is based on its polycationic nature that enables it to couple with nucleic acids and membrane phospholipids. Putrescine is also free radical scavenger and an antioxidant ^[28]. The importance of putrescine and other polyamines in the resistance of E. histolytica to OS has been proposed ^[25] but direct experimental evidences to support this suggestion are still missing. OS induces a strong inhibition of protein synthesis in the parasite ^[25]. Although the mechanism for this inhibition is still not understood, it probably involves a higher eukaryotes in the phosphorylation of the initiation factor (eIF-2α) ^[29]^[30] and the oxidation of components of the parasite’s translational machinery, such as ribosomal proteins and elongation factors which leads to their inhibition ^[25]^[31]. At the transcriptomics level, OS triggers a complex response in the parasite which involves the modulation of a large number of genes which encode proteins with roles in translation, signaling/regulatory processes, metabolic/repair processes, energy metabolism, stress response, and transport ^[8]^[32]. The regulation of expression of genes which are responsive to OS mediated by H2O2 is controlled by a transcription factor EHI_108720 that binds to the AAACCTCAATGAAGA motif which is enriched in promoters of H2O2-responsive genes ^[33].

4. Response of E. histolytica to OS in Presence of Bacteria

4.1. Effect of Bacteria on E. histolytica Transcriptome

It was proposed more than 30 years ago that bacteria can compensate the lack of antioxidant enzyme in E. histolytica by complementing the parasite with such enzymes ^[5]. Excluding this work, the knowledge about the role of the gut microbiota on the resistance of the parasite to OS was scant. Unexpected interactions between the parasite and the bacteria that contribute to the resistance of the parasite to OS has been recently highlighted. Interaction of E. histolytica with E. coli O55 (ratio 1:1000) confers resistance of the parasite to OS ^[8]. At the transcriptomic level, E. coli O55 has almost no effect on gene expression in the parasite. However, when the parasite is exposed to E. coli O55 and to OS, the combination of these two stimuli triggers a strong transcriptomic response that involves almost 50% of the parasite’s coding gene ^[8]. This transcriptomic response is very different to the response of the parasite exposed to the OS alone. A general pattern of this combined response is the “normalization” of the level of expression of many genes that have been downregulated (including many ribosomal proteins) or upregulated (including oxidoreductases and several metabolic enzymes like glyceraldehyde-3-phosphate dehydrogenase and malate dehydrogenase) by OS. Downregulation of ribosomal proteins expression is a conserved mechanism to shut down unnecessary protein synthesis during stress ^[34]. In contrast, the upregulation of oxidoreductases and metabolic enzymes expression is a mechanism that compensate the inhibition of activity of these essential enzymes for the parasite following their oxidation ^[35]. The same “normalization” mechanism on gene expression in the parasite has been observed with two other bacteria, Salmonella enterica and Enterococcus faecalis but not with the probiotic Lactobacillus acidophilus. It is possible that the production of H₂O₂ by L. acidophilus ^[36] is detrimental to the parasite already exposed to OS. The effect that bacteria have on gene expression in the parasite exposed to OS goes beyond the “normalization” mechanism described above. Many leucine-rich repeat (LRR) proteins that were downregulated in the presence of OS were upregulated in the presence of bacteria and OS ^[8]. These LRR proteins which belong to the BspA family of proteins present structural homologies with Toll-like receptors (TLRs). TLRs are usually expressed on sentinel cells such as macrophages and dendritic cells and are involved in the recognition of structurally conserved molecules derived from microbes ^[37]. The possibility that the ancient protozoan E. histolytica displays key characteristics of the antibacterial response present in higher eukaryotes has been recently discussed ^[38]^[8]. However, the strong homology of sequence between these LRR proteins will make very challenging the testing of their functionality as TLRs with the genetic tools that are actually available to manipulate gene expression in E. histolytica ^[39]. The recent success to make the CRISPR/Cas9 system work in E. histolytica at an episomal level provides hope for the future study of these LRR proteins ^[40].

4.2 Effect of Chemical Molecules Originating from Bacteria

4.2.1. Short-Chain Fatty Acids (SCFAs)

Gut microbial dysbiosis causes changes in SCFAs production leading, for example, to liver diseases ^[41] and neurodegenerative disorders ^[42]. The effect of chemical molecules originating from bacteria on the physiology of Entamoeba parasites has been pioneered by a study on SCFAs and their role in inhibiting encystation ^[43]. SCFAs are the main metabolites produced in the colon by bacterial fermentation of dietary fibers and resistant starch ^[44]. SCFAs inhibit OS in mammalian cells ^[45] and limit the genotoxic effect of H₂O₂ ^[46]. Based on this information, it will be very interesting to test in future the effect of different SCFAs like butyrate or propionate on the resistance of the parasite to OS.

4.2.2. Oxaloacetate

Alpha-keto acids pyruvate, oxaloacetate, and alpha-ketoglutarate have a good H₂O₂-scavenging activity ^[47]. The role of oxaloacetate produced by the enteropathogenic E. coli O55 in protecting E. histolytica against OS has been recently demonstrated ^[24]. Malate dehydrogenase (MDH), which catalyzes the formation of oxaloacetate from malate, is essential for the protective effect to OS that E. coli O55 confers to E. histolytica. Two mechanisms by which oxaloacetate is delivered to the parasite are possible: (i) Intrabacterial oxaloacetate reach the parasite by phagocytosis of the bacteria and (ii) secreted E. coli MDH are forming oxaloacetate in the environment and this oxaloacetate acts like a shield by scavenging H₂O₂ before it affects the parasite’s viability. Oxaloacetate also has a role in promoting the virulence of the parasite, which confirmed previous observations about the correlation between virulence of the parasite and its resistance to OS ^[23]. In future, it will be interesting to test the protective effect of other alpha keto-acids produced by the microbiota on the resistance of the parasite against OS. Other antioxidant metabolites are produced by the gut microbiota like glutathione and folic acid ^[48]. Entamoeba histolytica lacks glutathione reductase activity, the ability to synthesize glutathione de novo and the ability to form trypanothione from taken up glutathione ^[49]. Therefore, the relevance of glutathione produced by the gut microbiota to the resistance of the parasite to OS is probably weak. In contrast, folic acid is one of the vitamins, which is currently added to the culture media of E. histolytica [^[50]. In view of the ability of folic acid to scavenge free radical ^[51], it will be interesting to test its ability to protect the parasite against OS.

4.2.3. Queuine

Queuine and 7-(((4.5-cis-dihydroxy-2-cyclopenten-1-yl)-amino)-methyl)-7-deazaguanosine (queuosine—Q) are produced by bacteria. Q and its glycosylated derivatives occur in position 34 of the anticodon of tRNA^Asp, tRNA^His, tRNA^Asn,and tRNA^Tyr of eubacteria and eukaryotes except for Saccharomyces cerevisiae ^[52]^[53]. Q is highly conserved and found in plants, fishes, insects, and mammals. While many bacteria can synthesize queuine (the nucleobase of Q) de novo, salvaging the prokaryotic Q precursors preQ₀ and preQ₁ has recently been reported ^[54]. Eukaryotes are not capable of Q synthesis and they rely on salvaging the queuine base as a Q precursor either by nutrition or by the intestinal bacterial flora ^[55]^[56]^[57]. The effects of queuine on the physiology of E. histolytica have been recently studied ^[58]. Queuine protects the parasite against OS and it antagonizes the negative effect that OS has on translation by inducing the expression of genes involved in the OS response like heat shock protein 70 (Hsp70), antioxidant enzymes such as alcohol dehydrogenases, and proteins involved in the repair of oxidative DNA damage like RecQ helicase. On the other hand, queuine impairs E. histolytica virulence by downregulating the expression of cysteine proteases and other genes associated with virulence ^[58]. This is the first example in Eukaryotes of an effect of queuine on the regulation of gene expression. In contrast to oxaloacetate and other alpha-keto acids that rely on their ability to scavenge H₂O₂ to protect E. histolytica against OS, queuine uses a much more complex mechanism that depends on tRNA-guanine transglycosylase (TGT) activity. TGT is the main enzyme responsible for the formation of Q in the anticodon loop position 34 of tRNA^Asp, tRNA^His, tRNA^Asn, and tRNA^Tyr. The enzyme exchanges G34 for the precursors. In contrast to eubacterial TGT enzymes, all of which are homodimers, eukaryotic TGT enzymes, such as human TGT, are heterodimers and consist of a Q tRNA-ribosyltransferase 1 (QTRT1) and a Q tRNA-ribosyltransferase domain-containing 1 (QTRTD1) ^[59]^[60]. E. histolytica TGT enzyme has been recently identified and forms a heterodimer composed of EhQTRT1 and EhQTRTD1. EhTGT is catalytically active and incorporates queuine into E. histolytica tRNAs. Two mechanisms can possibly explain why queuine protects the parasite against OS. The first mechanism relies on the reprograming of gene expression in the parasite exposed to queuine. Genes involved in the resistance to OS like heat shock protein 70 (Hsp 70), antioxidant enzymes like alcohol dehydrogenases 2, and DNA repairing enzymes like RecQ helicases have their expression upregulated in the presence of queuine ^[58]. Why queuine leads to a reprograming of these genes is still an open question. It can be the result of an increased transcription of these genes triggered by transcription factor(s) and/or by an accumulation of these mRNAs in the parasite cultivated in presence of queuine. Work is in progress to address this question. In the second mechanism that relies on studies performed in S.pombe and mammals, Dnmt2 activity is stimulated by prior queuosine incorporation at G34 of tRNA^Asp_GUC ^[61]^[62]. Q-modified tRNA^Asp_GUC is protected against endonuclease cleavage and it is therefore preferentially used by the cells for the translation of stress proteins. Data supporting the presence of this mechanism is E. histolytica which includes: (i) The exogenous supplementation of E. histolytica trophozoites with queuine leads to hypermethylation of C38 in tRNA^Asp_GUC and (ii) hypermethylation of tRNA^Asp_GUC catalyzed by the E. histolytica Dnmt2 homolog Ehmeth correlates with the resistance of the parasite to OS ^[63] The two mechanisms may be connected as U (U-GUN) ending codons which are overrepresented in genes upregulated in the parasite exposed to queuine including possible transcription factors and proteins involved in OS resistance ^[58].

4.3 Response of E. histolytica to Nitrosative Stress (NS) and the Gut Microbiota

Following host invasion, the invading E. histolytica trophozoites are exposed to nanomolar concentrations of nitric oxide (NO) that is produced in intestinal epithelial cells by constitutive NO synthase ^[64] and as an intermediate in denitrification by the intestinal microbiota ^[65]. Although exposure to low NO concentrations is insufficient to kill the parasite ^[66], these low concentrations may strengthen its resistance to high NO concentrations. Amebiasis is characterized by acute inflammation of the intestine with the release of cytokines, such as tumor necrosis factor α, interleukin 8, interferon gamma, and interleukin β, and the generation of micromolar concentrations of ROS (discussed above) and reactive nitrogen species (RNS) from activated cells of the host’s immune system. NO in micromolar concentrations is cytotoxic for E. histolytica, and this cytotoxicity is implemented by S-nitrosylation of key metabolic enzymes and by fragmenting the endoplasmic reticulum (ER) ^[67]^[68]. NO also inhibits cysteine proteases ^[68], which are involved in differentiation, amino acid anabolism, inactivation of the host inflammatory response, lysosomal transport, and invasion of the host’s tissues ^[69]. NO can also regulate the activity and function of proteins by S-nitrosylation of their cysteine residues ^[70]. A high-throughput proteomic analysis of S-nitrosylated (SNO) proteins in NO-exposed E. histolytica using resin-assisted capture of SNO proteins ^[66], found that SNO proteins are involved in glycolysis, translation, protein transport, and virulence. E. histolytica can adapt to various stresses ^[71]^[72]^[73] including to progressive increases in the intestinal NO concentration ^[74], which may occur in patients with inflammation of the large intestine ^[64] or during the establishment of amebiasis ^[75].

Information about the role of the gut microbiota in protecting the host against NS is scanty. The role of acetate and butyrate, two SCFAs produced by the gut microbiota, to reduce NS in human islets and β cells after exposure to the apoptosis inducer and metabolic stressor streptozotocin ^[76] is one of the few examples available in the literature. In contrast, the ability of the gut microbiota to generate RNS is well discussed (for a recent review see ^[77]). The gut bacteria can convert nitrites into nitrosamines which have carcinogenic properties ^[78] and some food components present in meat and fish into trimethylamine. In the liver, trimethylamine is converted to its oxidized form (trimethylamine N-oxide) which have deleterious effects on cardiovascular and metabolic function ^[79].

Regarding E. histolytica, we did not found any protective effect of E. coli O55 on the resistance of the parasite to NS ^[8]. The lack of protection may be explained by the fact that E. coli O55 was not exposed to NS prior to its interaction with the parasite. E. coli possesses three major enzymes to overcome NS: the soluble flavohaemoglobin Hmp, the di-iron-center flavorubredoxin NorV with its NADH-dependent oxidoreductase NorW (NorVW) and the cytochrome c nitrite reductase NrfA. The expression of these enzymes is induced by the exposure of the bacteria to NS ^[80]. Consequently, it will be interesting to measure the effect of E. coli O55 on the resistance of E. histolytica to NS by using this time bacteria pre-exposed to NO. We have also addressed the role of queuine in protecting the parasite against NS. Queuine did protect the parasite against NS to some extend but the variability of the results among different experiments was very high (unpublished data).

4.4 E. histolytica Infection and Probiotics

Probiotics are live microorganisms that are intended to have health benefits when consumed or applied to the body ^[81]. It has been proposed that the use of probiotics, may present as complementary or as an alternative to the current treatment of amoebiasis. The possible effect of probiotics in preventing amebiasis has been recently reviewed ^[82]. A number of studies have been conducted to test the effectiveness of the probiotic at inhibiting adhesion of the protozoa to the intestinal mucosa surface ^[83]^[84]. More recently, it has been proposed that Lactobacillus acidophilus [18], Lactobacillus casei and Enterococcus faecium ^[85] are potent probiotics that can be used to fight amebiasis. How these probiotics work against the parasite is still not well understood. For L. acidophilus, it has been suggested that the ability of this bacteria to produce H₂O₂ [45] contributes to its amebicidal activity ^[8]. For Weissella paramesenteroides WpK, another lactic acid bacteria, amoebic lesions caused by Entamoeba dispar are reduced in presence of this bacteria. The authors proposed that W. paramesenteroides WpK4 works by strengthening the barrier function of the caecal mucosa ^[86].

5. Concluding Remarks

Beyond the predator-prey relationship that exists between the parasite and the gut microbiota evidences for a more complex interaction have emerged in the last decades. It is still not clear if the microbiota is paving the way for the development of amebiasis or if the disease is triggered by the dysbiosis caused by the parasite. It is probable that both scenarios are taking place. Small molecules originating from the bacteria like oxaloacetate, SCFA and queuine have proved to be important mediators between the bacteria and the parasite. These bacterial molecules which can control the different aspects of the physiology of the parasite may be exploited to manipulate the parasite and fight it. For example, the fact that queuine inhibits the virulence of E. histolytica may lead to new strategies for preventing and/or treating amebiasis by providing queuine to the host as a postbiotic (soluble factors secreted by live bacteria, or released after bacterial lysis that can be used to improve host health ^[87]) or via probiotics. Such strategy has been proposed for example with the gut bacteria Gordonibacter pamelaeae that produces the anticarcinogen urolithin ^[88]. SCFA, oxaloacetate and queuine represent probably the top of the iceberg of the molecules used between the microbiota and the parasite to communicate. It is essential to perform a systematic screen for such molecules in the future. Many challenges in studying the microbiome in the context of human diseases exists including the choice of appropriate experimental systems ^[89]. These challenges exist also in the study of the role of the microbiota in amebiasis. It is essential in the future to develop a simple model to study the interaction of the microbiota with the parasite in the gut. One such model that we are currently investigating is a three-dimensional intestinal model that replicates the general characteristics of the human colon. This model has been recently used to investigate the early stage of invasion of the gut by trophozoites ^[90]. Finally, what can be learned from the interaction taking place between E. histolytica and the microbiota is certainly relevant to other parasitic protozoa and helminths which are also in a tight relationship with the host’s intestinal microbiota. For example, the antioxidant properties of oxaloacetate which is produced by the gut microbiota is also valid for the protection of C. elegans by oxaloacetate against H2O2-induced oxidative stress ^[24].

References

Turkeltaub, J.A.; McCarty, T.R., 3rd; Hotez, P.J. The intestinal protozoa: Emerging impact on global health and development. Curr. Opin. Gastroenterol. 2015, 31, 38–44.
Bansal, D.; Sehgal, R.; Chawla, Y.; Mahajan, R.C.; Malla, N. In vitro activity of antiamoebic drugs against clinical isolates of Entamoeba histolytica and Entamoeba dispar. Ann. Clin. Microbiol. Antimicrob. 2004, 3, 27.
Iyer, L.R.; Verma, A.K.; Paul, J.; Bhattacharya, A. Phagocytosis of Gut Bacteria by Entamoeba histolytica. Front. Cell. Infect. Microbiol. 2019, 9, 34.
Burgess, S.L.; Petri, W.A., Jr. The Intestinal Bacterial Microbiome and E. histolytica Infection. Curr. Trop. Med. Rep. 2016, 3, 71–74.
Bracha, R.; Mirelman, D. Virulence of Entamoeba histolytica trophozoites. Effects of bacteria, microaerobic conditions, and metronidazole. J. Exp. Med. 1984, 160, 353–368.
Bhattacharya, A.; Ghildyal, R.; Prasad, J.; Bhattacharya, S.; Diamond, L.S. Modulation of a surface antigen of Entamoeba histolytica in response to bacteria. Infect. Immun. 1992, 60, 1711–1713.
Padilla-Vaca, F.; Ankri, S.; Bracha, R.; Koole, L.A.; Mirelman, D. Down regulation of Entamoeba histolytica virulence by monoxenic cultivation with Escherichia coli O55 is related to a decrease in expression of the light (35-kilodalton) subunit of the Gal/GalNAc lectin. Infect. Immun. 1999, 67, 2096–2102.
Varet, H.; Shaulov, Y.; Sismeiro, O.; Trebicz-Geffen, M.; Legendre, R.; Coppee, J.Y.; Ankri, S.; Guillen, N. Enteric bacteria boost defences against oxidative stress in Entamoeba histolytica. Sci. Rep. 2018, 8, 9042.
Galvan-Moroyoqui, J.M.; Dominguez-Robles, M.D.; Franco, E.; Meza, I. The interplay between Entamoeba and enteropathogenic bacteria modulates epithelial cell damage. PLoS Negl. Trop. Dis. 2008, 2, e266.
Verma, A.K.; Verma, R.; Ahuja, V.; Paul, J. Real-time analysis of gut flora in Entamoeba histolytica infected patients of Northern India. BMC Microbiol. 2012, 12, 183.
Morton, E.R.; Lynch, J.; Froment, A.; Lafosse, S.; Heyer, E.; Przeworski, M.; Blekhman, R.; Segurel, L. Variation in Rural African Gut Microbiota Is Strongly Correlated with Colonization by Entamoeba and Subsistence. PLoS Genet. 2015, 11, e1005658.
Morgan, X.C.; Tickle, T.L.; Sokol, H.; Gevers, D.; Devaney, K.L.; Ward, D.V.; Reyes, J.A.; Shah, S.A.; LeLeiko, N.; Snapper, S.B.; et al. Dysfunction of the intestinal microbiome in inflammatory bowel disease and treatment. Genome Biol. 2012, 13, R79.
Iljazovic, A.; Roy, U.; Galvez, E.J.C.; Lesker, T.R.; Zhao, B.; Gronow, A.; Amend, L.; Will, S.E.; Hofmann, J.D.; Pils, M.C.; et al. Perturbation of the gut microbiome by Prevotella spp. enhances host susceptibility to mucosal inflammation. Mucosal Immunol. 2021, 14, 113–124.
Burgess, S.L.; Buonomo, E.; Carey, M.; Cowardin, C.; Naylor, C.; Noor, Z.; Wills-Karp, M.; Petri, W.A., Jr. Bone marrow dendritic cells from mice with an altered microbiota provide interleukin 17A-dependent protection against Entamoeba histolytica colitis. mBio 2014, 5, e01817.
Aiken, C.T.; Kaake, R.M.; Wang, X.; Huang, L. Oxidative stress-mediated regulation of proteasome complexes. Mol. Cell Proteom. 2011, 10, R110.006924.
Shacter, E. Quantification and significance of protein oxidation in biological samples. Drug Metab. Rev. 2000, 32, 307–326.
Shaulov, Y.; Nagaraja, S.; Sarid, L.; Trebicz-Geffen, M.; Ankri, S. Formation of oxidised (OX) proteins in Entamoeba histolytica exposed to auranofin and consequences on the parasite virulence. Cell. Microbiol. 2020, 22, e13174.
Tekwani, B.L.; Mehlotra, R.K. Molecular basis of defence against oxidative stress in Entamoeba histolytica and Giardia lamblia. Microbes Infect. 1999, 1, 385–394.
Sen, A.; Chatterjee, N.S.; Akbar, M.A.; Nandi, N.; Das, P. The 29-kilodalton thiol-dependent peroxidase of Entamoeba histolytica is a factor involved in pathogenesis and survival of the parasite during oxidative stress. Eukaryot. Cell 2007, 6, 664–673.
Bruchhaus, I.; Tannich, E. Induction of the iron-containing superoxide dismutase in Entamoeba histolytica by a superoxide anion-generating system or by iron chelation. Mol. Biochem. Parasitol. 1994, 67, 281–288.
Iyer, L.R.; Singh, N.; Verma, A.K.; Paul, J. Differential expression and immunolocalization of antioxidant enzymes in Entamoeba histolytica isolates during metronidazole stress. Biomed. Res. Int. 2014, 2014, 704937.
Davis, P.H.; Zhang, X.; Guo, J.; Townsend, R.R.; Stanley, S.L., Jr. Comparative proteomic analysis of two Entamoeba histolytica strains with different virulence phenotypes identifies peroxiredoxin as an important component of amoebic virulence. Mol. Microbiol. 2006, 61, 1523–1532.
Rastew, E.; Vicente, J.B.; Singh, U. Oxidative stress resistance genes contribute to the pathogenic potential of the anaerobic protozoan parasite, Entamoeba histolytica. Int. J. Parasitol. 2012, 42, 1007–1015.
Shaulov, Y.; Shimokawa, C.; Trebicz-Geffen, M.; Nagaraja, S.; Methling, K.; Lalk, M.; Weiss-Cerem, L.; Lamm, A.T.; Hisaeda, H.; Ankri, S. Escherichia coli mediated resistance of Entamoeba histolytica to oxidative stress is triggered by oxaloacetate. PLoS Pathog. 2018, 14, e1007295.
Shahi, P.; Trebicz-Geffen, M.; Nagaraja, S.; Alterzon-Baumel, S.; Hertz, R.; Methling, K.; Lalk, M.; Ankri, S. Proteomic Identification of Oxidized Proteins in Entamoeba histolytica by Resin-Assisted Capture: Insights into the Role of Arginase in Resistance to Oxidative Stress. PLoS Negl. Trop. Dis. 2016, 10, e0004340.
Husain, A.; Sato, D.; Jeelani, G.; Soga, T.; Nozaki, T. Dramatic increase in glycerol biosynthesis upon oxidative stress in the anaerobic protozoan parasite Entamoeba histolytica. PLoS Negl. Trop. Dis. 2012, 6, e1831.
Phillips, M.A. Polyamines in protozoan pathogens. J. Biol. Chem. 2018, 293, 18746–18756.
Groppa, M.D.; Benavides, M.P. Polyamines and abiotic stress: Recent advances. Amino Acids 2008, 34, 35–45.
Walters, H.A.; Welter, B.H.; Sullivan, W.J., Jr.; Temesvari, L.A. Phosphorylation of eukaryotic initiation factor-2alpha in response to endoplasmic reticulum and nitrosative stress in the human protozoan parasite, Entamoeba histolytica. Mol. Biochem. Parasitol. 2019, 234, 111223.
Back, S.H.; Scheuner, D.; Han, J.; Song, B.; Ribick, M.; Wang, J.; Gildersleeve, R.D.; Pennathur, S.; Kaufman, R.J. Translation attenuation through eIF2alpha phosphorylation prevents oxidative stress and maintains the differentiated state in beta cells. Cell Metab. 2009, 10, 13–26.
Brandes, N.; Reichmann, D.; Tienson, H.; Leichert, L.I.; Jakob, U. Using quantitative redox proteomics to dissect the yeast redoxome. J. Biol. Chem. 2011, 286, 41893–41903.
Vicente, J.B.; Ehrenkaufer, G.M.; Saraiva, L.M.; Teixeira, M.; Singh, U. Entamoeba histolytica modulates a complex repertoire of novel genes in response to oxidative and nitrosative stresses: Implications for amebic pathogenesis. Cell. Microbiol. 2009, 11, 51–69.
Pearson, R.J.; Morf, L.; Singh, U. Regulation of H2O2 stress-responsive genes through a novel transcription factor in the protozoan pathogen Entamoeba histolytica. J. Biol. Chem. 2013, 288, 4462–4474.
Zencir, S.; Dilg, D.; Rueda, M.P.; Shore, D.; Albert, B. Mechanisms coordinating ribosomal protein gene transcription in response to stress. Nucleic Acids Res. 2020, 48, 11408–11420.
Shahi, P.; Trebicz-Geffen, M.; Nagaraja, S.; Alterzon-Baumel, S.; Hertz, R.; Methling, K.; Lalk, M.; Ankri, S. Proteomic Identification of Oxidized Proteins in Entamoeba histolytica by Resin-Assisted Capture: Insights into the Role of Arginase in Resistance to Oxidative Stress. PLoS Negl. Trop. Dis. 2016, 10, e0004340.
Hertzberger, R.; Arents, J.; Dekker, H.L.; Pridmore, R.D.; Gysler, C.; Kleerebezem, M.; de Mattos, M.J. H(2)O(2) production in species of the Lactobacillus acidophilus group: A central role for a novel NADH-dependent flavin reductase. Appl. Environ. Microbiol. 2014, 80, 2229–2239.
Kawasaki, T.; Kawai, T. Toll-like receptor signaling pathways. Front. Immunol. 2014, 5, 461.
Guillen, N. The interaction between Entamoeba histolytica and enterobacteria shed light on an ancient antibacterial response. Cell. Microbiol. 2019, 21, e13039.
Zhang, H.; Pompey, J.M.; Singh, U. RNA interference in Entamoeba histolytica: Implications for parasite biology and gene silencing. Future Microbiol. 2011, 6, 103–117.
Kangussu-Marcolino, M.M.; Morgado, P.; Manna, D.; Yee, H.; Singh, U. Development of a CRISPR/Cas9 system in Entamoeba histolytica: Proof of concept. Int. J. Parasitol. 2021, 51, 193–200.
Giuffre, M.; Campigotto, M.; Campisciano, G.; Comar, M.; Croce, L.S. A story of liver and gut microbes: How does the intestinal flora affect liver disease? A review of the literature. Am. J. Physiol. Gastr. Liver Physiol. 2020, 318, G889–G906.
Giuffre, M.; Moretti, R.; Campisciano, G.; da Silveira, A.B.M.; Monda, V.M.; Comar, M.; di Bella, S.; Antonello, R.M.; Luzzati, R.; Croce, L.S. You Talking to Me? Says the Enteric Nervous System (ENS) to the Microbe. How Intestinal Microbes Interact with the ENS. J. Clin. Med. 2020, 9, 3705.
Byers, J.; Faigle, W.; Eichinger, D. Colonic short-chain fatty acids inhibit encystation of Entamoeba invadens. Cell. Microbiol. 2005, 7, 269–279.
Sun, Y.; O’Riordan, M.X. Regulation of bacterial pathogenesis by intestinal short-chain Fatty acids. Adv. Appl. Microbiol. 2013, 85, 93–118.
Huang, W.; Guo, H.L.; Deng, X.; Zhu, T.T.; Xiong, J.F.; Xu, Y.H.; Xu, Y. Short-Chain Fatty Acids Inhibit Oxidative Stress and Inflammation in Mesangial Cells Induced by High Glucose and Lipopolysaccharide. Exp. Clin. Endocrinol. Diabetes 2017, 125, 98–105.
Abrahamse, S.L.; Pool-Zobel, B.L.; Rechkemmer, G. Potential of short chain fatty acids to modulate the induction of DNA damage and changes in the intracellular calcium concentration by oxidative stress in isolated rat distal colon cells. Carcinogenesis 1999, 20, 629–634.
Bayliak, M.M.; Lylyk, M.P.; Vytvytska, O.M.; Lushchak, V.I. Assessment of antioxidant properties of alpha-keto acids in vitro and in vivo. Eur. Food Res. Technol. 2016, 242, 179–188.
Wang, Y.; Wu, Y.; Wang, Y.; Xu, H.; Mei, X.; Yu, D.; Wang, Y.; Li, W. Antioxidant Properties of Probiotic Bacteria. Nutrients 2017, 9, 521.
Ariyanayagam, M.R.; Fairlamb, A.H. Entamoeba histolytica lacks trypanothione metabolism. Mol. Biochem. Parasitol. 1999, 103, 61–69.
Diamond, L.S.; Harlow, D.R.; Cunnick, C.C. A new medium for the axenic cultivation of Entamoeba histolytica and other Entamoeba. Trans. R. Soc. Trop. Med. Hyg. 1978, 72, 431–432.
Joshi, R.; Adhikari, S.; Patro, B.S.; Chattopadhyay, S.; Mukherjee, T. Free radical scavenging behavior of folic acid: Evidence for possible antioxidant activity. Free Radic. Bio Med. 2001, 30, 1390–1399.
Fergus, C.; Barnes, D.; Alqasem, M.A.; Kelly, V.P. The queuine micronutrient: Charting a course from microbe to man. Nutrients 2015, 7, 2897–2929.
Walden, T.; Reyniers, J.P.; Hiatt, V.; Farkas, W.R. Yeast cells cannot incorporate queuine into their tRNA. Proceedings of the Society for Experimental Biology and Medicine. Soc. Exp. Biol. Med. 1982, 170, 328–332.
Yuan, Y.; Zallot, R.; Grove, T.L.; Payan, D.J.; Martin-Verstraete, I.; Sepic, S.; Balamkundu, S.; Neelakandan, R.; Gadi, V.K.; Liu, C.F.; et al. Discovery of novel bacterial queuine salvage enzymes and pathways in human pathogens. Proc. Natl. Acad. Sci. USA 2019.
Katze, J.R.; Basile, B.; McCloskey, J.A. Queuine, a modified base incorporated posttranscriptionally into eukaryotic transfer RNA: Wide distribution in nature. Science 1982, 216, 55–56.
Ott, G.; Kersten, H.; Nishimura, S. Dictyostelium discoideum: A useful model system to evaluate the function of queuine and of the Q-family of tRNAs. FEBS Lett. 1982, 146, 311–314.
Farkas, W.R. Effect of diet on the queuosine family of tRNAs of germ-free mice. J. Biol. Chem. 1980, 255, 6832–6835.
Nagaraja, S.; Cai, M.W.; Sun, J.; Varet, H.; Sarid, L.; Trebicz-Geffen, M.; Ankri, S.; Shaulov, Y.; Mazumdar, M.; Legendre, R. Queuine is a nutritional regulator of Entamoeba histolytica response to oxidative stress and a virulence attenuator. mBio 2021, 12, 20.
Chen, Y.C.; Kelly, V.P.; Stachura, S.V.; Garcia, G.A. Characterization of the human tRNA-guanine transglycosylase: Confirmation of the heterodimeric subunit structure. RNA 2010, 16, 958–968.
Stengl, B.; Meyer, E.A.; Heine, A.; Brenk, R.; Diederich, F.; Klebe, G. Crystal structures of tRNA-guanine transglycosylase (TGT) in complex with novel and potent inhibitors unravel pronounced induced-fit adaptations and suggest dimer formation upon substrate binding. J. Mol. Biol. 2007, 370, 492–511.
Muller, M.; Hartmann, M.; Schuster, I.; Bender, S.; Thuring, K.L.; Helm, M.; Katze, J.R.; Nellen, W.; Lyko, F.; Ehrenhofer-Murray, A.E. Dynamic modulation of Dnmt2-dependent tRNA methylation by the micronutrient queuine. Nucleic Acids Res. 2015, 43, 10952–10962.
Ehrenhofer-Murray, A.E. Cross-Talk between Dnmt2-Dependent tRNA Methylation and Queuosine Modification. Biomolecules 2017, 7, 14.
Fisher, O.; Siman-Tov, R.; Ankri, S. Pleiotropic phenotype in Entamoeba histolytica overexpressing DNA methyltransferase (Ehmeth). Mol. Biochem. Parasitol. 2006, 147, 48–54.
Kolios, G.; Valatas, V.; Ward, S.G. Nitric oxide in inflammatory bowel disease: A universal messenger in an unsolved puzzle. Immunology 2004, 113, 427–437.
Vermeiren, J.; van de Wiele, T.; Verstraete, W.; Boeckx, P.; Boon, N. Nitric oxide production by the human intestinal microbiota by dissimilatory nitrate reduction to ammonium. J. Biomed. Biotechnol. 2009, 2009, 284718.
Hertz, R.; Lulu, S.B.; Shahi, P.; Trebicz-Geffen, M.; Benhar, M.; Ankri, S. Proteomic identification of S-nitrosylated proteins in the parasite Entamoeba histolytica by resin-assisted capture: Insights into the regulation of the Gal/GalNAc lectin by nitric oxide. PLoS ONE 2014, 9, e91518.
Lin, J.Y.; Chadee, K. Macrophage cytotoxicity against Entamoeba histolytica trophozoites is mediated by nitric oxide from L-arginine. J. Immunol. 1992, 148, 3999–4005.
Santi-Rocca, J.; Smith, S.; Weber, C.; Pineda, E.; Hon, C.C.; Saavedra, E.; Olivos-Garcia, A.; Rousseau, S.; Dillies, M.A.; Coppee, J.Y.; et al. Endoplasmic reticulum stress-sensing mechanism is activated in Entamoeba histolytica upon treatment with nitric oxide. PLoS ONE 2012, 7, e31777.
Serrano-Luna, J.; Pina-Vazquez, C.; Reyes-Lopez, M.; Ortiz-Estrada, G.; de la Garza, M. Proteases from Entamoeba spp. and Pathogenic Free-Living Amoebae as Virulence Factors. J. Trop. Med. 2013, 2013, 890603.
Gould, N.; Doulias, P.T.; Tenopoulou, M.; Raju, K.; Ischiropoulos, H. Regulation of Protein Function and Signaling by Reversible Cysteine S-Nitrosylation. J. Biol. Chem. 2013, 288, 26473–26479.
Baumel-Alterzon, S.; Weber, C.; Guillen, N.; Ankri, S. Identification of dihydropyrimidine dehydrogenase as a virulence factor essential for the survival of Entamoeba histolytica in glucose-poor environments. Cell. Microbiol. 2013, 15, 130–144.
Cabrera, H.A. Temperature adaptation of Entamoeba histolytica and its effect on virulence. Exp. Parasitol. 1958, 7, 276–284.
Wassmann, C.; Hellberg, A.; Tannich, E.; Bruchhaus, I. Metronidazole resistance in the protozoan parasite Entamoeba histolytica is associated with increased expression of iron-containing superoxide dismutase and peroxiredoxin and decreased expression of ferredoxin 1 and flavin reductase. J. Biol. Chem. 1999, 274, 26051–26056.
Trebicz-Geffen, M.; Shahi, P.; Nagaraja, S.; Vanunu, S.; Manor, S.; Avrahami, A.; Ankri, S. Identification of S-Nitrosylated (SNO) Proteins in Entamoeba histolytica Adapted to Nitrosative Stress: Insights into the Role of SNO Actin and In vitro Virulence. Front. Cell. Infect. Microbiol. 2017, 7, 192.
Mortimer, L.; Chadee, K. The immunopathogenesis of Entamoeba histolytica. Exp. Parasitol. 2010, 126, 366–380.
Hu, S.; Kuwabara, R.; de Haan, B.J.; Smink, A.M.; de Vos, P. Acetate and Butyrate Improve beta-cell Metabolism and Mitochondrial Respiration under Oxidative Stress. Int. J. Mol. Sci. 2020, 21, 1542.
Carlstrom, M.; Moretti, C.H.; Weitzberg, E.; Lundberg, J.O. Microbiota, diet and the generation of reactive nitrogen compounds. Free Radic. Biol. Med. 2020, 161, 321–325.
Rastogi, Y.R.; Saini, A.K.; Thakur, V.K.; Saini, R.V. New Insights into Molecular Links Between Microbiota and Gastrointestinal Cancers: A Literature Review. Int. J. Mol. Sci. 2020, 21, 3212. [Google Scholar] [CrossRef]
Zeisel, S.H.; Warrier, M. Trimethylamine N-Oxide, the Microbiome, and Heart and Kidney Disease. Annu. Rev. Nutr. 2017, 37, 157–181.
Arkenberg, A.; Runkel, S.; Richardson, D.J.; Rowley, G. The production and detoxification of a potent cytotoxin, nitric oxide, by pathogenic enteric bacteria. Biochem. Soc. Trans. 2011, 39, 1876–1879.
Ouwehand, A.C.; Salminen, S.; Isolauri, E. Probiotics: An overview of beneficial effects. Antonie Van Leeuwenhoek 2002, 82, 279–289.
Nagaraja, S.; Ankri, S. Target identification and intervention strategies against amebiasis. Drug Resist. Updates 2019, 44, 1–14.
Mansour-Ghanaei, F.; Dehbashi, N.; Yazdanparast, K.; Shafaghi, A. Efficacy of saccharomyces boulardii with antibiotics in acute amoebiasis. World J. Gastroenterol. 2003, 9, 1832–1833.
Rigothier, M.C.; Maccario, J.; Gayral, P. Inhibitory activity of saccharomyces yeasts on the adhesion of Entamoeba histolytica trophozoites to human erythrocytes in vitro. Parasitol. Res. 1994, 80, 10–15.
Sarjapuram, N.; Mekala, N.; Singh, M.; Tatu, U. The Potential of Lactobacillus casei and Entercoccus faecium Combination as a Preventive Probiotic Against Entamoeba. Probiotics Antimicrob. Proteins 2017, 9, 142–149.
Prado, G.K.S.; Torrinha, K.C.; Cruz, R.E.; Goncalves, A.B.B.; Silva, C.A.V.; Oliveira, F.M.S.; Nunes, A.C.; Gomes, M.A.; Caliari, M.V. Weissella paramesenteroides WpK4 ameliorate the experimental amoebic colitis by increasing the expression of MUC-2 and the intestinal epithelial regeneration. J. Appl. Microbiol. 2020, 129, 1706–1719.
Aguilar-Toala, J.E.; Garcia-Varela, R.; Garcia, H.S.; Mata-Haro, V.; Gonzalez-Cordova, A.F.; Vallejo-Cordoba, B.; Hernandez-Mendoza, A. Postbiotics: An evolving term within the functional foods field. Trends Food Sci. Technol. 2018, 75, 105–114.
Selma, M.V.; Beltran, D.; Garcia-Villalba, R.; Espin, J.C.; Tomas-Barberan, F.A. Description of urolithin production capacity from ellagic acid of two human intestinal Gordonibacter species. Food Funct. 2014, 5, 1779–1784.
Douglas, A.E. Which experimental systems should we use for human microbiome science? PLoS Biol. 2018, 16, e2005245.
Aguilar-Rojas, A.; Castellanos-Castro, S.; Matondo, M.; Gianetto, Q.G.; Varet, H.; Sismeiro, O.; Legendre, R.; Fernandes, J.; Hardy, D.; Coppee, J.Y.; et al. Insights into amebiasis using a human 3D-intestinal model. Cell. Microbiol. 2020, 22, e13203.

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Serge Ankri

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