Tissue Destruction Caused by Entamoeba histolytica Parasite: Cell Death, Inflammation, Invasion, and the Gut Microbiome
Purpose of Review
Entamoeba histolytica is a protozoan parasite that causes amebiasis, which remains a significant cause of morbidity and mortality worldwide. E. histolytica causes tissue destruction which leads to clinical disease. This review outlines some of the recent advances that have furthered our understanding of the processes that lead to the tissue damage caused by E. histolytica.
Recent studies have identified new mechanisms involved in E. histolytica–induced tissue damage. These include (i) new form of contact-dependent killing called trogocytosis; (ii) parasite-produced cytokine, macrophage migration inhibitory factor, that contributes to inflammation; (iii) exploitation of host immune response to promote invasion; and (iv) the contribution of the gut microbiome to clinical disease.
Targeting these mechanisms that result in tissue injury should be a focus of future research for the development of improved preventive and therapeutic strategies for amebiasis.
KeywordsAmebiasis Trogocytosis Microbiome Invasion E. histolytica macrophage migration inhibitory factor
E. histolytica–induced tissue damage is a result of 3 main events: host cell death, destructive inflammatory response, and parasite invasion.
Amebic trogocytosis is a recently discovered mechanism for host cell killing.
A specific parasite-encoded cytokine, E. histolytica macrophage migration inhibitory factor (EhMIF), mediates inflammation during amebiasis.
E. histolytica exploits the host inflammatory response to promote tissue invasion.
Gut microbiome influences the clinical outcomes of E.histolytica infection.
E. histolytica has the remarkable ability of direct killing of host cells. The mechanism of cell killing by E. histolytica has been the subject of intensive investigation for several decades. Adhesion to host cells is a critical factor for the killing activity of E. histolytica. Gal/GalNAC lectin is the major parasite adherence molecule that is required for the contact-dependent cell killing by E. histolytica. The process of cytotoxicity primarily involves programmed cell death (apoptosis) as demonstrated by TUNEL and annexin V staining showing DNA fragmentation and membrane blebbing. Several independent studies have shown that caspase-3 activation leads to the induction of programmed cell death , though the pathway that mediates this response is not fully understood. One theory is that parasite contact causes elevation of intracellular calcium in host cells, which ultimately leads to global protein tyrosine dephosphorylation and activation of caspase-3 .
What are the parasite cytotoxic effector molecules that trigger host cell death? It has been proposed that E. histolytica secretes proteins, such as amoebapores, that have cytotoxic effects on human cells. However, this theory is challenged by the failure of E. histolytica–secreted fractions to kill host cells.
E. histolytica is also capable of ingesting host cells by a process of phagocytosis. Phagocytosis is believed to play a crucial role in amebic pathogenesis as well as nutrient uptake . In vitro studies have shown that E. histolytica is capable of ingesting a variety of host cells. However, E. histolytica trophozoites obtained from clinical samples, including colonic ulcer biopsy, mainly consist of one cell type which is ingested red blood cells [1••].
More recently, real-time observation of cell killing by E. histolytica revealed that the parasite, prior to cell death, ingests distinct “bites” of live host cells by a process called “trogocytosis” [8••]. This leads to intracellular Ca2+ elevation and loss of membrane integrity in the host cells, ultimately causing cell death. Parasites were found to detach from the dead cells. Also, live host cells were preferentially ingested by amebic trogocytosis while pre-killed cells were taken up by phagocytosis. Although the molecular mechanism behind trogocytosis is not well understood, it was shown that the overlapping signaling pathways involving EhC2PK and PI3K, at least partially, regulate both phagocytic and trogocytic processes. Though there are several pathways common to both processes, differences likely exist. Researchers recently attempted to understand how trogocytosis was mechanistically distinct from phagocytosis. AGC family kinase 1 was found to be specifically involved in trogocytosis of live human cells and did not participate in phagocytosis of dead cells .
Biological processes equivalent of E. histolytica trogocytosis were previously identified in other human pathogens such as Naegleria fowleri. However, parasites like N. fowleri use a specialized cytoplasmic extension called “amoebostome” or “food-cup” for host cell attachment and ingestion . Structures homologous to Naegleria “food-cup” have not been found in E. histolytica, suggesting variations in this apparently similar process between organisms.
It appears that not all human epithelial cells are vulnerable to E. histolytica trogocytosis to the same levels. In a recent report, LS174T colonic epithelial cells, grown in monolayers, were rarely observed to undergo E. histolytica–mediated trogocytosis. The authors postulated that limited flexibility of the plasma membrane due to junctional complexes in cells grown in monolayers might limit trogocytosis by the parasite .
Inflammation and Macrophage Migration Inhibitory Factor Cytokine
Inflammation is a hallmark of amebic colitis; in fact, colitis literally means inflammation of the colon (Fig. 1). Amebic colitis is characterized by the secretion of pro-inflammatory cytokines and infiltration of the colon by immune cells, which would explain why it is often misdiagnosed as inflammatory bowel disease [2•]. The gut inflammatory response also contributes to the tissue destruction seen in amebic colitis . This notion was best exemplified in a previous study using a mouse model, which showed that persistent inflammation induced the classic flask-shaped ulcer of amebic colitis despite the lack of significant tissue invasion by E. histolytica parasites .
Neutrophils are one of the first responders to infiltrate the intestinal tract at the site of inflammation during amebic colitis [12, 14]. Neutrophils are implicated in both protection and pathology in amebic mouse models [15, 16]. Neutrophils generate oxygen free radicals that are capable of killing invading parasites, but are also responsible for collateral tissue damage during the inflammatory period, which might explain their protective and destructive role in amebiasis . This is further compounded by the fact that E. histolytica parasites have evolved strategies to evade the immune response and persist in the host, further exacerbating the damage caused by the lingering inflammatory response to invading parasites .
Intestinal epithelial cells are the first cell types to come into contact with E. histolytica (Fig. 2). It has been known for a while that before making cell contact, trophozoites secrete immunomodulatory proteins that stimulate epithelial cells, resulting in cytokine production and subsequent inflammatory cell infiltration [17, 18]. A variety of cells, including intestinal epithelial cells, produce interleukin-8 (IL-8), a potent neutrophil chemoattractant cytokine. In patients with amebic colitis, higher colonic tissue levels of IL-8 and neutrophils are associated with more severe disease [19, 20, 21]. Another cytokine that can result in undesirable effects when produced in excess is TNF-α. Higher TNF-α production was shown to correlate with E. histolytica diarrhea in children . TNF-α was also shown to mediate the tissue destruction seen in amebic liver abscess in a mouse model .
Many parasitic pathogens, including E. histolytica, express a homolog of the pro-inflammatory cytokine macrophage migration inhibitory factor (MIF) [24, 25, 26, 27, 28, 29••]. E. histolytica MIF (EhMIF) was recently shown to be a crucial parasite mediator of gut inflammation [29••]. A positive correlation was found between EhMIF levels and intestinal inflammation in persons with amebic colitis. EhMIF induced chemokine expression, neutrophil influx, and mucosal damage in cellular and mouse models of amebiasis [29••]. Also, EhMIF enhanced TNF-α production by macrophages . Infected children develop antibodies against EhMIF, which correlates with protection from future infection [25, 29••]. These studies suggest that EhMIF might have a role as an effective immunomodulatory target to prevent or reduce immunopathology in amebiasis.
Inflammasomes are key signaling platforms that detect pathogens and activate the pro-inflammatory cytokines IL-1β and IL-18 . The NLRP3 inflammasome is activated by E. histolytica; however, its role in immunopathology and tissue destruction is not yet fully understood . While a recent report found that MIF was required for NLRP3 inflammasome activation , the role of EhMIF in NLRP3 inflammasome activation remains unknown.
Nitroimidazoles antibiotics, such as metronidazole, are the mainstay therapy for amebic colitis [1••]. However, metronidazole alone is sometimes not enough for severe amebic colitis and even surgical removal of the inflamed colon may or may not prevent death [2•]. Studies in preclinical mouse models show that while metronidazole is very effective at killing ameba, it had little effect on E. histolytica–induced mucosal inflammation [33, 34]. Blocking parasite mediators of host inflammation such as EhMIF may help to attenuate disease, and these adjunctive anti-inflammatory strategies may lead to the improvement of the clinical outcomes of amebic colitis.
Tissue invasion by E. histolytica plays an important role in the pathogenesis of amebiasis. In clinicopathological studies of patients with severe amebic colitis, lesions extending beyond the cecum and depth of tissue invasion were associated with worse outcomes [35, 36].
The extracellular matrix (ECM) is a complex meshwork of proteins that provides support for tissues. The ECM can act as a physical barrier; thus, breakdown of the ECM is often required to promote cell movement through tissue. Matrix metalloproteinases (MMPs) are the main enzymes involved in ECM degradation, with at least 23 human MMPs identified so far .
MMPs are overexpressed in all protozoan infections . In the context of amebiasis, MMPs were among the top 5 most overexpressed genes in colonic tissue from patients suffering from intestinal amebiasis, and they were recently shown to be necessary for invasion. In a human colon explant model, inhibition of MMP activity blocked invasion of colonic mucosa by E. histolytica [14, 39••]. EhMIF has been found to influence the levels of MMP production. The inflammation induced by EhMIF resulted in an increase in MMP production [29••]. Therefore, E. histolytica parasites may produce MIF to exploit the host inflammatory response to promote tissue invasion.
Human Gut Microbiome and E. histolytica Infection
E. histolytica and bacteria have coevolved in the same intestinal environment over evolutionary time. Studies in microbiota-controlled animal models dating back more than half a century ago demonstrated that ulcerative lesions caused by E. histolytica were significantly enhanced in the presence of bacteria . The rapid expansion of human microbiome data has created opportunities for further understanding the role of the microbiota in amebiasis.
Recently, several human studies have revealed a significant change in the microbiota of patients with amebiasis. A strong correlation between the presence of E. histolytica and certain bacterial groups of the intestinal microbiota was found in an evaluation of the microbiota composition in rural populations of Cameroon . However, this study had several limitations, including the use of microscopy to detect Entamoeba. Microscopy does not distinguish nonpathogenic E. dispar from E. histolytica, the causative agents of amebiasis [1••]. Higher abundance of Prevotella copri, a species associated with gut inflammation, was found in children with diarrhea due to E. histolytica as compared with those with asymptomatic E. histolytica infection in a study conducted in an endemic area of Bangladesh [42••]. Also, a cross-sectional study of patients attending gastroenterology clinics in the Limpopo Province of South Africa found higher levels of P. copri in diarrhea due to E. histolytica when compared with nondiarrheal E. histolytica colonization . While these studies did not determine whether P. copri changes were the cause or effect of the disease, preliminary data suggest that P. copri expansion occurred prior to infection with E. histolytica and symptomatic disease .
Prevotella species are anaerobic gram-negative bacteria that constitute a major part of the normal flora of the mouth, gastrointestinal tract, and female genital tract. Interestingly, emerging studies have linked increased Prevotella abundance to inflammatory disorders . Prevotella spp. are capable of inducing IL-8 and IL-6 secretion by epithelial cells, resulting in Th17 responses and neutrophil recruitment in the intestinal mucosa . It is plausible that increased P. copri disrupts gut homeostasis and tips the balance toward a pro-inflammatory state which then amplifies E. histolyica–induced inflammation, resulting in immunopathology and symptomatic infection. Further studies, however, are needed to confirm this theory.
Genetic Tools for Investigating E. histolytica Pathogenesis
The molecular processes underlying the pathogenicity of E. histolytica are not fully understood. Therefore, genetic techniques are needed to further understand the pathogenesis of disease caused by E. histolytica. Here, we discuss the developments in the genetic methods applicable to E. histolytica.
Gene silencing has been achieved using a unique strain of E. histolytica called G3, where several amoebapore genes (ap-a, ap-b, and SAPLIP) were permanently silenced . Using this strain and the regulatory region of the endogenous ap-a gene, several different genes have been successfully silenced . However, this method does not allow for the silencing of a single gene. Gene silencing by exploiting the endogenous RNA interference pathway of eukaryotic cells has also been utilized in E. histolytica . Efficient but variable degrees of gene silencing are achieved by this approach. RNA interference methods that have been used successfully include antisense RNA expression  and RNAi “trigger”-based gene silencing .
In addition to knocking down gene expression, overexpression is often used to study the impact of gain of gene function in an organism. Different vector systems have been successfully used in E. histolytica for constitutive and inducible gene overexpression. For example, using the pKT3M vector, EhMIF gene was constitutively overexpressed in a virulent strain of E. histolytica, which was used to study its effect on mucosal inflammation in an amebic colitis mouse model [29••]. It is important to note that EhMIF is a soluble secreted and non-toxic protein which enabled successful constitutive overexpression [29••]. In addition, inducible systems such as pEhHYGB-Tet-0-CAT vector are available for tetracycline-induced overexpression . Furthermore, studies exploring E. histolytica virulent genes have overexpressed a dominant negative mutant protein to inhibit the endogenous protein function .
Despite all the current methods available for genetic manipulation, there is a need for developing a complete gene knockout system in E. histolytica. This has been achieved in other protist parasites [50, 51]. Efforts are underway to develop CRISPR-Cas9-mediated gene targeting in E. histolytica. So far, successful expression of the guide RNA and a modified version of Cas9 in E. histolytica trophozoites using a single plasmid approach has been achieved.
Are there host cell factors that promote resistance to trogocytosis?
Would nitroimidazoles antiprotozoal therapy in conjunction with anti-inflammatory strategies by blocking EhMIF activity prove superior to nitroimidazoles alone in reducing tissue damage and symptoms in severe amebiasis?
What is the mechanism by which increased P. copri abundance leads to symptomatic E. histolyica infection?
Will CRISPR genetic knockout develop into a reliable technique in E. histolyica?
We thank William Petri for his helpful advice. We apologize to all the colleagues we were unable to cite due to space limitations.
This work was supported by the National Institutes of Health (NIH) R01AI026649-27S1, K08AI119181, and the Robert Wood Johnson Foundation–Harold Amos Medical Faculty Development Program Award.
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The authors declare that they have no conflict of interest.
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This article does not contain any studies with human or animal subjects performed by any of the authors.
Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance
- 1.•• Shirley DT, Farr L, Watanabe K, Moonah S. A Review of the Global Burden, New Diagnostics, and Current Therapeutics for Amebiasis. Open Forum Infect Dis. 2018;5(7):ofy161). https://doi.org/10.1093/ofid/ofy161 The authors provide an updated clinical review of the epidemiology, clinical features, diagnosis, and treatment of amebiasis.
- 3.Swaminathan A, Torresi J, Schlagenhauf P, Thursky K, Wilder-Smith A, Connor BA, et al. A global study of pathogens and host risk factors associated with infectious gastrointestinal disease in returned international travellers. J Infect. 2009;59(1):19–27. https://doi.org/10.1016/j.jinf.2009.05.008.CrossRefGoogle Scholar
- 7.Somlata BS, Bhattacharya A. A C2 domain protein kinase initiates phagocytosis in the protozoan parasite Entamoeba histolytica. Nat Commun. 2011;2:230. https://doi.org/10.1038/ncomms1199 https://www.nature.com/articles/ncomms1199#supplementary-information.CrossRefGoogle Scholar
- 10.Grace E, Asbill S, Virga K. Naegleria fowleri: a review of the pathogenesis, diagnosis, and treatment options. Antimicrobial agents and chemotherapy. 2015:AAC. 01293–15.Google Scholar
- 13.Ghosh PK, Mancilla R, Ortiz-Ortiz L. Intestinal amebiasis: histopathologic features in experimentally infected mice. Arch Med Res. 1994;25(3):297–302.Google Scholar
- 29.•• Ngobeni R, Abhyankar MM, Jiang NM, Farr LA, Samie A, Haque R, et al. Entamoeba histolytica-encoded homolog of macrophage migration inhibitory factor contributes to mucosal inflammation during amebic colitis. J Infect Dis. 2017;215(8):1294–302. https://doi.org/10.1093/infdis/jix076 Identification of a specific parasite-encoded cytokine, E. histolytica migration inhibitory factor ( Eh MIF), which mediates inflammation during colitis.CrossRefGoogle Scholar
- 33.Debnath A, Parsonage D, Andrade RM, He C, Cobo ER, Hirata K, et al. A high-throughput drug screen for Entamoeba histolytica identifies a new lead and target. Nat Med. 2012;18(6):956–60 http://www.nature.com/nm/journal/v18/n6/abs/nm.2758.html#supplementary-information.CrossRefGoogle Scholar
- 39.•• Thibeaux R, Ave P, Bernier M, Morcelet M, Frileux P, Guillen N, et al. The parasite Entamoeba histolytica exploits the activities of human matrix metalloproteinases to invade colonic tissue. Nat Commun. 2014;5:5142. https://doi.org/10.1038/ncomms6142 Metalloproteinases (MMPs) are necessary for E. histolytica tissue invasion.CrossRefGoogle Scholar
- 42.•• Gilchrist CA, Petri SE, Schneider BN, Reichman DJ, Jiang N, Begum S, et al. Role of the gut microbiota of children in diarrhea due to the protozoan parasite Entamoeba histolytica. J Infect Dis. 2015;213(10):1579–85 Expansion of the Prevotella copri component of the human intestinal microbiome impacts the clinical outcome of E. histolytica infection.CrossRefGoogle Scholar
- 43.Ngobeni R, Samie A, Moonah S, Watanabe K, Petri WA Jr, Gilchrist C. Entamoeba species in South Africa: correlations with the host microbiome, parasite burdens, and first description of Entamoeba bangladeshi outside of Asia. J Infect Dis. 2017;216(12):1592–600. https://doi.org/10.1093/infdis/jix535.CrossRefGoogle Scholar
- 44.Gilchrist CA, Schneider BN, Alam M, Donowitz JR, Kabir M, Petri Jr WA et al., editors. Gut microbiome change prior to the onset of amebiasis. American Journal of Tropical Medicine and Hygiene; 2017: AMER SOC TROP MED & HYGIENE 8000 WESTPARK DR, STE 130, MCLEAN, VA 22101 USA.Google Scholar
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