Enterococcus faecium; a Suitable Probiotic Candidate for Modulation of Immune Responses Against Pathogens
Int J Basic Sci Med, 2(2), 77-82; DOI:10.15171/ijbsm.2017.15
Mini review
Enterococcus faecium; a Suitable Probiotic Candidate for Modulation of Immune Responses Against Pathogens
Soodabeh Khalkhali1,2, Naheed Mojgani3, *
1
Department of Microbiology, Shiraz Branch, Islamic Azad University, Shiraz, Iran
2
Department of Microbiology, Fars Research and Science Branch, Islamic Azad University, Fars, Iran
3
Department of Biotechnology, Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran
*Correspondence to
Naheed Mojgani, Department
of Biotechnology, Razi Vaccine
and Serum Research Institute,
Agricultural Research, Education and
Extension Organization (AREEO),
Karaj, Iran, Box: 31975/148.
Tel: +98 9121646063
Email: dnmoj@yahoo.com
Copyright © 2017 The Author(s);
Abstract
Probiotics are a set of nonpathogenic microorganisms without virulence which inhibit pathogen
growth in animals.
Enterococcus faecium has been introduced as a probiotic and its probiotic
characteristics have been evaluated in several investigations. Evidence suggests that probiotics
may modulate the immune system of the host to improve responses against pathogens. Thus,
this review aimed to present recent studies regarding the effects of the
E. faecium probiotic strain
on the host immune responses. It seems that
E. faecium AL41, CGMCC, NCIMB, SF68, Strain
26, JWS 833 and EF55 strains improve beneficially the immune responses of the host. However,
most studies have been performed on animal models, therefore, clinical trials on humans are
required to understand the beneficial mechanisms of
E. faecium on the human immune system.
Keywords: Probiotics, Enterococcus faecium, Immune responses
Please cite this article
as follows: Khalkhali S,
Mojgani N. Enterococcus
faecium; a suitable
probiotic candidate for
modulation of immune
responses against
pathogens. Int J Basic
Sci Med. 2017;2(2):77-
82. doi:10.15171/ijbms.2017.15.
Introduction
Probiotics are nonpathogenic microorganisms which have several benefits on human health or physiology.1 Probiotic is a Greek word ‘pro bios’ which means ‘for life’ as opposed to antibiotics which means ‘against life.’ Accordingly, it has been proposed that there are beneficial effects of probiotics on human health by a Russian researcher Ellie Metchnikoff. Probiotics have several positive and negative effects on the gut microflora and the microbial toxic activities, respectively.2,3 Both yeast and bacteria, especially lactic acid bacteria, are the main members of probiotics.1 Probiotics modulate endogenous flora, pathogenic micro-organisms and also the immune responses of hosts in either a direct or indirect manner.4 Accordingly, it has been hypothesized that probiotics can be considered as potential agents to prevent or help to cure human infectious diseases, especially intestinal disturbances.5
Enterococcus faecium is a strain of gram positive bacteria Firmicutes phylum, bacilli class, Lactobacillales order, Enterococcaceae family, Enterococcus genus, the E. faecium species, which exhibits some probiotic properties.6 Therefore, it has been proposed as a probiotic and several studies have evaluated the bacteria for treatment of several animal and human models.7-9 The following sections describe the bacteria in details. It has been hypothesized that probiotics, including E. faecium, fight the pathogenic microbes via several mechanisms.7 It appears that modulation of the immune responses against the pathogens is a plausible mechanism to fight against pathogens.10 Several probiotic strains including E. faecium SF68, AL41, EF55, JWS 833, Strain 26, NCIMB 10415 and CGMCC 2516 have been used to investigate the immunological modulation with focus on safety, anti-pathogenic and immunomodulatory properties which are listed in Table 1.
Table 1. The Major Effects of Enterococcus faecium Probiotic Strains on the Immune System of Hosts
|
Host | Effects on the Immune System | Strains | Ref.
|
Positive Results |
Mice | Increased phagocytic and digestive functions of macrophages | AL41 | 8 |
Chicken | Modulates the liver inflammatory molecules | CGMCC 2516 | 33 |
Ostrich | Mucosal immunity | AL41 | 12 |
Porcine | Increased intraepithelial lymphocyte numbers | NCIMB 10415 | 23 |
Holstein cows | Increased neutrophil infiltration and milk levels of MMP9 | SF68 | 13 |
Chicken | Increased serum levels of IgM | - | 25 |
Pig |
Increased humoral immune responses against the SIV vaccination and increased number of activated T
helper and cytotoxic T cell |
NCIMB 10415 | 26 |
Pig |
Regulation of the inflammatory molecules in the healthy animals.
Increased expression of IL-8 in response to pathogens |
NCIMB 10415 | 25 |
Holstein calves |
Increased numbers of T helper and cytotoxic as well as γδ T cells and their innate receptors such as
TLR2 |
Strain 26 | 27 |
Chicken | Up-regulated of the mucosal IL-4, TNF-α and IgA | - | 28 |
Fish | Increased myeloperoxidase and lysozyme activities | - | 16 |
Rabbit | Stimulation of the mucosal immunity | AL41 | 9 |
Mice | Increased production of NO, IL-1β and TNF-α | JWS 833 | 18 |
Chicken | Increased number of the peripheral blood lymphocytes and CD3, CD4, CD8, and IgM positive cells | EF55 | 29 |
Hen | Improvement of the intestine integrity | AL41 | 19 |
Chicken |
Increased humoral immunity to vaccination with the Newcastle disease virus and infectious bursal
disease
| - | 30 |
Fish | Increased expression levels of IL-1α, TNF-α and TGF-β | - | 17 |
Sow and piglet | Enhanced immune responses against Escherichia coli in CD8+ cytotoxic T cells independent manner SF68 31
Dog Increased production of specific IgA and IgG | SF68 | 32 |
Dog | Increased production of specific IgA and IgG | SF68 | 32 |
Human | Increased neutrophil phagocytosis and humoral immunity | - | 20 |
Dog |
Increased expression of pro-inflammatory cytokines (IL-17A, IL-22, IFN-γ and TNF-α) in the duodenal
biopsies and whole blood
| - | 21 |
|
Pig | Increased production of NO in response to swine influenza virus | NCIMB 10415 | 22 |
Negative Results |
Piglet |
Reduction in the cell density counts of α/βCD8+ intraepithelial and percentage of α/βCD8+ circulating
T cells
| - | 37 |
Dog | No differences in the IgA production | SF68 | 38 |
Dog | No alteration in the immune responses during the chronic enteropathy | NCIMB 10415 | 39 |
Although, there are several research and review articles related to E. faecium and its benefits for human, the interaction of the bacterium with the immune system has not been discussed previously. Additionally, E. faecium is now recognized as a probiotic, and hence, this review article collates recent information regarding the roles of E. faecium in modulation of the immune responses.
Enterococcus faecium and its Effects on the Immune Responses
Enterococcus faecium has been considered as a probiotic and several investigations have evaluated its effects on the immune responses in the human and animal models.11 The probiotic may modulate innate and adaptive immunity to either increase responses to infectious disease to clear them or modulate immune responses in inflammatory conditions to decrease their complications. Accordingly, investigations on the immunomodulatory effects of E. faecium have been categorized into three sections including (1) The effects of E. faecium on the innate immunity, (2) The effects of E. faecium on the adaptive immunity, and (3) the effects of E. faecium on the modulation of the immune responses during pro-inflammatory diseases.
The Effects of Enterococcus faecium on the Innate Immunity
Based on the probiotic effects of E. faecium, it seems that the bacterium not only considered as a foreign particle for immune system, but also can modulate innate immune system. Accordingly, Dvoroznakova et al have reported the effects of E. faecium on the innate immunity (monocytes, polymorphonuclear leukocytes, phagocytosis and oxidative burst) of Trichinella spiralis infected mice8 and have demonstrated that the administration of E. faecium to mice prior to T. spiralis infection led to increased innate immunity against the parasite and elevated prolonged phagocytic activities of the host leukocytes. The administration of E. faecium also increases the ingestion capacity of the innate immune cells, including macrophages.8 The E. faecium also plays key roles in the induction of an appropriate mucosal immunity against the pathogenic bacteria such as Salmonella typhimurium.12 Lauková et al also reported the positive effects of the E. faecium probiotic on the mucosal immunity of rabbits.9 Based on these results, Tiantong et alalso showed the beneficial effects of the E. faecium on the mucosal immunity and reported that the probiotic elevated the matrix metalloproteinase 9 (MMP9) and also improved the neutrophil infiltration to the infected glands of Holstein cows.13 In addition, Siepert et alshowed that pre-treatment of the animals by the E. faecium NCIMB 10415 before S. typhimurium challenge led to significantly increased expression levels of IL-8 in the mesenteric lymph nodes.14 IL-8 is a pro-inflammatory cytokine which recruits neutrophils to the infected sites.15 Therefore, it may be concluded that E. faecium fights against pathogens via the induction of the immune responses at the site of infection.
The E. faecium also affects the immune responses in a strain of fishes (Paralichthys olivaceus). Accordingly, Lee et alrevealed that the citrus by-products (CB) of fermentation with E. faecium enhanced the innate immunity of fish. Their results demonstrated that probiotic treatment led to increased myeloperoxidase and lysozyme activities in a dose-dependent manner.16 Another study on fish using rainbow trout, Oncorhynchus mykiss, as a model revealed that E. faecium enhanced leukocytes superoxide anion production and serum complement activities through the alternative pathway.17 The study also showed that expression levels of interleukin 1 alpha (IL-1α), Tumor necrosis factor-alpha (TNF-α) and transforming growth factor beta (TGF-β) were increased significantly in the spleen and the kidney.17 Choi et alused E. faecium JWS 833 isolated from the duck intestineand reported that the heat-killed JWS833 enhanced production of nitric oxide (NO), IL-1β and TNF-α by mouse peritoneal macrophages in response to Listeria monocytogenes.18 Using the E. faecium AL41 in hens also resulted in improvement of the intestine integrity, which is a part of the innate immunity against microbes.19 The probiotic also enhanced phagocytosis by neutrophils and production of antibodies in humans.20 Schmitz et al studied the dog’s duodenal biopsies and whole blood and demonstrated that E. faecium stimulated the expression of pro-inflammatory cytokines including IL-17A, IL-22, Interferon gamma (IFN-γ) and TNF-α in the duodenal biopsies and serum and subsequently enhanced the immune responses against pathogens.21 The probiotic form of E. faecium (NCIMB 10415) also increased the production of NO by the phagocyte cells of pigs.22 Based on the results, it appears that E. faecium modulates the innate immunity to fight against pathogens.
The Effects of Enterococcus faecium on the Adaptive Immunity
Enterococcus faecium also modulates the adaptive immunity. Rieger et al demonstrated that E. faecium treatment led to the improvement of the mucosal immunity against S. typhimurium by increasing the number of mucosal intraepithelial lymphocytes.23 Intraepithelial lymphocytes are the first line of cellular immunity against microbes and play key roles in the mucosal immunity.24
Ahmed et aldemonstrated that the administration of Citrus junos probiotics, a by-product of fermentation with E. faecium, to chicks showed that the product led to increased serum levels of immunoglobulin (Ig)M.25 Wang et al also demonstrated the immunomodulatory effects of the E. faecium reporting that the E. faecium NCIMB 10415 in combination with zinc oxide stimulated the humoral immune responses against trivalent influenza vaccination and also led to an increased numbers of activated T helper and cytotoxic T cells in pigs.26 Another study on Holstein calves using the E. faecium NCIMB 10415 showed that probiotic treatment led to increased numbers of the peripheral blood helper, cytotoxic and γδ T cells.27 Their study also demonstrated that the numbers of CD14(+), CD21(+) and TLR2(+) cells as well as the expression of IL-6, and IFN-γ were increased significantly in the probiotic treated animals on day 7.28 Treatment of chickens with E. faecium prior to challenge with the Escherichia coli K88 also led to up-regulation of IL-4, TNF-α and IgA in the mucosal immunity which eventually assisted in the eradication of the E. coli.29
Another study on chicks identified that the administration of E. faecium EF55 was associated with the elevated numbers of the peripheral blood lymphocytes and CD3, CD4, CD8, and IgM positive cells in response to Salmonella enterica serotype enteritidis phage type 4 (SE140 PT4).29 Talebi et al reported that the administration of E. faecium to chicken improved the humoral immunity responses to vaccination with the Newcastle disease virus and infectious bursal disease.30 Interestingly, the administration of E. faecium led to decreased numbers of intestinal CD8+ cytotoxic T cells and their results revealed that this was associated with suppression of the E. coli infection.31 It suggested that the probiotic enhances the immune responses against E. coli in a CD8+ cytotoxic T cells independent manner. E. faecium SF68 also increased fecal IgA and specific circulating IgG and IgA against the canine distemper virus (CDV) vaccine.32
In sum, it may be hypothesized that E. faecium modulate the mucosal adaptive immunity to fight against pathogens.
The Effects of Enterococcus faecium on the Modulation of the Immune Responses During Pro-inflammatory Diseases
Although, E. faecium plays key roles in induction of appropriate immune responses against pathogens, there are some evidences which confirm the roles played by E. faecium to modulate immune responses during pro-inflammatory based diseases. Another study investigated the roles of E. faecium on the liver functions of broiler chickens which revealed that the probiotic decreased the inflammatory responses ,damage associated with molecular patterns (PAMPs), and induced homeostasis.33 Siepert et al also used the E. faecium NCIMB 10415 strain to treat the pigs prior to the infection with S. typhimurium.14 They reported that treatment of healthy pigs with the E. faecium NCIMB 10415 led to reduced expression of IL-8, IL-10 and CD86/B7-2 (a co-stimulatory molecule present on activated antigen presenting cells, and interaction of CTLA-4 [cytotoxic T-lymphocyte antigen-4 or CD152] with CD86 inhibits human T-cell activation) (a co-stimulatory molecule) in the ileal Peyer’s patches and elevated serum levels of TGF-β.23 TGF-β is an anti-proliferative cytokine with angiogenesis properties and its strong chemotactic capacity.34,35 It is noteworthy to know that this cytokine is essential for the maintenance of mucosal integrity.36 Thus, it seems that E. faecium could play crucial roles in mucosal health programs. Thus, it seems that E. faecium may be considered as a therapeutic target for further investigations, especially on human subjects.
Figure 1 summarizes the immunoregulatory effects of
E. faecium.
Figure 1. Immunoregulatory Effects of Enterococcus faecium. E. faecium enhances mucosal immunity by increasing numbers of intraepithelial T lymphocytes (A) and production of IgA (B). It also stimulates macrophages and dendritic cells (DCs) to produce NO and digest microbes (C). The probiotic also increases infiltration of neutrophils to the breast and milk as well as milk levels of pro-inflammatory cytokines (D).
In contrast with the aforementioned investigations, Mafamane et al showed that the administration of E. faecium was associated with a reduction in the cell density counts of CD8+α/β intraepithelial and percentage of circulating T cells, and did not influence the control or proliferation of Salmonella growth in the piglets.37
In addition, short-term treatment of dogs suffering from giardiasis did not have any correlation with the associated response of IgA production against the worms.38 Furthermore, Schmitz et al,39 showed that E. faecium was unable to alter the immune responses during the chronic enteropathy in dogs.
Conclusion
The strong point of this review is that some strains of E. faecium can be considered as probiotics and can be used for the treatment against pathogens in the humans.
Some E. faecium strains can be used in vivo in a safe manner and either induce the innate and adaptive immune responses or inhibit the inflammatory related diseases. Thus, they may be useful for the immunomodulation of the human immune related diseases such as hypersensitivities, autoimmunity, transplantation and so on. However, some limited investigations revealed that the use of E. faecium was not associated with the improved immune responses and suggested negative results regarding the roles played by E. faecium against Salmonella growth in the piglets. Thus, it may be hypothesized that using short-term treatments, low doses of E. faecium or the use of the probiotic in chronic based disorders such as enteropathy, which is caused by a low grade chronic inflammation, are the main reasons for the negative results of E. faecium administration.
In sum, it seems that Enterococcus faecium AL41, CGMCC, NCIMB, SF68, Strain 26, JWS 833 and EF55 strains may use common mechanisms of action that are seen in other probiotics.
Ethical Approval
Not applicable.
Competing Interests
There is no conflict of interest to declare.
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