Efficacy and Enterococcal Consumption

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This entry is adapted from the peer-reviewed paper 10.3390/antibiotics12081327

Enterococci are often used in probiotics but can also cause nosocomial infections. As such, enterococcal consumption may have beneficial health effects, but a thorough evaluation of virulence absence and risk of antibiotic resistance spread is needed at the strain level.

enterococci probiotic VRE enterococcal consumption virulence factor antibiotic resistance

1. Introduction

The genus Enterococcus consists of lactic acid bacteria (LAB) found predominantly in the gut of humans and animals. Among enterococcal species, E. faecium and E. faecalis are the predominant species of the human gastrointestinal system. Enterococci are also involved in the fermentation process of various foods, including cheeses and sausages ^[1]. Additionally, certain species of Enterococcus are utilized as probiotics to maintain healthy gastrointestinal microbiota and reduce gastrointestinal inflammation. They also demonstrate the ability to produce bacteriocins, which are proteins produced by bacteria to inhibit growth or kill other competing bacteria ^[2]^[3]. However, enterococcal strains can carry plasmid-mediated resistance genes, which can be transferred between bacterial species, causing decreased susceptibility to common antibiotics ^[4]. These plasmid-mediated genes in enterococci have contributed to Vancomycin-Resistant Enterococci (VRE), which are problematic in the clinical setting ^[5].

2. Safety of Enterococcal Consumption: Virulence and Antibiotic Resistance

2.1. Opportunistic Pathogenicity of Enterococci

Although enterococci are commensal organisms that are part of the natural human gut flora, they have emerged as common pathogens causing nosocomial infections, such as endocarditis, bacteremia, urinary tract infections (UTIs), intra-abdominal and pelvic infections. Nearly 80% of these infections were associated with E. faecalis ^[6]. Most enterococcal strains are harmless, but some of the strains found in clinical settings are pathogenic because hospitals serve as reservoirs for antibiotic-resistant strains ^[7].

Enterococci are opportunistic pathogens, meaning that they are not usually pathogenic, but they can cause infections in individuals with weakened immune systems. Enterococci are harmless in their natural habitats (GI tract) but can exhibit pathogenicity outside this anatomical site ^[8]. For instance, translocation across intestinal mucosal surfaces to other tissues and systems, like the lung, liver, spleen, lymph nodes, and circulatory system, has been linked to numerous diseases and disorders ^[5]. Manfredo-Vieira et al. demonstrated that the translocation of E. gallinarum into systemic organs induced autoimmune responses in patients with systemic lupus erythematosus and autoimmune hepatitis ^[9]. In addition, Wang et al. showed that the translocation of E. faecalis had potentially mutagenic and carcinogenic effects in a cell culture model through the production of clastogens (chromosome-breaking factors). For example, the clastogen superoxide (O₂⁻) produced by E. faecalis mediated COX-2 expression, which caused macrophage-induced chromosomal instability and DNA damage in neighboring cells. ^[10].

2.2. Virulence Factors and Pathogenicity of Enterococcus in Probiotics

The existence of various virulence factors will lead to the pathogenicity of enterococci. These virulence factors can be classified by their functions: exoenzyme, adherence, exotoxin, immune modulation, and biofilm formation. Table 1 summarizes research investigating virulent factors and their functions.

Table 1. Virulence factors of enterococci classified by function.

Virulence Factors	Classification	Type of Research	Enterococcus strains	Functions	Reference
Adhesin to collagen of E. faecalis (Ace)	Adherence	Cell culture and analysis of clinical isolates from patients with endocarditis	E. faecium OG1RF	Ability to bind with collagen type I and IV, as well as laminin	Nallapareddy et al., 2000 ^[11]
Cell wall-anchored collagen membrane adhesin (Acm)	Adherence	Cell culture and analysis of isolates from patients with severe clinical infections	E. faecium TX0054 E. faecium TX2535 E. faecium TX2555	Ability to bind with collagen type I	Nallapareddy et al., 2003 ^[12]
Endocarditis- and biofilm-associated pili (Ebp)	Adherence	Analysis of isolates from rats	E. faecalis OG1RF	Contribution to biofilm formation and adherence to fibrinogen	Nallapareddy et al., 2006 ^[13]
Enterococcus collagen-binding adhesin (EcbA)	Adherence	Cell culture and analysis of hospital-acquired isolates in vitro	E. faecalis E1162	Ability to bind with collagen type I, IV, V, and fibrinogen	Hendrickx et al., 2009 ^[14]
E. faecalis antigen A (EfaA)	Adherence	In vitro analysis of clinical isolates from patients with endocarditis	E. faecalis EBH1	Potential function as an adhesin in the endocardium	Lowe et al., 1995 ^[15]
Extracellular surface protein (Esp)	Adherence	In vivo experiment regarding urinary tract infection with a mouse model	E. faecalis MMH94	Colonization and survival in the bladder	Shankar et al., 2001 ^[16]
Promotion aggregation complex (PrgB)	Adherence	In vitro experiment with PrgB (AS 10) wildtype and PrgB mutant	E. faecalis OG1RF	Promotion of aggregation and biofilm formation	Schmitt et al., 2018 ^[17]
Second collagen adhesin of E. faecium (Scm)	Adherence	Cell culture and analysis of endocarditis isolates	E. faecium TX0068 E. faecium TX0074	Ability to bind with specificity to collagen type V	Sillanpää et al., 2008 ^[18]
Serine glutamate repeat A (SgrA)	Adherence	Cell culture and analysis of hospital-acquired isolates in vitro	E. faecium U0317 E. faecium E1162	Potential contribution to biofilm formation by binding nidogen and fibrinogen	Hendrickx et al., 2009 ^[14]
Gelatinase (GelE)	Exoenzyme	Cell culture and analysis in vitro	E. faecalis (non-specified)	Cleavage of complement C3, resulting in activation of the complement system	Park et al., 2008 ^[19]
Serine Protease (SprE)	Exoenzyme	In vivo experiment with rabbit model of endophthalmitis	E. faecalis OG1RF	Activation of fsrABC by working together with GelE (Attenuation of endophthalmitis pathogenesis in rabbits with SprE-deficient mutant)	Engelbert et al., 2004 ^[20]
Cytolysin (Cyl)	Exotoxin	Translocation experiment in vitro	E. faecalis JH22, E. faecalis TX1322	Cleavage of complements C3 and iC3b	Zeng et al., 2005 ^[21]
Cytolysin (Cyl)		In vitro analysis of clinical isolates in patients	E. faecalis (non-specified)	Higher occurrence of Cyl among clinical pathogens	Huycke et al., 1995 ^[22]
Biofilm on plastic D (BopD)	Biofilm	In vivo experiment with mice	E. faecalis T9, E. faecalis 10D5, E. faecalis TDM	Contribution to biofilm formation	Creti et al., 2006 ^[23]
Quorum-sensing complex (FsrABC)	Biofilm	Comparative Transcriptional Analysis	E. faecalis OG1RF, E. faecalis TX5266	Encoding of a two-component signal transduction system for initiation of quorum sensing	Bourgogne et al., 2006 ^[24]
Capsular polysaccharides (Cps)	Immune Modulation	Cell culture and analysis in vitro	E. faecalis V583, E. faecalis LT02, E. faecalis LT06	Higher resistance to opsonophagocytosis	Thurlow et al., 2009 ^[25]

None of the above virulence factors have been reported in enterococci used in probiotics.

Despite growing concerns over the pathogenicity of enterococci in hospital settings, no reports have demonstrated virulence factors in enterococcal probiotics. Domann et al. sequenced and compared E. faecalis contained in the probiotic Symbioflor 1^® to clinical VRE isolates. E. faecalis strains in Symbioflor 1 were found to lack gene coding for essential virulence factors, such as cyl and esp. The E. faecium T110, a component of the probiotic BIO-THREE^®, was sequenced completely and compared to pathogenic and non-pathogenic enterococcal strains. The gene encoding virulence factors were not found in the genome of E. faecium T110. The genome was noticeably different from the pathogenic strains found in hospitals, which included VRE and pathogenicity genes. Of the 40 enterococcal virulence genes established in the VFDB database (http://www.mgc.ac.cn/VFs/main.htm (accessed on 30 May 2023), 32 genes were missing in the T110 genome, affirming its safety as a non-pathogenic strain. The eight virulence genes present in the genome were not well-characterized and did not seem to contribute much to its pathogenicity ^[26].

2.3. Antibiotic Resistance

Avoparcin, a glycopeptide antibiotic similar to vancomycin, has been used as a growth promoter in livestock feed since the 1970s. The use of avoparcin coincided with the emergence of VRE outbreaks in hospitals. This chain of events suggests the possibility of VRE originating from antibiotic use in livestock, which subsequently spread to humans and hospitals through consumption ^[27].

Enterococcal species can be divided into two major categories based on their susceptibility to antibiotics: clade A and clade B. Clade B strains are susceptible to antibiotics (i.e., ampicillin and vancomycin) and, therefore, are not problematic in treatment against enterococci. Clade A strains, on the other hand, are hospital-derived strains that have diverged from Clade B strains and have adapted antibiotic resistance to various antibiotics, such as ampicillin and vancomycin ^[27]^[28]. Persistent use of antibiotics in hospitals and veterinary medicine has created multi-drug-resistant strains of enterococci that may be problematic ^[5]. These multi-drug resistant strains may spread in hospital settings, mainly through the hands of healthcare workers as well as medical equipment, leading to problematic infections ^[7].

Of particular concern is the increase in the incidence of vancomycin-resistant strains, with over 30% of all nosocomial enterococcal infections having resistance to this antibiotic as of 2019 (CDC). Vancomycin is often used to treat ampicillin-resistant pathogens ^[6]. Therefore, VRE, when pathogenic, has been associated with higher mortality in patients after undergoing hematopoietic cell transplantation ^[29]. Vancomycin resistance is encoded by specific gene clusters with nine variants (vanA, vanB, vanC, vanD, vanE, vanG, vanL, vanM, vanN), which can be identified by PCR or DNA sequencing. ^[28]. The different variants display varying levels of resistance to vancomycin and similar glycopeptide antibiotics. VanA and B are commonly linked to high levels of resistance, whereas vanC, D, E, G, L, M, and N typically demonstrate resistance at lower levels. Each variant employs a unique mechanism to confer resistance to vancomycin. For instance, vanA, B, D, E, L, M, and N are associated with the production of modified peptidoglycan, resulting in reduced affinity towards vancomycin. On the other hand, vanC generates an altered target site that vancomycin struggles to bind effectively, while vanG combines the synthesis of modified peptidoglycan precursors with the alteration of the target site. Complete sequencing of two probiotic strains, E. faecium T110 (BIO-THREE^®) and E. faecalis (Symbioflor 1), showed the absence of antibiotic resistance genes ^[26]^[27].

Linezolid, daptomycin, and tigecycline are medications that can treat VRE. However, resistance to these three agents has emerged. According to the global Zyvox Annual Appraisal of Potency and Spectrum (ZAAPS) linezolid surveillance monitoring program, the number of linezolid-resistant enterococci (LRE) isolates has increased from 420 in 2002 to 813 in 2014. Similarly, the US Linezolid Experience and Accurate Determination of Resistance (LEADER) surveillance monitoring program reported that LRE faecium increased from 428 in 2004 to 589 in 2014, while LRE faecalis isolates increased from 196 to 239 in 2014 ^[30]. The prevalence of E. faecalis strains resistant to linezolid was found to be 2.8% in Asia, whereas, in the Americas, the prevalence of linezolid-resistant E. faecium was observed to be 3.4% ^[31]. The primary causes of LRE involve changes in the genetic material of the bacteria. These changes occur through mutations in specific genes responsible for producing 23S ribosomal RNA and regulatory genes that encode ribosomal proteins, namely rplC, D, and lV. These mutations result in the replacement of certain amino acids in various ribosomal proteins, including L3, L4, and L22 ^[32]^[33]^[34].

Daptomycin-resistant Enterococcus (DRE) has also been reported. Based on a meta-analysis in 2021 by Dadash et al., the prevalence of DRE (9%) is higher than that of LRE (2.2%). Multiple DRE mechanisms of resistance have been reported. However, two major categories of genes are found in DRE. These consist of regulatory genes for cell-envelope homeostasis and stress response, as well as genes that code for enzymes involved in the phospholipids of the cell membrane. Genes found in DRE faecalis are cls, liaFSR, and gdpD, whereas genes found in DRE faecium are cls, liaSR, and yycFG ^[35].

Tigecycline has been marked as a potential treatment option for complex soft tissue and intra-abdominal infections. However, it cannot be used for bloodstream infections due to inadequate antibiotic concentration in the bloodstream ^[36]. Dadash et al. also reported tigecycline-resistant Enterococcus (TRE) prevalence rates in Europe. TRE faecium was 3.9% and TRE faecalis was 0.4 ^[31]. Major genes that cause TRE are tet (M) and tet (L). Tet (M) is a ribosomal protection protein that alters the binding site of tigecycline, whereas tet (L) is an MFS-type efflux pump ^[35]^[36]. These tetracycline resistance genes also confer resistance to tigecycline ^[37]. Regarding the antibiotic-resistant risk of probiotic enterococci, no published research that sequences probiotic enterococci for the detection of these LRE, DRE, or DRE-related genes has been conducted.

2.4. Concern of Transfer of Virulence and Antibiotic Resistance

Enterococcal strains currently used in probiotics are not pathogenic, nor confer resistance to antibiotics. However, there is growing concern regarding the potential transfer of virulence and antibiotic-resistance genes between different enterococcal strains. Enterococci have a notable characteristic of possessing mobile genetic elements such as plasmids and transposons, which facilitate the efficient transfer of genes. This feature drives the evolution of certain strains, enabling them to adapt to different antibiotics found in clinical settings ^[38]. For instance, enterococcal strains can transfer genetic material like antibiotic resistance or virulence factors to each other or to other strains through the transfer of conjugative plasmids ^[5].

An example of such a transfer occurred in a study by de Niederhäusern et al., where they successfully transferred the vanA gene (associated with vancomycin resistance) from VRE to Staphylococcus aureus through the horizontal transfer of the Tn1546 transposon containing vanA. This discovery raised concerns about the horizontal transfer of vancomycin resistance, highlighting that VRE strains are capable of transferring their resistance to other pathogenic strains ^[39]. Another instance involved a clade B-classified E. faecium strain without vancomycin resistance. This clade B strain was found to possess the vanN gene and exhibited inducible vancomycin resistance. This finding suggests the potential transfer of vancomycin resistance from clade A to clade B strains, indicating that the extent of vancomycin resistance may be underestimated, especially in enterococcal strains previously described as lacking antibiotic resistance ^[28].

The highly efficient mechanism of gene transfer implies that a harmless enterococcal strain can acquire virulence or antibiotic resistance through conjugation with a pathogenic strain. In the case of probiotics, where enterococci are consumed in significant quantities, a large population of recipient bacteria is available for the transfer of virulence or antibiotic-resistance genes. This transfer can occur, for example, from pathogenic strains present in the human gastrointestinal tract to harmless probiotic strains ^[40]. Such transfer events can lead to the evolution of pathogenic or antibiotic-resistant probiotic strains, which can potentially cause problematic infections.

Olanrewaju et al. showed that conjugal transfer of resistance genes could result in an effect of biofiltration in the guts of zooplankton Daphnia magna and D. pulex. PCR and DNA sequencing was used to confirm that filter feeding in aquatic environments could lead to in vivo conjugative transfer of vanA resistance genes in Daphnia. These results showed that host enterococcal strains in Daphnia can acquire vanA simply through the consumption of vanA-containing bacteria in the aquatic environment. Such conclusions raise the possibility of humans being the end host of resistant enterococcal strains through the food chain ^[41].

In addition, Moubareck et al. demonstrated in vitro and in vivo conjugative transfer of the vanA resistance gene from vancomycin-resistant enterococcal strains isolated from pigs to vancomycin-susceptible human fecal isolates in gnotobiotic mice. The transfer event occurred in human isolates only 5 h after inoculation with the donor strain, suggesting that human bacteria may be able to acquire vancomycin resistance from enterococci of animal origin in a short time frame ^[42].

These findings suggest that the transfer of vancomycin resistance to human hosts is possible. Therefore, it is crucial to carefully monitor enterococcal strains currently deemed “safe” for any potential emergence of virulence or antibiotic resistance. Genetic changes can render these strains pathogenic at any time point in the future ^[38].

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