Genomic Insights of Enterococcus faecium UC7251, a Multi-Drug Resistant Strain From Ready-to-Eat Food, Highlight the Risk of Antimicrobial Resistance in the Food Chain

The presence of multi-drug resistant (MDR) bacteria in ready-to-eat foods comprises a threat for public health due to their ability to acquire and transfer antibiotic-resistant determinants that could settle in the microbiome of the human digestive tract. In this study, Enterococcus faecium UC7251 isolated from a fermented dry sausage was characterized phenotypically and genotypically to hold resistance to multiple antibiotics including aminoglycosides, macrolides, β-lactams, and tetracyclines. We further investigated this strain following a hybrid sequencing and assembly approach (short and long reads) and determined the presence of various mobile genetic elements (MGEs) responsible of horizontal gene transfer (HGT). On the chromosome of UC7251, we found one integrative and conjugative element (ICE) and a conjugative transposon Tn916-carrying tetracycline resistance. UC7251 carries two plasmids: one small plasmid harboring a rolling circle replication and one MDR megaplasmid. The latter was identified as mobilizable and containing a putative integrative and conjugative element-like region, prophage sequences, insertion sequences, heavy-metal resistance genes, and several antimicrobial resistance (AMR) genes, confirming the phenotypic resistance characteristics. The transmissibility potential of AMR markers was observed through mating experiments, where Tn916-carried tetracycline resistance was transferred at intra- and inter-species levels. This work highlights the significance of constant monitoring of products of animal origin, especially RTE foodstuffs, to stimulate the development of novel strategies in the race for constraining the spread of antibiotic resistance.

The presence of multi-drug resistant (MDR) bacteria in ready-to-eat foods comprises a threat for public health due to their ability to acquire and transfer antibiotic-resistant determinants that could settle in the microbiome of the human digestive tract. In this study, Enterococcus faecium UC7251 isolated from a fermented dry sausage was characterized phenotypically and genotypically to hold resistance to multiple antibiotics including aminoglycosides, macrolides, β-lactams, and tetracyclines. We further investigated this strain following a hybrid sequencing and assembly approach (short and long reads) and determined the presence of various mobile genetic elements (MGEs) responsible of horizontal gene transfer (HGT). On the chromosome of UC7251, we found one integrative and conjugative element (ICE) and a conjugative transposon Tn916-carrying tetracycline resistance. UC7251 carries two plasmids: one small plasmid harboring a rolling circle replication and one MDR megaplasmid. The latter was identified as mobilizable and containing a putative integrative and conjugative element-like region, prophage sequences, insertion sequences, heavy-metal resistance genes, and several antimicrobial resistance (AMR) genes, confirming the phenotypic resistance characteristics. The transmissibility potential of AMR markers was observed through mating experiments, where Tn916-carried tetracycline resistance was transferred at intra-and inter-species levels. This work highlights the significance of constant monitoring of products of animal origin, especially RTE foodstuffs, to stimulate the development of novel strategies in the race for constraining the spread of antibiotic resistance.

INTRODUCTION
Enterococcus faecium is an ubiquitous species found in a large number of foods, mainly fermented products of animal origin like cheeses and fermented sausages (Braïek et al., 2018). Some strains of this species have been also recognized as probiotics conferring benefits to their hosts (Ghattargi et al., 2018). Nevertheless, in the past three decades, E. faecium emerged as an important nosocomial multi-drug resistant (MDR) pathogen responsible for hospital-acquired infections (Gao et al., 2018). The duality of this species has led the European Food Safety Authority (EFSA) to state a safety assessment scheme based on the absence of genetic markers generally present in the hospitalassociated (HA) biotypes for those E. faecium strains that are intentionally introduced into the food chain (EFSA et al., 2018). Although E. faecium is extensively used as a probiotic and as part of the fermentation processes, it does not actually hold the qualified presumption of safety (QPS) status due to its potential pathogenicity (EFSA BIOHAZ Panel et al., 2021).
Previous studies indicated that the population structure of E. faecium is divided into three distinct clades: clade A1 bearing clinical isolates; clade A2 mainly represented by strains from animal and human commensals that might cause sporadic human infections, both carrying determinants for virulence and antimicrobial resistance (AMR); and clade B characterized by community-associated (CA) isolates lacking HA traits (Lebreton et al., 2013). Recently, clade B isolates were proposed to be reclassified as Enterococcus lactis because of their closer genomic proximity to this new species and lack of HA markers (Belloso Daza et al., 2021). The genetic transmission of HA markers among isolates, for instance, between farm animals and humans in the agricultural setting, revealed consequently the contamination of products of animal origin that affect the entire production and supply chain (Manyi-Loh et al., 2018). The rise of MDR enterococci in the food chain represents a major public health concern as they are easily disseminated through the environment (Serwecińska, 2020). Livestock animals and the farm environment exemplify an important reservoir of AMR bacteria due to the widely use of antibiotics , particularly in swine for prophylactic reasons (Pholwat et al., 2020). Also, resistance to heavy metals is a matter of concern because of possible co-selection of antibiotic resistance. Specifically, resistance toward copper is common in swine-derived isolates due to the use of copper sulfate as a growth promoter in the feed for pigs (Yu et al., 2017). Enterococci-harboring MDR genes have been frequently isolated from the swine samples (Tan et al., 2018), and their diffusion arises concerns about the potential transmission to meat-based ready-to-eat (RTE) foods, which proposes a risk because of the lack of microbial inactivation prior consumption (Chajecka-Wierzchowska et al., 2019). Considering the emergence of MDR enterococci and HA isolates, the current criteria for safety assessment are represented by an MIC of ampicillin of ≤ 2 mg/L and lack of IS16/esp/hyl genes, associated with plasticity, adhesion, and carbohydrate metabolism, respectively (EFSA et al., 2018). Further information on epidemiology and the population structure can be analyzed by applying the multilocus sequence typing (MLST) scheme. Following this, E. faecium can be classified in different sequence types (STs), where ST17 was identified as the ancestral clone of HA isolates, forming the clonal complex 17 (CC17) . Nonetheless, it is crucial to understand the distribution of other putative virulence markers (PVM) involved in colonization and resistance recognized in other studies (Freitas et al., 2018;Gao et al., 2018). Horizontal gene transfer (HGT) is one of the mechanisms at the base of AMR and virulence marker dissemination among bacteria that facilitates their survival and adaptation in stressful conditions. The HGT of AMR genes between E. faecium and other species has been investigated mostly in clinical settings; furthermore, gene exchange in food was also demonstrated (Chajecka-Wierzchowska et al., 2019). Additionally, the transfer of resistance toward linezolid (Tyson et al., 2018), oxazolidinone (Kang et al., 2019), aminoglycosides (Kim et al., 2019), glycopeptides, erythromycin, and tetracycline (Conwell et al., 2017) has been demonstrated between foodisolated strains. The detection of AMR has also reached the retail level with the presence of AMR dissemination in RTE foods such as dairy products (Chajecka-Wierzchowska et al., 2020), salads (Zhou et al., 2020), seafood (Igbinosa and Beshiru, 2019), meat products (Chajecka-Wierzchowska et al., 2016), and pork-origin products (Kim and Koo, 2020).
Whole-genome sequencing (WGS) has facilitated the understanding of the mechanisms that support the dissemination of mobile genetic elements (MGEs) in bacteria. The aim of this study is to investigate the genomic characteristics of a vancomycin-susceptible MDR (VSE-MDR) E. faecium strain isolated from ready-to-eat fermented sausage and to evaluate the potential transmissibility of AMR markers through MGEs.

Bacterial Strain, Cultivation, and Antibiotic Susceptibility Testing
The strain UC7251 was isolated from a dry fermented Italian salami on Slanetz and Bartley Medium (Oxoid) containing 4 µg/ml ampicillin (Sigma). The strain was subcultivated in brain heart infusion (Oxoid) overnight at 37 • C, and species-specific PCR using primers for the ddl gene (Supplementary Table 1S) was performed to confirm its taxonomical classification. Susceptibility to different antibiotics was determined by using the broth microdilution method according to EUCAST (EUCAST, 2022). The antimicrobial agents used were ampicillin, vancomycin, gentamycin, kanamycin, streptomycin, erythromycin, clindamycin, tylosin, tetracycline, and chloramphenicol. The antibiotics were obtained from Sigma (St. Louis, Missouri, USA). The minimum inhibitory concentrations (MICs) were compared to the breakpoints recommended by (EUCAST, 2022) (http://www.eucast.org/) and EFSA (EFSA et al., 2018).

Conjugal Transfer
In vitro conjugation experiments were performed as described before (Cocconcelli et al., 2003). UC7251 was used as a donor strain and 29 bacterial strains as recipients (see Supplementary Table 3S). Briefly, 1 ml of a culture (OD600 = 0.8) of donor and recipient strains was passed through a 0.45µm filter (MF-Millipore Membrane Filters, Merck). After that, the filter was placed onto non-selective agar plates favoring the growth of recipient strains and incubated at 37 • C for 24 h. Conjugation with Bacillus, Enterococcus, Listeria, Pseudomonas, and Staphylococcus as recipient strains was carried out onto BHI (Oxoid), Clostridium on RCM (Oxoid), for lactobacilli, Pediococcus and Weisella onto MRS (Difco). After the respective incubation period, the cells were resuspended from the filter using a saline solution and were diluted in a 10-fold dilution series and enumerated by spread plating onto appropriate agar mediums. Transconjugant selection was performed using the selective conditions reported in Supplementary Table 3S. Transconjugant colonies were randomly selected and analyzed to check the presence or absence of the antibiotic resistance genes, by extracting the DNA using a microLYSIS kit (Microzone) and performing PCR with primers for tetracycline and erythromycin resistance genes (Supplementary Table 1S). The passage of potential plasmid-borne antibiotic resistance genes coding for aminoglycosides(aad6, aph3-IIIa, aadE, satA, ant(6)-Ia), and lincosamides (IsaE, LnuB) resistance was also tested by PCR using the primers listed in Supplementary Table 1S.

Multilocus Sequence Typing (MLST) Analysis
Allelic profiles and sequence types were derived by PubMLST (Jolley et al., 2018). The obtained ST was analyzed using Phyloviz and the goeBURST algorithm to compute a spanning forest graph to build the relatedness between isolates based on single locus variants (SLV) to identify clonal complexes (Francisco et al., 2012). Furthermore, given that the resolution of MLST is limited, core genome MLST (cgMLST) was also determined using the cgmlst.org website. This method uses an allele numbering system for a scheme of 1423 cgMLST target genes, which confers a higher level of discrimination (De Been et al., 2015).

Detection of Markers Relevant for the Assessment of Safety and Antibiotic Resistance Determinants
The strain UC7251 was screened for the hospital-associated genetic markers IS16, hylEfm, and esp by PCR, using primers previously listed. Strains U0317 and E980 were used, respectively, as positive and negative controls. The presence of the antibiotic resistance determinants coding for the phenotypical resistances observed in UC7251 was investigated by PCR using the primers reported in Supplementary Table 1S. The complete pbp5 gene was amplified, sequenced, and analyzed, as described before (Pietta et al., 2014), while the amplification of ermB, tetM, tetL, aph3-IIIa, satA, ant(6)-Ia, and aadE was performed, as described elsewhere (Jacob et al., 1994;Olsvik et al., 1995;Swenson et al., 1995;Sutcliffe et al., 1996;Trzcinski et al., 2000;Ouoba et al., 2008). Here, new primers aad6_F and aad6_R for aad6 screening, Lnu-B_F and Lnu-B_R for Lnu(B) screening, and IsaE_F and lsaE_R for Isa(E) screening were designed de novo using Primer3 (Untergasser et al., 2012), and the amplification reaction was run with the following conditions: initial denaturation at 95 • C for 2 min; 35 cycles at 94 • C for 40 s, 53 • C for 45 s, and 72 • C for 50 s; and extension at 72 • C for 5 min.

Genome Sequencing and Database Submission
A hybrid sequencing approach (short and long reads) was followed to complete the assembly of UC7251. Genomic DNA was extracted from the cultured bacterium with NucleoSpin Tissue (Macherey-Nagel, Germany). Short-read resequencing was performed with Illumina MiSeq, 250 paired-end after Nextera XT paired-end library preparation. Long read sequencing was performed with PacBio Sequel II SMRT sequencing. After trimming the sequences using trimgalore! (GitHub -FelixKrueger/TrimGalore), hybrid assembly was carried out using Unicycler (Wick et al., 2017). The finished genome was deposited on the NCBI under assembly accession No. ASM41165v2.

Bioinformatics Analyses
A total of 74 E. faecium complete genomes, including reference strains, were selected to carry out phylogenetic and taxonomic analyses in comparison with UC7251 (Supplementary Table 2S). Assembled genomes were downloaded from the NCBI in September 2021 and were subsequently annotated using Prokka (Seemann, 2014). Annotation results were then submitted to pangenome and core genome analyses using Roary (Page et al., 2015). The phylogenetic tree was constructed using RAxML-NG, V1.0.0 (Kozlov et al., 2019), and iTOL was used to visualize and organize the tree (Letunic and Bork, 2019). The genomes were also submitted to digital DNA-DNA hybridization (dDDH) using the genome-to-genome distance calculator (GGDC) (Meier-Kolthoff et al., 2013). Average nucleotide identity (ANI) analysis was performed using fastANI (Jain et al., 2018).
In silico investigation of UC7251 was performed using the bioinformatics software platform Geneious Prime v. 10.1. The Basic Local Alignment Tool (BLAST) from the NCBI was used to investigate the presence and identity of different genetic markers contributing AMR, VF, and MGE. The genome was interrogated for the presence of AMR genes using the Comprehensive Antibiotic Resistance Database (CARD) (Alcock et al., 2020) and ResFinder (Bortolaia et al., 2020). Ampicillin resistance was studied by evaluating the allelic variation in the strain of interest, against the reference sequence for PBP5-S/R profiles. Virulence markers were investigated according to the latest guidelines of EFSA (EFSA et al., 2018) using manual annotation, VirulenceFinder (Joensen et al., 2014), and VFAnalyzer . HGT determinants were analyzed through MobileElementFinder (Johansson et al., 2021) and IslandViewer 4 (Bertelli et al., 2017). In addition, integrative and conjugative elements were predicted using ICEberg 2.0 (Liu et al., 2019), which detects the signature sequences of the integrative modules and conjugation modules based on the profile hidden Markov models (profile HMMs). The origin of transfer site (oriT) was determined with OriTFinder (Li et al., 2018). Last, the genome was screened for the presence of sequences of phage origin with Prophage Hunter (Song et al., 2019) and CRISPR-Cas sites using CRISPR-CasFinder (Couvin et al., 2018).

Isolation and Characterization of MDR E. faecium UC7251 From RTE Food
In the framework of risk assessment of MDR in ready-to-eat foods, UC7251 was isolated from a dry fermented sausage at a count of 3 x 10 5 CFU g-1 and identified as Enterococcus faecium by species-specific amplification of the ddl gene. This strain was resistant to ampicillin, streptomycin, kanamycin, erythromycin, clindamycin, tylosin, and tetracycline and presented an MIC higher than the cutoff values defined by EUCAST and EFSA ( Table 1). PCR analyses, using a pool of primer pairs targeted to the most common AMR genes found in enterococci (Supplementary Table 1S), identified the genetic determinants for these resistances. E. faecium UC7251 was identified as a MDR strain and harbored genes coding for aminoglycoside-modifying enzymes, three genes for macrolide resistance and two genes responsible for tetracycline resistance. Moreover, the sequence of the amplicon targeted to penicillin-binding protein 5 (PBP5), involved in β-lactams resistance, demonstrated that this strain showed the pbp5-S1/R20 allelic profile, conferring resistance to ampicillin (Galloway-Peña et al., 2011). E. faecium showed to be intrinsically resistant to low levels of ampicillin through cell wall synthesis protein complex PBP; pbp5 is part of this operon, and sequence variations allow to differentiate the two groups of E. faecium according to the allelic profile and expression levels (Pietta et al., 2014). Within the context of a study focusing on the detection of ampicillin-resistant E. faecium in ready-toeat fermented foods, a strain that presented resistance toward ampicillin with a MIC value of 64 µg/ml and carried the hybrid allelic profile PBP5-S1/R20 is of concern for the consumers' safety. It has been demonstrated that pbp5 may spread through horizontal gene transfer and specifically that pbp5 of resistant isolates was located on transferable chromosomal regions, which suggested its dissemination to the environment (Morroni et al., 2019).

Whole-Genome Sequence Analyses
UC7251 was submitted to genome sequencing following a hybrid approach using long-and short-read sequencing technology (GenBank assembly accession numbers for chromosome CP084886.1, plasmid pUC7251_1 CP084887.1, plasmid pUC7251_2 CP084888.1). The assembly of the genome of UC7251 built a total of 3 contigs, predicted as a 2.6 Mb chromosome and two plasmids, pUC7251_1 and UC7251_2 (192 kb and 1.9 kb, respectively). The presence of the two plasmids was also distinguished by total DNA extraction and pulsed-field gel electrophoresis (PFGE) (data not shown). The annotation of UC7251 resulted in 2662 coding sequences (CDS), of which 27% are hypothetical proteins and 73% have known functional assignments. It also contained genes coding for 18 rRNAs (six copies each of 23S rRNA, 16S rRNA, and 5s rRNA), 69 tRNAs, and 1 tmRNA. Compositional analysis resulted in 17 genomic islands (GIs), three active prophage sequences, and several VF and AMR genes distributed throughout the chromosome and plasmidome. Regarding mobile genetic elements, two mobile regions were predicted on the chromosome and one on pUC7251_1 (Supplementary Table 4S).
pUC7251_1 is a mobilizable megaplasmid as predicted by Plascad. According to OriTfinder, the origin of replication is 39 bp long and showed homology with oriT_pUB110. There are no predicted T4SS proteins and only one T4CP protein on locus tag UC7251_02595. The relaxase MobM is found on locus tag UC7251_02679. Mobilizable plasmids carry their own oriT and relaxase gene but lack genes required for T4SS formation and can therefore be transferred to cells that carry elements encoding a compatible T4SS (Guédon et al., 2017). This plasmid showed homology with plasmids pF88_1 (identity 83%), p17-318_1 (identity 83%), pE843-TC-299 (identity 82%), and pE843-171 (identity 80%). The first three are VSE-MDR plasmids carried by E. faecium strains of clade A2. These strains were isolated from environmental (pF88_1) and human samples (p17-318_1 and pE843-TC-299). The fourth plasmid, pE843-171, is carried by Enterococcus lactis E843, and it is characterized as VSE-MDR (Shan et al., 2022). According to these results, pUC7251_1 holds unique traits, and although the prevalence of VSE-MDR is high, none of the results on BLAST showed VSE-MDR from food origin. UC7251_2 harbors a single open reading frame that codes for a rolling circle REP (rep14a). Small plasmids of such size were also found in other E. faecium isolates, making it a common genomic feature.

Phylogenomics and Population Structure Show That Foodborne UC7251 Is Neighboring HA Isolates
For phylogenomic evaluation, UC7251 was compared with the other selected 74 E. faecium genomes (Figure 1). The interrogation of the pangenome has been recently regarded as a useful tool for species delimitation based on the identification of lineage-specific gene sets (Moldovan and Gelfand, 2018). Observing the distribution of core and accessory genomes of our analysis, isolates of clade A1 and, to a smaller extent, clade A2 have a high variability in their accessory genes. A highly variable accessory genome is conferred by the fact that E.
faecium has an open pangenome and therefore a higher genomic diversity (Lebreton et al., 2013). The adaptation of E. faecium to specific environmental factors, such as antimicrobial pressure, has increased the genomic diversity through horizontal gene transfer, genome rearrangement, and gene loss (Bonacina et al., 2017). Pangenome and core genome analyses uncovered an open pangenome, with a core genome consisting of 9.5% and an accessory genome of 90.5%. In this context, UC7251 contains 33 unique genes, mainly insertion sequences and hypothetical proteins located on the chromosome and on pUC7251_1. Transposases belonging to IS3, IS30, and IS256 families were detected as unique on both pUC7251_1 and chromosome. On the chromosome, we found unique gene arnB, which catalyzes the conversion of UDP-4-keto-arabinose to UDP-4-amino-4deoxy-L-arabinose. The modified arabinose is attached to lipid A and is required for resistance to polymyxin in Gram-negative bacteria (Lee and Sousa, 2014). Moreover, unique genes epsM and epsL coding for putative acetyltransferase and sugar transferase, respectively, were detected. They are involved in the production of the exopolysaccharide (EPS) component of the extracellular matrix during biofilm formation (Agius et al., 2021). Gene cbh_2, choloylglycine hydrolyse, catalyzes the de-conjugation of bile acids (Chand et al., 2018). In Enterococcus, bile salt hydrolase activity has a hypo-cholesterolemic effects on animal and human hosts, conferring probiotic properties (Singhal et al., 2019).
The population structure and location of UC7251 were also evaluated using MLST. The genome was submitted to PubMLST, and it was assigned to ST673. The latter clusters together with the clonal group of ST117, which is known to be a part of CC17 meroclone (Figure 1). Published data on PubMLST showed a unique isolate harboring ST673, which contains a strain from a non-hospitalized person collected in Spain in 2010. The MLST global scheme shows that UC7251, as other isolates from animal origin, belonged to hospital-associated clades (Gouliouris et al., 2018). Thus, E. faecium from CC17 have been also previously recovered from swine, poultry, and cow samples (Freitas et al., 2011;Werner et al., 2012;Getachew et al., 2013). The use of cgMLST, a clustering based on 1423 target genes of the core genome, indicated that UC7251 belonged to the unique cluster type CT745.
Subspeciation of E. faecium has been also studied considering the defense mechanisms against HGT, such as CRISPR-Cas systems and R-M systems (Koonin et al., 2017). CRISPR-Cas systems constitute endogenous barriers to HGT, and as a consequence, the presence of increased MGEs is associated with the complete absence or partial sequences of CRISPR-Cas systems (dos Santos et al., 2020). This has been observed in UC7251, where no complete CRISPR-Cas systems were detected. Differently, UC7251 carries, a type I R-M system with the allelic variations typical of clade A1 isolates, polymorphisms that are used for clade classification of E. faecium (Huo et al., 2019).

Antimicrobial Resistance Profile and Mobilome
Several AMR genes were detected on both the chromosome and pUC7251_1 ( Table 2). The intrinsic determinant coding for aminoglycoside 6 ′ -acetyltransferase enzyme (aac(6 ′ )-II), typical of E. faecium species (Chow, 2000), was found on the chromosome, together with the liaFSR operon, implicated in cell membrane-targeting lipopeptide antibiotic daptomycin (DAP) resistance. In previous studies, E. faecium isolates showed susceptibility and resistant allelic profiles of DAP (DAP-S and DAP-R, respectively) (Panesso et al., 2015); UC7251 harbors the complete liaFSR system with the DAP-S allelic variation. Interestingly, the occurrence of DAP resistance is inversely related to increased susceptibility to β-lactams, consistent with the ampicillin resistance in UC7251 (Diaz et al., 2014).
Genome sequencing and assembly following a hybrid approach elucidated various details about UC7251 mobilome, crucial to understand the AMR mechanisms in this food isolated strain. A total of two mobile regions were predicted on the FIGURE 1 | Maximum likelihood phylogenetic tree constructed using the core genome alignment of the selected 75 genomes and respective MLST and clonal complexes. E. faecium clade A1 strains are marked with red branches, clade A2 strains marked with blue, and clade B strains with green. Strain UC7251 (pointing arrow and text in red) is grouped among clade A2 isolates and belongs to ST673 part of CC117.
Frontiers in Microbiology | www.frontiersin.org chromosome. Region 1 is classified as a putative integrative and mobilizable element (IME) with an insertion site and attachment sites and no detected origin of transfer (oriT). Proteins T2SSE, T4CP, and VirB3 are also present within this region. T4CPs are phylogenetically and structurally associated with FtsK and SpoIIIE ATPases and the ability of translocating single-stranded DNA. Furthermore, type IV secretion protein VirB3 is an inner membrane protein and requires VirB4, VirB7, and VirB8 for stabilization (Álvarez-Rodríguez et al., 2020). The IME contains several carbohydrate metabolism genes, suggesting acquired mechanisms for survival in environmental conditions. Region 2 is classified as an integrative and conjugative element (ICE), including oriT, insertion, and attachments sites. Additionally, it harbors T4SS machinery, integrase, relaxase, and putative transposon Tn916. Tn916 is a well-described conjugative element that mediates tetracycline resistance (tetM) gene exchange principally among Gram-positive bacteria (Devirgiliis et al., 2009). In the same molecule, we found several inactive (score < 0.50), 2 ambiguous (score 0.5-0.79), and one putatively active (score >0.80) prophage sequences, according to the scores attributed by Prophage Hunter software. The active prophage candidate showed the closest homology to Halocynthia phage JM-2012 (identity of 78%). This phage is classified as a "jumbo" bacteriophage from the Myoviridae family, initially identified within marine Vibrio cyclitrophicus (Lavysh et al., 2016). Limitations of the database of the phage prediction tool may interfere with the estimation of the closest related phage. Phages from the Myoviridae family have been already identified in Enterococcus spp., making it a common feature within enterococci (Duerkop et al., 2014). Furthermore, pUC7251_1 harbors a large ICE-like gene (91 kb), with a total of four genomic islands (GIs) within (Figure 2). In detail, multiple AMR genes are found within GI2, GI3, and GI4 converting them in antibiotic resistance islands (ARI). ARI1 harbors against aminoglycoside coded by genes aph(3')-IIIa, satA, and ant(6')-Ia, found from UC7251_02667 to UC7251_02669. Interestingly, the insertion sequence IS1216E is found flanking this region. IS1216 is an enterococcal IS associated with resistance toward aminoglycosides, tetracyclines, macrolides, and glycopeptides in Gram-positive bacteria (Partridge et al., 2018). IS1216 has been identified as a vector for inter-plasmid recombination and dissemination of multi-drug elements in enterococci. Moreover, it has been found that IS1216 is responsible for passing vancomycin resistance with the help of transposon Tn1546 (Lin et al., 2020). Erythromycin resistance coded by ermB is found next to this region, and adjacently, the gene tetL is found next to relaxase MobM and the origin of transfer. It was reported that MobM has a dual role in autoregulation and initiation of transfer of plasmids or integrative mobilizable elements to other MGE members (Lorenzo-Díaz et al., 2018). Contiguous to this section, linezolid resistance genes LnuB and IsaE are found flanked by ISEfa5, which is typically found with a high copy number in E. faecium strains. According to a previous study, it is suggested that ISEfa5 may be contributing significantly to the genomic flexibility of the species with evidence of frequent integration and excision events (Bayjanov et al., 2019). Additional studies have investigated that plasmids harboring linezolid resistance genes acquired from other enterococcal plasmids through MGE are associated with the MDR phenotype (Sadowy, 2018;Elghaieb et al., 2020). Conjugation of these genes was also evidenced from Enterococcus to Staphylococcus, elucidating their transmission potential (Yan et al., 2021). ARI3 carries two genes coding for aminoglycoside resistance ant1, apt_3, and ant(6)-Ia, flanked by a putative recombinase and IS4 family transposase ISDha5. IS4 family transposases are typically found among important clinical lineages in E. faecium (Mikalsen et al., 2015). The presence of the complete operon for bacitracin resistance bcrABDR was found inside ARI4 flanked by IS1485. This is congruent with other studies suggesting the presence of this operon in swine isolates as it is used for prophylaxis and therapy in food animals. The plasmid co-location of this locus and other resistance gene clusters might accelerate their dissemination (Wang et al., 2015). Regarding prophage sequences, pUC7251_1 presented two sequence fragments with high homology (score > 0.8) to known prophage sequences, classified as active. These prophages show a high identity with Staphylococcus phage SP beta-like and Streptococcus phage phiJH1301-2 prophage sequences, genetic elements that are common in clade A1 isolates (Lisotto et al., 2021). The annotated genes for both prophage sequences code mainly for transposases and integrases, as well as RelE/ParE toxin/antitoxin systems. Additionally, three ambiguous and four inactive prophage sequences were detected. Interestingly, linezolid resistance genes IsaE, LnuB, and bacitracin resistance operon bcrABDR were predicted to be within inactive prophage sequences. Recent studies have elucidated the role of phages in HGT of AMR genes as they are often carried in prophage sequences and stably inherited in the host genome-carrying antibiotic-resistant determinants (Kondo et al., 2021). Inactive or defective phages, although categorized as non-functional, still may carry out important activities and functions like transposition and excision (Mitchell, 2014).
Copper resistance operon tcrYAZB was also found on an inactive prophage sequence. The swine industry is well-known for using copper as a feed additive. The presence of heavy metal resistance genes is a matter of concern also because of possible co-resistance with antibiotics (EFSA FEEDAP Panel, 2016; Ahmed and Baptiste, 2018). The genetic system of this phenotypic resistance is coded by the tcrYAZB operon, which enhances bacterial survival and plasmid maintenance against high concentrations of this heavy metal (Rebelo et al., 2021). After genomic identification of copper resistance, we performed a susceptibility test to determine the MIC value, which resulted in 16 mM, a level typical of high copper resistance. The mobility of this operon was evidenced by flanking IS1216E and IS1251, which are highly associated within vanA-type plasmids (Wongnak et al., 2021). A study by Silveira et al. (2014) elucidated the presence of copper resistance genes with co-occurrence of antibiotic resistance genes. Other heavy metal resistance genes were found in pUC7251_1. Zinc chloride, oxide, or sulfate compounds are currently approved in the EU (up to 2500 ppm) and used as additives in piglet feed (Murphy et al., 2017). Similar to copper, some regulatory genes and resistance mechanisms of Cu with known links to antibiotic resistance are also zinc-responsive (Poole, 2017). UC7251 has an MIC to Zn of 16 mM and harbors gene zosA, observed also in B. subtilis for facilitating homeostasis to Zn (Argudín et al., 2019). Moreover, resistance to Cd was also determined phenotypically at 2 mM and genotypically by identifying genes cadA, cadC, and cadD. The cad operons are typically found in Staphylococci carried by MGEs like plasmids and chromosomal cassettes and co-located with antibiotic resistance genes. Specifically, cadAC is known for conferring high resistance levels to Cd, and it has been also reported to be present in other bacteria like Lactococcus lactis, Streptococcus spp., and Listeria monocytogenes (Argudín et al., 2019). Furthermore, resistance to Hg was conferred by two genes merA and merR. In general, resistance to Hg, is given by a set of genes clustered at the mer operon (merRTPADE) and highly linked to AMR genes and MGEs (Argudín et al., 2019). The lack of the complete operon is also confirmed by the low levels of resistance determined by MIC testing, which was of 50 µM. Genes coding for resistance to Cu, Cd, Zn, and Hg carried by plasmids has been already observed in the plasmidome of other pig isolates (Wist et al., 2020).

Conjugation Experiments Suggest AMR Gene Transfer by Insertion Sequences
The MDR profile of UC7251 endorsed further evaluation of transmissibility of AMR genes, and we focused on tetracycline resistance coded by two genes on Tn916 and pUC7251_1 and the plasmid encoded erythromycin resistance. This was tested through conjugation experiments where gene exchange was demonstrated at inter-and intra-generic levels ( Table 2  and Supplementary Table 3S). Filter mating experiments demonstrated that tetracycline resistance was transferred from UC7251 to E. faecalis OG1rf, L. innocua L7, L. monocytogenes DSM 15675, S. aureus UC7180, and L. rhamnosus UC8647, with frequencies of transconjugants per donors varying from 6 x 10-3 to 5,7 x 10-6 CFU/ml. No gene transfer was observed toward Gram-negative species. The transfer of the tetM gene was confirmed by PCR assays, whereas tetL was absent in all tetracycline-positive transconjugants. The transfer of the tetM gene was found to be carried by chromosomal transposon Tn916 from E. faecalis. This operon was predicted in chromosomal locus UC7251_02362-02376. The nucleotide identity between the 18,032-bp sequence of Tn916 of UC7251 and E. faecalis (Genbank Accession No. U09422.1) sequences was of 99.97%.
It has been discovered that the presence of subinhibitory concentrations of specific classes of antibiotics can trigger the mobility of Tn916 as it has a broad inducibility of antibiotic resistance genes, implying that the dissemination of resistance genes is not necessarily linked to their selective pressure (Scornec et al., 2017).
No gene transfer for the genes coding for erythromycin resistance was observed, consistently with the characteristics of pUC7251_1, a mobilizable but non-conjugative plasmid lacking the complete conjugation apparatus.

Virulence Markers in the UC7251 Genome Show a Collection of Colonization Facilitators
The complete assembly and annotation of UC7251 genome allowed investigation of the presence of putative virulence markers ( Table 3). Adherence is an essential step in bacterial pathogenesis, required for colonization and attachment, and it is therefore considered a type of virulence marker. When scrutinizing the genome of UC7251, several microbial surface components, recognizing adhesive matrix molecules (MSCRAMMs) including LPXTG family cell wall-anchored surface proteins as well as fimbriae proteins such as pili, were identified. It is important to denote the presence of genes acm (cell wall-anchored collagen adhesin) and scm (second collagen adhesin). These proteins enhance initial adherence in vivo and interact with extracellular matrix components. Other genes associated with adhesion, efaA (E. faecium surface protein) and sagA (secreted antigen A), were detected. A novel class of cell surface proteins coded by WxL operon, found in clade A E. faecium isolates, with a functional role in virulence associated with endocarditis pathogenesis and bile salt resistance, was previously investigated (Galloway-Peña et al., 2015). The coding genes swpA (small WxL protein A), swpB (small WxL protein B), and swpC (small WxL protein C) were found in UC7251. Additionally, malR, a maltose-binding transcriptional regulator that increases biofilm production in the presence of this specific carbohydrate, was detected. Pili associated proteins, previously described as pilin gene clusters (PGC-1, PGC-2, PGC-3, PGC-4) (Freitas et al., 2018) were identified. PGC-1 is composed of the genes fms20 and fms21; both are present along with a sortase A. This loci/operon is located between UC7251_02853 and UC7251_02588 in pUC7251_1. In addition, PGC-3 was found with 100% of nucleotide identity containing the endocarditis and biofilm-associated pili genes ebpA, ebpB, and ebpC accompanied by srtC (sortase) and flanked by IS1216E. This region is encompassed from UC7251_02583 to UC7251_02589 in the chromosome. The PGC-4 cluster is incomplete, lacking operon fms11-19-16 and PGC-2-associated genes fms14-17-13. UC7251 does not express the capsular polysaccharide, presenting the capsule operon polymorphism CPS type 1 (Hufnagel et al., 2004), and does not harbor cytolysin (Top et al., 2008) and BoNT/En toxin, a botulin-type toxin found in a single strain of E. faecium (Zhang et al., 2018). E. faecium UC7251 lacks the putative HA virulence markers as defined by EFSA (EFSA et al., 2018) and  does not harbor the complete operons coding pili-associated proteins, which is typical of clade A1 isolates.

CONCLUSION
The presence of multi-drug resistant strains in ready-to-eat fermented food represents a risk of public health for the spread of AMR determinants in the food chain and in the gut microbiota of consumers. In silico bioinformatics evaluations derived from genomic data permitted to accurately assess the safety of UC7251, a strain of E. faecium clade A2 which does not carry virulence factors typical of HA strains but presents the co-location of several antimicrobial resistance genes with heavy metal resistances on the mobilizable plasmid pUC7251_1 and the conjugative transposon Tn916. This work emphasizes the importance of a surveillance for the presence of AMR bacteria in food, with particular attention to fermented RTE foods. Moreover, the presence of MDR strains carrying mobile AMR genetic elements incites the development of innovative strategies for the mitigation of the risk related to antimicrobial resistance diffusion in food.

DATA AVAILABILITY STATEMENT
The datasets presented in this study can be found in online repositories. writing-review and editing. DB: writingreview and editing, visualization, and supervision. PC: conceptualization, writing-review and editing, validation, visualization, supervision, and project administration. All authors contributed to the article and approved the submitted version.

FUNDING
This work was partially funded by the PRIMA programme, under BioProMedFood project (Reference  Number: 2019-SECTION2-4; CUP: J34I19004820005). The PRIMA programme was supported by the European Union H2020 programme and innovation programme.