Whole genome sequencing snapshot of multi-drug resistant Klebsiella pneumoniae strains from hospitals and receiving wastewater treatment plants in Southern Romania

We report on the genomic characterization of 47 multi-drug resistant, carbapenem resistant and ESBL-producing K. pneumoniae isolates from the influent (I) and effluent (E) of three wastewater treatment plants (WWTPs) and from Romanian hospital units which are discharging the wastewater in the sampled WWTPs. The K. pneumoniae whole genome sequences were analyzed for antibiotic resistance genes (ARGs), virulence genes and sequence types (STs) in order to compare their distribution in C, I and E samples. Both clinical and environmental samples harbored prevalent and widely distributed ESBL genes, i.e. blaSHV, blaOXA, blaTEM and blaCTX M. The most prevalent carbapenemase genes were blaNDM-1, blaOXA-48 and blaKPC-2. They were found in all types of isolates, while blaOXA-162, a rare blaOXA-48 variant, was found exclusively in water samples. A higher diversity of carbapenemases genes was seen in wastewater isolates. The aminoglycoside modifying enzymes (AME) genes found in all types of samples were aac(6’), ant(2'')Ia, aph(3'), aaD, aac(3) and aph(6). Quinolone resistance gene qnrS1 and the multi-drug resistance oqxA/B pump gene were found in all samples, while qnrD and qnrB were associated to aquatic isolates. The antiseptics resistance gene qacEdelta1 was found in all samples, while qacE was detected exclusively in the clinical ones. Trimethroprim-sulfamethoxazole (dfrA, sul1 and sul2), tetracyclines (tetA and tetD) and fosfomycin (fosA6, known to be located on a transpozon) resistance genes were found in all samples, while for choramphenicol and macrolides some ARGs were detected in all samples (catA1 and catB3 / mphA), while other (catA2, cmIA5 and aac(6’)Ib / mphE and msrE) only in wastewater samples. The rifampin resistance genes arr2 and 3 (both carried by class I integrons) were detected only in water samples. The highly prevalent ARGs preferentially associating with aquatic versus clinical samples could ascribe potential markers for the aquatic (blaSHV-145, qacEdelta1, sul1, aadA1, aadA2) and clinical (blaOXA-1, blaSHV-106,blaTEM-150, aac(3)Iia, dfrA14, oqxA10; oqxB17,catB3, tetD) reservoirs of AR. Moreover, some ARGs (oqxA10; blaSHV-145; blaSHV-100, aac(6')Il, aph(3')VI, armA, arr2, cmlA5, blaCMY-4, mphE, msrE, oqxB13, blaOXA-10) showing decreased prevalence in influent versus effluent wastewater samples could be used as markers for the efficiency of the WWTPs in eliminating AR bacteria and ARGs. The highest number of virulence genes (75) was recorded for the I samples, while for E and C samples it was reduced to half. The most prevalent belong to three functional groups: adherence (fim genes), iron acquisition (ent, fep, fyu, irp and ybt genes) and the secretion system (omp genes). However, none of the genes associated with hypervirulent K. pneumoniae have been found. A total of 14 STs were identified. The most prevalent clones were ST101, ST219 in clinical samples and ST258, ST395 in aquatic isolates. These STs were also the most frequently associated with integrons. ST45 and ST485 were exclusively associated with I samples, ST11, ST35, ST364 with E and ST1564 with C samples. The less frequent ST17 and ST307 aquatic isolates harbored blaOXA-162, which was co-expressed in our strains with blaCTX-M-15 and blaOXA-1.

Introduction Antibiotic resistance (AR) is presently considered one of the most serious global public health threats, with the potential to become significantly more problematic by 2020 [1] due to globalization, environmental, social and demographic changes and health system capacity [2]. One of the priority topics endorsed by WHO (Word Health Organization) and JPIAMR (The Joint Programme Initiative on Antimicrobial Resistance) for tackling AR is to determine the role played by the environment in the selection and dissemination of AR [3,4]. Wastewater treatment plants (WWTPs) have been recently suggested to be hotspots providing the perfect environment for the enrichment, recombination and selection of AR "super-bugs" which could eventually be discharged and subsequently impact adversely the environment and human health, thus highlighting the necessity for strategies of water quality improvement [5].
In 2018, a national consortium composed of the important Romanian institutions involved in water quality control and epidemiology of AR started the RADAR project, aiming to investigate the dynamics of AR and antibiotic resistance genes (ARGs) in ESKAPE pathogens (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumanii, Pseudomonas aeruginosa and Enterobacter sp.) isolated from clinical and wastewater samples [6].
Here we report results of a RADAR sub-study aiming the genomic characterization of carbapenem resistant and extended spectrum β-lactamase (ESBL)-producing K. pneumoniae isolates from the influent and effluent of three WWTPs compared to clinical isolates obtained from Romanian hospital units which are discharging the wastewater in the sampled WWTP influent in order to evaluate the contribution of WWTPs to the AR reservoir and to reveal potential transmission between the water and clinical compartments. The main reasons to choose K. pneumoniae is the high prevalence of infections with K. pneumoniae strains resistant to carbapenems (22.5%), 3 rd generation cephalosporins (62.55%) and multidrug resistant-MDR (55.4%) reported in Romania [7]. Moreover, the hospital effluents are often released in the urban WWTP influent, increasing the risk of antibiotic resistant bacteria to be disseminated in the environment. However, the epidemiology of resistant K. pneumoniae clinical strains in WWTPs in Romania is currently unknown. Moreover, K. pneumoniae is a good indicator of the transmission between clinical and environmental AR reservoirs, being an ubiquitous microorganism found in soil, surface water and on plants [8], but also one of the most important Gram-negative opportunistic pathogens, frequently associated with both hospital and community acquired severe infections. [9,10]; Moreover, K. pneumoniae could cumulate resistance (e.g. MDR, carbapenemase production) and hypervirulence (e.g. hypermucoviscosity) features could generate a new clinical crisis [11,12,13]. Isolation and characterization of K. pneumoniae strains. The analysed K. pneumoniae strains were isolated from influent and effluent water samples collected in sterile glass sample containers, transported to the laboratory at 5±3˚C and processed within less than 24 hours. The water samples were diluted and filtered through 0.45 μm pore size membrane filters (Millipore, France), as described in SR EN ISO 9308-2/2014 (for coliform bacteria), using the following antibiotic-enriched media (BioMérieux, France): ChromID ESBL agar for extended spectrum beta-lactamases (ESBL)-producing Enterobacteriaceae and non-Enterobacteriaceae strains, ChromID OXA-48 agar and ChromID CARBA agar for carbapenemase (CRE)-producing Enterobacteriaceae. The resistant colonies obtained after cultivation at 37˚C for 24 hours in aerobic conditions were subsequently inoculated on the selective media for the confirmation of the beta-lactam resistance phenotype. A total of 178 K. pneumoniae wastewater strains were recovered from the antibiotic-enriched media and identified using the MALDI--TOF-MS Bruker system: 96 from the influent and 82 from the effluent. The study also included 17 strains isolated during the same period from patients hospitalized in the clinical units discharging the wastewater in the sampled WWTPs. The antibiotic susceptibility profiles of K. pneumoniae strains were determined using the standard disc diffusion method according to The Clinical & Laboratory Standards Institute (CLSI) 2018 guidelines [14]. The antibiotics tested were: ampicillin (AMP), piperacillin (PRL), amoxicillin-clavulanic acid (AMC), aztreonam (ATM), meropenem (MEM), imipenem (IMP), ertapenem (ETP), cefuroxime (CXM), cefoxitin (FOX), ceftriaxone (CRO), cefepime (FEP), gentamicin (GEN), amikacin (AMK), tetracycline (TET), trimethoprim-sulfamethoxazole (SXT), ciprofloxacin (CIP).

Selection of K. pneumoniae strains for sequencing analyses.
From the total of 195 K. pneumoniae water and clinical strains, 47 strains (of which 18 from influent, 16 from effluent and 13 from clinical settings) were selected for sequencing. The water strains were selected to include all three geographical areas, both influent and effluent strains and isolates recovered from all three chromogenic media, i.e. ChromID ESBL agar (8 strains), ChromID OXA-48 (10 strains) and ChromID CARBA (18 strains) (S1 Table). The 13 clinical strains were selected from individual ESKAPE isolates collected during one month prior to wastewater collection in the three hospitals. The clinical strains displaying highly similar or identical resistance phenotypes with the water strains isolated from the same geographical area were given priority.

Next generation sequencing (NGS) setup
Bacterial DNA was extracted using DNeasy UltraClean Microbial Kit (Qiagen) and an inhouse protocol based on mechanical and chemical bacterial lysis followed by DNA precipitation with ethanol. The Nextera DNA Flex Library Prep Kit (Illumina) was further used according to the manufacturer recommendations. Before sequencing, the DNA pool libraries were checked for optimal quality (2100 Bioanalyser, Agilent) and quantity (Qubit 4 Fluorimeter, Thermo Fisher Scientific). Forty-seven bacterial isolates were sequenced on the Miseq platform (Illumina) by using the paired-end shotgun strategy and Miseq reagent kit v.3 (600 cycles). This ensures the highest output of all MiSeq kits and generates sequences up to 300 bp long.

Bioinformatics setup
K. pneumoniae whole genome sequences were analyzed using an NGS bioinformatics pipeline which runs on a Conda environment under Linux. Relevant information was extracted from NGS data by following the next steps: 1. The raw MiSeq Illumina pair-end (PE) reads were trimmed of the adaptor sequences using BBDuk program from the BBTools suite [15]; 2. The trimmed reads were assembled using SPAdes de novo assembler [16]; 3. Average Nucleotide Identity (ANI) was applied using the FastANI program [17] on the resulting scaffolds from SPAdes, in order to double-check the species against the K. pneumoniae complete assembled reference genomes downloaded from NCBI; 4. Antimicrobial resistance and virulence genes were identified in the de novo assembled scaffolds using the ABRicate program [18] to query the NCBI Bacterial Antimicrobial Resistance Reference Gene Database and the Virulence Factors database (VFDB), respectively. Plasmid replicon types were determined using the Plas-midFinder (implemented in ABRicate) [ The manipulation of the genomic information extracted from the MLST, resistance and virulence gene predictions, as well as plotting the resulting data was performed and computed in Excel, with the use of pivot tables and built-in functions.
The data have been filtered based on the extraction sites of the samples, on the number of wastewaters or clinical samples, on the MLST and based on the most important classes of antibiotic resistance and virulence genes.
The assembled sequences have been deposited in GenBank with Bioproject ID: PRJNA579879.

Antibiotic susceptibility testing
Out of the total of 178 K. pneumoniae strains recovered from the antibiotic-enriched media: 96 from the influent and 82 from the effluent, 34 water strains (18 from influent and16 from effluent) were selected for whole genome sequencing. The water strains have been recovered from chromogenic media, i.e. ChromID ESBL agar (8 strains), ChromID OXA-48 (10 strains) and ChromID CARBA (18 strains) (S1 Table). The in vitro antibiotic susceptibility profiles of the sequenced K. pneumoniae isolates confirmed the expected resistance phenotypes of the strains recovered from the ChromID ESBL agar (i.e. resistance to at least 3 rd generation cephalosporins) and ChromID OXA-48 and ChromID CARBA (i.e. resistance to at least one carbapenem). A number of 13 clinical strains isolated from the three hospitals on culture media currently used in the respective clinical settings has been included in the study (S1 Table). The great majority of the strains selected for sequencing were MDR (S1 Table).

Antimicrobial susceptibility profiles of the analysed strains
The antibiotic susceptibility assay of the tested strains has revealed that 92.30% of the clinical strains, and 87.5% and 82.3% respectively from the strains isolated from the WWTP effluent and influent were MDR. The clinical strains exhibited 92.30% resistance to AMP, PRL, ATM, FEP, and over 70% resistance to CXM, CIP, TET, SXT. The WWTP influent strains were 100% resistant to AMP, PRL and FEP and over 80% resistant to AMC, CXM, CRO, ATM, IMP, MEM, ETM, CIP, SXT, while the WWTP effluent strains were 100% resistant to AMP, SXT and over 80% resistant to PIP, AMC, CXM, FEP, ETP, ATM and CIP (S1 Table).

Antimicrobial resistance genes (ARGs) distribution
The most prevalent ARGs detected in the 47 K. pneumoniae isolates selected for analysis (18from influent, 16 from effluent and 13 from clinical samples) were as follows: a. In influent samples, the ARGs with prevalence >50% (n = 12, in decreasing order) are those which confer resistance to aminoglycosides and beta-lactams:  Table).
b. In effluent isolates, of the highly prevalent ARGs (n = 12), eight were similar to those found in the influent samples, i.  Table).
Among the quinolone resistance genes, qnrS1 was detected in all three types of samples from Bucharest, but was predominant in influent and effluent isolates. The qnrD (qnrD1) was detected exclusively in influent, while in the effluent samples the qnrB alleles were predominant. To these, the presence of the oqxA/B efflux pump, also responsible for resistance to antiseptics could explain the fluoroquinolone resistance. The most frequent antiseptics resistance genes were oqxA/B, followed by qacEdelta1, detected both in clinical and wastewater isolates and, with a much lower frequency, qacE, detected exclusively in clinical samples (Fig 3).
ARGs for other classes of antimicrobial substances were also identified: for SXT were represented by dfrA, sul1 and sul2, for tetracyclines by tetA and D, for choramphenicol by catA1 and catB3 (detected in all three types of samples), cat2, cmIA5 and aac(6')Ib (only in aquatic samples), for fosfomycin, by fosA (detected in all three types of samples), for macrolides by mph(A) (detected in all three types of samples) and mphE and msrE (only in wastewater samples) and for rifampin by arr2 and 3, detected only in water samples (Fig 4).

MLST distribution
Variations in MLST distribution among the three sample sets were observed and correlated both with geographical location and the sampling site (influent, effluent and clinical samples).
A total of 14 STs were identified in the K. pneumoniae strains analysed in this study. ST101 is the most prevalent clone (n = 13) closely followed by ST258 (n = 10). ST219 and ST395 have an equal prevalence (n = 5); ST307 (n = 3), ST1878 and ST17 (n = 2) have a low prevalence, while the following STs were identified only once: ST 219 like, ST45, ST485 only in influent (6%), ST11, ST35, ST364 only in effluent (6%) and ST1564 exclusively in the clinical isolates (S1 Fig). The ST with the highest prevalence, ST101, was mostly identified in the clinical isolates (54%), while the second most prevalent one, ST258, was found in only 8% of the clinical isolates and 28% and respectively 25% of the influent and effluent isolates. Only ST395 was found in all sampling points, but identified most frequently in the effluent (19%). ST219 and ST1878 were isolated from influent (22%/6%) and effluent samples (6%/6%) while ST307 from clinical (15%) and effluent (6%) samples. The most frequently encountered STs, i.e. 101, 258 and 219 were also among the ones in which class I integron sequences were most frequently detected (Fig 5).
The highest number of virulence genes (n = 75) was found in the influent strains, while those detected in the effluent and clinical samples were lower by about 40% and 50% respectively (S3 Table).

Discussions
Among the European countries, Romania is experiencing one of the highest rates of AR as revealed by the most recent data reported to EARSS (European Antimicrobial Resistance Surveillance System). The WWTPs are aquatic environments characterized by high-level selective pressure exerted by antibiotics and other chemical pollutants (such as heavy metals, drugs, metabolites); therefore, the comparative analysis of WWTPs and clinical isolates related in time and space could reveal trends of ARGs transmission and dissemination among the clinical and aquatic environment compartments. In this context, the RADAR national project has as a main goal to provide useful information and tools for bridging AR concerns in the hospital and the aquatic environment in Romania.
The main purpose of the current sub-study performed within the frame of RADAR project was to use WGS data for assessing the relatedness between clinical and environmental betalactam resistant K. pneumoniae isolates that could indicate the flow of ARGs from the hospital towards the environment and the reverse and thus providing a better understanding of the role of WWTP as an AR reservoir. The WGS data were obtained on K. pneumoniae isolates from three locations in southern Romania.
The strains isolated from Bucharest proved, as expected, a much higher rate of AR and diversity of ARGs and STs (S1 Fig) as compared to the other two geographical locations. This could be explained by the fact that the receiving WWTP from the capital city is much larger than those from Târgovişte and Galaţi. Moreover, Bucharest is by far more industrialized (therefore a higher selective pressure from pollutants can be expected inside WWTP, favouring the enrichment, recombination and selection of AR). The pathology in the Bucharest hospital unit is more diverse and more severe-cases from throughout the country are referred to the National Institute for Infectious Diseases "Matei Bals".
The ESBL-producing K. pneumoniae strains represent a serious public health issue globally and locally [25].
The ESBL-positive K. pneumoniae strains harboured the most frequent and clinically relevant ESBL genes belonging to SHV, CTX-M, OXA and TEM families. The preponderance of bla CTX-M-15 and bla SHV as the main ESBL genes in K. pneumoniae isolates confirms the results of other studies performed on Romanian clinical isolates, as well as the large worldwide distribution of these ESBL genes [26,27,28].
The most frequent carbapenemases genes (e.g. bla OXA-48, bla KPC-2, bla NDM-1 and bla OXA-162 ) found in the majority of the influent, effluent and clinical isolates are those reported as prevalent both in Romania and in other geographical areas [29]. Previous studies performed in Romania on carbapenem-non-susceptible Klebsiella pneumoniae clinical isolates have shown that bla OXA-48 was by far the most predominant genotype, followed by bla NDM-1 and bla KPC-2 [30,31,32]. The corresponding STs for the carbapenemase-producing isolates are: ST101 and ST258 (the most prevalent, as also reported in other studies including those performed on Romanian clinical strains by the authors of the present paper [11,33], followed by ST11, ST17, ST219, ST307 and ST395). It's worth mentioning that in two geographically different isolates from Bucharest (influent, ST17) and Galaţi (effluent, ST307) we have found bla OXA-162 , a rare bla OXA-48 variant, differing by a single amino acid substitution (Thr213Ala), and which is usually co-expressed with ESBL genes (such as bla TEM, bla SHV, bla CTX-M ), as in our case [34,35]. This particular carbapenemase remains extremely rare, with few reports from Turkey [36], Germany [37], Hungary [38] and Greece [35]. In Greece [35], bla OXA-162 has been found to be co-expressed with bla OXA-1 and bla DHA-1 in ST11 isolates. It is interesting to note that in our study, of the two isolates containing bla OXA-162 , one has also harboured bla OXA-1 . Also, similar to the German and Hungarian studies, bla OXA-162 is co-expressed in both isolates with the bla CTX-M-15 [29,38]. In contrast with other reports where bla OXA-162 was found in clinical isolates, in this study we have identified it in WWTP samples (both influent and effluent). To our knowledge, there is just one study that connects OXA-162 to the ST307 subtype [39] and there is none to connect it to ST17. On the other hand, we verified the possibility that detected bla OXA-162 gene in these two could be a sequencing artefact. Therefore, each assembled contig of these two isolates was further used as reference to map the corresponding raw Illumina PE reads onto. In the influent sample, the consensus sequence of bla OXA-162 gene was generated based on 8962 reads with a good coverage (mean = 269.6); In the effluent isolate, the contig was generated from 1483 reads having a satisfactory coverage (mean = 82.6).Performing comparative BLAST searches on both contigs resulted that both were identical (100% pairwise identity) with K. pneumoniae class D carbapenemases.
The most frequent STs in terms of frequency of isolation, geographical spreading and presence in both clinical and environmental compartments, i.e. 101, 258 and 219 were the most frequently associated with integrons. Class 1 integrons have been associated with the spread of resistance to antibiotics, disinfectants and heavy metals genes mainly in Gram-negative bacteria but also in Gram-positive strains. Furthermore, these mobile genetic elements represent a proxy for anthropogenic pollution [40].
Fluoroquinolones resistance rates are increasing, especially in Enterobacteriaceae, due to their broad use for treating both Gram-negative and Gram-positive bacterial infections. Of the known mechanisms of resistance to quinolones overexpression of efflux pumps and plasmid mediated resistance qnrB, D and S, which protect DNA gyrase from quinolone inhibition were detected in our strains. It is well known that plasmid mediated quinolones resistance (PMQR) plasmids may also carry ESBL genes, including those harboured by our strains, i.e. bla SHV , bla-TEM , bla CTX-M , bla OXA and bla KPC-2 , posing a great challenge for the treatment of the respective infections [53].
The most dominant aminoglycosides resistance gene was aac(6'), as also described in other studies [54], followed by ant(2"), aph(3") and aadA, either alone or in combination. The presence of these genes was higher in wastewater isolates, as compared to clinical ones, suggesting the important role of the aquatic environment as a reservoir of aminoglycosides resistance genes and the need for effective surveillance and strategies to reduce the selection pressure.
Similar to AME genes, trimethoprim-sulfamethoxazole resistance genes dfrA, sul1 and sul2 were also detected more frequently in wastewater samples, suggesting the need for careful surveillance of the aquatic reservoir for the presence of this type of resistance, particularly when taking into account that SXT is considered a low-cost alternative treatment by the Consortium on Resistance Against Carbapenems in Klebsiella and other Enterobacteriaceae (CRACKLE) [55,56] and that in K. pneumoniae, sul1 and dfr are highly prevalent in relation with class 1 integrons [57].
Similar to other studies, the most prevalent tetracyclines resistance genes were tetA and tetD [58].
Chloramphenicol resistance was mainly related to the presence of catB and catA genes, followed by cmIA5. Although cmr genes are reported by some studies as the most frequently found in clinical K. pneumoniae isolates [58], it was not present in the selected strains.
Although macrolides are not relevant for the treatment of Gram-negative infections, it has been suggested that commensal Gram-negative organisms may serve as a reservoir of ARGs that can be transferred to Gram-positive pathogens [59]. In our study, the most frequent macrolide ARG was mphA, followed by mphE and msrE.
Compared to other Gram-negative species, K. pneumoniae exhibits lower susceptibility to fosfomycin [60], and the most frequently reported mechanism is the production of the fosfomycin-inactivating enzyme fosA [61], which was identified in 99.7% of the K. pneumoniae genomes deposited in BLAST [62]. In our study fosA6 was identified with high frequency both in clinical and wastewater isolates. Taking into account that fosA6 is localized on a transposon and its transfer to a fosfomycin-resistant E. coli strain was already demonstrated [63], it can be suggested that K. pneumoniae isolates carrying the chromosomal fosA6 gene could serve as a reservoir of fosfomycin resistance in both clinical and aquatic environment.
The only rifampicin resistance mechanism harboured by our strains was the one linked to ADP-ribosyltransferase (arr) genes 2 and 3, revealed exclusively in the wastewater samples. The arr-1, arr-2 and arr-3 genes carried by class I integrons have been described in Gram-negative bacilli strains in Europe and Asia [64]. The arr-2 gene which was the most frequently detected in the selected strains, particularly in influent samples, has been reported to be associated with several transposons and integrons in K. pneumoniae strains [65]. This raises the concern of mobilization and transmission of rifampicin resistance from K. pneumoniae strains to other clinically important pathogens.
The effect of biocidal agents used for disinfection to enhance cross-resistance to antibiotics has been highlighted in different reports. In the case of K. pneumoniae, occurrence of resistance to different antibiotics, including colistin, has been revealed after exposure to benzalkonium chloride [66] and chlorhexidine digluconate [67,68]. Therefore, we have also followed the distribution of disinfectants resistance genes in the analyzed strains.
In our study, the qacEdelta and qacE genes have been more frequently associated with wastewater isolates, suggesting the selection of this type of resistance in the aquatic environment, probably due to the high selection pressure exerted by the presence of disinfectants. The qacdeltaE and qacE were isolated from a class I integron in the R751 plasmid, and were first documented in K. pneumoniae [69]. The qacE gene was, as expected, less encounteredsince it is predominantly associated with Gram-positive bacteria [70]. The most prevalent were the oqxA/B complex genes conferring resistance to multiple classes of antibiotics, but also to detergents and disinfectants. The oqxA/B complex can be located on chromosome and/or plasmids, flanked by IS26-like elements, posing thus a great risk for the public and environmental health, in terms of AMR horizontal transmission and selection of multiple-drug resistant phenotypes [71].
Besides its resistance mechanisms, K. pneumoniae can also present different virulence factors, some of them responsible for the occurrence of hypervirulent K. pneumoniae severe infections [72]. The hypervirulence-associated factors are including capsular serotypes (K1 and K2), certain STs (ST 23 and CC 23), the virulence plasmid pLVPK and KPHP1208 pathogenicity island, as well as RmpA and MagA required for the mucoid phenotype and aerobactin. Despite the high number of virulence genes harboured by our strains, none of the genes associated with the hypervirulent K. pneumoniae genotype was detected.
The presented results contribute to enriching the knowledge of the epidemiological context of ESKAPE pathogens at national and European level, a major step in the implementation of reliable surveillance and actions plans. Whole genome sequencing is an essential tool that could provide fast and rich data on resistance genes, mobile genetic elements and virulence profiles, very useful for tracking AR reservoirs and transmission.
Supporting information S1