Risks of Antibiotic Resistance Dissemination by Leachates from Municipal Landﬁlls of Different Ages

: Landﬁll leachate is regarded as a signiﬁcant point source of pollutants that may pose a hazard to the environment, particularly to surface and ground waters. Leachates are highly variable and heterogeneous. Our study was focused on the characterization of landﬁll leachates derived from young (YDS) and matured (MDS) dumpsites in terms of the abundance of micropollutants, antimicrobial resistance genes (ARG), and microbial community structure. The concentrations of poly-and perﬂuoroalkyl substances (PFASs) were found to be higher in MDS compared to YDS, i.e., 13.19 and 7.16 µ g/L, respectively. Among pharmaceutical compounds, ibuprofen was detected at the highest concentrations, i.e., 12.54, 12.81, and 13.13 µ g/L, in the leachates derived from MDS, YDS, and ponds. The distribution of bacteria, archaea, eukaryotes, and viruses in the three leachate samples was as follows: 85.15 ÷ 88.04%, 9.13 ÷ 12.29%, 2.20 ÷ 2.68%, and 0.12 ÷ 0.15%, respectively. In total, 31 distinct families of ARGs were identiﬁed, comprising a total of 80 ARGs. Incubation of P. putida MSCL650 in sterile leachate from the pond resulted in decreasing the minimum inhibitory concentrations for six antibiotics as compared to cells incubated in nutrient broth. Hydrological processes, i.e., runoff and inﬁltration, can increase the dissemination of ARGs.


Introduction
The worldwide use of antibiotics stimulates the evolution of bacterial resistance to antibiotics due to selection pressure, which poses a global health burden.In this respect, the dissemination paths of antibiotic resistance genes (ARG) from anthropogenic sources represent an important area of research.The main sources of antibiotics, antibiotic-resistant bacteria (ARB), and ARG are as follows: wastewater treatment plants, sewer runoff, pharmaceutical manufacturers, hospitals, agricultural and animal industrial sources, and estuaries, as well as landfill leachate [1][2][3].
According to EU Council recommendations in 2022, strengthening the environmental monitoring of antimicrobial resistance (AMR) in groundwater and surface waters is needed to combat AMR according to the One Health approach [4].
Furthermore, the role of environmental (ambient) waters in the development, transmission, and spread of AMR should be prioritized as well [5].Several critical issues related to effectively tackling the spread of AMR still remain unclear, e.g., (i) what kind and levels of ARGs in water carry a risk of acquiring resistant infections; (ii) what are the key hotspots for horizontal transfer of ARGs; (iii) which environmental factors elevate the selective pressure for maintenance of ARGs; and (iv) what are the best monitoring approaches [6,7].The impact of four domains, i.e., mankind, livestock, agriculture, and the ecosystem, should be recognized [8].
Since these stressors are present in wastewater almost everywhere at trace levels, controlling the conditions that cause stress is extremely difficult [13].
Over 1000 ARG subtypes have evolved and multiplied because of prolonged antibiotic treatments, and the diversity of the microbial communities in wastewater sludge has been reduced [2,9,14].The potential impact of PC on the spread of AMR through wastewater effluents can be evaluated by "predicted no-effect concentrations" (PNECs).The list of PCs currently published by the pharmaceutical manufacturing industry includes 125 antibiotics.However, this list does not encompass all known antibiotics [15].A recent statistical evaluation of the data has been performed using 0.05 µg/L of antibiotics as the default PNEC [15].
The high ubiquity, resistance to degradation, and potential toxicity of PFAS have recently received a lot of attention from environmental regulators and the general public.These micropollutants are derived from the textile finishing, semiconductor, paper, and chemical industries [10,16].
The EU Commission recently proposed to amend the Directive on Environmental Quality Standards (EQS) with additional quality standards for groundwater priority pollutants, e.g., PFAS (0.0044 PFOS equivalents), carbamazepine (0.25 µg/L), sulfamethoxazole (0.01 µg/L), a sum EQS for PC (0.25 µg/L), and a sum EQS for non-relevant pesticide metabolites (nrMs).It has been proposed by the Commission to assess PFAS substances, for which the sum of EQS shall be expressed as PFOA equivalents, using the Relative Potency Factor (RFP) approach [17].The total PFOA emissions from landfills in the United States in 2013 were estimated to be 52 kg/year [18].
At present, the assessment of AMR hazards in the community remains challenging due to the heterogeneity of the sources and the lack of data on the genomic, biochemical, and community levels [8].The relative impact of the environment versus the influence of different stress-inducing factors (e.g., bacteriophages, biocidal agents, heavy metals, detergents, pesticides, temperature, pH level, and others) should be evaluated in the context of AMR [8,19].The transmission routes of ARG in the environment are studied for informing and improving policy and monitoring systems, as well as identifying the relevant sampling locations and potential intervention points [20].Among the potential routes of ARG transmission are surface waters (designated bathing areas, lakes, estuaries), groundwater resources and their vulnerability, municipal water supplies, and others [20].
Landfill leachate is regarded as a significant point source of pollutants that may pose a hazard to the environment, particularly to surface and groundwater.In the context of AMR dissemination risks, recent studies have characterized landfill leachates in terms of microbial community structure [12], viral abundance and related bacterial hosts [21], AMR abundance [22], the concentration of micropollutants (e.g., PC and PFAS) [23][24][25][26], seasonal variations [27], and a comparison between different landfills [28].Nevertheless, more research is needed to evaluate the potential risks of AMR dissemination from landfills in order to reveal common trends and specific differences regarding local landfills.
Our study was performed with leachates from the Getlini landfill, which has served Riga and the surrounding municipalities since 1973, collecting about half of the municipal waste volume produced in Latvia.It was hypothesized that landfill leachates derived from young (YDS) and matured (MDS) dumpsites, as well as leachate ponds, would differ in terms of micropollution, ARG abundance, microbial community structure, and the risks of AMR induction by leachates.The dumpsites of different ages differed by waste composition and stage of waste decomposition and might have distinct differences in the aforementioned parameters.

Characterization of the Getlini Landfill and Leachate Collection
Landfill leachates were obtained at the Getlini municipal solid waste landfill, which is managed by SIA Getlini EKO (Riga, Latvia) (Figure 1).Getlini MSW landfill area is 87 hectares, and it currently receives 700-1000 tons of waste daily, amounting to ~215 thousand tons per year.Getlini landfill operations started in 1973 as a municipal and industrial waste dumpsite for the city of Riga.The initial dumpsite was located in an abandoned sand quarry, but later, it expanded on the adjacent Getlini Bog.Major changes in the landfill operation started in 1996 when a project financed by the World Bank was launched.The project included the closure and remediation of the old dumpsite (ODS in Figure 1) and the construction of modern, environmentally responsible waste disposal cells with leachate and landfill gas collection systems.Nowadays, the Getlini landfill continuously implements solutions that are environmentally friendly and minimize the volume of landfilled waste.The old dumpsite area does not have a leachate collection system, but some of the leachate seeping from the "waste hill" is collected in the leachate collection pond, where it mixes with the leachate from waste cells (MDS and YDS areas-see Figure 1).The MDS and YDS differ by waste composition and the duration of operation.In particular, the MDS has received mixed municipal wastes, inert wastes, and treated wastes for 10 years, then closed for 13 years until the sampling time.In turn, the YDS has received biological waste and operated since 2015 until the sampling time, i.e., May 2020.Leachate samples were taken in a collector manhole where outlets from the MDS leachate collection system (sample G1) and the YDS leachate collection system (sample G2) are accessible.A sample containing a mixture of all leachates, including leachate seeping from the old dumpsite area, was taken from the leachate collection pond (sample G4) (Figures 1 and A1).All three samples were taken on one day, and the composite samples were obtained from ten individual samples taken for one hour.
composition and stage of waste decomposition and might have distinct differences in the aforementioned parameters.

Characterization of the Getlini Landfill and Leachate Collection
Landfill leachates were obtained at the Getlini municipal solid waste landfill, which is managed by SIA Getlini EKO (Riga, Latvia) (Figure 1).Getlini MSW landfill area is 87 hectares, and it currently receives 700-1000 tons of waste daily, amounting to ~215 thousand tons per year.Getlini landfill operations started in 1973 as a municipal and industrial waste dumpsite for the city of Riga.The initial dumpsite was located in an abandoned sand quarry, but later, it expanded on the adjacent Getlini Bog.Major changes in the landfill operation started in 1996 when a project financed by the World Bank was launched.The project included the closure and remediation of the old dumpsite (ODS in Figure 1) and the construction of modern, environmentally responsible waste disposal cells with leachate and landfill gas collection systems.Nowadays, the Getlini landfill continuously implements solutions that are environmentally friendly and minimize the volume of landfilled waste.The old dumpsite area does not have a leachate collection system, but some of the leachate seeping from the "waste hill" is collected in the leachate collection pond, where it mixes with the leachate from waste cells (MDS and YDS areas-see Figure 1).The MDS and YDS differ by waste composition and the duration of operation.In particular, the MDS has received mixed municipal wastes, inert wastes, and treated wastes for 10 years, then closed for 13 years until the sampling time.In turn, the YDS has received biological waste and operated since 2015 until the sampling time, i.e., May 2020.Leachate samples were taken in a collector manhole where outlets from the MDS leachate collection system (sample G1) and the YDS leachate collection system (sample G2) are accessible.A sample containing a mixture of all leachates, including leachate seeping from the old dumpsite area, was taken from the leachate collection pond (sample G4) (Figures 1 and  A1).All three samples were taken on one day, and the composite samples were obtained from ten individual samples taken for one hour.

Physicochemical Testing of Leachates
The pH value and electrical conductivity (EC) were measured using a WTW Multi9620 IDS with the SenTix 940 P and TetraCon 925 electrodes, respectively.The total nitrogen concentration was measured by Koroleff's method and reaction with DMP, using a WTW photoLab S12 and WTW CR 420 thermoreactor, as well as the Spectroquant Nitrogen (total) 10-150 mg/L N kit (1.14763.0001).For measuring the N-NH 4 , a Spectroquant Ammonium Cell Test 4.0-80.0mg/L N-NH 4 kit (1.14559.0001)was applied based on the reaction with hypochlorites in a strong alkaline solution, followed by photometric determination with sodium nitroprusside using WTW photoLab S12.The chemical oxygen demand (COD) was determined using the Spectroquant COD Cell test 300-3500 mg/L kit (1.14691.0001)based on the reaction with potassium dichromate, sulfuric acid, and mercury (II) sulfate at 148 • C for 2 h, using the WTW photoLab S12 and WTW CR 420 thermoreactor.

Analytical Determination of Micropollutants
PFASs were analyzed according to the method described in [29], with some modifications in order to extend the scope of the analysis.Modifications were made in the HPLC gradient program, and detailed gradient ramps are provided below.Briefly, 5 mL of the leachate sample was diluted to 200 mL with ultrapure water and spiked with a methanolic solution containing 13 C-labeled PFAS surrogates (5 ng of each component).The resulting sample extract aliquots were added to Strata-X-AW 33 m 200 mg/3 mL SPE (Phenomenex, Torrance, CA, USA) cartridges that had been provisionally preconditioned with 3 mL of 1% NH 4 OH in MeOH, 3 mL of MeOH, and 3 mL of reagent grade water at a flow rate of less than 5 mL min −1 .After loading the columns with the sample, they were washed with 2% formic acid (1 mL) and MeOH (3 mL), dried for 30 min under vacuum, and then the analytes were eluted with 6 mL of 1% NH 4 OH in MeOH into a 10 mL glass vial.Before the HPLC-Orbitrap-MS analysis, the eluted extracts were concentrated to dryness under a moderate nitrogen stream at 30 • C and reconstituted with MeOH (100 µL).High-performance liquid chromatography coupled with Orbitrap high-resolution mass spectrometry (HPLC-Orbitrap-HRMS) was used for PFAS analysis.A Kinetex-C 18 reversedphase column (50 mm × 3.0 mm, 1.7 µm) was used to separate the target analytes with an injection volume of 5 µL for standard solutions and sample extracts.Analyte separation was performed at 40 • C with a mobile phase consisting of (A) 10 mM ammonium formate, 0.2% formic acid, methanol/water (1:9, v/v), and (B) methanol/acetonitrile (50:50 v/v).The effective gradient began at the initial composition (A/B) of 90:10 (v/v), which was held for 1.0 min, and then linearly ramped to an A/B ratio of 5:95 (v/v) over an 8.0 min period, where it was held for 4.0 min before returning to the initial conditions over 0.5 min.The column was equilibrated with the initial A/B ratio of 85:15 (v/v) for 3.0 min between the runs.The mobile phase flow rate was held constant at 0.3 mL min −1 .The heated electrospray interface (HESI-II) operating in negative ionization mode was applied for the analysis.The parameters of HESI-II were the following: capillary temperature, 250 • C; electrospray voltage, 4.5 kV; sheath gas flow rate, 20 arbitrary units (AU); auxiliary gas flow rate, 5 AU.The mass spectrometric ion detection was performed in parallel reaction monitoring (PRM) mode with a resolving power of 17,500 FWHM; automatic gain control (AGC), 1.0 × 10 5 with a maximum injection time of 200 ms.Two m/z → m/z transitions were used for each analyte.The isotopic peak ratios and retention periods of the monitored ion transitions were used to identify the analytes.The permissible range for the isotope ratio of the target and confirmation transitions was established at 30% of the average value attained for the calibration standards from the same sequence.Spiked samples and materials from earlier proficiency tests (PT) were routinely incorporated into the QC technique as well as each sample sequence to assess the continuous recovery of target analytes.In each sample sequence, procedural blanks with added internal standards were evaluated.These blanks were prepared without a matrix, using only the chemicals specified in the analytical protocol, and subjected to the full analytical procedure.
A previously described procedure was used to test the PC [30].Briefly, SPE and dilute-and-shoot techniques were used for sample preparation.On a 2D-HPLC-MS/MS device operating in PRM mode, instrumental analysis was performed by scanning two ion transitions for each chemical.On deionized water, multiple-level procedural calibration was used for quantification.In the reconstitution process, internal standards of salbutamol-d 3 and ibuprofen-d 3 were employed to account for the matrix effects in LC-MS/MS studies.

Characterization of Culturable Microorganisms
Using Biolog EcoPlate™ (Biolog, Inc., Biolog, Hayward, CA, USA), the catabolic diversity of the microbial population in leachates was identified.With EcoPlate™, the redox indicator tetrazolium dye produces a color that may be used to assess the metabolism of the substrate.Leachates were inoculated (100 µL) into each well, diluted with a sterile 0.85% NaCl solution, and then incubated for 72 h at 23 • C with periodic shaking and measurement (once per 24 h) using a TECAN Infinite F50 microplate reader (Switzerland).The results of Biolog profiles were presented by the Shannon diversity index, which was calculated by the following Eq1: H = −Σ p j log2 p j , where p j = relative color intensity of the individual well [31].The ratio of the usage of N-containing substrates in the EcoPlate™ to the overall substrate utilization was computed to determine the nitrogen use index (NUSE) [32,33].

Testing of Microbial DNA in Leachates 2.5.1. DNA Extraction and Shotgun Sequencing
Using the manufacturer's instructions, the FastDNA SPIN Kit for Soil (MP Bio-Medicals, Irvine, CA, USA) was used to isolate DNA from the samples.Normalized to the initial library input of 500 ng, DNA samples for the shotgun metagenomic studies were then sheared with a Covaris S220 Focused Ultrasonicator (Covaris, Woburn, MA, USA) to achieve an average fragment size of 400 bp.Following the manufacturer's instructions, libraries were created using the MGIEasy Universal DNA Library Prep Set V1.0 (MGI Tech Co., Shenzhen, China).Using the Agilent High Sensitivity DNA kit on an Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA) and the Qubit High Sensitivity dsDNA assay kit on a Qubit 2.0 instrument (both from Thermo Fisher Scientific, Waltham, MA, USA), quality control of the libraries was performed.The depth of the sequence was calculated to be at least 20 million reads per sample (paired-end read length of 150 bp).In order to prepare DNA nanoballs (DNBs), pooled and circularized libraries were employed as templates.The PE150 flow cell was loaded with DNBs via an automated DNB loading method.According to the established protocol, the libraries were sequenced with the DNBSEQ-G400 sequencer using the DNBSEQ-G400RS High-Throughput Sequencing Set (MGI Tech Co., Shenzhen, China).

Shotgun Sequencing Data Analysis
Trimmomatic v.0.39 [34] was used to perform quality trimming on the collected raw paired-end reads.Sequences less than 36 nt were ignored, and the leading and trailing quality levels were set to Q30 and Q30, respectively.Sequences were first quality-filtered, after which they were matched to the human genome reference (hg19), and bowtie2 [35] v.2.3.5.1 was used to eliminate complementary sequences.Sequences were then separated into paired files using bedtools2 and sorted by reading names using samtools [36].The Kraken2 [37] program and internal Kraken2 database, which comprise taxonomical reference data on bacterial, fungal, viral, and protozoan domains, were used to obtain the taxonomic profile.The R-based Pavian [38] v1.0 tool was used to perform taxonomical aggregation.MetaSPAdes [39] assembler was used to accomplish de novo read assembly into scaffolds.The generated assembly was evaluated using MetaQuast [40].The assembly database and the local alignment of input reads to assembly were performed using Bowtie2.

Identification of Microbial Resistance Genes
The Resistance Gene Identifier (RGI) v.5.1.1,the Comprehensive Antibiotic Resistance Database (CARD) [41], and the DIAMOND [42] alignment tool were used to create scaffolds to predict the resistome profile in the samples.The heat map function of RGI was used to organize resistance genes according to the drug class, gene family, and resistance mechanism in order to gather results for each sample.Additionally, hierarchical clustering was carried out to group samples according to how similar they were.

Risk of AMR Induction by Leachates
The changes in bacterial susceptibility to antibiotics after a 28-day incubation in leachates were tested.Leachate samples (MDS, YDS, and pond) were aseptically filtered using 0.22 µm syringe cellulose acetate filters (STARLAB International GmbH, Hamburg, Germany).A 24-hour-old culture of Pseudomonas putida MSCL 650 (previously obtained from the Microbial Strain Collection of Latvia (MSCL), University of Latvia) was used as a test bacterial culture.The inoculum was prepared in a liquid TSB broth with the following composition: g/L: tryptone 17.0 g; papaic digest of soybean meal 3.0 g; glucose 2.5 g; K 2 HPO 4 2.5 g; NaCl 5.0 g.The pH value of the ready-to-use media at 25 • C was 7.3 ± 0.2.After 24 h cultivation at 28 • C with periodic shaking, the cells were collected by centrifugation at 10,000 rpm and rinsed twice with 0.85% NaCl.A suspension of P. putida with a cell concentration of 10 7 cells/mL was added to sterile leachate (1 mL inoculum and 9 mL leachate).Incubation was performed in sterile 15 mL screw-cap tubes at 28 • C with periodic shaking.An additional tube with TSB served as a positive control.After 28 days of incubation, the cells were collected and rinsed, as mentioned above.The susceptibility of P. putida cells to antibiotics was tested using the MICROLATEST MIC ® , NEFERM kit (Cat.No. MLT00046, LACHEMA, Pliva, Czech Republic), according to the manufacturer's instructions.Each determination consisted of 12 antibiotics at 8 concentrations (Figure A3C).The results were read manually after 20 h incubation at 28 • C and expressed as the minimum inhibitory concentration (MIC).

Microscopy Study
The samples were analyzed using a Leica DM RA-2 confocal laser scanning microscope (CLSM) (Wetzlar, Germany) equipped with a TCS-SL confocal scanning head.The cell culture was washed twice with a sterile 0.95% NaCl solution and centrifuged at 10,000 rpm, then fixed with 70% ethanol and afterward stained with 20 mM propidium iodide (PI).The PI was excited at the 488 nm band, and fluorescence was detected between 600 nm and 640 nm.

Statistical Analysis
The data are provided as mean values with standard deviations.The Student's t-test and one-way analysis of variance (ANOVA) were used in an MS Excel 2308 environment to evaluate the differences between the treatments.The vegan v.2.5.6 package was used to compute the Chao1, Shannon, and Simpson indexes of alpha diversity, and the phyloseq v.1.30.0 program was used to visualize the results.

Physicochemical Characterization of Leachates
The physicochemical characteristics of leachates are presented in Table 1.Leachates from MDS, YDS, and pond slightly differed by N-NH 4 + and COD, with the lower values in YDS (Table 1).

Analytical Testing of Micropollutants
Two broad groups of micropollutants, i.e., PFAS and PC, were tested in the leachates.The abundance of PFAS in landfill leachates differed depending on the sampling site.In total, eight PFAS compounds were detected at the overall concentrations of 13.19, 7.16, and 11.14 µg/L in MDS, YDS, and pond, respectively (Figure 2A).Among the PFAS detected, PFBS prevailed in all three leachate samples, i.e., at 6.79, 2.73, and 5.28 µg/L levels in MDS, YDS, and pond, respectively.Other PFAS compounds varied in the range of 0.05 to 1.78 µg/L (Figure 2A).The testing of PC revealed an abundance of eleven compounds belonging to three drug classes, i.e., nonsteroidal anti-inflammatory drugs (NSAIDs), macrolides (clindamycin), and lincosamides (lincomycin), as well as sulfonamides.Among the PCs, NSAIDs were the most abundant in all three leachate samples.Particularly, the concentration of ibuprofen in MDS, YDS, and pond was 12.54, 12.81, and 13.13 µg/L, while diclofenac was 3.93, 4.52, and 6.08 µg/L, respectively (Figure 2B).

Analytical Testing of Micropollutants
Two broad groups of micropollutants, i.e., PFAS and PC, were tested in the leachates.The abundance of PFAS in landfill leachates differed depending on the sampling site.In total, eight PFAS compounds were detected at the overall concentrations of 13.19, 7.16, and 11.14 μg/L in MDS, YDS, and pond, respectively (Figure 2A).Among the PFAS detected, PFBS prevailed in all three leachate samples, i.e., at 6.79, 2.73, and 5.28 μg/L levels in MDS, YDS, and pond, respectively.Other PFAS compounds varied in the range of 0.05 to 1.78 μg/L (Figure 2A).The testing of PC revealed an abundance of eleven compounds belonging to three drug classes, i.e., nonsteroidal anti-inflammatory drugs (NSAIDs), macrolides (clindamycin), and lincosamides (lincomycin), as well as sulfonamides.Among the PCs, NSAIDs were the most abundant in all three leachate samples.Particularly, the concentration of ibuprofen in MDS, YDS, and pond was 12.54, 12.81, and 13.13 μg/L, while diclofenac was 3.93, 4.52, and 6.08 μg/L, respectively (Figure 2B).

Characterization of Culturable Microorganisms
We conducted the EcoPlate TM test to characterize the functional diversity of culturable microorganisms in the environmental samples collected at the MDS, YDS, and pond collection sites.The results of the EcoPlate TM test and Shannon index calculation indicated that the highest Shannon index at the 24 h mark was at the MDS collection site.However, there was no notable increase in the Shannon index between 24 h and 96 h, only ranging from 1.96 to 2.00.This could indicate that the microbial community in the sample consistently utilized the available carbon sources, pointing to the lower level of variation in the functional diversity of the microbial community compared to the other ones.The YDS collection site had a notable Shannon index growth from the 24 h mark to the 96 h mark, ranging from 1.33 to 1.82, although it was not as significant as the growth in samples from the pond collection site.The highest functional diversity of the microbial community was from the pond collection site, where the Shannon index ranged from 1.59 to 3.23,

Characterization of Culturable Microorganisms
We conducted the EcoPlate TM test to characterize the functional diversity of culturable microorganisms in the environmental samples collected at the MDS, YDS, and pond collection sites.The results of the EcoPlate TM test and Shannon index calculation indicated that the highest Shannon index at the 24 h mark was at the MDS collection site.However, there was no notable increase in the Shannon index between 24 h and 96 h, only ranging from 1.96 to 2.00.This could indicate that the microbial community in the sample consistently utilized the available carbon sources, pointing to the lower level of variation in the functional diversity of the microbial community compared to the other ones.The YDS collection site had a notable Shannon index growth from the 24 h mark to the 96 h mark, ranging from 1.33 to 1.82, although it was not as significant as the growth in samples from the pond collection site.The highest functional diversity of the microbial community was from the pond collection site, where the Shannon index ranged from 1.59 to 3.23, suggesting a diverse utilization of carbon sources by the microorganisms (Figure 3A).The nitrogen use index NUSE remained stable in leachates from YDS and ponds upon 96 h incubation, while in leachates from MDS, the NUSE was 0%, 57%, 36%, and 42% after 24 h, 48 h, 72 h, and 96 h, respectively (Figure 3B).
suggesting a diverse utilization of carbon sources by the microorganisms (Figure 3A).The nitrogen use index NUSE remained stable in leachates from YDS and ponds upon 96 h incubation, while in leachates from MDS, the NUSE was 0%, 57%, 36%, and 42% after 24 h, 48 h, 72 h, and 96 h, respectively (Figure 3B).
Regarding the alpha diversity of samples, the highest Chao1 measure was obtained for YDS-8885.95,followed by MDS and pond.On the contrary, the richness estimator, e.g., the Shannon index, was highest for the pond-7.23,followed by YDS and MDS.Similarly, the highest value of the evenness estimator-the Simpson index-was observed for the pond-0.99,followed by YDS and MDS (Figure 5).Regarding the alpha diversity of samples, the highest Chao1 measure was obtained for YDS-8885.95,followed by MDS and pond.On the contrary, the richness estimator, e.g., the Shannon index, was highest for the pond-7.23,followed by YDS and MDS.Similarly, the highest value of the evenness estimator-the Simpson index-was observed for the pond-0.99,followed by YDS and MDS (Figure 5).In the context of AMR, the species/genera/families from the list of antibiotic-resistant "priority pathogens" [43] have been selected from the sequencing results and summarized in Table A1.The most abundant family from this list was Enterobacteriaceae, found in MDS, YDS, and ponds at concentrations of 1.294, 0.984, and 1.324% (relative abundance).Also, the relative abundance of Campilobacter spp.exceeded 1% in the YDS leachate (Table A1).The abundance of viruses in the tested leachates is summarized in Table A2.

Antimicrobial Resistance Genes in Metagenomic Data
In the metagenomic analysis, we identified 31 distinct families of antimicrobial resistance genes (ARG), such as Erm 23S ribosomal RNA methyltransferase, glycopeptide resistance gene cluster, lincosamide nucleotidyltransferase, and tetracycline-resistant ribosomal protection protein, among others (Figure A1B).Collectively, these families encompass a total of 80 ARG genes, including aadA13, linG, mphE, qacEdelta1, adeF, sul2, and others.These ARG genes can be classified into five mechanism groups associated with resistance: antibiotic efflux, antibiotic inactivation, antibiotic target alteration, and antibi- In the context of AMR, the species/genera/families from the list of antibiotic-resistant "priority pathogens" [43] have been selected from the sequencing results and summarized in Table A1.The most abundant family from this list was Enterobacteriaceae, found in MDS, YDS, and ponds at concentrations of 1.294, 0.984, and 1.324% (relative abundance).Also, the relative abundance of Campilobacter spp.exceeded 1% in the YDS leachate (Table A1).The abundance of viruses in the tested leachates is summarized in Table A2.

Antimicrobial Resistance Genes in Metagenomic Data
In the metagenomic analysis, we identified 31 distinct families of antimicrobial resistance genes (ARG), such as Erm 23S ribosomal RNA methyltransferase, glycopeptide resistance gene cluster, lincosamide nucleotidyltransferase, and tetracycline-resistant ribo-Cell cultures incubated in different leachate samples and TSB slightly differed also by cell morphology.Specifically, the average cell length in the culture of P. putida after incubation in TSB was 1.07 ± 0.36 µm, while after incubation in leachates from MDS, YDS, and pond, the cell length was 1.11 ± 0.48 µm, 1.49 ± 0.50 µm, and 0.72 ± 0.34 µm, respectively (Figure 6).In the preparations with pond and MDS leachates, some long cells/chains were detected (up to 4.62 and 6.92 µm, respectively).However, these cells were not included in the counting of average cell length.

Discussion
The leachates generated at landfills differ greatly due to the heterogeneity of waste composition, treatment technologies, landfill/waste age, climatic conditions, and other parameters.The leachates derived from waste deposits aged <5 years, 5-10 years, and >15 years are considered acetogenic, intermediate, and methanogenic leachates, respectively, and differ by physicochemical characteristics [44,45].
Recently, it has been shown that pH values, the presence of nitrogen compounds, COD, and integrons are variables playing an important role in the abundance of ARGs [46].
Landfills represent a significant source of toxic substances in the environment [22].In our study, an emphasis was placed on two large groups of micropollutants, i.e., PFAS and PC, as they are known to concentrate in leachates [23,24].
Among PFAS, perfluorobutane sulfonic acid (PFBS) prevailed.This compound is proposed for National Primary Drinking Water Regulations by the US Environmental Protection Agency [47].A correlation between the physicochemical properties (i.e., alkalinity, total organic carbon, and ammonia) and the PFAS concentration in landfill leachates derived from 39 landfill facilities in Florida, USA, has been described [48].
The number and concentration of PCs in leachates can vary greatly, being site-specific.The concentration of PCs in the leachates in China varied in the range of 0.1 to 100 μg/L [25].Masoner et al. [23] analyzed leachates from 22 landfills in 12 states of the USA, and PCs were found in every sample, ranging in number from 1 to 58.The concentration of PCs was greater in leachates from active landfills compared to closed, unlined landfills [23].In our study, one dumping site (MDS) was closed by the sampling time, while an-

Discussion
The leachates generated at landfills differ greatly due to the heterogeneity of waste composition, treatment technologies, landfill/waste age, climatic conditions, and other parameters.The leachates derived from waste deposits aged <5 years, 5-10 years, and >15 years are considered acetogenic, intermediate, and methanogenic leachates, respectively, and differ by physicochemical characteristics [44,45].
Recently, it has been shown that pH values, the presence of nitrogen compounds, COD, and integrons are variables playing an important role in the abundance of ARGs [46].
Landfills represent a significant source of toxic substances in the environment [22].In our study, an emphasis was placed on two large groups of micropollutants, i.e., PFAS and PC, as they are known to concentrate in leachates [23,24].
Among PFAS, perfluorobutane sulfonic acid (PFBS) prevailed.This compound is proposed for National Primary Drinking Water Regulations by the US Environmental Protection Agency [47].A correlation between the physicochemical properties (i.e., alkalinity, total organic carbon, and ammonia) and the PFAS concentration in landfill leachates derived from 39 landfill facilities in Florida, USA, has been described [48].
The number and concentration of PCs in leachates can vary greatly, being site-specific.The concentration of PCs in the leachates in China varied in the range of 0.1 to 100 µg/L [25].Masoner et al. [23] analyzed leachates from 22 landfills in 12 states of the USA, and PCs were found in every sample, ranging in number from 1 to 58.The concentration of PCs was greater in leachates from active landfills compared to closed, unlined landfills [23].
In our study, one dumping site (MDS) was closed by the sampling time, while another (YDS) was active.Furthermore, these sites differed by waste composition.Nevertheless, no considerable differences between MDS and YDS were found.
The prevalence of ibuprofen among PCs in the tested leachate samples corroborates with other studies worldwide.The concentration range of ibuprofen in leachates from dumping sites of different ages was from 3.0 to 48.7 µg/L [26,49], while in hospital effluent, it was 3.9 µg/L [49].It was recently reported that ibuprofen, along with other non-antibiotic pharmaceuticals in therapeutically and environmentally relevant quantities, greatly increased the spread of ARGs via plasmid-borne bacterial conjugation [50].
Thus, the testing results on PFAS and PCs in leachates obtained at the Getlini landfill in Latvia corroborated those reported from other countries.
A metagenomic approach for the characterization of microbial biodiversity has revealed Proteobacteria as the dominant phylum in all three leachate samples tested (up to 50%).These data are in good agreement with reports by other authors who studied leachates and their aerobic treatment [28,[51][52][53][54]. Importantly, the majority of bacterial species mentioned in the list of antibiotic-resistant "priority pathogens" [43] belong to Proteobacteria (Table A1).In a study on soil bacterial communities, Proteobacteria was also emphasized as the most dominant phylum in the transconjugant pools in terms of horizontal transfer of ARGs [55].
Among important factors for ARG transmission, the viral [21,56] and archaea [57,58] community structures in landfill leachates should be emphasized.Thus, the physicochemical and microbial diversity in leachates provides a broad spectrum of mechanisms responsible for ARG transmission, including horizontal gene transfer [27].The genes sulI and sulII, found in MDS, YDS, and pond, have been mentioned by other authors as the most abundant antibiotic-resistance genes in leachates [51].In the studies where dynamic trends in the abundance of ARG in leachates were monitored, considerable variations were found.For example, the levels of sulI, tetO, and tetW in 2017 were reported to be 100 times higher than in 2018 [27].
The presence of ARGs in leachates may represent potential risks to public health and the environment, which are not yet fully understood.Mobile genetic elements can be released into local rivers and other receiving aquifers, where bacteria may quickly acquire antibiotic resistance [1,59].
ARGs are mobilized and transported primarily by hydrological processes such as runoff and infiltration [60].Furthermore, community access to drinking water and sanitation has a great impact on antibiotic resistance in humans [61].
Regarding the Watch List of Substances for Union-wide Monitoring in the Field of Water Policy, which was recently published by the EU Commission [62], only clindamycin has been detected in the tested leachates.Importantly, clindamycin was not detected in the pond, which confirms the efficiency of the primary treatment.
Among the limitations of our study, the absence of data on seasonal variables and differences over the years should be noted.Additionally, we lacked data on the concentration of additional micropollutant categories (e.g., heavy metals).Another limitation is the absence of standardized methods for sampling.These limitations can result in an underestimation of the abundance of ARGs and stress factors that promote their horizontal transfer.

Conclusions
By analyzing the chemical, biochemical, and microbiological composition of landfill leachates, we were able to characterize the abundance of micropollutants, ARGs, taxonomic groups of bacteria, viruses, and archaea, as well as compare leachates derived from solid waste dumping sites of different ages.The following conclusions were made:

•
Metagenomic analysis showed a prevalence of Proteobacteria (43.76-54.70%),followed by Firmicutes (8.51-13.11%)and Euryarchaeota (9.37-12.53%) in all three leachate samples.Regarding the inner diversity of samples, the highest Chao1 measure was obtained for YDS-8885.95,followed by MDS and pond, whereas the richness estimator, e.g., Shannon index, was the highest for pond-7.23,followed by YDS and MDS.Similarly, the highest value of the evenness estimator-the Simpson index-was observed for the pond-0.99,followed by YDS and MDS.

•
The number and composition of specific ARGs found in leachate samples derived from MDS, YDS, and ponds slightly varied.In total, 80 ARGs belonging to 31 distinct ARG families were identified.These ARGs are known to confer resistance against 19 different classes of antibiotics, such as aminoglycosides, glycopeptides, fluoroquinolones, lincosamides, macrolides, streptogramins, and tetracyclines, as well as disinfecting agents and antiseptics.

•
The incubation of P. putida MSCL650 in sterilized leachate derived from the pond resulted in a decrease in MIC for several antibiotics compared to the control.This effect can be explained by the high concentration of toxic compounds in leachates.
Leachates from MDS and YDS totally inhibited the cells of P. putida.

•
A comparison of two dumping sites tested in the study, which differed by waste composition and treatment and the duration of operations, did not reveal considerable differences in the microbial community structure and ARG abundance.The lower ecotoxicity in the leachate from the pond compared to those from MDS and YDS pointed to the effectiveness of solid waste treatment.

Figure 1 .
Figure 1.Location of sampling sites at the Getlini landfill.Figure 1. Location of sampling sites at the Getlini landfill.

Figure 1 .
Figure 1.Location of sampling sites at the Getlini landfill.Figure 1. Location of sampling sites at the Getlini landfill.

Figure 3 .
Figure 3. Changes in the functional diversity of the microbial community over a 96-h period in the three sources of infiltration: matured dumpsite (MDS), young dumpsite (YDS), and the pond.(A) Shannon diversity index; (B) NUSE index.The data are presented as the average of three replicate wells for each carbon substrate in EcoPlate TM .

Figure 3 .
Figure 3. Changes in the functional diversity of the microbial community over a 96-h period in the three sources of infiltration: matured dumpsite (MDS), young dumpsite (YDS), and the pond.(A) Shannon diversity index; (B) NUSE index.The data are presented as the average of three replicate wells for each carbon substrate in EcoPlate TM .

Figure 4 .
Figure 4.The microbial community structure at the phylum (A), order (B), genus (C), and species (D) levels in the leachates sampled at the matured dumpsite (MDS), young dumpsite (YDS), and pond.Only the taxon yields ≥ 1% in at least one sample are shown.

Figure 4 .
Figure 4.The microbial community structure at the phylum (A), order (B), genus (C), and species (D) levels in the leachates sampled at the matured dumpsite (MDS), young dumpsite (YDS), and pond.Only the taxon yields ≥ 1% in at least one sample are shown.Water 2023, 15, x FOR PEER REVIEW 10 of 21

Figure 5 .
Figure 5. Alpha diversity (E) is measured by the Chao1, Shannon, and Simpson indices.

Figure 5 .
Figure 5. Alpha diversity (E) is measured by the Chao1, Shannon, and Simpson indices.

Figure A1 .
Figure A1.Sampling of the leachates at Getlini solid waste landfill.Figure A1.Sampling of the leachates at Getlini solid waste landfill.

Figure A1 .
Figure A1.Sampling of the leachates at Getlini solid waste landfill.Figure A1.Sampling of the leachates at Getlini solid waste landfill.

Figure A2 .
Figure A2.The differences in specific ARG family presence in the leachates sampled at the matured dumpsite (MDS), young dumpsite (YDS), and pond.Dark blue color-100% sequence match, bluish color->90% match, bright color-not identified.Genes with asterisks (*) appear multiple times because they belong to more than one AMR gene family category in the Antibiotic Resistance Ontology.

Figure A3 .
Figure A3.The susceptibility of P. putida MSCL650 to antibiotics was tested by the MICROLATEST MIC ® kit, NEFERM.The results were read after 20 h incubation at 28 • C in TSB (A) and leachate from the pond (B).(C) the concentrations of antibiotics in the plate.

Table A2 .
The abundance (OTUs number) of viruses in leachates sampled at the matured dumpsite (MDS), young dumpsite (YDS), and pond.Only the taxons with OTUs ≥ 100 in at least one sample are shown.