Background

Mobile resistance factors accumulate in human pathogens via horizontal transfer, often from environmental bacteria or commensals [1]. To the best of our knowledge, every resistance factor that is a clinical problem today was discovered long after it irreversibly emerged and spread in pathogenic bacteria widely enough to cause treatment failures. After discovery, propagation can often be tracked in retrospect from country to country. One of the most prominent examples is the first detection of the mobile colistin resistance gene mcr-1 in 2015 followed by documentation of its worldwide presence [2].

If we could identify new resistance threats before they spread widely or even before they appear in pathogens, actions could be taken to reduce the risks of their emergence, spread and clinical consequences. Such actions include targeted monitoring, confinement and the addition of the new genes to genetics-based diagnostics. Moreover, the development of new antibiotics can benefit from the awareness of novel resistance mechanisms.

Large-scale functional screening of metagenomic DNA from microbial communities has revealed many unknown resistance genes in various environments [3, 4]. The approach is independent of the cultivability of the indigenous bacterial host and does not rely on similarity to known genes, making it suitable for the identification of novel resistance determinants [5]. Functional metagenomics cannot, however, easily discriminate between mobile and immobile genes, the latter having less potential of transfer to and between pathogens [6]. Moreover, common resistance genes will dominate the sequenced clones, reducing the likelihood of identifying rare, novel genes.

Integrons are genetic elements that acquire, shuffle and express promoter-less gene cassettes. Although not mobile themselves, integrons are often associated with mobile elements and located on conjugative plasmids [7]. This combination makes them ideal for acquisition and spread of resistance genes to and among pathogens, particularly integrons of class 1 [8].

The aim of this study was to discover rare, novel resistance determinants that may appear in pathogens or that have already emerged in pathogens but thus far escaped identification. We explored bacterial communities from river sediments contaminated with wastewater in a country with a high use of antibiotics (India) [9] by adapting a functional metagenomics approach focusing on amplicon libraries of integron gene cassettes. Blunt-end cloning into a plasmid under the control of a constitutively active promoter allowed us to screen for resistance against different antibiotics. To overcome sensitivity limitations, we did not analyse individual resistant clones but rather amplified and sequenced inserts of all growing bacteria on the plates via long-read technologies. We then filtered out highly abundant known resistance genes in silico to identify rare, new putative resistance genes.

Results and discussion

To identify mobilised novel resistance determinants, class 1 integron gene cassette libraries were prepared under control of the constitutively active Pbla promoter in E. coli DH10β pZE21-Pbla. Library sizes ranged from 5.0 × 109 to 1.8 × 1010 bp. The estimated average insert size of all libraries ranged from 600 to 1000 bp. Libraries were screened for functional resistance determinants on 13 different antibiotics at three different concentrations (Additional file 5). No resistance against tigecycline or nitrofurantoin was detected. The other antibiotics resulted in at least 15 to up to several thousand colonies on each screening plate. All colonies were scraped off and barcoded amplicons were prepared for long-read sequencing (PacBio Sequel). Amplicon sequencing resulted in 419,709 reads. Based on the retrieved barcodes, 382,332 could be assigned to the antibiotics and concentrations used to select resistant clones. We then predicted open reading frames (ORFs) and filtered out all reads containing known antibiotic resistance genes (ARGs) responsible for the respective phenotype. Known ARGs were defined as the ORFs with identity greater than 95% and coverage greater than 85% to their homologues in the ResFinder database. The remaining 147,151 reads consisted of 46,403 unique reads (11% of all reads) with an average length of 1540 bp and they included 48,562 unique predicted ORFs. Each of the selection amplicons resulted in an average of 1450 reads with no known ARGs. These were searched manually for resistance gene candidates.

To identify promising putative novel resistance genes, we used five criteria: An ORF needed to be (i) complete and (ii) highly abundant in its set of reads while (iii) not common in the other selection sets. To ensure that the ORF originated from an integron (iv) both binding sites for the primers used to amplify the gene cassettes should be present in the read. Furthermore, (v) the candidate ORF should be the only ORF present that could explain the resistance phenotype. Despite the large number of colonies growing during functional selection, only the gentamicin and β-lactam selection sets contained ORFs fulfilling all mentioned criteria (Table 1). Thus, the metagenomic DNA samples used in this study contain exceptionally high amounts of class 1 integrons carrying a multitude of antibiotic resistance genes [10, 11], but most of them were filtered out as known or close variants of known ARGs.

Table 1 Abundance of candidate ORFs for functional selection
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Using this approach, candidate ORFs with little or no resemblance to any known resistance factor were chosen for functional verification. The putative, completely novel resistance genes found in the read set selected by β-lactams did not confer resistance when synthesised and expressed in E. coli. It is possible that they were able to grow in close vicinity to resistant colonies during the functional selection, since β-lactamases are secreted into the periplasm and in outer membrane vesicles to inactivate β-lactam antibiotics [12,13,14]. Hence, they might simultaneously provide close-range protection for surrounding non-resistant bacteria, which appeared as false positives.

Resistance of the candidate gene highly selected on gentamicin (designated gar = garosamine-specific aminoglycoside resistance) was successfully verified in E. coli. The protein GAR (167 aa) has an overall negative charge (pI 4.6). Since cation concentrations profoundly influenced the minimal inhibitory concentrations (MICs) (Table S1), we performed all subsequent experiments in cation-adjusted Mueller-Hinton broth. The expression of gar resulted in a 2760-fold MIC increase of gentamicin (Fig. 1).

Fig. 1
figure 1

MIC values of GAR against several aminoglycosides. Molecular structures are shown in Table S2

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Aminoglycoside modifying enzymes (AMEs) are the most clinically important resistance mechanism against aminoglycosides [15]. AMEs are divided into three enzymatic classes targeting –OH or –NH2 groups: aminoglycoside N-acetyltransferases (AACs), –O-nucleotidyltransferases (ANTs) and –O-phosphotransferases (APHs). Each class possesses a unique pattern of activity against different aminoglycosides due to their specific targets in the molecular structure [16]. We therefore tested the effectiveness of GAR against at least one representative of each aminoglycoside subclass (Fig. 1). GAR conferred resistance specifically against all six tested 4,6-disubstituted 2-deoxystreptamine–aminoglycosides containing a garosamine residue (Table S2), suggesting that it is critical for recognition.

Aminoglycosides can cause mistranslation by targeting the negatively charged 16S rRNA close to the aminoacyl-tRNA site of the 30S subunit [17]. The negative charge and garosamine-specific resistance pattern make the ribosomal RNA an unlikely target for GAR. GAR contains the Walker A NTP-binding motif involved in various phosphorylation reactions [18]. It also harbours two DxD motifs (Fig. 2). Such a motif provides the ability to bind the required Mg2+ [18, 23, 26]. The presence of these two motifs and its negative charge strongly suggest that GAR is enzymatically active as a kinase with high affinity for positively charged targets. Aminoglycosides are indeed positively charged molecules that provide many hydroxyl residues for potential phosphorylation, including two at the garosamine moiety. One of these hydroxyl groups, located at the 4″ carbon atom, has not yet been described as a target for an AME.

Fig. 2
figure 2

Structural motifs of GAR and related proteins. a Alignment of GAR with related proteins. The two amino acids that differ between GAR variants (L9I, T75A) are framed in black. The ORF from Luteimonas sp. 83-4 (CP029556) with 100% identity to GAR has no annotation. OrfPa105 (AJ786649) from P. aeruginosa 105MG and the ORF from P. aeruginosa S742_C15_BS without annotation (NFFO01000062.1) are identical. They differ by two nucleotides and one amino acid (T75A) from GAR. The two ORFs from S. enterica ADRDL-2811 (AAKHBQ010000151.1) and S. enterica subsp. enterica serovar Johannesburg FSIS1609335 (AAIUOI010000042.1) are identical to each other, annotated as hypothetical proteins and differ by two nucleotides and one amino acid (L9I) from GAR. Tunicamycin resistance protein TmrB as harboured by Bacillus subtilis (WP_003246258.1), the C-terminal membrane anchor is underlined [19], TmrD from Deinococcus radiodurans (WP_010888058.1) [20]. The N-terminal Walker A motif occurs in TmrB and in GAR, but the absence of the membrane anchor hints to a cytoplasmic location of GAR. The NTP-binding motif G/AXXGXGKT/S (Walker A or P-loop) is marked by red rectangles [18, 21, 22]. Searching NCBI’s conserved domain database revealed an AAA domain (ATPases Associated with diverse cellular Activities, pfam13238) within GAR and similarity to gluconate kinases (COG3265). GAR harbours no Walker B motif, but two potential DxD motifs, which could be responsible for Mg2+ binding [23], marked by blue rectangles. b Protein structure model of GAR. According to the structure model, the first DxD motif (aa 31–33) is located in the same cavity as the P-loop and thus more likely to participate in the NTP-binding and hydrolysis. GAR is shorter than other aminoglycoside phosphotransferases (APHs) and seems to contain five N-terminal parallel β-sheets, while APHs contain five anti-parallel β-sheets in their N-terminal domain [24, 25]

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There is very little similarity between GAR and all known ARGs, including AMEs (less than 20% amino acid identity). The phylogenetic tree of GAR and related proteins (Fig. 3) shows that GAR is clearly separated from the known AMEs and is located among proteins mostly annotated as hypothetical or AAA-domain containing proteins (kinases). The closest related protein from the NCBI non-redundant protein database (51% identity, WP_135484108.1) is not assigned any function. GAR shares slight amino acid sequence identity (about 20%) to tunicamycin resistance proteins (Fig. 2). Resistance to tunicamycin, a toxic nucleoside analogue produced by several Streptomyces species, is caused by ATP-binding membrane proteins, which also have a suspected phosphorylation activity [20, 27].

Fig. 3
figure 3

Phylogenetic tree of aminoglycoside resistance enzymes, GAR and its 1000 closest related protein sequences. Clades are collapsed (dark circles) to improve visual comparisons

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Several studies have identified a range of new ARGs in environmental samples [4, 28,29,30,31,32]. However, the clinical implications are less clear, since only a minor fraction of these genes are likely to end up in pathogens, e. g. due to lack of mobility, limited ecological connectivity and high fitness costs [3, 6]. Searching gar against the GenBank database resulted in 100% and 99% nucleotide identity with chromosomal regions of the clinical isolates Luteimonas sp. 83-4 (CP029556.1, China) and P. aeruginosa 105MG [33] (AJ786649.2, Italy), respectively. We additionally found gar on contigs of the clinical isolate P. aeruginosa S742_C15_BS (NFFO01000062.1, Italy) and on contigs of the food-borne pathogens S. enterica ADRDL-2811 (AAKHBQ010000151.1, USA) and S. enterica subsp. enterica serovar Johannesburg FSIS1609335 (AAIUOI010000042.1, USA) isolated from poultry products. In neither case was the gar gene recognised as a resistance gene. We can show that gar appears as a gene cassette in several spatially, temporally and phylogenetically separated clinical isolates, so the gene has already overcome the barrier preventing most environmental ARGs from becoming clinically relevant. Combined with its absence in related isolates (none of the other currently available P. aeruginosa, Luteimonas sp. or S. enterica genomes or assemblies in GenBank contain gar), this provides evidence that the gar gene is mobile. Furthermore, P. aeruginosa 105MG and P. aeruginosa S742_C15_BS belong to the exceptionally successful multidrug-resistant P. aeruginosa ST235 and ST111 linages, respectively, which are predominant on five continents [34]. P. aeruginosa frequently causes nosocomial infections with high mortality rates, especially in patients with chronic diseases, due to the accumulation of resistances against aminoglycosides, β-lactams and fluoroquinolones [34, 35]. Salmonellosis is the most important food-borne illness in the USA and the second most common in the EU [36, 37]. Salmonella isolates have collected a multitude of aminoglycoside resistance genes, probably due to the long-term usage of this antibiotic class in food production [38]. Occurrence in several common multidrug-resistant pathogens increases the probability for horizontal gene transfer, (co-) selection and spread of gar.

The structure-specific resistance pattern of AMEs implies that a single resistance gene cannot confer resistance against all aminoglycosides. However, any ARG that adds resistance to any antibiotic, which could have been a treatment possibility, reduces clinical options for treatment. For instance, P. aeruginosa 105MG carries four AMEs (aph(3)-IIb, aac(6)-31, ant(3″)-Ia, aac(6)-Il) plus gar, a combination that results in resistance against all tested aminoglycosides with the exception of apramycin (Table S3). The five AMEs target streptomycin/spectinomycin (ant(3″)-Ia); the –OH(3′) of kanamycin, G418, isepamicin, paromomycin and ribostamycin (aph(3)-IIb) and the –NH2(6′) of kanamycin, gentamicin, netilmicin, sisomicin, isepamicin, amikacin, tobramycin and ribostamycin (aac(6)-31, aac(6)-Il) [16]. Thus, even in a strain already harbouring several AMEs, gar extends the resistance profile (micronomicin). Luteimonas sp. 83-4 contains two aminoglycoside resistance genes, an aph(3′)-XV and gar (Table S4). Here, gar adds resistance to gentamicin, netilmicin, sisomicin and micronomicin, exacerbating already observed clinical multi-resistance. Resistance against garosamine-containing aminoglycosides is particularly worrying, since the newest semisynthetic aminoglycoside plazomicin (FDA-approved for treatment of complicated urinary tract infections [39]), which is derived from sisomicin and designed to avoid most of the common AMEs [40], includes garosamine. In the light of more and more widespread resistance to e.g. all β-lactams, an increasing dependence on aminoglycosides presenting a target for gar implies a growing selective pressure for bacteria to acquire, keep and spread the gar gene.

To examine if gar is present on a conjugative element in the P. aeruginosa 105MG isolate available to us, we attempted to transfer its aminoglycoside resistance phenotype to E. coli or P. putida via conjugation, but could detect none. Nonetheless, considering that gar is harboured by three distantly related species, it can obviously move horizontally. To shed light on the mechanisms involved, the genome of P. aeruginosa 105MG (GenBank accession: VLOE00000000) was sequenced. The gar gene is located within a class 1 integron on a chromosomal scaffold of 1.18 Mb. The integron is flanked by Tn3 and Tn21 transposon elements, which are highly abundant in bacterial genomes [41,42,43]. Transposable elements can promote inter-cellular mobility of integrons by insertion into a conjugative plasmid or an integrative conjugative element (ICE). The contigs upstream of the class 1 integron of the two P. aeruginosa isolates containing the gar gene cassette are identical and harbour several genes encoding conjugal transfer proteins. Hence, the entire integron could have been aquired from a conjugative plasmid/ICE, e.g. via Tn21 [44]. There are currently 261 P. aeruginosa genomes in NCBI’s database of complete genomes, 74 of them (28%) contain the complete intI1 gene (query cover and identity ≥ 97%), ten (4%) of which are plasmid-borne, but only the 105MG isolate harbours gar. It is thus highly plausible that gar has been aquired as a cassette, probably from an integron located on a yet unidentified plasmid/ICE hosted transiently by P. aeruginosa 105MG.

We have identified gar in six gene cassette arrays in at least three species. These regions are within integrons and adjacent to known resistance gene cassettes, such as aph(3′)-XV, blaOXA-2 and blaVIM-1, providing resistance to a range of critically important antibiotics (Fig. 4). The identified genetic contexts show that gar has appeared as the first and only gene cassette in the integrons from PETL metagenomic samples, as the fifth in Luteimonas sp. 83-4, the third in P. aeruginosa 105MG, the fourth in P. aeruginosa S742_C15_BS and the first in both S. enterica isolates. Rearrangement of gene cassettes provides rapid adaptation in response to changing environments. The presence of gar in different contexts and pathogens not only shows that it could confer a selective advantage for its hosts, but that it is a gene cassette accessible to diverse microbial communities and pathogens. Integrons are present in 20% of the sequenced γ-proteobacterial genomes [45]. Class 1 integrons in particular have become very successful in pathogens and highly abundant in various human-impacted environments [46, 47]. Any compatible plasmid containing a class 1 integron could acquire the gar cassette and facilitate further spread. Therefore, if ecological connectivity allows, gar can be integrated into the genomes of diverse bacterial hosts.

Fig. 4
figure 4

Gar in the six identified genetic contexts. a PETL metagenomics DNA sample. Primers HS458-HS459 amplified the region between attI site and qacEΔ of a clinical class 1 integron (GenBank accession MN215968). bLuteimonas sp. 83-4 (CP029556.1), chromosomal, not annotated in the available contig sequence. cP. aeruginosa 105MG (AJ786649.2 and VLOE00000000), chromosomal, clinical class 1 integron, included in a Tn5051-like transposon. Gar variant of P. aeruginosa 105MG = orfPa105, previously annotated as hypothetical protein. dP. aeruginosa S742_C15_BS (NFFO01000062.1), clinical class 1 integron, downstream context identical to P. aeruginosa 105MG, but lacking the Tn21-like region upstream. eS. enterica subsp. enterica serovar Johannesburg FSIS1609335 (AAIUOI010000042.1), class 1 integron, downstream flanked by Tn21 elements, ISPa38 and IS110. f S. enterica ADRDL-2811 (AAKHBQ010000151.1), downstream flanked by Tn21 elements. a, d–f Entire contig shown. Attachment sites: attI, marked as blue rhomb; attC, marked as green rectangle; hp, hypothetical protein; aspA, aspartate ammonia lyase; catB3, chloramphenicol transferase; aph(3′)-XV, aminoglycoside phosphotransferase; xerC, tyrosine recombinase (integrase); IS1071 (Tn3 family): single element, including transposase and flanking inverted repeats; Tn5051-like tnp region consisting of tnpA: transposase, tnpR: resolvase and tnpM: putative transposition regulator; intI1, class 1 integron integrase; blaVIM-1, metallo-β-lactamase VIM-1; qacEΔ, quarternary ammonium compound resistance protein (truncated); GNAT, Gcn5-related N-acetyltransferase; tniA–tniR and urf-2, tni region (Tn21-like); aac(6′)-Ib, aminoglycoside acetyltransferase; blaOXA-2, class D β-lactamase OXA-2; ant(3″)-Ia, aminoglycoside nucleotidyltransferase; ISPa38 (Tn3 family); and an IS110 family element

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So far, gar is a rare but already widely dispersed gene in wastewater metagenomes from at least eight countries in Europe, Asia, Africa and Australia (Table S5). Additional transfer events to other pathogens are therefore plausible. Detection of gar only in wastewater-impacted environments, not in metagenomes from human individuals, is coherent with its presence in a small proportion of the human population. This implies that targeted investigations of wastewater would be suitable for both initial detection and monitoring, as a single sewage sample reflects the microbiota from a very large number of individuals [48].

Conclusions

Most clinically important resistance genes are discovered as a consequence of treatment failure or by screening clinical isolates. The combination of integron-focused functional metagenomics and in silico filtering of known resistances allowed us to explore environmental samples for already mobilised, novel resistance genes. With this approach, we discovered gar, a new mobile resistance gene providing high-level resistance against garosamine-containing aminoglycosides. Despite its presence in the clinics, gar has evaded discovery as it does not resemble previously known aminoglycoside resistance genes. The knowledge presented here offers possibilities for early surveillance, actions to reduce transmission, gene-based diagnostics and ultimately improved treatment.

Methods

Detailed material and methods with references are found in Additional file 5.

Bacterial strains

Metagenomic library construction and functional screenings were conducted in E. coli DH10β (NEB). Functional verifications were performed in E. coli C600Z1 (Expressys) and GAR-induced increases in aminoglycoside MICs were determined in E. coli BL21(DE3) (Invitrogen). P. aeruginosa 105MG [33] was kindly supplied by Professors C. Giske and G. Rossolini.

Metagenomic DNA samples

DNA was extracted, pooled and amplified with three sets of primers targeting the gene cassette array of class 1 integrons from sediment samples collected from Mutha River (Pune, Maharashtra, India) and Isakavagu/Nakkavagu River (Patancheru Enviro Tech Ltd. (PETL) near Hyderabad, India) as described before [9]. In contrast to the previously performed amplification of the same samples [9], 5′ phosphorylated primers were used to generate inserts for metagenomics libraries.

Metagenomic library preparation and functional selection

To identify mobilised novel resistance determinants, class 1 integron gene cassette libraries were prepared and screened following the protocol by Forsberg et al. [3] with some modifications. The plasmid pZE21-Pbla (pZE21-MCS1 harbouring the constitutively active promoter Pbla) was linearised, dephosphorylated and ligated with the amplified class 1 integron gene cassettes to create the libraries, which were electroporated into E. coli DH10β.

For functional selection, 100 μl of each metagenomic library was plated on LB + Kan50 agar containing one of 13 different antibiotics (ciprofloxacin, trimethoprim, gentamicin, tigecycline, chloramphenicol, nitrofurantoin, rifampicin, cefotaxime, ertapenem, imipenem, meropenem, sulfamethoxazole and colistin) at three different concentrations (4 × MIC, 8 × MIC and clinical breakpoint concentration). All colonies from a single plate were scraped off, resuspended in LB + 20% glycerol and frozen at − 80 °C.

Amplicon-PCR and sequencing

Pooled antibiotic resistant clone libraries were used as PCR templates to prepare amplicons with barcoded primers that allowed allocation of the antibiotics and concentrations used for selecting clones. Amplicons were combined into two pools (16 amplicons each), and sequencing libraries were prepared from each pool using SMRTbell™ Template Prep Kit 1.0-SPv3. The two libraries were sequenced on separate PacBio Sequel™ SMRT® cells in the Science for Life Laboratories (Uppsala, Sweden).

Integron amplicon read analysis

Open reading frames were predicted using Prodigal [49] (v2.6.3). The predicted ORFs were searched against NCBI’s non-redundant protein database (last update 13.04.2017) and ResFinder [50] (last update 15.04.2018) using Diamond [51] (v0.9.24.125). We defined known ARGs as ORFs with identities greater than 95% and coverage greater than 85% to their homologues in the ResFinder database. Reads that contained known ARGs responsible for the respective phenotype were filtered out.

To identify promising putative novel resistance genes, a manual search of the read sets for complete ORFs that were highly abundant in their set of reads followed. Presence of the cassette amplification primers was required to ensure that the ORF originated from an integron and that it was solely responsible for the resistance phenotype.

Functional verification of novel resistance genes

Resistance gene candidates were synthesised and tested in E. coli C600Z1 pZE21-MCS1 as described earlier [9]. Subsequently, gar was inserted into pUC19, replacing the bla gene and transformed into E. coli BL21(DE3) to test it in an expression system without any aminoglycoside resistance.

MIC determination

Minimal inhibitory concentrations (MICs) were determined by broth microdilution in cation-adjusted Mueller-Hinton medium. Serial dilutions of tested antibiotics were prepared in triplicate in 96-well plates and inoculated with 5 × 105 cells/ml per well (CLSI standard [52]) at a final volume of 200 μl. After 24 h incubation at 37 °C and 180 rpm, the optical density was measured and MIC was defined as the lowest concentration of an antimicrobial that reduced growth to OD650 ≤ 0.2 [53].

Whole genome sequencing

Genomic DNA was isolated using the DNeasy® Blood & Tissue Kit (Qiagen) and sent to FIMM Technology Centre in Helsinki, Finland, for next generation sequencing. The KAPA HyperPlus Kit was used for library preparation and paired-end sequencing was performed on a MiSeq® (Illumina). The paired-end datasets were filtered and trimmed using the Trim Galore (v0.4.4) software. SPAdes [54] (v3.12.0) was used to assemble the short reads into 134 contigs with a length greater than 500 bp. The regions around the gene (Fig. 4) were scaffolded from contigs 1, 3, 62, 83 and 89 using the previously recovered integron sequence (GenBank accession: AJ786649.2) and by manually exploring De Bruijn graphs with the Bandage software [55] (v0.8.1) as well as experimental control by PCR.

Multi-locus sequence typing

Contigs were searched against the PubMLST database [56]. P. aeruginosa 105MG was previously classified as ST227 [33], but whole genome sequencing resulted in a single nucleotide difference in the mutL allele changing the sequence type to ST235.

Metagenome search

The abundance of gar was searched in 1251 public metagenomic datasets (Additional file 2). Diamond [51] (v0.9.24.125) was used to map the reads to the reference protein with 100% identity and an ORF-length greater than 20 amino acids. To study the genetic context around the novel ARG, short reads from selected metagenomic datasets were mapped to the reference sequences from P. aeruginosa 105MG and Luteimonas sp. 83-4 using Bowtie 2 [57] (v2.2.9). Integron attachment sites were detected by identifying marginal paired-end reads using the Tablet software [58] (v1.19.05).

Phylogenetic trees

Sequences of the 1000 proteins most closely related to GAR were collected using three iterations of PSI-BLAST [59] on the NCBI non-redundant protein database. The retrieved proteins, GAR and all aminoglycoside resistance proteins from ResFinder were aligned with MAFFT [60] (v7.310). The phylogenetic tree was calculated by FastTree [61] (v2.1.9) using the maximum likelihood algorithm, Jones-Taylor-Thornton model, with 1000 bootstraps. Protein accession numbers and the full version of the tree are available in Additional files 3 and 4. The Interactive Tree Of Life (iTOL v4) online tool [62] was used to prepare the phylogenetic tree for display.

Protein model

The I-TASSER server for protein structure and function prediction was used to create models of GAR [63]. The model with the highest confidence score (C-score, − 0.21) is shown. DeepView/Swiss-PdbViewer [64] (v4.1.0) was used to create the ribbon presentation.