The draft genome of multidrug-resistant Aeromonas sp. ARM81 isolated from a wastewater treatment plant in Warsaw (Poland) was obtained. Sequence analysis revealed multiple genes conferring resistance to aminoglycosides, β-lactams or tetracycline. Three different β-lactamase genes were identified, including an extended-spectrum β-lactamase gene bla PER-1. The antibiotic susceptibility was experimentally tested. Genome sequencing also allowed us to investigate the plasmidome and transposable mobilome of ARM81. Four plasmids, of which two carry phenotypic modules (i.e., genes encoding a zinc transporter ZitB and a putative glucosyltransferase), and 28 putative transposase genes were identified. The mobility of three insertion sequences (isoforms of previously identified elements ISAs12, ISKpn9 and ISAs26) was confirmed using trap plasmids.
Aeromonas spp. are frequently recognized as pathogens of poikilothermic animals (e.g., Aeromonas salmonicida), but also humans (e.g., Aeromonas hydrophila) (Igbinosa et al. 2012). The pathogenesis of Aeromonas infections is multifactorial, as these bacteria produce a wide variety of virulence factors, e.g., hemolysins, entero- and endotoxins (Tomas 2012). Unfortunately, the increasing resistance to antimicrobial drugs among aeromonads threatens our ability to fight infections caused by these bacteria (Skwor et al. 2014).
Resistance to antibiotics and heavy metals is common in bacteria from wastewater treatment plants (WWTPs) (Li et al. 2015). Moreover, it has been suggested that this particular kind of environment is a specific reservoir of resistance genes (Munck et al. 2015). Aeromonads (which are commonly found in WWTPs) seem to be a good model for studies concerning the effect of water resource recovery facility effluents on the development and dissemination of antibiotic resistance. They can persist in the environment for a long time, are linked to a variety of human infections and carry multiple mobile genetic elements (MGEs) which may contribute to antibiotic resistance dissemination (Picao et al. 2013; Zhang et al. 2015).
As of August 20, 2016, according to the NCBI genome browser (http://www.ncbi.nlm.nih.gov/genome/browse/), 42 plasmids of Aeromonas spp. have been fully sequenced and analyzed. These plasmids are of various sizes (between 2524 and 198,307 bp) and some are cryptic (e.g., pAsa1, pAsa2 and pAsa3) (Attere et al. 2015), while others harbor virulence and/or antibiotic resistance genes (e.g., pAsa4 and pAsa5) (Vincent et al. 2014). Several other studies have investigated the transposable mobilome of Aeromonas spp., which led to the identification of novel transposons and insertion sequences [e.g., (Reith et al. 2008; Dobiasova et al. 2015)].
In this study, the draft genome of the multidrug-resistant strain Aeromonas sp. ARM81 isolated from a WWTP in Poland was investigated. Analyses of this genome provided insights into the resistome and mobilome of the strain.
Materials and methods
Standard molecular biology procedures
Plasmid DNA isolation by alkaline lysis and agarose gel electrophoresis was carried out according to the protocols described by Sambrook and Russell (2001). All PCRs were performed with Phusion high-fidelity DNA polymerase (Life Technologies). The active transposable elements were identified by performing PCRs with the trap plasmid insertion derivatives (as template DNAs) and a set of cassette-specific primers (Table S1, Supplementary materials) under the conditions described previously (Bartosik et al. 2003; Szuplewska and Bartosik 2009), followed by Sanger sequencing. Gaps within the plasmids and the Tn5393k transposon were closed by Sanger sequencing of amplicons obtained by PCRs performed with the primers listed in Table S1 (Supplementary material), under the following conditions: 35 cycles (denaturation at 96 °C for 30 s, annealing at 50 °C for 30 s, extension at 72 °C for 1 min) preceded by 3-min denaturation at 96 °C, and followed by 5-min extension at 72 °C. Amplified DNA fragments were analyzed by agarose gel electrophoresis and, if necessary, purified using a Gel Out kit (A&A Biotechnology) according to the manufacturer’s instructions.
Antibiotic susceptibility testing
Minimum inhibitory concentrations (MICs) for Aeromonas sp. ARM81 were determined on Mueller–Hinton agar plates (OXOID) using MIC Test Strips (Liofilchem) containing the following antimicrobial agents: ampicillin, ceftazidime, chloramphenicol, ciprofloxacin, erythromycin, gentamicin, kanamycin, meropenem, rifampicin, streptomycin, tetracycline or trimethoprim. MICs were read after incubation at 30 °C for 24 h.
Identification of active transposable elements (TEs)
For the identification of active TEs, two trap vectors were used: pGBG1 (Schneider et al. 2000) and pMAT1CM (constructed in this work). These vectors contain either the cI-tetA cassette or a levansucrase-coding gene (sacB), both enabling positive selection of transposition events (Dziewit et al. 2012). pMAT1CM was constructed by cloning the sacB gene (excised by the XbaI/PstI endonucleases) from the plasmid pEBB10 (Bartosik et al. 2008) into the broad host range plasmid pBBR1MCS (Kovach et al. 1994).
Each trap plasmid was introduced into a Rifr derivative of the strain ARM81 by triparental mating as described previously (Bartosik et al. 2001). The identification of functional TEs using each trap plasmid was performed according the scheme described previously (Dziewit et al. 2012).
Genomic DNA of ARM81 was isolated using the CTAB/Lysozyme method (Sambrook and Russell 2001). An Illumina TruSeq library was constructed following manufacturer’s instructions. Sequencing was performed on an Illumina MiSeq instrument using the v3 chemistry kit. Sequence reads were filtered for quality and assembled using Newbler version 3.0 software (Roche). Sanger sequencing of the ‘active’ transposable elements localized within trap plasmids as well as PCR amplicons obtained for the closing of gaps within plasmid and transposon sequences was performed on ABI3730xl Genetic Analyzer (Life Technologies) using BigDye Terminator Mix version 3.1 chemistry (Life Technologies).
The genome of ARM81 was automatically annotated using the RAST server (Aziz et al. 2008). To identify genetic determinants responsible for the resistance phenotype, the genome was screened using the Comprehensive Antibiotic Research Database (CARD) (McArthur et al. 2013)] and BacMet: antibacterial biocide and metal resistance genes database (Pal et al. 2014). Plasmid sequences were manually annotated using Artemis software (Rutherford et al. 2000). Similarity searches were performed using the BLAST programs (Altschul et al. 1997) and Pfam database (Finn et al. 2014). Putative ncRNA and tRNA sequences were identified using the Rfam (Nawrocki et al. 2014), tRNAScan-SE (Lowe and Eddy 1997) and ARAGORN programs (Laslett and Canback 2004). The BLAST and ISfinder (Siguier et al. 2006) database were used for identification and analysis of transposable elements. Plasmid and transposon annotations were visualized and compared using the Easyfig program (Sullivan et al. 2011).
Nucleotide sequence accession number
The whole-genome shotgun project has been deposited in the NCBI GenBank database under the accession number SAMN04225614.
Results and discussion
Aeromonas sp. ARM81 was isolated from a sample of mechanically pre-treated wastewater collected at a municipal WWTP in Warsaw (Poland). This isolate was randomly picked from bacteria that produced colonies on Luria–Bertani (LB) agar plates supplemented with 50 μg ml−1 kanamycin after overnight incubation at 30 °C. ARM81 was classified by 16S rRNA and rpoB genes analysis as Aeromonas sp., with the highest sequence similarity to Aeromonas caviae (punctata).
Illumina sequencing and assembly of the genome of Aeromonas sp. ARM81 gave 71 scaffolds consisting of 161 contigs with a total length of 4,640,951 bp. The GC content of the ARM81 draft genome was estimated as 61.3 %, which is in agreement with corresponding values for other Aeromonas genomes, ranging between 58.17 % (A. salmonicida subsp. salmonicida A449) and 62 % (A. hydrophila 4AK4). Automatic annotation using the RAST server identified 4240 genes with an average length of 925.8 bp (Table S2, Supplementary material). The total length of the predicted genes was 3,925,446 bp, which covers 84.6 % of the genome. Additionally, 94 tRNA genes were identified (Table S2, Supplementary material).
Aeromonas sp. ARM81 was initially identified on the basis of kanamycin resistance. However, antibiotic susceptibility testing performed using MIC Test Strips revealed that the strain also shows decreased susceptibility to other antimicrobials representing different classes, i.e., β-lactams, aminoglycosides and tetracyclines (Table 1).
Within the ARM81 genome, seven antibiotic resistance genes were found, namely: (1–3) three different phosphotransferases, aph(3′)-VIb, aph(3′′)-Ib and aph(6)-Id, conferring resistance to aminoglycosides (Ramirez and Tolmasky 2010); (4) tetA(E) encoding a tetracycline efflux protein (Li and Nikaido 2004); (5) an extended-spectrum β-lactamase gene bla PER-1, known for its ability to hydrolyze a broad range of β-lactams, excluding carbapenems, cephamycins and oxacillin (Poirel et al. 2005); (6) bla MOX-12 encoding an AmpC β-lactamase [MOX enzymes are thought to have originated in Aeromonas spp. and been mobilized onto plasmids among various bacteria (Philippon et al. 2002)]; and (7) a class D β-lactamase [this class groups OXA-like proteins, which may display an activity toward extended-spectrum cephalosporins and carbapenems (Bush and Fisher 2011)]. It is worth mentioning that bla PER-1, aph(3′)-VIb, aph(3′′)-Ib and aph(6)-Id are located within a non-composite transposon (named Tn5393k), which resembles Tn5393d from Alcaligenes faecalis FL-424/98 (Mantengoli and Rossolini 2005) and is flanked by 5-bp direct repeats (AAGAA). Tn5393k differs from Tn5393d only by a lack of one insertion sequence, ISPpu17 (Fig. 1). Based on the summarized results of antibiotic susceptibility testing and identification of genes conferring resistance to three different classes of antimicrobial agents, Aeromonas sp. ARM81 was defined as a multidrug-resistant strain.
In addition to antibiotic resistance genes, the BacMet database (Pal et al. 2014) predicted seven heavy metal resistance genetic modules, including: (1) the acr3 gene conferring resistance to arsenic (Bobrowicz et al. 1997); (2–4) two czcD genes and one czcAB gene cluster conferring resistance to cobalt, zinc and cadmium (Nies 1992); (v) the zitB gene for the zinc transporter (Lee et al. 2002); and (6–7) two zntA genes, conferring resistance to cadmium, lead and zinc (Rosen 2002).
Analyzing the draft genome of Aeromonas sp. ARM81, we also attempted to define its mobilome (i.e., plasmidome and transposable mobilome), since MGEs are frequent vehicles of horizontal transfer of various resistance genes, enabling their dissemination through microbiomes (von Wintersdorff et al. 2016). In Aeromonas sp. ARM81 genome, 28 predicted transposase genes were identified. Analysis revealed that they encode transposases of TEs belonging to 10 families described in the ISfinder database (Siguier et al. 2006), namely: ISAs1, IS4 (IS4, IS10 and ISH8 groups), IS5 (IS5 and IS903 groups), IS21, IS200/IS605, IS66, IS630, IS1595, IS1634 and Tn3.
To identify active (mobile) TEs, two trap vectors, pGBG1 and pMAT1CM (enabling positive selection of transposition events), were used. The analysis of 100 random insertional clones revealed only three types of insertion sequences. Sequencing showed that these were isoforms (98–99 % nucleotide sequence identity) of previously identified elements, i.e., ISAs12, ISKpn9, both belonging to ISAs1 family, and ISAs26 grouped within IS200/IS605 family.
Among the obtained contigs, four had much higher coverage than the average. We assumed that these corresponded to plasmids visible in agarose gel electrophoresis of the ARM81 DNA extracted by alkaline lysis procedure (data not shown). PCRs with primers designed on extremities of the contigs were used to close the plasmids. Linear representations of the plasmid genomes are shown in Fig. 2, and the summary of the genes and ncRNAs identified within the plasmids (including their position, transcriptional orientation, the size of the encoded proteins, and their closest known homologs) is presented in Table S3 (Supplementary Materials).
The smallest plasmid, ColE1-like pARM81P1, is 2890 bp and carries only two genes encoding replication (RepB) and mobilization (MobA) proteins. The second replicon, pARM81P2 (5281 bp), is another ColE1-like plasmid with repB and RNAI [which is known to regulate replication of ColE1 (Helmer-Citterich et al. 1988)] and six putative genes, including zitB encoding a zinc transporter gene and its putative regulator arsR. ZitB is a charge relay system for proton translocation, responsible for Zn(II) efflux, and therefore, it may confer resistance to zinc (Lee et al. 2002).
The third plasmid, pARM81P3 (6981 bp), shows some sequence similarity to plasmids previously identified in Aeromonas spp., e.g., pAhD4-2 and pAH06-06-2 (Fig. 1). Apparently, replication of such plasmids depends on a RepA protein whose expression is regulated by the upstream region PK-repBA (Athanasopoulos et al. 1999). Stable maintenance of this type of plasmids is probably ensured by a predicted type II (parDE-like) toxin–antitoxin system, while mobilization is apparently mediated by MobA and MobC proteins. Analysis also revealed a gene (gtr) encoding a putative glucosyltransferase, which might alter the structure and properties of lipopolysaccharides produced by the ARM81 strain (Lehane et al. 2005).
The largest plasmid, pARM81P4, is 7599 bp. Its nucleotide sequence and predicted genes do not show any significant similarity to sequences deposited in GenBank (NCBI); however, the predicted protein product of the largest gene contains two distinguishable domains: (1) PriCT-2 found in primases and (2) VirE of the virulence-associated proteins, which suggests that it may be a bifunctional protein.
Comparative genomic analyses of the ARM81 plasmids revealed that pARM81P2 and pARM81P3 are similar to several replicons found in Aeromonas spp., e.g., A. aquariorum AAK1 (Wu et al. 2012), A. hydrophila D4 (NCBI accession numbers: CP013967 and CP013969) and A. hydrophila AL06-06 (Tekedar et al. 2015), while pARM81P1 and pARM81P4 are unique, as they do not show homology with other known replicons (Fig. 2). The shared similarities between pARM81P2 and pARM81P3 and their homologs cover regions which might be defined as a ‘plasmid backbone,’ as they encode genes responsible for plasmid replication, maintenance and mobilization to conjugal transfer (Fig. 2). This is a common phenomenon observed in other bacterial plasmids harbored by representatives of a specific genus [e.g., plasmids of Paracoccus spp. (Maj et al. 2013) or Psychrobacter spp. (Dziewit et al. 2013)] or belonging to a particular incompatibility group [e.g., IncL/M plasmids (Adamczuk et al. 2015)], which supports the hypothesis that there is a clear distinction between the permanent members (genes) constituting plasmid backbones and the operative genes (additional load) that can be exchanged between replicating elements in the cell and are not conserved elements of plasmids (Norman et al. 2009).
WWTPs are known to be rich in nutrients and a mixture of toxic compounds/selective agents, including antibiotics and heavy metals (Baker-Austin et al. 2006). We are unable to say whether Aeromonas sp. ARM81 is permanently inhabiting this niche or it was just ‘passing through.’ Either way, insights into its genome content suggest that the strain is well adapted to unfavorable conditions as it contains multiple antibiotic and heavy metal resistance genes and a number of efflux transporters extruding a variety of compounds from the cell (data not shown). Identification of plasmids and various TEs (including the Tn5393d-like transposon with bla PER-1) in the ARM81 genome suggests that this strain actively participates in horizontal transfer of various genetic information (including antibiotic resistance genes) in the environment.
Adamczuk M, Zaleski P, Dziewit L, Wolinowska R, Nieckarz M, Wawrzyniak P, Kieryl P, Plucienniczak A, Bartosik D (2015) Diversity and global distribution of IncL/M plasmids enabling horizontal dissemination of β-lactam resistance genes among the Enterobacteriaceae. Biomed Res Int 2015:414681
Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25:3389–3402
Athanasopoulos V, Praszkier J, Pittard AJ (1999) Analysis of elements involved in pseudoknot-dependent expression and regulation of the repA gene of an IncL/M plasmid. J Bacteriol 181:1811–1819
Attere SA, Vincent AT, Trudel MV, Chanut R, Charette SJ (2015) Diversity and homogeneity among small plasmids of Aeromonas salmonicida subsp. salmonicida linked with geographical origin. Front Microbiol 6:1274
Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M, Meyer F, Olsen GJ, Olson R, Osterman AL, Overbeek RA, McNeil LK, Paarmann D, Paczian T, Parrello B, Pusch GD, Reich C, Stevens R, Vassieva O, Vonstein V, Wilke A, Zagnitko O (2008) The RAST server: rapid annotations using subsystems technology. BMC Genomics 9:75
Baker-Austin C, Wright MS, Stepanauskas R, McArthur JV (2006) Co-selection of antibiotic and metal resistance. Trends Microbiol 14:176–182
Bartosik D, Szymanik M, Wysocka E (2001) Identification of the partitioning site within the repABC-type replicon of the composite Paracoccus versutus plasmid pTAV1. J Bacteriol 183:6234–6243
Bartosik D, Sochacka M, Baj J (2003) Identification and characterization of transposable elements of Paracoccus pantotrophus. J Bacteriol 185:3753–3763
Bartosik D, Putyrski M, Dziewit L, Malewska E, Szymanik M, Jagiello E, Lukasik J, Baj J (2008) Transposable modules generated by a single copy of insertion sequence ISPme1 and their influence on structure and evolution of natural plasmids of Paracoccus methylutens DM12. J Bacteriol 190:3306–3313
Bobrowicz P, Wysocki R, Owsianik G, Goffeau A, Ulaszewski S (1997) Isolation of three contiguous genes, ACR1, ACR2 and ACR3, involved in resistance to arsenic compounds in the yeast Saccharomyces cerevisiae. Yeast 13:819–828
Bush K, Fisher JF (2011) Epidemiological expansion, structural studies, and clinical challenges of new β-lactamases from gram-negative bacteria. Annu Rev Microbiol 65:455–478
Dobiasova H, Videnska P, Dolejska M (2015) Complete sequences of IncU plasmids harboring quinolone resistance genes qnrS2 and aac(6′)-Ib-cr in Aeromonas spp. from ornamental fish. Antimicrob Agents Chemother 60:653–657
Dziewit L, Baj J, Szuplewska M, Maj A, Tabin M, Czyzkowska A, Skrzypczyk G, Adamczuk M, Sitarek T, Stawinski P, Tudek A, Wanasz K, Wardal E, Piechucka E, Bartosik D (2012) Insights into the transposable mobilome of Paracoccus spp. (Alphaproteobacteria). PLoS One 7:e32277
Dziewit L, Cegielski A, Romaniuk K, Uhrynowski W, Szych A, Niesiobedzki P, Zmuda-Baranowska MJ, Zdanowski MK, Bartosik D (2013) Plasmid diversity in arctic strains of Psychrobacter spp. Extremophiles 17:433–444
Finn RD, Bateman A, Clements J, Coggill P, Eberhardt RY, Eddy SR, Heger A, Hetherington K, Holm L, Mistry J, Sonnhammer EL, Tate J, Punta M (2014) Pfam: the protein families database. Nucleic Acids Res 42:D222–D230
Helmer-Citterich M, Anceschi MM, Banner DW, Cesareni G (1988) Control of ColE1 replication: low affinity specific binding of Rop (Rom) to RNAI and RNAII. EMBO J 7:557–566
Igbinosa IH, Igumbor EU, Aghdasi F, Tom M, Okoh AI (2012) Emerging Aeromonas species infections and their significance in public health. Sci World J 2012:625023
Kovach ME, Phillips RW, Elzer PH, Roop RM 2nd, Peterson KM (1994) pBBR1MCS: a broad-host-range cloning vector. Biotechniques 16:800–802
Laslett D, Canback B (2004) ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences. Nucleic Acids Res 32:11–16
Lee SM, Grass G, Haney CJ, Fan B, Rosen BP, Anton A, Nies DH, Rensing C (2002) Functional analysis of the Escherichia coli zinc transporter ZitB. FEMS Microbiol Lett 215:273–278
Lehane AM, Korres H, Verma NK (2005) Bacteriophage-encoded glucosyltransferase GtrII of Shigella flexneri: membrane topology and identification of critical residues. Biochem J 389:137–143
Li XZ, Nikaido H (2004) Efflux-mediated drug resistance in bacteria. Drugs 64:159–204
Li AD, Li LG, Zhang T (2015) Exploring antibiotic resistance genes and metal resistance genes in plasmid metagenomes from wastewater treatment plants. Front Microbiol 6:1025
Lowe TM, Eddy SR (1997) tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res 25:955–964
Maj A, Dziewit L, Czarnecki J, Wlodarczyk M, Baj J, Skrzypczyk G, Giersz D, Bartosik D (2013) Plasmids of carotenoid-producing Paracoccus spp. (Alphaproteobacteria)—structure, diversity and evolution. PLoS One 8:e80258
Mantengoli E, Rossolini GM (2005) Tn5393d, a complex Tn5393 derivative carrying the PER-1 extended-spectrum beta-lactamase gene and other resistance determinants. Antimicrob Agents Chemother 49:3289–3296
McArthur AG, Waglechner N, Nizam F, Yan A, Azad MA, Baylay AJ, Bhullar K, Canova MJ, De Pascale G, Ejim L, Kalan L, King AM, Koteva K, Morar M, Mulvey MR, O’Brien JS, Pawlowski AC, Piddock LJ, Spanogiannopoulos P, Sutherland AD, Tang I, Taylor PL, Thaker M, Wang W, Yan M, Yu T, Wright GD (2013) The comprehensive antibiotic resistance database. Antimicrob Agents Chemother 57:3348–3357
Munck C, Albertsen M, Telke A, Ellabaan M, Nielsen PH, Sommer MO (2015) Limited dissemination of the wastewater treatment plant core resistome. Nat. Commun. 6:8452
Nawrocki EP, Burge SW, Bateman A, Daub J, Eberhardt RY, Eddy SR, Floden EW, Gardner PP, Jones TA, Tate J, Finn RD (2014) Rfam 12.0: updates to the RNA families database. Nucleic Acids Res 43:D130–D137
Nies DH (1992) Resistance to cadmium, cobalt, zinc, and nickel in microbes. Plasmid 27:17–28
Norman A, Hansen LH, Sorensen SJ (2009) Conjugative plasmids: vessels of the communal gene pool. Philos Trans R Soc Lond B Biol Sci 364:2275–2289
Pal C, Bengtsson-Palme J, Rensing C, Kristiansson E, Larsson DG (2014) BacMet: antibacterial biocide and metal resistance genes database. Nucleic Acids Res 42:D737–D743
Philippon A, Arlet G, Jacoby GA (2002) Plasmid-determined AmpC-type beta-lactamases. Antimicrob Agents Chemother 46:1–11
Picao RC, Cardoso JP, Campana EH, Nicoletti AG, Petrolini FV, Assis DM, Juliano L, Gales AC (2013) The route of antimicrobial resistance from the hospital effluent to the environment: focus on the occurrence of KPC-producing Aeromonas spp. and Enterobacteriaceae in sewage. Diagn Microbiol Infect Dis 76:80–85
Poirel L, Cabanne L, Vahaboglu H, Nordmann P (2005) Genetic environment and expression of the extended-spectrum beta-lactamase blaPER-1 gene in gram-negative bacteria. Antimicrob Agents Chemother 49:1708–1713
Ramirez MS, Tolmasky ME (2010) Aminoglycoside modifying enzymes. Drug Resist Updates 13:151–171
Reith ME, Singh RK, Curtis B, Boyd JM, Bouevitch A, Kimball J, Munholland J, Murphy C, Sarty D, Williams J, Nash JH, Johnson SC, Brown LL (2008) The genome of Aeromonas salmonicida subsp. salmonicida A449: insights into the evolution of a fish pathogen. BMC Genomics 9:427
Rosen BP (2002) Transport and detoxification systems for transition metals, heavy metals and metalloids in eukaryotic and prokaryotic microbes. Comp Biochem Physiol A Mol Integr Physiol 133:689–693
Rutherford K, Parkhill J, Crook J, Horsnell T, Rice P, Rajandream MA, Barrell B (2000) Artemis: sequence visualization and annotation. Bioinformatics 16:944–945
Sambrook J, Russell DW (2001) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, New York
Schneider D, Faure D, Noirclerc-Savoye M, Barriere AC, Coursange E, Blot M (2000) A broad-host-range plasmid for isolating mobile genetic elements in gram-negative bacteria. Plasmid 44:201–207
Siguier P, Perochon J, Lestrade L, Mahillon J, Chandler M (2006) ISfinder: the reference centre for bacterial insertion sequences. Nucleic Acids Res 34:D32–D36
Skwor T, Shinko J, Augustyniak A, Gee C, Andraso G (2014) Aeromonas hydrophila and Aeromonas veronii predominate among potentially pathogenic ciprofloxacin- and tetracycline-resistant Aeromonas isolates from Lake Erie. Appl Environ Microbiol 80:841–848
Sullivan MJ, Petty NK, Beatson SA (2011) Easyfig: a genome comparison visualizer. Bioinformatics 27:1009–1010
Szuplewska M, Bartosik D (2009) Identification of a mosaic transposable element of Paracoccus marcusii composed of insertion sequence ISPmar4 (ISAs1 family) and an IS1247a-driven transposable module (TMo). FEMS Microbiol Lett 292:216–221
Tekedar HC, Karsi A, Akgul A, Kalindamar S, Waldbieser GC, Sonstegard T, Schroeder SG, Lawrence ML (2015) Complete genome sequence of fish pathogen Aeromonas hydrophila AL06-06. Genome Announc 3:e00368-e00415
Tomas JM (2012) The main Aeromonas pathogenic factors. ISRN Microbiol 2012:256261
Vincent AT, Trudel MV, Paquet VE, Boyle B, Tanaka KH, Dallaire-Dufresne S, Daher RK, Frenette M, Derome N, Charette SJ (2014) Detection of variants of the pRAS3, pAB5S9, and pSN254 plasmids in Aeromonas salmonicida subsp. salmonicida: multidrug resistance, interspecies exchanges, and plasmid reshaping. Antimicrob Agents Chemother 58:7367–7374
von Wintersdorff CJ, Penders J, van Niekerk JM, Mills ND, Majumder S, van Alphen LB, Savelkoul PH, Wolffs PF (2016) Dissemination of antimicrobial resistance in microbial ecosystems through horizontal gene transfer. Front Microbiol 7:173
Wu CJ, Wang HC, Chen CS, Shu HY, Kao AW, Chen PL, Ko WC (2012) Genome sequence of a novel human pathogen, Aeromonas aquariorum. J Bacteriol 194:4114–4115
Zhang S, Han B, Gu J, Wang C, Wang P, Ma Y, Cao J, He Z (2015) Fate of antibiotic resistant cultivable heterotrophic bacteria and antibiotic resistance genes in wastewater treatment processes. Chemosphere 135:138–145
This work was supported by the National Science Centre, Poland (DEC-2012/05/N/NZ9/01262). The genome sequencing was carried out in the DNA Sequencing and Oligonucleotide Synthesis Laboratory IBB PAS using the CePT infrastructure financed by the European Union—the European Regional Development Fund [Innovative economy 2007–2013, Agreement POIG.02.02.00-14-024/08-00].
Communicated by Yusuf Akhter.
About this article
Cite this article
Adamczuk, M., Dziewit, L. Genome-based insights into the resistome and mobilome of multidrug-resistant Aeromonas sp. ARM81 isolated from wastewater. Arch Microbiol 199, 177–183 (2017). https://doi.org/10.1007/s00203-016-1285-6
- Aeromonas sp. ARM81
- Antibiotic resistance gene
- Transposable element