BRIEF RESEARCH REPORT article
Genetic Features of Antarctic Acinetobacter radioresistens Strain A154 Harboring Multiple Antibiotic-Resistance Genes
- 1Laboratorio de Investigación en Agentes Antibacterianos (LIAA), Departamento de Microbiología, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile
- 2Millennium Nucleus for Collaborative Research on Bacterial Resistance (MICROB-R), Santiago, Chile
- 3Institute for Medical Microbiology, Immunology and Hygiene, University of Cologne, Cologne, Germany
- 4German Center for Infection Research (DZIF), Partner Site Bonn-Cologne, Cologne, Germany
- 5Departamento de Ciencias Biológicas y Químicas, Facultad de Medicina y Ciencia, Universidad San Sebastián, Concepción, Chile
While antibiotic-resistant bacteria have been detected in extreme environments, including Antarctica, to date there are no reports of Acinetobacter species isolated from this region. Here, we characterized by whole-genome sequencing (WGS) the genetic content of a single antibiotic-resistant Acinetobacter spp. isolate (A154) collected in Antarctica. The isolate was recovered in 2013 from soil samples at Fildes Peninsula, Antarctica, and was identified by detection of the intrinsic OXA-23 gene, and confirmed by Tetra Correlation Search (TCS) and WGS. The antibiotic susceptibility profile was determined by disc diffusion, E-test, and broth microdilution methods. From WGS data, the acquired resistome and insertion sequence (IS) content were identified by in silico analyses. Plasmids were studied by the alkaline lysis method followed by pulsed-field gel electrophoresis and conventional PCR. The A154 isolate was identified as A. radioresistens by WGS analysis and displayed >99.9 of similarity by TCS in relation with the databases. Moreover, it was resistant to ampicillin, ceftriaxone, ceftazidime, cefepime, cefotaxime, streptomycin, and kanamycin. Likewise, in addition to the intrinsic blaOXA−23−like gene, A154 harbored the plasmid-encoded antibiotic-resistance genes blaPER−2, tet(B), aph(3′)-Vla, strA, and strB, as well as a large diversity of ISs. This is the first report of antibiotic-resistant A. radioresistens in Antarctica. Our findings show the presence of several resistance genes which could be either intrinsic or acquired in the region.
Antarctica possesses one of the most extreme environmental conditions on earth, where low temperatures, high levels of UV radiation, and low water availability, limit the growth of living organisms, including bacteria (Convey et al., 2008). In these ecosystems, diverse survival strategies to ward off competing microorganisms are present, including the production of antibiotics by environmental microbiota (Aronson et al., 2011). Lately, it has been determined that antibiotic production and resistance have ancient origins in nature, ranging from 2 billion years to 40 million years (Dcosta et al., 2011). In this sense, several antibiotic resistance genes (ARGs) have been identified in uncontaminated soil in Antarctica, confirming that this continent possesses a natural microbial community associated with a local resistome (Van Goethem et al., 2018). Although this natural phenomenon is old, the high use of antibiotics in human practice, as well as the rise of anthropic activity around the globe, have favored to increase the selection and dissemination of antibiotic resistant bacteria and antibiotic resistance determinants (Rabbia et al., 2016).
Although Antarctica has been historically considered as a pristine unexplored continent, the anthropogenic activity has been increasing recently, which could potentially have an impact on the resistome of the natural bacterial community (Rabbia et al., 2016). It has been demonstrated that the presence of military bases, scientific programs, and tourism, promotes the dissemination of ARGs possibly due to the introduction of human-related microorganisms (Hernandez and González-Acuña, 2016). For instance, we recently found that Escherichia coli isolates collected from seawater and waste-water treatment plants located in the Antarctic Treaty area showed resistance to β-lactams, aminoglycosides, tetracycline, and trimethoprim-sulphonamide, which is probably associated with discharged of inefficiently treated water emanating from waste-water plants (Rabbia et al., 2016).
Acinetobacter radioresistens is able to survive extreme levels of oxidative stress, desiccation, and irradiation (Touchon et al., 2014; Sacher et al., 2018) and has primarily been isolated from environmental sources (i.e., cotton, water, and soil), and has also been identified as part of the human skin microbiota of healthy people (Seifert et al., 1997), as well as from fecal samples from chickens (Ngaiganam et al., 2019). Few studies on the presence of ARGs in A. radioresistens are published, and the species is considered largely susceptible to antibiotics.
A. radioresistens isolate A154 was collected from a soil sample in Antarctica in 2013. Interestingly, it displayed an unusual resistance pattern to diverse antibiotics, including β-lactams and aminoglycosides. Hence, to further understand the genetic features of the Antarctic A154 isolate containing multiple ARGs, we report its genome sequence.
Materials and Methods
Acinetobacter spp. isolate A154 was recovered from ornitogenic soil (superficial layer) in Ardley Island (−62°12′60.00″S −58°55′59.99″W) in Fildes Peninsula, Antarctica, during a scientific expedition in 2013. Specifically, the isolate was recovered in a soil sample from a lagoon shore. Fildes Peninsula is located on King George Island and holds the largest number of scientific research bases in the Antarctic Treaty Area (Rabbia et al., 2016). The isolate was grown on trypticase soy agar incubated overnight at 30°C.
Total DNA was extracted by the boiling water method and utilized as template for preliminary species identification by the detection of the intrinsic chromosomally-encoded blaOXA−23−like gene.
Susceptibility testing were performed by disc diffusion following the CLSI recommendations, for ampicillin (AMP, 10 μg), cefotaxime (CTX, 30 μg), ceftriaxone (CRO, 30 μg), ceftazidime (CAZ, 30 μg), cefepime (FEP, 30 μg), imipenem (IPM, 10 μg), meropenem (MEM, 10 μg), gentamicin (GEN, 10 μg), amikacin (AMK, 30 μg), kanamycin (KAN, 30 μg), streptomycin (STR, 10 μg), tetracycline (TET, 30 μg), and ciprofloxacin (CIP, 5 μg) (Clinical Laboratory Standards Institute, 2017). Minimum inhibitory concentrations (MICs) were determined by E-test and broth microdilution for AMP, CTX, IPM, MEM, GEN, AMK, and KAN (Clinical Laboratory Standards Institute, 2017).
Total DNA for whole-genome sequencing (WGS) was extracted using the Wizard® Genomic DNA Purification kit (Promega, USA) following the manufacturer's protocol. DNA concentration and integrity were verified using a Take3 plate (BioTek Instruments). WGS was performed by the Illumina MiSeq platform (2 × 250 bp paired end reads) with libraries prepared by the NexteraXT kit (Illumina).
In silico Genome Analyses
De novo assembly was performed by using the SPades software version 3.9 available at the CGE server (https://cge.cbs.dtu.dk/services/SPAdes/), utilizing default values (Nurk et al., 2013). Species identification was carried out by the SpeciesFinder service, version 1.3 (https://cge.cbs.dtu.dk/services/SpeciesFinder/), which is based on the 16S rRNA sequence. Genome annotation was accomplished using the NCBI Prokaryotic Genome Annotation Pipeline (PGAP) web-service (http://www.ncbi.nlm.nih.gov/genome/annotation_prok). Moreover, the draft genome was analyzed by the Comprehensive Genome Analysis service (https://www.patricbrc.org/app/ComprehensiveGenomeAnalysis), which incorporates the RAST tool kit (RASTtk). The genetic contexts of the contigs in which plasmid-encoded ARGs were detected, were plotted using the Artemis software, version 18.0.2 (Carver et al., 2012).
In order to establish the taxonomic relatedness of A154, we used the Tetra Correlation Search (TCS), which allows to compare the draft genome of this isolate against the genomes reference database GenomesDB (http://jspecies.ribohost.com/jspeciesws/#genomesdb), which contains >30.000 whole and draft genomes with pre-calculated overall genome relatedness indices (Richter et al., 2015). In addition, we determined the acquired resistome, insertion sequences (ISs) content and toxin-antitoxin (TA) systems through ResFinder (https://cge.cbs.dtu.dk/services/ResFinder/), RASTtk and Pathosystems Resource Integration Center (PATRIC) platforms. Plasmid replicons were searched using the PlasmidFinder tool (Carattoli et al., 2014) and the PATRIC platform. The genome of the isolate A154 was deposited at DDBJ/EMBL/GenBank under the accession number PXJD00000000.1.
Additionally, from WGS data we extracted the seven alleles according to the Pasteur MLST scheme which were submitted to the PubMLST database (https://pubmlst.org/) in order to assign a specific sequence type (ST).
Plasmids were isolated by the alkaline lysis method according to a standard protocol (Kado and Liu, 1981). Afterwards, DNA concentration of the plasmids extracts were measured by spectrophotometry (BioTek Instruments) and chromosomal contamination was evaluated by detecting the 16S rDNA gene, which is chromosomally encoded. After, ARGs previously detected in total DNA were screened using the pure DNA plasmids extracts. Moreover, we performed mating and plasmid curing experiments (Trevors, 1986; Leungtongkam et al., 2018).
Results and Discussion
The A154 isolate was identified as A. radioresistens according to its 16S rRNA sequence, and displayed >99.9 of similarity by TCS with the genome of A. radioresistens strain SK82 (NCBI: txid596318), thus confirming that A154 belongs to this species. Additionally, it was resistant to AMP, CRO, CTX, CAZ, FEP, KAN, and STR, intermediate to GEN, and susceptible to IMP, MEM, CIP, TET, and AMK. MICs values of AMP, CAZ, CTX, FEP, GEN, and KAN were >128, >128, 128, 32, 8, and 128 μg/mL, respectively (Table 1).
From in silico analyses, we determined that the WGS data generated resulted in 205 contigs and a N50 contig size of 131,303 bp. Moreover, A154 genome comprised 3,448,645 bp with an average GC content of 41.5%, 3,444 coding sequences (CDS), 64 transfer RNA (tRNA) genes, and 8 ribosomal RNA (rRNA) genes.
From RASTtk results, we determined that the resistome of A154 was comprised of aminoglycoside modifying enzymes (AMEs) encoded by aph(3′)-VIa, aac(3)-IIa, strA (aph(3″)-Ia), and strB (aph(6)-Id), as well as the β-lactamase genes blaOXA−23−like (intrinsic to this species), blaTEM−1B, blaSCO−1 and blaPER−2, and the tetracycline-resistance gene tet(B) (Table 1). ARGs positions on the genome of A154 are shown in Figure 1. Interestingly, the blaOXA−23−like allele identified in A154 did not match with any variant from the database, sharing a 98.18% identity with blaOXA−565 (accession number KY883665). SCO-1 encodes for a RTG-type carbenicillinase identified in Escherichia coli and Acinetobacter spp. (Papagiannitsis et al., 2007; Poirel et al., 2007). To the author's knowledge, the single report of this enzyme in Acinetobacter genus occurred in isolates collected in Argentina (Poirel et al., 2007); thus its presence could be associated to isolates from South America and nearby regions. According to Van Goethem et al. (2018), resistance determinants present in environmental soil, especially from extreme and remote ecosystems, are still underrepresented, thus our findings represent the very first description of A. radioresistens resistant to multiple antibiotics in this area.
Figure 1. Circular representation of A154 draft genome. Circles from the outermost are as follows: contigs; forward CDS; reverse CDS; GC content; GC skew. Red lines: antibiotic-resistance genes; blue lines: transposase genes.
Importantly, A. radioresistens has been rarely associated with human infections and the species is normally highly susceptible to antibiotics. In this sense, Visca et al. described a community-acquired bacteraemia caused by this species, but the isolate was susceptible to cephalosporins and aminoglycosides (Visca et al., 2001). Similarly, Poirel et al. published a study that included five A. radioresistens isolates that were fully susceptible to all antibiotics tested, including penicillins and carbapenems, despite the detection of blaOXA−23−like gene (Poirel et al., 2008). On the other hand, Higgins et al. identified two carbapenem-resistant A. radioresistens isolates that were recovered from the same patient 17 days apart, which were also resistant to fluoroquinolones (Higgins et al., 2013). Additionally, two A. radioresistens isolates collected from companion animal infections, which harbored blaIMP−1, sul1, aadA1, and aac(6)-31, were resistant to carbapenems and fluoroquinolones (Kimura et al., 2017), but despite the presence of AMEs, the isolates were susceptible to GEN and AMK.
Our findings show that the isolate A154 was resistant to β-lactams, except carbapenems, which could be explained by the presence of the blaTEM−1B, blaPER−2, and blaSCO−1 genes. Interestingly, PER-2 corresponds to an extended-spectrum β-lactamase (Pasteran et al., 2006; Gutkind et al., 2012), while TEM-1B and SCO-1 are class A narrow-spectrum β-lactamases (Poirel et al., 2007), which could be mediating the resistance displayed against β-lactams, such as cephalosporins (Gutkind et al., 2012). These findings are particularly interesting since although β-lactamase genes are common components of the soil resistome, they are not highly abundant. Accordingly, a study of soil samples from the Mackay Glacier in Antarctica showed a very low β-lactamase abundance (Van Goethem et al., 2018). The same study also demonstrated that β-lactamase genes are more common in soil samples from regions that are more likely to have been exposed to human activity (Van Goethem et al., 2018), representing a possible source of selective pressure.
Importantly, A154 was resistant to KAN and STR, and intermediate to GEN. Although the isolate was classified as AMK susceptible, the MIC value (16 μg/mL) was only one dilution below the CLSI breakpoint for intermediate (32 μg/mL). This particular phenotype is mainly explained by the activity the APH(3′)-VIa enzyme, which was originally described in A. baumannii and confers resistance to AMK and KAN (Ramirez and Tolmasky, 2010). Additionally, other AME genes detected were strA and strB which confer resistance to STR (Ramirez and Tolmasky, 2010), in concordance with the observed phenotype. We also identified the aac(3)-IIa gene, which is related to resistance to GEN and tobramycin (TOB) (Ramirez and Tolmasky, 2010). Similarly, the identified resistome included the tet(B) gene, however, the isolate was susceptible to tetracycline. These inconsistencies suggest that A. radioresistens might need a complementary mechanism of aminoglycosides/tetracycline resistance or to regulate the expression of ARGs to develop the resistance phenotype. This assumption is reaffirmed by the presence of the intrinsic blaOXA−23−like gene in carbapenem-susceptible A. radioresistens, which when present in A. baumannii, confers resistance to carbapenems (Evans and Amyes, 2014), when over-expressed (Higgins et al., 2013). Therefore, expression experiments of the ARGs are required in order to understand the potential influence of these determinants on the resistance level to antimicrobials in the species described.
On the other hand, A154 was assigned to the ST1207 in PubMLST (https://pubmlst.org/), which corresponds to a novel ST. This is a novel lineage which corresponds to a singleton, since is not associated to any described ST of the database. Accordingly, it is important to analyze a larger collection of isolates from regions with and without human influence in order to determine whether this ST is endemic/prevalent to this area or it was introduced. This is particularly important since we have previously determined that antibiotic-resistant E. coli isolates in Antarctica are more frequent in regions with a significant anthropic influence (Rabbia et al., 2016). In the case of A154, it was collected from the same region of the study mentioned above, thus the local microbiome and resistome are probably affected by human activity. However, since the soil from which the isolate was recovered corresponded to surface soil, which is determined by the influence of organic matter from animals, it is possible that it could be carried by migrating birds (Segawa et al., 2013), which might be playing an important role in the genetic contamination of this region.
Moreover, no plasmid replicons were detected by PlasmidFinder and PATRIC. However, we detected a large plasmid of ca. 280 kb which was not detected in silico from WGS (data not shown). Moreover, the plasmid could not be transferred by conjugation and neither cured by temperature. The latter could be explained by the presence of the type II toxin-antitoxin systems RelB/DinJ (accession number PSD36295.1) and RelE/ParE (accession number PSD36025.1), which were detected from WGS. Interestingly, the RelE/ParE genes were located adjacent to strA and strB genes (Figure 2), which suggests that both are contained in the same plasmid. The toxin-antitoxin systems are defined as plasmid maintenance systems present in almost all free-living bacteria (Kang et al., 2018), which could confer stability against curing agents. Conjugation experiments under different conditions should be performed in order to determine the ability of the plasmid to be mobilized.
Figure 2. Linear map of A154 contigs 35 (A) and 10 (B). DNA strands sense and anti-sense are represented. Hyp., hypothetical protein. The linear representation was generated by using Artemis software.
Remarkably, a large diversity of IS-family transposases was found on the genomes of A154. Specifically, its IS content was composed by fifteen copies of IS/IS1182 transposase, twelve of IS6, 11 of IS30, eight of IS4, four of ISL3, two each of IS3-like and IS5-like, and a single copy each of IS982, IS200/IS605, ISNCY, IS481, and IS1. IS-elements are capable of mobilizing and controlling the expression of ARGs, among other functions, therefore the isolate has an important potential to acquire/disseminate and over-express resistance determinants (Siguier et al., 2014). Notably, the blaPER−2; aph(3′)-VIa; strA; strB; tet(B) were identified in the plasmid extract obtained from alkaline lysis, and are also located in the same region of the genome in which diverse ISs were also located (Figure 1). This suggests that they could has been incorporated by A154 by horizontal-gene transfer mediated by plasmids and/or IS-elements. As shown in Figure 2, the plasmid-encoded ARGs were located in different contigs from WGS, in which also several IS-elements were located, reaffirming the potential role of these mobile-genetic elements in their mobilization. The contig in which aph(3′)-VIa is located, was not represented since it was contained in a short contig, which harbored only two genes.
An important limitation of our study is the Illumina platform generates short reads, making it difficult to determine the entire sequence and structure of the plasmid contained by A154 (Roosaare et al., 2018). In consequence, the use of this sequencing technology to predict plasmids (i.e., by PlasmidFinder) is limited, being only possible to search for the incompatibility groups detected in the genome which are deposited on the databases. A potential solution for this problem, is to isolate the plasmid and sequence it or use new sequencing technologies, such as Oxford Nanopore Technology (ONT) (Lemon et al., 2017).
In conclusion, our results represent the first description of A. radioresistens in Antarctica containing several ARGs, in an isolate recovered from a region under both human and animal influences, thus these factors could be contributing to the introduction of ARGs in Antarctica. These findings contribute to better understand the knowledge of the biology of Acinetobacter as well as to add more data about the content of ARGs in the region.
The raw data supporting the conclusions of this manuscript will be made available by the authors, without undue reservation, to any qualified researcher.
AO-C, PG-M, PH, and JW contributed to the acquisition, analysis, and interpretation of the data. AO-C, CC, PG-M, and MQ-A made important contributions to the design of the work. HS, MD-Y, HB-T, LV, and GG-R provided approval for publication of the content and contributed drafting the work and critically revisiting the manuscript.
This work was funded by the post-doctoral project N°3150286 from The National Fund for Scientific and Technological Development (FONDECYT) and the Chilean Antarctic Institute (INACH) project number RT_06_12.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The authors highly appreciate the support from the Chilean National Commission for Scientific and Technological Research (CONICYT), the Chilean Antarctic Institute (INACH), and the Millennium Science Initiative of the Ministry of Economy, Development and Tourism, Chile.
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Keywords: antibiotic-resistance genes, Acinetobacter, Antarctica, whole-genome sequencing, resistance plasmid, ecotoxicology
Citation: Opazo-Capurro A, Higgins PG, Wille J, Seifert H, Cigarroa C, González-Muñoz P, Quezada-Aguiluz M, Domínguez-Yévenes M, Bello-Toledo H, Vergara L and González-Rocha G (2019) Genetic Features of Antarctic Acinetobacter radioresistens Strain A154 Harboring Multiple Antibiotic-Resistance Genes. Front. Cell. Infect. Microbiol. 9:328. doi: 10.3389/fcimb.2019.00328
Received: 14 June 2019; Accepted: 02 September 2019;
Published: 13 September 2019.
Edited by:Xiangmin Lin, Fujian Agriculture and Forestry University, China
Reviewed by:Hossam Abdelhamed, Mississippi State University, United States
José Alejandro Di Conza, University of Buenos Aires, Argentina
Copyright © 2019 Opazo-Capurro, Higgins, Wille, Seifert, Cigarroa, González-Muñoz, Quezada-Aguiluz, Domínguez-Yévenes, Bello-Toledo, Vergara and González-Rocha. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Gerardo González-Rocha, firstname.lastname@example.org