- Open Access
Conserved phylogenetic distribution and limited antibiotic resistance of class 1 integrons revealed by assessing the bacterial genome and plasmid collection
Microbiome volume 6, Article number: 130 (2018)
Integrons, especially the class 1 integrons, are major contributors to the acquisition and dissemination of antibiotic resistance genes (ARGs). However, comprehensive knowledge of the types, content, and distribution of integrons in bacterial taxa is lacking to evaluate their contribution.
We have constructed a new integrase database and developed a pipeline that provides comprehensive recovery of class 1 integrons. Previous PCR-based techniques might only detect one fourth of the integron-integrases and integrons recovered in this study. By exploring the class 1 integrons in over 73,000 currently available complete and draft bacterial genomes, the contribution of class 1 integrons in spreading and acquiring ARGs was evaluated. Firstly, the host species of class 1 integrons are highly conserved within (96%) in class Gammaproteobacteria, dominated by four pathogenic species of “ESKAPE.” Secondly, more than half of class 1 integrons are embedded in chromosomes with less potential for horizontal gene transfer. Finally, ARGs that have been acquired by these integrons only cover 11% of all the ARG genotypes detected in bacterial genomes.
The above observations indicated that there are both biological and ecological limitations to class 1 integrons in acquiring and spreading ARGs across different classes of the domain Bacteria.
Integrons are the major contributors to the acquisition and dissemination of antibiotic resistance genes (ARGs) [1, 2], and class 1 integrons are the central agents. They have been so successful at spreading into diverse clinically relevant taxa that they have been likened to invasive species . Their subsequent spread into multiple environments has also led to suggestions that the class 1 integron-integrase gene (intI1) could be used as a proxy for anthropogenic pollution . Thus, this study mainly focused on the class 1 integrons with typical structure and well-known intI1, which are considered to have a significant contribution to the spreading of ARGs.
Class 1 integrons were initially discovered in clinical isolates. However, as more and more metagenomic and qPCR analyses regularly detect intI1 in different environments [4,5,6,7,8], the comprehensive recovery of integrons in metagenomic data has become a demanding task. The first bottleneck lies in the lack of a well-organized pipeline for integron identification, coupled with a well-curated intI1 database. Previous studies on class 1 integrons and intI1 in environments mainly relied on PCR-based sequencing [6, 7, 9, 10], but biases from primers would result in incomplete information. Besides, PCR-independent methods were often designed to target separate integron elements, such as attC sites  and intI1 , but not whole integrons. Recently, a program targeting whole integrons, the IntegronFinder , was designed for complete genomes and does not support draft genomes and metagenomic data.
Without comprehensive databases and methods, it is difficult to evaluate the phylogenetic distribution, ARG content, and the environmental landscape of integrons. Such knowledge is needed to understand their contribution in acquiring and spreading ARGs in environments. To address this goal, we asked two fundamental questions using bacterial whole genomes: (1) what is the potential of class 1 integrons as invasive species across the current bacterial taxa? and (2) what is the contribution of class 1 integrons to the acquisition of antibiotic resistance. Previous studies have revealed that the class 1 integrons carry diverse ARGs and are wildly distributed in more than 70 species [3, 13], especially gram-negative bacterial pathogens. A more comprehensive survey into 2500 complete genomes  indicates the heterogeneous distribution of integrons in Proteobacteria. This whole genome analysis avoids the bias from PCR primers, while another concern arises of the limited genomes and the exclusion of draft genomes. The NCBI bacterial whole genome database (WGD) and plasmid database  have been rapidly expanded to now 73,655 complete and draft (≥ 50% completeness [15, 16] on May 11, 2018) genomes and 12,733 plasmids. Even though these genomes do not represent the uncultured species in the environments, they can serve as representatives of the microbes of interest to microbiologists and clinicians. Bioinformatic analyses based on WGD may provide essential information for interpreting the environments, as demonstrated in recent studies by the construction of database [17, 18] and benchmark references for metagenomic analysis [19,20,21,22,23]. Similarly, the identification of class 1 integrons and their ARGs in WGD would help define their roles in horizontal gene transfer (HGT). Thus, a bioinformatics pipeline was developed to systematically identify class 1 integrons and applied to WGD. The deeper understanding revealed in this study would help future studies to better interpret the functions and potential risks of integrons in environments.
Integrase database construction and classification
The previous intI1 databases [6, 12] were evaluated against all curated class 1 integrons and a subset of potential clinical class 1 integrons from the INTEGRALL , which reveals a coverage of less than 30 and 70%, respectively (Additional file 1: Table S1). Thus, the first task was to construct a new intI1 database to allow a more comprehensive identification of integrons.
A new method is introduced here to construct databases integrating both WGD and NCBI nr database  (Fig. 1), by keyword search (Additional file 1: Table S2), sequence-based search, and phylogenetic topology. The WGD collected in this study contains 73,655 complete and draft (≥ 50% completeness on May 11, 2018) genomes (Additional file 1: Table S3). Compared to nr database, WGD has more rigorous and standardized annotations of genes (keyword search) and can provide the information of related or neighboring genes (further filtering). Meanwhile, nr database can provide more abundant sources of both positive- and false-positive sequences for curation and expansion (sequence-based search). Integrases were firstly extracted from WGD by their annotations. After curation and expansion by nr database  using BLASTP , an integrase database was constructed with 3384 non-redundant sequences (Additional file 1: Figure S1). Together, the previous databases only cover 15% of the integrase database and 70% of the intI1 database in this study. To avoid false positives caused by misannotation, we removed integrases with no neighboring attC site (≤ 4 kb in distance).
The integrases were classified into intI1 and non-intI1 by their phylogenetic relationship to references (of classes I to V, XerC, and XerD) from the NCBI database (Additional file 1: Figure S1). Totally, 922 integrases were identified as intI1 (Fig. 2a) to populate the intI1 sub-database and were validated to have both high specificity and coverage. The specificity was evaluated as 100% by searching against WGD using BLASTP . The coverage was evaluated to be 90% (Additional file 1: Table S1) of all clinical class 1 integrons from the INTEGRALL .
Briefly, the Integron Visualization and Identification Pipeline (I-VIP) is a well-organized pipeline to identify, classify, annotate, and visualize class 1 integrons (Fig. 3 and Additional file 1: Figure S2, Additional file 1: Supplementary Methods) in complete/draft genomes and assembled metagenomes. To facilitate flexible application by the users, I-VIP was separated into two modules: module A for integron identification and classification (orange framework in Fig. 3) and module B for integron extraction, annotation, and visualization (blue framework in Fig. 3).
Firstly, three elements were selected to identify integrons (Additional file 1: Figure S3), which are the intI1 as the 5′conserved segment (5′-CS), the attC site associated with gene cassettes (Gcs), and the sulfonamide resistance gene (sulI) as the 3′conserved segment (3′-CS) of class 1 integrons. This identification is conducted using sequence-based searching against three reference databases, the attC cite , the integrase (this study), and sulI  databases. Since these databases were constructed by nr database, they included sequences from both cultured and not-yet-cultured bacteria. Thus, the I-VIP is not limited to complete genomes but can also cover integrons from draft genomes and environmental metagenomes. However, a functional integron should be further evaluated by the other integron elements, such as promoters and regulatory genes [1, 27].
In module A, integron elements within a distance of 4 kb (twice the size of the longest Gcs in class 1 integrons ) are clustered into one candidate integron. The longest Gc found in WGD was 2.6 kb, indicating that the length criterion of 4 kb for clustering should be sufficient. In this study, an integron is defined as a segment of sequence containing at least two neighboring (≤ 4 kb in distance) integron elements (integrase, attC site, or sulI) and the genes entrained among these elements. Qualified integrons are then classified into types A to E based on the integron elements they carry (Additional file 1: Figure S3). Integrons with both intI1 and sulI are classified as type A, and integrons with only intI1 but no sulI are classified as type B. Type C integrons refer to integrons carrying integrases of other classes. The classification of types A–C is introduced in this study to differentiate the potential class 1 integrons (types A and B) and integrons of other classes (type C). The class 1 integrons are further separated into types A and B based on the presence of sulI. A type A integron has a typical structure of clinical class 1 integrons, while a type B integron could be a potential pre-clinical class 1 integron  or could be caused by the deletion of 3′-CS . Since the activity of an integron ultimately hinges on the possession of the functional platform (an integrase and an attI site), integrons carrying no integrases are classified into types D (with sulI genes) and E (without sulI genes) as non-functional integrons. Types D and E integrons are proposed as the sources of Gcs for integrase-carrying integrons (types A to C) or as a means of stabilizing Gcs in genomes . The identification of types D and E integrons at the extremities of assembled contigs should be treated with caution since they could be caused by the inefficient assembly.
For further analysis, the sequences of whole integrons and their integrases and Gcs are extracted using module B. The Gcs are annotated using Structured ARG (SARG)  and ComMet  databases for potential ARGs and the metal resistant genes (MRGs). The structure of integrons is generated based on the arrangement of integron elements and Gcs and is visualized using the phylogenetic tree of the hosts as the skeleton.
The I-VIP was compared to the IntegronFinder  applying compatible settings, using a set of 5436 complete genomes. The classification of intI1 genes from other integrases and the inclusion of sulI as an anchoring element enable the I-VIP to differentiate the potential clinical and pre-clinical class 1 integrons (types A and B) from the integrons of other classes (type C). In contrast, the types A–C integrons are generally identified as complete integrons by IntegronFinder (Additional file 1: Table S4 and Figure S4). Besides, single integrases and single attC sites, which are identified as In0 and CALIN with single attC by IntegronFinder, are not defined as integrons by I-VIP and are excluded from the results to avoid false positives caused by misannotation. In details, the I-VIP and IntegronFinder recovered 1320 and 920 integrons (not considering the single integrases and single attC cites), respectively, from the set of complete genomes. Totally, 845 integrons (153 type A, 38 type B, 154 type C, 34 type D, and 466 type E) are shared by two approaches, with minor differences in the number of Gcs. However, the attC sites of 34 type A–C integrons are missed by IntegronFinder and therefore classified as In0. Moreover, the difference of the integrase databases used by two approaches resulted in the missing of the integrases on 294 integrons by IntegronFinder compared to 99 missing integrases by I-VIP. The integrase database in this study also recovered 69 type C integrons, which were not detected by the IntegronFinder.
Integrons in WGD and plasmid database
Because of the uniqueness and dynamics of bacterial genomes [15, 31], the inclusion of draft genomes would largely expand the diversity of genome reservoirs, especially for mobile gene elements (MGEs) like integrons. Thus, the I-VIP was designed to be applicable to both complete and draft genomes in the current bacterial WGD. To further assess the potential for HGT, especially by conjugative transformation , all sequences in WGD were classified into chromosomes and plasmids according to the GenBank annotation and were curated by PlasFlow  (Additional file 1: Table S3). As a supplement to the plasmids retrieved from WGD, the NCBI plasmid database containing totally 12,733 plasmids was downloaded and analyzed by I-VIP. Although some MGEs, such as transposons, would facilitate the transfer of chromosomal integrons, the identification of such elements and the evaluation of their mobility are not the focus of this study.
Totally, 2977 integrons were identified from the WGD and plasmid database (Table 1 and Additional file 1: Table S5). The integrons were classified into types A to E based on their integron elements (Table 1) and more than two thirds of the integrons (2137) carry the integrases (types A–C). The class 1 integrons account for half of all the identified integrons, consisting of 1039 clinical class 1 integrons (type A) and 431 pre-clinical class 1 integrons (type B). Approximately 50% of the class 1 integrons (types A and B) are carried by plasmids, showing a potential of HGT by conjugative transformation; while more than 90% of the integrons of other classes (type C) are embedded in chromosomes.
Phylogenetic distribution of integrons in WGD
Among those 2440 integrons identified in WGD, 2295 integrons are hosted by the phylum Proteobacteria (30,593 genomes), mainly by Gammaproteobacteria (93%) (Additional file 1: Table S6). In contrast, the phyla Tenericutes (392 genomes) and Chlamydiae (336 genomes) encode no integron. This is not surprising because Tenericutes and Chlamydiae are known to have limited capacity for HGT. Moreover, it is intriguing to find a heterogeneous distribution of integrons in phylogenetically close clades under the same taxonomic level. For example, there are only a few integrons detected in Alphaproteobacteria (5 in 2879 available genomes) and Betaproteobacteria (109 in 3401 genomes) while their sister class Gammaproteobacteria harbors 2142 integrons (among 21,986 genomes) in total, in agreement with a previous study into 2500 complete genomes .
To avoid the bias caused by heterogeneous sequencing and pseudo-replication of draft genomes, especially in pathogenic species, all genomes within a species were integrated to count the occurrence of integrons. The integron copy number was normalized against the species level, that is, one copy integron per species was counted if any one of the genomes within that species is carrying an integron (Additional file 1: Table S7). For type A (clinical class 1) integrons, it demonstrates a clear trend that they are highly dominant in pathogenic hosts and frequently carried ARGs, which indicate their primary roles in HGT of ARGs (Fig. 4). Firstly, the host species of type A integrons reveals a significant pathogenic prevalence of 58%, which means that 58% of the bacterial species harboring type A integrons are potential human pathogens. It is almost seven times compared to the percentage of the pathogenic species in WGD (Table 2). Although the hosts of type A integrons are dominant in class Gammaproteobacteria and family Enterobacteriaceae with high percentage of pathogenic species (14 and 25%), the significantly higher pathogenic prevalence of type A integrons (60 and 54%) clearly implies the ecological adaptations of clinical class 1 integrons in bacteria of medical importance. In addition, more than half of type A integrons are chromosomal integrons (Table 1) showing less mobility of HGT by conjugative transformation. These observations may indicate that so far, the HGT of clinical class 1 integrons could be restricted even within Gammaproteobacteria. Although the current WGD is biased to more easily cultured and pathogenic strains, and the HGT of class 1 integrons is variable to the bacterial communities and the environments, the very strong trend is suggestive that there could be a biological  barrier (i.e., mechanistic gene transfer [32, 34, 35]) and ecological barrier (i.e., host fitness effects ) to broad HGT of class 1 integrons. Furthermore, almost all (99%) type A integrons carry at least one ARG, mainly harbored by the pathogenic species such as Acinetobacter baumannii, Pseudomonas aeruginosa, Shigella flexneri, Klebsiella oxytoca, Klebsiella pneumoniae, Enterobacter species, and Escherichia coli (of Proteobacteria), covering four of the species named “ESKAPE” pathogens . In contrast, the other two species in the “ESKAPE” group, the Enterococcus faecium and Staphylococcus aureus (of phylum Firmicutes), carry only four types D and E integrons (without ARG). It suggests that for human pathogenic species, the biological barrier (across phyla) could have played a greater role than the ecological barrier as the limitation for HGT of clinical class 1 integrons.
In WGD, the majority (90%) of the hosts carry one copy of type A integrons on either chromosomes or plasmids (Additional file 1: Figure S5). It is intriguing that eight hosts from the genus of Klebsiella and Salmonella carry both chromosomal and plasmid type A integrons. It is not surprising that 88% of the plasmid type A integrons in WGD are hosted by pathogenic species (Additional file 1: Table S5), as they were originally isolated from clinical settings. The non-pathogenic species harboring the remaining 12% type A plasmid integrons are highly dominated by the close relatives of pathogens (especially in the family of Enterobacteriaceae). These integrons all carry ARGs and could serve as an important reservoir for HGT of ARGs into human pathogens , especially since they occupy the same habitats.
ARGs on class 1 integrons
Types A and B integrons generally carry 0 to 11 Gcs, with a total size of 1 to 14 kb (from 3′-CS to 5′-CS, Fig. 5). The majority (99%) of type A integrons have the size of 3 to 10 kb. Overall, most (81%) of the ARG-carrying integrons are type A and type B integrons (class 1 integrons), pointing out that the class 1 integrons play the central role in the dissemination and the acquisition of ARGs, compared to the integrons of other classes. Specifically, almost all (98%) class 1 integrons carry at least one ARG, and more than half of them carry multiple (2–6) ARGs. Moreover, 48% of the Gcs on class 1 integrons are annotated with the function of antibiotic resistance. Although ARGs have been frequently captured by class 1 integrons, it reveals a limited diversity and heterogeneous distribution of totally 60 ARG genotypes and 9 ARG phenotypes, compared to a total of 1209 genotypes and 24 phenotypes in SARG database . ARGs resistant to aminoglycoside, beta-lactam, chloramphenicol, and trimethoprim are widely distributed in both chromosomal and plasmid class 1 integrons (Fig. 4 and Additional file 1: Table S8). In contrast, macrolide-lincosamide-streptogramin (MLS)-, quinolone-, and tetracycline-resistant genes were rarely detected on the class 1 integrons. Regardless of the high occurrence of tetracycline-resistant genes in bacterial genomes and in the environments [30, 38], only one tetracycline resistance protein was discovered to be acquired by a plasmid type B integron. Besides, the plasmid class 1 integrons harbor a more diverse reservoir of ARGs (59 genotypes) than the chromosomal class 1 integrons (45 genotypes), including the medically relevant ARGs of TEM-1 and VIM-1 resistant to beta-lactam .
The phylogenetic conservation of intI1
To identify the host of intI1, the intI1 sequences of class 1 integrons in WGD were extracted and further classified into two subgroups, i.e., (1) the type A intI1 carried by the type A integrons and (2) the type B intI1 carried by the type B integrons. The amino acid sequence identity in the type A intI1 varies from 56 to 100%, indicating that these clinical class 1 integrons may not originate from one common ancestor . The mutational inactivation to be adapted to different hosts could have exaggerated the divergence within the type A intI1 genes . Figure 2b displays the phylogenetic relationship among 693 type A intI1 genes and type B 155 intI1 genes, which demonstrates that (1) the intI1 is harbored mostly (85%) by the Enterobacteriaceae family in Gammaproteobacteria and (2) almost all (96%) intI1 is embedded in ARG-carrying integrons and more than half (53%) of intI1 is leading multiple ARGs. It is intriguing that a large portion (74% on Fig. 2b) of intI1 shows no phylogenetic difference, distributed in both pathogenic and non-pathogenic hosts in Enterobacteriaceae, Pseudomonadaceae, Moraxellaceae, and other families, indicating the potential for HGT of these intI1 across the family level.
In this study, two databases (integron and integrase) were rigorously constructed and curated using the bioinformatic pipeline and whole genome analysis, which overcome the inherent limitation and biases of databases constructed from PCR-generated sequences. With the rapid expansion of available genomes, periodic updates of these databases could be performed through the automatic pipeline developed in this study, enabling a comprehensive survey on integrons.
The integrase database (Additional file 1: Supplementary File S1) contained 3384 complete and non-redundant integrases with an aa inter-group identity of 17–100%. A total of 922 integrases were classified as intI1 to generate a sub-database, the intI1 database. The low coverage (26%) of previous intI1 primers  (HS464/HS463a) against the corresponding intI1 nucleotide (nt) database in this study indicates that the currently available primer  may only identify a limited spectrum (Fig. 2a red edges, Additional file 1: Table S9) of the intI1 database. Thus, new primer sets will be necessary for a more comprehensive identification and quantification of intI1 from clinical and environmental samples.
The integron database is a compact database of both sequences and associated information for 2153 non-redundant whole integrons (Additional file 1: Table S5), 66% of which have not been included by the INTEGRALL  (95% aa identity and 90% hit length, Additional file 1: Table S10). A total of 502 type A and 283 type B non-redundant integrons dramatically expand the diversity of class 1 integrons in the INTEGRALL database with an addition of 61% new sequences. However, the INTEGRALL database also contributes new integron sequences with a variation of gene cassettes (but not new integrases), and the integration of these two databases would provide the abundant and representative resources for future studies. Moreover, the available PCR primer sets [5, 40,41,42] have very low coverages of 0 to 24% (Additional file 1: Table S9) of the integron database in this study, indicating that a large proportion of integrons in the environments may be missed using those primer sets.
Discussion and conclusions
By exploring the integrons from a WGD of 73,655 complete and draft bacterial genomes and a plasmid database of 12,733 plasmids using the I-VIP pipeline developed in this study, the contribution of class 1 integrons was evaluated to spread and acquire ARGs.
Firstly, the host species of class 1 integrons are found to be highly conserved within one narrow bacterial lineage in Gammaproteobacteria, especially in three families of Enterobacteriaceae, Pseudomonadaceae, and Moraxellaceae. By extracting the metadata of their hosts from the IMG database, the habitat information was recovered for 20% of the class 1 integrons, which revealed that most of these 20% class 1 integrons distributed in human-associated habitats. The significantly high prevalence of clinical class 1 integrons in potential human pathogens was observed (with sevenfold of the percentage of pathogenic bacterial species in WGD), but they are also commonly distributed (the remaining 42%) in closely related non-pathogenic Gammaproteobacteria. Moreover, more than half of the class 1 integrons are embedded in chromosomes, which indicates less potential of HGT by conjugative transformation. This strongly suggests that the contribution of class 1 integrons on the ARG dissemination might be limited, in terms of the biological potential of HGT (mainly within Gammaproteobacteria), but critical, in terms of exchanging Gcs between non-pathogens and pathogens.
The role of integrons is well established in supplying adaptive traits via HGT to bacteria under various selection pressures [2, 3]. However, this does not mean that integrons harbor resistance to all antimicrobial agents. In fact, after exploring the ARGs already acquired by the integrons on chromosomes and plasmids, the ARGs harbored on all types of integrons are surprisingly limited to only 69 genotypes from 9 phenotypes of ARGs (Additional file 1: Table S8), i.e., the aminoglycosides, sulfonamide, trimethoprim, beta-lactam, chloramphenicol, and rifamycin. Among 11 phenotypes of globally used antibiotics , the resistant genes to tetracycline, vancomycin, and polymyxin and multidrug-resistant genes are rarely captured on the integrons. In contrast, ARGs from 627 genotypes and 24 phenotypes are found to be widely distributed across the bacterial taxa in WGD. It seemed that 89% of the ARG genotypes in bacterial genomes are not likely to be acquired and expressed via the integrons. This result is consistent with a previous environmental survey that reported limited genotypes of ARGs carried by class 1 integrons . These observations suggest that high co-occurrence of intI1 and ARGs of other genotypes [4, 44] could be caused by the co-enrichment and co-localization of class 1 integrons and these ARGs on the same transposons or plasmids. Although it deserves confirmation in the further studies, the datasets of WGD and plasmid database used in this study could serve as appropriate representatives for natural environments.
The above two observations, which are (1) the potential of class 1 integrons as invasive species is constrained within Gammaproteobacteria and (2) the contribution of class 1 integrons to the acquisition of antibiotic resistance is limited to 69 genotypes (11% of the ARG genotypes identified in WGD), indicate that there are both biological and ecological limitations to class 1 integrons in acquiring and spreading ARGs across different classes of the domain Bacteria by HGT.
The complete genomes used in this study are mainly obtained from culturable species of practical importance to humans. To investigate the environmental microbes, especially the not-yet-cultured species, all the draft genomes from NCBI genome database, including 7351 bacterial genomes obtained in a previous study from environmental and non-human gastrointestinal samples , were downloaded and analyzed by I-VIP. By recovering the metadata of 10,733 genomes (Additional file 1: Table S3) from the columns “Cultured,” “Ecosystem,” and “Ecosystem Subtype” in IMG database, the proportion of not-yet-cultured genomes was evaluated to be 26% in WGD, which were obtained from 36 diverse environmental and engineered habitats. Although these genomes represent bacterial phylogeny quite well (34 phyla excluding unclassified and Candidatus phyla), they do not represent the diversity of the very large not-yet-cultured species in nature. Moreover, the limitation of assembly methods may result in more incomplete integrons (types B, D, and E). To maintain the high quality of contigs, draft genomes with less than 50% completeness [15, 16] were abandoned. Additionally, the impact of short-read assembly on the recovery of complete integrons was assessed by comparing the proportion of types B, D, and E integrons obtained from the complete genomes against the draft genomes within the same family of Enterobacteriaceae. The results show no significant enrichment of the types B, D, and E integrons in the draft genomes (40% in complete genomes compared with 42% in draft genomes). Furthermore, the development of long-read sequencing, i.e., PacBio  and MinION nanopore , and of assembly-facilitated technologies, i.e., inverse PCR  and Hi-C [48, 49], will help obtain draft or nearly complete genomes with high quality, as demonstrated by previous studies into the pure cultures [50, 51]. In addition, the I-VIP pipeline can rapidly take advantage of the expanding WGD to broaden the bacterial taxa examined and incorporate new metagenomic datasets. These data will be crucial for understanding the distribution and dissemination of integrons under the continuing influence of anthropogenic impacts. Besides, the approach used in this study focuses on the classical class 1 integrons that are already known and well investigated. But it is probably just a small part of the class 1 integron distribution and will not reflect its biology to a full extent. Moreover, it is challenging to unravel the complex resistance regions computationally.
The overall technical flow of this study is summarized in Fig. 3.
This database contains a collection of 73,655 bacterial genomes (10,112 complete genomes and 63,543 draft genomes with ≥ 50% completeness [15, 16]) and 12,733 plasmids (ftp://ftp.ncbi.nlm.nih.gov/genomes/genbank/bacteria) and NCBI plasmid database (ftp://ftp.ncbi.nlm.nih.gov/genomes/refseq/plasmid)  (on May 11, 2018). The taxonomy information of all genomes was curated and summarized in Additional file 1: Table S3. The potential pathogenicity of bacterial genomes was obtained by matching their taxonomic information with a database of all recognized species of human bacterial pathogens . If either one of the taxonomic annotations of species or strain level was matched to the human pathogen list , the genome was labeled as a potential human pathogen [30, 53]. Those genomes without the taxonomic annotations down to the genus level were treated as non-pathogens. The information of habitats and isolates was extracted from IMG database (on May 10, 2018) combining the columns of “Cultured,” “Ecosystem,” “Ecosystem Category,” “Ecosystem Subtype,” “Ecosystem Type,” and “Relevance.” By mapping the organism name of genomes, the metadata of 10,733 genomes was recovered with valid information of the columns “Cultured,” “Ecosystem,” and “Ecosystem Subtype” (Additional file 1: Table S3). All sequences/contigs with the size larger than 1 kb in WGD (both the complete and draft genomes) were classified into chromosomes and plasmids by the PlasFlow 1.0  using the default threshold of 0.7 for probability filtering.
Integrase database construction
A new method was developed here to construct databases by integrating WGD and NCBI nr database  (Fig. 1, Additional file 1: Supplementary Methods), which could facilitate future studies to construct databases of other functional genes. Candidate integrases (containing true-positive keywords and no false-positive keyword) were firstly extracted from WGD by keyword search (Additional file 1: Table S2) against their annotation (red framework in Fig. 1). Then, sequences containing integrases were searched for attC site  (e value 1) by cmsearch 1.1.1 , and candidate integrases neighboring attC sites (≤ 4 kb in distance) were kept as seed sequences for curation by nr database (blue framework in Fig. 1). The seed sequences were sequentially searched against nr database by BLASTP 2.2.28+  (e value 1e−3, 80% aa similarity over 50% aa hit length), and the output sequences from nr database were treated as daughter sequences. The annotation of the daughter sequences was used to evaluate their seed sequences by calculating the ratio of false-positive daughter sequences. In other words, those seed sequences were abandoned if larger than 1% of their daughter sequences contained false-positive keywords or did not contain any true-positive keyword. All the daughter sequences of true-positive seed sequences were treated as new seed sequences for the next cycle of curation by nr database. After curation, all true-positive sequences were classified into subgroups, and one representative for each subgroup was manually checked by online BLASTP  (orange framework in Fig. 1). Those subgroups with false-positive representative were abandoned. After manually checking, the candidate database was expanded against nr database using usearchv8  (e value 1e−3, 70% aa similarity over 50% aa hit length). All daughter sequences were treated as new seed sequences and were curated one by one using the same method described before (blue framework in Fig. 1). The cycles of curation and expansion (blue and orange framework in Fig. 1) were ended if no new seed sequence was found. Finally, the intI1 genes were classified by the phylogenetic tree, using default parameters of MUSCLE v3.8.31  and FastTree 2.1.10  (green framework in Fig. 1).
The coverage of the integrase databases constructed in previous studies and this study was evaluated against all curated class 1 integrons from INTEGRALL  (http://integrall.bio.ua.pt/IntegronNumbering-lastestUpdate.xls), while still it could be heavily biased to mobile integrons with ARGs. The cutoff for different databases was consistent with the original studies (e value 1e−5, 90% nt similarity over 50% nt hit length for ; e value 1e−3 over 50% aa hit length for ) and this study (e value 1e−3, 80% aa similarity over 50% aa hit length). The in silico coverage of previously designed primers to intI1 nucleotide (nt) database and the class 1 integron database was evaluated by self-written scripts and PRISE2 , allowing no mismatch.
Integron identification and visualization
The integrons were identified, classified, annotated, and visualized by I-VIP (Fig. 3 and Additional file 1: Figure S2, Additional file 1: Supplementary Methods), allowing multiple inputs (available on https://github.com/caozhichongchong/I-VIP/releases). The identification was conducted against three reference databases, by cmsearch 1.1.1  against the attC database  (e value 1 for 2 Mb), by BLASTP 2.2.28+  against the integrase database (this study, e value 1e−3, 80% aa similarity over 50% aa hit length), and sulI database  (e value 1e−3, 90% aa similarity over 80% aa hit length). To maintain the consistency of the e value for cmsearch, all genomes were split into 2 Mb. In this study, to avoid potential misidentification by similarity search, integrons with only one integron element (integrase, attC cite, or sulI) were excluded. The Gcs on integrons were extracted and annotated by BLASTP 2.2.28+  against SARG  (e value 1e−5, 90% aa similarity over 80% aa hit length) and ComMet database  (e value 1e−5, 80% aa similarity over 90% aa hit length). Finally, combining the taxonomic information of their hosts, the phylogenetic distribution and the structure of integrons were plotted together as an integron phylogram by Hierarchic or Tree layout in Cytoscape 3.3.0 , using the phylogenetic tree of the hosts as the skeleton.
Since global searches for attC sites by cmsearch (module A1) were computationally time-consuming, an alternative process (local search module A2) was developed and compared with module A1. Briefly, module A1 searched the whole profile of the input file for all three integron elements (attC, integrase, and sulI), while module A2 firstly searched the integrase and then searched the attC sites and sulI on integrase-containing sequences. Hence, integrons without integrases (types D and E) would not be identified by module A2. However, types A to C integrons were retrieved with 100% specificity and 100% coverage as by module A1 while saving 96% of computation time (evaluated by 10,112 complete genomes). Module A2 could dramatically save time and resources for cmsearch, without sacrificing the accuracy and coverage. The integrons in a set of 5436 complete genomes were identified by IntegronFinder v1.4  applying default settings.
Gillings MR. Integrons: past, present, and future. Microbiol Mol Biol Rev. 2014;78:257–77.
Gillings MR, Boucher Y, Labbate M, Holmes A, Krishnan S, Holley M, Stokes HW. The evolution of class 1 integrons and the rise of antibiotic resistance. J Bacteriol. 2008;190:5095–100.
Gillings MR. Class 1 integrons as invasive species. Curr Opin Microbiol. 2017;38:10–5.
Gillings MR, Gaze WH, Pruden A, Smalla K, Tiedje JM, Zhu YG. Using the class 1 integron-integrase gene as a proxy for anthropogenic pollution. ISME J. 2015;9:1269–79.
Holmes AJ, Gillings MR, Nield BS, Mabbutt BC, Nevalainen K, Stokes H. The gene cassette metagenome is a basic resource for bacterial genome evolution. Environ Microbiol. 2003;5:383–94.
Ma L, Li A-D, Yin X-L, Zhang T. The prevalence of integrons as the carrier of antibiotic resistance genes in natural and man-made environments. Environ Sci Technol. 2017;51:5721–8.
Gatica J, Tripathi V, Green S, Manaia CM, Berendonk T, Cacace D, Merlin C, Kreuzinger N, Schwartz T, Fatta-Kassinos D, et al. High throughput analysis of integron gene cassettes in wastewater environments. Environ Sci Technol. 2016;50:11825–36.
Stalder T, Barraud O, Casellas M, Dagot C, Ploy M-C. Integron involvement in environmental spread of antibiotic resistance. Front Microbiol. 2012;3
Hardwick SA, Stokes HW, Findlay S, Taylor M, Gillings MR. Quantification of class 1 integron abundance in natural environments using real-time quantitative PCR. FEMS Microbiol Lett. 2008;278:207–12.
Abella J, Bielen A, Huang L, Delmont TO, Vujaklija D, Duran R, Cagnon C. Integron diversity in marine environments. Environ Sci Pollut Res Int. 2015;22:15360–9.
Tsafnat G, Coiera E, Partridge SR, Schaeffer J, Iredell JR. Context-driven discovery of gene cassettes in mobile integrons using a computational grammar. BMC Bioinformatics. 2009;10:281.
Cury J, Jové T, Touchon M, Néron B, Rocha EP. Identification and analysis of integrons and cassette arrays in bacterial genomes. Nucleic Acids Res. 2016;44:4539–50.
Domingues S, da Silva GJ, Nielsen KM. Global dissemination patterns of common gene cassette arrays in class 1 integrons. Microbiology. 2015;161:1313–37.
Sayers EW, Barrett T, Benson DA, Bolton E, Bryant SH, Canese K, Chetvernin V, Church DM, DiCuccio M, Federhen S. Database resources of the national center for biotechnology information. Nucleic Acids Res. 2012;40:D13–25.
Parks DH, Rinke C, Chuvochina M, Chaumeil PA, Woodcroft BJ, Evans PN, Hugenholtz P, Tyson GW. Recovery of nearly 8,000 metagenome-assembled genomes substantially expands the tree of life. Nat Microbiol. 2017;2(11):1533–42.
Chain P, Grafham D, Fulton R, Fitzgerald M, Hostetler J, Muzny D, Ali J, Birren B, Bruce D, Buhay C. Genome project standards in a new era of sequencing. Science. 2009;326:236–7.
Chan PP, Lowe TM. GtRNAdb 2.0: an expanded database of transfer RNA genes identified in complete and draft genomes. Nucleic Acids Res. 2016;44:D184–9.
Blin K, Medema MH, Kottmann R, Lee SY, Weber T. The antiSMASH database, a comprehensive database of microbial secondary metabolite biosynthetic gene clusters. Nucleic Acids Res. 2016;45:D1.
Parks DH, Imelfort M, Skennerton CT, Hugenholtz P, Tyson GW. CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res. 2015;25:1043–55.
MacDonald NJ, Parks DH, Beiko RG. Rapid identification of high-confidence taxonomic assignments for metagenomic data. Nucleic Acids Res. 2012;40:e111.
Krause L, Diaz NN, Goesmann A, Kelley S, Nattkemper TW, Rohwer F, Edwards RA, Stoye J. Phylogenetic classification of short environmental DNA fragments. Nucleic Acids Res. 2008;36:2230–9.
Parks DH, MacDonald NJ, Beiko RG. Classifying short genomic fragments from novel lineages using composition and homology. BMC Bioinformatics. 2011;12:328.
Huson DH, Auch AF, Qi J, Schuster SC. MEGAN analysis of metagenomic data. Genome Res. 2007;17:377–86.
Moura A, Soares M, Pereira C, Leitao N, Henriques I, Correia A. INTEGRALL: a database and search engine for integrons, integrases and gene cassettes. Bioinformatics. 2009;25:1096–8.
Camacho C, Coulouris G, Avagyan V, Ma N, Papadopoulos J, Bealer K, Madden TL. BLAST+: architecture and applications. BMC Bioinformatics. 2009;10:421.
Yang Y, Jiang X, Chai B, Ma L, Li B, Zhang A, Cole JR, Tiedje JM, Zhang T. ARGs-OAP: online analysis pipeline for antibiotic resistance genes detection from metagenomic data using an integrated structured ARG-database. Bioinformatics. 2016;32:15.
Ghaly TM, Chow L, Asher AJ, Waldron LS, Gillings MR. Evolution of class 1 integrons: mobilization and dispersal via food-borne bacteria. PLoS One. 2017;12:e0179169.
Joss MJ, Koenig JE, Labbate M, Polz MF, Gillings MR, Stokes HW, Doolittle WF, Boucher Y. ACID: annotation of cassette and integron data. BMC Bioinformatics. 2009;10:118.
Dawes FE, Kuzevski A, Bettelheim KA, Hornitzky MA, Djordjevic SP, Walker MJ. Distribution of class 1 integrons with IS26-mediated deletions in their 3′-conserved segments in Escherichia coli of human and animal origin. PLoS One. 2010;5:e12754.
Li L-G, Xia Y, Zhang T. Co-occurrence of antibiotic and metal resistance genes revealed in complete genome collection. ISME J. 2017;11:651–62.
Lapierre P, Gogarten JP. Estimating the size of the bacterial pan-genome. Trends Genet. 2009;25:107–10.
Thomas CM, Nielsen KM. Mechanisms of, and barriers to, horizontal gene transfer between bacteria. Nat Rev Microbiol. 2005;3:711–21.
Krawczyk PS, Lipinski L, Dziembowski A. PlasFlow: predicting plasmid sequences in metagenomic data using genome signatures. Nucleic Acids Res. 2018;
Frost LS, Leplae R, Summers AO, Toussaint A. Mobile genetic elements: the agents of open source evolution. Nat Rev Microbiol. 2005;3:722–32.
Zaneveld JR, Nemergut DR, Knight R. Are all horizontal gene transfers created equal? Prospects for mechanism-based studies of HGT patterns. Microbiology. 2008;154:1–15.
Starikova I, Harms K, Haugen P, Lunde TT, Primicerio R, Samuelsen Ø, Nielsen KM, Johnsen PJ. A trade-off between the fitness cost of functional integrases and long-term stability of integrons. PLoS Pathog. 2012;8:e1003043.
Boucher HW, Talbot GH, Bradley JS, Edwards JE, Gilbert D, Rice LB, Scheld M, Spellberg B, Bartlett J. Bad bugs, no drugs: no ESKAPE! An update from the Infectious Diseases Society of America. Clin Infect Dis. 2009;48:1–12.
Li B, Yang Y, Ma L, Ju F, Guo F, Tiedje JM, Zhang T. Metagenomic and network analysis reveal wide distribution and co-occurrence of environmental antibiotic resistance genes. ISME J. 2015;9:2490–502.
Martinez JL, Coque TM, Baquero F. What is a resistance gene? Ranking risk in resistomes. Nat Rev Microbiol. 2015;13:116–23.
Levesque C, Piche L, Larose C, Roy PH. PCR mapping of integrons reveals several novel combinations of resistance genes. Antimicrob Agents Chemother. 1995;39:185–91.
Gillings MR, Xuejun D, Hardwick SA, Holley MP, Stokes HW. Gene cassettes encoding resistance to quaternary ammonium compounds: a role in the origin of clinical class 1 integrons? ISME J. 2009;3:209–15.
Rosser SJ, Young H-K. Identification and characterization of class 1 integrons in bacteria from an aquatic environment. J Antimicrob Chemother. 1999;44:11–8.
Van Boeckel TP, Gandra S, Ashok A, Caudron Q, Grenfell BT, Levin SA, Laxminarayan R. Global antibiotic consumption 2000 to 2010: an analysis of national pharmaceutical sales data. Lancet Infect Dis. 2014;14:742–50.
Johnson TA, Stedtfeld RD, Wang Q, Cole JR, Hashsham SA, Looft T, Zhu Y-G, Tiedje JM. Clusters of antibiotic resistance genes enriched together stay together in swine agriculture. MBio. 2016;7:e02214–5.
Rhoads A, Au KF. PacBio sequencing and its applications. Genomics Prot Bioinform. 2015;13:278–89.
Jain M, Fiddes IT, Miga KH, Olsen HE, Paten B, Akeson M. Improved data analysis for the MinION nanopore sequencer. Nat Methods. 2015;12:351–6.
Siebert PD, Chenchik A, Kellogg DE, Lukyanov KA, Lukyanov SA. An improved PCR method for walking in uncloned genomic DNA. Nucleic Acids Res. 1995;23:1087.
Mifsud B, Tavares-Cadete F, Young AN, Sugar R, Schoenfelder S, Ferreira L, Wingett SW, Andrews S, Grey W, Ewels PA. Mapping long-range promoter contacts in human cells with high-resolution capture Hi-C. Nat Genet. 2015;47:598–606.
Nagano T, Lubling Y, Stevens TJ, Schoenfelder S, Yaffe E, Dean W, Laue ED, Tanay A, Fraser P. Single-cell Hi-C reveals cell-to-cell variability in chromosome structure. Nature. 2013;502:59–64.
van der Helm E, Imamovic L, Hashim Ellabaan MM, van Schaik W, Koza A, Sommer MO. Rapid resistome mapping using nanopore sequencing. Nucleic Acids Res. 2017;45:e61.
Schmidt K, Mwaigwisya S, Crossman L, Doumith M, Munroe D, Pires C, Khan A, Woodford N, Saunders N, Wain J. Identification of bacterial pathogens and antimicrobial resistance directly from clinical urines by nanopore-based metagenomic sequencing. J Antimicrob Chemother. 2016;72:104–14.
Woolhouse ME, Gowtage-Sequeria S. Host range and emerging and reemerging pathogens. Emerg Infect Dis. 2005;11:1842.
Ma L, Xia Y, Li B, Yang Y, Li L-G, Tiedje JM, Zhang T. Metagenomic assembly reveals hosts of antibiotic resistance genes and the shared resistome in pig, chicken, and human feces. Environ Sci Technol. 2015;50:420–7.
Nawrocki EP, Eddy SR. Infernal 1.1: 100-fold faster RNA homology searches. Bioinformatics. 2013;29:2933–5.
Edgar RC. Search and clustering orders of magnitude faster than BLAST. Bioinformatics. 2010;26:2460–1.
Edgar RC. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 2004;32:1792–7.
Price MN, Dehal PS, Arkin AP. FastTree 2—approximately maximum-likelihood trees for large alignments. PLoS One. 2010;5:e9490.
Huang YT, Yang J-I, Chrobak M, Borneman J. PRISE2: software for designing sequence-selective PCR primers and probes. BMC Bioinformatics. 2014;15:317.
Shannon P, Markiel A, Ozier O, Baliga NS, Wang JT, Ramage D, Amin N, Schwikowski B, Ideker T. Cytoscape: a software environment for integrated models of biomolecular interaction networks. Genome Res. 2003;13:2498–504.
Miss A.N. Zhang, Dr. L.G Li, and Dr. L.P. Ma acknowledge the University of Hong Kong for the postgraduate studentship and postdoctoral fellowship. The authors appreciate the help of Vicky Fung, and thank Lilian Y L Chan for technical assistance of High Performance Computing & Grid Computint System.
The authors would like to thank the Hong Kong General Research Fund (172057/15E) for the financial support.
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The integron-integrase database constructed and curated using bioinformatics pipeline and whole genome analysis in this study, covering 3,384 complete and non-redundant integrases. (ZIP 11490 kb)
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Zhang, A.N., Li, LG., Ma, L. et al. Conserved phylogenetic distribution and limited antibiotic resistance of class 1 integrons revealed by assessing the bacterial genome and plasmid collection. Microbiome 6, 130 (2018). https://doi.org/10.1186/s40168-018-0516-2
- Class 1 integrons
- Antibiotic resistance
- Whole genome analysis
- Database construction