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Article

Phylogenetic Grouping of Human Ocular Escherichia coli Based on Whole-Genome Sequence Analysis

by
Konduri Ranjith
,
Chinthala Reddy SaiAbhilash
,
Gumpili Sai Prashanthi
,
Shalem Raj Padakandla
,
Savitri Sharma
and
Sisinthy Shivaji
*
Jhaveri Microbiology Centre, Prof. Brien Holden Eye Research Centre, L. V. Prasad Eye Institute, Kallam Anji Reddy campus, Hyderabad, Telangana 500034, India
*
Author to whom correspondence should be addressed.
Microorganisms 2020, 8(3), 422; https://doi.org/10.3390/microorganisms8030422
Submission received: 2 January 2020 / Revised: 10 March 2020 / Accepted: 14 March 2020 / Published: 17 March 2020
(This article belongs to the Section Systems Microbiology)
Browse Figure
Versions Notes

Abstract

:
Escherichia coli is a predominant bacterium in the intestinal tracts of animals. Phylogenetically, strains have been classified into seven phylogroups, A, B1, B2, C, D, E, and F. Pathogenic strains have been categorized into several pathotypes such as Enteropathogenic (EPEC), Enterotoxigenic (ETEC), Enteroinvasive (EIEC), Enteroaggregative (EAEC), Diffusely adherent (DAEC), Uropathogenic (UPEC), Shiga-toxin producing (STEC) or Enterohemorrhagic (EHEC) and Extra-intestinal pathogenic E. coli (ExPEC). E. coli also survives as a commensal on the ocular surface. However, under conditions of trauma and immune-compromised states, E. coli causes conjunctivitis, keratitis, endopthalmitis, dacyrocystitis, etc. The phylogenetic affiliation and the pathotype status of these ocular E. coli strains is not known. For this purpose, the whole-genome sequencing of the 10 ocular E. coli strains was accomplished. Based on whole-genome SNP variation, the ocular E. coli strains were assigned to phylogenetic groups A (two isolates), B2 (seven isolates), and C (one isolate). Furthermore, results indicated that ocular E. coli originated either from feces (enteropathogenic and enterotoxigenic), urine (uropathogenic), or from extra-intestinal sources (extra-intestinal pathogenic). A high concordance was observed between the presence of AMR (Antimicrobial Resistance) genes and antibiotic resistance in the ocular E. coli strains. Furthermore, several virulent genes (fimB to fimI, papB to papX, etc.) and prophages (Enterobacteria phage HK97, Enterobacteria phage P1, Escherichia phage D108 etc.) were unique to ocular E. coli. This is the first report on a whole-genome analysis of ocular E. coli strains.

1. Introduction

The human eye is sterile prior to birth, but immediately after birth the ocular surface acquires several bacteria from the mother and the environment, and these survive on the ocular surface as commensals. The ocular surface commensal bacteria include Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, Micrococcus luteus, Neisseria spp., Moraxella spp., Bacillus spp., Rhodococcus erythropolis, Propionibacterium acnes, Klebsiella oxytoca, Escherichia coli, Proteus mirabilis, Enterobacter agglomerans, Klebsiella spp. etc. More recently, based on 16S rRNA gene sequencing, a greater bacterial diversity has been observed associated with the lid margin and lower conjunctival sac [1,2,3]. These bacteria are normally harmless and do not cause any infections. However, under conditions of trauma and when the host’s immunity is compromised, these commensal bacteria become infective and cause diseases like conjunctivitis, keratitis, or endopthalmitis [4,5,6]. In general, transformation from a commensal to a virulent form depends on several attributes, such as the ability to swim, adhere, form a biofilm, produce toxins, and avoid host defense mechanisms [7]. Virulence is also enhanced by virulent factors [8], the presence of prophages, plasmids, ability to conjugate, etc. [9]. These studies also suggested that transposons, plasmids and insertion sequences contribute to the plasticity of the E. coli genome, resulting in an extremely large pangenome [10].
The origin of ocular E. coli is not very clear, but ocular microbiologists believe that they most likely originate from fecal or urine contamination or from an extra-intestinal source. It is possible that these ocular E. coli are related to one or more of the known eight pathotypes of E. coli, namely enteropathogenic (EPEC), enterotoxigenic (ETEC), enteroinvasive (EIEC), enteroaggregative (EAEC), diffusely adherent (DAEC), uropathogenic (UPEC), Shiga-toxin producing (STEC), or enterohemorrhagic (EHEC) and extra-intestinal pathogenic E. coli (ExPEC) [11]. Phylogenetically, these ocular E. coli could be affiliated with the already characterized phylogenetic groups designated A, B1, B2, C, D, E, and F [12,13,14,15,16,17], and strains affiliated to B2 and D often carry virulence determinants that are lacking in group A and B1 strains [15,17]. In a recent study, Raimondi et al. [12] demonstrated that the ExPEC strains residing as commensals in the guts of healthy subjects mostly belonged to phylogroup B2, followed by A, B1, D, E, and F phylogroups. Several other features like the presence of virulent genes, ability to form biofilm, resistance to antibiotics, and toxin production were also checked [12]. In the present study, susceptibility of the 10 ocular E. coli isolates to 29 antibiotics belonging to 11 different classes was ascertained via phenotypic tests. Furthermore, whole-genome sequencing (WGS) of the 10 ocular surface E. coli isolates was accomplished and based on whole-genome SNP variation, the isolates were assigned to one or more of the nearest E. coli phylogenetic groups (A, B1, B2, C, D, E, and F) and to one or more of the eight pathotypes (EPEC, ETEC, EIEC, EAEC, DAEC, UPEC, STEC, or EHEC and ExPEC). Additional information on the presence of AMR genes, prophages, and genes involved in quorum sensing, biofilm formation, motility, and stress response, which contribute to AMR and pathogenicity, were also determined. This is the first report on the whole-genome analysis of 10 ocular E. coli strains.

2. Materials and Methods

2.1. Ethics

This study was approved by the Ethics Committee of L V Prasad Eye Institute, Hyderabad, India (ECR/468/Inst./AP/2013, Ref No: LEC 03-15-029 (14th May 2018)).

2.2. Bacterial Strains and Antibiotic Susceptibility of the Ocular E. coli

The details of the patients from whom the 10 ocular strains of E. coli were isolated are given in Table S11. Two isolates were from the conjunctival swabs of two patients with conjunctivitis, two were from corneal scrapings of two patients with infectious keratitis, five were isolated from the vitreous fluid of five patients with endophthalmitis, and one from the pus of a patient with orbital cellulitis. The taxonomic characterization of the 10 ocular E. coli isolates was determined as described previously [18]. The 10 E. coli infections were community infections and presented with the infection when they visited the hospital.
The susceptibility of the 10 isolates to 29 antibiotics (Table 1) was determined using the Vitek2 (BioMérieux, Paris, France) method and the serial dilution method [19,20,21]. The pattern of susceptibility was assigned as per European Committee on Antimicrobial Susceptibility Testing (EUCAST).

2.3. DNA Extraction and Whole-Genome Analysis

Genomic DNA was extracted from an overnight culture using a DNA isolation kit (Qiagen, Heilden, Germany), quality checked on 0.8% agarose gel run at 110 V for 30 min, and the concentration was determined using Qubit® 2.0 Fluorometer [18].Whole-genome sequencing (WGS) was performed on the Illumina HiSeq 2500 platform at Xcelris Genomics Pvt. Ltd., Ahmedabad, India. Good quality genomic DNA (200 ng) was used for the preparation of the paired-end sequencing library using a Truseq Nano DNA Library Prep kit (Illumina, CA 92122, USA).

2.4. Data Availability

All genome sequence data were submitted to the National Center for Biotechnology Information (NCBI) under Bioproject accession number PRJNA543974.

2.5. Assembly of Genomes

Genomes were assembled both by reference-based and de-novo-based assembly. In the former method, high-quality reads were mapped to a reference genome of E. coli strain K-12 substrain MG1655 (henceforth E. coli MG1655) genome (https://www.ncbi.nlm.nih.gov/nuccore/U00096.3/) [22] using BWA version 0.7.5a. Subsequently, SAM tools were used to call the consensus from the resultant BAM file. In de novo assembly, all 10 samples were de novo assembled separately using Velvet (v 1.2.10) assembler [19] at different k-mer ranges. Assemblies determined to be robust in terms of number of contigs, N50, and maximum scaffold length were selected for downstream analysis. The assembly elements were computed using in-house Perl script. The quality of the microbial genomes was based on the estimates of completeness and contamination, as monitored by CheckM [23].

2.6. Annotation of the Genomes and Pathway Analysis

BLAST v2.2.28+ was used for annotation of genes involved in antimicrobial resistance, virulence, prophages, motility, biofilm, quorum sensing, etc. The predicted proteins were also identified using the BLAST algorithm. Pathway analysis of the genes was performed using the KEGG automatic annotation server database using BLASTP with a default value of 60.

2.7. Non-Coding RNA Prediction

tRNAscan-SE v.1.31 [24,25] was used for identification of probable tRNA genes. These results were also validated using ARAGORN, a computer program which identifies tRNA and tmRNA (transfer-messenger RNA) genes. [26]. The location of ribosomal RNA genes was predicted using the Basic Rapid Ribosomal RNA Predictor.

2.8. Identification of Acquired Antimicrobial Resistance Genes, Plasmids, Virulence Genes, and Prophages

AMR genes including chromosomal mutations conferring AMR were detected using ResFinder 3.2 [27], plasmids using PlasmidFinder database (https://cge.cbs.dtu.dk/services/PlasmidFinder/version2.0) [28], and virulence genes using ABRicate (https://github.com/tseemann/abricate) and VFDB (Virulence Factor Data Base)database [29] as a reference. All the above genes were identified with a minimum coverage of 60% and minimum identity of 90%. Prophages in the genomes were identified using PHASTER (Phage Search Tool Enhanced Release) (http://phaster.ca/) [30,31]. Genes with 90% identity and 90% prophage sequence length coverage were considered for comparison of genomes.

2.9. SNP Detection and Phylogenetic Tree Construction

A whole-genome single nucleotide polymorphism (SNP)-based phylogenetic tree was constructed using kSNP3.0 software [32]. K-chooser was used to identify the optimal kmer length as 21 and to calculate the fraction of core kmers. We included genomes from all isolates and reference genomes belonging to phylogenetic groups A, B1, B2, C, D, E, and F. The parsimony tree was estimated based on SNP loci that occurred in at least 50% of the strains. Each strain was assigned to a phylogenetic group or a cryptic clade based on its position in the phylogenetic tree. In addition, Clermont typing was also used to determine the phylogroups of the ocular isolates [33,34], and the MLST 2.0 (Multi-Locus Sequence Typing 2.0) tool of Centre for Genomic Epidemiology was used to determine the sequence types (STs) of the ocular isolates [35].

2.10. Comparison of E. coli Genomes

BRIG (Blast Ring Image Generator) [36] was used to ascertain the similarities between a central reference sequence, the 10 ocular isolates, and reference sequences of E. coli phylogenetic groups A, B2, and C. L-2594/2017 was used as the reference sequence.

3. Results and Discussion

3.1. Whole-Genome Analysis and Antimicrobial Resistance Genes

Tyson et al. [37] and Moran et al. [38] suggested that a combination of whole-genome analysis (WGA) and phenotypic data would be most suitable to understand antimicrobial resistance. Accordingly the genomes of the 10 ocular strains were sequenced and compared with that of E. coli MG1655 with respect to several characteristics like genome coverage, completeness, the number of genes, the G+C% content of DNA, and number of tRNA genes (Table 1 and Table S1) which indicated a high degree of similarity and that majority of the genes were affiliated to E. coli MG1655. KEGG (Kyoto Encyclopedia of Genes and Genomes) pathway analysis also confirmed that majority of the genes were affiliated to E. coli and the mapped proteins represented metabolic pathways of major biomolecules and genes involved in genetic information processing, environmental information processing, cellular processes, drug resistance, etc. (Table S2).
Resfinder 3.2. was used to identify 22 AMR genes conferring resistance to eight different classes of antibiotics (Table 2A) in the 10 ocular E. coli isolates. Isolate L-2594/2017 was the only isolate that possessed genes that conferred resistance to all the eight classes of antibiotics. Phenotypic studies were carried out to correlate the phenotypic susceptibility/resistance pattern to antibiotics with the absence or presence of AMR genes in the 10 isolates. When comparing the results in Table 2 and Table 3, certain generalizations emerged. The first was that in several cases, the presence of an AMR gene positively correlated with resistance to a particular antibiotic. For instance, resistance to one penicillin (ampicillin) and six cephalosporins (cefuroxime, cefuroxime axetil, ceftriaxone, cefepime, cefazolin, and ceftazidime) could be attributed to genes conferring resistance to penicillin (like blaCTX-M-15 and dfrA17) and to the six cephalosporins (like aadA2, aadA5, blaOXA-1, blaNDM-5, dfrA12, dfrA17, blaCTX-M-15, blaTEM-1B, blaOXA-1) that were detected (Table 2A and Table 3). Isolate L-1216/2010 was the most sensitive of all the 10 isolates and was resistant to only five antibiotics, namely nalidixic acid due to the presence of blaTEM-1B, and clindamycin and lincomycin due to the presence of mdfA, but resistant genes for minocycline and sulfanilamide were not detected, implying that resistance was due to some unknown genes (Table 2). It has been reported that mdfA also confers resistance to a broad range of antibiotics including tetracycline, chloramphenicol, erythromycin, daunomycin, puromycin, benzalkonium, rifampin, some aminoglycosides and fluoroquinolones, and organic cations such as ethidium bromide and tetraphenylphosphonium [39], and its presence in L-1216/2010 may therefore compensate for the absence of the specific genes conferring resistance to minocycline, a tetracycline antibiotic. It was also observed that sensitivity to an antibiotic could be attributed to the absence of a gene that confers resistance. For instance, all the isolates were susceptible to tigecycline, nitrofurantoin, and colistin, and they did not possess the corresponding resistant genes. In a recent study, Sun et al. [40] reported that tigecycline resistance was mediated by tet(X4) associated with IncQ1 plasmid in E. coli. Further the resistance to colistin, the polymixin antibiotic, could be attributed to the fact that lipid A modification, which is a prominent feature of polymyxin resistance, probably did not occur [41,42]. The second generalization was that the presence of an AMR gene may not result in a resistance phenotype if the gene is not expressed. For instance, L-1534/2017 was sensitive to ceftazidime although it possessed the AMR gene blaTEM-1B. We also observed resistance even in the absence of the AMR gene, implying that other undiscovered genes may be conferring resistance. In the ocular strains L-1534/2016 and L-3137/2017, we detected blaTEM-1B, which confers resistance to ampicillin. Intriguingly, seven other isolates did not possess blaTEM-1B but were still resistant to ampicillin, indicating that another β-lactamase gene may be involved. This other β-lactamase gene is likely to be blaCTX-M-15 or blaOXA-1, which were detected in this study. A similar observation was also made with respect to susceptibility to fluoroquinolones. The AMR gene for fluoroquinolone is aac(6’)-1b-cr. Six isolates did not have this gene, but exhibited resistance to one or more of the six antibiotics tested, implying the existence of other genes conferring resistance to fluoroquinolones (Table 2 and Table 3). The additional possibility is that these organisms may have had chromosomal mutations conferring resistance to fluoroquinolones. Accordingly, we detected chromosomal mutations inparE, gyrA, and parC that conferred resistance to fluoroquinolones like nalidixic acid and ciprofloxacin (Table 2B).We observed one or more of these three generalizations across all the antibiotic groups studied (Table 2A,B and Table 3A). These results were in accordance with earlier results that demonstrated the presence of blaCTX-M-15 in E. coli strains from India [43,44] and from Europe, Asia, Canada, and United Kingdom [45,46,47,48]. We also confirmed that the plasmids harboring the blaCTX-M-15 gene were of the incompatibility group FII in 7 of the 10 isolates. We also detected the IncX3 plasmid, which plays an important role in the dissemination of blaNDM-5 [49]. The observed resistance to nalidixic acid could be attributable to the presence of emrB, which extrudes nalidixic acid. The mphA gene, which confers resistance to erythromycin and azithromycin, was also present in a few of the ocular isolates. Two of the three genes that confer resistance to sulfonamides, namely sul1 and sul2, were also detected in a few of the ocular isolates. Studies on sulfonamide-resistant Escherichia coli from various animals and humans have indicated that sul2 is the most prevalent, and sul3 is restricted mainly to porcine E. coli isolates [50]. Sul-carrying plasmids belonged to diverse replicon types, and IncFII seems to be the dominant replicon type in sul2-carrying plasmids [51]. dfrA genes are known to confer resistance to trimethoprim, and their prevalence in E. coli isolates of human and animal origin has been well established [52,53]. The above results confirmed earlier studies pointing to a high concordance between the presence of genes conferring resistance to antibiotics and the phenotypic observation of antibiotic resistance. We compared the resistance profile of the ocular and urine isolates of E. coli from patients with ocular disease to different antimicrobial agents, and observed that both the ocular and urine isolates were more resistant to fluoroquinolones (73–90%) and cephalosporins (60–80%), but showed reduced resistance to aminoglycoside (10–23%), amphenicols (10–15%), and carbapenems (10–15%) (Table 3B). The urine isolates were more resistant than the ocular isolates to the antibiotics tested.

3.2. Plasmids and Virulence Genes

In this study, 11 different types of plasmid were identified (Table 4), with 7 affiliated to the Inc group, 3 to the Col group, and 1 to the repB plasmid group. Earlier studies have indicated that plasmids from Enterobacteriaceae contain antibiotic resistance genes [54,55,56,57], and a vast majority of these plasmids (>75%) can be classified into Inc groups or Rep types [54]. It is intriguing that E. coli L-1149/2016 was the only ocular strain without any plasmids, although it was resistant to 12 of the antibiotics tested (Table 1). In E. coli MG1655, we failed to detect any plasmids with either PlasmidFinder [28] or PlasmidSpades (https://github.com/ablab/spades) [20]. This study also confirmed that all the AMR genes were associated with a specific plasmid (Table S3), except that plasmid pT7-5, which harbors mdfA, was not detected. Furthermore, the STEC plasmid was not detected in the 10 ocular isolates (Table 5), confirming that STEC plasmid was rare in non-STEC strains of E. coli [21,58].
A total of 114 different virulent genes were detected across the 10 ocular isolates (Table 5) and 25 out of 114 were shared across all the isolates. Several virulent genes detected in this study were similar to those reported earlier [21], including aerobactin siderophore biosynthesis protein, cytotoxic necrotizing factor, secreted auto-transporter toxin, enterotoxin, yersiniabactin, enterobactin, aerobactin, adhesin, fimbriae, pilus, ABC transporter, type III secretion system effectors, hemoglobin proteases, serine protease, hemolysine genes, outer membrane protein genes, etc. (Table 5). It was observed that L-3003/2015 and L-2594/2017, which are affiliated to phylogenetic group A, possessed all the genes found in NA635, a group A reference strain, except espY1. At the same time, it was observed that fimB to fimI and papB to papX genes were present only in the ocular isolates (Tables S4 and S5). The majority of the virulent genes in the seven ocular isolates affiliated to phylogenetic group B2 were shared with the B2 reference strain CFT073. We also identified several gspC and gspK in these seven ocular isolates affiliated to phylogenetic group B2 (Table S4). We also compared the virulent genes of the 10 ocular isolates with type strains of the phylogenetic groups B1, B3, D, E, and F of E. coli, and the differences appeared to be more pronounced (Table S5).

3.3. Prophages in Ocular E. coli

We report for the first time 24 prophages in 10 ocular E. coli (Table S6). Eleven out of the 24 prophages were unique and were detected only in a single isolate (Table S6). Enterobacteria phage lambda and Enterobacteria phage mEp460 were shared by eight isolates. Comparison of the prophages with other E. coli isolates indicated that four phages, namely Enterobacteria phage lambda, Enterobacteria phage mEp460, Enterobacteria phage P2, and Enterobacteria phage P4 were shared by all the groups of E. coli (ocular, EPEC, ETEC, ExPEC, UPEC, and environmental) in at least one strain, and five prophages, namely Bacillus phage G, Enterobacteria phage HK97, Enterobacteria phage P1, Escherichia phage D108, Escherichia Stx1 converting phage, and Escherichia phage vB_EcoM-ep3 were unique to the ocular E. coli isolates (Table S7). We observed that the genome sizes of the 10 ocular isolates were larger than E. coli MG 1655 (Table 2), maybe due to the presence of prophages. This was in accordance with Perna et al. [59] and Hayashi et al. [60,61], who reported that the genomes of E. coli O157:H7 (strains EDL933 and RIMD0509952) were approximately 880 and 860 kb larger compared to E. coli MG1655, partly because these contained prophages and prophage-like elements. It was suggested that prophage sequences are beneficial since they confer AMR, help to overcome various types of stresses, and facilitate increase in growth and biofilm formation [62].

3.4. Genes Involved in Quorum Sensing, Biofilm Formation, and Motility in Ocular E. coli

Genes for quorum sensing (QS) (Table S8), genes facilitating biofilm formation (Table S9), and genes involved in motility (Table S10), which are important for AMR, were also identified. We have no direct proof of the involvement of these genes in AMR in ocular E. coli, but it is unequivocally established in the literature that QS biofilm formation [63,64,65] and motility [66,67,68,69] are linked to AMR. In a recent review, Rossi et al. [70] highlighted that motility is also downregulated in biofilm cells with simultaneous upregulation of adhesion factors [71]. In two earlier studies, we demonstrated biofilm formation potential in 7 of the above 10 ocular isolates, their increased resistance to antibiotics in the biofilm phase, identified genes that were overexpressed in the biofilm phase, and also identified five genes (bdcR, mhpA, mhpB, ryfA, and tolA) required for biofilm formation [18,72]. Studies have also implicated stress response regulators Dgk, sigma B, and rpoS in Staphylococcus aureus and in E. coli in biofilm formation [73,74,75,76]. Genes spoT and relA were present in 6 out of 10 ocular strains, and both these genes are involved in the stringent response in E. coli [77,78].

3.5. Phylogenetic Grouping of Ocular E. coli Based on BRIG

BLAST Ring Image Generator (BRIG) was used to compare the whole genomes of the 10 ocular E. coli strains (Figure 1) with strains selected from phylogenetic groups A, B2, and C with respect to gaps in the genomes (like G1 and G2) indicative of the absence of a gene(s), presence/absence of virulence genes (blue), resistance genes (black), phages (red), and plasmids (green). Virulent genes (blue) were distributed across the genomes, and several of them were present as clusters (1 to 5). Clusters 1 and 2 were present in all the isolates and in the reference strains of phylogenetic groups A, B2 and C whereas genes in Clusters 3–5 were differentially distributed. It was also observed that L-3003/2015 (Ring 4) was very similar to phylogroup A reference strain NA635 (Ring 3), L-1010/2018 (Ring 6) to phylogroup C (Ring 5), and the remaining seven isolates (Rings 8-13 and15) were similar to phylogroup B2 (Rings 7 and 14). Perna et al. [59] and Hayashi et al. [60,61] previously reported that the genomes of pathogenic E. coli O157:H7 (strains EDL933 and RIMD0509952) were larger compared to E. coli MG1655, partly because of these prophages and prophage-like elements.

3.6. Phylogenetic Affiliation of the Ten Ocular E. coli Isolates with Other Phylogenomic Groups

This study raised the question as to the origin of the ocular E. coli. For this purpose, the genomes of the 10 ocular E. coli isolates were subjected to phylogroup identification using Clermont typing, which indicated that the 10 isolates were affiliated to three phylogenetic groups, A (L-2594/2017 and L-3003/2015), B2 (L-1339/2013, L-494/2011, L-3137/2017, L-1149/2016, L-1216/2010, L-1534/2016, and GMRV-476/2017), and C (L-1010/2018). Identical results were also obtained via phylogenetic analysis of whole-genome single nucleotide polymorphism (SNP) patterns using kSNP3.0 software [32] (data not shown). The tree also indicated that six strains were affiliated to ExPEC, two to EPEC, one to ETEC, and one to UPEC. These studies thus indicated a lack of concordance between the pathotype and phylogenetic group. Sequence typing also indicated that five isolates (L-1339/2013, L-494/2011, L-3137/2017, L-1149/2016, and GMRV-476/2017 ) were affiliated to ST131, and the remaining five were affiliated to ST10 (L-3003/2015), ST73 (L-1216/2010), ST410 (L-1010/2018), ST617 (L-2594/2017), and ST1193 (L-1534/2016), confirming a lack of concordance.). Our findings were partially in agreement with earlier studies indicating that extra-intestinal pathogenic E. coli are affiliated to phylogenetic groups A and B2 groups [32,79,80,81,82,83,84]. Phylogenetic groups B2 and D have been demonstrated to be linked to virulence determinants [17,85], antibiotic resistance [86,87,88], and possess virulence properties such as biofilm formation and hemolysin secretion when compared with phylogroup A and B1 isolates [87,89]. In this study, all the isolates, irrespective of their phylogenetic affiliations, had several AMR and virulent genes, biofilm genes, QS genes, etc., which facilitate their survival and pathogenic function. Further, it was observed as predicted that the 10 ocular E. coli isolates originated from fecal (EPEC and ETEC) or urine contamination (UPEC), or from extra-intestinal sources (ExPEC).

4. Conclusions

1. Whole-genome sequencing of 10 ocular strains of E. coli indicated increases in the genome length and the number of genes compared to a laboratory strain of E. coli.
2. Five of the 10 isolates were resistant to more than three classes of antibiotics, implying that these strains were MDR (Multi Drug Resistant) E. coli.
3. AMR genes were identified and a high concordance was observed between the presence of AMR genes and antibiotic resistance.
4. All the AMR genes were associated with a specific plasmid affiliated to the Inc group, the Col group, or the repB plasmid.
5. It was observed that the virulent genes fimB to fimI, papB to papX, and gspC and gspK genes were unique to the ocular isolates.
6. Prophages, namely Bacillus phage G, Enterobacteria phage HK97, Enterobacteria phage P1, Escherichia phage D108, Escherichia Stx1 converting phage, and Escherichia phage vB_EcoM-ep3 were also unique to the ocular E. coli isolates.
7. Prophages and genes involved in quorum sensing and biofilm formation, which contribute to AMR and pathogenicity, were also detected in ocular E. coli.
8. The 10 ocular E. coli were affiliated to phylogenetic groups A (two isolates), B2 (seven isolates), and C (one isolate).
9. The data also indicated that the 10 ocular E. coli isolates most likely originated from fecal (EPEC and ETEC), urine (UPEC), or from extra-intestinal sources (ExPEC), as per our prediction.

Supplementary Materials

The following are available online at https://www.mdpi.com/2076-2607/8/3/422/s1, Table S1: Identification of probable tRNA genes* in the 10 ocular E. coli isolates. Table S2: Enrichment of genes* in the 10 ocular E. coli isolates. Table S3: Antimicrobial-resistant genes associated with the plasmids in the 10 ocular E. coli isolates. Table S4: Comparison of virulent genes in the 10 ocular E. coli isolates and E. coli type strains associated with phylogenomic groups A, B2, and C. Table S5: Comparison of virulent genes in the 10 ocular E. coli isolates and E. coli type strains associated with phylogenomic groups A to F. Table S6: Comparison of prophages in ocular, EPEC, ETEC, ExPEC, UPEC, and environmental E. coli strains. Table S7: Characteristics of patients from whom the 10 ocular E. coli isolates were collected. Table S8: Number of quorum sensing genes * in ocular E. coli isolates. Table S9: Biofilm genes * in ocular E. coli isolates. Table S10: Motility genes * in ocular E. coli isolates. Table S11: Characteristics of patients from whom the 10 ocular E. coli were isolated.

Author Contributions

Conceptualization, S.S. (Sisinthy Shivaji); methodology, K.R., C.R.S., S.R.P.; software, K.R., G.S.P., S.R.P.; validation, K.R.; formal analysis, K.R.; investigation K.R.; resources, S.S. (Sisinthy Shivaji), S.S. (Savitri Sharma); writing—original draft, S.S. (Sisinthy Shivaji); writing—review and editing, S.S. (Sisinthy Shivaji); visualization, S.S. (Sisinthy Shivaji); supervision, S.S. (Sisinthy Shivaji); project administration, S.S. (Sisinthy Shivaji); funding acquisition, S.S. (Sisinthy Shivaji). All authors have read and agreed to the published version of the manuscript.

Funding

This research received in house funding from L.V. Prasad Eye Institute. It was not funded by any outside agency.

Acknowledgments

KR thanks ICMR (2017-2836/CMB-BMS) for the SRF fellowship.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

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Microorganisms 08 00422 g001 550
Figure 1. Comparison of ocular E. coli genomes and reference genomes of different phylogenetic groups. Ocular isolate L-2594/2017 was used as a reference. In the outermost ring, blue, black, red, and green indicate virulence genes, resistance genes, phages, and plasmids, respectively. Numerals 1 to 5 indicate the five clusters of virulent genes. BLASTn matches with less than 30% identity appear as blank spaces (gaps) in each ring. G1 and G2 indicate the gaps in the genomes. The image was prepared using Blast Ring Image Generator. Ring 1: Reference genome—L-2594/2017, Ring 2: E. coli MG1655, Ring 3: NA635, Ring 4: L-3003/2015, Ring 5: TW14425, Ring 6: L-1010/2018, Ring 7: SE15, Ring 8: L-3137/2017, Ring 9: L-494/2011, Ring 10: GMRV-476/2017, Ring 11: L-1339/2013, Ring 12: L-1149/2016, Ring 13: L-1534/2016, Ring 14: CFT073, and Ring 15: L-1216/2010.
Figure 1. Comparison of ocular E. coli genomes and reference genomes of different phylogenetic groups. Ocular isolate L-2594/2017 was used as a reference. In the outermost ring, blue, black, red, and green indicate virulence genes, resistance genes, phages, and plasmids, respectively. Numerals 1 to 5 indicate the five clusters of virulent genes. BLASTn matches with less than 30% identity appear as blank spaces (gaps) in each ring. G1 and G2 indicate the gaps in the genomes. The image was prepared using Blast Ring Image Generator. Ring 1: Reference genome—L-2594/2017, Ring 2: E. coli MG1655, Ring 3: NA635, Ring 4: L-3003/2015, Ring 5: TW14425, Ring 6: L-1010/2018, Ring 7: SE15, Ring 8: L-3137/2017, Ring 9: L-494/2011, Ring 10: GMRV-476/2017, Ring 11: L-1339/2013, Ring 12: L-1149/2016, Ring 13: L-1534/2016, Ring 14: CFT073, and Ring 15: L-1216/2010.
Microorganisms 08 00422 g001
Table
Table 1. Characteristics of the whole-genome sequences of the 10 ocular Escherichia coli isolates.
Table 1. Characteristics of the whole-genome sequences of the 10 ocular Escherichia coli isolates.
Sl. No.E. coli StrainL-1339/
2013		L-2594/
2017		L-494/
2011		L-3003/
2015		L-1010/
2018		L-3137/
2017		L-1149/
2016		GMRV-476/
2017		L-1534/
2016		L-1216/
2010		K-12 MG1655
1Sequencing data (GB)0.830.831.631.871.041.090.881.031.020.88
2Completeness99.9799.9799.9799.9799.6299.9799.9799.9799.9199.9799.97
3Contamination0.330.090.370.450.260.330.330.330.390.080.04
4DNA coding sequence (%)86.9293.0386.9192.5693.2086.9486.8986.8687.3585.9589
5Genome length (kbp)53515018542047464864526451195502504652394639
6Total number of tRNAs8587858887858485858487
7G+C content of DNA (%)50.650.750.750.750.650.750.750.650.650.550.8 *
8Genes encoding a protein51564816532144674664507448695402483750084583 **
* Data were from https://www.pnas.org/content/103/34/12879.short#sec-8; ** Data from https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi? mode=Info & id=511145.
Table 2. (A) Identification of antimicrobial resistance genes in 10 ocular E. coli * isolates; (B) Chromosomal mutations in parE, gyrA, and parC in the 10 ocular E. coli isolates conferring resistance to naldixic acid and ciprofloxacin.
Table
(A)
(A)
S.No.Class of AntibioticResistance GeneL-1339/
2013		L-2594/
2017		L-494/
2011		L-3003/
2015		L-1010/
2018		L-3137/
2017		L-1149/
2016		GMRV-476/
2017		L-1534/
2016		L-1216/
2010		Count
1Aminoglycosideaph(3’’)-Ib-+------+-2
aph(6)-Id-+------+-2
aac(6’)-Ib-cr++-+---+--4
aadA5+++-+-----4
aac(3)-IIa+-+-------2
aadA2-+--------1
2AmphenicolcatB3++++------4
catA1-+--------1
3Beta-lactamblaCTX-M-15++++++++--8
blaNDM-5-+--------1
blaTEM-1B-----+--+-2
blaOXA-1++++---+--5
4Fluoroquinoloneaac(6’)-Ib-cr++-+---+--4
5Lincosamidemph(A)++--+-----3
emrB---+------1
mdfA-+++++++++9
6Sulfonamidesul2-+------+-2
sul1+++-+-----4
7Tetracyclinetet(B)-+--------1
tet(A)----+--+--2
8TrimethoprimdfrA17+++-+-----4
dfrA12-+--------1
Total22101887732651
* Genes were identified from the whole-genome sequence using ResFinder 3.2 (https://cge.cbs.dtu.dk/services/ResFinder/). (+) and (-) indicate presence and absence of gene, respectively.
Table
(B)
(B)
S. No. E. coli IsolateChromosomal Mutation *
parEgyrAparC
1L-1339/2013 I529LS83L, D87NS80I, E84V
2L-2594/2017 S458AS83L, D87NS80I
3L-494/2011 I529LS83L, D87NS80I, E84V
4L-3003/2015 I529LS83L, D87NS80I, E84V
5L-1010/2018 No mutationS83LG78D
6L-3137/2017 S458AS83L, D87NS80I
7L-1149/2016 S458AS83L, D87NS80I
8GMRV-476/2017 L416FS83L, D87NS80I
9L-1534/2016 I529LS83L, D87NS80I, E84V
10L-1216/2010 I529LS83L, D87NS80I, E84V
* Chromosomal mutations were identified from the whole-genome sequence using ResFinder 3.2 (https://cge.cbs.dtu.dk/services/ResFinder/).
Table 3. (A) Susceptibility of the 10 ocular E. coli isolates * to 29 different antimicrobial agents belonging to seven different classes; (B) Comparison of the resistance profile of the ocular and urine isolates of E. coli from patients with ocular disease to 11 different antimicrobial agents.
Table
(A)
(A)
Sl. No.Antibiotic and ClassL-1339/
2013 (CjS)		L-2594/
2017 (V)		L-494/
2011 (V)		L-3003/
2015 (CrS)		L-1010/
2018 (PC)		L-3137/
2017 (V)		L-1149/
2016 (CrS)		GMRV-476/
2017 (V)		L-1534/
2016 (CjS)		L-1216/
2010 (V)		Resistance Genes
1Aminoglycosides
1Amikacin RSSSSSSSSSaac(6’)-Ib-cr
2Gentamicin RSRSSSSSSSaadA5, aac(3)-Iia
3TobramycinRRSRSSSRSSaph(3’’)-Ib,aph(6)-Id,aac(6’)-Ib-cr,aadA5,aac(3)-IIa
2Amphenicols
4ChloramphenicolSRSSSSSSSScatB, cat A1
3β-lactam
Penicillins
5AmpicillinRRRRRRRRRSblaCTX-M-15, dfrA17
Cephalosporins
6CefuroximeRRRRRRRRSSaadA5, aadA2, dfrA12, dfrA17, blaNDM-5, blaOXA-1
7Cefuroxime axetilRRRRRRRRSSaadA5, aadA2, dfrA12, dfrA17, blaNDM-5, blaOXA-1
8CeftriaxoneRRRRRRRRSSblaTEM-1B, blaCTX-M-15, blaOXA-1
9CefepimeRRRRRRSRSSblaTEM-1B, blaCTX-M-15, blaOXA-1
10CefazolinRRRRRRRRRSblaTEM-1B
11CeftazidimeRRRRRRRRSSblaTEM-1B
3Carbapenems
12ErtapenemSRSSSSSSSSblaCTX-M-15, blaNDM-5, blaOXA-1
13ImipenemSRSSSSSSSSblaNDM-5, blaOXA-1
14MeropenemSRSSSSSSSSblaNDM-5, blaOXA-1
4Fluoroquinolones
15GatifloxacinRRRRRRRRRS
16MoxifloxacinRRRRRRRRRS
17CiprofloxacinRRRRRSRRRSaac(6’)-Ib-cr
18OfloxacinRRRRRRRRRS
19NorfloxacinRRRRRRRRRScat A1
20Nalidixic AcidRRRRRRRRRRblaTEM-1B
5Glycylcyclines
21TigecyclineSSSSSSSSSS
6Nitrofurans
22NitrofurantoinSSSSSSSSSS
7Polymyxins
23ColistinSSSSSSSSSS
8Tetracycline
24DoxycyclineSRSSRRRRRStet(A), tet(B)
25MinocyclineSSSSSSSSSRtet(A), tet(B)
9Lincosamide
26ClindamycinRRRRRRRRRRmph(A), emrB, mdfA
27LincomycinRRRRRRRRRRmph(A), emrB, mdfA
10Sulfanilamide
28SulfanilamideRRRRRRRRRRsul1, sul2
11Trimethoprim
29TrimethoprimRRRRSSSSRSdfrA17, dfrA12
Resistant (29 antibiotics tested)2023181817161618135
Resistant to number of classes5565444553
* Sample: CjS: conjunctival swab; V; vitreous; CrS: corneal scraping; PC: pus-orbital cellulitius. S: Sensitive; R: resistant.
Table
(B)
(B)
Antibiotic Antibiotics (Number of Urine Samples Tested)Resistance in Urine Isolates (%)Resistance in Ocular Isolates (%)
AminoglycosideGentamycin (26)23.0820
Amikacin (86)16.2810
AmphenicolsChloramphenicol (86)15.1210
CephalosporinsCeftazidime (84)66.6780
Cefuroxime (25)60.0080
CarbapenemsImipenem (67)15.3810
FluoroquinolonesCiprofloxacin (86)82.5680
Ofloxacin (86)75.5890
Moxifloxacin (86)77.9190
Gatifloxacin (86)73.2690
Norfloxacin (67)79.1090
Table
Table 4. Plasmids in the 10 ocular E. coli * isolates.
Table 4. Plasmids in the 10 ocular E. coli * isolates.
Sl. No.PlasmidL-1339/2013L-2594/2017L-494/2011L-3003/2015L-1010/2018L-3137/2017L-1149/2016GMRV-476/2017L-1534/2016L-1216/2010Count
1Col(BS512)-+-----++-3
2Col(MG828)-----+----1
3Col156----++--++4
4IncFIA+++++--++-7
5IncFIB(AP001918)++++++-+++9
6IncFII++++++-+--7
7IncFII(29)---------+1
8IncQ1--------+-1
9IncX4+---------1
10IncY--+-------1
11p0111/repB-------+--1
Total4443440553
* Plasmids were detected using PlasmidFinder 2.1 (https://cge.cbs.dtu.dk/services/Plasmid Finder/). (+) and (-) indicate presence and absence of plasmid respectively.
Table
Table 5. Virulence genes * in 10 ocular E. coli isolates.
Table 5. Virulence genes * in 10 ocular E. coli isolates.
Sl. No.Protein and GenePlasmidL-1339/
2013		L-2594/
2017		L-494/
2011		L-3003/
2015		L-1010/
2018		L-1037/
2017		L-1149/
2016		GMRV-457/
2017		L-1534/
2016		L-1216/
2010		Count
1AdhesinfdeCpITS 24++++++++++10
2Secreted auto transpoter toxinSat55989p+-+--++++-6
3Aerobactin receptoriutApAPEC-O2-ColV-------+--1
4Aerobactin siderophore biosynthesis proteiniucA, iucB, iucCpO83_CORR+++++++++-9
5A fimbrial adhesinafaA, afaB-I, afaC-I, afaD, afaE-IpILL1101, pO86A1----+-----1
6polysaccharide export ATP-binding proteinkpsT, kpsD, kpsMpCP53-92k, pSR128+-+--+++++7
7Cytotoxic necrotizing factor 1cnf1pVir68------+--+2
8Daaf proteindaaF-----+-----1
9DradhesinsdraP-----+-----1
10E. coli common pilus chaperoneyagV/ecpE, yagX/ecpC, yagY/ecpB, yagZ/ecpA-+++-++++++9
11Enterobactin synthase multienzyme complexentA, entB, entC, entD, entE, entF, entSpITS 12, pITS 1, pITS 24, pITS 31, pITS 21++++++++++10
12Enterobactin/ferric enterobactin esteraseFespAPEC-1++++++++++10
13EnterotoxinsenBpEC14_114----++--++4
14F1C major fimbrial subunit precursorfocA, focF, focG, focHpPKL143---------+1
15Ferrienterobactin ABC transporter permeasefepA, fepB, fepC, fepD, fepGpITS24, pTBnb2, pAPEC-O103-ColBM++++++++++10
16Fimbrial switch regulatory proteinsfaB, sfaC, sfaF----------+1
17General secretion pathway protein C, D, E, L, F, G, H, I, J, K, MgspC, gspD, gspE, gspL, gspF, gspG, gspH, gspI, gspJ, gspK, gspMp14EC047c, p2009C-4207, pMRE600-1, p2009C-4207--+--++-++5
18GlucosyltransferaseiroB, iroC, iroE, iroD, iroNp2HS-C-2,pSA186_2---------+1
19Haemoglobin proteaseVat---------++2
20Hemolysin A, B, C, DhlyA, hlyB, hlyC, hlyDpO157, pO158--+--++--+4
21Outer membrane proteinompApO113++++++++++10
22Pesticin/yersiniabactin receptor proteinfyuA-++++++++++10
23Pilus assembly proteinpapB, papD, papC, papI, papX, papF, papG, papH, papJ, papKpDD3, pDD4, p600468_158, p503829_52, p300709_60,+++--+++-+7
24Polymerized tip adhesin of ECP fibersyagW/ecpDpVir68+++-++++++9
25Putative arylsulfataseaslAp5C10++++-+++++9
26Putative heme-binding proteinchuA, chuS, chuT, chuU, chuV, chuW, chuX, chuYpYUK1+-+--+++++7
27Regulator protein ecprykgK/ecpR-+++-++++++9
28Serine protease precursorPicpHUSEC41-2---------+1
29Tir-domain-containing proteintcpCpNB10---------+1
30Fimbriae regulatory proteinfimA, fimB, fimC, fimD, fimE, fimF, fimG, fimH, fimIpSLD203, pWRS17-4Z7, pfimF, pVir68, pORN160, pWRS1-17, pORN310, pEsST410_NW_4+-++++++++9
31Type III secretion system effectorespL1, espL4, espX1, espX4, espX5pO157-+-++-----3
32Yersiniabactin proteinirp1, irp2pUC18++++++++++10
33Yersiniabactin transcriptional regulatorybtA, ybtE, ybtP, ybtQ, ybtS, ybtT, ybtU, ybtXpET3c-YbtA, pCP1, pPSN345, pEUYbtP, pSDR498.1++++++++++10
Total18152012182121192026
* Abricate virulence finder database (https://github.com/tseemann/abricate) was used for the presence (+) or absence (-) of a gene.

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Ranjith, K.; SaiAbhilash, C.R.; Sai Prashanthi, G.; Padakandla, S.R.; Sharma, S.; Shivaji, S. Phylogenetic Grouping of Human Ocular Escherichia coli Based on Whole-Genome Sequence Analysis. Microorganisms 2020, 8, 422. https://doi.org/10.3390/microorganisms8030422

AMA Style

Ranjith K, SaiAbhilash CR, Sai Prashanthi G, Padakandla SR, Sharma S, Shivaji S. Phylogenetic Grouping of Human Ocular Escherichia coli Based on Whole-Genome Sequence Analysis. Microorganisms. 2020; 8(3):422. https://doi.org/10.3390/microorganisms8030422

Chicago/Turabian Style

Ranjith, Konduri, Chinthala Reddy SaiAbhilash, Gumpili Sai Prashanthi, Shalem Raj Padakandla, Savitri Sharma, and Sisinthy Shivaji. 2020. "Phylogenetic Grouping of Human Ocular Escherichia coli Based on Whole-Genome Sequence Analysis" Microorganisms 8, no. 3: 422. https://doi.org/10.3390/microorganisms8030422

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