The origin and population structure of Borrelia burgdorferi sensu stricto (s.s.), the agent of Lyme disease, remain obscure. This tick-transmitted bacterial species occurs in both North America and Europe. We sequenced 17 European isolates (representing the most frequently found sequence types in Europe) and compared these with 17 North American strains. We show that trans-Atlantic exchanges have occurred in the evolutionary history of this species and that a European origin of B. burgdorferi s.s. is marginally more likely than a USA origin. The data further suggest that some European human patients may have acquired their infection in North America. We found three distinct genetically differentiated groups: i) the outgroup species Borrelia bissettii, ii) two divergent strains from Europe, and iii) a group composed of strains from both the USA and Europe. Phylogenetic analysis indicated that different genotypes were likely to have been introduced several times into the same area. Our results demonstrate that irrespective of whether B. burgdorferi s.s. originated in Europe or the USA, later trans-Atlantic exchange(s) have occurred and have shaped the population structure of this genospecies. This study clearly shows the utility of next generation sequencing to obtain a better understanding of the phylogeography of this bacterial species.
Genome sequencing has drastically changed our understanding of microbial microevolution over the past decades. This is particularly the case for bacteria causing infectious diseases. Furthermore, the advent of next-generation sequencing (NGS) has allowed scientists to handle large population samples and to address a variety of biological questions concerning the evolution and ecology of bacterial pathogens. For example, NGS data has been used to study pathogen evolution within a single patient1, transmission chains within a single hospital2,3 and clonal diversification over time and space4,5. Without any doubt the unprecedented resolution provided by NGS is changing the way in which evolutionary biology and molecular epidemiology studies are conducted4,5,6.
Borrelia burgdorferi sensu stricto, a tick-borne spirochete bacterium, belongs to the species complex B. burgdorferi sensu lato (s.l.) that now comprises more than 20 accepted and proposed species of which five are regularly isolated from human patients7,8. The species that cause Lyme Borreliosis (LB) (also called Lyme disease) include B. burgdorferi s.s., B. afzelii, B. spielmanii, B. garinii and B. bavariensis. LB can be regarded as a multi-systemic disease, because it presents different symptoms in patients, such as erythema migrans (EM), arthritis, neurological manifestations (neuroborreliosis) or lymphocytoma9,10,11. So far, B. burgdorferi s.s. is the only human pathogenic Borrelia species of the Lyme borreliosis group of spirochetes in North America9 and symptoms described in the USA differ somewhat from those in Europe11,12,13.
LB is a zoonotic vector-borne disease, hence, the natural transmission cycles of these bacteria depend on vertebrate reservoir hosts and vector ticks of the Ixodes persulcatus species complex14,15. This ecological dependence determines the geographic distribution of the bacteria (and the disease) to the temperate zones of the northern hemisphere (roughly from latitude 40 degree - 60 degree N). Within this geographic range of vector and host occurrence, the distribution of Borrelia species is not uniform. Some Borrelia species (e.g. B. garinii, B. afzelii and B. bavariensis) are only found in Eurasia, whereas B. burgdorferi s.s. occurs on both sides of the Atlantic Ocean16.
Understanding the movement or spread of bacterial pathogens is important for epidemiological surveillance and monitoring and to predict the spread of such pathogens into new geographic regions. Researchers have used B. burgdorferi s.s. to understand the movement of these bacteria within endemic areas but also into new geographic regions17,18,19,20,21,22,23,24. Depending on the molecular markers used, the origin of the genospecies B. burgdorferi s.s. has been suggested to be in the USA (ospC23,25) or Europe (multilocus sequence typing [MLST]20). Furthermore, population level studies using ospC suggested that ospC type A strains crossed the Atlantic Ocean approximately 200 years ago23. Although B. burgdorferi s.s. was one of the first bacterial species being sequenced26, completed genomes are available only for 17 isolates, mainly originate from the USA (14 out of 17)27,28,29,30.
In this study, we exploit the high resolution of NGS to obtain a better understanding of the relatedness of populations from Europe and the USA, with a particular view on human patient isolates from Europe, and to re-address the question of the origin of B. burgdorferi s.s.. We included in our analysis some previously sequenced strains to create a more comprehensive data set for this species in terms of genome sequences and geographic origin.
The data set and genome sequencing
We sequenced 17 European isolates (Table 1) using the Illumina MiSeq technology to compare them to fully sequenced genomes available in GenBank, the majority of these strains originated from the USA (see http://borreliabase.org/). As we aimed to infer the evolutionary history of strains, we chose to analyse the main chromosome, which contains the genetic information of the core genome. In general, the reads mapped uniformly to the B31 main linear chromosome with more than 90 percent of the chromosome covered. Mean median coverage was 221× (minimum coverage 34× for sample PLue, maximum coverage 419× for sample PAli) (Supplementary Table 1). Regardless of coverage, we observed an alignment gap in the region corresponding to 435 kbp to 442 kbp of B31 (with some variation between strains) for all strains. In B31 this region contains the 5S–23S ribosomal DNA which is duplicated in LB spirochetes31 and this duplication evidently presents a problem for proper mapping of NGS sequence reads. We included in our analyses 17 genome sequences that are publicly available (Table 2); most of them are from the USA (n = 14) while three are from Europe (Bol26, SV1, and ZS7) and the closely related species B. bissettii strain DN127 was used as an outgroup. We used progressive Mauve32 to align the chromosomal genomes of our newly sequenced strains as well as those from the previously published strains. We found 92 locally colinear blocks (LCBs), eight of them contain DNA conserved in all the strains and were used for downstream analysis; these eight LCBs are described in Supplementary Table 2. Of note, we observed similar levels of genetic variation across the eight LCBs (see Supplementary Table 2). In summary, we compiled a data set of 35 strains that contained isolates from both Europe and the USA (including an outgroup).
Three genetically differentiated groups
To visualize the genetic relationships among the strains, we first employed a neighbor net (Fig. 1), as this approach accounts for the possibility of recombination. It is known that significant amounts of variation on plasmids of B. burgdorferi s.s. have arisen by recombination33, and our analysis showed that some recombination seems to occur on the main chromosome (Fig. 1). As would be expected if recombination occurs, the network showed some reticulation reflecting conflicting phylogenetic signals; corroborating this result, the PhiTest gave significant signals for recombination (p < 0.001). Neither the European strains (blue) nor the American strains (red) formed a monophyletic group (Fig. 1). Actually, there were several clades that contained both European and American strains. Strains SV1 and Z41293 (which were both isolated from I. ricinus ticks) clustered together and were well separated from the rest of the strains, suggesting that these two strains comprised divergent strains of B. burgdorferi s.s.. All B. burgdorferi s.s. strains were clearly differentiated from the outgroup and although SV1 and Z41293 were considerably separated from the other B. burgdorferi s.s. strains, they were much closer to the rest of the B. burgdorferi s.s. strains than to the B. bissettii outgroup. To further study the genetic relationships of these strains we used the Bayesian Analysis of Population Structure software (BAPS)34. Three genetically differentiated groups were found (Fig. 2). The smallest group (BAPS group 3) contained exclusively the outgroup strain (black bar) and another small group (BAPS group 2) had the two divergent strains (dark grey bars). BAPS group 1 is the largest group and contained all the remaining strains (light grey bars). Notably, neither the American strains nor the European strains formed particular clusters; this result is consistent with genetic exchange/migration between European and North American populations of B. burgdorferi s.s.. Remarkably, we did not detect any signals of admixture between the different BAPS groups. Taken together, these results indicate population structuring and trans-Atlantic exchange between Europe and the USA.
Agreement between chromosomal phylogeny and MLST
We used phylogenetic analysis to provide additional insights into the population structure of B. burgdorferi s.s.. Given the distorting effects of recombination on phylogenetic analysis, we first identified the recombination events between genomes via BRATNextGen35; this software implements a Bayesian analysis for detecting recombination events in whole-genome sequences. This analysis suggested that 8,321 out of 68,158 (~12%) of the SNPs reside in regions of the genome that have undergone recombination. Using the remaining SNPs not affected by recombination (the SNP alignment is available upon request), we constructed both Bayesian and Maximum Likelihood (ML) phylogenies, which showed very similar topologies; for simplicity only the Bayesian phylogeny is presented (Fig. 3, Supplementary Figures 1 and 2). All three groups identified by BAPS show very strong node support (posterior probabilities ranged from 1.00 to 0.79).
Given the tree topologies of our Bayesian and ML phylogenies, we wanted to ensure that this result was not due to long-branch attraction (LBA); the wrong grouping of two or more long non-sister branches in a tree due to homoplasies36. Specifically, we wanted to corroborate that the position of the divergent group was not a result of LBA and, hence, we conducted two exploratory analyses. The rationale of the long-branch extraction strategy (our first approach) is to take out the long branches - the ones allegedly causing the LBA - one at time, and see whether this disturbs the groupings present in the tree37. Therefore, we constructed one ML phylogeny without B. bissettii and another without SV1 and Z41293 (see methods). Notably, the groupings in the trees were hardly affected when either B. bissettii or SV1 and Z41293 were removed (Supplementary Figure 4) and the trees were very similar to those in our initial Bayesian and ML phylogenies; thus LBA does not seem to affect our phylogenetic reconstructions. However, to provide additional independent support, we also carried out a partition analysis where the idea is to eliminate the fast-evolving sites, the ones most contributing to LBA. Thus, we created a phylogeny based on the SNP alignment without the fast-evolving sites (see methods); this phylogeny shows identical groups to the Bayesian and ML phylogenies and was very similar to the phylogenies from the previous analysis (see Supplementary Figure 5). These two exploratory analyses convincingly show that LBA is not affecting our data and that the position of the divergent group with respect to the outgroup is not an artifact.
Our tree suggested that different genotypes are likely to have been introduced several times into the same area. For instance, PLue, is genetically distant from PDri, PKifI and PKifII, even though all four strains were collected in Munich. The same applies for the USA strains; for example, although strains CA8 and CA382 were both collected in California, these strains are located on distant branches of the tree. Furthermore, this phylogeny strongly suggests that intercontinental exchanges might have occurred from the USA to EU. By way of illustration, PAbe, PAli, and PHas (all from Germany) cluster within a group that also includes B31 and CA382 (from New York and California, respectively). Another example is 156a, which was collected from New York and clusters with PLue, a German isolate. Given the topology of our tree, at least four trans-Atlantic migrations might have happened, all of them within BAPS group 1. Our phylogenetic analysis is in good agreement with the pattern of genetic relatedness among the strains that had been previously shown using MLST based on eight chromosomally located housekeeping genes20 (Supplementary Figure 3) suggesting that MLST provides a good approximation of strain relatedness. Furthermore, the phylogenetic analysis gives additional support to the suggestion that Borrelia populations are genetically structured, have experienced trans-Atlantic exchange and that SV1 and Z412 are the most divergent strains within the B. burgdorferi s.s. species. As most of our strains originated from human patients, we used the MLST data to compare the strains analysed here with tick-derived strains in the MLST database (Supplementary Figure 6). All but two STs (i.e. ST1 and ST3, which have so far been only found in human patients) are also found in the European tick vector. The majority of STs found in ticks and humans in the USA differ from those found in Europe, the exception being ST1 and ST3.
To infer the geographic origin of B. burgdorferi s.s., we conducted an ancestral state reconstruction analysis using SIMMAP38; the results of this analysis are summarized in Fig. 3. This figure shows that a European origin is moderately more probable than a North American origin for the ancestor of all the B. burgdorferi s.s. strains (marginal posterior probability (MPP) of EU origin 0.69) but is highly likely for the group composed of the two divergent strains included in BAPS group 2 (MPP of EU origin 0.95). The directionality of subsequent movements is, however, not straightforward. According to our analysis, we were able to detect several trans-Atlantic exchanges and most of them seem to go from the USA to Europe. For instance, if only the three strains PAli, PAbe and PHas are considered in the analysis – a tight cluster of strains from Munich – a European origin is very plausible (MPP of EU origin 0.999). However, if the closest related strain (namely B31 from New York) to those three strains is included, the situation is reversed and now a North American origin is much more likely (MPP of USA origin 0.978, Table 3); this implies an introduction from the USA into Europe. Similarly, given that the ancestor of the group composed of 156s and PLue seems to have been in the USA (MPP of USA origin 0.85, see Fig. 3), PLue may reflect a recent introduction to Europe from the USA. The MLST Sequence Types (ST) were ST1 for B31, PAli, PAbe, PHas and ST3 for PLue. In this context it is noteworthy that both STs have frequently been found in I. scapularis ticks in the USA (but not in I. ricinus ticks in Europe) further supporting an American origin of the respective clades. Interestingly, STs that are found in European ticks (e.g. ST20, ST24) form their own cluster within the phylogeny and these STs have not been described in either patients or ticks in the USA (Supplementary Figure 6). Thus, the ancestral state reconstruction analysis suggests a moderately more likely European origin for the original population and also clarifies the probable directionality of some of the trans-Atlantic exchanges.
In this study we sequenced 17 European B. burgdorferi s.s. strains isolated from human patients and from a tick via NGS. We also included previously sequenced strains into our analyses (to produce a data set of 34 strains) to obtain a better understanding of the relationship of strains between Europe and the USA and the origin of B. burgdorferi s.s.. Importantly this dataset, although limited in extent, includes both human and tick isolates from both Europe and the USA (see Tables 1 and 2); without considering the outgroup, 11 isolates (~33%) came from ticks and 13 isolates (~39%) were collected in the USA. Even though the newly sequenced isolates included in the study originated mainly from German patients, they do represent the most frequently found MLST STs of B. burgdorferi s.s. in Europe, which have been found in ticks in various regions such as Latvia, France and UK (39,40, www.pubmlst.org/borrelia/).
We focused on the main linear chromosome because it is more likely to reflect the core genome28 and may be less prone to horizontal transfer than plasmid-encoded genes27,33,41. However, we found that a significant amount of the SNPs (12%) were located on regions inferred to be affected by recombination. This result was not unexpected as previous studies suggested recombination to mutation rates of 3:1 in B. burgdorferi s.s., although this ratio was found in plasmids rather than the main linear chromosome33. However, more recent population genomics studies using the main linear chromosome and two plasmids of European strains of B. burgdorferi s.s. suggested recombination to mutation ratios of 1.7 42. These data reinforce the view that recombination is one of the forces creating novel combinations of alleles within this species.
Strain clustering in phylogenetic analysis correlated only poorly with geography. Notably, of three well-differentiated genetic groups, one comprised both European and American strains, supporting the idea of trans-Atlantic exchange33. In addition, phylogenetic analysis showed that strains from Europe are nested within the USA clades suggesting that at least four intercontinental migration events have occurred in that direction (i.e. from the USA to Europe). The routes and vehicles of these exchanges are unknown and deserve further investigation (see below) though our data suggest that some European patients may have acquired their infection in North America. One ancestral migration might have occurred at a more basal position of the tree resulting in the split between BAPS1 and BAPS2 clades, an event that gave rise to the USA population. Apart from this, our phylogenetic analysis demonstrates that multiple introductions, with different genotypes, might have occurred into the same geographic area. This is also supported by the BAPS analysis, as we found that strains from sites that are in geographic close proximity belong to different BAPS groups. In accordance with this, no admixture was detected between the BAPS groups, not even between BAPS groups 2 and 1, both of which have B. burgdorferi s.s. strains. Therefore, besides geography with intercontinental exchange, additional unknown factors probably operate to generate population structuring.
Whether the divergence of the two strains from BAPS group 2 reflects also differences in ecology is currently unknown. Strains related to Z41293 (here abbreviated Z412) have been found in I. ricinus ticks in Switzerland and France20, but further ecological information on these strains is not available. Z41293 and related strains have been used to determine the species threshold for B. burgdorferi s.l.39,43. Strain Z41293 and related strains were considered “borderline” B. burgdorferi s.s.43 because DNA-DNA hybridization studies found that this strain showed 74 percent similarity and a Tm of 2 °C to strain B31. Using MLST, strain SV1 also falls within the borders of B. burgdorferi s.s. species. As the former strains served to set the threshold for species delineation, in our view it is problematic to designate them as a new species44. Despite the contentious status of Z41293 and related strains, these divergent strains have so far only been detected in Europe, but not in North America supporting the idea of a European origin of B. burgdorferi s.s..
We conducted an ancestral state reconstruction analysis to infer the geographic origin of the species and it suggests that the ancestor of all the strains is moderately more likely to have had a European origin than a North American origin. This relates to the fact that the most divergent group (BAPS group 2) has a probable European origin. In this context, we would like to point out that, in order to correct for the sampling bias (more European isolates), we employed an equal prior so that a priori both a European and a USA origin had an equal probability of occurrence. This finding combined with the fact that these strains have been found only in Europe further supports the notion that the seminal population originated in Europe as suggested previously by20. Our analysis also implies that after the origin of the primordial population, several trans-Atlantic exchanges have evidently occurred.
However, considering the position of B. burgdorferi s.s. in a whole species tree7, a number of potential alternative scenarios can be considered: A) the common ancestor of B. burgdorferi s.s. originated in Europe and following the split from the divergent clade (BAPS group 2), the resulting B. burgdorferi s.s. migrated to North America. Since then several trans-Atlantic migrations have occurred forming the European subpopulations and a North American subpopulation. B) Another possibility is that all B. burgdorferi s.s. evolved in North America. The divergent group migrated to Europe and died out in North America. C) B. burgdorferi s.s. evolved in North America and the divergent group still exists in North America but at very low frequency and has simply not been found in natural transmission cycles. It needs to be emphasized that the species tree shown by 7 was based on eight chromosomal housekeeping loci and may change if more genetic information is incorporated. We acknowledge that denser sampling from both Europe and the USA – especially of isolates from this divergent group – and time dating of population migrations is needed to be able to resolve these issues unambiguously. We also suggest that in order to resolve the phylogeography of B. burgdorferi s.s., other genospecies of the LB group of spirochetes need to be included into future phylogenetic investigations.
It is difficult to reconcile the population structure of B. burgdorferi s.s. with natural transmission cycles. Two different tick vector species maintain the transmission cycles in Europe and North America, namely I. ricinus and I. scapularis, respectively. Trans-Atlantic migration and mixing of tick vector species has not been reported suggesting that the Atlantic Ocean represents a barrier to migration/mixing of vector species14. Although B. burgdorferi s.s. can utilize many hosts as reservoirs including rodents, insectivores and birds16, none of these hosts is known to regularly migrate East-to-West or vice versa across the Atlantic. Whether sea birds may be involved in transcontinental migration of B. burgdorferi s.s.45 needs to be further investigated. We would like to highlight that strains of B. burgdorferi s.s. found in Europe - and showing the same ST as North American strains (ST1 and ST3) - have only been isolated from human patients (see below) (23,46, and this study), so humans are potentially the vehicle to transport strains of B. burgdorferi s.s. between continents. If this is the case, these strains are highly unlikely to enter natural transmission cycles as humans are not considered to contribute to the natural transmission of Borrelia14. Intriguingly, ST1 strains of B. burgdorferi s.s. are commonly found in ticks and patients in the USA, but they have not been reported from ticks in Europe (see pubmlst.org/borrelia/ database46). There are several possible scenarios that might explain the finding of such closely related strains to B31 in patients in Europe. First, these patients may have acquired their Borrelia infections while travelling in the USA. Second, such strains may be present at a very low prevalence in ticks in Southern Germany as ticks investigated for B. burgdorferi s.s. had been collected in Latvia, Scotland, France or Italy and this ST has not been found47,48. As pointed out before, B. burgdorferi s.s. is not very prevalent in Europe; LB species such as B. garinii or B. afzelii are much more common than B. burgdorferi s.s.49. In this scenario, the fact that B31-related strains are not found in ticks but only in patients might suggest a high potential for establishing an infection in humans. However, a discrepancy between tick and human isolates has been observed in the USA, not all STs isolated from human patients have been detected in ticks50 suggesting that some strains although rare in natural transmission cycles can be found in human patients.
The NGS data provided very robust phylogenies and it was interesting that the distribution of STs matched well with clades generated by MLST analysis. This suggests that MLST can be used as a good approximation to explore/investigate the relationship of B. burgdorferi strains, although some authors reported otherwise28. Interestingly and, in contrast to other bacterial pathogens, there was a limited amount of variation between strains belonging to the same ST. For example, strains that belonged to ST1 (PAli, PAbe, PHas) differed in only 63, 64 and 261 SNPs, respectively, to B31 on the main linear chromosome. In comparison, an ST (i.e. ST239) of Staphylococcus aureus strains comprising identical MLST types differed in more than 4,000 SNPs51. On the other hand, due to the high resolution provided by NGS, no two strains show the same genotype – not even FheI and FheII that were collected from the same patient at the same time. That was still true when only the non-recombinant SNPs were considered.
In conclusion, our study shows that population structuring and trans-Atlantic exchanges have occurred during the evolutionary history of B. burgdorferi s.s. and may still occur today. However, we do acknowledge that more data are required to infer migration routes and transport vehicles. Importantly, it seems that some European patients may have acquired their infection in North America. Thus, our study clearly gives a demonstration of the utility of NGS platforms for studying the evolutionary history of vector-borne bacterial pathogens, especially for those where genetic variation is low.
Materials and Methods
The data set and genome sequencing
We analyzed 17 strains that were previously typed to be B. burgdorferi s.s. and were available at the German National Reference Centre for Borrelia (Table 1). B. burgdorferi s.s. is less common in Europe than in North America (13% of all European species in the MLST database). The strains included in the study were chosen to account for the genetic variation found by MLST in European B. burgdorferi s.s. to attempt to limit phylogenetic discovery bias52. The MLST STs included were ST20, ST21, ST24, ST284 and ST27, which represent the most common STs in Ixodes ricinus ticks from Germany, Latvia, UK, France and human patients (see PubMLST.org/datbase/borrelia/). ST27 represents a divergent strain, which was used to determine the species threshold in Borrelia39. ST1 was frequently found in human patients and was included to determine its relationship to strains found in North America23. Strains were isolated between 1985 and 2010 from patients and one I. ricinus tick. Details are given in Table 1. Borrelia cultures grown under standard conditions53 were used for DNA extraction via a Maxwell® 16 genomic DNA purification kit (Promega, Germany). Following DNA quantification, libraries were prepared according to the Nextera DNA sample preparation guide (Qiagen, Germany). The samples were diluted to a concentration of 50 ng per microliter and “tagmented” by simultaneously fragmenting DNA using transposomes as provided by the manufacturer and adding adapters. After tagmentation, samples having adapters on both ends underwent 5 PCR cycles to amplify the product and to add index primers. The resulting libraries were then validated using an Agilent 2100 Bioanalyzer (Agilent, Germany). Paired end sequence reads (250 bp) were generated using an Illumina Miseq platform (Illumina, San Diego CA, USA). We used the B31 and SV1 main linear chromosomes (B31, GenBank accession number NC001318; SV1, GenBank accession number NZ ABJZ00000000.2) as reference. We concentrated on the main chromosome because it most likely represents the core genome for Borrelia27 which is best suited to infer the evolutionary history of strains. For de novo assembly, reads were quality checked and filtered using FastQ Trimmer (window size 10, step size 2, Q score 20)54, kmernator (k-mer size 31) and velvetoptimizer55 implemented in the Galaxy platform56,57 provided by the Gene Centre, LMU, Munich, Germany. The following parameters were used in velvetoptimiser: start Hash length 35, end hash length 85, no. of threads 4, k-mer optimization metric N50. Resulting contigs were mapped onto the reference chromosomes with Burrows-Wheeler Aligner (BWA)58 and re-arranged and sorted using the Mauve Contig Mover algorithm59 which is within the Mauve Genome Alignment Software60. The reference chromosomes were B31 for 16 strains and SV1 for strain Z41293. Contigs that did not align to the main linear chromosome were discarded. Some of the publicly available genomes are in a draft status and we therefore used the Mauve Contig Mover to order the contigs; in such cases B31 was used as the reference genome. We used progressive Mauve32 to align the chromosome genomes of our newly sequenced strains as well as those from the previously published strains. We employed the default parameters and a SNP file was created; 92 colinear sub-alignments (LCBs) were found, but only eight of them contained DNA conserved in all the strains. An SNP alignment was created which is available upon request. For comparison with the MLST scheme used by20 and50, sequence data of the eight housekeeping loci (clpA, clpX, nifS, pepX, pyrG, recG, rplB, uvrA) were extracted from whole genome sequences if not already available from the MLST database hosted at the University of Oxford (PubMLST.org).
Neighbor net and detection of recombination
We employed SplitTree4 software on the SNP alignment to construct a Neighbor Net61, the uncorrected P distance was used. We use the BRATNextGen software35 to identify the recombination events exclusively in the eight LCBs that contained DNA conserved in all the strains. We used similar settings as those used by Castillo-Ramirez et al.4. A p-value of less than 0.01 was set to determine the significance of the recombinant segments, this was done via a bootstrap test with 100 replicates.
Maximum Likelihood and Bayesian phylogenies
We constructed phylogenies by means of PhyML (Maximum Likelihood; ML)62 and MrBayes63. The multiple alignment on which the phylogenies were run, contained only SNPs that were located in the eight conserved LCBs and that were not present in regions affected by recombination. We used the GTR model and, because we only considered SNPs, we did not include a proportion of invariable sites. Base frequencies as well as the relative substitution rates between them were calculated by maximizing the likelihood of the phylogeny. We set the GTR model, allowing gamma-distributed rate variation across sites. We ran the analysis for 8,000,000 generations, sampling every 1000 generations −25% were discarded as burn-in. To ensure that two runs had converged we checked that the average standard deviation of the split frequencies were below 0.01.
Bayesian Analysis of Population Structure (BAPS)
The mixture and admixture analyses were implemented through BAPS 534. To conduct the population mixture analysis we selected the “Clustering of individuals” module. To properly evaluate the number of genetically diverged groups, we ran the analysis several times with different values for the maximum number of genetically diverged groups; these values ranged from 2–20. We chose the “Admixture based on mixture clustering” module to implement the population admixture analysis. The minimum population size was set to 2; we used 100 iterations to calculate the admixture coefficient for the individuals and the number of reference individuals from each population was set to 200. Finally, 20 iterations were used to calculate the admixture coefficient for the reference individuals.
Ancestral Reconstruction Analysis
The ancestral state reconstruction analysis was carried out by means of SIMMAP38. The ancestral state reconstruction module was employed on the trees that were derived from a Bayesian analysis conducted with MrBayes. The geographic source of the strains was coded as 1 (Europe) and 0 (USA) and we configured the models as follows: for the bias parameter we selected an equal prior (1/k) – this was in order to not bias our analysis given the overrepresentation of European strains - and for the rate parameter we specified a gamma distribution with an alpha of 1.25, beta of 0.25 and k equal to 90.
Detecting long-branch attraction (LBA)
We used two strategies to detect LBA. First, we conducted a long-branch extraction approach37 in which the branches that are potential candidates for causing LBA are extracted one at time. If LBA is the problem this should affect the clustering pattern in the remaining taxa. Therefore, we constructed two new ML phylogenies: one without the outgroup and another without strains SV1 and Z41293 that are located on the second longest branch (see Supplementary Figure 4). As a second strategy, we conducted a partition analysis, in which the fast-evolving sites are discarded as these mostly contribute to LAB. For this, MEGA664 was used to estimate position-by-position rates under the GTR model employing a discrete Gamma distribution (with 5 categories) to model the rate differences across the SNPs. Then, a new alignment was created that included only the SNPs with slower relative evolutionary rates than the two fast evolving categories from the discrete Gamma distribution. A ML phylogeny was made on this alignment (see Supplementary Figure 5).
How to cite this article: Castillo-Ramírez, S. et al. Trans-Atlantic exchanges have shaped the population structure of the Lyme disease agent Borrelia burgdorferi sensu stricto. Sci. Rep. 6, 22794; doi: 10.1038/srep22794 (2016).
Mwangi, M. M. et al. Tracking the in vivo evolution of multidrug resistance in Staphylococcus aureus by whole-genome sequencing. Proc Natl Acad Sci USA 104, 9451–9456 (2007).
Snitkin, E. S. et al. Tracking a hospital outbreak of carbapenem-resistant Klebsiella pneumoniae with whole-genome sequencing. Science translational medicine 4, 148ra116 (2012).
Torok, M. E. et al. Rapid whole-genome sequencing for investigation of a suspected tuberculosis outbreak. J Clin Microbiol 51, 611–614 (2013).
Castillo-Ramirez, S. et al. Phylogeographic variation in recombination rates within a global clone of methicillin-resistant Staphylococcus aureus. Genome Biol 13, R126 (2012).
Holden, M. T. et al. A genomic portrait of the emergence, evolution, and global spread of a methicillin-resistant Staphylococcus aureus pandemic. Genome Res 23, 653–664 (2013).
Croucher, N. J. et al. Rapid pneumococcal evolution in response to clinical interventions. Science 331, 430–434 (2011).
Margos, G., Vollmer, S. A., Ogden, N. H. & Fish, D. Population genetics, taxonomy, phylogeny and evolution of Borrelia burgdorferi sensu lato. Infect Genet Evol 11, 1545–1563 (2011).
Rudenko, N., Golovchenko, M., Grubhoffer, L. & Oliver, J. H., Jr. Updates on Borrelia burgdorferi sensu lato complex with respect to public health. Ticks Tick Borne Dis 2, 123–128 (2011).
Bacon, R. M., Kugeler, K. J. & Mead, P. S. Surveillance for Lyme disease–United States, 1992–2006. MMWR Surveill Summ 57, 1–9 (2008).
Stanek, G. et al. Lyme borreliosis: Clinical case definitions for diagnosis and management in Europe. Clin Microbiol Infect 17, 69–79 (2010).
Steere, A. C. Lyme borreliosis in 2005, 30 years after initial observations in Lyme Connecticut. Wien Klin Wochenschr 118, 625–633 (2006).
Strle, F. & Stanek, G. Clinical manifestations and diagnosis of Lyme borreliosis. Current Problems in Dermatology 37, 51–110 (2009).
Steere, A. C. Lyme disease. N Engl J Med 345, 115–125 (2001).
Kurtenbach, K. et al. In Bacterial Population Genetics in Infectious Disease, Edn. 1. (eds D. A. Robinson, D. Falush & E. J. Feil ) (John Wiley & Sons, Inc., 2010).
Radolf, J. D., Caimano, M. J., Stevenson, B. & Hu, L. T. Of ticks, mice and men: understanding the dual-host lifestyle of Lyme disease spirochaetes. Nat Rev Microbiol 10, 87–99 (2012).
Piesman, J. & Gern, L. Lyme borreliosis in Europe and North America. Parasitology 129 Suppl, S191–220 (2004).
Brisson, D. et al. Evolution of northeastern and midwestern Borrelia burgdorferi, United States. Emerg Infect Dis 16, 911–917 (2010).
Hoen, A. G. et al. Phylogeography of Borrelia burgdorferi in the eastern United States reflects multiple independent Lyme disease emergence events. Proc Natl Acad Sci USA 106, 15013–15018 (2009).
Margos, G., Castillo-Ramirez, S. & Hoen, A. G. Phylogeography of Lyme borreliosis-group spirochetes and methicillin-resistant Staphylococcus aureus. Parasitology 139, 1952–1965 (2012).
Margos, G. et al. MLST of housekeeping genes captures geographic population structure and suggests a European origin of Borrelia burgdorferi . Proc Natl Acad Sci USA 105, 8730–8735 (2008).
Mechai, S. et al. Phylogeographic analysis reveals a complex population structure of Borrelia burgdorferi in southeastern and south central Canada. Appl Environ Microbiol (2014).
Ogden, N. H. et al. Investigation of genotypes of Borrelia burgdorferi in Ixodes scapularis ticks collected in surveillance in Canada. Appl Environ Microbiol 77, 3244–3254 (2011).
Qiu, W. G. et al. Wide distribution of a high-virulence Borrelia burgdorferi clone in Europe and North America. Emerg Infect Dis 14, 1097–1104 (2008).
Qiu, W. G., Dykhuizen, D. E., Acosta, M. S. & Luft, B. J. Geographic uniformity of the Lyme disease spirochete (Borrelia burgdorferi) and its shared history with tick vector (Ixodes scapularis) in the Northeastern United States. Genetics 160, 833–849 (2002).
Marti Ras, N., Postic, D., Foretz, M. & Baranton, G. Borrelia burgdorferi sensu stricto, a bacterial species “made in the U.S.A.”? Int J Syst Bacteriol 47, 1112–1117 (1997).
Fraser, C. M. et al. Genomic sequence of a Lyme disease spirochaete, Borrelia burgdorferi. Nature 390, 580–586 (1997).
Casjens, S. R. et al. Genome stability of Lyme disease spirochetes: comparative genomics of Borrelia burgdorferi plasmids. PloS ONE 7, e33280 (2012).
Mongodin, E. F. et al. Inter- and intra-specific pan-genomes of Borrelia burgdorferi sensu lato: genome stability and adaptive radiation. BMC Genomics 14, 693 (2013).
Schutzer, S. E. et al. Whole-genome sequences of Borrelia bissettii, Borrelia valaisiana, and Borrelia spielmanii. J Bacteriol 194, 545–546 (2012).
Schutzer, S. E. et al. Whole-genome sequences of thirteen isolates of Borrelia burgdorferi . J Bacteriol 193, 1018–1020 (2011).
Schwartz, J. J., Gazumyan, A. & Schwartz, I. rRNA gene organization in the Lyme disease spirochete, Borrelia burgdorferi. J Bacteriol 174, 3757–3765 (1992).
Darling, A. E., Mau, B. & Perna, N. T. progressiveMauve: multiple genome alignment with gene gain, loss and rearrangement. PLoS One 5, e11147 (2010).
Qiu, W. G. et al. Genetic exchange and plasmid transfers in Borrelia burgdorferi sensu stricto revealed by three-way genome comparisons and multilocus sequence typing. Proc Natl Acad Sci USA 101, 14150–14155 (2004).
Tang, J., Hanage, W. P., Fraser, C. & Corander, J. Identifying currents in the gene pool for bacterial populations using an integrative approach. PLoS computational biology 5, e1000455 (2009).
Marttinen, P. et al. Detection of recombination events in bacterial genomes from large population samples. Nucleic acids research 40, e6 (2012).
Bergsten, J. A review of long-branch attraction. Cladistics 21, 163–193 (2005).
Siddall, M. E. & Whiting, M. F. Lang-Branch Abstractions. Cladistics 15, 9–24 (1999).
Bollback, J. P. SIMMAP: stochastic character mapping of discrete traits on phylogenies. BMC Bioinformatics 7, 88 (2006).
Margos, G. et al. A new Borrelia species defined by Multilocus Sequence Analysis of Housekeeping Genes. Appl Environ Microbiol 75, 5410–5416 (2009).
Vollmer, S. A. et al. Host migration impacts on the phylogeography of Lyme Borreliosis spirochaete species in Europe. Environ Microbiol 13, 184–192 (2011).
Seifert, S. N., Khatchikian, C. E., Zhou, W. & Brisson, D. Evolution and population genomics of the Lyme borreliosis pathogen, Borrelia burgdorferi. Trends in genetics : TIG 31, 201–207 (2015).
Jacquot, M. et al. Comparative population genomics of the Borrelia burgdorferi species complex reveals high degree of genetic isolation among species and underscores benefits and constraints to studying intra-specific epidemiological processes. PloS ONE 9, e94384 (2014).
Postic, D., Garnier, M. & Baranton, G. Multilocus sequence analysis of atypical Borrelia burgdorferi sensu lato isolates - description of Borrelia californiensis sp. nov., and genomospecies 1 and 2. Int J Med Microbiol 297, 263–271 (2007).
Casjens, S. R. et al. Whole genome sequence of an unusual Borrelia burgdorferi sensu lato isolate. J Bacteriol 193, 1489–1490 (2011).
Duneau, D. et al. Prevalence and diversity of Lyme borreliosis bacteria in marine birds. Infect Genet Evol 8, 352–359 (2008).
Crowder, C. D. et al. Genotypic variation and mixtures of Lyme Borrelia in Ixodes ticks from North America and Europe. PLoS One 5, e10650 (2010).
James, M. C., Gilbert, L., Bowman, A. S. & Forbes, K. J. The Heterogeneity, Distribution, and Environmental Associations of Borrelia burgdorferi Sensu Lato, the Agent of Lyme Borreliosis, in Scotland. Frontiers in public health 2, 129 (2014).
Vollmer, S. A. et al. Spatial spread and demographic expansion of Lyme borreliosis spirochaetes in Eurasia. Infect Genet Evol 14C, 147–155 (2013).
Rauter, C. & Hartung, T. Prevalence of Borrelia burgdorferi sensu lato genospecies in Ixodes ricinus ticks in Europe: A metaanalysis. Appl Environ Microbiol 71, 7203–7216 (2005).
Hanincova, K. et al. Multilocus sequence typing of Borrelia burgdorferi suggests existence of lineages with differential pathogenic properties in humans. PLoS One 8, e73066 (2013).
Harris, S. R. et al. Evolution of MRSA During Hospital Transmission and Intercontinental Spread. Science 327, 469–474 (2010).
Pearson, T. et al. Phylogenetic discovery bias in Bacillus anthracis using single-nucleotide polymorphisms from whole-genome sequencing. Proc Natl Acad Sci USA 101, 13536–13541 (2004).
Ruzic-Sabljic, E. & Strle, F. Comparison of growth of Borrelia afzelii, B. garinii, and B. burgdorferi sensu stricto in MKP and BSK-II medium. Int J Med Microbiol 294, 407–412 (2004).
Blankenberg, D. et al. Manipulation of FASTQ data with Galaxy. Bioinformatics 26, 1783–1785 (2010).
Zerbino, D. R. & Birney, E. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 18, 821–829 (2008).
Giardine, B. et al. Galaxy: a platform for interactive large-scale genome analysis. Genome Res 15, 1451–1455 (2005).
Goecks, J., Nekrutenko, A. & Taylor, J. Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences. Genome Biol 11, R86 (2010).
Li, H. et al. The sequence alignment/map format and SAMtools. Bioinformatics 25, 2078–2079 (2009).
Rissman, A. I. et al. Reordering contigs of draft genomes using the Mauve aligner. Bioinformatics 25, 2071–2073 (2009).
Darling, A. E., Tritt, A., Eisen, J. A. & Facciotti, M. T. Mauve assembly metrics. Bioinformatics 27, 2756–2757 (2011).
Huson, D. H. & Bryant, D. Application of phylogenetic networks in evolutionary studies. Mol Biol Evol 23, 254–267 (2006).
Guindon, S. & Gascuel, O. A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol 52, 696–704 (2003).
Ronquist, F. et al. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst Biol 61, 539–542 (2012).
Tamura, K. et al. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Mol Biol Evol 30, 2725–2729 (2013).
The study was supported by the Bavarian Ministry for Health and Care and by the German Federal Ministry of Health via the Robert Koch-Institute and its National Reference Laboratories Network. This work was partially supported by “Programa de Apoyo a Proyectos de Investigación e Innovación Tecnológica PAPIIT”, grant number IA200515 to S.C.R. The authors would like to thank Cecilia Hizo-Teufel and Silvia Stockmeier for excellent technical assistance. V.F., A.S. and G.M. are members of ESGBOR. S.C.R. would like to dedicate this work to the 43 trainee teachers from Ayotzinapa, who were abducted in September 2014 in the town of Iguala, Mexico.
The authors declare no competing financial interests.
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Castillo-Ramírez, S., Fingerle, V., Jungnick, S. et al. Trans-Atlantic exchanges have shaped the population structure of the Lyme disease agent Borrelia burgdorferi sensu stricto. Sci Rep 6, 22794 (2016). https://doi.org/10.1038/srep22794
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