The genetic diversity of Borrelia afzelii is not maintained by the diversity of the rodent hosts
Small mammals are essential in the enzootic cycle of many tick-borne pathogens (TBP). To understand their contribution to the genetic diversity of Borrelia afzelii, the most prevalent TBP in questing Ixodes ricinus, we compared the genetic variants of B. afzelii at three distinct genetic loci. We chose two plasmid loci, dbpA and ospC, and a chromosomal one, IGS.
While the larvae that fed on shrews (Sorex sp.) tested negative for B. afzelii, those fed on bank voles (Myodes glareolus) and wood mice (Apodemus sylvaticus) showed high infection prevalences of 0.13 and 0.27, respectively. Despite the high genetic diversity within B. afzelii, there was no difference between wood mice and bank voles in the number and types of B. afzelii haplotypes they transmit.
The genetic diversity in B. afzelii cannot be explained by separate enzootic cycles in wood mice and bank voles.
KeywordsBorrelia burgdorferi (s.l.) Ixodes ricinus larvae Rodents IGS ospC dbpA
decorin binding protein A
5S-23S rDNA intergenic spacer region
outer surface protein A
outer surface protein C
Borrelia burgdorferi (sensu lato) is a bacterial complex whose members are causative agents of Lyme borreliosis, the most widespread vector-borne disease in Europe. The genospecies that accounts for the majority of Lyme borreliosis cases is Borrelia afzelii . The enzootic transmission cycle of B. afzelii predominantly involves small mammals and I. ricinus ticks, in which it is also the most prevalent Borrelia genospecies [2, 3].
The high genetic diversity of B. burgdorferi (s.l.), at both inter- and intra-specific level, is partly the reason for the multiple clinical manifestations that the infection with these bacteria can display in humans [4, 5, 6, 7]. An important role in the maintenance of the intraspecific genetic diversity of B. burgdorferi (s.l.) has been attributed to the host community. One of the underlying mechanisms is the multiple-niche polymorphism balancing selection where various vertebrate hosts can act as ecological niches for some genotypes of a species [8, 9]. This balancing selection entails that the bacteria have different fitness in different vertebrate hosts. Changes in the vertebrate host composition could therefore result in changes in the abundance of the more pathogenic bacteria [10, 11, 12].
Genes such as the outer surface protein C gene (ospC) and ribosomal protein L2 gene (rplB) have been used in studies addressing the genetic diversity of B. afzelii [13, 14, 15, 16] in either skin biopsies from rodents, or questing I. ricinus. While rodents could get infected by certain Borrelia genotypes, it is not necessary that they transmit them with equal efficiencies to the ticks feeding on them. Likewise, the presence of the genotypes with multiple sources in questing ticks cannot indicate which of the sources contributed most to the abundance of those respective genotypes. A manner to overcome these issues is to study the distribution of the various genotypes in the engorged larvae attached to their hosts. This has been done in two European studies highlighting the existence of co-infection with multiple ospC haplotypes of B. afzelii in fed larvae [17, 18]; these studies, however, did not address the question of differential roles of small mammal species in the maintenance of B. afzelii genetic polymorphism. To our knowledge, the only comparative studies on fed larvae from various rodent species were performed on B. burgdorferi (sensu stricto) (s.s.) [19, 20]. There they found that certain genotypes of B. burgdorferi (s.s.) are associated to certain vertebrate hosts, supporting the hypotheses that host adaptation is an important determinant for the genetic differentiation of B. burgdorferi (s.s.) and potentially also for its variation in pathogenicity in humans.
In this study, we tested the hypothesis of host driven multiple-niche polymorphism of B. afzelii. We did this by testing fed larvae collected from five small mammal species: the wood mouse (Apodemus sylvaticus), bank vole (Myodes glareolus), field vole (Microtus agrestis), common shrew (Sorex araneus) and pygmy shrew (Sorex minutus). While the first two are among the most abundant rodent species in northwestern Europe [21, 22, 23] and recognized as the most important reservoirs for B. afzelii [3, 24], the field vole and shrews are less studied in this context. To this end, we chose two protein-coding genes, whose products are active elicitors of the immune response of the rodent hosts [25, 26]: ospC and decorin binding protein A (dbpA). According to the niche-polymorphism model, we expected to find distinct haplotypes of the genes in the larvae collected from the small mammals. In order to be able to identify the Borrelia burgdorferi (s.l.) genospecies we additionally used the 5S-23S intergenic spacer region (IGS), which is located on the chromosome and is evolving neutrally .
We trapped rodents and shrews with small mammal live-traps (Heslinga Traps, Groningen, The Netherlands) baited with grain, carrot and mealworms (as in ). Traps were checked at 12 h intervals. The sampling was performed between July 2013 and August 2014 at 11 different sites located in ten forests in The Netherlands (Additional file 1: Table S1). Each animal was thoroughly examined for ticks and then released at the site of capture. Animals that accidentally died in the traps were brought to the laboratory for a thorough examination for ticks (see Additional file 2: Table S2 for an overview of which animals were checked alive, and which were checked dead). Each tick was collected and placed in a separate tube. For each tick we registered the species, the development stage (larva, nymph, adult) and the feeding status (fed/unfed). An overview of the tick burdens per species can be found in Additional file 3: Table S3. The samples were stored at -20 °C until DNA extraction.
DNA extraction and qPCR detection of microorganisms
Total DNA was extracted from engorged larvae only. The level of engorgement was determined based on visual inspection under a stereomicroscope, where the flat larvae were assigned as unfed, while the partly- or fully-fed were assigned as engorged. This was done to ensure that the Borrelia burgdorferi (s.l.) detected in the larvae came from the vertebrate hosts they were feeding on at that moment, considering that transovarial transmission of these bacteria is absent or very low [29, 30]. The extraction was performed using the Qiagen DNeasy 96 Blood & Tissue Kit (Qiagen, Venlo, The Netherlands).
For the detection of B. burgdorferi (s.l.), a triplex qPCR, targeting ospA and flaB genes of B. burgdorferi (s.l.) and the flaB gene of B. miyamotoi, was used. The sequences of primers and probes are given in Additional file 4: Table S4. qPCRs were performed using the iQ Multiplex Powermix PCR reagent kit (Bio-Rad Laboratories, Hercules, USA), in a LightCycler 480 Real-Time PCR System (F. Hoffmann-La Roche, Basel, Switzerland). The triplex reaction mix for Borrelia species consisted of iQ multiplex Powermix, 100 nM of the B-FlaB-Rc and B-FlaB-Rt primers, 200 nM of the B-FlaB-F, FlabBm.motoiF2, and FlabB.m.motoiR3 primers, 400 nM of the B-OspA_modF and B-OspA_borAS primers, 100 nM of the B-OspAmodPatto probe, 200 nM of the B-FlaB-Patto and FlabBm.motoiPro probes, and 3 μl of template DNA in a final volume of 20 μl. Analysis was performed using the second derivative calculations for crossing point values. For each run three positive controls, two negative controls, and two blank samples were included.
Conventional PCR and sequencing
We targeted three genes located on different genetic elements of B. afzelii: (i) 5S-23S intergenic spacer region (IGS) located on the chromosome, (ii) dbpA located on plasmid lp54, and (iii) ospC located on plasmid cp26. In order to build a phylogeny of the spirochetes found in the rodent ticks, we used the 5S-23S rDNA intergenic spacer (IGS). The PCR was performed according to the protocol described in Coipan et al. .
Conventional PCR for ospC was performed using the forward primer (OC6) described by Qiu et al.  and a modification of the reverse primer (OC602) described by the same author, in a final concentration per reaction of 0.4 μM. The sequences of the primers are given in Additional file 4: Table S4. The PCR reaction was done using the HotStar Master Mix Kit (Qiagen), with the following conditions: 15 min at 94 °C, then cycles of 20 s at 94 °C, 30 s at 70 °C, 30 s at 72 °C lowering the annealing temperature 1 °C each cycle until reaching 60 °C, then 40 cycles at this annealing temperature and ending with 7 min at 72 °C. Due to the high sequence variability of dbpA, the conventional PCR for this gene was performed using three primer pairs, described in Additional file 5: Table S5. The PCR reaction mix and conditions were the same as for ospC.
PCR products were sequenced using an ABI PRISM BigDye Terminator Cycle sequencing Ready Reaction kit (Applied Biosystems, Foster City, California). Sequences were confirmed by sequencing both strands . Storage, trimming and cleaning of the sequences were performed in BioNumerics version 7.0 (Applied Math, Sint-Martens-Latem, Belgium).
Sequences were aligned by MAFFT v.7.222 . Phylogenetic trees of all three genes were constructed by using a maximum likelihood algorithm, in RAxML, run under RDP 4.56 , with 100 bootstraps. Based on the clustering in the phylogenetic trees each allele of the three genes received a unique ID number/name.
The ospC alleles were named according to Durand et al. . To identify similarities with sequences from other areas of Europe we downloaded IGS, dbpA and ospC sequences available in GenBank. The phylogenetic trees of IGS and ospC were rooted with B. garinii. For data visualization we constructed phylogenetic trees linked with heatmaps of the rodent species, using the functions implemented in the ggtree package .
We tested for genetic differentiation between the various sites and rodent species using the AMOVA test implemented in Arlequin 3.5 , where we defined the rodent species as a group and the various sampling locations as populations. We used R 3.4.4 to test for differences in tick burden using a generalized linear model with a negative binomial distribution and a log-link function .
Full body inspection for ticks was performed on 120 small mammals (Additional file 2: Table S2). The small mammals carried a total of 4292 larval and 94 nymphal Ixodes ricinus, with variable infestation levels between the various species (Additional file 3: Table S3). Wood mice did not have a significantly higher mean larval burden (mean ± SD, 48.1 ± 51.9) than bank voles (32.2 ± 39) (nbGLM: Z = 1.8, P = 0.08). Field voles had the highest mean larval burden (91.2 ± 165.5), which was higher than bank voles (nbGLM with bank voles: Z = 2.06, P = 0.05) but not than wood mice (nbGLM with wood mice; Z = 1.24, P = 0.22).
Tick burden and prevalence of infection of the five small mammalian species
Larval/nymphal tick burden median (range)
B. burgdorferi (s.l.) prevalence of infection (positive/tested)
Results of AMOVA test for the three selected genes
Percentage of variation (degrees of freedom)
Between samples within genus
In this study, we tested whether the three most common rodent species in northwestern Europe transmit different variants of B. afzelii, by comparing the haplotypes of B. afzelii at three distinct genetic loci in engorging larvae removed from rodents. Two main assumptions were made in the analysis of the data: (i) the newly hatched larvae that are questing for a vertebrate host are B. burgdorferi (s.l.) free, as previous studies have shown transovarial transmission to be close to null [38, 39] and (ii) all larvae have been attached to their hosts long enough to get infected with the bacteria of interest for our study . Recent studies  have shown that transovarial transmission of B. burgdorferi (s.l.) might be the reason that 0.62% of the larvae are infected. We argue that, at this prevalence, the transovarially transmitted Borrelia burgdorferi (s.l.) in our study would represent only a minor fraction (8–9 positive larvae) and would, therefore, not be a major bias in our results.
Our comparison of the infection prevalence in the larvae feeding on the various small mammals indicated that B. afzelii is more prevalent in larvae feeding on bank voles than in those feeding on wood mice. While previous studies have indicated this with xenodiagnostic data [40, 41], our data confirm that the bank voles are better transmitters of B. afzelii than wood mice using field data.
We also find that bank voles and wood mice transmit the same B. burgdorferi (s.l.) genotypes to the larvae they feed. The existence of multiple genotypes with divergent nucleotide sequences at several loci in the genome of Borrelia could be explained, among others, by the multiple-niche polymorphism balancing selection, where the bacteria have evolved to be adapted to various vertebrate hosts. Borrelia burgdorferi (s.s.) bacteria in North America have been shown to confirm to this hypothesis, with host-specific bacterial strains [19, 20]. The same hypothesis was tested on the European B. afzelii using tissues from various rodent species [13, 14] but the results indicated that B. afzelii does not exhibit host specificity. One might argue, however, that using animal tissues will allow the detection of Borrelia genotypes that cause systemic infection in the rodents but will miss an important fraction of the B. afzelii genotypes: those transmitted via co-feeding . In order to circumvent this potential bias, we tested engorged larvae collected from small mammals. Our analysis indicated that most IGS, dbpA and ospC B. afzelii haplotypes are maintained by both wood mice and bank voles (Fig. 1). Furthermore, the high degree of linkage disequilibrium between the alleles at the three loci implies that the horizontal gene transfer does not occur often in these bacteria and that the spirochetes have evolved to have equal fitness for both species of the main rodent hosts. This implies that the innate immune response of the various small rodents exempts a more or less similar selective pressure on B. afzelii. The absence or scarcity of a haplotype in a rodent species in our study could be the result of a small sample size, so that the sampled rodents were infected with some haplotypes only, due to chance. On the other hand, our sample size could have been insufficient to capture the whole spectrum of haplotypes, so that we cannot exclude the possibility that other haplotypes of B. afzelii exist and those would show a different distribution pattern across the vertebrate hosts.
Another reason for the genetic variation at the selected loci could be, as pointed out previously [13, 27], geographical differentiation. Our data indicated that there is genetic variation among the sampling locations but this is lower than the genetic variation within the locations for all three genetic loci (Table 2). We conclude, thus, that geographical differentiation at the local scale of B. afzelii strains at these three loci plays a minor role in the observed polymorphism. There are, however, differences in the frequencies of the haplotypes at various sampling sites. This can be explained by a negative frequency-dependent mechanism in which no genotype has a maximum fitness within a certain host species but that initial infection of a host triggers an immune response that will be protective against subsequent infections with genetically similar bacterial genotypes [42, 43]. The genotype that is most abundant at some point in time will be gradually decreased in frequency by negative selection from the host, favouring another one to become more frequent, with the ensuing fluctuations in time and space of the genotype’s frequencies .
In general, a third reason for the maintenance of the genetic variation at some genetic loci of B. afzelii could be the interaction bacterium-tick species. While some Ixodes species transmit multiple B. burgdorferi (s.l.) genospecies, other tick-Borrelia associations seem to be less efficient . Different tick receptors for Borrelia proteins could account for different attachment rates of the spirochaetes to the tick midgut and, hence, for their abundance in enzootic cycles [46, 47, 48, 49]. Since in our study we only looked at I. ricinus larvae, which were only very seldom co-feeding with other Ixodes spp., we can exclude the possibility of selection of Borrelia genotypes by the tick species.
Several studies have shown that there are B. afzelii multilocus sequence types that are overrepresented in human samples, as compared to the tick samples [7, 50]. The natural question that ensues is: What is the provenience of those sequence types? Is there a vertebrate host in nature that can act as main reservoir for these sequence types? Our study suggests that the differential virulence of the B. afzelii sequence types is not the result of maintenance of the bacteria in distinct vertebrate hosts in enzootic cycles. The various rodent species were capable of transmitting or allowing transmission of many overlapping B. afzelii haplotypes. This finding, together with the variety of the transmission cycles of B. afzelii throughout Europe , have direct implications for the control of B. afzelii, in the sense that interventions on the diversity of small mammal hosts would have limited, if any, effect in reducing the density of ticks infected with a certain bacterial haplotype. This is in contrast to what the “dilution effect”, according to which more diverse host communities would lead to a reduction of the strains with increased pathogenicity for humans due to a decrease in the relative abundances of the competent reservoir hosts [10, 11, 12], would predict. Instead, the overall number of ticks feeding on the rodents could be decreased indirectly, by increasing the number of predators  or excluding propagation hosts (e.g. deer) at small spatial scales .
We show that small rodents do not contribute differently to the genetic diversity of B. afzelii at neither chromosomal nor plasmid loci. The results of the genetic analysis indicate that the existence of multiple haplotypes at plasmid loci that are responsible for the microorganism-host interaction is unlikely to be the result of niche-polymorphism balancing selection. It is possible that another form of balancing selection, such as negative frequency-dependent selection, is responsible for maintaining the genetic diversity at various loci in the B. afzelii genome. Further studies are necessary to elucidate the ecological factors that drive and maintain the genetic differentiation of Lyme disease spirochetes at an intraspecific level.
We give thanks to Willem Takken for fruitful discussions on the analysis and the results of our study.
This study was financially supported by the Dutch Ministry of Health, Welfare and Sport (VWS).
Availability of data and materials
All data generated or analysed during this study are included in this published article and its additional files.
Part of the data from this study was published in a modified form as a chapter in the first author’s doctoral thesis (ECC). ECC and HS designed the study. TH and GvD collected field data, ECC performed molecular and statistical analyses and drafted the manuscript. HS conceived the study. All authors improved the draft manuscript and read and approved the final manuscript.
All experimental handling procedures were approved by the Animal Experiments Committee of Wageningen University (WUR- 2013055, WUR-2014019 and WUR-2012065) and by the Netherlands Ministry of Economic Affairs (FF/75A/2013/003).
Consent for publication
The authors declare that they have no competing interests.
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