Tick-transmitted diseases are an emerging health problem, and the hard tick Ixodes ricinus is the main vector for Borrelia spp., tick-borne encephalitis virus and most of the spotted fever Rickettsiae in Europe. The aim of the present study was to examine the incidence of rickettsial infection in the southernmost and south central parts of Sweden and the Åland Islands in Finland, the risk of infection in humans and its correlation with a bite of a Rickettsia-infected tick, the self-reported symptoms of rickettsial disease, and the prevalence of co-infection between Rickettsia spp. and Borrelia spp. Persons with a recent tick bite were enrolled through public media and asked to answer a questionnaire, provide a blood sample and bring detached ticks at enlistment and at follow-up three months later. Blood samples were previously analysed for Borrelia spp. antibodies and, for this report, analysed for antibodies to Rickettsia spp. by immunofluorescence and in 16 cases also using Western Blot. Ninety-six (44.0%) of the 218 participants were seropositive for IgG antibodies to Rickettsia spp. Forty (18.3%) of the seropositive participants had increased titres at the follow-up, indicating recent/current infection, while four (1.8%) had titres indicating probable recent/current infection (≥1:256). Of 472 ticks, 39 (8.3%) were Rickettsia sp. positive. Five (31.3%) of 16 participants bitten by a Rickettsia-infected tick seroconverted. Experience of the self-reported symptoms nausea (p = 0.006) and radiating pain (p = 0.041) was more common among those with recent, current or probable infection compared to those who did not seroconvert. Participants who showed seroreactivity or seroconversion to Rickettsia spp. had more symptoms than those who were seronegative. Seven (3.2%) participants showed seroconversion to Borrelia spp., and three (1.4%) of these showed seroconversion to both Rickettsia spp. and Borrelia spp., in accordance with previous studies in Sweden. Symptoms of rickettsial disease were in most of the cases vague and general that were difficult to differentiate from other tick-borne diseases.
Citation: Lindblom A, Wallménius K, Sjöwall J, Fryland L, Wilhelmsson P, Lindgren P-E, et al. (2016) Prevalence of Rickettsia spp. in Ticks and Serological and Clinical Outcomes in Tick-Bitten Individuals in Sweden and on the Åland Islands. PLoS ONE 11(11): e0166653. https://doi.org/10.1371/journal.pone.0166653
Editor: Ben J. Mans, Onderstepoort Veterinary Institute, SOUTH AFRICA
Received: August 7, 2016; Accepted: November 1, 2016; Published: November 15, 2016
Copyright: © 2016 Lindblom et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: The study was financially supported by grants from the Swedish Research Council Branch of Medicine (grant no. K2008-58X-14631-06-3)(PF); the EU Interreg IV A project ScandTick (grant no. 167226)(PEL); the County Council of Östergötland (grant no. LIO-56191)(PF); Stiftelsen Olle Engqvist Byggmästare (11877)(KN); Uppsala-Örebro-Regional Research 324 Council (25021)(KN); the Center for Clinical Research Dalarna (9028)(KN). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Several tick-transmitted microorganisms can cause human disease, among them members of the Borrelia burgdorferi sensu lato group, including B. afzelii, B. garinii, tick-borne encephalitis virus, Anaplasma spp., Candidatus Neoehrlichia mikurensis, and most of the species of the spotted fever group of rickettsiae (SFGR). The main vector in Sweden and other European countries is the hard tick, Ixodes ricinus. At least 22 species of SFGR are known, 17 of which are identified as human pathogens . The predominant SFG Rickettsia in ticks in Sweden is Rickettsia helvetica, which appears at a prevalence between 1.7–22% in ticks collected from different areas, whereas R. sibirica has in one occasion also been detected in I. ricinus ticks in Sweden [2, 3]. R. helvetica infection is primarily considered a self-limited disease with fever, myalgia and headache, in some cases with a rash and eschar. However, the infection can present more severe symptoms, including neurological symptoms as well as perimyocarditis [4–12]. Only a limited number of patients with serology-based diagnosis have been reported to date. For this reason, more studies are needed to understand all clinical manifestations of R. helvetica . In addition to R. helvetica, R. felis, whose main vector is the cat flea (Ctenophalides felis), has also been associated with meningitis .
Ticks may harbour and be simultaneously infested with many microorganisms [14–16]. In a study from Italy, the most frequently observed double infestation in ticks was SFG Rickettsiae and Borrelia burgdorferi sensu lato . Despite the fact that several agents appear in ticks, co-infections in humans have rarely been studied, although a few surveys have been conducted that included co-infections with different Rickettsia species [18–23].
The aims of the present study were: 1) to examine the prevalence of rickettsial disease in humans with a confirmed tick bite, 2) to calculate the risk of infection after being bitten by a Rickettsia infected tick, 3) to describe the clinical manifestations of rickettsial disease, and 4) to chart the extent to which a serological response to both Rickettsia spp. and Borrelia spp. occurs following a tick bite.
Materials and Methods
The Tick-Borne Disease (TBD) STING study is a prospective study following recently tick-bitten individuals for a 3-month study period [24,25]. Individuals ≥ 18 years of age with an observed and recent tick bite were asked through local public media to bring the tick, after detachment, to their Primary Health Care (PHC) centre. In the present study, a total of 222 participants were enrolled from May 2008 to September 2009. Four participants were excluded from the study: two were being treated with antibiotics at the time of enrolment and two failed to show up for the follow-up visit. All participants who visited the PHC centre were, after giving their written informed consent, asked to complete a questionnaire, to provide a blood sample and to donate their ticks for further investigation. They were followed up with a second visit to the PHC centre three months later, at which time they completed a second questionnaire, provided a new blood sample and brought ticks from additional tick bites. All samples were transported to Linköping University and frozen within 3 days at -70°C for later analyses.
The questionnaire completed at enrolment included information about the number of tick bites, geographical location at which the tick bite occurred and medical history regarding previous tick-borne diseases . The second questionnaire completed at the follow-up visit included questions about new tick bites, non-specific symptoms associated with tick-borne diseases and whether the participants had sought medical care. The symptoms listed included fatigue, headache, loss of appetite, weight loss, nausea, fever, neck pain, vertigo myalgia/arthralgia, numbness, radiating pain and cognitive difficulties. Medical records were examined to determine whether the patients had been diagnosed with a tick-borne infection. The regions participating in the current study were located in the south central parts of Sweden represented by: Västra Götaland (Lidköping); Östergötland (Söderköping; Kisa; Vikbolandet) Jönköping County (Bankeryd), southernmost Sweden (Kalmar) and the Åland Islands in Finland (Fig 1). These areas were selected because they are known to be high endemic tick areas identified in previous studies [24, 25].
A total of 472 ticks detached from the participants were collected from the different locations (98 ticks in Lidköping, 97 in Jönköping, 98 in Östergötland, 82 in Kalmar and 97 on the Åland Islands). Some participants delivered additional detached ticks during the 3-month follow-up period. From participants who seroconverted and presented a Rickettsia negative tick at inclusion, additional ticks were analysed using PCR to determine whether infection occurred after recruitment. Ticks were photographed and measured dorsally and ventrally to determine species; all belonged to I. ricinus [24, 25, 27]. Life cycle stages of the ticks were determined. Blood feeding time of nymphs and female adults were estimated using the scutal and coxal indices .
Serology (Immunofluorescence assay)
R. helvetica-infected Vero cells supplemented with 10% yolk sac solution were used as antigen. The antigen solution was applied to each well of the microscope slides, dried, and fixed in acetone, where after the serum was serially diluted in titres 1/64, 1/128 and 1/256, respectively, and incubated as previously described . Human blood donor serum was used as a negative control, and serum from a patient with proven end-point titres of 1:256 and 1:128 of IgG/IgM, respectively, was used as a positive control. Fluorescein isothio-cyanate-conjugated (FITC) γ–and mu-chain-specific polyclonal rabbit anti-human IgG and IgM (Ref.: F0202 and FF0203, Dako, Denmark) were used for detection of IgG and IgM antibodies, the latter after pretreatment with rheumatoid factor absorbent (Immunkemi, Stockholm, Sweden). The participants were divided into four groups based on their serologic results. As done at the Rickettsia laboratory in Marseille (Unité des Rickettsies), IgG titres ≥ 128 was judged as indicative of infection and a titre ≥ 1:256 was assumed to be the result of a current rather than a past infection . Group 1 (confirmed case): four-fold or greater rise in IgG titre between the first and second sera. Group 2 (probable case): single or repeatable IgG endpoint titres of ≥1:256 were regarded as evidence of a recent or current infection. Group 3 (seroreactive): IgG and/or IgM titres ≥ 1:64 and ≤ 1:128 were considered indicative of either past infection or early response (IgM) to infection, while persisting IgG titres with or without IgM reactivity were considered to indicate a past infection. Persisting IgM antibodies alone were interpreted as non-specific cross-reactivity due to exposure to other organisms or autoimmune responses or possibly as a sign of previous exposure . Group 4: IgG/IgM titres <1:64 were considered negative. All groups were evaluated separately. However, for the evaluation of symptoms, we combined the serological groups with findings on rickettsial DNA in the ticks.
Western Blot (WB)
Sera from 16 of the IgG-positive participants (Pat. nos. K7, K9, K46, K56, L16, L43, L46, S71. S72, S75, V6, Å16, Å23 and Å35 (Group 1) and K13 and Å13 (Group 2) were diluted to titres 1:200 and tested for WB with R. helvetica whole-cell antigen using Amersham WB system (GE Healthcare) with the secondary antibody Antihuman IgG DyLight™549 (Rockland Inc. cat.no 609-142-123) in the concentration of 1:10,000 in accordance with the manufacturer’s instructions. A serum from a patient with a proven end-point IgG/IgM of 1:512/1:128 to R. helvetica was used.with served as the positive control. The secondary antibody alone served as the negative control together with serum sample from a healthy blood donor
All cDNA samples from the ticks were individually assayed using a real-time PCR targeting the citrate synthase (gltA) gene of Rickettsia spp., as previously described [2, 14, 27]. Two to five μl cDNA was used as a template in each reaction, together with 0.25 μl LC Uracil-DNA glycosylase (UNG) (Roche Diagnostics, Mannheim, Germany) to minimize the risk of contamination. The reactions were run in a Rotor-Gene 3000 (Qiagen, Sydney, Australia) using LightCycler® TaqMan® Master (Roche Diagnostics, Mannheim, Germany). In each amplification trial, a negative control, sterile water and a positive standard plasmid constructed by cloning the 74 bp PCR product of the gltA gene into a PCR 4-TOPO vector (TOPO® TA Cloning® kit for Sequencing, Invitrogen, Carlsbad, CA, USA) and containing the cloned 74 bp fragment of the gltA gene were included in 10-fold serial dilutions. All samples that were positive in real-time PCR were further amplified for analysis of a fragment of the genes coding for the outer membrane protein B, ompB, 17-kDa or using a semi-nested PCR targeting the gltA gene, as previously described [2, 14]. All PCR products considered for sequencing were cleansed using Exonuclease I and FastAP™ Thermosensitive Alkaline Phosphatase (Fermentas GmbH). Sequencing analysis of PCR products was performed at Macrogen Inc. (Macrogen Europe, Amsterdam, Netherlands). DNA Baser version 2.80.0 (HeracleSoftware, Lilienthal, Germany) and BioEdit Sequence Alignment Editor Version 220.127.116.11 (Ibis Therapeutics, Carlsbad, CA) were used for sequence alignments. For species identification, sequences were examined using the Basic Local Alignment Search Tool (BLAST). A summary of primers, probe, sequences and products is provided in Table 1.
The Fischer’s exact test was used to compare the proportions between the Rickettsia seropositive and seronegative group concerning symptoms, as well as to examine the differences in seroreactivity between the geographical areas. The statistical analyses were conducted using IBM SPSS Statistics version 21. A p-value ≤ 0.05 (two-tailed) was considered statistically significant.
Of the 218 participants included in the study, 82 (37.6%) were men and 136 (62.4%) women. The median age was 64 years (range 19 to 92), with 66 years for men (range 34 to 87) and 63 years for women (range 19 to 92). One hundred and four (47.7%) of the participants reported tick bites earlier in the season before enrolment, and 129 (59.2%) reported tick bites during the 3-month interval between inclusion and follow-up.
At follow-up, serological results regarding Rickettsia showed that 96 of 218 participants (44.0%) had IgG equal to or higher than the cut-off titre of 1:64. Out of the 96 participants, 40 (18.3%) seroconverted with a titre of at least 1:128 or showed a four-fold increase in IgG titre (Group 1), another four (1.8%) showed a single titre equal to or above 1:256 (Group 2), 52 (23.8%) had an IgG titre between 1:64 and 1:128 (Group 3), and 122 (56.0%) were seronegative (Group 4). In summary, 44 (20.2%) participants showed either a seroconversion with a four-fold increase in titre or a titre ≥ 1:256, thus indicating a recent or current infection (Tables 2–4).
WB for patient’s nos. K7, K9, K46, K56, L16, L43, L46, S71. S72, S75, V6, Å16, Å23 and Å35 (Group 1) and K13 and Å13 (Group 2) showed a specific response against lipopolysaccharide (LPS) and protein antigens in the 110–150 kDa region for IgG to whole cell antigen of R. helvetica (Fig 2). Negative controls in the form of serum from a healthy blood donor and IFA negative participant showed no specific reactions.
Lane A-P demonstrates the lipopolysaccaride ladders and specific reactions against R. helvetica proteins in the 110-150-kDa region for serum 2 for patients (Lane) V16(A), V43(B), V46 (C)(Area V); S71(D), S72(E), S75(F), V6(G) (Area Ö); K7(H), K9(I), K14(J), K46(K) K56(L) (Area K); Å13(M), Å16(N), Å23(O), Å35(P) (Area Å) in titres 1:200. Lane P(h) demonstrates specific proteins and the lipopolysaccharide (LPS) ladders reacting with a human antiserum from a patient diagnosed with rickettsial infection and N(h) a healthy negative blood donor. Mw = molecular weight marker. “Fig 2” is compiled of four figure panels representing the groups of lanes that originated from different gels/blots (Gel A-D). The short vertical lines of “Fig 2” divide the individual non-adjacent lanes in the gels. The original analyses are presented in S1–S4 Figs with Gels A-D as Supporting Information.
In the four regions representing south central and southernmost Sweden, there were no statistically significant differences between the groups (1–4) compared to the Åland Islands regarding serologic findings showing antibodies to Rickettsia spp. (Table 5). Of the collected 472 ticks that had bitten humans, 39 (8.3%) were positive for Rickettsia, as indicated by real-time PCR. All of these amplicons were further analysed using PCR targeting at least one of the genes encoding for ompB, citrate synthase (gltA) or the 17kDa protein followed by sequencing. Twenty-three amplicons showed a sequence with a 100% match to the deposited sequences in Gen Bank representing R. helvetica. The other 16 samples had weak signals in real-time PCR and showed no product by amplification with the other PCR assays. The ticks with confirmed infestation with R. helvetica were 11/98 (11.2%) from Lidköping, which was significantly higher than for the other areas, 4/98 (4.1%) from Östergötland, 7/97 (7.2%) from Jönköping, 1/82 (1,2%) from Kalmar and 0/98 (0%) from the Åland Islands. Of the ticks that were identified by stage, 90 were adults, 288 nymphs and 14 larvae and correlated with Group 1–4, as shown in Table 6.
Blood feeding duration was calculated in 327 ticks, 90 of which belonged to Group 1, four to Group 2, 117 to Group 3, and 116 to Group 4. The median blood feeding time was 27 hours (h) in Group 1, 32 h in Group 2, 32 h in Group 3 and 34 h in Group 4. Sixteen (7.3%) of the participants had been bitten by at least one Rickettsia-infected tick. Five of the 40 (12.5%) participants in Group 1 had been bitten by a Rickettsia-infected tick, no one in Group 2, seven of 52 (13.5%) in Group 3, and 3 of 122 (2.5%) in Group 4. Of the total of 16 participants bitten by a Rickettsia-infected tick, five (31.3%) seroconverted or had a four-fold increase in antibody titres. Of the 10 ticks in which R. helvetica was quantified by PCR, the mean value for Group 1 (4 ticks) was 12793 copies/μl reaction and for Group 4 (13 ticks) 35847 copies/μl. Symptoms of the participants bitten by rickettsial-positive ticks are listed in Table 7.
Forty-seven (21.6%) of the participants self-reported at least one non-specific symptom at the follow-up visit (Table 8). The symptoms were consistently unspecific, and only a few participants sought medical care for their symptoms, though none was diagnosed with tick-borne diseases. Most of the symptoms were equally distributed in all groups, but nausea (p = 0.006) and radiating pain (p = 0.041) were more common in Group 1 and 2 combined than in Group 4. Only three participants developed erythema migrans (EM), one each in Group 1, 3 and 4 (Table 8). Only the participant in Group 1 had been bitten by a rickettsial-positive tick. In this case, Borrelia serology was negative. In Group 3, the participant was seroreactive for both Borrelia and Rickettsia, but did not seroconvert. The participant in Group 4 seroconverted to Borrelia. Among those who seroconverted (Group 1) and were bitten by a Rickettsia spp.-positive tick, 20.0% reported more than three non-specific symptoms (Table 2). The corresponding percentage for participants who seroconverted and had been bitten by a Rickettsia spp.-negative tick was 16.7%, compared to 42.9% for participants who showed seroreactivity and also had been bitten by a Rickettsia spp.-positive tick (Tables 3 and 7). For those who were seronegative (Group 4), only 10.7% reported more than three non-specific symptoms. The participants who showed seroreactivity and had been bitten by a Rickettsia spp.-positive tick (Table 7) had significantly more non-specific symptoms compared to the seronegative group (Group 4) (p = 0.041).
Ninety-five (43.6%) of the participants were seropositive to Borrelia spp. Of these seven participants (3.2%) showed seroconversion against Borrelia spp. (Table 8). Three of them belonged to Group 1; 1.4% seroconverted to both Rickettsia spp. and Borrelia spp., and four belonged to Group 4. In addition, 88 participants (40.4%) were seropositive to Borrelia spp., of whom 17 of 40 (42.5%) were positive in Group 1, three of 4 (75.0%) in Group 2, 24 of 52 (46.2%) in Group 3, and 44 of 122 (36.1%) in Group 4.
The current study presents the prevalence of Rickettsia sp. in ticks, serological results and symptoms on tick-bitten individuals in Sweden and on the Åland Islands. All amplicons that were sequenced represented R. helvetica sequences. Previous studies in Sweden have shown a prevalence of Rickettsia-positive ticks collected from nature of between 1.7% and 22.1%, with a median between 9% and 11% [2, 3]. The present study supports previous findings showing that R. helvetica is the most prevalent Rickettsia sp. and, besides an occasional finding of R. slovaca, thus far the only reported tick-borne Rickettsia sp. to have infected humans in Sweden. Seroconversion after tick-bites should therefore primarily reflect antibodies to R. helvetica.
The results are in accordance with findings from previous surveys in high endemic areas in Sweden. In a previous study of recruits in Sweden, a four-fold increase in titre or seroconversion was found in 22.9% of participants . Although there were fewer participants in that study, the results are similar to the present findings and probably represent a baseline for what can be expected in individuals frequently exposed to ticks in Sweden.
Seroconversion to Rickettsia spp. was more common than seroconversion to Borrelia spp., suggesting that, in these areas, the risk of becoming infected with Rickettsia spp. after a tick bite is higher than for Borrelia spp. Ninety-five (43.6%) of the participants were either seropositive or showed seroconversion to Borrelia spp., compared to 96 (44.0%) for Rickettsia spp. Seroconversion was more common to Rickettsia spp. than to Borrelia spp., but the number of participants with antibodies to both agents was equal. Antibodies to Borrelia can remain for years while antibodies to Rickettsia seem to remain for a shorter period, where IgG can persist for at least 8–12 months [31–33]. The latter may be of importance in explaining why participants with a recent or current co-infection with Borrelia spp. and Rickettsia spp., based on seroconversion, were fewer in the present study compared to findings from earlier studies where co-infection was based on sero-reactivity [18, 20].
The blood feeding time required for transmission of rickettsial bacteria to the vertebrate host has been reported to be between 10 minutes and ≥10 hours . The blood feeding time in our study was almost equal in all groups (1–4), with a median time over 24 hours. A longer blood feeding time did not correlate with a higher infection rate, which is consistent with previously reported data . When measuring the number of bacteria infesting the ticks, using PCR quantification, lower numbers of rickettsia DNA copies per μl reaction were found in Group 1 than in Group 4. According to these results, there was no correlation between higher numbers of DNA copies/μl and seroconversion.
Surprisingly, none of the ticks collected from the Åland Islands contained Rickettsia spp., although the participants showed the same percentage of seroconversion and seroreactivity as those in the other study areas. All participants from the Åland Islands reported having acquired their tick bites in that area. The Åland Islands are known to be a very high endemic area for ticks, and the participants from this area had an average of 2.7 ticks collected per person in comparison to 1.7 ticks collected per person among the Swedish participants. The explanation could be that although the prevalence of Rickettsia spp. in ticks on the Åland Islands is lower than in the Swedish areas, the citizens of Åland get more tick bites and thus an equal amount of exposure to Rickettsia spp. ticks as the other study participants.
Most of the ticks in Group 1 were not infected by Rickettsia spp, but the absence of ticks positive does not imply that the person was not bitten by another overlooked positive tick. For this reason, it seems likely that these participants had been bitten by a number of ticks during the season and that the ticks collected at study enrolment were not the ticks that caused the infection. Therefore, based on the present data, it is difficult to draw conclusions concerning the exact risk of becoming infected when bitten by a Rickettsia-positive tick.
Regarding self-reported non-specific symptoms, we only found that nausea and radiating pain were more common among participants in Group 1 and 2 combined compared to those in Group 4. Among the participants with several non-specific symptoms, those who showed seroreactivity and had been bitten by a Rickettsia spp.-positive tick had a greater number of non-specific symptoms than did the seronegative participants (Group 4). However, the groups were small, and the self-reporting of symoptims may not always be accurate, meaning that no certain conclusions can be drawn. EM was not common and the participants presenting with EM were few, why any conclusion regarding the possibility that EM could be caused by tick-borne agents other than Borrelia spp. cannot be drawn.
Our findings on clinical manifestations support the assumption that R. helvetica is primarily a subclinical disease with non-specific symptoms, likely leading to an under-estimation of human cases. However, severe symptoms may develop as well (meningitis, septicaemia and myocarditis) and be misinterpreted as another tick-borne disease. More knowledge about the course and frequency of the infection is needed but the present study shows that rickettsial infection is a common tick-borne infection in Sweden and should be considered among tick-bitten persons.
S1 Fig. Gel A.
Patients(lane) V16(A), V43(B), V46 (C); S71(D), S72(E). Western Blot analysis of IgG antibodies against R. helvetica whole cell antigen for serum 2 in titres 1:200. Mw = molecular weight marker. P(h) and N(h) represent positive and negative human control sera.
S2 Fig. Gel B.
Patients(lane) S75(F), V6(G). x-s = extra serum. Western Blot analysis of IgG antibodies against R. helvetica whole cell antigen for serum 2 in titres 1:200. Mw = molecular weight marker. P(h) and N(h) represent positive and negative human control sera.
S3 Fig. Gel C.
Patients(lane) K7(H), K9(I), K14(J), K46(K), K55(Table 4). Western Blot analysis of IgG antibodies against R. helvetica whole cell antigen for serum 2 in titres 1:200. Mw = molecular weight marker. P(h) and N(h) represent positive and negative human control sera.
S4 Fig. Gel D.
Patients(lane) K56(L); Å13(M), Å16(N), Å23(O), Å35(P). Western Blot analysis of IgG antibodies against R. helvetica whole cell antigen for serum 2 in titres 1:200. Mw = molecular weight marker. P(h) and N(h) represent positive and negative human control sera.
We thank the employees in the PHC centres and our colleagues in the TBD STING-study group for valuable contributions during the study period.
- Conceptualization: AL PEL PF KN.
- Data curation: AL KW LF PW PEL PF KN.
- Formal analysis: AL PW PF LF PEL KN.
- Funding acquisition: PEL PF KN.
- Investigation: AL KW JS PW PEL PF KN.
- Methodology: AL KW JS LF PW PF KN.
- Project administration: PF KN.
- Resources: PEL PF KN.
- Supervision: PF KN.
- Validation: AL KW KN.
- Visualization: PF KN.
- Writing – original draft: AL LF PW PEL PF KN.
- Writing – review & editing: KN.
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