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Applied and Environmental Microbiology, February 2009, p. 596-602, Vol. 75, No. 3
0099-2240/09/$08.00+0     doi:10.1128/AEM.01674-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Differential Role of Passerine Birds in Distribution of Borrelia Spirochetes, Based on Data from Ticks Collected from Birds during the Postbreeding Migration Period in Central Europe

Lenka Dubska,^1* Ivan Literak,¹ Elena Kocianova,² Veronika Taragelova,³ and Oldrich Sychra¹

Department of Biology and Wildlife Diseases, Faculty of Veterinary Hygiene and Ecology, University of Veterinary and Pharmaceutical Sciences, Palackeho 1-3, 612 42 Brno, Czech Republic,¹ Institute of Virology, Slovak Academy of Sciences, Dubravska cesta 9, 842 45 Bratislava, Slovakia,² Institute of Zoology, Slovak Academy of Sciences, Dubravska cesta 9, 845 06 Bratislava, Slovakia³

Received 19 July 2008/ Accepted 1 December 2008

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Borrelia spirochetes in bird-feeding ticks were studied in the Czech Republic. During the postbreeding period (July to September 2005), 1,080 passerine birds infested by 2,240 Ixodes ricinus subadult ticks were examined. Borrelia garinii was detected in 22.2% of the ticks, Borrelia valaisiana was detected in 12.8% of the ticks, Borrelia afzelii was detected in 1.6% of the ticks, and Borrelia burgdorferi sensu stricto was detected in 0.3% of the ticks. After analysis of infections in which the blood meal volume and the stage of the ticks were considered, we concluded that Eurasian blackbirds (Turdus merula), song thrushes (Turdus philomelos), and great tits (Parus major) are capable of transmitting B. garinii; that juvenile blackbirds and song thrushes are prominent reservoirs for B. garinii spirochetes; that some other passerine birds investigated play minor roles in transmitting B. garinii; and that the presence B. afzelii in ticks results from infection in a former stage. Thus, while B. garinii transmission is associated with only a few passerine bird species, these birds have the potential to distribute millions of Lyme disease spirochetes between urban areas.

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Lyme borreliosis, the most frequent tick-borne human disease in the northern hemisphere, is a multisystemic disorder caused by spirochetes belonging to the genus Borrelia (12). At least seven Borrelia species have been obtained from the tick Ixodes ricinus (Acari: Ixodidae) in Europe: B. afzelii, B. bissettii, B. burgdorferi, B. garinii, B. lusitaniae, B. spielmanii, and B. valaisiana (30, 33). Various reservoir hosts seem to harbor different Borrelia species, which is explained by differential properties of the hosts' complement systems (17). Generally, B. afzelii is a rodent specialist, B. garinii and B. valaisiana are associated with birds, and B. lusitaniae is associated with lizards (7, 16, 22, 32). The clinical manifestations of Lyme borreliosis in humans differ depending on the Borrelia species; B. garinii is associated with neurological diseases, while B. burgdorferi and B. afzelii are more likely to cause arthritis and cutaneous symptoms, respectively (2, 4, 5, 36).

Ixodid ticks may attach to a host for 24 to 48 h, which is sufficient time for some birds to travel hundreds of kilometers along migration routes before ticks complete their feeding and drop off (31). The role of migratory birds in distributing Lyme disease spirochetes to new areas has been established in North America (25, 28, 37).

Recently, it has become clear that the bird host competency for maintaining and transmitting Borrelia spirochetes is different in different bird species. Pheasants in the United Kingdom (15, 16) and blackbirds and song thrushes in Central Europe (13, 35) have been shown to be important reservoirs of B. garinii and B. valaisiana. However, little is known about the other migrating passerine bird species with respect to their competence as Lyme disease reservoirs and transmission abilities.

Here we characterized tick infestation in migratory passerine bird species captured in the northeastern part of the Czech Republic during the postbreeding migration period. Further, we investigated the incidence of B. garinii, B. valaisiana, B. afzelii, and B. burgdorferi (B. burgdorferi sensu stricto) in bird-feeding ticks and in questing ticks from the same area in order to evaluate the importance of migrating passerine species as reservoirs and disseminators of Lyme disease spirochetes.

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Study site, birds, and tick collection and determination.
The field investigation was conducted at Certak (49°34'N, 17°59'E) in the northeastern part of the Czech Republic. Details concerning the location have been described by Kulich et al. (14). Birds were collected with mist nets during the postbreeding period from 29 July 2005 to 24 September 2005. The birds were identified, examined, and released back into the wild as quickly as possible to minimize disturbance. Ticks were collected from birds using tweezers. On 16 April 2006, host-seeking unfed ticks (nymphs and adults) were collected by dragging a blanket in lower vegetation at the same location. The ticks were placed in 70% ethanol. In the laboratory, the ticks were removed from the ethanol, and the species, stage, and sex of adults were determined using a stereomicroscope. The ticks were classified as "unfed" if there was no marked increase in body volume, as "half-fed" if there was a marked increase, and "fully fed" if the volume of the body was the maximum volume.

DNA isolation and identification and genotyping of Borrelia species.
Genomic DNA was extracted from ticks by alkaline hydrolysis (8). The mitochondrial cytochrome b gene was amplified as a control for DNA extraction for randomly selected Borrelia-negative samples (1), which revealed that the efficacy of the DNA isolation procedure was more than 95%. All samples were then subjected to nested PCR targeting a fragment of the rrf (5S)-rrl (23S) intergenic spacer (IGS) of B. burgdorferi sensu lato (16). Diluted B. garinii or B. valaisiana DNA was used as a positive control.

The PCR products were analyzed further by performing a reverse line blot assay using DNA probes specific for B. afzelii, B. bissettii, B. burgdorferi sensu lato, B. burgdorferi sensu stricto, B. garinii, and B. valaisiana, as described previously (10, 16). As positive controls, amplicons derived from cultured B. afzelii, B. burgdorferi sensu stricto, B. garinii, and B. valaisiana were blotted.

A subset of PCR-positive B. burgdorferi sensu lato samples that could not be assigned to species based on the reverse line blot assay results was subjected to nucleotide sequencing of the IGS and/or the flagellin B locus (flaB). A partial flagellin gene was amplified by using primers described by Fukunaga et al. (6) and the following PCR conditions: 35 cycles consisting of 94°C for 15 s, 52°C for 30 s, and 70°C for 90 s and then a final extension for 5 min at 70°C. The products of the IGS and flaB PCR were purified using a Wizard SV gel and PCR clean-up system (Promega). Both strands of the IGS PCR products were sequenced using the inner primers for the nested PCR. flaB PCR products were purified and sequenced in both directions using primers described by Fukunaga et al. (6).

Ability of the host to transmit Borrelia to ticks.
As Borrelia spirochetes are rarely transmitted transovarially (21) or by cofeeding (27), their presence in feeding larvae suggests that they were acquired from the host. Thus, we assumed that a higher proportion of infected fed larvae than of infected unfed larvae supported the conclusion that the host was able to transmit Borrelia to ticks.

Data analysis and statistics.
We used standard parametric statistics (Student's t test and analysis of variance) and determined means and 95% confidence intervals (95% CI). Proportions were evaluated by using odds ratio (OR) procedures with a 95% CI. To estimate the ability to transmit Borrelia spirochetes to ticks feeding on birds that might be infected, we calculated a noninfectivity coefficient (n-I) by determining the proportion of noninfected larvae among larvae feeding on a bird carrying 1 infected tick; an n-I of 1 suggested that a bird species was not able to transmit Borrelia spirochetes. Coefficients were calculated for each Borrelia species.

Nucleotide sequence accession numbers.
Sequences of Borrelia DNA have been deposited in the GenBank database under accession numbers EU401776, EU401777, EU401778, EU401779, EU401780, and EU401781 (5S-23S rRNA IGS), as well as EU401782, EU401783, and EU401784 (flaB gene).

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Tick infestation of birds.
The total number of birds captured was 1,084. Of these, 1,080 (99.6%) were passerines (order Passeriformes), 2 (0.2%) were members of the order Piciformes, 1 (0.1%) was common kingfisher (Alcedo atthis) (Coraciiformes), and 1 was a corncrake (Crex crex) (Gruiformes). Ringing data showed that 857 of the trapped birds were trapped for the first time, while 227 of them had been trapped previously. Both birds that were trapped for the first time and birds that had been trapped previously were examined. The most common birds were blackcaps (Sylvia atricapilla) and European robins (Erithacus rubecula), which accounted for 29.8 and 18.2% of all examinations, respectively.

Overall, 2,240 ticks were removed from 446 (41.1%) of the 1,084 birds (Table 1). No overall significant decrease in the prevalence of infestation (38.0% in originally trapped birds versus 52.0% in birds that had been trapped previously) or in the infestation level (1.96 ticks/originally trapped bird versus 2.48 ticks/bird that had been trapped previously) was observed for birds that were disinfested and trapped again. Therefore, birds that had been trapped previously were not excluded from the analysis. A total of 273 (25%) of the 1,084 birds were identified as males (172 birds) or females (101 birds). No difference in infestation level between males (1.9 ticks/bird) and females (1.8 ticks/bird) was observed. A total of 1,023 (94%) of the 1,084 birds were identified as young (born in the year when they were examined) (785 birds) or adult (1 year old) (238 birds). The infestation level was 2.0 ticks/young bird and 2.5 ticks/adult bird, and there was no significant difference in the level of infestation between birds that were different ages.

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TABLE 1. Birds captured in the Czech Republic during the postbreeding migration period and data on their infestation with I. ricinus ticks

The highest prevalences of infestation were found for Eurasian blackbirds (Turdus merula) (90.3%; n = 579; mean infestation level, 20.7 ticks per infested bird), dunnocks (Prunella modularis) (90.9%; n = 412; mean infestation level, 8.24 ticks per infested bird), song thrushes (Turdus philomelos) (77.4%; n = 264; mean infestation level, 6.4 ticks per infested bird), and winter wrens (Troglodytes troglodytes) (75.8%; n = 145; mean infestation level, 5.8 ticks per infested bird). The mean number of ticks for ground-foraging birds (winter wrens, dunnocks, European robins, song thrushes, bullfinches, gray wagtails, blackbirds, hawfinches, yellowhammers, and marsh warblers) was 4.2 ticks per infested bird, and it was 0.8 tick per infested bird for other bird species.

All ticks found on birds were identified as I. ricinus subadults. A total 1,547 (70%) of these ticks were larvae and 676 (30%) were nymphs, and the levels of infestation were 3.5 larvae/infested bird and 1.5 nymphs/infested bird. There were no differences between originally trapped birds and birds that had been trapped previously in the proportions of larvae (68% of all ticks on originally trapped birds and 74% of all ticks on birds that had been trapped previously) and nymphs (32% of the ticks on originally trapped birds and 26% of the ticks on birds that had been trapped previously) or the number of larvae (3.4 larvae/originally trapped infested bird and 4.1 larvae/infested bird that had been trapped previously) or nymphs (1.5 nymphs/originally trapped infested bird and 1.4 nymphs/infested bird that had been trapped previously). However, we observed bird species-related differences in the proportions of larvae and nymphs; most significantly, there were lower proportions of larvae in song thrushes (57%; OR 0.5; 95% CI, 0.4 to 0.7) and dunnocks (60%; OR, 0.6; 95% CI, 0.5 to 0.7) and higher proportions of larvae in winter wrens (95%; OR, 8.9; 95% CI, 4.1 to 19.0). Based on their volumes, 41% of the ticks were identified as unfed, 49% of the ticks were identified as half-fed, and as 9% of the ticks were identified as fully fed. There were no overall differences in proportions among bird species except that dunnocks had significantly higher proportions of unfed ticks (98%; P < 0.001).

Borrelia infection in bird-feeding ticks.
Borrelia spirochetes were found in 613 (27.4%) of 2,240 I. ricinus subadults. For these 613 infected ticks, we detected 856 infection events resulting from infection or coinfection with various Borrelia genospecies, and the mean number of infection events was 1.40 events per infected tick. Borrelia spirochetes were more common in nymphs than in larvae (31.4% versus 22.4%; OR, 1.6; 95% CI, 1.3 to 1.9), and there was 0.45 infection event per infected nymph, compared with 0.31 infection event per infected larva. The greater infection rate in nymphs was observed for European robins (OR, 12.0; 95% CI, 1.3 to 127.3) and dunnocks (OR, 2.9; 95% CI, 1.3 to 6.5) but not for other bird species.

B. garinii infections were found in 22.2% (497) of the ticks, and the prevalence was higher in nymphs (27.2%) than in larvae (20.2%) (OR, 1.5; 95% CI, 1.2 to 1.8) (Table 2). B. garinii DNA was detected far more often in ticks infesting Eurasian blackbirds (55.0%) and song thrushes (50.2%). Intermediate prevalence was observed for great tits (Parus major) (15.5% of the ticks were infected) and winter wrens (6.2% of the ticks were infected). The lowest n-I for B. garinii were obtained for song thrushes (0.34), great tits (0.42), and blackbirds (0.45). Although we did not find B. garinii in cofeeding nymphs, we detected B. garinii in 25 larvae from eight Eurasian blackbirds, in 9 larvae from four song thrushes, in 2 larvae from two European robins, in 1 larva from a blackcap, in 6 larvae from four dunnocks, in 3 larvae from 3 winter wrens, in 5 larvae from 2 great tits, and in 1 larva from a common treecreeper (Certhia familiaris). The prevalence of B. garinii was significantly higher in larvae feeding on young birds than in larvae feeding on birds more than 1 year old for Eurasian blackbirds (72% versus 6%; OR, 42.2; 95% CI, 17.7 to 100.5) and for song thrushes (63% versus 20%; OR, 6.0; 95% CI, 2.5 to 14.3).

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TABLE 2. Birds with B. garinii spirochete-infected subadult ticks

B. valaisiana was found in 12.7% (285) of the ticks, and there was no statistically significant difference between the prevalence in nymphs (14.3%) and the prevalence in larvae (12.2%) (OR, 1.1; 95% CI, 0.9 to 1.5) (Table 3). For song thrushes and dunnocks, we observed a lower level of infection in nymphs than in larvae. B. valaisiana was detected mostly in ticks infesting Eurasian blackbirds (37.0%), and the prevalence in ticks infesting song thrushes was intermediate (18.6%). In ticks feeding on other bird species, including great tits and winter wrens, the level of B. valaisiana infection was low. For all bird species, the n-I of B. valaisiana was greater than the n-I of B. garinii, and the lowest values were obtained for song thrushes (0.60), great tits (0.62), and blackbirds (0.64). Although we did not find B. valaisiana in cofeeding nymphs, we detected B. valaisiana in 23 larvae from six Eurasian blackbirds, in 11 larvae from seven song thrushes, in 2 larvae from two blackcaps, in 4 larvae from two dunnocks, in 3 larvae from three winter wrens, and in 5 larvae from a great tit. A higher prevalence of B. valaisiana in larvae feeding on young birds was observed for Eurasian blackbirds (71% versus 17%; OR, 12.2; 95% CI, 6.9 to 22.0) but not for song thrushes (20% versus 27%; OR, 0.7; 95% CI, 0.3 to 1.6).

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TABLE 3. Birds with B. valaisiana spirochete-infected subadult ticks

B. afzelii infection was found in 1.6% (36) of the ticks, and the prevalence was substantially higher in nymphs (5.0%) than in larvae (0.1%) (OR, 40.0; 95% CI, 9.8 to 170.8) (Table 4). The levels of infection with B. afzelii were approximately equal in ticks infesting great tits (2.3%), dunnocks (2.4%), song thrushes (1.1%), and Eurasian blackbirds (1.9%). B. afzelii was not present in ticks feeding on blackcaps and winter wrens. B. afzelii was detected in 2.3% of the unfed nymphs and in only 1.0% of the nymphs whose body volume was markedly increased (OR, 2.35; P < 0.02). Estimated absolute noninfectivity was observed for all bird species except great tits (n-I, 0.92). Although we did not find B. afzelii in cofeeding nymphs, we detected B. afzelii in one larva from a great tit and in one larva from a gray wagtail (Motacilla cinerea).

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TABLE 4. Birds with B. afzelii spirochete-infected subadult ticks

B. burgdorferi was found in only 0.3% (6) of the ticks feeding on birds, and there was not a striking association with a particular bird species (Table 5). Although we did not find B. burgdorferi in cofeeding nymphs, we detected B. burgdorferi in two larvae from a winter wren, for which the n-I was 0.91.

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TABLE 5. Birds with B. burgdorferi sensu stricto spirochete-infected subadult ticks

The reverse line blotting technique allowed identification of spirochete species in all cases except organisms that infected 10 ticks that were identified by sequencing of the flagellin or 16S rRNA gene as B. garinii for nine bird-infesting ticks and one case of B. afzelii in an adult questing tick. Two variants of B. garinii (accession numbers EU401782 and EU401783) isolated from two ticks infesting a song thrush were identical to isolates obtained by Taragel’ova et al. (35) and to a spirochete found in I. ricinus in Moscow province (23). Using BLAST searches, we found a B. afzelii partial flaB sequence (accession number EU401784) from a questing male tick that differed from the sequences of the most similar isolates by two nucleotides.

Greater infection in fed (half-fed and fully fed) larvae than in unfed larvae was observed for Eurasian blackbirds (OR, 4.6; 95% CI, 2.9 to 7.3) and for song thrushes (OR, 2.5; 95% CI, 1.2 to 5.3), as well as (without statistical significance) for great tits (OR, 2.4; 95% CI, 0.5 to 11.5) and for winter wrens (OR, 1.5; 95% CI, 0.5 to 4.0). Specifically, for Eurasian blackbirds and song thrushes, the correlation between the volume of larvae and Borrelia infection was stronger for B. valaisiana, for which the OR was 5.7 and the 95% CI was 3.1 to 10.3 for blackbirds and the OR was 9.0 and the 95% CI was 2.1 to 39.7 for song thrushes, than for B. garinii, for which the OR was 3.1 and the 95% CI was 2.0 to 4.9 for blackbirds and the OR was 2.1 and the 95% CI was 1.0 to 4.4 for song thrushes.

We also frequently observed mixed infections with Borrelia species. If infection with Borrelia spirochetes in ticks were independent, we would expect that 2.8% of the ticks would be infected with both B. garinii and B. valaisiana; in fact, the value was substantially higher, 10.4%. Infections with three species, mostly infections with B. garinii, B. valaisiana, and B. afzelii, were also detected for nine ticks.

Borrelia spirochetes in host-seeking unfed ticks.
A total of 109 questing ticks (24 unfed nymphs, 39 adult males, and 46 adult females) were collected from vegetation by dragging a blanket. B. afzelii was detected in seven ticks (6.4%), including three nymphs, three adult males, and one adult female. Moreover, we detected a tick containing both B. garinii and B. valaisiana (one female tick [0.9%]).

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In this paper, we report data obtained in a large-scale study of Borrelia spirochete distribution in passerine bird-feeding ticks collected from birds during the postbreeding migration period, and we assess the roles of certain bird species as reservoirs and distributors of Borrelia species. We found significantly higher infestation rates in ticks on ground-feeding birds connected with high levels of infection with Borrelia spirochetes in Eurasian blackbirds and song thrushes, but not dunnocks or European robins. Interestingly, dunnocks were heavily infested with ticks, but their infection rates were very low, which may have been associated with the fact that 98% of the ticks on dunnocks were starving. On the other hand, over 60% of the ticks feeding on European robins had a blood meal. Thus, ground-foraging behavior in birds results in a significantly greater risk of tick infestation. It is not, however, the crucial biological determinant for competence for transmission of Borrelia spirochetes to I. ricinus.

Overall, the Borrelia infection data for ticks obtained from passerine birds in our study were equivalent to findings for birds captured during 2001 and 2002 in Slovakian woodlands (35), but the values were substantially higher than the values for ticks obtained from birds examined in the spring and autumn of 2001 in southeastern Sweden (3). This suggests that migratory passerine birds from Central Europe are prominent reservoir hosts of Borrelia species. Almost 90% of B. garinii infections were detected in song thrushes and Eurasian blackbirds. The significantly higher proportion of B. garinii in larvae feeding on young song thrushes and Eurasian blackbirds than in larvae feeding on adult birds suggests that juvenile birds are prone to spirochetemia. It has been shown that migratory restlessness in young redwing thrushes (Turdus iliacus) can reactivate a latent B. garinii infection (9). This may be due to an increase in endogenous glucocorticoids during migratory restlessness (19) that adversely affects the immune system and leads to a decrease in the bactericidal response (24). Juvenile birds might have substantial migration-associated hormonal changes or less developed immune responses (20, 29) that increase their susceptibility to infectious diseases.

Based on noninfectivity ability and the cluster of B. garinii infections in great tits, we concluded that these passerine birds can also transmit B. garinii to feeding ticks under certain conditions. Interestingly, all five great tits yielding three to nine B. garinii-infected larvae had previously been captured. And for one great tit examined for the first time there was 1 nymph among the 16 ticks infected with B. garinii; then after capture on days 9, 10, and 12, 16 of 17 new larvae were infected. This suggests that trap-induced stress may have been a triggering mechanism for spirochetemia (9, 24). The n-I less than 1 for other passerine birds and the presence of infected larvae but not B. garinii-infected nymphs suggest that blackcaps, European robins, dunnocks, and treecreepers may play minor roles in transmitting B. garinii. Compared to the noninfectivity of B. garinii, however, the noninfectivity of B. valaisiana was higher, and Eurasian blackbirds and song thrushes were key reservoirs of this spirochete species. Moreover, our data suggest that juvenile Eurasian blackbirds, but not juvenile song thrushes, comprise a subgroup that is very efficient for B. valaisiana transmission. The role of other passerine birds as reservoirs of B. valaisiana is minor, and transmission competence is likely restricted to a few individuals.

The prevalence of B. afzelii in bird-feeding ticks was low, and there was no robust evidence that birds had transmission competence for this spirochete species. Together with the fact that the vast majority of infections were detected in nymphs, we suggest that these ticks were infected with B. afzelii as larvae feeding on nonbird hosts (likely rodents). Moreover, the significantly higher prevalence of B. afzelii in unfed nymphs supports the conclusion of Kurtenbach et al. (18) that avian blood induces selective complement killing of B. afzelii in ticks. Nevertheless, our finding that 13 bird-feeding nymphs were infected with B. afzelii suggests that the immune elimination of this Borrelia species by a bird host is not absolute. However, we observed two larvae positive for B. afzelii, one from a great tit and one from a gray wagtail, which may be attributed to a low transmission rate of B. afzelii in birds, to transovarial transmission, or to cofeeding transmission (26).

B. burgdorferi sensu stricto was rare in bird-feeding ticks. However, since we found two larvae containing B. burgdorferi on a treecreeper, we cannot exclude the possibility that birds have the potential to transmit this Borrelia genospecies.

Based on data for bird-feeding subadult ticks and questing adult ticks and nymphs, the estimated transstadial transmission is more significant for B. afzelii than for other Borrelia genospecies. Compared to the strikingly higher prevalence of B. afzelii in nymphs as a result of accumulated infection in the former stage during consecutive feeding events, we found a less markedly higher proportion of B. garinii in nymphs, and there was no difference between nymph infection with B. valaisiana and larva infection with B. valaisiana. This suggests that B. garinii and B. valaisiana spirochetes are transmitted in ticks transstadially with lower efficiency and possibly that their levels decrease during blood meal digestion, which is supported by the fact that there was a strong correlation between the tick volume and the presence of B. valaisiana.

Thus, we concluded that migratory passerine birds, specifically Eurasian blackbirds, song thrushes, and great tits, are competent for transmitting the Lyme disease spirochete B. garinii, and that migratory restlessness may influence the infectivity (9, 35). The Eurasian blackbird, the song thrush, and the great tit commonly inhabit Central Europe, from lowlands up to the upper tree line at 1,400 m above sea level (34). The Eurasian blackbird population density is highest in urban areas, especially in parks. The total number of pairs in the Czech Republic is estimated to 2 to 4 million, and this population shows long-term stability. From the data collected in this study, we estimated that the Czech population of blackbirds may contain as many as 50 x 10⁶ B. garinii-infected I. ricinus subadult ticks. The total population of the song thrush in the Czech Republic is estimated to be 400,000 to 800,000, also shows long-term stability, and carries approximately 2 x 10⁶ B. garinii-infected I. ricinus subadult ticks. The total population of the great tit in the Czech Republic is estimated to be 3 to 6 million and carries approximately 1 x 10⁶ to 2 x 10⁶ B. garinii-infected I. ricinus subadult ticks. Synanthropization processes are obvious in the cases of the Eurasian blackbird, song thrush, and great tit, and thus their roles in the natural cycle of B. garinii may substantially impact the epidemiology of Lyme disease. However, the transstadial transmission of B. garinii spirochetes is a crucial step that influences the risk of infection for humans, and the efficiency of this process in I. ricinus ticks remains to be fully elucidated. The passerine bird migration habits need to be considered in the ecology of Borrelia spirochetes. Eurasian blackbirds from the Czech Republic winter mainly in France and northern Italy. Although only one-third to two-thirds of Czech Eurasian blackbirds migrate seasonally, they potentially carry millions of Lyme disease spirochete-infected ticks. In addition, the entire Czech population of song thrushes winters in France, northern Italy, and the Mediterranean, including Spain and North Africa. The vast majority of great tits reside in the Czech Republic, and a minor part of the population migrates southwest to Germany, Austria, northern Italy, and eastern France (11). Thus, we concluded that passerine birds play different roles in transmitting Lyme neuroborreliosis agents. Eurasian blackbirds, song thrushes, and great tits are transmission-competent hosts of B. garinii and prominent reservoirs of this spirochete due to their high densities in urban habitats and high rates of infestation by I. ricinus. During migration periods, moreover, they may transfer millions of Borrelia-infected ticks and thus establish new endemic foci of Lyme disease in southwest Europe and North Africa.

 
This study was funded by the Ministry of Education, Youth and Sports of the Czech Republic (grant MSM6215712402) and by the Czech Science Foundation (grant 524-08-P139). V.T. received funds from the Slovak Research and Development Agency (grant APVV-51-009205), and E.K. was funded by the Scientific Grant Agency of the Ministry of Education and the Slovak Academy of Sciences (grant 2/7020).

We thank Eva Suchanova for her excellent technical cooperation.

 
* Corresponding author. Mailing address: Department of Biology and Wildlife Diseases, University of Veterinary and Pharmaceutical Sciences, Palackeho 1/3, 612 42 Brno, Czech Republic. Phone: 420 543 136 730. Fax: 420 541 562 631. E-mail: dubska{at}mou.cz

Published ahead of print on 5 December 2008.

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Applied and Environmental Microbiology, February 2009, p. 596-602, Vol. 75, No. 3
0099-2240/09/$08.00+0     doi:10.1128/AEM.01674-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

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