Applied and Environmental Microbiology, May 2003, p . 3008-3010, Vol . 69, No . 5

Three forest sites around Riga, Latvia, were selected . Site 1 (Jaunciems; longitude, 24° 09'; latitude, 57° 03') is peridomestic and close to a suburb of Riga . Site 2 (Kemeri; longitude, 23° 29'; latitude, 56° 56';) is also peridomestic and represents a mixed forest habitat along marshes . Site 3 (Babite; longitude, 23° 48'; latitude, 56° 50') is truly sylvatic . Questing I . ricinus nymphs and adults were collected in May 1999 and 2000 by blanket dragging (13) . The 5S-23S intergenic spacer of B . burgdorferi sensu lato was amplified from ticks by PCR, and the genospecies were determined using DNA probes specific for the whole group of Lyme borreliosis spirochetes as well as for B . burgdorferi sensu stricto, B . afzelii, B . garinii, B . valaisiana, and Borrelia lusitaniae (14, 20) . As B . garinii comprises different ecotypes (12), the ospA gene of randomly selected B . garinii was also amplified, and DNA sequences were determined .

Of the 505 questing I . ricinus ticks analyzed, 141 (28%) were infected with B . burgdorferi sensu lato, with no significant difference between the years (Table 1) . When comparing site and developmental stage of the tick, significant differences in the infection prevalence between site and stage, but not between the years, were observed with a significant site-to-stage interaction (² = 14.5; df = 2; P = 0.0007) . B . burgdorferi sensu lato was more prevalent in nymphs than in adult ticks in site 1 but more prevalent in adult ticks than in nymphs in sites 2 and 3 . The four genospecies B . afzelii, B . garinii, B . valaisiana, and B . burgdorferi sensu stricto were identified . Some amplicons that reacted with the B . burgdorferi sensu lato-specific probe did not react with the genospecies-specific probes and were considered to be untypeable . For B . afzelii, no significant difference in prevalence of infection between nymphs and adults was observed in any site, but the overall infection prevalence of this genospecies was significantly lower in site 3 than in sites 1 and 2 (² = 20.8; df = 2; P = 0.00003) . For B . garinii, both the site and the developmental stage of the tick were significantly different (² = 11.5, df = 1, P = 0.0007; ² = 14.93, df = 2, P = 0.0006; scale parameter = 2.31) . A similar pattern has been observed for B . valaisiana (² = 8.73; df = 1; P = 0.003; for site: ² = 14.6; df = 2; P = 0.0007) . No significant trend was found for B . burgdorferi sensu stricto, as this genospecies was too rare . The overall increase in prevalence of infection of B . burgdorferi sensu lato from nymphs to adults as seen in sites 2 and 3 is, therefore, due to the increase of B . garinii and B . valaisiana . The ospA genes of 12 randomly selected B . garinii samples were sequenced, and 9 alleles were found . Eight alleles were found to represent OspA serotypes other than OspA serotype 4 (3, 6) . One sample derived from a questing nymph collected in site 1 represented OspA serotype 4 (Table 2) .

 
The study shows a high degree of local variation in the distribution of B . burgdorferi sensu lato genospecies . The distances between the sites studied (>40 km) suggest that the populations of small mammals are effectively separated from each other (1, 2) . However, since larger mammals and many bird species have greater activity ranges, it is likely that tick migration occurs between the sites (17, 18) . Therefore, we had expected to find a more homogeneous distribution pattern of B . burgdorferi sensu lato genospecies across the sites . The substantial heterogeneity in the genospecies distribution suggests that strong ecological factors operate which maintain a habitat-specific diversity of the bacteria . Since B . burgdorferi sensu lato is host associated, it is predicted that the structure of the host community differs substantially between the sites and that rodents are dominant in site 1 and ground-feeding birds are dominant in sites 2 and 3 . Preliminary, qualitative observations support this as they indicate that ground-feeding or ground-nesting birds are highly abundant in sites 2 and 3 (A . Bormane, personal observations) . The most frequently observed species include the chaffinch (Fringilla coelebs), robin (Erithacus rubecula), wood warbler (Phylloscopus sibilatrix) and thrush species (Turdus spp.) . Furthermore, most of the sequenced B . garinii samples represent OspA serotypes other than serotype 4, as deduced from their sequences . In vivo and in vitro evidence indicates that such strains are bird associated (3, 9, 12, 14, 15, 16, 21) . Furthermore, larvae of I . ricinus are more likely to feed on small mammals, but nymphs are more likely to feed on certain birds and larger mammals, such as rabbits, hares, or deer (18, 19) . Thus, it is likely that the relative proportion of each life stage of I . ricinus feeding on each host species and the different efficiencies with which the strains of Borrelia are transmitted are the main factors shaping the local genospecies diversity in the developmental stages of questing ticks .

OspA serotype 4 strains of B . garinii are hyperinvasive, and isolates have so far mainly been obtained from human patients . Therefore, it seems to be rare in Europe (6, 8) . The detection of one OspA serotype 4 sample in field-collected ticks in this study may indicate that such strains become more prevalent towards Asia . Unlike the other OspA serotypes of B . garinii, OspA serotype 4 strains are associated with rodents (6, 8), suggesting that their ecology is similar to that of B . afzelii (5) . However, the reason for the low prevalence of OspA serotype 4 strains in Europe remains obscure .

The present study shows that the migration rates of I . ricinus are not sufficient to homogenize the frequency distribution of B . burgdorferi sensu lato genotypes between ecologically distinct sites . We conclude that the structure of the host community determines the population structure of Lyme borreliosis spirochetes in Europe .

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12. Kurtenbach, K., S . De Michelis, S . Etti, S . M . Schäfer, H.-S . Sewell, V . Brade, and P . Kraiczy. 2002 . Host association of Borrelia burgdorferi sensu lato—the key role of host complement . Trends Microbiol . 10:74-79.
13. Kurtenbach, K., H . Kampen, A . Dizij, S . Arndt, H . M . Seitz, U . E . Schaible, and M . M . Simon. 1995 . Infestation of rodents with larval Ixodes ricinus L . (Acari:Ixodidae) is an important factor in the transmission cycle of Borrelia burgdorferi sensu lato in German woodlands . J . Med . Entomol . 32:807-817.
14. Kurtenbach, K., M . Peacey, S . G . T . Rijpkema, A . N . Hoodless, P . A . Nuttall, and S . E . Randolph. 1998 . Differential transmission of the genospecies of Borrelia burgdorferi sensu lato by game birds and small rodents in England . Appl . Environ . Microbiol . 64:1169-1174.
15. Kurtenbach, K., S . M . Schäfer, H.-S . Sewell, M . Peacey, A . Hoodless, P . A . Nuttall, and S . E . Randolph. 2002 . Differential survival of Lyme borreliosis spirochetes in ticks that feed on birds . Infect . Immun . 70:5893-5895.
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