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Applied and Environmental Microbiology, May 2003, p. 3008-3010, Vol. 69, No. 5
0099-2240/03/$08.00+0 DOI: 10.1128/AEM.69.5.3008-3010.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Habitat-Specific Diversity of Borrelia burgdorferi Sensu Lato in Europe, Exemplified by Data from Latvia
Susanne Etti,1 Rosie Hails,2 Stefanie M. Schäfer,1,2,3 Simona De Michelis,3 Henna-Sisko Sewell,1,3 Antra Bormane,4 Michael Donaghy,5 and Klaus Kurtenbach1*
Department of Infectious Disease Epidemiology, Imperial College of Science, Technology and Medicine, St. Mary's Campus, London,1
NERC Centre of Ecology and Hydrology,2
Department of Zoology,3
Department of Clinical Neurology, Radcliffe Infirmary, University of Oxford, Oxford, United Kingdom,5
Public Health Agency of the Ministry of Welfare of the Republic of Latvia, Riga, Latvia4
Received 11 July 2002/
Accepted 20 February 2003

ABSTRACT
The distribution of
Borrelia burgdorferi sensu lato genospecies
in questing
Ixodes ricinus ticks from ecologically distinct
habitats in Latvia was analyzed. A significant variation in
the frequency of the genospecies across sites was observed,
pointing to the importance of the host community in the ecology
of Lyme borreliosis.

INTRODUCTION
Borrelia afzelii,
Borrelia garinii, and
Borrelia valaisiana are the most prevalent genospecies of
Borrelia burgdorferi sensu
lato in questing
Ixodes ricinus ticks from Europe (
4,
5,
7).
Little is known about the scale of the geographical variation
in the distribution of the
B. burgdorferi sensu lato genospecies
and their strains (
10,
11). The genospecies of
B. burgdorferi sensu lato, and some of their variants, are known to be host
associated, which is determined by host complement (
9,
12,
14-
16,
21). Differences in the composition of the host community could,
therefore, lead to a pronounced local variation in the diversity
of
B. burgdorferi sensu lato. However, migration of larger mammals
or birds that carry immature ticks could have adverse effects,
homogenizing the frequency distribution of spirochetal strains
across sites. The aim of this study was to analyze the spatial
variation in the distribution of the
B. burgdorferi sensu lato
genospecies in questing ticks in a region of East Europe.
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).
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TABLE 1. B. burgdorferi sensu lato genospecies in questing I. ricinus ticks collected in the years 1999 and 2000a
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TABLE 2. OspA alleles of 12 B. garinii samples amplified from questing ticks and their relationships with reference strains
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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.

ACKNOWLEDGMENTS
This study was funded by The Wellcome Trust, London, United
Kingdom (grants 050854/Z/97/Z and 054292/Z/98/Z), and the German
Academic Exchange Service (DAAD).

FOOTNOTES
* Corresponding author. Mailing address: Department of Infectious Disease Epidemiology, Imperial College of Science, Technology and Medicine, Norfolk Pl., London W2 1PG, United Kingdom. Phone: 44 20 7594 3787. Fax: 44 20 7594 3693. E-mail:
k.kurtenbach{at}ic.ac.uk.


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Applied and Environmental Microbiology, May 2003, p. 3008-3010, Vol. 69, No. 5
0099-2240/03/$08.00+0 DOI: 10.1128/AEM.69.5.3008-3010.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
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