Email updates

Keep up to date with the latest news and content from Parasites & Vectors and BioMed Central.

Open Access Highly Accessed Research

Babesia spp. and Anaplasma phagocytophilum in questing ticks, ticks parasitizing rodents and the parasitized rodents – Analyzing the host-pathogen-vector interface in a metropolitan area

Cornelia Silaghi1*, Dietlinde Woll2, Dietmar Hamel1, Kurt Pfister1, Monia Mahling3 and Martin Pfeffer2

Author Affiliations

1 Comparative Tropical Medicine and Parasitology, Ludwig-Maximilians-Universität München, Munich, Germany

2 Institute of Animal Hygiene and Veterinary Public Health, University Leipzig, Leipzig, Germany

3 Statistical Consulting Unit, Department of Statistics, Ludwig-Maximilians-Universität München, Munich, Germany

For all author emails, please log on.

Parasites & Vectors 2012, 5:191  doi:10.1186/1756-3305-5-191

The electronic version of this article is the complete one and can be found online at: http://www.parasitesandvectors.com/content/5/1/191


Received:5 April 2012
Accepted:7 August 2012
Published:5 September 2012

© 2012 Silaghi et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

The aims of this study were to evaluate the host-tick-pathogen interface of Babesia spp. and Anaplasma phagocytophilum in restored areas in both questing and host-attached Ixodes ricinus and Dermacentor reticulatus and their small mammalian hosts.

Methods

Questing ticks were collected from 5 sites within the city of Leipzig, Germany, in 2009. Small mammals were trapped at 3 of the 5 sites during 2010 and 2011. DNA extracts of questing and host-attached I. ricinus and D. reticulatus and of several tissue types of small mammals (the majority bank voles and yellow-necked mice), were investigated by PCR followed by sequencing for the occurrence of DNA of Babesia spp. and by real-time PCR for A. phagocytophilum. A selected number of samples positive for A. phagocytophilum were further investigated for variants of the partial 16S rRNA gene. Co-infection with Rickettsia spp. in the questing ticks was additionally investigated.

Results

4.1% of questing I. ricinus ticks, but no D. reticulatus, were positive for Babesia sp. and 8.7% of I. ricinus for A. phagocytophilum. Sequencing revealed B. microti, B. capreoli and Babesia spp. EU1 in Leipzig and sequence analysis of the partial 16S RNA gene of A. phagocytophilum revealed variants either rarely reported in human cases or associated with cervid hosts. The statistical analysis revealed significantly less ticks infected with A. phagocytophilum in a city park in Leipzig as compared to the other sampling sites. A. phagocytophilum-DNA was detected in 2 bank voles, DNA of B. microti in 1 striped field-mouse and of Babesia sp. EU1 in the skin tissue of a mole. Co-infections were detected.

Conclusion

Our results show the involvement of small mammals in the natural endemic cycles of tick-borne pathogens. A more thorough understanding of the interactions of ticks, pathogens and hosts is the essential basis for effective preventive control measures.

Keywords:
Babesia spp; Anaplasma phagocytophilum; Ixodes ricinus; Dermacentor reticulatus; Bank vole; Yellow-necked mouse; Recreational area; Host survey; Vector-host relation

Background

Tick-borne disease agents form complex life cycles involving an arthropod and vertebrate host. The complexity is enhanced by the diversity of hosts in different biotopes, which depends on factors like type of vegetation, climate and/or human influence, such as restoration of former industrial sites which leads to the development of new biotopes. Thus, on the one hand, new habitats for plants and animals including ticks, and on the other hand, new interfaces for humans and nature are created.

In contrast to Ixodes ricinus, the most common tick in Europe, Dermacentor reticulatus has a focal distribution. I. ricinus is an important vector for pathogens such as Borrelia burgdorferi sensu lato and the tick-borne encephalitis virus, but also for so-called emerging pathogens like Anaplasma phagocytophilum and Babesia spp. [1]. D. reticulatus as well serves as a vector for pathogens of human and veterinary concern, e. g. for Rickettsia raoultii (causing Tick-Borne Lymphadenopathy - TIBOLA) and Babesia canis canis (one of the causative agents of canine babesiosis) [2,3]. Canine babesiosis can be a mild to serious disease in dogs, leading even to organ failure and death [2]. In the USA, human babesiosis is primarily caused by B. microti, in Europe by B. divergens and few cases caused by B. microti and Babesia sp. EU1 have been described [4-7]. Whereas ticks as well as cattle and roe deer can serve as a reservoir for B. divergens and Babesia sp. EU1 due to transovarial transmission, B. microti is not transmitted transovarially and small mammals are the reservoir [8-11]. A. phagocytophilum causes granulocytic anaplasmosis in dogs, horses and humans [12]. Transovarial transmission of A. phagocytophilum has not been proven in I. ricinus, and several mammalian species are under discussion as reservoir hosts [12]. Previous infection rates of Babesia spp. and A. phagocytophilum detected in questing I. ricinus in Germany are listed in Tables  1 and 2. Comparison of Babesia prevalences from previous studies shows that infection rates are generally lower, by a factor of 5 to 10, in the South of Germany (Table 1). Both babesiosis and granulocytic anaplasmosis are zoonotic diseases with a natural enzootic cycle involving the agent itself, the tick and the host. For both tick species and disease agents, humans can be considered accidental hosts acquiring the respective infection during interaction with the natural enzootic cycle. In this context, recreationally used urban and suburban green areas are intriguing habitats due to the strong influence that humans exert on them and thus, these areas should be given special consideration with regard to host-pathogen-vector interactions. We have previously shown high prevalences of spotted fever group rickettsiae in questing I. ricinus and D. reticulatus in recreationally used renatured areas [13]. The aims of the present study were the evaluation of the tick-host-pathogen interface in recreational areas in Leipzig, Germany. Therefore we attempted (i) to identify Babesia infections in questing and host-attached I. ricinus and D. reticulatus populations, (ii) to identify the infection rate with A. phagocytophilum in questing and host-attached I. ricinus, (iii) to identify possible small mammalian reservoir hosts in the investigated areas and (iv) to evaluate co-infections with Rickettsia spp. in the same questing ticks which had been investigated for Rickettsia spp. in a previous study [13].

Table 1. Previously identified infection rates of Babesia spp. in questing Ixodes ricinus in Germany

Table 2. Previously identified infection rates with Anaplasma phagocytophilum in questing Ixodes ricinus in Germany

Methods

Sampling sites and questing tick collection

Questing ticks were collected with the flagging method in 5 sites (E-I) in Leipzig (Saxony, Germany), all located within the city or close to suburban residential areas (Figure 1). Sites E-G are part of the “Leipziger Neuseenland” ( http://www.leipzigerneuseenland.de/ webcite), a restored area of former pit holes of a brown coal surface mining site. Brown coal was mined till 1990 and flooding of the area started in 1993. When fully flooded, the area will contain 18 lakes. Ticks were collected around Lake Cospuden (Sites E-G; fully flooded since 2000; 436 ha in size). Site E is located on the Eastern, Site F on the Northern and site G on the Western shore. The area is popular for hiking, jogging, cycling and dog walking.

thumbnailFigure 1 . Sampling sites in the Saarland, Bavaria and sites E-I in the city area of Leipzig are indicated with red rings; the * marks the site where additional animals were caught by a cat.

Further ticks were collected in the recreational city park “Lößnig-Dölitz” (site H; ( http://www.leipzig.de/de/buerger/freizeit/leipzig/parks/park_loessnig/ webcite), containing several small ponds. This park is located in an area which was used for underground brown coal mining up to 1959 and was also created by renaturation in the 1980s . To the North it borders to the city of Leipzig and to the South, where a renatured waste disposal mountain is located, it merges directly into forest areas. Site I is located in one of the largest riparian forest areas in Germany, within the city of Leipzig ( http://www.leipziger-auwald.de webcite). A 42 ha game park ( http://www.leipzig.de/de/buerger/freizeit/leipzig/parks/wildpark/wissen/ webcite) with about 250 animals (amongst them roe deer, red deer, fallow deer, wild boar, mustelids and several bird species) is situated within this forest.

For comparison, one site in Bavaria, located 20 km north of the city of Munich in a riparian forest on the Eastern banks of the river Isar was chosen. The area is popular for hiking, biking and dog walking.

Ticks were collected in April and September/October 2009 and were stored as described [13]. Further I. ricinus ticks were available from a previous study [14] from an area in the Saarland of altogether 150 km2 west of Saarbrücken (collection from March to September 2008). That previous study was concerned primarily with D. reticulatus and the I. ricinus were collected but kept aside.

Trapping of small mammals

Small mammals were trapped at 3 out of 5 sites in Leipzig with Sherman live traps baited with apple pieces (August 2010 sites E and I; October 2010 / March 2011 site H; June 2011 sites E, H, I). Usually twenty traps per site were placed along natural structures or directly in front of holes in the ground. The number of traps per night never exceeded 75 and they all were checked twice daily. Captured animals were anesthetized with CO2 exposure and killed humanely according to the German Animal Protection Act after blood was drawn by heart puncture. After recording trapping site, species, gender, and health status, rodents were dissected under BSL-2 conditions in the laboratory and stored at −80°C. Ticks were collected from the small mammals and stored at −80°C separately for each individual animal until species identification.

DNA extraction

Species identification of ticks was carried out with standard taxonomic keys [15-17] and DNA was extracted from the ticks as described [13] and from tissues and body liquids with the Qiagen DNA Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer’s instruction for either animal tissue or blood. Tissue lysis was carried out over night at 56°C in a thermomixer (Eppendorf, Hamburg, Germany). Quality and quantity of extracted DNA were tested with a spectrophotometer (NanoDrop ND-1000, Erlangen, Germany).

PCR methods

Detection of Babesia spp.-DNA in all tick and small mammal samples was carried out with a conventional PCR targeting the 18S rRNA gene followed by gel electrophoresis as described [18,19]. Detection of A. phagocytophilum was carried out in I. ricinus ticks only and in the small mammals with a real-time PCR as described [20,21]. For a subsample of the A. phagocytophilum positive samples, a nested PCR targeting a 497 bp region of the 16S rRNA gene was performed as previously described [22,23]. Genomic DNA from A. phagocytophilum cell culture and from B. microti from continuous culture in BALB/c mice (courtesy of Prof. Dr. E. Siński) were used as positive controls and molecular grade water as negative controls and were included in each PCR run.

Sequence analysis

PCR products of the partial Babesia spp. 18S rRNA gene and of the partial 16S rRNA gene of A. phagocytophilum were purified with the QIAquick PCR Purification Kit (Qiagen, Hilden, Germany) and sequenced bidirectionally at Eurofins MWG Operon (Martinsried, Germany). The analysis of the obtained sequences was performed as described [24].

Co-infections and statistical analysis of questing tick results

Exact confidence intervals of the prevalences (CI 95%) were computed with the Clopper and Pearson method. For pooled samples the confidence interval was calculated for the minimal infection, taking into account the nymphal pools and assuming that only one of the nymphs in one pool was infected.

Differences in the infection rates with Anaplasma phagocytophilum, Babesia spp. and Rickettsia spp. (data in the same questing ticks from a previous study [13]) between sex of ticks, collection sites and region were computed with logistic regression (generalized linear models with binominal distribution and logit link) using R 2.13.1 [25]. Separate models had to be computed to investigate the effect of collection sites and region. Moreover, separate models were used for the two species. However, a variable containing the information about the developmental stage and the sex of ticks was included as covariate in all models. P-values <0.05 were regarded as statistically significant. Co-infections of the questing ticks with Rickettsia spp. were investigated as data on this pathogen in the same ticks was available from a previous study [13]. As the trapping of small mammals took place at irregular intervals, no statistical analysis was attempted for the infestations of small mammals with ticks.

GenBank accession numbers

Sequences from this study were deposited in GenBank [accession nos. B. microti: JQ886033- JQ886058, Babesia spp. EU1: JQ886024-JQ886032, B. divergens: JQ886059-JQ886060, B. capreoli: JQ886061, Hepatozoon spp.: JQ886023, Sarcocystis spp.: JQ886022, A. phagocytophilum: JQ886009 - JQ886021].

Results

Questing tick collection

A total of 1.256 I. ricinus (506 females, 519 males, 231 nymphs) and 814 D. reticulatus (503 females, 311 males) were collected in recreational areas in Leipzig (Sites E-I; Table 3). At the comparative site in Bavaria, 331 I. ricinus (109 females, 159 males, 63 nymphs) and 153 D. reticulatus (102 females, 51 males) were collected. From the Saarland, 115 I. ricinus (43 females, 36 males, 36 nymphs) were available [13,14]. DNA was successfully extracted from 804 D. reticulatus in Leipzig and 135 D. reticulatus in Bavaria. DNA from only a part of the I. ricinus was extracted (for detailed numbers, see Table 4).

Table 3. Results of the questing tick collection at recreational areas of Leipzig in spring and autumn 2009

Table 4. Infection rates with Babesia spp. and Anaplasma phagocytophilum in ticks from recreational areas within the city limits of Leipzig, Saxony and at comparative sites in Bavaria and the Saarland

Small mammals

Overall, 72 animals of 4 species were trapped: bank vole (Myodes glareolus; n = 36), yellow-necked mouse (Apodemus flavicollis; n = 32), and striped field mouse (A. agrarius; n = 3). One common shrew (Sorex araneus) was found dead in a trap. 21 animals were trapped at site E (16 in 2010; 5 in 2011; 14 bank voles, 6 yellow-necked mice, 1 common shrew), 21 animals at site I (17 in 2010; 4 in 2011; 14 bank voles, 7 yellow-necked mice), and 30 animals at site H (14 in 2010, 16 in 2011; 8 bank voles, 19 yellow-necked mice, 3 striped field mice). The average trapping success during the nine trapping days was 12% (2.5%-19%). A further 8 animals of three additional species captured by a cat at a different location within the renatured brown coal surface mining sites were investigated (* in Figure  1): water voles (Arvicola terrestris, n = 3); shrews (Crocidura russula, n = 4) and a common mole (Talpa europaea, n = 1). DNA from blood (n = 31), transudates (n = 80), spleens (n = 79), kidneys (n = 80) and ears (n = 80) were used for the molecular analysis in this study.

Tick infestation on small mammals

Overall, 365 ticks were collected from 50 of the 80 small mammals. The infested mammals were 15 out of 31 females and 35 out of 49 males. Species identification revealed 232 I. ricinus (44 nymphs, 188 larvae) and 117 D. reticulatus (112 nymphs, 5 larvae) (Table 5). One I. trianguliceps larva was identified on a bank vole at site I. A further 12 ticks were identified as Ixodes spp., 1 as Dermacentor spp. and for 2, identification was not possible due to damage. Ixodes spp. were obtained on 6 small mammal species (except S. araneus) at all 3 trapping sites during all trapping months (Table 6). Comparable numbers of them had tick infestation (slightly more in yellow-necked mice), and of those, comparable numbers were infested with I. ricinus larvae and nymphs with comparable median numbers of ticks (Table 6). In contrast, D. reticulatus were obtained on bank voles only (apart from 1 nymph on one yellow-necked mouse), exclusively during the month of August and only at sites E and I, even though at the latter no questing D. reticulatus had been detected (Table 3). The median of D. reticulatus nymphs was higher than that of I. ricinus larvae and nymphs on bank voles. 95.4% (n = 21) out of the 22 tick-infested yellow-necked mice were infested with I. ricinus larvae, 36.4% with I. ricinus nymphs and 4.5% (1 individual) with a D. reticulatus nymph. 80.1% out of the 21 tick-infested bank voles were infested with I. ricinus larvae, 28.6% with I. ricinus nymphs, 4.8% with D. reticulatus larvae and 62% with D. reticulatus nymphs.

Table 5. Small mammals trapped at recreational areas of Leipzig during 2010 and 2011: PCR results of the investigations for Babesia spp. and Anaplasma phagocytophilum and their tick infestationa

Table 6. Small mammals trapped at recreational areas of Leipzig during 2010 and 2011: detailed results of their tick infestation and results of the PCR screening of the ticks for Babesia spp. and Anaplasma phagocytophilum*

Co-infestation and thus co-feeding of I. ricinus nymphs and larvae was observed on 7 yellow-necked mice, 8 bank voles, 1 striped field mouse and 1 shrew (C. russula). One of those yellow-necked mice and 5 bank voles were additionally infested with D. reticulatus nymphs and one bank vole with D. reticulatus larvae. 3 bank voles carried I. ricinus larvae and D. reticulatus nymphs and 1 bank vole I. ricinus larvae and an I. trianguliceps larva. The rest were single infestations of I. ricinus larvae (14 yellow-necked mice, 6 bank voles, 1 striped field mouse, 1 great white-toothed shrew, 1 common mole), I. ricinus nymphs (1 yellow-necked mouse, 2 European water voles) and D. reticulatus nymphs (4 bank voles). DNA was extracted individually from all host-attached nymphs.

PCR analysis for Babesia spp

Questing ticks

Overall, 4.1% of I. ricinus (22/539; 95% CI: 2.6 to 6.1) were positive for DNA of Babesia spp. in Leipzig (Table 4). Average infection rates were 3.4% (5/148; 95% CI: 1.1 to 7.7) at sites E-G (Lake Cospuden), 8.7% (15/172; 95% CI: 5.0 to 14.0) at site H and 0.9% (2/219 95% CI: 0.1 to 3.5) at site I. In Bavaria, 5.5% of I. ricinus (7/128; 95% CI: 2.2 to 10.9) were positive, and in the Saarland, 6.1% (7/115; 95% CI 2.5 to 12.1). No statistically significant differences were observed between sites or developmental stages. Sequencing revealed B. microti (n = 3) and Babesia sp. EU1 (n = 2) at site E, B. microti (n = 14) and B. capreoli (n = 1) at site H and B. microti (n = 1) and Babesia spp. EU1 (n = 1) at site I. In questing ticks in Bavaria, the detected species were B. microti (n = 3), B. divergens (n = 2) and Babesia sp. EU1 (n = 2) and in the Saarland B. microti (n = 4), Babesia spp. (n = 2) and Babesia sp. EU1 (n = 1). All 939 questing adult D. reticulatus, for which DNA was successfully extracted, were negative for Babesia-DNA.

Small mammals and host-attached ticks

The Babesia spp.-PCR was positive for the kidney and transudate of one striped field mouse from site H (B. microti), for the ear tissue of the European mole (Babesia sp. EU1) and for the transudates of a bank vole and a shrew from site E (Table 5). The latter two PCR-products revealed greatest similarity (99%) to Hepatozoon spp. BV1 [GenBank AY600626] for the bank vole and to Sarcocystis spp. isolate 5 [GenBank AF513487] for the shrew. The blood and spleens were all negative.

In two host-attached I. ricinus nymphs DNA of Babesia sp. EU1 was detected, the host-attached larvae were all negative (Table 6). The juvenile stages of D. reticulatus from small mammals were negative for DNA of Babesia spp.

Sequence analysis

All 495 bp sequences from B. microti were 100% similar amongst each other and 100% similar to B. microti from M. glareolus (Germany), I. ricinus (Belgium, Switzerland and Germany) and also from the recently published first European case of human babesiosis due to B. microti in Germany (isolate Jena/Germany) [GenBank: AB085191, AF231349, AY144692, GQ856653] [5]. For one B. microti, only 465 bp could be evaluated. The 409 bp sequences of Babesia sp. EU1 were 100% identical to each other and to Babesia sp. EU1 from I. ricinus (Belgium), from I. persulcatus (Russia) and from roe deer (France and Austria) [GenBank: JF776414, GQ856657, HQ830266, GU734773, JN543171]. The sequence from the nymph collected from A. flavicollis differed in 1 nt position. The B. capreoli sequence (468 bp) from site H was 100% identical in the amplified part to the recently described B. capreoli including two of the 3 B. capreoli typical nucleotide (nt) positions at 631 (G) and 663 (T) of the 18S rRNA gene [GenBank: FJ944828] [26]. For B. divergens sequences from Bavaria 463 bp and 325 bp were available and they were 100% identical to B. divergens with nucleotides AA at positions 631 and 663 [FJ944826] as described [26].

PCR analysis for Anaplasma phagocytophilum

Questing ticks

A total of 8.7% (47/539; 95% CI: 6.5 to 11.4) of I. ricinus were positive for A. phagocytophilum in Leipzig (Table 4). Average prevalences were 8.1% (12/148; 95% CI: 4.3 to 13.7) at site E-G (Lake Cospuden), 2.3% (4/172; 95% CI: 0.6 to 5.8) at site H and 14.2% (31/219; 95% CI: 9.8 to 19.4) at site I. Nymphs were significantly less often infected than adult ticks (p < 0.05) (Table 4). Significantly less I. ricinus were infected with A. phagocytophilum at site H compared to the site E in Leipzig (p = 0.01). A total of 9.4% (12/128; 95% CI: 4.9 to 15.8) and 17.4% (20/115; 95% CI for the minimal infection rate: 11.0-25.6) I. ricinus were also positive for A. phagocytophilum-DNA in Bavaria and the Saarland, respectively (Table 4). Looking at the regions under investigation, there was no difference in the overall infection rate between Bavaria and Leipzig, but the ticks in the Saarland were significantly more often infected (p = 0.01).

Small mammals and host-attached ticks

All blood and tissue samples of the small mammals were negative for A. phagocytophilum-DNA, but it was detected in the transudates of 2 bank voles from site E (Table 5). From one of them the kidney sample was also positive. One I. ricinus nymph collected from a bank vole from site E and from a yellow-necked mouse from site I were positive for A. phagocytophilum, all other host-attached ticks were negative (Table 6).

Sequence analysis

Sequencing of 13 partial 16S rRNA gene sequences from questing ticks revealed 4 gene variants. Variant “A” was detected at site I (n = 7) and in the Saarland (n = 1), variant “S” in Bavaria (n = 1), variant “X” at site E (n = 1) and I (n = 1) and variant “Y” in the Saarland (n = 2). This nomenclature is not official but has been used previously for comparison of 16S rRNA variants [21,23,24]. Variant “A” has previously been detected in ticks, hedgehogs, dogs, horses, a cat and a human patient [GenBank: JF893935, FJ829748, HM138366] [24,27-31]. Variant “S” has previously been detected for example in horses, dogs, roe deer, red deer and ibex [GenBank: JF893934, FJ829790, FJ812391-FJ812397] [23,24,28]. The potentially apathogenic variants “X” and “Y” [GenBank: FJ538288, FJ538289, FJ812405, FJ812406] seem to be typical for roe deer and goats [23,32].

Co-infections

Co-infections of Babesia spp. and A. phagocytophilum were not detected in 539 questing I. ricinus in Leipzig and in 128 questing I. ricinus in Bavaria, whereas in the Saarland 1/115 (0.9%; one adult male) was infected with B. microti and A. phagocytophilum.

With regard to co-infections and differences in prevalence patterns we also statistically analysed data from a previous study in the same questing ticks which were investigated for Rickettsia spp. (R. helvetica in I. ricinus and R. raoultii in D. reticulatus) [13]. In Leipzig, 7/539 I. ricinus (1.3%; 3 adult male and one adult female from site I; one adult male and two females from site E) were coinfected with R. helvetica and A. phagocytophilum, and 1/539 (0.2%; one adult female) from site H was coinfected with B. microti and R. helvetica. In Bavaria, 1/128 I. ricinus (0.8%; one adult male) was coinfected with R. helvetica and A. phagocytophilum. In the Saarland, altogether 6 I. ricinus samples (5.2%; 4 males, 1 female, 1 nymphal pool containing two nymphs) were coinfected with R. helvetica and A. phagocytophilum, one adult female with R. helvetica and B. microti and one nymph pool (containing two nymphs) with Babesia spp. and R. helvetica. Triple infections were not detected [13]. The comparison of the single collection sites amongst each other revealed for I. ricinus a significant difference in the infection rates with R. helvetica between site E and I in Leipzig (p = 0.02). For D. reticulatus, the collection sites in the Saarland and Bavaria, as well as the site G revealed a lower prevalence compared to site E which was used as a reference site for the analysis. The comparison of the three regions showed significantly higher prevalences in I. ricinus in comparison to Leipzig for Bavaria (p = 0.001) and the Saarland (p < 0.001), whereas for D. reticulatus, the infection was significantly higher in Leipzig compared to Bavaria and the Saarland (for both p < 0.001).

Discussion

To investigate the host-pathogen-vector interface in urban recreational areas in the city of Leipzig, Germany, questing I. ricinus and D. reticulatus ticks, small mammals and the ticks infesting them were screened by molecular methods for the presence of zoonotic Babesia spp. and A. phagocytophilum. Additionally, questing ticks from Bavaria and the Saarland were collected for comparative purposes. The questing tick collection revealed a coexistence of I. ricinus and D. reticulatus in recreationally used renatured areas in Leipzig. Reports on the existence of D. reticulatus in Eastern Germany date back to the first half of the 20th century [33,34], but recently reports about their abundance in new or renewed habitats are accumulating [13,35-39]. Climatic change or changes in landscape structure or land use are being discussed for its geographical expansion and our findings in a newly created renatured area adds evidence to this [13,40].

PCR results for Babesia spp

Average detection rates in questing I. ricinus ticks of DNA of Babesia spp. were 4.1% in Leipzig, 5.5% in Bavaria and 6.1% the Saarland) and the species B. capreoli, B. divergens, B. microti, Babesia sp. EU1 and Babesia spp. were identified by sequencing. We detected DNA of B. microti also in the kidney of only one A. agrarius but not in its other tissues. Previous PCR-detections of B. microti in small mammals in Europe ranged from 1.6% to 42% in microtine voles and from 1% to 11.8% in A. flavicollis[41-45] and generally voles seem to be infected more often with B. microti than mice [46]. Thus, voles and shrews, but not mice are considered as reservoirs [43]. These small mammalian species all live in urban environments, but the abundance of Apodemus spp. is considered to be higher than that of M. glareolus[46,47]. As expected, at site H in the present study (an urban park) more Apodemus spp. were trapped than voles (this was the opposite for sites E and I), nonetheless in questing I. ricinus ticks a high prevalence of B. microti was found at site H. This is a rather surprising result and shows that further systematic investigations in this geographic area are needed, but also that the choice of tissue for investigation has a strong influence on the outcome of a study.

The presence of Babesia sp. EU1 was shown for the first time in questing ticks in the Middle of Germany in the present study. The mammalian reservoir for Babesia sp. EU1 is unknown, but roe deer has also been suggested [8]. This may explain the predominance of this Babesia species around Lake Cospuden where roe deer has found a new habitat. We detected Babesia sp. EU1-DNA in two nymphs collected from rodents and in the ear tissue of a common mole, which is the first detection of this Babesia species in this insectivore. Whether this is a rare coincidence or whether T. europaea, or other rodents and insectivores, play a role in the life cycle of Babesia sp. EU1 remains to be investigated. Apicomplexan parasites as well as trypanosomes have been shown in the red blood cells of the common mole before [48,49]. Isolation of the tick-borne encephalitis virus was achieved from a common mole, showing that this insectivore species may indeed play a role in the life cycle of some tick-borne pathogens [50]. It is interesting in this context that we are not aware of any description of Babesia spp. other than B. microti in small mammals thus far. We cannot tell whether this is because other investigators specifically look for B. microti or do not differentiate the Babesia spp., but the Babesia sp. EU1 detection in the European mole is a new and interesting finding in this regard. The detection of three zoonotic Babesia species in actively questing I. ricinus in recreational areas in Germany has considerable public health implications even though, in Europe, human babesiosis occurs almost exclusively in splenectomised or otherwise immunocompromised individuals [4,11].

In the present study, no evidence was found in the investigated D. reticulatus populations in Leipzig and Bavaria for infection with B. canis even though reports on autochthonous cases of canine babesiosis occur occasionally in Germany [51]. Discussion is ongoing that the import of persistently infected dogs may provide a source and could contribute to the creation of new endemic cycles in previously Babesia-free D. reticulatus populations [52].

It is noteworthy that both a Hepatozoon spp. and a Sarcocystis spp. were identified in a bank vole and a shrew due to two reasons, respectively. Firstly, this shows that in an apparently genus-specific PCR other genera of closely related protozoa may also be amplified and highlights the importance of sequencing in such screenings. In our particular case, this would have resulted in doubling the prevalence of Babesia spp. in the small mammals investigated. Secondly and even more importantly, it also shows that rodents and insectivores are hosts to a very large parasitical and bacterial fauna.

PCR results for Anaplasma phagocytophilum

The average prevalence of A. phagocytophilum in Ixodes ricinus in the investigated areas in Leipzig (8.7%) was considerably higher than most previously detected average infection rates in Germany (see Table 2) and was most similar to average prevalences recorded from city parks in Bavaria [29,53]. The presence of a different reservoir host had been hypothesised as a reason for this in areas with a city park character. However, in Leipzig, a city park (Site H) had the lowest prevalence (2.3%). The highest prevalence (14.2%) was observed close to the game park (site I). The presence of cervids might lead to a higher prevalence of A. phagocytophilum in ticks, as for example roe deer is frequently infested with ticks and is discussed as a potential reservoir host [12,54]. Similarly high prevalences of up to 17.1% have been detected in Norway in sites with a high density of wild cervids [55]. Surprisingly, and also on the contrary to the “city park” hypothesis, an infection rate of 9.4% was recognized in the alluvial forest north of Munich along the river Isar. The prevalence in an earlier study in the same region was remarkably lower (females 4.1%, males 0.75%) [29]. The difference in prevalence rates may also be based on a year-to-year fluctuation, as has been shown in other studies [56,57]. For Borrelia spp., a correlation was observed between peak abundance of rodent populations and an increase of infection in ticks in following years [58].

Significantly less nymphs than adults were infected with A. phagocytophilum in the present study. This result is well explained by the lack of transovarial transmission of A. phagocytophilum and has been shown in previous studies as well [29,53]. Apart from roe deer, small mammals have been suggested as reservoir hosts for A. phagocytophilum. In the present study, transudates of two bank voles were positive for DNA of A. phagocytophilum as well as one kidney sample. In the U.K., where A. phagocytophilum was found in field voles, bank voles and wood mice, the infection rate was generally higher in voles. Higher infection was further observed in sites with occurrence of I. trianguliceps. Rodents were not or less infected in sites where only I. ricinus occurred [59,60]. A separate endemic niche cycle involving voles and I. trianguliceps was suggested for A. phagocytophilum[59-61]. When individual voles were investigated several times during one study, A. phagocytophilum infection seemed short-lived whereas rodents were persistently infected with B. microti[45,59]. Only voles were infected with A. phagocytophilum in this study which coincides with this hypothesis. This could be the reason for the low prevalence with A. phagocytophilum in this study.

Larvae are free of A. phagocytophilum as no transovarial transmission occurs and adult ticks do not generally feed on rodents. Consequently, larvae need to acquire the infection from rodents and following this, nymphs have to give it back to the rodents to keep up the endemic cycle. Keeping in mind that small rodents are themselves short-lived animals and that the infection with A. phagocytophilum is transient, the question has to be raised if they would provide a suitable reservoir for keeping an endemic cycle. We observed a high percentage of co-feeding ticks on the trapped small mammals and similar to Borrelia spp. or the TBE-virus, this could be part of the endemic cycle [62,63].

Anaplasma phagocytophilum 16S rRNA gene variants

Four genetic variants of the partial 16S rRNA of A. phagocytophilum were detected in questing ticks in this study, all of which have been previously described. Interestingly, the human pathogenic prototype variant “B” [equalling GenBank U02521 in the amplified part] was not detected. About one-fourth of the A. phagocytophilum positive samples were sequenced and the variant “A” was the most prevalent variant (8 of 13). This variant is very common in ticks in Germany and has also been detected as the most common variant in hedgehogs [29,30,53]. Variant “A” is also known to cause granulocytic anaplasmosis in humans, horses and dogs, but apparently to a lesser extent [24,27,28,31]. Variant “S” has been previously detected in clinical cases of dogs and horses [24,28]. Variants “X” and “Y” seem to be typical for caprines and cervids, and have also been previously detected in ticks [23,27,32,53]. Due to the low occurrence of seemingly pathogenic variants, the high prevalences and the resulting actual risk for human beings to develop clinical disease has to be carefully evaluated. In the USA, human granulocytic anaplasmosis (HGA) is the second most important tick-borne disease after Lyme Borreliosis, whereas in Europe only about 70 cases have been reported [64]. Even though human cases have to date not been reported in Germany, seroprevalence studies have shown that the human population is exposed to the agent [65,66] and granulocytic anaplasmosis cases have been reported from dogs and horses [67-69]. Around Germany, HGA cases have been reported, for example from Slovenia, Austria and Poland [70-72].

Co-infections

The rates of co-infections detected in this study were less than 1% of investigated ticks and similar to previously detected ones [18]. The lowest co-infection rate seems to occur between Babesia spp. and Rickettsia spp., and the highest between Rickettsia spp. and A. phagocytophilum[18]. The co-infection rate of Rickettsia spp. and A. phagocytophilum was especially high in the Saarland (5.2%), and can be lead back to the fact that 17.4% I. ricinus ticks were infected with A. phagocytophilum. Co-infections between the pathogens investigated in this study have also been detected in other European countries [73-80].

Tick infestation on small mammals

Developmental stages of D. reticulatus were observed almost exclusively on bank voles. Similar results were obtained previously [62,81]. Furthermore, they were only observed during trapping in the month of August. This reflects the seasonal dynamics of this tick species, with developmental stages being active during the months of July and August [16], whereas adults have their activity peak in spring and autumn [15]. The developmental stages have an endophilic life cycle adapted to their small mammalian hosts and are therefore not obtained by the flagging method.

Co-feeding of both developmental stages of I. ricinus and additionally co-infestation with both hard tick species was frequently observed, especially in bank voles. This finding highlights the importance of rodent species in the developmental cycles of ticks and consequently for tick-borne pathogens. Larvae and nymphs of I. ricinus originate most probably from different tick generations, based on the life cycle of this tick species, whereas Dermacentor spp. can complete its entire life cycle within one year [16] which may result in different dynamics of the involved pathogens. I. ricinus is the main vector in Europe for A. phagocytophilum, R. helvetica and the Babesia species detected in this study. Even though I. trianguliceps may also act as a vector for A. phagocytophilum, its occurrence is relatively rare in Central and Eastern Europe, and therefore its importance is less apparent [59]. Furthermore, I. trianguliceps rarely feeds on humans whereas this is regularly the case for I. ricinus. In contrast, the distribution of D. reticulatus is highly focally. Its developmental stages do not attack humans, and the adult stages only rarely do. Therefore the public health risk of I. ricinus-borne pathogens has to be considered way higher by comparison, especially as co-infections with several pathogens can be detected. However, D. reticulatus is a tick frequently observed on dogs, thus posing a health threat for the canine population.

Conclusion

In conclusion, three zoonotic Babesia species and A. phagocytophilum as well as co-infections between the two and with Rickettsia spp. were detected in three areas of Germany – Leipzig, north of Munich and the Saarland. As the areas under investigation are recreational, the detection of A. phagocytophilum has both implications for human and animal health and the detection of the zoonotic Babesia spp. is of importance for humans. Although we provide new data regarding the distribution patterns of the described pathogens, we still lack a thorough understanding of the epidemiology and interplay of the ticks, their feeding sources and pathogens. In particular, knowledge about the role of co-feeding in the transmission cycles, as well as the specific hosts and potential reservoir animals in these areas, is the essential basis for the development of effective preventive control measures.

Competing interests

The authors declare that they have no conflict of interest of any kind.

Authors’ contributions

CS and MP conceived the idea and design of the study. CS, DW, MP and DH carried out field and laboratory work. CS analysed the data and wrote the manuscript. MM performed the statistical analysis. MP and KP critically revised the manuscript. All authors read and approved the final version of the manuscript.

Acknowledgments

The authors thank Claudia Thiel for excellent technical assistance, Dr. Matthias Kiefer for advice on the identification of developmental stages of Dermacentor spp., and Prof. Dr. Edward Siński (Department of Parasitology, Faculty of Biology, Warsaw, Poland) for providing the positive control of B. microti (from BALB/c mice – King’s College strain from S. Randolph).

References

  1. Stanek G: Pandora's Box: pathogens in Ixodes ricinus ticks in Central Europe.

    Wien Klin Wochenschr 2009, 121:673-683. PubMed Abstract | Publisher Full Text OpenURL

  2. Irwin PJ: Canine babesiosis: from molecular taxonomy to control.

    Parasit Vectors 2009, 2(Suppl 1):S4. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  3. Parola P, Rovery C, Rolain JM, Brouqui P, Davoust B, Raoult D: Rickettsia slovaca and R. raoultii in tick-borne Rickettsioses.

    Emerg Infect Dis 2009, 15:1105-1108. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  4. Gray J, Zintl A, Hildebrandt A, Hunfeld KP, Weiss L: Zoonotic babesiosis: Overview of the disease and novel aspects of pathogen identity.

    Ticks Tick-borne Dis 2010, 1:3-10. PubMed Abstract | Publisher Full Text OpenURL

  5. Hildebrandt A, Hunfeld KP, Baier M, Krumbholz A, Sachse S, Lorenzen T, Kiehntopf M, Fricke HJ, Straube E: First confirmed autochthonous case of human Babesia microti infection in Europe.

    Eur J Clin Microbiol Infect Dis 2007, 26:595-601. PubMed Abstract | Publisher Full Text OpenURL

  6. Herwaldt BL, Caccio S, Gherlinzoni F, Aspöck H, Slemenda SB, Piccaluga P, Martinelli G, Edelhofer R, Hollenstein U, Poletti G, et al.: Molecular characterization of a non-Babesia divergens organism causing zoonotic babesiosis in Europe.

    Emerg Infect Dis 2003, 9:942-948. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  7. Häselbarth K, Tenter AM, Brade V, Krieger G, Hunfeld KP: First case of human babesiosis in Germany - Clinical presentation and molecular characterisation of the pathogen.

    Int J Med Microbiol 2007, 297:197-204. PubMed Abstract | Publisher Full Text OpenURL

  8. Bonnet S, Jouglin M, L'Hostis M, Chauvin A: Babesia sp. EU1 from roe deer and transmission within Ixodes ricinus.

    Emerg Infect Dis 2007, 13:1208-1210. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  9. Bonnet S, Brisseau N, Hermouet A, Jouglin M, Chauvin A: Experimental in vitro transmission of Babesia sp. (EU1) by Ixodes ricinus.

    Vet Res 2009, 40:21. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  10. Bonnet S, Jouglin M, Malandrin L, Becker C, Agoulon A, L'Hostis M, Chauvin A: Transstadial and transovarial persistence of Babesia divergens DNA in Ixodes ricinus ticks fed on infected blood in a new skin-feeding technique.

    Parasitology 2007, 134:197-207. PubMed Abstract | Publisher Full Text OpenURL

  11. Homer MJ, Aguilar-Delfin I, Telford SR 3rd, Krause PJ, Persing DH: Babesiosis.

    Clin Microbiol Rev 2000, 13:451-469. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  12. Woldehiwet Z: The natural history of Anaplasma phagocytophilum.

    Veterinary Parasitolology 2010, 167:108-122. Publisher Full Text OpenURL

  13. Silaghi C, Hamel D, Thiel C, Pfister K, Pfeffer M: Spotted fever group rickettsiae in ticks, Germany.

    Emerg Infect Dis 2011, 17:890-892. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  14. Beelitz P, Schumacher S, Marholdt F, Pfister K, Silaghi C: Untersuchungen zur Prävalenz von Babesia canis canis in Auwaldzecken (Dermacentor reticulatus) im Saarland.

    Berl Munch Tierarztl Wochenschr 2012, 125:168-171. PubMed Abstract OpenURL

  15. Hillyard PD: Ticks of North-West Europe. The Dorset Press, Dorchester; 1996. OpenURL

  16. Arthur DR: Ticks - A monograph of the Ixodoidea. Cambridge University Press, London, UK; 1960. OpenURL

  17. Rosicky B, Minar J, Cerny V, Daniel M, Dusbábek F, Gregor F, Hájkova Z, Honzakova F: Cizopasní clenovci skotu na pastvinách.

    Academia,Praha 1983, 167pp. OpenURL

  18. Schorn S, Pfister K, Reulen H, Mahling M, Silaghi C: Occurrence of Babesia spp., Rickettsia spp. and Bartonella spp. in Ixodes ricinus in Bavarian public parks, Germany.

    Parasites & Vectors 2011, 4:135. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  19. Casati S, Sager H, Gern L, Piffaretti JC: Presence of potentially pathogenic Babesia sp. for human in Ixodes ricinus in Switzerland.

    Ann Agric Environ Med 2006, 13:65-70. PubMed Abstract | Publisher Full Text OpenURL

  20. Courtney JW, Kostelnik LM, Zeidner NS, Massung RF: Multiplex real-time PCR for detection of Anaplasma phagocytophilum and Borrelia burgdorferi.

    J Clin Microbiol 2004, 42:3164-3168. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  21. Silaghi C, Kauffmann M, Passos LMF, Pfister K, Zweygarth E: Isolation, propagation and preliminary characterisation of Anaplasma phagocytophilum from roe deer (Capreolus capreolus) in the tick cell line IDE8.

    Ticks and Tick-borne Diseases 2011, 2:204-208. PubMed Abstract | Publisher Full Text OpenURL

  22. Massung RF, Slater K, Owens JH, Nicholson WL, Mather TN, Solberg VB, Olson JG: Nested PCR assay for detection of granulocytic ehrlichiae.

    J Clin Microbiol 1998, 36:1090-1095. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  23. Silaghi C, Hamel D, Thiel C, Pfister K, Passos LM, Rehbein S: Genetic variants of Anaplasma phagocytophilum in wild caprine and cervid ungulates from the Alps in Tyrol, Austria.

    Vector Borne Zoonotic Dis 2011, 11:355-362. PubMed Abstract | Publisher Full Text OpenURL

  24. Silaghi C, Liebisch G, Pfister K: Genetic variants of Anaplasma phagocytophilum from 14 equine granulocytic anaplasmosis cases.

    Parasites & Vectors 2011, 4:161. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  25. Team RDC: R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria; 2011. OpenURL

  26. Malandrin L, Jouglin M, Sun Y, Brisseau N, Chauvin A: Redescription of Babesia capreoli (Enigk and Friedhoff, 1962) from roe deer (Capreolus capreolus): isolation, cultivation, host specificity, molecular characterisation and differentiation from Babesia divergens.

    Int J Parasitol 2010, 40:277-284. PubMed Abstract | Publisher Full Text OpenURL

  27. Scharf W, Schauer S, Freyburger F, Petrovec M, Schaarschmidt-Kiener D, Liebisch G, Runge M, Ganter M, Kehl A, Dumler JS, et al.: Distinct host species correlate with Anaplasma phagocytophilum ankA gene clusters.

    J Clin Microbiol 2011, 49:790-796. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  28. Silaghi C, Kohn B, Chirek A, Thiel C, Nolte I, Liebisch G, Pfister K: Investigations on the relationship of molecular and clinical findings of Anaplasma phagocytophilum involved in natural infections of dogs.

    J Clin Microbiol 2011, 49:4413-4414. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  29. Silaghi C, Gilles J, Höhle M, Fingerle V, Just FT, Pfister K: Anaplasma phagocytophilum infection in Ixodes ricinus, Bavaria, Germany.

    Emerg Infect Dis 2008, 14:972-974. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  30. Von Loewenich FD, Baumgarten BU, Schröppel K, Geissdörfer W, Röllinghoff M, Bogdan C: High diversity of ankA sequences of Anaplasma phagocytophilum among Ixodes ricinus ticks in Germany.

    J Clin Microbiol 2003, 41:5033-5040. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  31. Silaghi C, Skuballa J, Thiel C, Pfister K, Petney T, Pfäffle M, Taraschewski H, Passos LM: The European hedgehog (Erinaceus europaeus) - A suitable reservoir for variants of Anaplasma phagocytophilum?

    Ticks and Tick-borne Diseases 2012, 3:49-54. PubMed Abstract | Publisher Full Text OpenURL

  32. Silaghi C, Scheuerle MC, Friche Passos LM, Thiel C, Pfister K: PCR detection of Anaplasma phagocytophilum in goat flocks in an area endemic for tick-borne fever in Switzerland.

    Parasite 2011, 18:57-62. PubMed Abstract OpenURL

  33. Bauch RJ, Danner G: Funde von Dermancentor reticulatus (Ixodida, Ixodidae) in den DDR-Bezirken Leipzig und Halle.

    Angew Parasitol 1988, 29:250-254. PubMed Abstract OpenURL

  34. Schulze P: Endemisches Vorkommen einer Mediterranen Zecke (Dermacentor reticulatus F.) in Deutschland.

    Zoomorphology 1925, 3:704-705. OpenURL

  35. Dautel H, Dippel C, Oehme R, Hartelt K, Schettler E: Evidence for an increased geographical distribution of Dermacentor reticulatus in Germany and detection of Rickettsia sp. RpA4.

    Int J Med Microbiol 2006, 296(Suppl 40):149-156. PubMed Abstract | Publisher Full Text OpenURL

  36. Pluta S, Tewald F, Hartelt K, Oehme R, Kimmig P, Mackenstedt U: Rickettsia slovaca in Dermacentor marginatus ticks, Germany.

    Emerg Infect Dis 2009, 15:2077-2078. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  37. Menn B: Untersuchungen zur Verbreitung und Ökologie von Dermacentor spec. (Ixodidae, Acari) in Deutschland. Friedrich-Wilhelms-Universität, Diploma Thesis; 2006. OpenURL

  38. Siroky P, Kubelová M, Bednář M, Modrý D, Hubálek Z, Tkadlec E: The distribution and spreading pattern of Dermacentor reticulatus over its threshold area in the Czech Republic-How much is range of this vector expanding?

    Vet Parasitol 2011, 183:130-135. PubMed Abstract | Publisher Full Text OpenURL

  39. Kubelová M, Tkadlec E, Bednář M, Roubalová E, Široký P: West-to-east differences of Babesia canis canis prevalence in Dermacentor reticulatus ticks in Slovakia.

    Vet Parasitol 2011, 180:191-196. PubMed Abstract | Publisher Full Text OpenURL

  40. Gray JS, Dautel H, Estrada-Peña A, Kahl O, Lindgren E: Effects of climate change on ticks and tick-borne diseases in europe.

    Interdiscip Perspect Infect Dis 2009, 2009:593232. PubMed Abstract | PubMed Central Full Text OpenURL

  41. Hartelt K, Pluta S, Oehme R, Kimmig P: Spread of ticks and tick-borne diseases in Germany due to global warming.

    Parasitol Res 2008, 103(Suppl 1):S109-S116. PubMed Abstract | Publisher Full Text OpenURL

  42. Beck R, Vojta L, Curkovic S, Mrljak V, Margaletic J, Habrun B: Molecular Survey of Babesia microti in Wild Rodents in Central Croatia.

    Vector Borne Zoonotic Dis 2011, 11:81-83. PubMed Abstract | Publisher Full Text OpenURL

  43. Siński E, Bajer A, Welc R, Pawelczyk A, Ogrzewalska M, Behnke JM: Babesia microti: prevalence in wild rodents and Ixodes ricinus ticks from the Mazury Lakes District of North-Eastern Poland.

    Int J Med Microbiol 2006, 296(Suppl 40):137-143. PubMed Abstract | Publisher Full Text OpenURL

  44. Duh D, Petrovec M, Trilar T, Avsic-Županc T: The molecular evidence of Babesia microti infection in small mammals collected in Slovenia.

    Parasitology 2003, 126:113-117. PubMed Abstract | Publisher Full Text OpenURL

  45. Bown KJ, Lambin X, Telford GR, Ogden NH, Telfer S, Woldehiwet Z, Birtles RJ: Relative importance of Ixodes ricinus and Ixodes trianguliceps as vectors for Anaplasma phagocytophilum and Babesia microti in field vole (Microtus agrestis) populations.

    Appl Environ Microbiol 2008, 74:7118-7125. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  46. Karbowiak G: Zoonotic reservoir of Babesia microti in Poland.

    Pol J Microbiol 2004, 53(Suppl):61-65. PubMed Abstract OpenURL

  47. Dickman CR, Doncaster CP: The ecology of small mammals in urban habitats. I. Populations in a patchy environment.

    J Animal Ecol 1987, 56:629-640. Publisher Full Text OpenURL

  48. Mohamed HA, Molyneux DH: Elleipsisoma thomsoni Franca, 1912: an Apicomplexan parasite in the red blood cells of the mole (Talpa europaea).

    Parasitology 1984, 89(Pt 3):407-415. PubMed Abstract OpenURL

  49. Sebek Z: Blood parasites of small wild mammals in Czechoslovakia.

    Folia Parasitol (Praha) 1975, 22:11-20. OpenURL

  50. Kozuch O, Grulich I, Nosek J, Albrecht P: Isolation of tick-borne encephalitis virus from the blood of the mole (Talpa europaea) in a natural focus of infection.

    Acta Virol 1966, 10:84. PubMed Abstract OpenURL

  51. Barutzki D, Reule M, Scheunemann R, Heile C, Schein E: Die Babesiose des Hundes - Eine autochthone Erkrankung in Deutschland.

    Deutsches Tierärzteblatt 2007, 3:284-293. OpenURL

  52. Menn B, Lorentz S, Naucke TJ: Imported and travelling dogs as carriers of canine vector-borne pathogens in Germany.

    Parasit Vectors 2010, 3:34. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  53. Schorn S, Pfister K, Reulen H, Mahling M, Manitz J, Thiel C, Silaghi C: Prevalence of Anaplasma phagocytophilum in Ixodes ricinus in Bavarian public parks, Germany.

    Ticks Tick Borne Dis 2011, 2:196-203. PubMed Abstract | Publisher Full Text OpenURL

  54. Vor T, Kiffner C, Hagedorn P, Niedrig M, Ruhe F: Tick burden on European roe deer (Capreolus capreolus).

    Exp Appl Acarol 2010, 51:405-417. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  55. Rosef O, Paulauskas A, Radzijevskaja J: Prevalence of Borrelia burgdorferi sensu lato and Anaplasma phagocytophilum in questing Ixodes ricinus ticks in relation to the density of wild cervids.

    Acta Vet Scand 2009, 51:47. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  56. Grzeszczuk A, Stanczak J: Highly variable year-to-year prevalence of Anaplasma phagocytophilum in Ixodes ricinus ticks in northeastern Poland: a 4-year follow-up.

    Ann N Y Acad Sci 2006, 1078:309-311. PubMed Abstract | Publisher Full Text OpenURL

  57. Wielinga PR, Gaasenbeek C, Fonville M, de Boer A, de Vries A, Dimmers W, Akkerhuis Op Jagers G, Schouls LM, Borgsteede F, van der Giessen JW: Longitudinal analysis of tick densities and Borrelia, Anaplasma, and Ehrlichia infections of Ixodes ricinus ticks in different habitat areas in The Netherlands.

    Appl Environ Microbiol 2006, 72:7594-7601. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  58. Ostfeld RS, Canham CD, Oggenfuss K, Winchcombe RJ, Keesing F: Climate, deer, rodents, and acorns as determinants of variation in lyme-disease risk.

    PLoS Biol 2006, 4:e145. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  59. Bown KJ, Begon M, Bennett M, Woldehiwet Z, Ogden NH: Seasonal dynamics of Anaplasma phagocytophila in a rodent-tick (Ixodes trianguliceps) system, United Kingdom.

    Emerg Infect Dis 2003, 9:63-70. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  60. Bown KJ, Lambin X, Ogden NH, Begon M, Telford G, Woldehiwet Z, Birtles RJ: Delineating Anaplasma phagocytophilum ecotypes in coexisting, discrete enzootic cycles.

    Emerg Infect Dis 2009, 15:1948-1954. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  61. Ogden NH, Bown K, Horrocks BK, Woldehiwet Z, Bennett M: Granulocytic Ehrlichia infection in ixodid ticks and mammals in woodlands and uplands of the U.K.

    Med Vet Entomol 1998, 12:423-429. PubMed Abstract | Publisher Full Text OpenURL

  62. Kiffner C, Vor T, Hagedorn P, Niedrig M, Rühe F: Factors affecting patterns of tick parasitism on forest rodents in tick-borne encephalitis risk areas, Germany.

    Parasitol Res 2011, 108:323-335. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  63. Randolph SE, Gern L, Nuttall PA: Co-feeding ticks: Epidemiological significance for tick-borne pathogen transmission.

    Parasitol Today 1996, 12:472-479. PubMed Abstract | Publisher Full Text OpenURL

  64. Doudier B, Olano J, Parola P, Brouqui P: Factors contributing to emergence of Ehrlichia and Anaplasma spp. as human pathogens.

    Vet Parasitol 2010, 167:149-154. PubMed Abstract | Publisher Full Text OpenURL

  65. Hunfeld KP, Brade V: Prevalence of antibodies against the human granulocytic ehrlichiosis agent in Lyme borreliosis patients from Germany.

    Eur J Clin Microbiol Infect Dis 1999, 18:221-224. PubMed Abstract | Publisher Full Text OpenURL

  66. Fingerle V, Goodman JL, Johnson RC, Kurtti TJ, Munderloh UG, Wilske B: Human granulocytic ehrlichiosis in southern Germany: increased seroprevalence in high-risk groups.

    J Clin Microbiol 1997, 35:3244-3247. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  67. Kohn B, Silaghi C, Galke D, Arndt G, Pfister K: Infections with Anaplasma phagocytophilum in dogs in Germany.

    Res Vet Sci 2011, 91:71-76. PubMed Abstract | Publisher Full Text OpenURL

  68. Jensen J, Simon D, Murua Escobar H, Soller JT, Bullerdiek J, Beelitz P, Pfister K, Nolte I: Anaplasma phagocytophilum in dogs in Germany.

    Zoonoses Public Health 2007, 54:94-101. PubMed Abstract | Publisher Full Text OpenURL

  69. Von Loewenich FD, Stumpf G, Baumgarten BU, Röllinghoff M, Dumler JS, Bogdan C: A case of equine granulocytic ehrlichiosis provides molecular evidence for the presence of pathogenic Anaplasma phagocytophilum (HGE agent) in Germany.

    Eur J Clin Microbiol Infect Dis 2003, 22:303-305. PubMed Abstract | Publisher Full Text OpenURL

  70. Walder G, Falkensammer B, Aigner J, Tiwald G, Dierich MP, Wurzner R, Lechleitner P: First documented case of human granulocytic ehrlichiosis in Austria.

    Wien Klin Wochenschr 2003, 115:263-266. PubMed Abstract | Publisher Full Text OpenURL

  71. Tylewska-Wierzbanowska S, Chmielewski T, Kondrusik M, Hermanowska-Szpakowicz T, Sawicki W, Sulek K: First cases of acute human granulocytic ehrlichiosis in Poland.

    Eur J Clin Microbiol Infect Dis 2001, 20:196-198. PubMed Abstract | Publisher Full Text OpenURL

  72. Lotrič-Furlan S, Rojko T, Petrovec M, Avšič-Županc T, Strle F: Epidemiological, clinical and laboratory characteristics of patients with human granulocytic anaplasmosis in Slovenia.

    Wien Klin Wochenschr 2006, 118:708-713. PubMed Abstract | Publisher Full Text OpenURL

  73. Hildebrandt A, Kramer A, Sachse S, Straube E: Detection of Rickettsia spp. and Anaplasma phagocytophilum in Ixodes ricinus ticks in a region of Middle Germany (Thuringia).

    Ticks Tick Borne Dis 2010, 1:52-56. PubMed Abstract | Publisher Full Text OpenURL

  74. Movila A, Rolain JM, Podavalenko A, Toderas I, Tkachenco L, Naglov V, Raoult D: Detection of spotted fever group rickettsiae and family Anaplasmataceae in Ixodes ricinus ticks from Republic of Moldova and Eastern Ukraine.

    Clin Microbiol Infect 2009, 15(Suppl 2):32-33. PubMed Abstract OpenURL

  75. Severinsson K, Jaenson TG, Pettersson J, Falk K, Nilsson K: Detection and prevalence of Anaplasma phagocytophilum and Rickettsia helvetica in Ixodes ricinus ticks in seven study areas in Sweden.

    Parasit Vectors 2010, 3:66. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  76. Halos L, Bord S, Cotté V, Gasqui P, Abrial D, Barnouin J, Boulouis HJ, Vayssier-Taussat M, Vourc'h G: Ecological factors characterizing the prevalence of bacterial tick-borne pathogens in Ixodes ricinus ticks in pastures and woodlands.

    Appl Environ Microbiol 2010, 76:4413-4420. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  77. Reye AL, Hübschen JM, Sausy A, Müller CP: Prevalence and seasonality of tick-borne pathogens in questing Ixodes ricinus ticks from Luxembourg.

    Appl Environ Microbiol 2010, 76:2923-2931. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  78. Hartelt K, Oehme R, Frank H, Brockmann SO, Hassler D, Kimmig P: Pathogens and symbionts in ticks: prevalence of Anaplasma phagocytophilum (Ehrlichia sp.), Wolbachia sp., Rickettsia sp., and Babesia sp. in Southern Germany.

    Int J Med Microbiol 2004, 293(Suppl 37):86-92. PubMed Abstract OpenURL

  79. Franke J, Fritzsch J, Tomaso H, Straube E, Dorn W, Hildebrandt A: Coexistence of pathogens in host-seeking and feeding ticks within a single natural habitat in Central Germany.

    Appl Environ Microbiol 2010, 76:6829-6836. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  80. Piccolin G, Benedetti G, Doglioni C, Lorenzato C, Mancuso S, Papa N, Pitton L, Ramon MC, Zasio C, Bertiato G: A study of the presence of B. burgdorferi, Anaplasma (previously Ehrlichia) phagocytophilum, Rickettsia, and Babesia in Ixodes ricinus collected within the territory of Belluno, Italy.

    Vector Borne Zoonotic Dis 2006, 6:24-31. PubMed Abstract | Publisher Full Text OpenURL

  81. Paziewska A, Zwolińska L, Harris PD, Bajer A, Siński E: Utilisation of rodent species by larvae and nymphs of hard ticks (Ixodidae) in two habitats in NE Poland.

    Exp Appl Acarol 2010, 50:79-91. PubMed Abstract | Publisher Full Text OpenURL

  82. Pichon B, Kahl O, Hammer B, Gray JS: Pathogens and host DNA in Ixodes ricinus nymphal ticks from a German forest.

    Vector Borne Zoonotic Dis 2006, 6:382-387. PubMed Abstract | Publisher Full Text OpenURL

  83. Hildebrandt A, Pauliks K, Sachse S, Straube E: Coexistence of Borrelia spp. and Babesia spp. in Ixodes ricinus ticks in Middle Germany.

    Vector Borne Zoonotic Dis 2010, 10:831-837. PubMed Abstract | Publisher Full Text OpenURL

  84. Leonhard S: Untersuchungen zur Häufigkeit von Borrelia burgdorferi sensu lato. Anaplasma phagocytophilum and Babesia spp. in Ixodes ricinus aus Bayern und Baden-Württemberg. Doctoral thesis, Ludwig-Maximilians-Universität, Tierärztliche Fakultät; 2005. OpenURL

  85. Schicht S, Junge S, Schnieder T, Strube C: Prevalence of Anaplasma phagocytophilum and Coinfection with Borrelia burgdorferi Sensu Lato in the Hard Tick Ixodes ricinus in the City of Hanover (Germany).

    Vector Borne Zoonotic Dis 2011, 11:1595-1597. PubMed Abstract | Publisher Full Text OpenURL

  86. Hildebrandt A, Schmidt KH, Fingerle V, Wilske B, Straube E: Prevalence of granulocytic Ehrlichiae in Ixodes ricinus ticks in Middle Germany (Thuringia) detected by PCR and sequencing of a 16S ribosomal DNA fragment.

    FEMS Microbiol Lett 2002, 211:225-230. PubMed Abstract | Publisher Full Text OpenURL

  87. Fingerle V, Munderloh UG, Liegl G, Wilske B: Coexistence of ehrlichiae of the phagocytophila group with Borrelia burgdorferi in Ixodes ricinus from Southern Germany.

    Med Microbiol Immunol 1999, 188:145-149. PubMed Abstract | Publisher Full Text OpenURL

  88. Oehme R, Hartelt K, Backe H, Brockmann S, Kimmig P: Foci of tick-borne diseases in southwest Germany.

    Int J Med Microbiol 2002, 291(Suppl 33):22-29. PubMed Abstract OpenURL