Detection of selected pathogens in ticks collected from cats and dogs in the Wrocław Agglomeration, South-West Poland
Parasites & Vectors volume 9, Article number: 351 (2016)
Tick-borne infections are no longer confined to rural areas, they are documented with increasing frequency in urban settlements across the world. They are known to cause diseases in humans as well as in their companion animals.
During a period of 2 years, from January 2013 until December 2014, ticks were collected from dogs and cats in 18 veterinary clinics in the Wrocław Agglomeration, Poland. In total, 1455 ticks were found on 931 pets: 760 domestic dogs and 171 cats. For molecular examinations 127 I. ricinus ticks (115 females and 12 males) were randomly selected, all collected I. hexagonus (n = 137, 32 females, 98 nymphs, 7 larvae) and all collected D. reticulatus (n = 46, 31 females, 15 males) were taken. Ixodes ricinus and I. hexagonus ticks were tested for Rickettsia spp., Anaplasma phagocytophilum, Candidatus Neoehrlichia mikurensis and Babesia spp., while D. reticulatus ticks were investigated for Rickettsia spp. and Babesia spp. only.
In total, 65.4 % I. ricinus ticks were infected with at least one pathogen. Over 50 % of I. ricinus were positive for Rickettsia spp. (R. helvetica and R. monacensis). The infection level with A. phagocytophilum was 21.3 %. DNA of Cand. N. mikurensis was detected in 8.1 % I. ricinus ticks. Interestingly only female ticks were infected. The prevalence of Babesia spp. was confirmed in 9.0 % of I. ricinus involving the species B. microti and B. venatorum. A total of nineteen double, one triple and two quadruple infections were found in I. ricinus ticks only. Almost 11 % of I. hexagonus ticks were positive for at least one of the tested pathogens. Rickettsia spp. infection was found in 2.2 %, while A. phagocytophilum was detected in 8.1 % of I. hexagonus ticks. Only one nymph was positive for Cand. N. mikurensis and none of I. hexagonus ticks harbored a Babesia spp. Over 60 % of D. reticulatus ticks were positive for rickettsial DNA, exclusively belonging to the species R. raoultii.
The high tick infestation rates and the prevalence of pathogens found in these ticks demonstrate a serious level of encounter to tick-borne diseases in urban dogs in the Wroclaw area, and provide evidence that dogs and cats themselves may substantially contribute to the circulation of the ticks and pathogens in the urban area.
Tick-borne pathogens, such as Anaplasma phagocytophilum, Candidatus Neoehrlichia mikurensis and Rickettsia spp., belong to the order Rickettsiales, while such as Babesia spp. are parasitic protozoans. All these pathogens, are known to cause diseases in humans as well as in their companion animals, and are considered to be emerging across Europe and other parts of the world [1–6].
Rickettsia spp. are divided into four groups: the spotted fever group (SFG), the typhus group, the Rickettsia bellii group, and the Rickettsia canadensis group . Rickettsiae of the SFG are known to be transmitted by ticks and cause DEBONEL (Dermacentor-borne necrosis erythema lymphadenopathy), also known as TIBOLA (tick-borne lymphadenopathy) in humans . In Poland, rickettsioses caused by rickettsiae of the SFG were described in forest workers, dogs and ticks [9–11].
Anaplasma phagocytophilum and Candidatus Neoehrlichia mikurensis are gram-negative obligate intracellular bacteria. Anaplasma phagocytophilum may cause granulocytic anaplasmosis in humans, dogs, horses and ruminants . Anaplasmosis has been reported in dogs, cats and humans from Poland with evidence of autochthonous human cases [12–15]. Neoehrlichiosis was described in immunodeficient and previously healthy humans but also in immunodeficient dogs [1, 3, 16]. The presence of Cand. Neoehrlichia mikurensis has been proven in Ixodes ricinus ticks and in asymptomatic humans from Poland [17, 18].
Babesiosis is a zoonotic disease occurring worldwide which is caused by intraerythrocytic parasites of the genus Babesia . In Europe, Babesia divergens-like organisms are mainly responsible for the disease in humans. Babesia spp. are reported in Ixodes ricinus and Dermacentor reticulatus from Poland . Nowadays, cases caused by tick-borne pathogens are emerging in urban regions in Europe [20, 21]. Dogs and cats should be taken into account as important hosts of ticks in urban areas [21, 22].
In Poland, 5 of the 19 detected tick species (I. ricinus Linnaeus, 1758, I. hexagonus Leach, 1815, I. crenulatus Koch, 1844, I. rugicollis Schulze et Schlottke, 1929, and D. reticulatus Fabricius, 1794) parasitize on cats and dogs . Most commonly, however, I. ricinus and D. reticulatus, the important vectors of Rickettsia spp., Anaplasma phagocytophilum and Babesia spp., are detected on pets [21, 24–28]. In a previous study, ticks collected from cats and dogs from the Wrocław Agglomeration, SW Poland, were tested for the presence of Borrelia spp. .
The aim of this follow-up study was to evaluate the prevalence of Babesia spp., A. phagocytophilum, Cand. Neoehrlichia mikurensis and Rickettsia spp. in ticks collected from cats and dogs in the Wrocław Agglomeration, Poland.
During a period of 2 years, from January 2013 till December 2014, ticks were collected from dogs and cats in the veterinary clinics in the Wrocław Agglomeration, Poland. Wrocław city (c292.8 km2) is located in the south-west of Poland (51°07'N, 17°02'E). Tick collection from 2013  was extended with specimens collected in the next year. In total, 18 veterinary clinics submitted 1455 ticks found on 931 pets: 760 domestic dogs and 171 cats (Table 1). Tick specimens were determined by life stage, sex and species . Tick collection consisted of: 46 D. reticulatus ticks (31 females, 15 males), 137 I. hexagonus (32 females, 98 nymphs, 7 larvae), and 1272 I. ricinus (1160 females, 103 males, 9 nymphs).
DNA isolation and biological material
All collected ticks were kept in 70 % ethanol until isolation of DNA was performed. Before DNA extraction, ticks were washed in sterile water. All ticks were individually homogenized using sterile polystyrene pistils and then genomic DNA was extracted by using a Tissue Genomic Extraction GPB Mini Kit with proteinase K (Genoplast Biochemicals, Poland) according to the manufacturer’s instructions. All of the obtained lysates were stored at -20 °C until examined.
For further examinations 310 ticks were selected: 127 randomly chosen I. ricinus ticks (115 females and 12 males), all collected I. hexagonus ticks (n = 137; 32 females, 98 nymphs, 7 larvae) and D. reticulatus ticks (n = 46; 31 females, 15 males) (Table 2). Ixodes ricinus and I. hexagonus ticks were tested for Rickettsia spp., Anaplasma phagocytophilum, Candidatus Neoehrlichia mikurensis and Babesia spp., while D. reticulatus ticks were only investigated for Rickettsia spp. and Babesia spp.
Molecular detection of Rickettsia spp., Anaplasma phagocytophilum, Candidatus Neoehrlichia mikurensis and Babesia spp.
For detection of Rickettsia spp., a real-time PCR targeting the gltA genome region (70 bp) was used . A real-time PCR targeting msp2 gene fragment (77 bp) was performed to detect A. phagocytophilum . In order to detect Candidatus Neoehrlichia mikurensis, a real-time PCR targeting the partial groEL gene (99 bp) was used [33, 34]. All PCR methods were carried out using the Mx3000P real-time cycler (Stratagene).
For detection of Babesia spp., a conventional PCR amplification of the small 18S subunit of the rRNA gene (411–452 bp) with primers BJ1 and BN2 was performed . Samples positive for Rickettsia spp. DNA by real-time PCR were further investigated using a conventional PCR in which a 811-bp fragment of the ompB gene was amplified . The PCR products were visualized by electrophoresis on 1.5 % agarose gels stained with Midori Green (NIPPON Genetics, Düren, Germany). Randomly selected positive PCR products (n = 22) were purified using the NucleoSpin® and PCR Clean-up Kit (MACHEREY-NAGEL, Düren, Germany) according to the manufacturer’s instructions. Purified PCR products were sequenced (Interdisziplinäres Zentrum für Klinische Forschung, Leipzig, Germany) with forward and reverse primers, and analyzed with Chromas Lite (Technelysium Pty Ltd, Australia). Nucleotide sequences were compared with GenBank entries using NCBI BLAST.
The chi-square test was used to compare infected and not infected ticks (STATISTICA ver. 9.0). Yates’ correction was used for 1-df tests when expected frequencies were less than 5. The significance level was set at 0.05.
The most common infection was Rickettsia spp., which was found in 30.6 % (n = 95) of all tick species (Table 3). The highest infection level was detected in D. reticulatus ticks (60.9 %), followed by I. ricinus (50.4 %) and I. hexagonus (2.2 %). The differences in prevalence between tick species were statistically significant (χ 2 = 95.268, df = 2, P < 0.001). Rickettsia raoultii was found in 100 % sequenced D. reticulatus samples (100 % identity to acc. no. JX298077.1). In I. ricinus ticks, the distribution of Rickettsia spp. was 80 % for R. helvetica (100 % identity to acc. no. KR150781.1) and 20 % for R. monacensis (100 % identity to KC137254.1). DNA from I. hexagonus was not tested due to high CT values previously obtained by RT-PCR (CT > 35). The prevalence of A. phagocytophilum was detected in 14.4 % (n = 37) of Ixodes species. Further, 21.3 % of I. ricinus, and 8.1 % of I. hexagonus were positive for this pathogen. The infection level was statistically higher in I. ricinus ticks than I. hexagonus (χ 2 = 9.01, df = 1, P = 0.003). Candidatus N. mikurensis was found in 4.2 % of Ixodes samples. It was detected in 8.1 % of I. ricinus and 0.7 % of I. hexagonus (the difference being statistically significant, χ 2 = 8.599, df = 1, P = 0.003). The prevalence of Babesia spp. was the lowest among the tested pathogens, 3.6 % (n = 11) for all tick species, but only I. ricinus ticks (9.0 %) were infected (χ 2 = 16.934, df = 2, P < 0.001). Babesia microti was detected in 83.3 % (all samples with identity over 96 % to acc. no. JQ711225.1), and B. venatorum in 16.7 % (identical with 99 % to acc. no. KR493907.1 and 98 % to KF500410.1) of sequenced I. ricinus samples.
Ixodes ricinus ticks were more often infected, with minimum one pathogen, than I. hexagonus or D. reticulatus (χ 2 = 90.019, df = 2, P < 0.001). In total, 65.4 % (n = 83) I. ricinus ticks were positive for at least a single infection. The most often detected pathogen was Rickettsia spp. (χ 2 = 84.505, df = 3, P < 0.0001), in 50.4 % of I. ricinus (n = 64; Table 3). There were no significant differences in infection levels between females and males (χ 2 = 0.404, df = 1, P = 0.525) nor ticks collected from cats or dogs (χ 2 = 0.694, df = 1, P = 0.405). Anaplasma phagocytophilum was verified in 21.3 % specimens (n = 26, no statistically significant differences were observed between females and males, χ 2 = 0.259, df = 1, P = 0.611, or between ticks parasitizing cats or dogs, χ 2 = 0.002, df = 1, P = 0.964). Candidatus N. mikurensis was detected in 8.1 % I. ricinus (n = 10), only females were infected (χ 2 = 0.202, df = 1, P = 0.653); infection level of ticks collected from pets was not statistically significant (χ 2 = 0.097, df = 1, P = 0.755). The prevalence of Babesia spp. was confirmed in 9.0 % of specimens (n = 11); there were neither significant differences between females and males (χ 2 = 0.214, df = 1, P = 0.644) nor ticks infesting cats or dogs (χ 2 = 3,086, df = 1, P = 0.079).
In total, 10.9 % (n = 15) I. hexagonus ticks were positive for at least one of the tested pathogens. Anaplasma phagocytophilum was the most common infection in these ticks (χ 2 = 20.661, df = 3, P < 0.001), it was detected in 8.1 % of ticks (n = 11); no statistically significant differences were observed between life stages (χ 2 = 0.473, df = 2, P = 0.789) or for ticks parasitizing cats or dogs (χ 2 = 1.373, df = 1, P = 0.241). Rickettsia spp. infection was found in 2.2 % ticks (n = 3), there were no statistically significant differences between life stages, (χ 2 = 3.245, df = 2, P = 0.197) or for ticks from different hosts (χ 2 = 0.166, df = 1, P = 0.684). Only one nymph specimen (0.7 %) was positive for Cand. N. mikurensis, with no statistical differences in infection levels between different life stages (χ 2 = 0.405, df = 2, P = 0.817) or ticks collected from pets (χ 2 = 0.052, df = 1, P = 0.82). None of the I. hexagonus ticks was found to be infected by Babesia spp.
Among D. reticulatus only Rickettsia spp. was detected; 60.9 % of ticks were positive (n = 28). Statistically significant differences were not detected in infection levels between males and females (χ 2 = 0.007, df = 1, P = 0.933) or ticks from cats or dogs (χ 2 = 0.175, df = 1, P = 0.676). Babesia spp. DNA was not amplified in any of D. reticulatus sample.
Co-infections were detected only in I. ricinus ticks, mainly females. Only one male tick had a double-infection with Rickettsia spp. and A. phagocytophilum. The most common pathogen combination was Rickettsia spp. + A. phagocytophilum, followed by Rickettsia spp. + Cand. N. mikurensis, Rickettsia spp. + Babesia spp. and one of Cand. N. mikurensis + Babesia spp. (Table 4). Apart from these, two quadruple-infections and one triple-infection (Rickettsia spp., Cand. N. mikurensis, A. phagocytophilum.)
From three ticks species identified as parasites of dogs and cats in the Wrocław Agglomeration, Ixodes ricinus was predominant, followed by I. hexagonus and D. reticulatus. Similar findings were obtained in Belgium , Switzerland , Germany  and Great Britain , as well as in Bosnia and Herzegovina .
The prevalence of pathogens differed between the tick species. Ixodes ricinus individuals were the most often infected species. The lowest infection levels were observed in I. hexagonus ticks. From all tested pathogens (Rickettsia spp., Babesia spp., Candidatus Neoehrlichia mikurensis and Anaplasma phagocytophilum), rickettsial infections were the most common. The infection levels of A. phagocytophilum, Cand. N. mikurensis and Babesia spp. (B. microti, B. venatorum) were the highest in I. ricinus ticks and co-infections were detected only in this species. Interestingly, Babesia spp. DNA was only found in I. ricinus ticks, none of the D. reticulatus, the main vector for B. canis , was infected. The most often detected pathogen in I. hexagonus specimens was A. phagocytophilum. There were no statistically significant differences in infection levels between different tick life stages and between ticks collected from cats and dogs in any case. In Switzerland , researchers observed a difference in Rickettsia spp. infection levels between ticks from cats (40 %) and dogs (18 %), which was not found in this study.
Rickettsia spp. was dominant among D. reticulatus ticks (only R. raoultii) with prevalence over 60 % and I. ricinus (only R. helvetica and R. monacensis) - over 50 %. Only 2 % of Ixodes hexagonus ticks were infected. In Europe, prevalence of Rickettsia spp. in ticks infesting urban animals reached levels, e.g. 14–61 % in I. ricinus, 1–44 % of I. hexagonus, 14–39 % of D. reticulatus [37, 44–46]. In Poland, the infection levels in the questing I. ricinus ticks were much lower than results obtained in this study; they differed from 6 to 23 % [47, 48] but prevalence in D. reticulatus was similar, 57 % .
Anaplasma phagocytophilum infection levels of I. ricinus in this research were comparable to those reported in Belgium but much lower for I. hexagonus . However, in The Netherlands and Germany, the prevalence was lower in I. ricinus ticks but similar to I. hexagonus [44, 50]. In Poland, also in Lower Silesia, the infection of I. ricinus ticks (questing as well as collected from dogs) was lower than the data presented here [51–53].
Candidatus N. mikurensis was previously found in ticks in Poland , however, the detection in feeding I. hexagonus is the first one in the country. In Germany, the prevalence of this pathogen in I. ricinus and I. hexagonus from pets was 4 % and 6 %, respectively , while in Denmark only 1 % of I. ricinus was infected . The prevalence in I. hexagonus ticks in the present study (0.7 %) is lower than in other countries; however, it is comparable to results obtained in a former study from Poland conducted on other tick species, I. ricinus (0.5 %) .
The prevalence of Babesia spp. (B. microti and B. venatorum) in I. ricinus was higher than in Belgium  and Germany , where the infection was also detected in I. hexagonus ticks. In Poland, also in Lower Silesia, only 1–3 % of questing I. ricinus ticks were infected [52, 53, 55]. Similar to our results, all tested D. reticulatus in Germany were free of babesial parasites . However, 11 % of D. reticulatus ticks infesting dogs in central Poland were infected ; in Austria 2 of 6 specimens and in Hungary almost 30 % of D. reticulatus (only female ticks) were positive for B. canis [56, 57].
As results of this study show, the risk of tick-borne diseases (TBD) is high in the Wrocław Agglomeration. However, due to the limitation of this study (no blood samples of dogs and cats were investigated for the pathogens), the tick-borne situation among pets in this area is not fully estimated. In Poland, canine tick-borne diseases pose an emerging veterinary problem. The most common TBD among dogs are B. canis and A. phagocytophilum reaching levels of 28 and 12 %, respectively [58, 59]. Apart from the above, dogs were infected with Borrelia burgdorferi (s.l.), and Ehrlichia canis.
The high infection levels were detected for Rickettsia spp. (R. raoultii, R. helvetica and R. monacensis), Anaplasma phagocytophilum, Candidatus Neoehrlichia mikurensis and Babesia spp. (B. microti and B. venatorum) in ticks infesting dogs and cats in the Wrocław Agglomeration, Poland. These findings, as well as the high tick infestation rates, demonstrate a serious level of encounter to tick-borne diseases in urban dogs and cats in the Wrocław area, and provide evidence that dogs and cats themselves may substantially contribute to the circulation of the ticks and the pathogens in the urban area.
DEBONEL, dermacentor-borne necrosis erythema lymphadenopathy; SFG, spotted fever group; TBD, tick-borne disease; TIBOLA, tick-borne lymphadenopathy
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This study was partially financed by the European Union through the European Social Fund as well as by the University of Wrocław (grants numbers 1145/M/IGM/13 and 2113/M/IGM/14). This paper has been sponsored by Bayer Animal Health in the framework of the 11th CVBD World Forum Symposium.
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NK organized the collection of samples, carried out the morphologic determination of ticks, and prepared the samples in the laboratory. MP, AO and NK designed, planned and organized the study. NK and AO tested the samples for pathogens, performed the sequence analysis. NK conducted data analysis. NK, AO, MP, DK and EL drafted the manuscript and wrote the final version. MP, DK and EL contributed to acquire funding. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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Król, N., Obiegala, A., Pfeffer, M. et al. Detection of selected pathogens in ticks collected from cats and dogs in the Wrocław Agglomeration, South-West Poland. Parasites Vectors 9, 351 (2016). https://doi.org/10.1186/s13071-016-1632-0