Abstract
BackgroundThe present study investigated the prevalence of Borrelia burgdorferi sensu lato (s.l.) genospecies in Ixodes ricinus ticks collected in Hanover, Northern Germany, in 2010. At the same time the study served as fifth-year-follow-up study for data comparison with 2005.MethodsA total of 2100 questing ticks were collected and analysed by quantitative real-time PCR (qPCR) with subsequent species differentiation via Reverse Line Blot and Sanger sequencing. Simultaneously, results obtained in 2010 were compared to infection rates from 2005 to evaluate the development of B. burgdorferi s.l. infection rates in Hanoverian ticks.ResultsOverall, 22.7% (476/2,100) of collected ticks were tested positive for B. burgdorferi s.l. infections. Adult ticks showed an infection rate of 33.3% (124/372), subdivided into 29.6% (58/196) positive males and 37.5% (66/176) positive females. Nymph and larvae infection rates were found to be 20.3% (344/1,697) and 25.8% (8/31), respectively. Species identification was successful for 59.2% (282/476) of positive ticks with B. afzelii as the most frequently detected genospecies, followed by B. garinii (including B. bavariensis) and B. spielmanii. B. burgdorferi sensu stricto (s.s.), B. bissettii, B. valaisiana and B. lusitaniae were also identified. Significant differences concerning seasonal fluctuations as well as local differences were observed. Comparing infection rates of Hanoverian ticks between years, a significant increase (P = 0.002) could be observed for larvae with 1.7% positives (2/60) in 2005 and 25.8% positives (8/31) in 2010. In the latter year, coinfections with Borrelia and Rickettsiales were detected in a total of 7.8% (163/2,100) of collected ticks. Of these, 7.3% (153/2,100) were coinfected with Rickettsia spp., 0.3% (7/2,100) with A. phagocytophilum and 0.1% (3/2,100) were coinfected with all three pathogens. Between years 2005 and 2010, no statistically significant differences in coinfection rates were found.ConclusionsComparing B. burgdorferi s.l. infections in Hanoverian I. ricinus ticks in 2010 with data from 2005, a statistically significant increase of infected larvae was noted, whereas the other stages revealed no statistically significant differences. Whether the increased larvae infection rate is an isolated event or results from factual circumstances, e.g. increasing effectiveness of transovarial transmission due to unknown factors, has to be evaluated in further studies.
Highlights
The present study investigated the prevalence of Borrelia burgdorferi sensu lato (s.l.) genospecies in Ixodes ricinus ticks collected in Hanover, Northern Germany, in 2010
Detection of B. burgdorferi s.l. was achieved by minor groove binder probe-based quantitative real-time PCR (qPCR) targeting the 5S-23S intergenic spacer (IGS) region described by Strube et al [37] with the modification that Absolute Blue QPCR low ROX mix (Thermo Fisher; containing Thermo-StartTM DNA Polymerase) was used and tick DNA template was increased to 10 μl
Collection of 2,100 questing ticks resulted in 372 adult ticks (196 males and 176 females), 1,697 nymphs and 31 larvae all identified as I. ricinus
Summary
The present study investigated the prevalence of Borrelia burgdorferi sensu lato (s.l.) genospecies in Ixodes ricinus ticks collected in Hanover, Northern Germany, in 2010. The hard tick Ixodes ricinus Linné 1758, known as vector for different pathogenic agents, serves as the main vector for spirochetes of the Borrelia burgdorferi sensu lato (s.l.) complex in Central Europe [1]. This genospecies complex includes the causative agents for Lyme borreliosis, the most frequent arthropod-borne human disease in the temperate northern hemisphere [2]. 2,100 ticks were collected in different recreational areas in 2010 in the northern German city of Hanover and subsequently analysed for B. burgdorferi s.l. infections
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