Abstract

In Europe, the hard tick Ixodes ricinus is considered the most important vector of human zoonotic diseases. Human pathogenic agents spread by I. ricinus in Sweden include Borrelia burgdorferi sensu lato (s.l.), Anaplasma phagocytophilum, Rickettsia helvetica, the recently described Neoehrlichia mikurensis, Borrelia miyamotoi, tick-borne encephalitis virus (TBEV), and Babesia spp. (Babesia microti, Babesia venatorum and Babesia divergens). Since these pathogens share the same vector, co-infections with more than one tick-borne pathogen may occur and thus complicate the diagnosis and clinical management of the patient due to possibly altered symptomatology. Borrelia burgdorferi s.l., TBEV and B. miyamotoi are well-known to cause infections of the central nervous system (CNS), whereas the abilities of other tick-borne pathogens to invade the CNS are largely unknown. The aim of this study was to investigate the presence and clinical impact of tick-borne pathogens other than B. burgdorferi s.l. in the cerebrospinal fluid (CSF) and serum samples of patients who were under investigation for Lyme neuroborreliosis (LNB) in a tick-endemic region of South-eastern Sweden. CSF and serum samples from 600 patients, recruited from the Regions of Östergötland County, Jönköping County and Kalmar County in South-eastern Sweden and investigated for LNB during the period of 2009–2013, were retrospectively collected for analysis. The samples were analysed by real-time PCR for the presence of nucleic acid from B. burgdorferi s.l., B. miyamotoi, A. phagocytophilum, Rickettsia spp., N. mikurensis, TBEV and Babesia spp. Serological analyses were conducted in CSF and serum samples for all patients regarding B. burgdorferi s.l., and for the patients with CSF mononuclear pleocytosis, analyses of antibodies to B. miyamotoi, A. phagocytophilum, spotted fever group (SFG) rickettsiae, TBEV and B. microti in serum were performed. The medical charts of all the patients with CSF mononuclear pleocytosis and patients with positive PCR findings were reviewed. Of the 600 patients, 55 (9%) presented with CSF mononuclear pleocytosis, 13 (2%) of whom had Borrelia-specific antibodies in the CSF. One patient was PCR-positive for N. mikurensis, and another one was PCR-positive for Borrelia spp. in serum. No pathogens were detected by PCR in the CSF samples. Four patients had serum antibodies to B. miyamotoi, four patients to A. phagocytophilum, five patients to SFG rickettsiae, and six patients to TBEV. One patient, with antibodies to SFG rickettsiae, had both clinical and laboratory signs suggestive of a current infection. Nine patients had serum antibodies to more than one pathogen, although none of these was assessed as a current co-infection. We can conclude from this study that tick-borne co-infections are uncommon in patients who are being investigated for suspected LNB in South-eastern Sweden, an area endemic for borreliosis and TBE.

Highlights

  • Tick-borne infections are increasing in the Northern hemisphere, and new pathogens causing human disease are being identified (Socolovschi et al, 2009)

  • The aim of the present study was to investigate the presence of tickborne pathogens other than B. burgdorferi s.l. in the cerebrospinal fluid (CSF), using both molecular and serological methods, in patients who have been investigated for Lyme neuroborreliosis (LNB)

  • White blood cell counts in the CSF and serological ana­ lyses regarding B. burgdorferi s.l. were performed as part of the initial investigation at the time of sampling

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Summary

Introduction

Tick-borne infections are increasing in the Northern hemisphere, and new pathogens causing human disease are being identified (Socolovschi et al, 2009). L.) group of spirochaetes, Borrelia miyamotoi, Anaplasma phag­ ocytophilum, Neoehrlichia mikurensis, and several species of the spotted fever group (SFG) rickettsiae (Socolovschi et al, 2009; Wass et al, 2019; Welinder-Olsson et al, 2010). These microorganisms have all been re­ ported with different prevalence in collected ticks in Sweden (Ander­ sson et al, 2013; (Henningsson et al, 2015b); Lindblom et al, 2016; Wilhelmsson et al, 2013). Since the CNS symptoms of these three in­ fections are similar, they can be difficult to distinguish clinically

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