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Ahead of Print -Human Exposure to Tickborne Relapsing Fever Spirochete Borrelia miyamotoi, the Netherlands - Volume 20, Number 7—July 2014 - Emerging Infectious Disease journal - CDC

Ahead of Print -Human Exposure to Tickborne Relapsing Fever Spirochete Borrelia miyamotoi, the Netherlands - Volume 20, Number 7—July 2014 - Emerging Infectious Disease journal - CDC



Volume 20, Number 7—July 2014

Letter

Human Exposure to Tickborne Relapsing Fever SpirocheteBorrelia miyamotoi, the Netherlands

To the Editor: Borrelia miyamotoi is a relatively novel tickborne relapsing fever spirochete, and is a different species than B. burgdorferi sensu lato, the causative pathogen of Lyme borreliosis (1). B. miyamotoi was first isolated in 1995 from Ixodes persulcatus ticks in Japan, after which it was detected in ticks in North America, Europe, and Russia (1,2). Bmiyamotoi infections among humans were first reported in Russia in 2011 (3), and in 2013 in the United States (4). Recently, the first patient infected with the tickborne pathogen B. miyamotoi was reported in the Netherlands (5). Conditions reported to be associated withBmiyamotoi infection were systemic, including malaise and fever, meningoencephalitis, and neurologic symptoms. Because of the nature of these manifestations and because regular diagnostic tests for B. burgdorferi will most probably not detect Bmiyamotoi infections (3,5), Bmiyamotoi infections may remain undiagnosed. Nevertheless, the relationship between Bmiyamotoi infection and illness is not very well established; the case-patients reported, including the patient in the Netherlands, were usually hospitalized, severely ill, and often immunocompromised (35). The extent to which B.miyamotoi causes infection and disease in immunocompetent persons is unknown. As a first step to indicate the population at risk for infection, we investigated human exposure to B.miyamotoi in the Netherlands.
To do this, we assessed the Bmiyamotoi infection rate of ticks that had bitten humans. Earlier studies included ticks collected through flagging an area (1,2); this study provides specific information about the infection rate of ticks feeding on humans. The ticks were collected from persons who reported their tick bites on the tracking website, http://www.tekenradar.nlExternal Web Site Icon. After removal of the ticks from the skin, the ticks were submitted to the National Institute of Public Health and the Environment. For 1,040 ticks gathered during April–June 2012, we determined tick species, stage of development, and gender by microscopic examination.
We defined the degree of engorgement in 4 categories from unengorged (score 0) to fully engorged (score 3), as visually determined. To isolate DNA, we boiled the ticks with engorgement scores of 0­1 in ammonium hydroxide (6); for ticks with engorgement scores of 2–3, we used the QIAGEN (Valencia, CA . USA) blood and tissue DNA-extraction kit (7). We used aBmiyamotoi–specific real-time PCR based on the flagellin gene for detection of the bacteria (5). Quantitative PCR-positive tick lysates were tested with a conventional PCR, which amplifies a fragment of glycerophosphodiester phosphodiesterase (glpQ) gene, to confirm the outcome (5). These PCR products were sequenced and were identical to B. miyamotoi sequences filed in GenBank (AB824855). We determined the presence of Bburgdorferi DNA with a duplex quantitative PCR using fragments of the outer membrane protein A gene and the flagellin B gene as targets (7).
All 1,040 ticks were identified as Ixodes ricinus, the most common tick that transmits B. burgdorferi in northern Europe (8). We detected Bmiyamotoi DNA in 37 ticks (3.6%) using real-time PCR targeting the flagellin gene, which was confirmed for 32 ticks (3.1%) in the conventional PCR targeting the glpQ gene. (Technical Appendix Adobe PDF file [PDF - 17 KB - 1 page] Table). In 9 of the 37 ticks positive for BmiyamotoiBburgdorferi was also detected. Similar to B. burgdorferi, the risk of transmission of B. miyamotoi is likely to become higher if ticks become engorged with blood; 23 of the 37 (62.2%) B. miyamotoi–infected ticks were somewhat engorged (score 1–3) and thus had such an increased risk for transmission. All glpQ sequences of the detected Bmiyamotoi isolates were identical to the sequence detected in the sample from the patient reported in the Netherlands this year by Hovius et al. (5). B. burgdorferi DNA was detected in 190 ticks (18.3%) compared with 11.8% detected in a study that included ticks collected through flagging (9).
Figure
Thumbnail of Locations of ticks collected through the website http://www.tekenradar.nl in the Netherlands during summer 2012,. Ticks included in the study were submitted from all parts of the country; ticks positive for Borrelia miyamotoi and B. burgdorferi were found in almost every region.
Figure. Locations of ticks collected through the websitehttp://www.tekenradar.nlExternal Web Site Iconin the Netherlands during summer 2012,Ticks included in the study were submitted from all parts of the country; ticks positive for Borrelia...
Figure shows that ticks included in the study were submitted from all parts of the country; B. miyamotoi– and B. burgdorferi–positive ticks were found in almost every region. Of the ≈1 million tick bites per year in the Netherlands (10), an estimated 36,000 were by ticks that were infected with B. miyamotoi, and 183,000 were by ticks infected with B. burgdorferi. This substantial human exposure to B. miyamotoi and the reported cases in Russia, the United States, and, recently, the Netherlands (35) raises the question “To what extent does exposure to B. miyamotoi lead to human disease in the general population?” These results call for the development of sensitive and specific serologic and molecular tests for B. miyamotoito identify possible patients, which will lead to a better understanding of the clinical spectrum of B. miyamotoi–induced disease.
Manoj Fonville, Ingrid.H.M. Friesema, Paul D. Hengeveld, Arieke Docters van Leeuwen, Seta Jahfari, Margriet G. Harms, Arnold J.H. van Vliet, Agnetha Hofhuis, Wilfrid van Pelt, Hein Sprong, and Cees C. van den WijngaardComments to Author 
Author affiliations: National Institute of Public Health and the Environment, Bilthoven, the Netherlands (M. Fonville, I.H.M. Friesema, P.D. Hengeveld, A. Docters van Leeuwen, S. Jahfari, M.G. Harms, A. Hofhuis, W. van Pelt, H. Sprong, C.C. van den Wijngaard)Wageningen University, Wageningen, the Netherlands, (A.J.H. van Vliet)

Acknowledgment

This study was financed by the Ministry of Health, Welfare and Sport, the Netherlands.

References

  1. Fukunaga MTakahashi YTsuruta YMatsushita ORalph DMcClelland MGenetic and phenotypic analysis of Borrelia miyamotoi sp. nov., isolated from the ixodid tick Ixodes persulcatus, the vector for Lyme disease in Japan. Int J Syst Bacteriol1995;45:80410 . DOIExternal Web Site IconPubMedExternal Web Site Icon
  2. Geller JNazarova LKatargina OJarvekulg LFomenko NGolovljova IDetection and genetic characterization of relapsing fever spirochete Borrelia miyamotoi in Estonian ticks. PLoS ONE2012;7:e51914 . DOIExternal Web Site IconPubMedExternal Web Site Icon
  3. Platonov AEKaran LSKolyasnikova NMMakhneva NAToporkova MGMaleev VV,Humans infected with relapsing fever spirochete Borrelia miyamotoi, Russia. Emerg Infect Dis2011;17:181623 . DOIExternal Web Site IconPubMedExternal Web Site Icon
  4. Gugliotta JLGoethert HKBerardi VPTelford SR IIIMeningoencephalitis from Borrelia miyamotoi in an immunocompromised patient. N Engl J Med2013;368:2405DOIExternal Web Site IconPubMedExternal Web Site Icon
  5. Hovius JWde Wever BSohne MBrouwer MCCoumou JWagemakers AA case of meningoencephalitis by the relapsing fever spirochaete Borrelia miyamotoi in Europe.Lancet2013;382:658 . DOIExternal Web Site IconPubMedExternal Web Site Icon
  6. Schouls LMVan De Pol IRijpkema SGSchot CSDetection and identification of Ehrlichia, Borrelia burgdorferi sensu lato, and Bartonella species in Dutch Ixodes ricinus ticks. J Clin Microbiol1999;37:221522 .PubMedExternal Web Site Icon
  7. Heylen DTijsse EFonville MMatthysen ESprong HTransmission dynamics of Borrelia burgdorferi s.l. in a bird tick community. Environ Microbiol2013;15:66373DOIExternal Web Site IconPubMedExternal Web Site Icon
  8. Heyman PCochez CHofhuis Avan der Giessen JSprong HPorter SRA clear and present danger: tick-borne diseases in Europe. Expert Rev Anti Infect Ther.2010;8:3350 . DOIExternal Web Site IconPubMedExternal Web Site Icon
  9. Coipan ECJahfari SFonville MMaassen CBvan der Giessen JTakken W,Spatiotemporal dynamics of emerging pathogens in questing Ixodes ricinus. Front cell infect microbiol. 2013;3:36.External Web Site Icon
  10. Hofhuis AHarms MGvan der Giessen JWBSprong HNotermans DWvan Pelt W. [Lyme disease in the Netherlands 1994 - 2009]. Infectieziektebulletin 2010;21(3):84–7 [cited 2014 Feb 27]http://www.rivm.nl/Bibliotheek/Algemeen_Actueel/Uitgaven/Infectieziekten_Bulletin/Archief_jaargangenExternal Web Site Icon.

Figure

Technical Appendix

Suggested citation for this article: Fonville M, Friesema IHM, Hengeveld PD, Docters van Leeuwen A, Jahfari S, Harms MG, et al. Human exposure to tickborne relapsing fever spirochete Borreliamiyamotoi, the Netherlands [letter]. Emerg Infect Dis. 2014 Jul [date cited].http://dx.doi.org/10.3201/eid2007.131525External Web Site Icon
DOI: 10.3201/eid2007.131525

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