Literature DB >> 24963562

Human exposure to tickborne relapsing fever spirochete Borrelia miyamotoi, the Netherlands.

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, Cees C van den Wijngaard.   

Abstract

Entities:  

Keywords:  B. burgdorferi sensu lato; Borrelia; Lyme disease; Tickborne diseases; borreliosis; miyamotoi; relapsing fever; the Netherlands; zoonoses

Mesh:

Year:  2014        PMID: 24963562      PMCID: PMC4073841          DOI: 10.3201/eid2007.131525

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


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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 (). 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 (,). B. miyamotoi infections among humans were first reported in Russia in 2011 (), and in 2013 in the United States (). Recently, the first patient infected with B. miyamotoi was reported in the Netherlands (). Conditions reported to be associated with B. miyamotoi 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 B. miyamotoi infections (,), B. miyamotoi infections may remain undiagnosed. Nevertheless, the relationship between B. miyamotoi 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 (–). 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 B. miyamotoi infection rate of ticks that had bitten humans. Earlier studies included ticks collected through flagging an area (,); our 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 website http://www.tekenradar.nl. 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 0­–1 in ammonium hydroxide (); for ticks with engorgement scores of 2–3, we used the QIAGEN (Valencia, CA . USA) blood and tissue DNA-extraction kit (). We used a B. miyamotoi–specific real-time PCR based on the flagellin gene for detection of the bacteria (). Quantitative PCR-positive tick lysates were tested with a conventional PCR, which amplifies a fragment of glycerophosphodiester phosphodiesterase (glpQ) gene, to confirm the outcome (). These PCR products were sequenced and were identical to B. miyamotoi sequences filed in GenBank (AB824855). We determined the presence of B. burgdorferi DNA with a duplex quantitative PCR using fragments of the outer membrane protein A gene and the flagellin B gene as targets (). All 1,040 ticks were identified as Ixodes ricinus, the most common tick that transmits B. burgdorferi in northern Europe (). We detected B. miyamotoi 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 Table). In 9 of the 37 ticks positive for B. miyamotoi, B. burgdorferi 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 B. miyamotoi isolates were identical to the sequence detected in the sample from the patient reported in the Netherlands this year by Hovius et al. (). B. burgdorferi DNA was detected in 190 ticks (18.3%) compared with 11.8% detected in a study that included ticks collected through flagging (). 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 (), 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 (–) raises the question to what extent exposure to B. miyamotoi leads to human disease in the general population? These results call for the development of sensitive and specific serologic and molecular tests for B. miyamotoi to identify possible patients, which will lead to a better understanding of the clinical spectrum of B. miyamotoi–induced disease.
Figure

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.

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.

Technical Appendix

Infection rates of Ixodes ricinus ticks with Borrelia miyamotoi and B. burgdorferi
  9 in total

Review 1.  A clear and present danger: tick-borne diseases in Europe.

Authors:  Paul Heyman; Christel Cochez; Agnetha Hofhuis; Joke van der Giessen; Hein Sprong; Sarah Rebecca Porter; Bertrand Losson; Claude Saegerman; Oliver Donoso-Mantke; Matthias Niedrig; Anna Papa
Journal:  Expert Rev Anti Infect Ther       Date:  2010-01       Impact factor: 5.091

2.  Detection and identification of Ehrlichia, Borrelia burgdorferi sensu lato, and Bartonella species in Dutch Ixodes ricinus ticks.

Authors:  L M Schouls; I Van De Pol; S G Rijpkema; C S Schot
Journal:  J Clin Microbiol       Date:  1999-07       Impact factor: 5.948

3.  Transmission dynamics of Borrelia burgdorferi s.l. in a bird tick community.

Authors:  Dieter Heylen; Ellen Tijsse; Manoj Fonville; Erik Matthysen; Hein Sprong
Journal:  Environ Microbiol       Date:  2012-12-23       Impact factor: 5.491

4.  A case of meningoencephalitis by the relapsing fever spirochaete Borrelia miyamotoi in Europe.

Authors:  Joppe W R Hovius; Bob de Wever; Maaike Sohne; Matthijs C Brouwer; Jeroen Coumou; Alex Wagemakers; Anneke Oei; Henrike Knol; Sukanya Narasimhan; Caspar J Hodiamont; Setareh Jahfari; Steven T Pals; Hugo M Horlings; Erol Fikrig; Hein Sprong; Marinus H J van Oers
Journal:  Lancet       Date:  2013-08-17       Impact factor: 79.321

5.  Meningoencephalitis from Borrelia miyamotoi in an immunocompromised patient.

Authors:  Joseph L Gugliotta; Heidi K Goethert; Victor P Berardi; Sam R Telford
Journal:  N Engl J Med       Date:  2013-01-17       Impact factor: 91.245

6.  Genetic and phenotypic analysis of Borrelia miyamotoi sp. nov., isolated from the ixodid tick Ixodes persulcatus, the vector for Lyme disease in Japan.

Authors:  M Fukunaga; Y Takahashi; Y Tsuruta; O Matsushita; D Ralph; M McClelland; M Nakao
Journal:  Int J Syst Bacteriol       Date:  1995-10

7.  Humans infected with relapsing fever spirochete Borrelia miyamotoi, Russia.

Authors:  Alexander E Platonov; Ludmila S Karan; Nadezhda M Kolyasnikova; Natalya A Makhneva; Marina G Toporkova; Victor V Maleev; Durland Fish; Peter J Krause
Journal:  Emerg Infect Dis       Date:  2011-10       Impact factor: 6.883

8.  Spatiotemporal dynamics of emerging pathogens in questing Ixodes ricinus.

Authors:  Elena Claudia Coipan; Setareh Jahfari; Manoj Fonville; Catharina B Maassen; Joke van der Giessen; Willem Takken; Katsuhisa Takumi; Hein Sprong
Journal:  Front Cell Infect Microbiol       Date:  2013-07-30       Impact factor: 5.293

9.  Detection and genetic characterization of relapsing fever spirochete Borrelia miyamotoi in Estonian ticks.

Authors:  Julia Geller; Lidia Nazarova; Olga Katargina; Lilian Järvekülg; Natalya Fomenko; Irina Golovljova
Journal:  PLoS One       Date:  2012-12-14       Impact factor: 3.240

  9 in total
  15 in total

1.  Borrelia miyamotoi and Co-Infection with Borrelia afzelii in Ixodes ricinus Ticks and Rodents from Slovakia.

Authors:  Zuzana Hamšíková; Claudia Coipan; Lenka Mahríková; Lenka Minichová; Hein Sprong; Mária Kazimírová
Journal:  Microb Ecol       Date:  2016-12-19       Impact factor: 4.552

Review 2.  Neoehrlichiosis: an emerging tick-borne zoonosis caused by Candidatus Neoehrlichia mikurensis.

Authors:  Cornelia Silaghi; Relja Beck; José A Oteo; Martin Pfeffer; Hein Sprong
Journal:  Exp Appl Acarol       Date:  2015-06-17       Impact factor: 2.132

3.  Ticking on Pandora's box: a prospective case-control study into 'other' tick-borne diseases.

Authors:  D Hoornstra; M G Harms; S A Gauw; A Wagemakers; T Azagi; K Kremer; H Sprong; C C van den Wijngaard; J W Hovius
Journal:  BMC Infect Dis       Date:  2021-05-29       Impact factor: 3.090

4.  Presence of zoonotic agents in engorged ticks and hedgehog faeces from Erinaceus europaeus in (sub) urban areas.

Authors:  Aleksandra I Krawczyk; Arieke Docters van Leeuwen; Wilma Jacobs-Reitsma; Lucas M Wijnands; El Bouw; Setareh Jahfari; Angela H A M van Hoek; Joke W B van der Giessen; Jeroen H Roelfsema; Michiel Kroes; Jenny Kleve; Yolanda Dullemont; Hein Sprong; Arnout de Bruin
Journal:  Parasit Vectors       Date:  2015-04-09       Impact factor: 3.876

5.  High seroprevalence of Borrelia miyamotoi antibodies in forestry workers and individuals suspected of human granulocytic anaplasmosis in the Netherlands.

Authors:  S Jahfari; T Herremans; A E Platonov; H Kuiper; L S Karan; O Vasilieva; M P G Koopmans; J W R Hovius; H Sprong
Journal:  New Microbes New Infect       Date:  2014-09-06

6.  Multiple and Diverse vsp and vlp Sequences in Borrelia miyamotoi, a Hard Tick-Borne Zoonotic Pathogen.

Authors:  Alan G Barbour
Journal:  PLoS One       Date:  2016-01-19       Impact factor: 3.240

7.  Borrelia miyamotoi Infections in Humans and Ticks, Northeastern China.

Authors:  Bao-Gui Jiang; Na Jia; Jia-Fu Jiang; Yuan-Chun Zheng; Yan-Li Chu; Rui-Ruo Jiang; Ya-Wei Wang; Hong-Bo Liu; Ran Wei; Wen-Hui Zhang; Yan Li; Xiao-Wei Xu; Jin-Ling Ye; Nan-Nan Yao; Xiao-Jing Liu; Qiu-Bo Huo; Yi Sun; Ju-Liang Song; Wei Liu; Wu-Chun Cao
Journal:  Emerg Infect Dis       Date:  2018-02       Impact factor: 6.883

8.  Predicting the risk of Lyme borreliosis after a tick bite, using a structural equation model.

Authors:  Agnetha Hofhuis; Jan van de Kassteele; Hein Sprong; Cees C van den Wijngaard; Margriet G Harms; Manoj Fonville; Arieke Docters van Leeuwen; Mariana Simões; Wilfrid van Pelt
Journal:  PLoS One       Date:  2017-07-24       Impact factor: 3.240

Review 9.  Dermacentor reticulatus: a vector on the rise.

Authors:  Gábor Földvári; Pavel Široký; Sándor Szekeres; Gábor Majoros; Hein Sprong
Journal:  Parasit Vectors       Date:  2016-06-01       Impact factor: 3.876

10.  Borrelia miyamotoi and Candidatus Neoehrlichia mikurensis in Ixodes ricinus Ticks, Romania.

Authors:  Zsuzsa Kalmár; Hein Sprong; Andrei D Mihalca; Călin M Gherman; Mirabela O Dumitrache; Elena C Coipan; Manoj Fonville; Vasile Cozma
Journal:  Emerg Infect Dis       Date:  2016-03       Impact factor: 6.883

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