Literature DB >> 17979540

Ticks and associated pathogens collected from domestic animals in the Netherlands.

Ard M Nijhof1, Christa Bodaan, Milagros Postigo, Hans Nieuwenhuijs, Marieke Opsteegh, Linda Franssen, Florian Jebbink, Frans Jongejan.   

Abstract

Following an outbreak of autochthonous canine babesiosis in the Netherlands, a request made to veterinarians and the public to collect ticks from companion animals resulted in 4298 ticks submitted between July 2005 and October 2006 to our center. Ticks were identified as Ixodes ricinus adults (2907/4298, 67.6%), Ixodes sp. nymphs (529/4298, 12.3%) and Ixodes sp. larvae (385/4298, 9.0%), I. hexagonus adults (328/4298, 7.6%), Dermacentor reticulatus (72/4298, 1.7%), and several other exotic tick species such as Amblyomma flavomaculatum (formerly Aponomma flavomaculatum), Hyalomma marginatum rufipes, Rhipicephalus sanguineus, and R. turanicus (55/4298, 1.3%). Eight localities were surveyed for the presence of local D. reticulatus, a tick not indigenous to the Netherlands, based on multiple submissions of D. reticulatus ticks from these areas. D. reticulatus was collected from the vegetation in six of these localities, confirming the presence of populations of this tick in the Netherlands. Adult I. ricinus (n=251), I. hexagonus (n=237), and D. reticulatus (n=344) ticks were selected at random and subsequently screened by polymerase chain reaction (PCR) and reverse line blot (RLB) hybridization for the presence of Borrelia, Babesia, Theileria, Anaplasma, Ehrlichia, and Rickettsia species. I. ricinus ticks were infected with Rickettsia helvetica (24.7%), spirochetes belonging to the Borrelia burgdorferi sensu lato group (7.2%), the Ehrlichia-like "Schotii" variant (2.4%), Anaplasma phagocytophilum (1.6%), Babesia sp. (EU1) (1.2%), Babesia divergens (0.4%), and Babesia microti (0.4%). A. phagocytophilum (5.9%) and R. helvetica (0.8%) were also detected in adult I. hexagonus ticks. Spotted fever group Rickettsiae, previously reported as Rickettsia sp. DnS14/RpA4 (14.0%), and Borrelia burgdorferi sensu lato (0.3%) were detected in the D. reticulatus ticks, which appeared to be free from B. canis infection. We concluded that a much broader spectrum of ticks and tick-borne pathogens is present in the Netherlands than previously thought, including several potential zoonotic pathogens.

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Year:  2007        PMID: 17979540     DOI: 10.1089/vbz.2007.0130

Source DB:  PubMed          Journal:  Vector Borne Zoonotic Dis        ISSN: 1530-3667            Impact factor:   2.133


  68 in total

1.  Canine babesiosis in Romania due to Babesia canis and Babesia vogeli: a molecular approach.

Authors:  Mariana Ionita; Ioan Liviu Mitrea; Kurt Pfister; Dietmar Hamel; Catalin Marius Buzatu; Cornelia Silaghi
Journal:  Parasitol Res       Date:  2011-10-18       Impact factor: 2.289

2.  Approaches for Reverse Line Blot-Based Detection of Microbial Pathogens in Ixodes ricinus Ticks Collected in Austria and Impact of the Chosen Method.

Authors:  Anna-Margarita Schötta; Michiel Wijnveld; Hannes Stockinger; Gerold Stanek
Journal:  Appl Environ Microbiol       Date:  2017-06-16       Impact factor: 4.792

Review 3.  The role of ticks in the maintenance and transmission of Crimean-Congo hemorrhagic fever virus: A review of published field and laboratory studies.

Authors:  Aysen Gargili; Agustin Estrada-Peña; Jessica R Spengler; Alexander Lukashev; Patricia A Nuttall; Dennis A Bente
Journal:  Antiviral Res       Date:  2017-06-01       Impact factor: 5.970

4.  Close geographic association of human neoehrlichiosis and tick populations carrying "Candidatus Neoehrlichia mikurensis" in eastern Switzerland.

Authors:  Florian P Maurer; Peter M Keller; Christian Beuret; Cornelia Joha; Yvonne Achermann; Jacques Gubler; Daniela Bircher; Urs Karrer; Jan Fehr; Lukas Zimmerli; Guido V Bloemberg
Journal:  J Clin Microbiol       Date:  2012-10-31       Impact factor: 5.948

5.  Molecular detection of Anaplasma platys, Anaplasma phagocytophilum and Wolbachia sp. but not Ehrlichia canis in Croatian dogs.

Authors:  Doroteja Huber; Irena Reil; Sanja Duvnjak; Daria Jurković; Damir Lukačević; Miroslav Pilat; Ana Beck; Željko Mihaljević; Lea Vojta; Adam Polkinghorne; Relja Beck
Journal:  Parasitol Res       Date:  2017-09-14       Impact factor: 2.289

6.  Experimental in vitro transmission of Babesia sp. (EU1) by Ixodes ricinus.

Authors:  Sarah Bonnet; Nadine Brisseau; Axelle Hermouet; Maggy Jouglin; Alain Chauvin
Journal:  Vet Res       Date:  2009-02-13       Impact factor: 3.683

7.  Ectoparasites of dogs and cats in Albania.

Authors:  Dashamir Xhaxhiu; Ilir Kusi; Dhimiter Rapti; Martin Visser; Martin Knaus; Thomas Lindner; Steffen Rehbein
Journal:  Parasitol Res       Date:  2009-08-19       Impact factor: 2.289

8.  Natural transmission of Zoonotic Babesia spp. by Ixodes ricinus ticks.

Authors:  Claire A M Becker; Agnès Bouju-Albert; Maggy Jouglin; Alain Chauvin; Laurence Malandrin
Journal:  Emerg Infect Dis       Date:  2009-02       Impact factor: 6.883

9.  Ixodes ricinus ticks are reservoir hosts for Rickettsia helvetica and potentially carry flea-borne Rickettsia species.

Authors:  Hein Sprong; Peter R Wielinga; Manoj Fonville; Chantal Reusken; Afke H Brandenburg; Fred Borgsteede; Cor Gaasenbeek; Joke Wb van der Giessen
Journal:  Parasit Vectors       Date:  2009-09-04       Impact factor: 3.876

10.  Rickettsia slovaca and R. raoultii in tick-borne Rickettsioses.

Authors:  Philippe Parola; Clarisse Rovery; Jean Marc Rolain; Philippe Brouqui; Bernard Davoust; Didier Raoult
Journal:  Emerg Infect Dis       Date:  2009-07       Impact factor: 6.883

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