Literature DB >> 23891104

Rodent species as natural reservoirs of Borrelia burgdorferi sensu lato in different habitats of Ixodes ricinus in The Netherlands.

Fedor Gassner1, Willem Takken, Carin Lombaers-van der Plas, Pieter Kastelein, Arno J Hoetmer, Maarten Holdinga, Leonard S van Overbeek.   

Abstract

Rodents are natural reservoirs for human pathogenic spirochaetes of the Borrelia burgdorferi complex [B. burgdorferi sensu lato (s.l.)], and the pathogens are transmitted by Ixodes ricinus ticks to humans in The Netherlands. B. burgdorferi s.l. infection prevalence in questing ticks, rodents, and ticks feeding on these rodents, all sampled within the same short time span of five days in three different areas in The Netherlands, were compared in order to establish the relationship between ticks, reservoir hosts, and B. burgdorferi s.l. Questing nymphs were found in all 3 areas and numbers differed per area and even per site within areas. Infection prevalence in questing nymphs ranged between 0 and 20%. Apodemus sylvaticus and Myodes glareolus were the dominant rodents captured, and their numbers differed per area. Infection prevalence, determined by ear biopsies, ranged between 0 and 33.3% for both rodent species. Larvae were most frequently found feeding on these rodents, and their Borrelia infection prevalence ranged between 0 and 6.3% (A. sylvaticus) and between 0 and 29.4% (M. glareolus). The burden of nymphs feeding on rodents was low and varied per area with only 2 of 42 nymphs infected. Comparisons made on the basis of infection prevalence indicated that there was no clear relationship between rodents and questing nymphs when sampled within the same short time span. However, a possible relationship was present when questing ticks were sampled over longer periods in time (months) within or near the same areas (range of infection prevalence between 3.7 and 39.4). Confounding factors thus play a role in the interaction between rodents, ticks, and B. burgdorferi s.l., and it is very likely that other reservoir host species are responsible for the observed fluctuations. It is concluded that the local variations in rodent-Borrelia-tick interactions only partially explain the Lyme borreliosis risk in the sites studied and that other ecological determinants, notably vertebrate hosts and vegetation structure, should be incorporated in future studies of Lyme borreliosis risk.
Copyright © 2013 Elsevier GmbH. All rights reserved.

Entities:  

Keywords:  Apodemus sylvaticus; Borrelia afzelii; Borrelia burgdorferi sensu lato; Ixodes ricinus; Myodes glareolus; Reservoir host; Rodent

Mesh:

Substances:

Year:  2013        PMID: 23891104     DOI: 10.1016/j.ttbdis.2012.11.017

Source DB:  PubMed          Journal:  Ticks Tick Borne Dis        ISSN: 1877-959X            Impact factor:   3.744


  11 in total

1.  Europe-Wide Meta-Analysis of Borrelia burgdorferi Sensu Lato Prevalence in Questing Ixodes ricinus Ticks.

Authors:  Martin Strnad; Václav Hönig; Daniel Růžek; Libor Grubhoffer; Ryan O M Rego
Journal:  Appl Environ Microbiol       Date:  2017-07-17       Impact factor: 4.792

2.  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 3.  Multi-trophic interactions driving the transmission cycle of Borrelia afzelii between Ixodes ricinus and rodents: a review.

Authors:  Gilian van Duijvendijk; Hein Sprong; Willem Takken
Journal:  Parasit Vectors       Date:  2015-12-18       Impact factor: 3.876

4.  Larvae of Ixodes ricinus transmit Borrelia afzelii and B. miyamotoi to vertebrate hosts.

Authors:  Gilian van Duijvendijk; Claudia Coipan; Alex Wagemakers; Manoj Fonville; Jasmin Ersöz; Anneke Oei; Gábor Földvári; Joppe Hovius; Willem Takken; Hein Sprong
Journal:  Parasit Vectors       Date:  2016-02-20       Impact factor: 3.876

5.  Functional Redundancy and Ecological Innovation Shape the Circulation of Tick-Transmitted Pathogens.

Authors:  Agustín Estrada-Peña; José de la Fuente; Alejandro Cabezas-Cruz
Journal:  Front Cell Infect Microbiol       Date:  2017-05-31       Impact factor: 5.293

6.  The enzootic life-cycle of Borrelia burgdorferi (sensu lato) and tick-borne rickettsiae: an epidemiological study on wild-living small mammals and their ticks from Saxony, Germany.

Authors:  Anna Obiegala; Nina Król; Carolin Oltersdorf; Julian Nader; Martin Pfeffer
Journal:  Parasit Vectors       Date:  2017-03-13       Impact factor: 3.876

7.  Cascading effects of predator activity on tick-borne disease risk.

Authors:  Tim R Hofmeester; Patrick A Jansen; Hendrikus J Wijnen; Elena C Coipan; Manoj Fonville; Herbert H T Prins; Hein Sprong; Sipke E van Wieren
Journal:  Proc Biol Sci       Date:  2017-07-26       Impact factor: 5.349

8.  A cross-sectional study of small mammals for tick-borne pathogen infection in northern Mongolia.

Authors:  Laura A Pulscher; Thomas C Moore; Luke Caddell; Lkhagvatseren Sukhbaatar; Michael E von Fricken; Benjamin D Anderson; Battsetseg Gonchigoo; Gregory C Gray
Journal:  Infect Ecol Epidemiol       Date:  2018-03-16

9.  The genetic diversity of Borrelia afzelii is not maintained by the diversity of the rodent hosts.

Authors:  Claudia E Coipan; Gilian L A van Duijvendijk; Tim R Hofmeester; Katsuhisa Takumi; Hein Sprong
Journal:  Parasit Vectors       Date:  2018-08-06       Impact factor: 3.876

10.  Effect of rodent density on tick and tick-borne pathogen populations: consequences for infectious disease risk.

Authors:  Aleksandra I Krawczyk; Gilian L A van Duijvendijk; Arno Swart; Dieter Heylen; Ryanne I Jaarsma; Frans H H Jacobs; Manoj Fonville; Hein Sprong; Willem Takken
Journal:  Parasit Vectors       Date:  2020-01-20       Impact factor: 3.876

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