Literature DB >> 18639947

The phenology and population dynamics of Culicoides spp. in different ecosystems in The Netherlands.

Willem Takken1, Niels Verhulst, Ernst-Jan Scholte, Frans Jacobs, Yde Jongema, Ron van Lammeren.   

Abstract

The Netherlands has enjoyed a relatively free state of vector-borne diseases of economic importance for more than one century. Emerging infectious diseases may change this situation, threatening the health of humans, domestic livestock and wildlife. In order to be prepared for the potential outbreak of vector-borne diseases, a study was undertaken to investigate the distribution and seasonal dynamics of candidate vectors of infectious diseases with emphasis on bluetongue vectors (Culicoides spp.). The study focused primarily on the relationship between characteristic ecosystems suitable for bluetongue vectors and climate, as well as on the phenology and population dynamics of these vectors. Twelve locations were selected, distributed over four distinct habitats: a wetland area, three riverine systems, four peat land areas and four livestock farms. Culicoides populations were sampled continuously using CO(2)-baited counterflow traps from July 2005 until August 2006, with an interruption from November 2005 to March 2006. All vectors were identified to species level. Meteorological and environmental data were collected at each location. Culicoides species were found in all four different habitat types studied. Wetland areas and peat bogs were rich in Culicoides spp. The taxonomic groups Culicoides obsoletus (Meigen) and Culicoides pulicaris (Linnaeus) were strongly associated with farms. Eighty-eight percent of all Culicoides consisted of the taxon C. obsoletus/Culicoides scoticus. On the livestock farms, 3% of Culicoides existed of the alleged bluetongue vector Culicoides dewulfi Goetghebuer. Culicoides impunctatus Goetghebuer was strongly associated with wetland and peat bog. Many Culicoides species were found until late in the phenological season and their activity was strongly associated with climate throughout the year. High annual variations in population dynamics were observed within the same study areas, which were probably caused by annual variations in environmental conditions. The study demonstrates that candidate vectors of bluetongue virus are present in natural and livestock-farm habitats in the Netherlands, distributed widely across the country. Under favourable climatic conditions, following virus introduction, bluetongue can spread among livestock (cattle, sheep and goats), depending on the nature of the viral serotype. The question now arises whether the virus can survive the winter conditions in north-western Europe and whether measures can be taken that effectively halt further spread of the disease.

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Year:  2008        PMID: 18639947     DOI: 10.1016/j.prevetmed.2008.06.015

Source DB:  PubMed          Journal:  Prev Vet Med        ISSN: 0167-5877            Impact factor:   2.670


  22 in total

1.  Molecular differentiation of Culicoides biting midges (Diptera: Ceratopogonidae) from the subgenus Culicoides Latreille in Denmark.

Authors:  S B Lassen; S Achim Nielsen; H Skovgård; M Kristensen
Journal:  Parasitol Res       Date:  2011-10-29       Impact factor: 2.289

2.  Community analysis of biting midges (Culicoides Latr.) on livestock farms in Denmark.

Authors:  S A Nielsen; G Banta; A-M Rasmussen; H Skovgård
Journal:  Parasitol Res       Date:  2014-10-19       Impact factor: 2.289

Review 3.  Present and future arboviral threats.

Authors:  Scott C Weaver; William K Reisen
Journal:  Antiviral Res       Date:  2009-10-24       Impact factor: 5.970

4.  Sticky-trapping biting midges (Culicoides spp.) alighting on cattle and sheep: effects of trap colour and evidence for host preference.

Authors:  G M Thompson; S Jess; A W Gordon; A K Murchie
Journal:  Parasitol Res       Date:  2014-06-10       Impact factor: 2.289

5.  Identity and diversity of blood meal hosts of biting midges (Diptera: Ceratopogonidae: Culicoides Latreille) in Denmark.

Authors:  Sandra B Lassen; Søren Achim Nielsen; Michael Kristensen
Journal:  Parasit Vectors       Date:  2012-07-23       Impact factor: 3.876

6.  Are bogs reservoirs for emerging disease vectors? Evaluation of culicoides populations in the Hautes Fagnes Nature Reserve (Belgium).

Authors:  Jean-Yves Zimmer; François Smeets; Grégory Simonon; Jean Fagot; Eric Haubruge; Frédéric Francis; Bertrand Losson
Journal:  PLoS One       Date:  2013-06-14       Impact factor: 3.240

7.  Estimating front-wave velocity of infectious diseases: a simple, efficient method applied to bluetongue.

Authors:  Maryline Pioz; Hélène Guis; Didier Calavas; Benoît Durand; David Abrial; Christian Ducrot
Journal:  Vet Res       Date:  2011-04-20       Impact factor: 3.683

8.  Spatio-temporal occurrence of Culicoides biting midges in the climatic regions of Switzerland, along with large scale species identification by MALDI-TOF mass spectrometry.

Authors:  Christian Kaufmann; Irene C Steinmann; Daniel Hegglin; Francis Schaffner; Alexander Mathis
Journal:  Parasit Vectors       Date:  2012-10-31       Impact factor: 3.876

9.  The range of attraction for light traps catching Culicoides biting midges (Diptera: Ceratopogonidae).

Authors:  Carsten Kirkeby; Kaare Græsbøll; Anders Stockmarr; Lasse E Christiansen; René Bødker
Journal:  Parasit Vectors       Date:  2013-03-15       Impact factor: 3.876

10.  Development and field evaluation of the sentinel mosquito arbovirus capture kit (SMACK).

Authors:  Brian J Johnson; Tim Kerlin; Sonja Hall-Mendelin; Andrew F van den Hurk; Giles Cortis; Stephen L Doggett; Cheryl Toi; Ken Fall; Jamie L McMahon; Michael Townsend; Scott A Ritchie
Journal:  Parasit Vectors       Date:  2015-10-06       Impact factor: 3.876

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