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Medical and veterinary entomology2025; doi: 10.1111/mve.70016

Investigation of the global transportation of Culicoides biting midges, vectors of livestock and equid arboviruses, from flower-packing plants in Kenya.

Abstract: In recent decades there has been a huge increase in the export of cut flowers from countries in Africa and elsewhere to European flower markets, with the vast majority first entering the Netherlands for local use or for export. Coincidentally, three significant livestock disease outbreaks caused by viruses associated with Africa or other tropical regions were first detected in the Netherlands (bluetongue virus serotype 8 (BTV-8), 2006, and BTV-3, 2023) and in western Germany about 200 km from the Netherlands border (Schmallenberg virus, SBV, 2011). This study aimed to determine whether Culicoides biting midges (Diptera: Ceratopogonidae), the vectors of BTV and SBV, are present within flower-packaging plants in East Africa, and therefore whether Culicoides could be unknowingly exported during the shipping of cut flowers. Field sampling was undertaken at a flower-packaging facility in Kenya, East Africa. The facility undertook all stages of cut flower production from maintaining rootstock through to packaging and shipping to an airport for international export. Trapping was undertaken at each stage of production (rootstock, propagation, inside growing greenhouses, in the packing-house, inside cold-storage rooms, during transportation) using Centers for Disease Control and Prevention (CDC) Light Emitting Diode (LED) light traps. Hand-held aspirators were used to obtain individual insects directly from flowers and around composting sites, while emergence traps studied insect emergence from compost, leaf litter and flowers discarded at quality control checkpoints. A maximum nightly catch of 269 Culicoides was identified on a half-acre smallholding, containing 15 ruminants and 40 birds, located 20 m from the nearest greenhouse. The greatest numbers of Culicoides were trapped at a pond (n = 23) and leaf-litter compost site (n = 19) within the curtilage of the flower-packaging plant. Of the seven greenhouses sampled, three had Culicoides trapped overnight (mean = 4, range: 1-9), and no Culicoides were trapped in the propagation units. No Culicoides were trapped in the pack house, cold-store, or during transportation of the flowers to the airport for shipment. No Culicoides emerged from emergence traps or were trapped when aspirating directly from flowers. This is the first study to investigate whether Culicoides are present within flower packaging plants in Africa. The results highlight that although present in small numbers both outside and within greenhouses, the presence of Culicoides declined with each stage of production. Therefore, the risk of exporting Culicoides with packaged cut flowers is non-zero but likely very small.
Publication Date: 2025-10-08 PubMed ID: 41058475DOI: 10.1111/mve.70016Google Scholar: Lookup
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  • Journal Article

Summary

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Overview

  • This study investigates whether Culicoides biting midges, which can transmit livestock viruses, are present in flower-packaging plants in Kenya and if they could be unintentionally exported with cut flowers.
  • It examines the potential risk of transporting these vectors internationally via the cut flower trade, particularly to European markets.

Background

  • There has been a significant increase in the export of cut flowers from African countries, including Kenya, to European flower markets, with many flowers first arriving in the Netherlands.
  • Several livestock disease outbreaks linked to viruses from Africa or tropical regions (e.g., bluetongue virus serotype 8 in 2006, BTV-3 in 2023, Schmallenberg virus in 2011) were first detected in Europe near major flower import hubs.
  • Culicoides biting midges are known vectors of these viruses affecting livestock, raising concerns that these insects may be transported alongside the flower shipments.

Research Objective

  • To determine if Culicoides biting midges are present within flower-packaging plants in East Africa (Kenya).
  • To assess the likelihood of these midges being exported unintentionally as part of cut flower shipments.

Methodology

  • Field sampling was conducted at a flower-packaging facility in Kenya that included all stages of cut flower production, from maintaining rootstock to shipping.
  • Trapping methods included:
    • CDC LED light traps at different production stages: rootstock, propagation units, greenhouses, packing-house, cold-storage, and transport.
    • Hand-held aspirators to capture insects directly from flowers and composting areas.
    • Emergence traps placed over compost, leaf litter, and discarded flowers to detect newly emerging insects.
  • A nearby smallholding with livestock and birds served as a comparative habitat for trapping maximum Culicoides numbers.

Results

  • A maximum of 269 Culicoides were caught in one night on the smallholding, highlighting ideal conditions for Culicoides abundance near livestock.
  • Within the flower-packaging plant premises:
    • The highest counts were at a pond (23 midges) and leaf-litter compost site (19 midges).
    • Three out of seven greenhouses had low numbers of Culicoides overnight (mean 4, range 1-9).
    • No midges were trapped in propagation units, packing house, cold storage, or during transport to the airport.
    • Emergence traps and aspirators found no Culicoides emerging from or directly on flowers.

Conclusions

  • This is the first study to examine the presence of Culicoides biting midges within African flower-packaging plants.
  • Culicoides are present in small numbers outside and inside some greenhouses but their numbers decline significantly during later production stages.
  • The absence of Culicoides in packing, storage, and transport steps reduces the likelihood of their export on cut flowers to very low but not zero levels.
  • Therefore, while there is some risk of unintentional global transport of these disease vectors via flower shipments, it appears to be minimal according to this study.

Implications

  • Understanding the potential for transporting disease vectors through international trade can improve biosecurity measures.
  • Further monitoring and control protocols at flower packaging and shipment points can help lower the risk of spreading arboviruses that affect livestock and equids.
  • This research supports the need for integrated vector management and routine surveillance in global flower export industries to prevent disease outbreaks in importing countries.

Cite This Article

APA
Stokes JE, Labuschagne K, Fèvre EM, Baylis M. (2025). Investigation of the global transportation of Culicoides biting midges, vectors of livestock and equid arboviruses, from flower-packing plants in Kenya. Med Vet Entomol. https://doi.org/10.1111/mve.70016

Publication

ISSN: 1365-2915
NlmUniqueID: 8708682
Country: England
Language: English

Researcher Affiliations

Stokes, Jessica Eleanor
  • Liverpool University Climate and Infectious Diseases of Animals (LUCINDA) Group, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Leahurst Campus, Neston, Cheshire, UK.
Labuschagne, Karien
  • ARC - Onderstepoort Veterinary Research, EPV, Onderstepoort, South Africa.
Fèvre, Eric Maurice
  • Liverpool University Climate and Infectious Diseases of Animals (LUCINDA) Group, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Leahurst Campus, Neston, Cheshire, UK.
  • International Livestock Research Institute, Nairobi, Kenya.
Baylis, Matthew
  • Liverpool University Climate and Infectious Diseases of Animals (LUCINDA) Group, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Leahurst Campus, Neston, Cheshire, UK.
  • National Institute for Health Research, Health Protection Research Unit in Emerging and Zoonotic Infections, University of Liverpool, Liverpool, UK.

Grant Funding

  • University of Liverpool

References

This article includes 22 references
  1. Anon. Kenya flower industry on a boom trajectory. FarmBiz Africa .
  2. Anon. CBI trade statistics: cut flowers and foliage. CBI Market Intelligence, The Hague .
  3. Anon. Final pest risk analysis for cut flower and foliage imports—part 1. Department of Agriculture Canberra .
  4. Baylis M, Stokes JE, Labuschagne K, Fèvre EM, Kluiters G. Kenyan flower data deposit. University of Liverpool repository .
  5. Dyce AL. Biting midges (Diptera: Ceratopogonidae) reared from rotting cactus in Australia. Mosquito News 29, 644–649.
  6. Elbers ARW, Backx A, Meroc E, Gerbier G, Staubach C, Hendrickx G. Field observations during the bluetongue serotype 8 epidemic in 2006 – I. Detection of first outbreaks and clinical signs in sheep and cattle in Belgium, France and The Netherlands. Preventive Veterinary Medicine 87, 21–30.
  7. Glick JI. Culicoides biting midges (Diptera: Ceratopogonidae) of Kenya. Journal of Medical Entomology 27, 85–195.
  8. Hinsley A, Hughes AC, van Valkenburg J, Stark T, van Delft J, Sutherland W. Understanding the environmental and social risks from the international trade in ornamental plants. BioScience 75, biae124.
  9. Hoffmann B, Scheuch M, Hoeper D, Jungblut R, Holsteg M, Schirrmeier H. Novel orthobunyavirus in cattle, Europe, 2011. Emerging Infectious Diseases 18, 469–472.
  10. Holwerda M, Santman‐Berends IM, Harders F, Engelsma M, Vloet RP, Dijkstra E. Emergence of bluetongue virus serotype 3, the Netherlands, September 2023. Emerging Infectious Diseases 30, 1552.
  11. Ibáñez‐Justicia A, Koenraadt CJ, Stroo A, Van Lammeren R, Takken W. Risk‐based and adaptive invasive mosquito surveillance at lucky bamboo and used tire importers in The Netherlands. Journal of the American Mosquito Control Association 36, 89–98.
  12. Maan S, Maan NS, Ross‐Smith N, Batten CA, Shaw AE, Anthony SJ. Sequence analysis of bluetongue virus serotype 8 from The Netherlands 2006 and comparison to other European strains. Virology 377, 308–318.
  13. Meiswinkel R, Gomulski LM, Delecolle JC, Goffredo M, Gasperi G. The taxonomy of Culicoides vector complexes – unfinished business. Veterinaria Italiana 40, 151–159.
  14. Meiswinkel R, Labuschagne K, Goffredo M. Christopher Columbus and Culicoides: was C. jamaicensis Edwards, 1922 introduced into the Mediterranean 500 years ago and later re‐named C. paolae Boorman 1996. Veterinaria Italiana 40, 340–344.
  15. Mellor PS, Boorman J, Baylis M. Culicoides biting midges: their role as arbovirus vectors. Annual Review of Entomology 45, 307–340.
  16. Mellor PS, Carpenter S, Harrup L, Baylis M, Mertens PPC. Bluetongue in Europe and the Mediterranean Basin: history of occurrence prior to 2006. Preventive Veterinary Medicine 87, 4–20.
  17. Mintiens K, Meroc E, Mellor PS, Staubach C, Gerbier G, Elbers ARW. Possible routes of introduction of bluetongue virus serotype 8 into the epicentre of the 2006 epidemic in North‐Western Europe. Preventive Veterinary Medicine 87, 131–144.
  18. Saeed MF, Li L, Wang H, Weaver SC, Barrett AD. Phylogeny of the Simbu serogroup of the genus Bunyavirus. Journal of General Virology 82, 2173–2181.
  19. van den Brom R, Santman‐Berends I, van der Heijden MG, Harders F, Engelsma M, van Gennip RG. Bluetongue virus serotype 12 in sheep and cattle in The Netherlands in 2024 – a BTV serotype reported in Europe for the first time. Veterinary Microbiology 301, 110365.
  20. Walker AR, Davies FG. A preliminary survey of the epidemiology of bluetongue in Kenya. Journal of Hygiene 69, 47–60.
  21. Wernike K, Holsteg M, Schirrmeier H, Hoffmann B, Beer M. Natural infection of pregnant cows with Schmallenberg virus – a follow‐up study. PLoS One 9, e98223.
  22. Yanase T, Kato T, Aizawa M, Shuto Y, Shirafuji H, Yamakawa M. Genetic reassortment between Sathuperi and Shamonda viruses of the genus Orthobunyavirus in nature: implications for their genetic relationship to Schmallenberg virus. Archives of Virology 157, 1611–1616.

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