• Aucun résultat trouvé

Glossina palpalis gambiensis (Tsetse Fly)

N/A
N/A
Protected

Academic year: 2021

Partager "Glossina palpalis gambiensis (Tsetse Fly)"

Copied!
3
0
0

Texte intégral

(1)

HAL Id: cirad-02879787

http://hal.cirad.fr/cirad-02879787

Submitted on 24 Jun 2020

HAL is a multi-disciplinary open access

archive for the deposit and dissemination of

sci-entific research documents, whether they are

pub-lished or not. The documents may come from

teaching and research institutions in France or

abroad, or from public or private research centers.

L’archive ouverte pluridisciplinaire HAL, est

destinée au dépôt et à la diffusion de documents

scientifiques de niveau recherche, publiés ou non,

émanant des établissements d’enseignement et de

recherche français ou étrangers, des laboratoires

publics ou privés.

Distributed under a Creative Commons Attribution - NonCommercial - NoDerivatives| 4.0

International License

Glossina palpalis gambiensis (Tsetse Fly)

Jérémy Bouyer

To cite this version:

Jérémy Bouyer. Glossina palpalis gambiensis (Tsetse Fly). Trends in Parasitology, Elsevier, 2020,

�10.1016/j.pt.2020.05.010�. �cirad-02879787�

(2)

UNCORRECTED PR

OOF

Glossina palpalis gambiensis (Tsetse Fly)

Jérémy Bouyer

1,2,3,

*

1

Insect Pest Control Laboratory, Joint FAO/IAEA Programme of Nuclear Techniques in Food and Agriculture, Wagramerstrasse 5, A-1400, Vienna, Austria

2

Unité Mixte de Recherche‘Animal, Santé, Territoires, Risques et Ecosystèmes’, Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD), 34398, Montpellier, France

3

Unité Mixte de Recherche‘Interactions hôtes-vecteurs-parasites-environnement dans les maladies tropicales négligées dues aux trypanosomatides’, Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD), 34398 Montpellier, France

Trends

Trends inin ParasitologyParasitology

Glossina palpalis gambiensis is a riverine tsetse species endemic in West Africa and thriving in riparian vegeta-tion of the savannah areas from Burkina Faso and Mali to Guinea and Senegal. It is a major vector of human and animal trypanosomosis (sleeping sickness and nagana, respectively) in that region. G. p. gambiensis is an opportunistic species, feeding on a wide range of hosts from reptiles to pigs and cattle, with humans as one of its preferred hosts. Like most tsetse species, it has a narrow range of acceptable temperature and humidity, a low reproduction rate, and is thus very sensitive to climate change but can adapt to human modification of its environment and survive in polluted and densely populated areas. Its presence in the Niayes area of Senegal, where rainfall is below 500 mm a year, and in the Parc de Hahn of Dakar reveals an extraordinary plasticity. In the Niayes area it is presently targeted by an eradication program, including a sterile insect technique component.

Trends

Trends inin ParasitologyParasitology

TRANSMISSION FACTS:

G. p. gambiensis can transmit all Trypanosoma spp., particularly Trypanosoma brucei gambiense in humans and Trypanosoma vivax in cattle. It picks up the bloodstream form of trypanosomes from a host and injects the metacyclic form into the skin of another host after an extrinsic cycle of 10–30 days depending on the parasite species. It is a day-biter, with a peak of activity conditioned by temperature. Its distribution, density, lifespan and infection rate are also temperature-dependent. Its learning capability increases the hunting efficiency of older flies, that is, the host selected for thefirst bloodmeal can influence host selection for the second meal.

CONTROL FACTS:

Conventional control relies on insecticide-baited traps. Cattle are generally treated with pyrethroid pour-ons.

In Guinea, its control was instrumental in reducing the incidence of sleeping sickness. Its ecology and preferred habitats (riverine and dense forest vegetation) partially protect it against sequential aerosol spraying of insecticides that is more efficient against savannah tsetse species. It was eradicated from a 3000 km2area in

Burkina Faso (Sidéradougou) in the 1980s using an integrated strategy including the sterile insect technique, but the cleared area was then reinvaded because the target area was not isolated.

TAXONOMY AND CLASSIFICATION PHYLUM:Arthropoda

CLASS:Insecta

ORDER:Diptera

FAMILY:Glossinidae

GENUS:Glossina

SPECIES:G. palpalis gambiensis

(Vanderplank 1949)

*Correspondence:

j.bouyer@iaea.org(J. Bouyer).

Trends in Parasitology, Month 2020, Vol. xx, No. xx © 2020 The Author. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). https://doi.org/10.1016/j.pt.2020.05.010 1

(3)

UNCORRECTED PR

OOF

Acknowledgments

J.B. is funded by the European Research Council under the European Union’s Horizon 2020 research and innovation program (grant agreement no. 682387–REVOLINC). This article reflects only the author's views, and the agency is not responsible for any use that may be made of the information it contains. J.B. is grateful to Dominique Cuisance for his original drawing of the tsetse habitat and Awuoche et al. for their drawing of the cycle of Trypanosoma congolense in the tsetsefly in Figure 1.

Resources

www.fao.org/paat/resources/atlases/tsetse-and-aat/en/ https://books.openedition.org/irdeditions/10532?lang=fr www.anipedia.org/resources/vectors-tsetse-flies/1109

Literature

1. Van den Bossche, P. et al. (2010) A changing environment and the epidemiology of tsetse-transmitted livestock trypanosomiasis. Trends Parasitol. 26, 236–243 2. Solano, P. et al. (2010) Cyclical vectors of trypanosomosis. In Infectious and Parasitic Diseases of Livestock (Lefèvre, P.-C. et al., eds), pp. 155–183, Éditions Lavoisier

(Tec & Doc)

3. Bouyer, J. et al. (2007) Learning influences host choice in tsetse. Biol. Lett. 3, 113–116

4. Awuoche, E.O. et al. (2017) Molecular characterization of tsetse’s proboscis and its response to Trypanosoma congolense infection. PLoS Negl. Trop. Dis. 11, e0006057

5. Diall, O. et al. (2017) Developing a progressive control pathway for African animal trypanosomosis. Trends Parasitol. 33, 499–509

6. Courtin, F. et al. (2015) Reducing human–tsetse contact significantly enhances the efficacy of sleeping sickness active screening campaigns: a promising result in the context of elimination. PLoS Negl. Trop. Dis. 9, e0003727

7. De Deken, R. and Bouyer, J. (2018) Can sequential aerosol technique be used against riverine tsetse? PLoS Negl. Trop. Dis. 12, e0006768

8. Cuisance, D. et al. (1984) Les lâchers de mâles irradiés dans la campagne de lutte intégrée contre les glossines dans la zone pastorale de Sidéradougou, Burkina Faso. Rev. Elev. Méd. vét. Pays trop. 37, 449–468 (in French)

9. Dicko, A.H. et al. (2014) Using species distribution models to optimize vector control: the tsetse eradication campaign in Senegal. Proc. Natl. Acad. Sci. U. S. A. 111, 10149–10154

10. Bouyer, J. et al. (2015) Mapping landscape friction to locate isolated tsetse populations candidate for elimination. Proc. Natl. Acad. Sci. U. S. A. 112, 14575–14580

Trends in Parasitology

| Vector of the Month

2 Trends in Parasitology, Month 2020, Vol. xx, No. xx © 2020 The Author. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). https://doi.org/10.1016/j.pt.2020.05.010

Références

Documents relatifs

gambiensis populations within the Niayes was also assessed to determine if the different populations of the Niayes can be targeted at the same time (if it is a single panmictic

Glossina palpalis gambiensis is a riverine tsetse species endemic in West Africa and thriving in riparian vegeta- tion of the savannah areas from Burkina Faso and Mali to Guinea

Saini, R.K., et al., Identification of major components of larviposition pheromone from larvae of tsetse flies Glossina morsitans morsitans westwood and Glossina morsitans

In order to assess the effect of irradiation on male pupae of Glossina palpalis gambiensis, we assessed quality parameters of the irradiated male pupae, notably the hatching rate

La présente étude a été menée pour évaluer l’impact de la durée de congélation du sang utilisé pour les repas sanguin sur les performances des glossines afin de décider

In grouped larviposition experiments, females selected significantly more often for sites with pupae (P < 0.05), but were not able to discriminate between

The mean dispersal distances observed here are much higher than those estimated be- tween river basins in Burkina Faso using population genetics (19–26 m) [10] but in line with

palpalis populations in the three affected areas within Abidjan, we used both genetic (microsatellite DNA) and phenetic (geometric morphometrics) markers on the same specimens,