scholarly journals Rhipicephalus microplus and its vector-borne haemoparasites in Guinea: further species expansion in West Africa

Author(s):  
Marat T. Makenov ◽  
Aboubakar H. Toure ◽  
Mikhail G. Korneev ◽  
Noumany Sacko ◽  
Aleksander M. Porshakov ◽  
...  
Author(s):  
MT Makenov ◽  
AH Toure ◽  
MG Korneev ◽  
N Sacko ◽  
AM Porshakov ◽  
...  

AbstractRhipicephalus microplus is an ixodid tick with a pantropical distribution that represents a serious threat to livestock. West Africa was free of this tick until 2007, when its introduction into Benin was reported. Shortly thereafter, the further invasion of this tick into West African countries was demonstrated. In this paper, we describe the first detection of R. microplus in Guinea and list the vector-borne haemoparasites that were detected in the invader and indigenous Boophilus species.In 2018, we conducted a small-scale survey of ticks infesting cattle in three administrative regions of Guinea: N`Zerekore, Faranah, and Kankan. The tick species were identified by examining their morphological characteristics and by sequencing their COI gene and ITS-2 gene fragments. R. microplus was found in each studied region. In the ticks, we found DNA of Babesia bigemina, Anaplasma marginale, Anaplasma platys, and Ehrlichia spp. The results of this study indicate that R. microplus was introduced into Guinea with cows from Mali and/or Ivory Coast.


Parasitology ◽  
1993 ◽  
Vol 106 (S1) ◽  
pp. S55-S75 ◽  
Author(s):  
J. F. Walsh ◽  
D. H. Molyneux ◽  
M. H. Birley

SUMMARYThis review addresses' changes in the ecology of vectors and epidemiology of vector-borne diseases which result from deforestation. Selected examples are considered from viral and parasitic infections (arboviruses, malaria, the leishmaniases, nlariases, Chagas Disease and schistosomiasis) where disease patterns have been directly or indirectly influenced by loss of natural tropical forests. A wide range of activities have resulted in deforestation. These include colonisation and settlement, transmigrant programmes, logging, agricultural activities to provide for cash crops, mining, hydropower development and fuelwood collection. Each activity influences the prevalence, incidence and distribution of vector-borne disease. Three main regions are considered – South America, West & Central Africa and South-East Asia. In each, documented changes in vector ecology and behaviour and disease pattern have occurred. Such changes result from human activity at the forest interface and within the forest. They include both deforestation and reafforestation programmes. Deforestation, or activities associated with it, have produced new habitats for Anopheles darlingi mosquitoes and have caused malaria epidemics in South America. The different species complexes in South-East Asia (A. dirus, A. minimus, A. balabacensis) have been affected in different ways by forest clearance with different impacts on malaria incidence. The ability of zoophilic vectors to adapt to human blood as an alternative source of food and to become associated with human dwellings (peridomestic behaviour) have influenced the distribution of the leishmaniases in South America. Certain species of sandflies (Lutzomyia intermedia, Lu. longipalpis, Lu. whitmani), which were originally zoophilic and sylvatic, have adapted to feeding on humans in peridomestic and even periurban situations. The changes in behaviour of reservoir hosts and the ability of pathogens to adapt to new reservoir hosts in the newly-created habitats also influence the patterns of disease. In anthroponotic infections, such as Plasmodium, Onchocerca and Wuchereria, changes in disease patterns and vector ecology may be more difficult to detect. Detailed knowledge of vector species and species complexes is needed in relation to changing climate associated with deforestation. The distributions of the Anopheles gambiae and Simulium damnosum species complexes in West Africa are examples. There have been detailed longitudinal studies of Anopheles gambiae populations in different ecological zones of West Africa. Studies on Simulium damnosum cytoforms (using chromosome identification methods) in the Onchocerciasis Control Programme were necessary to detect changes in distribution of species in relation to changed habitats. These examples underline the need for studies on the taxonomy of medically-important insects in parallel with long-term observations on changing habitats. In some circumstances, destruction of the forest has reduced or even removed disease transmission (e.g. S. neavei-transmitted Onchocerca in Kenya). Whilst the process of deforestation can be expected to continue, hopefully at a decreased rate, it is expected that unpredictable and sometimes rapid changes in disease patterns will pose problems for the public health services.


2013 ◽  
pp. 132-133
Author(s):  
Gloria Ines Palma ◽  
Sofía Duque Bernal ◽  
Ruben Santiago Nicholls

Onchocerciasis, also known as River Blindness, is a parasitic disease caused by the nematode Onchocerca volvulus and transmitted by black flies of the genus Simulium. It is endemic in Africa, where an estimated 37 million people are infected. It is almost certain that the slave trade in the 17th and 18th centuries brought onchocerciasis from West Africa to the Americas (1), where transmission foci where established in six countries: Mexico, Guatemala, Venezuela, Brazil, Ecuador and Colombia. Since the beginning of the 20th century it was suspected that this vector borne disease was present in Colombia but the first confirmed case was not reported until 1965. The exact location of the single focus in the country was confirmed almost thirty years later in the locality of Naicioná, on the stream that bears the same name


2013 ◽  
Vol 61 (3) ◽  
pp. 383-386 ◽  
Author(s):  
H. Adakal ◽  
A. Biguezoton ◽  
S. Zoungrana ◽  
F. Courtin ◽  
E. M. De Clercq ◽  
...  

2016 ◽  
Vol 9 (1) ◽  
Author(s):  
Abel Biguezoton ◽  
Valerie Noel ◽  
Safiou Adehan ◽  
Hassane Adakal ◽  
Guiguigbaza-Kossigan Dayo ◽  
...  

2018 ◽  
Vol 9 (3) ◽  
pp. 665-671 ◽  
Author(s):  
Roland Eric Yessinou ◽  
Yao Akpo ◽  
Aboubakar Sidick ◽  
Camus Adoligbe ◽  
Issaka Youssao Abdou Karim ◽  
...  

2021 ◽  
Vol 10 (1) ◽  
pp. 113-116
Author(s):  
Andrey Vladimirovich Mishchenko ◽  
Elena Aleksandrovna Artemyeva

The paper discusses the food supply of the vector of malaria mosquitoes of the genus Anopheles, which are birds of tropical regions of West Africa. Birds, as distant migrants, penetrate high latitudes and contribute to the spread of malaria in Europe and other countries of the northern hemisphere. The results of the studies show that the main role in the choice of prey objects by female Anopheles gambiae mosquitoes birds is played by the nesting and forage biotopes of birds, which are comfortable for mosquito breeding. Probably, female mosquitoes use non-feathered parts of the body of adult birds for feeding unfeathered or weakly feathered chicks in nests. The circulation of Plasmodium falciparum includes populations of birds, primarily water, near-water and marsh complexes, as well as birds, the development of which takes place in specific conditions of a closed space in holes, hollows and closed nests. The Anopheles gambiae mosquito in this system plays the role of a carrier of Plasmodium falciparum not only among populations of birds and mammals, but also among humans, which determines the range of tropical malaria, which is a natural focal vector-borne disease. The authors have identified 37 species of birds carriers of malaria in natural and anthropogenic biocoenoses of Mali (West Africa). The most numerous during the migration and nesting period are birds of the aquatic, near-water and meadow-bog complexes (herons, herons, waders) distant migrants on the territory of Russia and neighboring countries. The risk areas include, first of all, the southern regions Astrakhan Region, Rostov Region and Krasnodar Region.


2013 ◽  
Vol 8 (1) ◽  
pp. 301 ◽  
Author(s):  
Eva M. De Clercq ◽  
Agustin Estrada-Peña ◽  
Safiou Adehan ◽  
Maxime Madder ◽  
Sophie O. Vanwambeke

2012 ◽  
Vol 56 (4) ◽  
pp. 385-390 ◽  
Author(s):  
M. Madder ◽  
S. Adehan ◽  
R. De Deken ◽  
R. Adehan ◽  
R. Lokossou

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