Rahmatoulaye Maiga
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Rahmatoulaye Maiga has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Abdoul-Aziz Maiga
Laboratoire d'Entomologie Fondamentale et Appliquée Université Joseph Ki‐Zerbo Ouagadougou Burkina Faso
1 shared publication - Aboubacar Sombié
Laboratoire d’Entomologie Fondamentale et Appliquée, Université Joseph Ki-Zerbo, Ouagadougou, Burkina Faso
1 shared publication - Ali Doumma
Département de Biologie, Faculté des Sciences et Techniques, Université Abdou Moumouni, Niamey BP 10896, Niger
1 shared publication - Antoine Sanon
Laboratoire d’Entomologie Fondamentale et Appliquée, Université Joseph Ki-Zerbo, Ouagadougou, Burkina Faso
1 shared publication - Athanase Badolo
Laboratoire d'Entomologie Fondamentale et Appliquée Université Joseph Ki‐Zerbo Ouagadougou Burkina Faso
1 shared publication - Maman Laminou Ibrahim
Unité de Paludologie et d’Entomologie Médicale, Centre de Recherche Médicale et Sanitaire, Niamey BP 10887, Niger
1 shared publication
Latest Publications
- Open Access
Susceptibility of Aedes aegypti Larvae to Temephos and Fenitrothion in Niamey (Niger) and Ouagadougou (Burkina Faso), Two West African Cities Recently Affected by Dengue
In the absence of commercialized vaccines for most arboviruses, including dengue, chikungunya, and Zika, which are transmitted by Aedes aegypti, the management of vector populations to prevent disease transmission remains the cornerstone of arbovirus control strategies. Larviciding targets the early stages of the mosquito life cycle and subsequently reduces the capacity of adult population to transmit pathogens. Here, we report the susceptibility profile of Ae. aegypti larval populations from two West Africa cities, namely Niamey and Ouagadougou, to organophosphates larvicides. In Niamey, sampling was carried out using ovitraps at two sites, whereas in Ouagadougou, larvae were collected from three different types of larval containers at a single site. Temephos and fenitrothion were tested at six different concentrations each. Mosquito populations from Niamey and Ouagadougou were found susceptible to temephos and fenitrothion, with LD50 < 0.015 mg/L and RR50 < 5. However, Ae. aegypti populations from Ouagadougou showed reduced susceptibility to temephos compared to baseline data from 2016, as indicated by RR50 values. This observation highlights the need for regular surveillance of larval susceptibility, as it may signal the emergence of temephos resistance in Ouagadougou. The acetylcholinesterase (AChE) mutation and the expression levels of metabolic genes Carboxy-/Cholinesterase (CCE) should be characterized to understand the molecular mechanisms underlying the observed phenotype response. Our results provide up-to-date data that could inform the potential deployment of these larvicides for the prevention and control of dengue and chikungunya outbreaks in Ouagadougou and Niamey.
Open AccessSusceptibility of Aedes aegypti Larvae to Temephos and Fenitrothion in Niamey (Niger) and Ouagadougou (Burkina Faso), Two West African Cities Recently Affected by Dengue
In the absence of commercialized vaccines for most arboviruses, including dengue, chikungunya, and Zika, which are transmitted by Aedes aegypti, the management of vector populations to prevent disease transmission remains the cornerstone of arbovirus control strategies. Larviciding targets the early stages of the mosquito life cycle and subsequently reduces the capacity of adult population to transmit pathogens. Here, we report the susceptibility profile of Ae. aegypti larval populations from two West Africa cities, namely Niamey and Ouagadougou, to organophosphates larvicides. In Niamey, sampling was carried out using ovitraps at two sites, whereas in Ouagadougou, larvae were collected from three different types of larval containers at a single site. Temephos and fenitrothion were tested at six different concentrations each. Mosquito populations from Niamey and Ouagadougou were found susceptible to temephos and fenitrothion, with LD50 < 0.015 mg/L and RR50 < 5. However, Ae. aegypti populations from Ouagadougou showed reduced susceptibility to temephos compared to baseline data from 2016, as indicated by RR50 values. This observation highlights the need for regular surveillance of larval susceptibility, as it may signal the emergence of temephos resistance in Ouagadougou. The acetylcholinesterase (AChE) mutation and the expression levels of metabolic genes Carboxy-/Cholinesterase (CCE) should be characterized to understand the molecular mechanisms underlying the observed phenotype response. Our results provide up-to-date data that could inform the potential deployment of these larvicides for the prevention and control of dengue and chikungunya outbreaks in Ouagadougou and Niamey.