Abstract

BackgroundAnopheles arabiensis and A. gambiae (sensu stricto) are the most prolific Afrotropical malaria vectors. Population control efforts of these two vectors have been hampered by extremely diverse larval breeding sites and widespread resistance to currently available insecticides. Control of mosquito larval stages using bioactive compounds of plant origin has the potential to suppress vector populations leading to concomitant reduction in disease transmission rates. In this study, we evaluated the efficacy of Camellia sinensis crude leaf extract and its fraction against the larvae of A. arabiensis and A. gambiae (s.s.).MethodsLate third/early fourth instar larvae (L3/L4) of A. arabiensis and A. gambiae (s.s.) were exposed to increasing doses of C. sinensis leaf extract and its active fraction for 72 h, with mortality rates recorded every 24 h in both control and test groups. Ultra performance liquid chromatography electron spray ionization quadruple time of flight coupled with mass spectrometry (UPLC/ESI-Qtof/MS) was used to determine the main active constituents in the fraction.ResultsThe major bioactive chemical constituents in the C. sinensis leaf extract were identified to be proanthocyanidins. The extract significantly interfered with larval survival and adult emergence in both species (ANOVA, F(5,24) = 1435.92, P < 0.001). Additionally, larval exposure to crude extract at 250 ppm and 500 ppm for 24 h resulted in larval mortality rates of over 90 % in A. gambiae (s.s.) and 75 % in A. arabiensis. A relatively lower concentration of 100 ppm resulted in moderate mortality rates of < 50 % in both species, but induced growth disruption effects evident as abnormal larval-pupal intermediates and disrupted adult emergence. The estimated LC50 concentrations of the crude leaf extract against A. arabiensis and A. gambiae (s.s.) larvae at 24 h were 154.58 ppm (95 % CI: 152.37–158.22) and 117.15 ppm (95 % CI: 112.86–127.04), respectively. The bioactive polar fraction caused 100 % larval mortality in both vector species at 25 ppm.ConclusionsOur findings demonstrate the potential of green tea extract and its active constituents in disrupting mosquito larval development. This could contribute to the control of mosquito populations and improved management of malaria.

Highlights

  • Anopheles arabiensis and A. gambiae are the most prolific Afrotropical malaria vectors

  • Malaria vector control relies on integrated vector management (IVM) approaches such as targeting adult stages using long-lasting insecticide treated nets (LLINs) and indoor residual spraying (IRS), environmental management and larval source reduction [1, 3, 4]

  • All the vector control strategies have limitations prompting the need for application of multiple control methods to reduce malaria transmission rates as well as offset insecticide resistance [8, 9]

Read more

Summary

Introduction

Anopheles arabiensis and A. gambiae (sensu stricto) are the most prolific Afrotropical malaria vectors. Population control efforts of these two vectors have been hampered by extremely diverse larval breeding sites and widespread resistance to currently available insecticides. Control of mosquito larval stages using bioactive compounds of plant origin has the potential to suppress vector populations leading to concomitant reduction in disease transmission rates. Malaria vector control relies on integrated vector management (IVM) approaches such as targeting adult stages using long-lasting insecticide treated nets (LLINs) and indoor residual spraying (IRS), environmental management and larval source reduction [1, 3, 4]. All the vector control strategies have limitations prompting the need for application of multiple control methods to reduce malaria transmission rates as well as offset insecticide resistance [8, 9]. There is renewed interest in the search for novel chemicals that have reduced chances of development of resistance, especially ecofriendly natural compounds that are less toxic, or selectively toxic to mosquitoes [10]

Objectives
Methods
Results
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call