Age physiologique et cycle d'agressivité chez Anopheles gambiae Giles et A. funestus Giles dans la région de Bobo-Dioulasso (Haute-Volta) [Dipt. Culicidae]

1964 ◽  
Vol 69 (5) ◽  
pp. 110-121
Author(s):  
J. Hamon ◽  
S. Sales ◽  
Jean-Paul Adam ◽  
P. Grenier
Keyword(s):  
Anopheles Gambiae ◽  
Bobo Dioulasso ◽  
Anopheles Gambiae Giles

scholarly journals Human biting rhythm of Anopheles gambiae Giles, 1902 (Diptera: Culicidae) and sleeping behaviour of pregnant women in a lagoon area in Southern Benin

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Armel Djènontin ◽  
Aziz Bouraima ◽  
Christophe Soares ◽  
Seun Egbinola ◽  
Gilles Cottrell
Keyword(s):  
Plasmodium Falciparum ◽  
Pregnant Women ◽  
Anopheles Gambiae ◽  
Early Morning ◽  
Allelic Frequency ◽  
Malaria Vectors ◽  
Mosquito Nets ◽  
Anopheles Gambiae Giles ◽  
Almost All ◽  
Southern Benin

Abstract Objective In the framework of EVALMOUS study aiming to assess the use and effectiveness of mosquito nets by pregnant women and other members of their household in a lagoon area in southern Benin, the behaviour of pregnant women relative to the time they go to bed using the net were recorded. Malaria vectors biting rhythm, Plasmodium falciparum infection and insecticide resistance genes in malaria vectors were also determined. Results Overall, 3848 females of Anopheles gambiae s. l were collected and 280 pregnant women responded to the survey. Almost all Anopheles gambiae s. l. tested were Anopheles coluzzi Coetzee and Wilkerson 2013 (Diptera: Culicidae). The CSP index in malaria vector was 1.85% and the allelic frequency of kdr gene was 74.4%. Around 90% of bites and Plasmodium falciparum Welch, 1897 (Haemosporida: Plasmodiidae) transmission occurred between 10 p.m. and 6 a.m., which coincides with the period when more than 80% of pregnant women were under bednet. Despite a slight early evening and early morning biting activity of malaria vectors in the study area, the good use of nets might remain a useful protection tool against mosquito biting and malaria transmission.

Studies of House Leaving and Outside Resting of Anopheles gambiae Giles and Anopheles funestus Giles in East Africa. I.—The Outside Resting Population

1954 ◽  
Vol 45 (2) ◽  
pp. 361-373 ◽  
Author(s):  
M. T. Gillies
Keyword(s):  
Anopheles Gambiae ◽  
Anopheles Funestus ◽  
Drastic Reduction ◽  
Natural Conditions ◽  
Resting Sites ◽  
Lowland Area ◽  
Set Up ◽  
Anopheles Gambiae Giles ◽  
Gravid Females ◽  
Periodic Examination

The behaviour of Anopheles gambiae Giles and A. funestus Giles was studied under natural conditions in a lowland area of Tanganyika.Studies on the outside resting population were carried out by direct searching for natural resting sites, and by the use of artificial box shelters partly buried in the ground in shaded localities. Catches in these give a valid sample when set up at some distance from houses.Fed and gravid females comprised 67 per cent. of the outside resting gambiae population, the latter group being between 12 and 4·5 times as numerous as the former. Rather less than half the funestus females caught were unfed, the remainder of the population being mainly composed of gravid females.Precipitin tests on the small numbers of fed females caught outside were nearly all positive for man.The identification of gravid funestus females was confirmed by periodic examination of the eggs.Entry of females into outside shelters did not occur solely in the period around sunrise. An appreciable number of funestus females did not enter before 07.00 hours and this was particularly so in shaded shelters.The building of a hut in the vicinity of a box shelter caused a drastic reduction in the numbers of mosquitos resting in the latter.Outside biting activity in these two species is of negligible importance as a source of females resting outside.

scholarly journals Characterizing Permethrin and Etofenprox Resistance in Two Common Laboratory Strains of Anopheles gambiae (Diptera: Culicidae)

Insects ◽  
2018 ◽  
Vol 9 (4) ◽  
pp. 146 ◽  
Author(s):  
Aaron Gross ◽  
Jeffrey Bloomquist
Keyword(s):  
Anopheles Gambiae ◽  
Pyrethroid Resistance ◽  
Laboratory Strain ◽  
Pyrethroid Insecticide ◽  
Sub Saharan Africa ◽  
Cross Resistance ◽  
Type I ◽  
Mosquito Vector ◽  
Sub Saharan ◽  
Anopheles Gambiae Giles

Anopheles gambiae Giles (Diptera: Culicidae) is the most prolific malaria vector in sub-Saharan Africa, where widespread insecticide resistance has been reported. An. gambiae laboratory strains are commonly used to study the basic biology of this important mosquito vector, and also in new insecticide discovery programs, where insecticide-susceptible and -resistant strains are often used to screen new molecules for potency and cross-resistance, respectively. This study investigated the toxicity of permethrin, a Type-I pyrethroid insecticide, and etofenprox, a non-ester containing pyrethroid insecticide, against An. gambiae at three life stages. This characterization was performed with susceptible (G3; MRA-112) and resistant (Akdr; MRA-1280) An. gambiae strains; the Akdr strain is known to contain the L1014F mutation in the voltage-sensitive sodium channel. Surprisingly, etofenprox displays a lower level of resistance than permethrin against all stages of mosquitoes, except in a headless larval paralysis assay designed to minimize penetration factors. In first-instar An. gambiae larvae, permethrin had significant resistance, determined by the resistance ratio (RR50 = 5), but etofenprox was not significantly different (RR50 = 3.4) from the wild-type strain. Fourth-instar larvae displayed the highest level of resistance for permethrin (RR50 = 108) and etofenprox (RR50 = 35). Permethrin (PC50 = 2 ppb) and etofenprox (PC50 = 9 ppb) resulted in headless larval paralysis (5-h), but resistance, albeit lower, was still present for permethrin (RR50 = 5) and etofenprox (RR50 = 6.9). In adult female mosquitoes, permethrin displayed higher resistance (RR50 = 14) compared to etofenprox (RR50 = 4.3). The level of etofenprox resistance was different from that previously reported for a similar Akron An. gambiae laboratory strain (MRA-913). The chemical synergists piperonyl butoxide (PBO) and diethyl maleate (DEM) were able to synergize permethrin, but not etofenprox in the resistant strain (Akdr). In conclusion, multiple mechanisms are likely involved in pyrethroid resistance, but resistance profiles are dependent upon selection. Etofenprox is an effective insecticide against An. gambiae in the lab but will likely suffer from resistance in the field.

Enzyme variation in the Anopheles gambiae Giles group of species (Diptera: Culicidae)

1978 ◽  
Vol 68 (1) ◽  
pp. 85-97 ◽  
Author(s):  
S. J. Miles
Keyword(s):  
Anopheles Gambiae ◽  
Natural Populations ◽  
Lactic Dehydrogenase ◽  
Starch Gel Electrophoresis ◽  
Malic Dehydrogenase ◽  
Glycerophosphate Dehydrogenase ◽  
Starch Gel ◽  
Anopheles Gambiae Giles ◽  
Species Specific ◽  
Glucose 6 Phosphate Dehydrogenase

AbstractThe genotypes of chromosomally-identified individuals from natural populations of the known species of the group of Anopheles gambiae Giles were scored for the enzyme protein structural loci coding for adenylate kinase (Adk), α-naphthyl acetate esterase (Est-1, Est-2, Est-3), glutamic-oxaloacetic transaminase (Got), α-glycerophosphate dehydrogenase (αGpd), hexokinase (Hk), isocitric dehydrogenase (Idh), lactic dehydrogenase (Ldh), ‘leucine’ aminopeptidase (Lap-2), malic enzyme (Me), octanol dehydrogenase (Odh), phosphoglucomutase (Pgm-1, Pgm-2), 6-phosphogluconic dehydrogenase (6-Pgd), phosphohexose isomerase (Phi) and superoxide dismutase (Sod), following starch gel electrophoresis. In the material examined, Est-1, Est-2, Est-3, Got, ldh, Lap-2, Odh, Pgm-1, Pgm-2 and Sod were segregating for two or more alleles; unique alleles at the Est-1, Got and Sod loci produced species-specific phenotypes in A. melas (Theo.), species C and species D, respectively. The further sampling of A. merus Dön, populations supported the presence of a unique SOD phenotype by which this species can also be identified. Of the other enzyme systems examined, no activity following electrophoresis was detected for aldolase and fructose-1,6-diphosphatase, and the resolution of acid and alkaline phosphatase, glyceraldehyde-3-phosphate dehydrogenase, glucose-6-phosphate dehydrogenase, malic dehydrogenase and xanthine dehydrogenase was too poor under the particular electrophoretic conditions for genetic analyses of the enzyme phenotypes.

scholarly journals A Cage Colony of Anopheles gambiæ Giles

Nature ◽  
1937 ◽  
Vol 140 (3540) ◽  
pp. 428-428
Author(s):  
BOTHA DE MEILLON
Keyword(s):  
Anopheles Gambiae ◽  
Anopheles Gambiae Giles

scholarly journals Plasmodium falciparum (Haemosporodia: Plasmodiidae) and O’nyong-nyong Virus Development in a Transgenic Anopheles gambiae (Diptera: Culicidae) Strain

2019 ◽  
Vol 56 (4) ◽  
pp. 936-941 ◽  
Author(s):  
John D Mumford ◽  
Carole A Long ◽  
Scott C Weaver ◽  
Katzutoyo Miura ◽  
Eryu Wang ◽  
...  
Keyword(s):  
Plasmodium Falciparum ◽  
Anopheles Gambiae ◽  
Genetic Background ◽  
Homing Endonuclease ◽  
Virus Titer ◽  
Consistent Difference ◽  
Human Pathogens ◽  
Infectious Dose ◽  
Anopheles Gambiae Giles ◽  
Transgenic Mosquitoes

Abstract Transgenic Anopheles gambiae Giles (Diptera: Culicidae) mosquitoes have been developed that confer sexual sterility on males that carry a transgene encoding a protein which cuts ribosomal DNA. A relevant risk concern with transgenic mosquitoes is that their capacity to transmit known pathogens could be greater than the unmodified form. In this study, the ability to develop two human pathogens in these transgenic mosquitoes carrying a homing endonuclease which is expressed in the testes was compared with its nontransgenic siblings. Infections were performed with Plasmodium falciparum (Welch) and o’nyong-nyong virus (ONNV) and the results between the transgenic and nontransgenic sibling females were compared. There was no difference observed with ONNV isolate SG650 in intrathoracic infections or the 50% oral infectious dose measured at 14 d postinfection or in mean body titers. Some significant differences were observed for leg titers at the medium and highest doses for those individuals in which virus titer could be detected. No consistent difference was observed between the transgenic and nontransgenic comparator females in their ability to develop P. falciparum NF54 strain parasites. This particular transgene caused no significant effect in the ability of mosquitoes to become infected by these two pathogens in this genetic background. These results are discussed in the context of risk to human health if these transgenic individuals were present in the environment.

Comparative studies on sibling species of the Anopheles gambiae Giles complex (Dipt., Culicidae): bionomics and vectorial activity of species A and species B at Segera, Tanzania

1972 ◽  
Vol 62 (2) ◽  
pp. 295-317 ◽  
Author(s):  
G. B. White ◽  
S. A. Magayuka ◽  
P. F. L. Boreham
Keyword(s):  
Survival Rate ◽  
Anopheles Gambiae ◽  
Sibling Species ◽  
Malaria Vectors ◽  
Daily Survival Rate ◽  
Filarial Infection ◽  
Blood Indices ◽  
Biting Rate ◽  
Short Rains ◽  
Anopheles Gambiae Giles

Collections of Anopheles gambiae Giles complex, A. funestus Giles group and other mosquitoes were made by spray-catch from twelve catching stations indoors and by hand-catch from pit shelters at two catching stations at Segera, Tanzania, between January 1970 and June 1971. Females of A. gambiae were identified cytotaxonomically as sibling species A or B of the complex. In houses during 1970, A. gambiae species B was more numerous at first than A, but A became predominant during the long rains of March-May. In the cool dry weather of June-November both A and B densities declined and the A:B ratio surpassed 50:1. The short rains in December produced a population explosion of species B and less multiplication of species A, the B:A ratio reaching >11:1. In 1971, hot dry weather during January-March caused declines of species A and B with a maximum B: A ratio of 13:1. Long rains, coming in late March, provoked a resurgence of A and a concurrent decline of B, so that the A:B ratio again reached 20:1 in June. Similar cycles of species A and B were observed outdoors, although the relative numbers outdoors/indoors averaged 2·3 times more for species B than for species A. In A. funestus, A. gambiae species A and A. gambiae species B Human Blood Indices were 97·5%, 91·2% and 60·9% indoors and 24%, 2% and 7% outdoors, respectively. Respective malaria sporozoite rates were 1·62%, 4·23% and 0·32% and minimum rates of stage-Ill filarial infection were 0·33%, 0·44% and 0·57%. Sporozoite-positive and sporozoite-negative mosquitoes exhibited similar HBF's in species A and discrepant HBI's in species B. The HBI's were higher in filariapositive A and B females than in filaria-negative females. Gregarines occurred in 1·36% of species A and 0·38% of species B. Trematode cysts were seen in two specimens of species A.Of A and B females 28% and 4%, respectively, had four-banded palps. It is shown mathematically that the discrepant malaria sporozoite rates in species A and B may be explained by extrapolating from the man-biting rate and probable daily survival rate for each species. This implies that no unrecognised factors play a major role in causing the contrasting efficiency of these two sibling species as malaria vectors.

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