scholarly journals Temporal Distribution and Abundance of Mosquito Vectors in Dhaka City

2021 ◽  
Vol 46 (1) ◽  
pp. 27-35
Author(s):  
MG Sharower ◽  
MA Latif ◽  
SM Uddin
Keyword(s):  
Anopheles Gambiae ◽  
Sibling Species ◽  
Rainy Season ◽  
Temporal Distribution ◽  
Malaria Vectors ◽  
Dhaka City ◽  
Mosquito Vectors ◽  
Anopheles Gambiae S.S ◽  
Culex Fatigans ◽  
Highly Correlated

Species of Anopheles, Aedes and Culex mosquitoes showed that Anopheles gambiae s.s had the highest number (43.5%) out of the three malaria vectors (viz. Anopheles gambiae, An. arabiensis and An. funestus). For Aedes and Culex species, Aedes aegypti (37.6%) and Culex fatigans (37.1%) had the highest prevalence out of their sibling species. Temperature and rainfall were highly correlated with the abundance of mosquito vectors. It was observed that the rainy season (March to October) recorded the highest number (Total 11 specie) of mosquito vectors collected with the peak (Aedes aegypty, 140) in the months of July (932) and August (976) while the lowest (333) collection was in the dry season (November to February) with lowest (333) in the month of February when there was little or no rains. Asiat. Soc. Bangladesh, Sci. 46(1): 27-35, June 2020

scholarly journals Phenotypic Insecticide Resistance in Anopheles gambiae (Diptera: Culicidae): Specific Characterization of Underlying Resistance Mechanisms Still Matters

2020 ◽  
Author(s):  
Adandé A Medjigbodo ◽  
Luc S Djogbenou ◽  
Aubin A Koumba ◽  
Laurette Djossou ◽  
Athanase Badolo ◽  
...  
Keyword(s):  
Insecticide Resistance ◽  
Anopheles Gambiae ◽  
Resistance Mechanisms ◽  
Malaria Vectors ◽  
Effective Control ◽  
Anopheles Coluzzii ◽  
Anopheles Gambiae S.S ◽  
Diagnostic Dose ◽  
Pirimiphos Methyl ◽  
Old Adult

Abstract An effective control of malaria vectors requires an extensive knowledge of mechanisms underlying the resistance-phenotypes developed by these vectors against insecticides. We investigated Anopheles gambiae mosquitoes from Benin and Togo for their intensity of insecticide resistance and we discussed the involvement of genotyped mechanisms in the resistance-phenotypes observed. Three- to five-day-old adult mosquitoes emerged from field and laboratory An. gambiae larvae were assayed using WHO tube intensity tests against various doses of deltamethrin: 1× (0.05%); 2× (0.1%); 5× (0.25%); 7.5× (0.375%) and those of pirimiphos-methyl: 0.5× (0.125%); 1× (0.25%). Members of An. gambiae complex were screened in field populations using polymerase chain reaction (PCR) assays. The presence of kdrR(1014F/1014S) and ace-1R(119S) mutations was also investigated using TaqMan and PCR-RFLP techniques, respectively. Anopheles gambiae from field were very resistant to deltamethrin, whereas KisKdr and AcerKdrKis strains displayed 100% mortality rates at 2× the diagnostic dose. In contrast, the field mosquitoes displayed a low resistance-intensity against 1× the diagnostic dose of pirimiphos-methyl, whereas AcerKis and AcerKdrKis strains showed susceptibility at 0.5× the diagnostic dose. Anopheles gambiae s.s., Anopheles coluzzii, and Anopheles arabiensis were identified. Allelic frequencies of kdrR (1014F) and ace-1R (119S) mutations in the field populations varied from 0.65 to 1 and 0 to 0.84, respectively. The field An. gambiae displayed high-resistance levels against deltamethrin and pirimiphos-methyl when compared with those of the laboratory An. gambiae-resistant strains. These results exhibit the complexity of underlying insecticide resistance mechanisms in these field malaria vectors.

scholarly journals Rapid high throughput SYBR green assay for identifying the malaria vectors Anopheles arabiensis, Anopheles coluzzii and Anopheles gambiae s.s. Giles

PLoS ONE ◽  
2019 ◽  
Vol 14 (4) ◽  
pp. e0215669 ◽  
Author(s):  
Joseph Chabi ◽  
Arjen Van’t Hof ◽  
Louis K. N’dri ◽  
Alex Datsomor ◽  
Dora Okyere ◽  
...  
Keyword(s):  
Anopheles Gambiae ◽  
High Throughput ◽  
Anopheles Arabiensis ◽  
Sybr Green ◽  
Malaria Vectors ◽  
Anopheles Coluzzii ◽  
Anopheles Gambiae S.S ◽  
Sybr Green Assay

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.

High Levels of Knockdown Resistance in Anopheles coluzzii and Anopheles gambiae (Diptera: Culicidae), Major Malaria Vectors in Togo, West Africa: A 2011 Monitoring Report

2019 ◽  
Vol 56 (4) ◽  
pp. 1159-1164
Author(s):  
Koffi Mensah Ahadji-Dabla ◽  
Adjovi Djifa Amoudji ◽  
Seth Wolali Nyamador ◽  
Georges Yawo Apétogbo ◽  
Joseph Chabi ◽  
...  
Keyword(s):  
West Africa ◽  
Anopheles Gambiae ◽  
National Malaria Control Programme ◽  
Control Programme ◽  
World Health ◽  
Malaria Vectors ◽  
Malaria Control Programme ◽  
Anopheles Coluzzii ◽  
Knockdown Resistance ◽  
Anopheles Gambiae S.S

Abstract A survey of susceptibility to DDT, deltamethrin, bendiocarb, and chlorpyrifos-methyl was conducted in five localities in 2011 in Togo, West Africa, to assess the insecticide resistance status of Anopheles gambiae s.l. (Diptera: Culicidae). Female populations of An. gambaie s.l. emerged from collected larvae (F0) were exposed to insecticide-impregnated papers using World Health Organization test kits for adult mosquitoes; the susceptible reference strain Kisumu was used as a control. Resistance to DDT and deltamethrin was observed within the mosquito populations tested. Anopheles gambiae s.s. and Anopheles coluzzii represented the only species recorded in the study sites. The frequency of knockdown resistance (kdr L1014F) mutation determined using polymerase chain reaction diagnostic tests was lower in An. gambiae than in An. coluzzii in all of the localities except Kolokopé. Further investigations of An. gambiae s.l. resistance are needed in Togo to help the National Malaria Control Programme in vector control decision making and implementation of resistance management strategy.

scholarly journals Malaria Transmission, Vector Diversity, and Insecticide Resistance at a Peri-Urban Site in the Forest Zone of Ghana

2021 ◽  
Vol 2 ◽  
Author(s):  
Yaw Akuamoah-Boateng ◽  
Ruth C. Brenyah ◽  
Sandra A. Kwarteng ◽  
Patrick Obuam ◽  
Isaac Owusu-Frimpong ◽  
...  
Keyword(s):  
Insecticide Resistance ◽  
Anopheles Gambiae ◽  
Malaria Transmission ◽  
Urban Setting ◽  
World Health ◽  
Malaria Vectors ◽  
Urban Site ◽  
Human Landing Catch ◽  
Anopheles Coluzzii ◽  
Anopheles Gambiae S.S

IntroductionRecent surge of Anopheles resistance to major classes of World Health Organization (WHO)-approved insecticides globally necessitates the need for information about local malaria vector populations. It is believed that insecticide efficacy loss may lead to operational failure of control interventions and an increase in malaria infection transmission. We investigated the susceptibility levels of malaria vectors to all classes of WHO-approved vector control insecticides and described the dynamics of malaria transmission in a peri-urban setting.MethodsFit 3–5-day-old adults that emerged from Anopheles larvae collected from several different sites in the study area were subjected to the WHO bioassay for detecting insecticide resistance. The knockdown resistance gene (kdr) mutations within the vector populations were detected using PCR. Entomological inoculation rates were determined using the human landing catch technique and Plasmodium falciparum circumsporozoite ELISA.ResultsThe malaria vectors from the study area were resistant to all classes of insecticides tested. Out of the 284 Anopheles complex specimen assayed for the resistance study, 265 (93.30%) were identified as Anopheles gambiae s.s. The kdr gene was detected in 90% of the Anopheles gambiae s.s. assayed. In an area where Anopheles coluzzii resistance to insecticides had never been reported, the kdr gene was detected in 78% of the Anopheles coluzzii sampled. The entomological inoculation rate (EIR) for the dry season was 1.44 ib/m/n, whereas the EIR for the rainy season was 2.69 ib/m/n.ConclusionsThis study provides information on the high parasite inoculation rate and insecticide resistance of malaria vectors in a peri-urban community, which is critical in the development of an insecticide resistance management program for the community.

scholarly journals Anopheles gambiae s. l. larval control: An important method for malaria control

2021 ◽  
Vol 6 (3) ◽  
pp. 027-034
Author(s):  
Nazaire Aïzoun
Keyword(s):  
Anopheles Gambiae ◽  
Malaria Control ◽  
Malaria Elimination ◽  
Rainy Season ◽  
Enzyme Inhibitor ◽  
Integrated Control ◽  
Detoxification Enzymes ◽  
Malaria Vectors ◽  
Important Method ◽  
Susceptibility Tests

The current study aimed to investigate on the control tools against larvae and adults of Anopheles gambiae s. l. and then explore the detoxification enzymes mechanisms conferring permethrin tolerance in Anopheles gambiae s. l. larvae in Benin. Larvae and pupae were collected from March to July and August to November 2018 during the rainy season in Bopa district in Mono department in south-western Benin, West Africa. Larval bioassays were performed on these collected Anopheles gambiae s. l. larvae using permethrin as larvicide and synergist piperonyl butoxide (PBO) as enzyme inhibitor or synergist. WHO susceptibility tests were also conducted on adult unfed female mosquitoes aged 3-5 days old with impregnated papers of permethrin (0.75%). The results showed that malaria elimination in Benin needs integrated control. Both larvae or pupae and adults malaria vectors must be controlled.

scholarly journals Multimodal Pyrethroid Resistance in Malaria Vectors, Anopheles gambiae s.s., Anopheles arabiensis, and Anopheles funestus s.s. in Western Kenya

PLoS ONE ◽  
2011 ◽  
Vol 6 (8) ◽  
pp. e22574 ◽  
Author(s):  
Hitoshi Kawada ◽  
Gabriel O. Dida ◽  
Kazunori Ohashi ◽  
Osamu Komagata ◽  
Shinji Kasai ◽  
...  
Keyword(s):  
Anopheles Gambiae ◽  
Anopheles Arabiensis ◽  
Pyrethroid Resistance ◽  
Anopheles Funestus ◽  
Malaria Vectors ◽  
Anopheles Gambiae S.S ◽  
Western Kenya

scholarly journals Sporozoite Infection Rate and Identification of the Infective and Refractory Species of Anopheles gambiae (Giles) Complex

2014 ◽  
Vol 6 (4) ◽  
pp. 407-413
Author(s):  
Music Temitope OBEMBE ◽  
Idowu J. AWOPETU
Keyword(s):  
Anopheles Gambiae ◽  
Infection Rate ◽  
Sibling Species ◽  
Sensu Stricto ◽  
Malaria Vectors ◽  
Southwestern Nigeria ◽  
Complex Span ◽  
Gambiae Complex ◽  
Anopheles Gambiae Complex ◽  
Sporozoite Infection

The ability of Anopheles gambiae complex mosquitoes to transmit Plasmodium infection is known to be variable within sibling species of the complex with strains that cannot transmit the parasite. High sporozoite infection rate recorded showed that A. gambiae mosquitoes are potent malaria vectors in southwestern Nigeria. The aim of this study was to identify the infective and refractory strains of A. gambiae mosquitoes and to determine the sporozoite infection rate in this area. The infective strains were A. gambiae (sensu stricto) and A. arabiensis, while the refractory strains were A. gambiae (sensu stricto). However, ovarian polytene chromosome banding patterns could not be used to distinguish between the infective and refractory strains of A. gambiae (sensu stricto). This study showed that the refractory strains of Anopheles gambiae complex are present, but in low frequencies, in southwestern Nigeria, and that the sibling species of Anopheles gambiae (A. gambiae s.s. and A. arabiensis) are potent malaria vectors.

scholarly journals Behavioral Responses of Pyrethroid-resistant Anopheles Gambiae Mosquitoes to Insecticide-treated Bed Net

2021 ◽  
Author(s):  
Maxwell G. Machani ◽  
Eric Ochomo ◽  
Fred Amimo ◽  
Andrew K. Githeko ◽  
Guiyun Yan ◽  
...  
Keyword(s):  
Insecticide Resistance ◽  
Anopheles Gambiae ◽  
Malaria Transmission ◽  
Malaria Vectors ◽  
Bed Net ◽  
Anopheles Gambiae S.S ◽  
Field Environment ◽  
Host Seeking ◽  
Seeking Behavior ◽  
Vector Behavior

Abstract Background: Long-lasting insecticidal nets are an effective tool in reducing malaria transmission. However, with increasing insecticide resistance little is known about how physiologically resistant malaria vectors behave around a human-occupied bed net, despite their importance in malaria transmission. We assessed the host-seeking behavior of the major malaria vector Anopheles gambiae s.s, when an intact human-occupied treated bed net is in place, with respect to their insecticide resistance status under semi-field conditions. Methods: Pyrethroid resistant and susceptible colonies of female Anopheles gambiae s.s aged 3-5 days that have been bred in our insectary, were color-marked with fluorescent powder and released inside a semi-field environment housing a hut which was occupied by a human host. Inside the hut, the occupant slept under an insecticide-treated bed net trap or untreated bed net trap. The window exit trap was installed to catch mosquitoes exiting the hut. A prokopack aspirator was used to collect indoor and outdoor resting mosquitoes in the morning. Clay pots were placed outside the hut to collect mosquitoes resting outdoors. Results: The proportion of resistant mosquitoes caught in the treated bed net trap was higher 43% (95% CI= [40.6-45.3]) compared to the susceptible mosquitoes 28.3% (OR=1.445; P<0.00019). The proportion of susceptible mosquitoes caught in the untreated bed net trap was higher 51.3% (95% CI= [48.8-53.6]) compared to the treated bed net trap 28.3% (95% CI= [26.3-30.5]) (OR=2.65; P<0.0001). Resistant mosquitoes were less likely to exit the house when a treated bed net was present (5.2%; 95% CI= [4.2-6.4]) compared to the susceptible mosquitoes (11.5%; 95% CI= [9.6-12.6]). The proportion of susceptible mosquitoes avoiding contact with the treated bed net and caught resting indoors in the hut (53.8%) and outdoors (64.5%) was higher compared to the resistant mosquitoes (indoors: 46.2%, outdoor: 35.4%). The susceptible females were 2.3 times more likely to stay outdoors away from the treated bed net (OR=2.25; 95% CI= [1.7-2.9]; P<0.0001).Conclusion: The results show that in the presence of a treated net, the host-seeking performance was not altered for the resistant mosquitoes, unlike the susceptible females that were observed to exit the house and remained outdoors when a treated net was used. However, further investigations of the behavior of resistant mosquitoes under natural conditions should be undertaken to confirm these observations and improve the current intervention which are threatened by insecticide resistance and altered vector behavior.

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