Influence of geographical location on abundance assortment of Anopheles mosquito species (Diptera: Culicidae) on malaria parasite rate in Enugu State, Nigeria

2021 ◽  
Vol 42 (1) ◽  
pp. 31-40
Author(s):  
G.I. Ngwu ◽  
F.C. Okafor ◽  
J.E. Eyo ◽  
M.I. Ngwu
Keyword(s):  
Malaria Parasite ◽  
Mosquito Species ◽  
Geographical Location ◽  
Sensu Stricto ◽  
Anopheles Mosquito ◽  
Malaria Vectors ◽  
Malaria Control Programme ◽  
Anopheles Coluzzii ◽  
Anopheles Gambiae S.S ◽  
Enugu State

Assessment of geographical distribution of malaria vectors is essential to effective malaria parasite control. This study evaluated the influence of geographical locations on distribution of Anopheles mosquito species and malaria parasite vectorial efficacy in Enugu State, Nigeria. Mosquitoes were collected, using indoor resting pyrethrum spray collection (IRPSC) method. They were morphologically identified and molecularly (PCR) characterised. The M form (now called Anopheles coluzzii) and S form (now called nominotypical Anopheles gambiae s.s.), were identified using Restriction Fragment Length Polymorphism (RFLP). Plasmodium falciparum sporozoite rates of sampled mosquitoes and malaria status of households were evaluated microscopically and by using rapid diagnostic kits. An. gambiae Giles (sensu stricto), and bands resembling An. melas and An. arabiensisspecies complexes were observed. Out of 300 An. gambiae s.l. identified using PCR, 243 were An. gambiae Giles (sensu stricto), 6 were An. melas and 5 were An. arabiensis. Out of the 243 An. gambiae Giles (sensu stricto), 184 were M form (now An. coluzzii) and 59 were S form (now nominotypical An. gambiae s.s).The M form (now An. coluzzii) constituted 99% of Anopheles mosquitoes from southernmost part of the study area while northernmost part showed 100% S form (An. gambiae s.s.). The median location had the M form (An. coluzzii) and S form (An. gambiae s.s.) in  sympatric. Sporozoite rate in northernmost area was highest when compared with median and southernmost parts. The S form (An. gambiae s.s.) was observed as more important malaria parasite vector, and the results revealed that geographical location affected species diversities which is an important consideration for malaria control  programme. Keywords: Anopheles, distribution, sporozoite, malaria parasite

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 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

scholarly journals Pollutants and insecticides drive local adaptation in African malaria mosquitoes

2016 ◽  
Author(s):  
Colince Kamdem ◽  
Caroline Fouet ◽  
Stephanie Gamez ◽  
Bradley J. White
Keyword(s):  
Anopheles Gambiae ◽  
Local Adaptation ◽  
Mosquito Species ◽  
Sensu Stricto ◽  
Detoxification Enzymes ◽  
Malaria Vectors ◽  
Breeding Sites ◽  
Reduced Representation ◽  
Malaria Epidemiology ◽  
Rural And Urban

ABSTRACTThe Anopheles gambiae complex contains a number of highly anthropophilic mosquito species that have acquired exceptional ability to thrive in complex human habitats. Thus, examining the evolutionary history of this Afrotropical mosquito may yield vital information on the selective processes that occurred during the adaptation to human-dominated environments. We performed reduced representation sequencing on 941 mosquitoes of the Anopheles gambiae complex collected across four ecogeographic zones in Cameroon. We find evidence for genetic and geographic subdivision within An. coluzzii and An. gambiae sensu stricto – the two most significant malaria vectors in the region. Importantly, in both species, rural and urban populations are genetically differentiated. Genome scans reveal pervasive signatures of selection centered on genes involved in xenobiotic resistance. Notably, a selective sweep containing detoxification enzymes is prominent in urban mosquitoes that exploit polluted breeding sites. Overall, our study suggests that recent anthropogenic environmental modifications and widespread use of insecticides are driving population differentiation and local adaptation in vectors with potentially significant consequences for malaria epidemiology.

scholarly journals Quantifying flight aptitude variation in wild A. gambiae s.l. in order to identify long-distance migrants

2020 ◽  
Author(s):  
Roy Faiman ◽  
Alpha Seydou YARO ◽  
Moussa Diallo ◽  
Adama Dao ◽  
Djibril Samake ◽  
...  
Keyword(s):  
Sensu Stricto ◽  
Flight Activity ◽  
Malaria Vectors ◽  
Anopheles Coluzzii ◽  
Wing Size ◽  
Wet Season ◽  
Long Distance ◽  
Flight Duration ◽  
Tethered Flight ◽  
Gravid Females

Abstract Background In the West African Sahel, mosquito reproduction is halted during the 5-7 month-long dry season, due to the absence of surface waters required for larval development. However, recent studies have suggested that both Anopheles gambiae sensu stricto (s.s.) and Anopheles arabiensis repopulate this region via migration from distant locations where larval sites are perennial. Anopheles coluzzii engages in more regional migration, presumably within the Sahel, following shifting resources correlating with the ever-changing patterns of Sahelian rainfall. Understanding mosquito migration is key to controlling malaria—a disease that continues to claim more than 400,000 lives annually, especially those of African children. Using tethered flight data of wild mosquitoes, the distribution of flight parameters were evaluated as indicators of long-range migrants versus appetitive flyers, and the species specific seasonal differences and gonotrophic states compared between two flight activity modalities. Morphometrical differences were evaluated in the wings of mosquitoes exhibiting high flight activity (HFA) vs. low flight activity (LFA).Methods A novel tethered-flight assay was used to characterize flight in the three primary malaria vectors- An. arabiensis, An. coluzzii and An. gambiae s.s. The flights of tethered wild mosquitoes were audio-recorded from 21:00h to 05:00h in the following morning and three flight aptitude indices were examined: total flight duration, longest flight bout, and the number of flight bouts during the assay.Results The distributions of all flight indices were strongly skewed to the right, indicating that the population consisted of a majority of low-flight activity (LFA) mosquitoes and a minority of high-flight activity (HFA) mosquitoes. The median total flight was 586 seconds and the maximum value was 16,110 seconds (~4.5 h). In accordance with recent results, flight aptitude peaked in the wet season, and was higher in gravid females than in non-blood-fed females. Flight aptitude was also found to be higher in An. coluzzii compared to An. arabiensis, with intermediate values in An. gambiae s.s., but displaying no statistical difference. Evaluating differences in wing size and shape between LFA individuals and HFA ones, the wing size of HFA An. coluzzii was larger than that of LFAs during the wet season—its length was wider than predicted by allometry alone, indicating a change in wing shape. No statistically significant differences were found in the wing size/shape of An. gambiae s.s. or An. arabiensis.Conclusions The partial agreement between the tethered flight results and recent results based on aerial sampling of these species suggest a degree of discrimination between appetitive flyers and long-distance migrants although identifying HFAs as long-distance migrants is not recommended without further investigation.

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 Malaria vector species composition and relative abundance in Mutare and Mutasa districts, Zimbabwe

2015 ◽  
Vol 47 (3) ◽  
pp. 79 ◽  
Author(s):  
S. Sande ◽  
M. Zimba ◽  
P. Chinwada ◽  
H.T. Masendu ◽  
A. Makuwaza
Keyword(s):  
Species Composition ◽  
Relative Abundance ◽  
Malaria Vector ◽  
Sibling Species ◽  
Mosquito Species ◽  
Sensu Stricto ◽  
Malaria Vectors ◽  
Morphological Identification ◽  
Vector Species ◽  
Vector Behaviour

Regular entomological monitoring is important to determine changes in mosquito species composition and relative densities of malaria vectors in relation to vector control interventions. A study to gain insights into malaria vector species composition and relative abundance was undertaken in Mutare and Mutasa districts, Zimbabwe. Two methods; indoor resting catches and larval sampling were used to collect indoor resting adults and larvae from May 2013 to April 2014. Mosquitoes collected as adults and reared from larvae that were identified morphologically as potential malaria vectors were further processed to sibling species by polymerase chain reaction (PCR). Morphological identification of anopheline mosquitoes showed presence of two complexes: <em>An. funestus</em> and <em>An. gambiae</em>. The total number of female members of the <em>An. funestus</em> group and <em>An. gambiae</em> complex collected by both methods from the two sites was 840 and 31 respectively. Malaria vector species of both complexes were more abundant in Mutare than in Mutasa. The PCR-based assays showed the presence of four sibling species: <em>An. funestus</em> <em>sensu</em> <em>stricto</em> (90.8%, 267/294) and <em>An. leesoni</em> (5.1%, 15/294), of <em>An. funestus</em> group; <em>An. arabiensis</em> (41.9%, 13/31) and <em>An. quadriannulatus</em> (48.4%, 15/31) of the <em>An. gambiae</em> complex. About 4% and 5% of specimens of <em>An. gambiae</em> complex and A<em>n. funestus</em> group respectively did not amplify. Of the two identified malaria vector sibling species, An. funestus sensu stricto was more abundant (95.4%, 267/280) than <em>An. arabiensis</em> (4.6%, 13/280), suggesting the replacement to secondary vector of <em>An. arabiensis</em>, which was previously the predominant vector species. <em>An. funestus</em> <em>sensu</em> <em>stricto</em> and <em>An</em>. <em>arabiensis</em>, the most important vectors of human malaria were identified in this study, but their resting and biting habits as well as insecticide susceptibility are unclear. Further studies on vector behaviour are therefore recommended.

scholarly journals Evidence for Divergent Selection on Immune Genes between the African Malaria Vectors, Anopheles coluzzii and A. gambiae

Insects ◽  
2020 ◽  
Vol 11 (12) ◽  
pp. 893
Author(s):  
Yoosook Lee ◽  
Lattha Souvannaseng ◽  
Travis C. Collier ◽  
Bradley J. Main ◽  
Laura C. Norris ◽  
...  
Keyword(s):  
Permutation Test ◽  
Wide Distribution ◽  
Sensu Stricto ◽  
Life Cycles ◽  
Malaria Vectors ◽  
Immune Gene ◽  
Anopheles Coluzzii ◽  
Potential Force ◽  
Larval Habitats ◽  
Immune Genes

During their life cycles, microbes infecting mosquitoes encounter components of the mosquito anti-microbial innate immune defenses. Many of these immune responses also mediate susceptibility to malaria parasite infection. In West Africa, the primary malaria vectors are Anopheles coluzzii and A. gambiae sensu stricto, which is subdivided into the Bamako and Savanna sub-taxa. Here, we performed whole genome comparisons of the three taxa as well as genotyping of 333 putatively functional SNPs located in 58 immune signaling genes. Genome data support significantly higher differentiation in immune genes compared with a randomly selected set of non-immune genes among the three taxa (permutation test p < 0.001). Among the 58 genes studied, the majority had one or more segregating mutations (72.9%) that were significantly diverged among the three taxa. Genes detected to be under selection include MAP2K4 and Raf. Despite the genome-wide distribution of immune genes, a high level of linkage disequilibrium (r2 > 0.8) was detected in over 27% of SNP pairs. We discuss the potential role of immune gene divergence as adaptations to the different larval habitats associated with A. gambiae taxa and as a potential force driving ecological speciation in this group of mosquitoes.

scholarly journals Evolution of the Pyrethroids Target-Site Resistance Mechanisms in Senegal: Early Stage of the Vgsc-1014F and Vgsc-1014S Allelic Frequencies Shift

Genes ◽  
2021 ◽  
Vol 12 (12) ◽  
pp. 1948
Author(s):  
Moussa Diallo ◽  
Majidah Hamid-Adiamoh ◽  
Ousmane Sy ◽  
Pape Cheikh Sarr ◽  
Jarra Manneh ◽  
...  
Keyword(s):  
Insecticide Resistance ◽  
Anopheles Gambiae ◽  
Pyrethroid Resistance ◽  
Early Stage ◽  
Resistance Mechanisms ◽  
Sub Saharan Africa ◽  
Malaria Vectors ◽  
Malaria Control Programme ◽  
Anopheles Coluzzii ◽  
Resistance Mutations

The evolution and spread of insecticide resistance mechanisms amongst malaria vectors across the sub-Saharan Africa threaten the effectiveness and sustainability of current insecticide-based vector control interventions. However, a successful insecticide resistance management plan relies strongly on evidence of historical and contemporary mechanisms circulating. This study aims to retrospectively determine the evolution and spread of pyrethroid resistance mechanisms among natural Anopheles gambiae s.l. populations in Senegal. Samples were randomly drawn from an existing mosquito sample, collected in 2013, 2017, and 2018 from 10 sentinel sites monitored by the Senegalese National Malaria Control Programme (NMCP). Molecular species of An. gambiae s.l. and the resistance mutations at the Voltage-gated Sodium Channel 1014 (Vgsc-1014) locus were characterised using PCR-based assays. The genetic diversity of the Vgsc gene was further analyzed by sequencing. The overall species composition revealed the predominance of Anopheles arabiensis (73.08%) followed by An. gambiae s.s. (14.48%), Anopheles coluzzii (10.94%) and Anopheles gambiae–coluzii hybrids (1.48%). Both Vgsc-1014F and Vgsc-1014S mutations were found in all studied populations with a spatial variation of allele frequencies from 3% to 90%; and 7% to 41%, respectively. The two mutations have been detected since 2013 across all the selected health districts, with Vgsc-L1014S frequency increasing over the years while Vgsc-1014F decreasing. At species level, the Vgsc-1014F and Vgsc-1014S alleles were more frequent amongst An. gambiae s.s. (70%) and An. arabiensis (20%). The Vgsc gene was found to be highly diversified with eight different haplotypes shared between Vgsc-1014F and Vgsc-1014S. The observed co-occurrence of Vgsc-1014F and Vgsc-1014S mutations suggest that pyrethroid resistance is becoming a widespread phenomenon amongst malaria vector populations, and the NMCP needs to address this issue to sustain the gain made in controlling malaria.

scholarly journals Chromosome-level genome assemblies of the malaria vectors Anopheles coluzzii and Anopheles arabiensis

GigaScience ◽  
2021 ◽  
Vol 10 (3) ◽  
Author(s):  
Anton Zamyatin ◽  
Pavel Avdeyev ◽  
Jiangtao Liang ◽  
Atashi Sharma ◽  
Chujia Chen ◽  
...  
Keyword(s):  
Anopheles Arabiensis ◽  
De Novo ◽  
Mosquito Species ◽  
Sub Saharan Africa ◽  
Malaria Vectors ◽  
Anopheles Coluzzii ◽  
Reference Quality ◽  
Sub Saharan ◽  
Genome Assemblies ◽  
Chromosome Level

Abstract Background Anopheles coluzzii and Anopheles arabiensis belong to the Anopheles gambiae complex and are among the major malaria vectors in sub-Saharan Africa. However, chromosome-level reference genome assemblies are still lacking for these medically important mosquito species. Findings In this study, we produced de novo chromosome-level genome assemblies for A. coluzzii and A. arabiensis using the long-read Oxford Nanopore sequencing technology and the Hi-C scaffolding approach. We obtained 273.4 and 256.8 Mb of the total assemblies for A. coluzzii and A. arabiensis, respectively. Each assembly consists of 3 chromosome-scale scaffolds (X, 2, 3), complete mitochondrion, and unordered contigs identified as autosomal pericentromeric DNA, X pericentromeric DNA, and Y sequences. Comparison of these assemblies with the existing assemblies for these species demonstrated that we obtained improved reference-quality genomes. The new assemblies allowed us to identify genomic coordinates for the breakpoint regions of fixed and polymorphic chromosomal inversions in A. coluzzii and A. arabiensis. Conclusion The new chromosome-level assemblies will facilitate functional and population genomic studies in A. coluzzii and A. arabiensis. The presented assembly pipeline will accelerate progress toward creating high-quality genome references for other disease vectors.

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