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Machani, M. G.

Publications and source records attributed to Machani, M. G..

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Local trait responses and aquatic microclimates increase projected habitat suitability for field-collected Anopheles stephensi in southern Ethiopia

BackgroundTrait-based models of mosquito environmental suitability commonly use global thermal performance curves compiled from laboratory studies. These curves may misrepresent suitability when local populations or larval habitats differ from globally synthesised expectations. This issue is particularly relevant for Anopheles stephensi, an urban malaria vector expanding in the Horn of Africa, where artificial aquatic habitats may generate microclimates poorly represented by global trait datasets or gridded air-temperature products. Methodology/Principal FindingsWe compared juvenile survival, development, and projected maximal population growth rate, rm, using locally measured data from field-collected Ethiopian An. stephensi and a global comparator combining pub-lished juvenile trait data. We fitted thermal performance curves for juvenile survival and development, used these curves to estimate temperature-dependent rm as a metric of habitat suitability, and projected rm across two matched temperature inputs: logger-measured larval habitat water temperature and ERA5-Land 2 m air temperature. Local juvenile trait responses produced higher projected rm than the global comparator across monitored habitats. Measured aquatic temperatures were warmer than ERA5-Land air temperatures, with a mean daily water-air offset of 3.26{whitebullet}C, and were more spatially heterogeneous among habitats. ERA5-Land resolved only two unique temperature series across the six monitored habitats. Sensitivity analyses showed that the Local-Global difference was robust for logger-measured water temperatures, whereas the ERA5-based difference was partly amplified by cooler temperatures below the local experimental range. Conclusions/SignificanceThis study provides the first locally derived juvenile thermal performance curves and temperature-dependent population growth estimates for field-collected An. stephensi in Africa, demonstrating that locally measured juvenile traits consistently predict higher habitat suitability than globally synthesised trait data. These find-ings highlight the importance of incorporating local mosquito trait data and aquatic microclimate measure-ments into predictive models to improve assessments of An. stephensi establishment, spread, and malaria risk in newly invaded urban environments. Author SummaryAnopheles stephensi is an invasive malaria mosquito that is rapidly spreading in urban areas of Africa. Pre-dicting where this species can establish is difficult because many models use mosquito temperature-response data from long-maintained laboratory colonies rather than from recently collected African populations. We measured juvenile survival and development in An. stephensi collected from Ethiopia, and compared pro-jections based on these local data with projections based on published laboratory-colony data. We also compared field-measured larval habitat water temperature with ERA5-Land air temperature. We found that local juvenile trait responses produced higher projected population growth than the global comparator across monitored habitats. Field-measured water temperatures were warmer and more variable among habitats than gridded air temperatures, which reduced habitat-level differences. These findings show that local mosquito biology and larval habitat microclimate measurements can change fine-scale estimates of suitability. This matters for surveillance and control because urban water containers may create suitable conditions that are poorly represented by broad climate datasets.

ecology↗

Early-evening biting by Anopheles stephensi in Southern Ethiopia: A Challenge for Bed Net Use as Vector Control in Africa

Anopheles stephensi is rapidly expanding across Africa, posing new challenges for malaria control. Its biting time patterns, however, remain poorly characterized, raising uncertainty about the effectiveness of bed nets against this invasive vector. To address this gap, we investigated diel biting activity, feeding propensity, and flight behavior using complementary behavioral assays on females reared from wild-caught larvae in Hawassa City, southern Ethiopia. Flight monitoring assays revealed that An. stephensi exhibited pronounced activity at dusk, beginning between 18:00 and 19:00 with the onset of scotophase, and little to no activity during the photophase. Blood-feeding propensity, defined as the proportion of mosquitoes taking a blood meal when offered, peaked during the early scotophase (18:00-22:00) at 33.3-51.7%, but was markedly reduced during daylight hours (0-16.7%). Human landing catches in large-cage enclosures confirmed this early evening activity: 83.5% of total landings occurred between 18:00 and 22:00 with a sharp peak at 18:00-19:00, corresponding to a mean biting rate of 17.8 bites per person per hour. These findings demonstrate that invasive An. stephensi primarily seek hosts and bite during the early evening, a time when people are often unprotected by bed nets. This behavior reduces the protective impact of conventional net-based interventions and underscores the need for African National Malaria Control Programs to deploy complementary measures such as spatial repellents and larval source management to mitigate early-evening transmission. Moreover, this study highlights the utility of integrated behavioral assays for estimating biting time, offering approaches that can be extended to other vector species across Africa.

zoology↗

Biting time of day in malaria mosquitoes is modulated by nutritional status

BackgroundTransmission of vector-borne pathogens follows daily rhythms, occurring at the time of day that vectors forage for blood. Control measures such as insecticide-treated bed nets (ITNs) have been particularly successful for reducing malaria transmission, because they exploit the nocturnal biting behaviour of the Anopheles spp. that vector malaria. However, shifts in biting behaviour to earlier or later hours when people are unprotected can undermine the efficacy of ITNs. Despite the implications for malaria transmission, the mechanisms underlying these shifts remain poorly understood. Because food availability mediates activity and foraging rhythms, and ITNs block access to human blood as a food source, we hypothesized that nutritional deprivation could cause mosquitoes to shift their biting behaviour to earlier or later in the diel cycle. MethodsWe provided female Anopheles gambiae s.l. mosquitoes with a blood meal on day 3 post-emergence, and access to one of three feeding treatments that varied in nutritional resources: (i) 0.5% sucrose, (ii) 10% sucrose, or (iii) 10% sucrose plus an additional blood meal on day 6. We released mosquitoes into a semi-field system on day 10 with human-mimic traps to investigate how food availability impacted the time of day that mosquitoes host seek. ResultsNutritional resources determine both the likelihood and time of day that host seeking occurs. Specifically, low-resourced mosquitoes were 2-3 fold more likely to host seek overall, and 5-10 fold more likely to host seek at an earlier time of day than well-resourced mosquitoes (fed 10% sucrose with and without an additional blood meal), which predominantly sought a host in the second half of the night time. ConclusionsWe reveal that mosquito nutritional condition drives plasticity in biting time of day, suggesting it is an underappreciated contributor to residual malaria transmission. Furthermore, our results suggest that targeting mosquito nutrition (e.g. sugar-baited traps) could influence mosquito behaviour in ways that affect the success of ITNs. More broadly, understanding the drivers of biting time of day variation is crucial for the future success of vector control tools and controlling malaria transmission.

ecology↗

Insecticide resistance and its intensity in urban Anopheles arabiensis in Kisumu City, Western Kenya: Implications for malaria control in urban areas

BackgroundThe rise of insecticide resistance poses a growing challenge to the effectiveness of vector control tools, particularly in rural areas. However, the urban setting has received comparatively less focus despite its significance in attracting rural to urban migration. Unplanned urbanization, often overlooked, exacerbates insecticide resistance as Anopheles mosquitoes adapt to the polluted environments of rapidly expanding cities. This study aimed to assess the insecticide susceptibility status of malaria vectors and identify potential underlying mechanisms across three distinct ecological settings characterized by differing levels of urbanization in Kisumu County, Kenya. MethodsField-derived An. gambiae (s.l.) larvae collected from a long stretch of urban-to-rural continuum were phenotyped as either resistant or susceptible to six different insecticides using the World Health Organization (WHO) susceptibility test. Polymerase chain reaction (PCR) techniques were used to identify the species of the An. gambiae complex and screened for mutations at voltage-gated sodium channels (Vgsc-1014F, Vgsc-1014S, Vgsc-1575Y) and acetylcholinesterase Ace1-119S. Metabolic enzymes activities (non-specific {beta}-esterases and monooxygenases) were evaluated in mosquitoes not exposed to insecticides using microplate assays. Additionally, during larval sampling, a retrospective questionnaire survey was conducted to determine pesticide usage by the local inhabitants. ResultsAnopheles arabiensis dominated in urban (96.2%) and peri-urban (96.8%) areas, while An. gambiae (s.s.) was abundant in rural settings (82.7%). Urban mosquito populations showed high resistance intensity to deltamethrin (Mortality rate: 85.2% at 10x) and suspected resistance to Pirimiphos-methyl and bendiocarb while peri-urban and rural populations exhibited moderate resistance intensity to deltamethrin (mortality rate >98% at 10x). Preexposure of mosquitoes to a synergist piperonyl butoxide (PBO) significantly increased mortality rates: from 40.7% to 88.5% in urban, 51.9% to 90.3% in peri-urban, and 55.4% to 87.6% in rural populations for deltamethrin, and from 41.4% to 78.8% in urban, 43.7% to 90.7% in peri-urban, and 35% to 84.2% in rural populations for permethrin. In contrast, 100% mortality to chlorfenapyr and clothianidin was observed in all the populations tested. The prevalence of L1014F mutation was notably higher in urban An. arabiensis (0.22) unlike the peri-urban (0.11) and rural (0.14) populations while the L1014S mutation was more prevalent in rural An. gambiae (0.93). Additionally, urban An. arabiensis exhibited elevated levels of mixed function oxidases (0.8/mg protein) and non-specific esterases (2.12/mg protein) compared to peri-urban (0.57/mg protein and 1.5/mg protein, respectively) and rural populations (0.6/mg protein and 1.8/mg protein, respectively). Pyrethroids, apart from their use in public health through LLINs, were being highly used for agricultural purposes across all ecological settings (urban 38%, peri-urban 36% and rural 37%) followed by amidine group, with organophosphates, neonicotinoids and carbamates being of secondary importance. ConclusionThese findings show high resistance of An. arabiensis to insecticides commonly used for vector control, linked with increased levels of detoxification enzymes. The observed intensity of resistance underscores the pressing issue of insecticide resistance in urban areas, potentially compromising the effectiveness of vector control measures, especially pyrethroid-treated LLINs. Given the species unique behavior and ecology compared to An. gambiae, tailored vector control strategies are needed to address this concern in urban settings.

ecology↗

Insecticide resistance status of indoor and outdoor resting malaria vectors in a highland and lowland site in Western Kenya

BackgroundLong Lasting Insecticidal Nets (LLINs) and indoor residual spraying (IRS) represent powerful tools for controlling malaria vectors in sub-Saharan Africa. The success of these interventions relies on their capability to inhibit indoor feeding and resting of malaria mosquitoes. This study sought to understand the interaction of insecticide resistance with indoor and outdoor resting behavioral responses of malaria vectors from Western Kenya. MethodsThe status of insecticide resistance among indoor and outdoor resting anopheline mosquitoes was compared in Anopheles mosquitoes collected from Kisumu and Bungoma counties in Western Kenya. The level and intensity of resistance were measured using WHO-tube and CDC-bottle bioassays, respectively. The synergist piperonyl butoxide (PBO) was used to determine if metabolic activity (monooxygenase enzymes) explained the resistance observed. The mutations at the voltage-gated sodium channel (Vgsc) gene and Ace 1 gene were characterized using PCR methods. Microplate assays were used to measure levels of detoxification enzymes if present. ResultsA total of 1094 samples were discriminated within Anopheles gambiae s.l. and 289 within An. funestus s.l. In Kisian (Kisumu county), the dominant species was Anopheles arabiensis 75.2% (391/520) while in Kimaeti (Bungoma county) collections the dominant sibling species was Anopheles gambiae s.s 96.5% (554/574). The An. funestus s.l samples analysed were all An. funestus s.s from both sites. Pyrethroid resistance of An.gambiae s.l F1 progeny was observed in all sites. Lower mortality was observed against deltamethrin for the progeny of indoor resting mosquitoes compared to outdoor resting mosquitoes (Mortality rate: 37% vs 51%, P=0.044). The intensity assays showed moderate-intensity resistance to deltamethrin in the progeny of mosquitoes collected from indoors and outdoors in both study sites. In Kisian, the frequency of vgsc-L1014S and vgsc-L1014F mutation was 0.14 and 0.19 respectively in indoor resting malaria mosquitoes while those of the outdoor resting mosquitoes were 0.12 and 0.12 respectively. The ace 1 mutation was present in higher frequency in the F1 of mosquitoes resting indoors (0.23) compared to those of mosquitoes resting outdoors (0.12). In Kimaeti, the frequencies of vgsc-L1014S and vgsc-L1014F were 0.75 and 0.05 respectively for the F1 of mosquitoes collected indoors whereas those of outdoor resting ones were 0.67 and 0.03 respectively. The ace 1 G119S mutation was present in progeny of mosquitoes from Kimaeti resting indoors (0.05) whereas it was absent in those resting outdoors. Monooxygenase activity was elevated by 1.83 folds in Kisian and by 1.33 folds in Kimaeti for mosquitoes resting indoors than those resting outdoors respectively. ConclusionThe study recorded high phenotypic, metabolic and genotypic insecticide resistance in indoor resting populations of malaria vectors compared to their outdoor resting counterparts. The indication of moderate resistance intensity for the indoor resting mosquitoes is alarming as it could have an operational impact on the efficacy of the existing pyrethroid based vector control tools. The use of synergist (PBO) in LLINs may be a better alternative for widespread use in these regions recording high insecticide resistance.

zoology↗

Resting behaviour of malaria vectors in a highland and a lowland site of western Kenya: Implication on malaria vector control measures

BackgroundUnderstanding the interactions between increased insecticide resistance in field malaria vector populations and the subsequent resting behaviour patterns is important for planning adequate vector control measures in a specific context and sustaining the current vector interventions. The aim of this study was to investigate the resting behavior, host preference and infection with Plasmodium falciparum sporozoites by malaria vectors in different ecological settings of western Kenya with different levels of insecticide resistance. MethodsIndoor and outdoor resting Anopheline mosquitoes were sampled during the dry and rainy seasons in Kisian (lowland site) and Bungoma (highland site), both in western Kenya. WHO tube bioassay was used to determine levels of phenotypic resistance of first generation offspring (F1 progeny) of malaria vectors resting indoors and outdoors to deltamethrin. PCR-based molecular diagnostics were used for mosquito speciation, genotype for resistance mutations and to determine specific host blood meal origins. Enzyme-linked Immunosorbent Assay (ELISA) was used to determine mosquito sporozoite infections. ResultsOverall, 3,566 female Anopheles mosquitoes were collected with Anopheles gambiae s.l [In Bungoma, An. gambiae s.s (90.9%), An arabiensis (7.6%) and in Kisian, An. gambiae s.s (38.9%), An. arabiensis (60.2%)] being the most abundant species (74.7%) followed by An. funestus s.l (25.3%). The majority of An. gambiae s.l (85.4 and 58%) and An. funestus (96.6 and 91.1%) were caught resting indoors in Bungoma and Kisian respectively.Vgsc-1014S was observed at a slightly higher frequency in An. gambiae s.s hereafter(An. gambiae) resting indoor than outdoor (89.7 vs 84.6% and 71.5 vs 61.1%) in Bungoma and Kisian respectively. For An. arabiensis, Vgsc-1014S was 18.2% indoor and outdoor (17.9%) in Kisian. In Bungoma, the Vgsc-1014S was only detected in An. arabiensis resting indoors with a frequency of 10%. The Vgsc-1014F mutation was only present in An. gambiae resting indoors from both sites, but at very low frequencies in Kisian compared to Bungoma (0.8 and 9.2% respectively. In Bungoma, the sporozoite rates for An. funestus, An. gambiae, and An. arabiensis resting indoors were 10.9, 7.6 and 3.4 % respectively. For outdoor resting, An. gambiae and An. arabiensis in Bungoma, the sporozoite rates were 4.7 and 2.9 % respectively.Overall, in Bungoma, the sporozoite rate for indoor resting mosquitoes was 8.6% and 4.2% for outdoors. In Kisian the sporozoite rate was 0.9% for indoor resting An. gambiae. None of the outdoor collected mosquitoes in Kisian tested positive for sporozoite infections. ConclusionThe study reports high densities of insecticide-resistant An. gambiae and An. funestus resting indoors and the persistence of malaria transmission indoors with high entomological inoculation rates (EIR) regardless of the use of Long-lasting insecticidal nets (LLINs). These findings underline the difficulties of controlling malaria vectors resting and biting indoors using the current interventions. Supplemental vector control tools and implementation of sustainable insecticide resistance management strategies are needed in western Kenya.

zoology↗