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      Effect of physicochemical parameters on Anopheles and Culex mosquito larvae abundance in different breeding sites in a rural setting of Muheza, Tanzania

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          Translated abstract

          Background

          Malaria and lymphatic filariasis (LF) are diseases of great public health important in East Africa. Malaria is transmitted by Anopheles while LF is transmitted by both Anopheles and Culex mosquitoes. There is limited evidence on the effects of physicochemical parameters on these mosquitoes in rural settings of Tanzania. This study aimed at assessing the effects of physicochemical parameters on Anopheles and Culex larvae abundance in different breeding sites in a rural setting of Muheza district .

          Methods

          A cross-sectional study was conducted in 13 villages in Muheza district, between December 2015 and May 2016. Mosquito larvae were sampled using standard dipping techniques. Physicochemical parameters were measured by a Multi-parameter pH meter in different mosquito breeding sites. Mosquito larvae and pupa densities were compared between the ≤33th (lower) and ≥67th (upper) percentiles of physicochemical parameters. An. gambiae ( s.l.) and An. funestus were identified by polymerase chain reaction (PCR) to reveal their sibling species.

          Results

          Abundance of Anopheles larvae was significantly higher (76.6%) than Culex (66.9%) χ 2 = 5.73, df = 1, P = 0.017). The presence of late instars of Anopheles was significantly higher (78.2%) than that of Culex (64.5%) ( χ 2 = 0.984, df = 1, P = 0.017). A model adjusted for larval stage showed that the likelihood of finding Culex larvae was lower by 38.2% (95% CI: 16.9–54.1, df = 1, P = 0.001) compared to Anopheles. Upper percentiles of salinity (OR = 7.05; 95% CI: 1.19–41.88, P = 0.032) and conductivity (OR = 5.47; 95% CI: 1.01–29.67, P = 0.056) were significantly associated with the presence and with increased density of Anopheles larvae. PCR results showed that, within the gambiae complex, 53.3% ( n = 136) were An. gambiae ( s.s.) and 46.7% ( n = 119) were An. arabiensis. In An. funestus group, 91.1% ( n = 41) were An. funestus ( s.s.) , 4.4% ( n = 2) were An. rivulorum, 2.2% ( n = 1) were An. leesoni and 2.2% ( n = 1) were An. parensis.

          Conclusion

          High salinity and conductivity were significantly associated with increased density of Anopheles larvae. To our knowledge, this is the first study to demonstrate the occurrence of Anopheles larvae in polluted breeding sites in rural settings of Tanzania. The study has found both Anopheles and Culex mosquito larvae co-existed in breeding sites. The possible reasons for tolerance to a higher level of physicochemical parameters among Anopheles mosquitoes need to be ascertained.

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          Most cited references33

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          Impact of environment on mosquito response to pyrethroid insecticides: facts, evidences and prospects.

          By transmitting major human diseases such as malaria, dengue fever and filariasis, mosquito species represent a serious threat worldwide in terms of public health, and pose a significant economic burden for the African continent and developing tropical regions. Most vector control programmes aiming at controlling life-threatening mosquitoes rely on the use of chemical insecticides, mainly belonging to the pyrethroid class. However, resistance of mosquito populations to pyrethroids is increasing at a dramatic rate, threatening the efficacy of control programmes throughout insecticide-treated areas, where mosquito-borne diseases are still prevalent. In the absence of new insecticides and efficient alternative vector control methods, resistance management strategies are therefore critical, but these require a deep understanding of adaptive mechanisms underlying resistance. Although insecticide resistance mechanisms are intensively studied in mosquitoes, such adaptation is often considered as the unique result of the selection pressure caused by insecticides used for vector control. Indeed, additional environmental parameters, such as insecticides/pesticides usage in agriculture, the presence of anthropogenic or natural xenobiotics, and biotic interactions between vectors and other organisms, may affect both the overall mosquito responses to pyrethroids and the selection of resistance mechanisms. In this context, the present work aims at updating current knowledge on pyrethroid resistance mechanisms in mosquitoes and compiling available data, often from different research fields, on the impact of the environment on mosquito response to pyrethroids. Key environmental factors, such as the presence of urban or agricultural pollutants and biotic interactions between mosquitoes and their microbiome are discussed, and research perspectives to fill in knowledge gaps are suggested. Copyright © 2012 Elsevier Ltd. All rights reserved.
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            Insecticide resistance mechanisms associated with different environments in the malaria vector Anopheles gambiae: a case study in Tanzania

            Background Resistance of mosquitoes to insecticides is a growing concern in Africa. Since only a few insecticides are used for public health and limited development of new molecules is expected in the next decade, maintaining the efficacy of control programmes mostly relies on resistance management strategies. Developing such strategies requires a deep understanding of factors influencing resistance together with characterizing the mechanisms involved. Among factors likely to influence insecticide resistance in mosquitoes, agriculture and urbanization have been implicated but rarely studied in detail. The present study aimed at comparing insecticide resistance levels and associated mechanisms across multiple Anopheles gambiae sensu lato populations from different environments. Methods Nine populations were sampled in three areas of Tanzania showing contrasting agriculture activity, urbanization and usage of insecticides for vector control. Insecticide resistance levels were measured in larvae and adults through bioassays with deltamethrin, DDT and bendiocarb. The distribution of An. gambiae sub-species and pyrethroid target-site mutations (kdr) were investigated using molecular assays. A microarray approach was used for identifying transcription level variations associated to different environments and insecticide resistance. Results Elevated resistance levels to deltamethrin and DDT were identified in agriculture and urban areas as compared to the susceptible strain Kisumu. A significant correlation was found between adult deltamethrin resistance and agriculture activity. The subspecies Anopheles arabiensis was predominant with only few An. gambiae sensu stricto identified in the urban area of Dar es Salaam. The L1014S kdr mutation was detected at elevated frequency in An gambiae s.s. in the urban area but remains sporadic in An. arabiensis specimens. Microarrays identified 416 transcripts differentially expressed in any area versus the susceptible reference strain and supported the impact of agriculture on resistance mechanisms with multiple genes encoding pesticide targets, detoxification enzymes and proteins linked to neurotransmitter activity affected. In contrast, resistance mechanisms found in the urban area appeared more specific and more related to the use of insecticides for vector control. Conclusions Overall, this study confirmed the role of the environment in shaping insecticide resistance in mosquitoes with a major impact of agriculture activities. Results are discussed in relation to resistance mechanisms and the optimization of resistance management strategies.
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              Influence of host and larval habitat distribution on the abundance of African malaria vectors in western Kenya.

              The abundance of anopheline mosquitoes varies substantially among houses within the same villages. Anopheles gambiae sensu stricto is highly anthropophilic, and Anopheles arabiensis is zoophilic; thus, it is often hypothesized that the abundance of An. gambiae and An. arabiensis in a house is associated with the distribution of livestock and humans. In this paper we examined the influence of livestock and human host availability on the distribution and abundance of malaria vectors in the basin region of Lake Victoria in western Kenya. Larvae and adults of An. gambiae, An. arabiensis and Anopheles funestus were collected in the beginning and the end of the rainy season in 1999. Anopheles gambiae was the predominant species in both larval and adult samples. Multiple regression analyses found that the ratio of distance between houses and larval habitats to distance between cowsheds and larval habitats had a significant and negative association with the relative abundance of An. gambiae larvae for both sampling periods. The ratio of human density to cow density was positively correlated with the relative abundance of An. gambiae larvae in the late rainy period. For the adult samples, distance from a house to its nearest larval habitats was the only variable that showed a significant correlation with the An. gambiae density in houses in both sample periods. More than 90% of anopheline adults were found in the houses within 300 meters from the nearest larval habitats. Anopheline mosquito density was not correlated to the density of cows or humans, or the distance to cowsheds from houses. These results suggest that livestock and human host availability affect the relative abundance of An. gambiae larvae in aquatic habitats, but the distribution of anopheline adults in houses is determined by the distance from houses to larval habitats.
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                Author and article information

                Contributors
                ebasi2002@gmail.com
                wnkisinza@gmail.com
                b.mmbando@yahoo.com
                r_malima@hotmail.com
                fwmosha@gmail.com
                Journal
                Parasit Vectors
                Parasit Vectors
                Parasites & Vectors
                BioMed Central (London )
                1756-3305
                24 June 2017
                24 June 2017
                2017
                : 10
                : 304
                Affiliations
                [1 ]ISNI 0000 0004 0648 0439, GRID grid.412898.e, , Kilimanjaro Christian Medical University College, ; P.O. Box 2240, Moshi, Tanzania
                [2 ]ISNI 0000 0004 0367 5636, GRID grid.416716.3, , National Institute for Medical Research, Headquarters, ; P.O. Box 9653, Dar es Salaam, Tanzania
                [3 ]ISNI 0000 0004 0367 5636, GRID grid.416716.3, , National Institute for Medical Research, Amani Centre, ; P.O. Box 81, Muheza, Tanzania
                [4 ]ISNI 0000 0004 0367 5636, GRID grid.416716.3, , National Institute for Medical Research, Tanga Centre, ; P.O. Box 5004, Tanga, Tanzania
                Article
                2238
                10.1186/s13071-017-2238-x
                5482952
                28645303
                180d4137-762d-40e3-b80d-005b92a01557
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 11 November 2016
                : 11 June 2017
                Categories
                Research
                Custom metadata
                © The Author(s) 2017

                Parasitology
                anopheles,culex,mosquitoes,breeding sites,physicochemical parameters,muheza,tanzania
                Parasitology
                anopheles, culex, mosquitoes, breeding sites, physicochemical parameters, muheza, tanzania

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