scholarly journals Indoor and outdoor malaria vector surveillance in western Kenya: implications for better understanding of residual transmission

2017 ◽  
Vol 16 (1) ◽  
Author(s):  
Teshome Degefa ◽  
Delenasaw Yewhalaw ◽  
Guofa Zhou ◽  
Ming-chieh Lee ◽  
Harrysone Atieli ◽  
...  
2019 ◽  
Author(s):  
Maxwell G. Machani ◽  
Eric Ochomo ◽  
Fred Amimo ◽  
Jackline Kosgei ◽  
Stephen Munga ◽  
...  

AbstractBackgroundUnderstanding 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.


2019 ◽  
Vol 12 (1) ◽  
Author(s):  
Teshome Degefa ◽  
Delenasaw Yewhalaw ◽  
Guofa Zhou ◽  
Ming-Chieh Lee ◽  
Harrysone Atieli ◽  
...  

2017 ◽  
Vol 10 (1) ◽  
Author(s):  
Margaret M. Njoroge ◽  
Inaki Tirados ◽  
Steven W. Lindsay ◽  
Glyn A. Vale ◽  
Stephen J. Torr ◽  
...  

2020 ◽  
Vol 9 (1) ◽  
Author(s):  
Guofa Zhou ◽  
Eugenia Lo ◽  
Andrew K. Githeko ◽  
Yaw A. Afrane ◽  
Guiyun Yan

AbstractThe issues of pyrethroid resistance and outdoor malaria parasite transmission have prompted the WHO to call for the development and adoption of viable alternative vector control methods. Larval source management is one of the core malaria vector interventions recommended by the Ministry of Health in many African countries, but it is rarely implemented due to concerns on its cost-effectiveness. New long-lasting microbial larvicide can be a promising cost-effective supplement to current vector control and elimination methods because microbial larvicide uses killing mechanisms different from pyrethroids and other chemical insecticides. It has been shown to be effective in reducing the overall vector abundance and thus both indoor and outdoor transmission. In our opinion, the long-lasting formulation can potentially reduce the cost of larvicide field application, and should be evaluated for its cost-effectiveness, resistance development, and impact on non-target organisms when integrating with other malaria vector control measures. In this opinion, we highlight that long-lasting microbial larvicide can be a potential cost-effective product that complements current front-line long-lasting insecticidal nets (LLINs) and indoor residual spraying (IRS) programs for malaria control and elimination. Microbial larviciding targets immature mosquitoes, reduces both indoor and outdoor transmission and is not affected by vector resistance to synthetic insecticides. This control method is a shift from the conventional LLINs and IRS programs that mainly target indoor-biting and resting adult mosquitoes.


PLoS ONE ◽  
2020 ◽  
Vol 15 (2) ◽  
pp. e0224718 ◽  
Author(s):  
Maxwell G. Machani ◽  
Eric Ochomo ◽  
Fred Amimo ◽  
Jackline Kosgei ◽  
Stephen Munga ◽  
...  

2017 ◽  
Vol 10 (1) ◽  
Author(s):  
Alongkot Ponlawat ◽  
Patcharee Khongtak ◽  
Boonsong Jaichapor ◽  
Arissara Pongsiri ◽  
Brian P. Evans

2020 ◽  
Vol 47 (4) ◽  
Author(s):  
Riyani Setiyaningsih

Abstract The target of malaria elimination in Indonesia is expected to be achieved in 2030. One of the activities to support malaria elimination is vector surveillance. Several districts in Indonesia have certificates of malaria, including Jembrana, Bali Province, Bulukumba, South Sulawesi Province, and Bengkalis, Riau Province. Analysis of the presence of malaria vectors and Plasmodium needs to be done for the potential occurances of malaria transmission in eliminated malaria areas. Bioecology study of malaria vectors were conducted to determine receptivity status and others risk factors and the potential for malaria transmission based on ecosystems in Jembrana, Bulukumba and Bengkalis districts. As part of national research of disease vector and reservoir (Rikhus Vektora), mosquitoes and larval field-collection methods, molecular plasmodium detection and blood meal analyses were carried out according Rikhus vektora guidelines. The result showed that Anopheles kochi and An. tesselatus were positive confirmed with Plasmodium falciparum by using PCR in Jembrana, Bali province, which were found in non-forest ecosystems near settlements and beaches near settlements. In addition, Anopheles barbirostris, Anopheles vagus, and Anopheles peditaeniatus were also positive confirmed with P. falciparum by using similar methods in Bulukumba, South Sulawesi province. An. barbirostris was found in forest ecosystems near settlement, Anopheles vagus was found in remote forest ecosystems of settlements and beaches near settlements, and Anopheles peditaenistus was found in non-forest ecosystems near settlements. While Anopheles sinensis was confirmed positive with P. falciparum in Bengkalis, Riau province. Jembrana, Bulukumba and Bengkalis districts are recognized as receptive areas and have potential for re-transmission of malaria. Vector surveillance and the implementation of approriate vector control and migration surveillance are needed to ascertain wheter the positive Anopheles with positives Plasmodium falciparum getting the parasites from imported cases or there has been a local transmission (indigenous) in these areas. This information is needed to prevent malaria re-transmission in the eliminated areas. Keywords : elimination, malaria, vector Abstrak Target eliminasi malaria di Indonesia harapannya dapat dicapai tahun 2030. Salah satu kegiatan yang dilakukan untuk menunjang elimnasi malaria adalah surveilans vektor. Beberapa Kabupaten di Indonesia telah memperoleh serfikat eliminasi malaria diantaranya Kabupaten Jembrana Propinsi Bali, Bulukumba Propinsi Sulawesi Selatan, dan Bengkalis Propinsi Riau. Analisis keberadaan vektor dan patogen malaria perlu dilakukan untuk melihat potensi terjadinya penularan malaria kembali di daerah yang telah mendapatkan sertifikat eliminasi malaria. Studi bioekologi vektor malaria dilakukan untuk mengetahui status reseptivitas dan faktor risiko lainnya, serta potensi penularan malaria berbasis ekosistem di daerah tersebut. Sebagai bagian dari dari Riset khusus (rikhus) vektora, koleksi lapangan nyamuk dan jentik, prosedur deteksi melekuler plasmodium dan analisis pakan darah dilakukan dengan menggunakan pedoman Rikhus vektora. Hasil studi menunjukkan bahwa Anopheles kochi dan Anopheles tesselatus, yang masing-masing ditemukan di eksoistem non hutan dekat pemukiman dan pantai dekat pemukiman ditemukan positif mengandung Plasmodium falciparum di Kabupaten Jembrana, Bali. Sedangkan di Kabupaten Bulukumba, Sulawesi Selatan, Anopheles barbirostris, Anopheles vagus, dan Anopheles peditaeniatus merupakan spesies Anopheles yang terkonfirmasi positif mengandung P. falciparum. An. barbirostris ditemukan di ekosistem hutan dekat pemukiman, Anopheles vagus ditemukan di ekosistem hutan jauh pemukiman dan pantai dekat pemukiman, dan Anopheles peditaenistus ditemukan di ekosistem non hutan dekat pemukiman. Sedangkan Anopheles sinensis merupakan satu-satunya spesies Anopheles yang ditemukan positif mengandung P. falciparum di Kabupaten Bengkalis, Riau. Dari hasil studi menunjukkan, Kabupaten Jembrana, Bulukumba, dan Bengkalis merupakan daerah reseptif dan berpotensi terjadinya penularan kembali malaria. Surveilans vektor dan implementasi pengendalian vektor yang tepat serta surveilans migrasi secara ketat diperlukan untuk memastikan apakah Anopheles yang positif tersebut mendapatkan parasit P. falciparum dari kasus import ataukah memang sudah terjadi transmisi secara lokal (indigenous) di wilayah tersebut. Hal ini perlu dilakukan agar tidak terjadi penularan kembali malaria di daerah yang sudah tereliminasi tersebut. Kata kunci: eliminasi, malaria, vektor


2012 ◽  
Vol 6 (08) ◽  
pp. 637-643 ◽  
Author(s):  
Andrew Ambogo Obala ◽  
Helen L Kutima ◽  
Henry D.N. Nyamogoba ◽  
Anne W Mwangi ◽  
Chrispinus J Simiyu ◽  
...  

Introduction: This study was conducted in a sugar belt region of western Kenya interfacing epidemic and endemic malaria transmission. We investigated Anopheles gambiae sensu stricto (ss) and Anopheles arabiensis species compositions and densities, human host choice, and infectivity. Methodology: Mosquitoes were captured using pyrethrum spray catch technique and first identified based on morphology; species were confirmed by PCR. Blood meal preference and sporozoite rates were determined by ELISA. Parity rates and entomological inoculation rates (EIR) were determined. Seasonal densities were compared against environmental temperatures, relative humidity and rainfall. Results: In total 2,426 An. gambiae were collected.  Out of 1,687 female blood-fed mosquitoes, 272 were randomly selected for entomological tests. An. gambiae ss and An. arabiensis comprised 75% (205/272) and 25% (68/272) of the selection, respectively. An. gambiae ss had higher preference for human blood (97%; n=263/272) compared with An. arabiensis, which mostly fed on bovines (88%; n=239/272).  The sporozoite and parity rates were 6% (16/272) and 66% (179/272) for An. gambiae ss and 2% (4/272) and 53% (144/272) for An. arabiensis respectively, while EIR was 0.78 infective bites/person/night.  Climate (ANOVA; F=14.2; DF=23) and temperature alone (r=0.626; t=3.75; p=0.001) were significantly correlated with vector densities. Conclusion: An. gambiae ss are the most efficient malaria vector mosquito species in Kopere village. Because An. gambiae ss largely rests and feeds indoors, use of indoor residual spray and insecticide-treated nets is likely the most suitable approach to malaria vector control in Kopere village and other parts of Kenya where this species is abundant. 


2016 ◽  
Vol 5 (3) ◽  
Author(s):  
Rezka Gustya Sari ◽  
Nurhayati Nurhayati ◽  
Rosfita Rasyid

AbstrakMalaria adalah penyakit infeksi parasit yang disebabkan oleh protozoa obligat intraselular dari genus Plasmodium yang ditularkan nyamuk Anopheles. Bungus merupakan salah satu kecamatan dengan kasus malaria tinggi di Kota Padang, terdapat 69 kasus malaria pada tahun 2011. Pengendalian vektor malaria dibutuhkan pengetahuan mengenai spesies vector. Tujuan penelitian ini adalah menentukan spesies nyamuk tersangka vektor malaria. Penelitian dilaksanakan dari Oktober sampai November 2011. Nyamuk Anopheles di tangkap di dalam dan di luar ruangan menggunakan light trap dan umpan orang menggunakan aspirator. Penangkapan dilakukan pada malam hari pada jam 18.00 - 06.00 dan pagi hari pada jam 07.00 - 09.00. Semua nyamuk yang berhasil tertangkap diidentifikasi di bawah mikroskop. Bedasarkan penelitian yang telah dilakukan didapatkan nyamuk An.subpictus, An.sundaicus dan An.aconitus dengan persentase (49,5%), (29,4%) dan (14,7%). Hal ini menunjukkan bahwa An.sundaicus, An.subpictus dan An.aconitus memiliki potensi yang besar dalam penularan penyakit malaria.                                 Kata kunci: malaria, vektor malaria AbstractMalaria is a disease caused by intracellular obligate protozoa, genus of plasmodium which is a parasite is carried by Anopheles mosquito. Bungus subdistrict is one of the areas that has high case of malaria in Padang district of Sumatera Barat Province, there were 69 case of malaria. Determination of method of control requires an understanding on the species of mosquito which serves as the vector and its behavior. The objective of this study was to assess fauna and the activity of Anopheles spp as suspected malaria vector. This research had done on October to November 2011. The Anopheles mosquitoes were collected indoor and outdoor by using light trap and human landing collection in the evening starting from 6 p.m - 6 a.m, in the morning from 7 - 9 a.m. All the Moquitoes were  brougt to the laboratory for identifications. The resut showed that An. subpictus (49.5%) An. sundaicus (29.4%) and A. aconitus (14.7%). were the suspected malaria vector that has important role in tranmission of malaria in this area.Keywords: malaria, malaria vektor


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