Anopheles collections in the health districts of Korhogo (Côte d'Ivoire) and Diébougou (Burkina Faso) (2016-2018)

データ レコード

この sampling event リソース内のデータは、1 つまたは複数のデータ テーブルとして生物多様性データを共有するための標準化された形式であるダーウィン コア アーカイブ (DwC-A) として公開されています。 コア データ テーブルには、1,683 レコードが含まれています。

拡張データ テーブルは3 件存在しています。拡張レコードは、コアのレコードについての追加情報を提供するものです。 各拡張データ テーブル内のレコード数を以下に示します。

この IPT はデータをアーカイブし、データ リポジトリとして機能します。データとリソースのメタデータは、 ダウンロード セクションからダウンロードできます。 バージョン テーブルから公開可能な他のバージョンを閲覧でき、リソースに加えられた変更を知ることができます。

バージョン

次の表は、公にアクセス可能な公開バージョンのリソースのみ表示しています。

引用方法

研究者はこの研究内容を以下のように引用する必要があります。:

Soma D D, Zogo B, Taconet P, Mouline K, Ahoua Alou L P, Dabiré R K, Amanan Koffi A, Pennetier C, Moiroux N (2024). Anopheles collections in the health districts of Korhogo (Côte d'Ivoire) and Diébougou (Burkina Faso) (2016-2018). Version 1.1. IRD - Institute of Research for Development. Samplingevent dataset. https://ipt.gbif.fr/resource?r=anopheles_collections_react_project&v=1.1

権利

研究者は権利に関する下記ステートメントを尊重する必要があります。:

パブリッシャーとライセンス保持者権利者は IRD - Institute of Research for Development。 This work is licensed under a Creative Commons Attribution (CC-BY 4.0) License.

GBIF登録

このリソースをはGBIF と登録されており GBIF UUID: 9f6ad2af-34cb-4f69-8436-1a41c2b43c62が割り当てられています。   GBIF France によって承認されたデータ パブリッシャーとして GBIF に登録されているIRD - Institute of Research for Development が、このリソースをパブリッシュしました。

キーワード

samplingEvent; malaria ; vectors ; resistance ; human landing catch ; exophagy ; endophagy ; biting behaviour

連絡先

地理的範囲

The geographic coverage includes the health districts of Korhogo (Nothern Côte d'Ivoire) and Diébougou (South-West Burkina Faso). Each study area is around 2500 squared km.

生物分類学的範囲

Several anopheles mosquitoes are included

時間的範囲

収集方法

Several villages (27 in Burkina Faso, 28 in Côte d'Ivoire) were selected within each area at the beginning of the project according to the following criteria : accessibility during the rainy season, 200 to 500 inhabitants per village, and distance between villages greater than 2 km. In each village, several rounds of mosquito collections (surveys) were carried out using the Human Landing Catch (HLC) sampling method. The procedure for conducting HLC was for a person to sit on a stool, and mosquitoes to alight on his exposed legs where they were then collected using a hemolysis tube. Mosquitoes were collected from 17:00 to 09:00 both indoors and outdoors at 4 sites per village. Collectors were organized into two teams of eight persons in each village; the first group collected from 17:00 to 01:00 and the second from 01:00 to 09:00. Collectors were rotated between indoor and outdoor collection sites every hour at each selected house to reduce potential collector bias. Indoor collection points were rooms that meet the following criteria: being usually inhabited; quiet without excessive movement of peoples; open to the outside through a door or a window. Outdoor collection was conducted in areas usually occupied by people but are sheltered from wind, traffic, fires and are not large meeting areas. The distance between collection sites was at least 50 m. The distance between indoors and outdoors collection points in one site was at least 10 m to minimize competition between mosquito collectors. Mosquitoes were collected in individual tubes plugged with cotton and stored in hourly bags. Morphological identification : All captured mosquitoes were morphologically identified in the field to genus and where possible to species levels according to established taxonomic keys. Molecular analysis : In the Burkina Faso area, for all the entomological surveys : - a subsample of 100 non blood-fed Anopheles spp. individuals was randomly selected per survey and per village and dissected to identify their parity state (parous or nulliparous) (parous female are those that have laid eggs at least once); - all individuals belonging to the Funestus group or Anopheles gambiae complex were identified to species by PCR; - DNA extracted from head-thorax of Anopheles spp. individuals was used to detect Plasmodium falciparum infection using quantitative polymerase chain reaction (qPCR) assay; - PCR assay were carried out on all mosquitoes belonging to the An. gambiae complex to detect the L1014F (kdr-w), G119S (ace-1), and L1014S (kdr-e) mutations (kdr-w and kdr-e mutations confer insecticide resistance to pyrethroids whereas ace-1 confers resistance to carbamates and organophosphates). In the Côte d'Ivoire area, for the first four entomological surveys : due to the very large numbers of vectors collected, a subsample of Anopheles spp. vectors from six villages randomly chosen out of the 28 villages included in the study were further analyzed : - For all the individuals belonging to the Anopheles nili complex or An. funestus group collected in these six villages : Plasmodium falciparum infection was detected using quantitative polymerase chain reaction (qPCR); - For one individual of Anopheles gambiae complex randomly selected per hour per collection site (indoor/outdoor) during each survey in these six villages : identification of species (PCR), Plasmodium falciparum infection (qPCR), L1014F (kdr-w) and G119S (ace-1) mutations (qPCR). In the Côte d'Ivoire area, for the last four entomological surveys : - For all the individuals belonging to the Anopheles nili complex or An. funestus group : identification of Plasmodium falciparum infection (qPCR); - For a subsample representing 25% of the total of the Anopheles gambiae captured : identification of species (PCR), Plasmodium falciparum infection (qPCR), L1014F (kdr-w) and G119S (ace-1) mutations (qPCR). The results of the molecular analysis are made available in the Extended Measurement or Facts extension. This extension also includes the place of collection of each mosquito (indoors or outdoors). In addition, a set of environmental data were extracted at the places and times of samplings from Earth-observation satellite products. These data are made available in the Measurement or Facts extension. The following measurements are provided : % of landscape occupied by each land cover type in a 2-km radius buffer zone around the sampling site, weekly rainfall and weekly land surface temperature up to 6 weeks before each collection date.

Method step description:

1. Several villages were selected as detailed in the Sampling Method section.
2. In each village, several rounds of mosquito collections (surveys) were carried out using the Human Landing Catch (HLC) sampling method between 2016 and 2018 as detailed in the Sampling Method section.
3. Morphological identification of the captured mosquitoes was performed as detailed in the Sampling Method section. Methods used are detailed in the following publications : Gillies MT. 1987. A supplement to the Anophelinae of Africa south of the Sahara (Afrotropical Region). Publications of the South African Institute for Medical Research, 55, 1–143. Gillies M, Meillon D. 1968. The Anophelinae of Africa south of the Sahara. Publication of the South African Institute for Medical Research, Johannesburg, 54, 1–343. Mattingly PF, Rageau J, La CA, Des F, Du M, Xii SA. Contributions de la faune des moustiques du Sud-Est Asiatique. XII. Contrib Am Entomol Inst. 1973; 7.
4. Molecular analysis of some of the captured anopheles was performed as detailed in the Sampling Method section. Methods used are detailed in the following publications : Detection of the L1014F (kdr-w) mutation by PCR in the Burkina Faso area : https://doi.org/10.1046/j.1365-2583.1998.72062.x Detection of the L1014S (kdr-e) mutation by PCR in the Burkina Faso area : https://doi.org/10.1046/j.1365-2583.2000.00209.x Detection of the G119S (ace-1) mutation by qPCR in the Burkina Faso area : https://doi.org/10.1186/1475-2875-12-404 Detection of Plasmodium falciparum infection by qPCR in the Burkina Faso area : https://doi.org/10.1371/journal.pone.0054820 Detection of the L1014F (kdr-w) mutation by PCR in the Côte d'Ivoire area : https://doi.org/10.1186/1475-2875-6-111 Detection of the G119S (ace-1) mutation by qPCR in the Côte d'Ivoire area : https://doi.org/10.1186/1475-2875-12-404 Detection of Plasmodium falciparum infection by qPCR in the Côte d'Ivoire area : https://doi.org/10.1371/journal.pone.0054820
5. Environmental data were collected and prepared as detailed in the Sampling Method section. Methods used are detailed in the following publication : https://doi.org/10.1186/s13071-021-04851-x
6. The collected data were digitized when relevant.
7. A custom R script was created to map the original data to Darwin Core as an event core with the relevant extensions (occurrence, Measurements or Facts, and Extended Measurements or Facts).
8. The Darwin Core files were connected to the French IPT and documented with metadata.
9. The data was published and registered with GBIF

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