학술논문

A next-generation (DNA) sequencing (NGS)-based method for identifying the sources of sugar meals in mosquito vectors of West Nile virus in Israel.
Document Type
Academic Journal
Author
Abbasi I; Department of Microbiology and Molecular Genetics, The Institute for Medical Research Israel-Canada (IMRIC), The Kuvin Centre for the Study of Infectious and Tropical Diseases, The Hebrew University of Jerusalem, 91120, Israel, ibrahima@ekmd.huji.ac.il.; Akad F; Laboratory of Entomology, Central Laboratories Jerusalem, Ministry of Health, Israel.; Studentsky L; Laboratory of Entomology, Central Laboratories Jerusalem, Ministry of Health, Israel.; Avi IB; Laboratory of Entomology, Central Laboratories Jerusalem, Ministry of Health, Israel.; Orshan L; Laboratory of Entomology, Central Laboratories Jerusalem, Ministry of Health, Israel.; Warburg A; Department of Microbiology and Molecular Genetics, The Institute for Medical Research Israel-Canada (IMRIC), The Kuvin Centre for the Study of Infectious and Tropical Diseases, The Hebrew University of Jerusalem, 91120, Israel.
Source
Publisher: BioOne Country of Publication: United States NLM ID: 9512496 Publication Model: Print Cited Medium: Internet ISSN: 1948-7134 (Electronic) Linking ISSN: 10811710 NLM ISO Abbreviation: J Vector Ecol Subsets: MEDLINE
Subject
Language
English
Abstract
Mosquitoes of the genus Culex comprise important vectors of pathogenic arboviruses in our region, including West Nile and Rift Valley Fever viruses. To improve our understanding of the epidemiology and transmission dynamics of arboviruses, we need to study the behavior and ecology of their vectors. The feeding patterns of the vector mosquitoes can be very useful in determining how and where to focus control efforts. For example, determining the preferred blood hosts of the females can assist in the implementation of potentially efficacious strategies for focused control of mosquito females. Determining the plants from which both sexes derive their sugar meals can comprise the initial step towards the formulation of efficient lures for trapping mosquitoes. In the past, plant meal identification was based mainly on chemical detection of fructose and microscopical observations of cellulose particles in mosquito guts. More recent studies have utilized DNA barcoding capable of identifying plant food sources. In the current study, we identify multiple plant species from which large numbers of mosquitoes obtained their sugar meals in one experimental procedure. We employed next generation DNA sequencing to sequence the chloroplast specific plant genes atpB and rbcL.