Stable and heritable gene silencing in the malaria vector Anopheles stephensi.
نویسندگان
چکیده
Heritable RNA interference (RNAi), triggered from stably expressed transgenes with an inverted repeat (IR) configuration, is an important tool for reverse genetic studies. Here we report on the development of stable RNAi in Anopheles stephensi mosquitoes, the major vector of human malaria in Asia. Trans genic mosquitoes stably expressing a RNAi transgene, designed to produce intron-spliced double-stranded RNA (dsRNA) targeting the green fluorescent protein EGFP gene, were crossed to an EGFP-expressing target line. EGFP expression was dramatically reduced at both the protein and RNA levels. The levels of gene silencing depended upon the RNAi gene copy number and its site of integration. These results demonstrate that specific RNAi-mediated knockdown of gene function can be achieved with high efficiency in Anopheles . This will be invaluable to systematically unravel the function of Anopheles genes determining the vectorial capacity of the malaria parasite.
منابع مشابه
Determination of Glutathione S-Transferase e2 Region (GSTe2) in DDT Susceptible and Resistant Anopheles stephensi Populations: Significance and Application of Nucleotide and Amino Acid Comparison
Glutathione S-transferases (GSTs) are a major family of detoxification enzymes which possess a wide range of substrate specificities. Interest in insect GSTs has primarily focused on their role in insecticide resistance. In this study, following World Health Organization (WHO) routine susceptibility test, DNA was extracted from specimens of Anopheles stephensi collected from the Kazeroon distri...
متن کاملSusceptibility Status of Anopheles Stephensi Liston the Main Malaria Vector, to Deltamethrin and Bacillus Thuringiensis in the Endemic Malarious Area of Hormozgan Province, Southern Iran
Background & Aims: Anopheles stephensi is one of the most important malaria vectors in Hormozgan province, southern Iran. This species with high density has an effective role in malaria transmission, especially in plain and coastal areas. At present, the country malaria vector control program in areas with local transmission is using deltamethrin 5% and Bacillus thuringiensis as insecticide ...
متن کاملMonitoring Pyrethroid Insecticide Resistance in Major Malaria Vector Anopheles culicifacies: Comparison of Molecular Tools and Conventional Susceptibility Test
<Anopheles culicifacies is a main malaria vector in southeastern part of Iran, bordring Afghanistan and Pakistan. So far, resistance to DDT, dieldrin, malathion and partial tolerance to pyrethroids has been reported in An. stephensi, but nothing confirmed on resistance status of An. culicifacies in Iran. Methods: In current study, along with WHO routine susceptibility test with DDT (4%), di...
متن کاملLaboratory and semi-field evaluation of Bacillus thuringiensis (Bioflash®) against Anopheles stephensi (Diptera: Culicidae) in an endemic malarious area of Iran
Background: Anopheles stephensi is considered to be the main malaria vector in the Middle East area including Iran. We aimed to evaluate the efficiency of a granule 10% formulation of Bacillus thuringiensis against this species under laboratory and semi-field conditions in an endemic malarious area of Iran. Method: After collecting mosquitos ...
متن کاملLarvicidal activity of Ferulago carduchorum Boiss. & Hausskn. against the main malaria vector, Anopheles stephensi
Background and objectives: Malaria is a remarkable cause of death in the world. Several ways are used by researchers to control or to decrease the detrimental effects of the disease, in which natural insecticides with less malaria vectors resistance and lower environmental damages are considered in last decades.The objective of this study was to assess the larvicidal activity of the whole flowe...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Nucleic acids research
دوره 31 15 شماره
صفحات -
تاریخ انتشار 2003