Towards genetic manipulation of wild mosquito populations to combat malaria: advances and challenges

被引:42
作者
Riehle, MA [1 ]
Srinivasan, P [1 ]
Moreira, CK [1 ]
Jacobs-Lorena, M [1 ]
机构
[1] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
关键词
Plasmodium; genetic engineering; paratransgenesis; genetic drive mechanisms; genetic sexing; fitness; mosquito;
D O I
10.1242/jeb.00609
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Malaria kills millions of people every year, yet there has been little progress in controlling this disease. For transmission to occur, the malaria parasite has to complete a complex developmental cycle in the mosquito. The mosquito is therefore a potential weak link in malaria transmission, and generating mosquito populations that are refractory to the parasite is a potential means of controlling the disease. There has been considerable progress over the last decade towards developing the tools for creating a refractory mosquito. Accomplishments include germline transformation of several important mosquito vectors, the completed genomes of the mosquito Anopheles gambiae and the malaria parasite Plasmodium falciparum, and the identification of promoters and effector genes that confer resistance in the mosquito. These tools have provided researchers with the ability to engineer a refractory mosquito vector, but there are fundamental gaps in our knowledge of how to transfer this technology safely and effectively into field populations. This review considers strategies for interfering with Plasmodium development in the mosquito, together with issues related to the transfer of laboratory-acquired knowledge to the field, such as minimization of transgene fitness load to the mosquito, driving genes through populations, avoiding the selection of resistant strains, and how to produce and release populations of males only.
引用
收藏
页码:3809 / 3816
页数:8
相关论文
共 54 条
[1]   Dominant lethality and insect population control [J].
Alphey, L ;
Andreasen, M .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2002, 121 (02) :173-178
[2]  
ANXOLABEHERE D, 1988, MOL BIOL EVOL, V5, P252
[3]   Tet repressor-based system for regulated gene expression in eukaryotic cells: Principles and advances [J].
Baron, U ;
Bujard, H .
APPLICATIONS OF CHIMERIC GENES AND HYBRID PROTEINS PT B: CELL BIOLOGY AND PHYSIOLOGY, 2000, 327 :401-421
[4]   Bacterial symbiosis in arthropods and the control of disease transmission [J].
Beard, CB ;
Durvasula, RV ;
Richards, FF .
EMERGING INFECTIOUS DISEASES, 1998, 4 (04) :581-591
[5]   Bacterial symbionts of the triatominae and their potential use in control of Chagas disease transmission [J].
Ben Beard, C ;
Cordon-Rosales, C ;
Durvasula, RV .
ANNUAL REVIEW OF ENTOMOLOGY, 2002, 47 :123-141
[6]   Evolutionary ideas about genetically manipulated mosquitoes and malaria control [J].
Boëte, C ;
Koella, JC .
TRENDS IN PARASITOLOGY, 2003, 19 (01) :32-38
[8]   Virus-expressed, recombinant single-chain antibody blocks sporozoite infection of salivary glands in Plasmodium gallinaceum-infected Aedes aegypti [J].
Capurro, MD ;
Coleman, J ;
Beerntsen, BT ;
Myles, KM ;
Olson, KE ;
Rocha, E ;
Krettli, AU ;
James, AA .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2000, 62 (04) :427-433
[9]   Transmission blocking malaria vaccines [J].
Carter, R .
VACCINE, 2001, 19 (17-19) :2309-2314
[10]   Stable germline transformation of the malaria mosquito Anopheles stephensi [J].
Catteruccia, F ;
Nolan, T ;
Loukeris, TG ;
Blass, C ;
Savakis, C ;
Kafatos, FC ;
Crisanti, A .
NATURE, 2000, 405 (6789) :959-962