Olson K E, Myles K M, Seabaugh R C, Higgs S, Carlson J O, Beaty B J
Arthropod-Borne and Infectious Diseases Laboratory, Department of Microbiology, Colorado State University, Ft. Collins, CO 80523, USA.
Insect Mol Biol. 2000 Feb;9(1):57-65. doi: 10.1046/j.1365-2583.2000.00162.x.
A double subgenomic Sindbis (dsSIN) virus, MRE/3'2 J/GFP, was constructed to efficiently express green fluorescent protein (GFP) in the midgut of Aedes aegypti following per os infection. The MRE/3'2 J/GFP RNA genome contained the nonstructural genes and cis-acting sequences of the dsSIN virus, TE/3'2 J/GFP, but had the structural genes of MRE16 SIN virus. MRE/3'2 J/GFP virus, unlike TE/3'2 J/GFP virus, efficiently infected mosquitoes orally. At 1-2 days postinfection, GFP was observed as multiple foci of expression on the lumenal side of the midgut. At 10-12 days postinfection, thirteen of fifteen mosquitoes infected with MRE/3'2 J/GFP virus had high levels of GFP expression in the mosquito midgut. The MRE3'2 J dsSIN expression system should be an important tool for efficient gene expression in Ae. aegypti midguts.
构建了一种双亚基因组辛德毕斯病毒(dsSIN),即MRE/3'2 J/GFP,以便在经口感染后在埃及伊蚊中肠高效表达绿色荧光蛋白(GFP)。MRE/3'2 J/GFP RNA基因组包含dsSIN病毒TE/3'2 J/GFP的非结构基因和顺式作用序列,但具有MRE16 SIN病毒的结构基因。与TE/3'2 J/GFP病毒不同,MRE/3'2 J/GFP病毒能有效地经口感染蚊子。感染后1至2天,在中肠腔侧观察到GFP呈多个表达灶。感染后10至12天,感染MRE/3'2 J/GFP病毒的15只蚊子中有13只在蚊子中肠中有高水平的GFP表达。MRE3'2 J dsSIN表达系统应是在埃及伊蚊中肠高效表达基因的重要工具。