Pierro Dennis J, Powers Erik L, Olson Ken E
Arthropod-Borne and Infectious Disease Laboratory, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO 80523, USA.
J Gen Virol. 2007 May;88(Pt 5):1545-1554. doi: 10.1099/vir.0.82577-0.
Mosquito midgut epithelial cells (MEC) play a major role in determining whether an arbovirus can successfully infect and be transmitted by mosquitoes. The Sindbis virus (SINV) strain TR339 efficiently infects Aedes aegypti MEC but the SINV strain TE/5'2J poorly infects MEC. SINV determinants for MEC infection have been localized to the E2 glycoprotein. The E2 amino acid sequences of TR339 and TE/5'2J differ at two sites, E2-55 and E2-70. We have altered the TE/5'2J virus genome by site-directed mutagenesis to contain two TR339 residues, E2-55 H-->Q (histidine to glutamine) and E2-70 K-->E (lysine to glutamic acid). We have characterized the growth patterns of derived viruses in cell culture and determined the midgut infection rate (MIR) in A. aegypti mosquitoes. Our results clearly show that the E2-55 H-->Q and the E2-70 K-->E mutations in the TE/5'2J virus increase MIR both independently and in combination. TE/5'2J virus containing both TR339 E2 residues had MIRs similar to the parental TR339 virus. In addition, SINV propagated in a mammalian cell line had a significantly lower A. aegypti midgut 50 % infectious dose than virus propagated in a mosquito cell line.
蚊子中肠上皮细胞(MEC)在决定虫媒病毒能否成功感染蚊子并由蚊子传播方面起着主要作用。辛德毕斯病毒(SINV)毒株TR339能有效感染埃及伊蚊MEC,但SINV毒株TE/5'2J对MEC的感染能力较差。MEC感染的SINV决定因素已定位到E2糖蛋白。TR339和TE/5'2J的E2氨基酸序列在两个位点E2-55和E2-70处不同。我们通过定点诱变改变了TE/5'2J病毒基因组,使其包含两个TR339残基,即E2-55 H→Q(组氨酸变为谷氨酰胺)和E2-70 K→E(赖氨酸变为谷氨酸)。我们已经在细胞培养中对衍生病毒的生长模式进行了表征,并测定了埃及伊蚊中肠感染率(MIR)。我们的结果清楚地表明,TE/5'2J病毒中的E2-55 H→Q和E2-70 K→E突变单独或联合作用均能提高MIR。含有两个TR339 E2残基的TE/5'2J病毒的MIR与亲本TR339病毒相似。此外,在哺乳动物细胞系中繁殖的SINV的埃及伊蚊中肠50%感染剂量显著低于在蚊子细胞系中繁殖的病毒。