Quantitative Trait Loci That Control Vector Competence for Dengue-2 Virus in the Mosquito Aedes aegypti

• Published in: Genetics (Austin) Vol. 156; no. 2; pp. 687 - 698
• Main Authors: Bosio, Christopher F, Fulton, Ruth E, Salasek, Mike L, Beaty, Barry J, Black, William C., , IV
• Format: Journal Article
• Language: English
• Published: United States Genetics Soc America 01.10.2000; Genetics Society of America
• Subjects: Aedes - genetics; Aedes - virology; Aedes aegypti; Animals; chromosome I; chromosome II; chromosome III; Chromosome Mapping; Crosses, Genetic; Culicidae; Dengue Virus - physiology; Dengue virus 2; Digestive System - virology; Disease; Female; Genetic Markers; Genetic Vectors; Genetics; Male; Microsatellite Repeats; Mosquitoes; Polymorphism, Single-Stranded Conformational; Quantitative Trait, Heritable; Random Amplified Polymorphic DNA Technique; Vaccines; Africa
• ISSN: 0016-6731; 1943-2631; 1943-2631
• DOI: 10.1093/genetics/156.2.687

Quantitative trait loci (QTL) affecting the ability of the mosquito Aedes aegypti to become infected with dengue-2 virus were mapped in an F(1) intercross. Dengue-susceptible A. aegypti aegypti were crossed with dengue refractory A. aegypti formosus. F(2) offspring were analyzed for midgut infection and escape barriers. In P(1) and F(1) parents and in 207 F(2) individuals, regions of 14 cDNA loci were analyzed with single-strand conformation polymorphism analysis to identify and orient linkage groups with respect to chromosomes I-III. Genotypes were also scored at 57 RAPD-SSCP loci, 5 (TAG)(n) microsatellite loci, and 6 sequence-tagged RAPD loci. Dengue infection phenotypes were scored in 86 F(2) females. Two QTL for a midgut infection barrier were detected with standard and composite interval mapping on chromosomes II and III that accounted for approximately 30% of the phenotypic variance (sigma(2)(p)) in dengue infection and these accounted for 44 and 56%, respectively, of the overall genetic variance (sigma(2)(g)). QTL of minor effect were detected on chromosomes I and III, but these were not detected with composite interval mapping. Evidence for a QTL for midgut escape barrier was detected with standard interval mapping but not with composite interval mapping on chromosome III.