Development of an Enzyme-Linked Immunosorbent Assay (ELISA) as a tool to detect NS1 of dengue virus serotype 2 in female Aedes aegypti eggs for the surveillance of dengue fever transmission

被引:3
作者
Argotte-Ramos, Rocio [1 ]
Cime-Castillo, Jorge [1 ]
Vargas, Valeria [1 ]
Lanz-Mendoza, Humberto [1 ]
Rodriguez, Mario H. [1 ]
Rodriguez, Maria Carmen [1 ]
机构
[1] Inst Nacl Salud Publ, Ctr Invest Enfermedades Infecciosas, Av Univ 655, Cuernavaca 62100, Morelos, Mexico
关键词
Aedes aegypti; Dengue virus; Surveillance; ELISA; NS1; Egg homogenates; NATURAL VERTICAL TRANSMISSION; TRANS-OVARIAL TRANSMISSION; MOSQUITOS; ALBOPICTUS; ANTIGEN; STRAINS; PROTEIN; GROWTH;
D O I
10.1016/j.heliyon.2024.e29329
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dengue is a significant disease transmitted by Aedes mosquitoes in the tropics and subtropics worldwide. The disease is caused by four virus (DENV) serotypes and is transmitted to humans by female Aedes aegypti mosquito bites infected with the virus and vertically to their progeny. Current strategies to control dengue transmission focus on the vector. In this study, we describe an indirect Enzyme-Linked Immunosorbent Assay (ELISA), using a monoclonal antibody against the non-structural dengue virus protein 1 (NS1), to detect DENV2 in Ae. aegypti eggs. The assay detects NS1 in eggs homogenates with 87.5% sensitivity and 75.0% specificity and it is proposed as a tool for the routine entomovirological surveillance of DENV 2 in field mosquito populations.
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