4.6 Article

A novel strategy for screening mutations in the voltage-gated sodium channel gene of Aedes albopictus based on multiplex PCR-mass spectrometry minisequencing technology

Journal

INFECTIOUS DISEASES OF POVERTY
Volume 12, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s40249-023-01122-y

Keywords

Aedes albopictus; VGSC gene; Mutation; Single nucleotide polymorphisms; Multiplex polymerase chain reaction-mass spectrometry mini-sequencing

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This study developed a novel strategy for detecting mutations in the VGSC gene in Ae. albopictus using MPCR-MS minisequencing technology. The results showed that this method can simultaneously detect multiple mutation sites of the VGSC gene in 96 samples of Ae. albopictus, with high sensitivity and high throughput. Compared with conventional sequencing, this method is more economical and efficient, and of great value for insecticide resistance surveillance in high-risk areas of vector-borne diseases.
Background The current prevention and control strategy for Aedes albopictus heavily relies on comprehensive management, such as environmental management and chemical control. However, the wide application of pyrethroids has facilitated the development of insecticide resistance, primarily via mutations in the voltage-gated sodium channel (VGSC) gene. This study aims to develop a novel strategy for detecting mutations in the VGSC gene in Ae. albopictus using multiplex PCR-mass spectrometry (MPCR-MS) minisequencing technology. Methods We established a new strategy for detecting mutations in the VGSC gene in Ae. albopictus using MPCR-MS minisequencing technology. MPCR amplification and mass probe extension (MPE) were first used, followed by single nucleotide polymorphism (SNP) typing mass spectrometry, which allows the simultaneous detection of multiple mutation sites of the VGSC gene in 96 samples of Ae. albopictus. A total of 70 wild-collected Ae. albopictus were used to evaluate the performance of the method by comparing it with other methods. Results Three target sites (1016, 1532, 1534) in the VGSC gene can be detected simultaneously by double PCR amplification combined with matrix-assisted laser desorption ionization-time-of-flight mass spectrometry, achieving a detection limit of 20 fg/mu l. We applied this method to 70 wild-collected Ae. albopictus, and the obtained genotypes were consistent with the routine sequencing results, suggesting the accuracy of our method. Conclusions MPCR-MS minisequencing technology provides a sensitive and high-throughput approach to Ae. albopictus VGSC gene mutation screening. Compared with conventional sequencing, this method is economical and timesaving. It is of great value for insecticide resistance surveillance in areas with a high risk of vector-borne disease.

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