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dc.contributor.authorAbadi, M. Mashlawi
dc.contributor.authorAshwaq, M. Al‑Nazawi
dc.contributor.authorElsiddig, M. Noureldin
dc.contributor.authorHussain, Alqahtani
dc.contributor.authorJazem, A. Mahyoub
dc.contributor.authorJassada, Saingamsook
dc.contributor.authorMustapha, Debboun
dc.contributor.authorMartha, Kaddumukasa
dc.contributor.authorHesham, M. Al‑Mekhlafi
dc.contributor.authorCatherine, Walton
dc.date.accessioned2024-02-07T09:47:50Z
dc.date.available2024-02-07T09:47:50Z
dc.date.issued2022
dc.identifier.citationMashlawi, A. M., Al-Nazawi, A. M., Noureldin, E. M., Alqahtani, H., Mahyoub, J. A., Saingamsook, J., ... & Walton, C. (2022). Molecular analysis of knockdown resistance (kdr) mutations in the voltage-gated sodium channel gene of Aedes aegypti populations from Saudi Arabia. Parasites & Vectors, 15(1), 1-13.en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12504/1599
dc.description.abstractBackground: The Aedes aegypti mosquito is the primary vector for dengue, chikungunya, yellow fever and Zika viruses worldwide. The first record of Ae. aegypti in southwestern Saudi Arabia was in 1956. However, the first outbreak and cases of dengue fever were reported in 1994, and cases have increased in recent years. Vector control for Ae. aegypti mainly uses pyrethroid insecticides in outdoor and indoor space spraying. The constant use of pyrethroids has exerted intense selection pressure for developing target-site mutations in the voltage-gated sodium channel (vgsc) gene in Ae. Aegypti against pyrethroids—mutations that have led to knockdown resistance (kdr). Methods: Aedes aegypti field populations from five regions (Jazan, Sahil, Makkah, Jeddah and Madinah) of southwestern Saudi Arabia were genotyped for known kdr mutations in domains IIS6 and IIIS6 of the vgsc gene using polymerase chain reaction (PCR) amplification and sequencing. We estimated the frequency of kdr mutations and genotypes from Saudi Arabia as well as from other countries, Thailand, Myanmar (Southeast Asia) and Uganda (East Africa). We constructed haplotype networks to infer the evolutionary relationships of these gene regions. Results: The three known kdr mutations, S989P, V1016G (IIS6) and F1534C (IIIS6), were detected in all five regions of Saudi Arabia. Interestingly, the triple homozygous wild genotype was reported for the first time in two individuals from the highlands of the Jazan region and one from the Al-Quoz, Sahil region. Overall, nine genotypes comprising four haplotypes were observed in southwestern Saudi Arabia. The median-joining haplotype networks of eight populations from Saudi Arabia, Southeast Asia and East Africa for both the IIS6 and IIIS6 domains revealed that haplotype diversity was highest in Uganda and in the Jazan and Sahil regions of Saudi Arabia, whereas haplotype diversity was low in the Jeddah, Makkah and Madinah regions. Median-joining haplotype networks of both domains indicated selection acting on the kdr-mutation containing haplotypes in Saudi Arabia. Conclusions: The presence of wild type haplotypes without any of the three kdr mutations, i.e. that are fully susceptible, in Saudi Arabia indicates that further consideration should be given to insecticide resistance management strategies that could restore pyrethroid sensitivity to the populations of Ae. aegypti in Saudi Arabia as part of an integrative vector control strategy.en_US
dc.language.isoenen_US
dc.publisherBMC Parasites & Vectorsen_US
dc.subjectAedes aegyptien_US
dc.subjectInsecticide resistanceen_US
dc.subjectKnockdown resistanceen_US
dc.subjectMutationsen_US
dc.subjectMedian-joining haplotype networken_US
dc.subjectHaplotypeen_US
dc.subjectSaudi Arabiaen_US
dc.titleMolecular analysis of knockdown resistance (kdr) mutations in the voltage‑gated sodium channel gene of Aedes aegypti populations from Saudi Arabiaen_US
dc.typeArticleen_US


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