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Relationship between deltamethrin resistance and gut symbiotic bacteria of Aedes albopictus by 16S rDNA sequencing.
Sun, Yingbo; Li, Tingting; Zhou, Guofa; Zhou, Yunfei; Wu, Yuhong; Xu, Jiabao; Chen, Jiarong; Zhong, Saifeng; Zhong, Daibin; Liu, Rui; Lu, Gang; Li, Yiji.
Afiliação
  • Sun Y; Key Laboratory of Tropical Translational Medicine of Ministry of Education, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
  • Li T; Tropical Diseases Research Center, Department of Pathogen Biology, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
  • Zhou G; Hainan Medical University-The University of Hong Kong Joint Laboratory of Tropical Infectious Diseases, Hainan Medical University, Haikou, 571199, China.
  • Zhou Y; Key Laboratory of Tropical Translational Medicine of Ministry of Education, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
  • Wu Y; Tropical Diseases Research Center, Department of Pathogen Biology, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
  • Xu J; Hainan Medical University-The University of Hong Kong Joint Laboratory of Tropical Infectious Diseases, Hainan Medical University, Haikou, 571199, China.
  • Chen J; Program in Public Health, College of Health Sciences, University of California at Irvine, Irvine, CA, 92617, USA.
  • Zhong S; Tropical Diseases Research Center, Department of Pathogen Biology, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
  • Zhong D; Tropical Diseases Research Center, Department of Pathogen Biology, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
  • Liu R; Department of Immunology and Microbiology, School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, Zhejiang, China.
  • Lu G; Tropical Diseases Research Center, Department of Pathogen Biology, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
  • Li Y; Key Laboratory of Tropical Translational Medicine of Ministry of Education, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
Parasit Vectors ; 17(1): 330, 2024 Aug 05.
Article em En | MEDLINE | ID: mdl-39103931
ABSTRACT

BACKGROUND:

Aedes albopictus is an important vector for pathogens such as dengue, Zika, and chikungunya viruses. While insecticides is the mainstay for mosquito control, their widespread and excessive use has led to the increased resistance in Ae. albopictus globally. Gut symbiotic bacteria are believed to play a potential role in insect physiology, potentially linking to mosquitoes' metabolic resistance against insecticides.

METHODS:

We investigated the role of symbiotic bacteria in the development of resistance in Ae. albopictus by comparing gut symbiotic bacteria between deltamethrin-sensitive and deltamethrin-resistant populations. Adults were reared from field-collected larvae. Sensitive and resistant mosquitoes were screened using 0.03% and 0.09% deltamethrin, respectively, on the basis of the World Health Organization (WHO) tube bioassay. Sensitive and resistant field-collected larvae were screened using 5 × LC50 (lethal concentration at 50% mortality) and 20 × LC50 concentration of deltamethrin, respectively. Laboratory strain deltamethrin-sensitive adults and larvae were used as controls. The DNA of gut samples from these mosquitoes were extracted using the magnetic bead method. Bacterial 16S rDNA was sequenced using BGISEQ method. We isolated and cultured gut microorganisms from adult and larvae mosquitoes using four different media Luria Bertani (LB), brain heart infusion (BHI), nutrient agar (NA), and salmonella shigella (SS).

RESULTS:

Sequencing revealed significantly higher gut microbial diversity in field-resistant larvae compared with field-sensitive and laboratory-sensitive larvae (P < 0.01). Conversely, gut microorganism diversity in field-resistant and field-sensitive adults was significantly lower compared with laboratory-sensitive adults (P < 0.01). At the species level, 25 and 12 bacterial species were isolated from the gut of field resistant larvae and adults, respectively. The abundance of Flavobacterium spp., Gemmobacter spp., and Dysgonomonas spp. was significantly higher in the gut of field-resistant larvae compared with sensitive larvae (all P < 0.05). Furthermore, the abundance of Flavobacterium spp., Pantoea spp., and Aeromonas spp. was significantly higher in the gut of field-resistant adults compared with sensitive adults (all P < 0.05). The dominant and differentially occurring microorganisms were also different between resistant larval and adult mosquitoes. These findings suggest that the gut commensal bacteria of Ae. albopictus adults and larvae may play distinct roles in their deltamethrin resistance.

CONCLUSIONS:

This study provides an empirical basis for further exploration of the mechanisms underlying the role of gut microbial in insecticide resistance, potentially opening a new prospect for mosquito control strategies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Piretrinas / Simbiose / Bactérias / Resistência a Inseticidas / RNA Ribossômico 16S / Aedes / Inseticidas / Larva / Nitrilas Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Piretrinas / Simbiose / Bactérias / Resistência a Inseticidas / RNA Ribossômico 16S / Aedes / Inseticidas / Larva / Nitrilas Idioma: En Ano de publicação: 2024 Tipo de documento: Article