Evidence map›Paper›PMID 39103931›Full record

ArticleParasites & vectors2024

Relationship between deltamethrin resistance and gut symbiotic bacteria of Aedes albopictus by 16S rDNA sequencing.

Yingbo Sun, Tingting Li, Guofa Zhou, Yunfei Zhou, Yuhong Wu, Jiabao Xu, Jiarong Chen, Saifeng Zhong, Daibin Zhong, Rui Liu and 2 more

Abstract read
In one paragraph

Article in Parasites & vectors, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Microbial gatekeepers: midgut bacteria inFrontiers in microbiology · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Yingbo Sun *Key Laboratory of Tropical Translational Medicine of Ministry of Education, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
Tingting Li *Key Laboratory of Tropical Translational Medicine of Ministry of Education, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
Guofa ZhouProgram in Public Health, College of Health Sciences, University of California at Irvine, Irvine, CA, 92617, USA.
Yunfei ZhouTropical Diseases Research Center, Department of Pathogen Biology, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
Yuhong WuTropical Diseases Research Center, Department of Pathogen Biology, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
Jiabao XuDepartment of Immunology and Microbiology, School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, Zhejiang, China.
Jiarong ChenTropical Diseases Research Center, Department of Pathogen Biology, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
Saifeng ZhongKey Laboratory of Tropical Translational Medicine of Ministry of Education, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China.
Daibin ZhongProgram in Public Health, College of Health Sciences, University of California at Irvine, Irvine, CA, 92617, USA.
Rui LiuDepartment of Infectious and Tropical Diseases, The Second Affiliated Hospital of Hainan Medical University, Haikou, 570311, People's Republic of China.
Gang LuKey Laboratory of Tropical Translational Medicine of Ministry of Education, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China. luganghn@163.com.
Yiji LiKey Laboratory of Tropical Translational Medicine of Ministry of Education, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou, 571199, China. bdlyj06@163.com.

Funding

Hainan Provincial Natural Science Foundation 820RC653Hainan Provincial Ordinary Higher Education Institutions Graduate Students' Innovative Scientific Research Projects Qhys2022-293National Natural Science Foundation of China 82060375National Natural Science Foundation of China 82060379Natural Science Foundation of Hainan Province 824RC516Talent Introduction Fund of Hainan Medical University XRC220012
6 · The paper itself

Abstract

backgroundAedes 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.

methodsWe 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 × LC

resultsSequencing 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.

conclusionsThis 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.

Indexed as

AedesBacteriaInsecticide ResistanceInsecticidesLarvaNitrilesPyrethrinsRNA, Ribosomal, 16SSymbiosisAnimalsDNA, BacterialDNA, RibosomalFemaleGastrointestinal MicrobiomeGastrointestinal TractMosquito VectorsdecamethrinDNA, BacterialDNA, RibosomalInsecticidesNitrilesPyrethrinsRNA, Ribosomal, 16S16S rDNAAedes albopictusDeltamethrinGut commensal bacteriaInsecticide resistance

Identifiers

PMID39103931
PMCPMC11299273

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.