Evidence map›Paper›PMID 36804043›Full record

ArticleParasites & vectors2023

Inhibition of alternative oxidase disrupts the development and oviposition of Biomphalaria glabrata snails.

Sha Xu, Yang-Wen-Qing Zhang, Mohamed R Habib, Shi-Zhu Li, Yi Yuan, Wei Hao Ke, Ni Jiang, Huifen Dong, Qin-Ping Zhao

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.8field-weighted citation impact, top 33% of its field
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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

9 authors at 4 institutions in 2 countries.

Sha Xu *Department of Parasitology, School of Basic Medical Sciences, Wuhan University, Wuhan, Hubei Province, China.
Yang-Wen-Qing Zhang *Department of Parasitology, School of Basic Medical Sciences, Wuhan University, Wuhan, Hubei Province, China.
Mohamed R HabibMedical Malacology Laboratory, Theodor Bilharz Research Institute, Giza, Egypt.
Shi-Zhu LiNational Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention, National Center for Tropical Diseases Research, WHO Collaborating Center for Tropical Diseases, Key Laboratory of Parasite and Vector Biology, Ministry of Health, Shanghai, China.
Yi YuanHubei Center for Disease Control and Prevention, Wuhan, Hubei Province, China.
Wei Hao KeDepartment of Parasitology, School of Basic Medical Sciences, Wuhan University, Wuhan, Hubei Province, China.
Ni JiangDepartment of Parasitology, School of Basic Medical Sciences, Wuhan University, Wuhan, Hubei Province, China.
Huifen DongDepartment of Parasitology, School of Basic Medical Sciences, Wuhan University, Wuhan, Hubei Province, China.
Qin-Ping ZhaoDepartment of Parasitology, School of Basic Medical Sciences, Wuhan University, Wuhan, Hubei Province, China. zhaoqinping@whu.edu.cn.
Wuhan University · CNHubei Provincial Center for Disease Control and Prevention · CNNational Institute for Parasitic Diseases · CNTheodor Bilharz Research Institute · EG

Funding

Key Laboratory of Parasite and Vector Biology, Ministry of Health WSBKFKT-201801National Natural Science Foundation of China 32170506Seed Fund Program for Sino-Foreign Joint Scientific Research Platform of Wuhan University WHUZZJJ202231
6 · The paper itself

Abstract

backgroundBiomphalaria glabrata is one of the main intermediate hosts of Schistosoma mansoni, the most widespread species of Schistosoma. Our previous studies proved that alternative oxidase (AOX), the terminal oxidase in the mitochondrial respiratory chain, widely exists in several species of intermediate host snails of Schistosoma. Meanwhile, inhibition of AOX activity in Oncomelania hupensis snails could dramatically enhance the molluscicidal effect of niclosamide. As a hermaphroditic aquatic mollusc, the high fecundity and population density of B. glabrata increase the difficulty of snail control, which is one of the critical strategies for schistosomiasis elimination. The present study aimed to investigate the possible role of AOX in the development and fecundity of B. glabrata snail, which could be manipulated more manageable than other species of intermediate host snails of Schistosoma.

methodsThe dynamic expression of the AOX gene was investigated in different developmental stages and tissues of B. glabrata, with morphological change and oviposition behaviour observed from juvenile to adult snails. Furtherly, dsRNA-mediated knockdown of BgAOX mRNA and the AOX protein activity inhibiting was performed to investigate the effect of AOX on the development and oviposition of snails.

resultsThe BgAOX gene expression profile is highly related to the development from late juveniles to adults, especially to the reproductive system of snails, with a positive correlation of 0.975 between egg production and BgAOX relative expression in ovotestis of snails. The inhibition of BgAOX at the transcriptional level and AOX activity could efficiently inhibit snail growth. However, the interference at the BgAOX protein activity level led to more severe tissue damage and more significant inhibition of oviposition than at the transcriptional level. This inhibition of growth and oviposition decreased gradually with the increase in the snail size.

conclusionsThe inhibition of AOX could efficiently disrupt the development and oviposition of B. glabrata snails, and the intervention targeting AOX at the juvenile stage is more effective for snails. This investigation explored the role of AOX in the growth and development of snails. It would benefit snail control in the future by providing a potential target while using molluscicides more efficiently.

Indexed as

BiomphalariaAlternative OxidaseAnimalsFemaleOvipositionOxidoreductasesSchistosoma mansoniAlternative OxidaseOxidoreductasesAlternative oxidaseBiomphalaria glabrataDevelopmentOvipositionReproductive systemRNA interference

Identifiers

PMID36804043
PMCPMC9938623
OpenAlexW4321214496

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.