Evidence map›Paper›PMID 41286025›Full record

ArticleScientific reports2025

Microbiota and their functional profiling across the life cycle of the blow fly Hemipyrellia ligurriens.

Pluemkamon Phuwanatsarunya, Rutchanee Rodpai, Sophit Khanthawong, Ketsarin Thipphet, Rapee Thummeepak, Sudarat Onsurathum, Kabkaew L Sukontason, Wanchai Maleewong, Tongjit Thanchomnang, Nophawan Bunchu

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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
–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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Pluemkamon PhuwanatsarunyaDepartment of Microbiology and Parasitology, Faculty of Medical Science, Naresuan University, Muang district, Phitsanulok, 65000, Thailand.
Rutchanee RodpaiDepartment of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand.
Sophit KhanthawongDepartment of Microbiology and Parasitology, Faculty of Medical Science, Naresuan University, Muang district, Phitsanulok, 65000, Thailand.
Ketsarin ThipphetDepartment of Microbiology and Parasitology, Faculty of Medical Science, Naresuan University, Muang district, Phitsanulok, 65000, Thailand.
Rapee ThummeepakDepartment of Microbiology and Parasitology, Faculty of Medical Science, Naresuan University, Muang district, Phitsanulok, 65000, Thailand.
Sudarat OnsurathumDepartment of Microbiology and Parasitology, Faculty of Medical Science, Naresuan University, Muang district, Phitsanulok, 65000, Thailand.
Kabkaew L SukontasonDepartment of Parasitology, Faculty of Medicine, Chiang Mai University, Chiang Mai, 50200, Thailand.
Wanchai MaleewongDepartment of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand.
Tongjit Thanchomnang *Faculty of Medicine and Biomedical Science Research Unit, Mahasarakham University, Maha Sarakham, 44000, Thailand. tongjit.t@msu.ac.th.
Nophawan Bunchu *Department of Microbiology and Parasitology, Faculty of Medical Science, Naresuan University, Muang district, Phitsanulok, 65000, Thailand. nophawanb@nu.ac.th.

Funding

National Research Council of Thailand N41A640214
6 · The paper itself

Abstract

The blow fly, Hemipyrellia ligurriens (Diptera: Calliphoridae), is an ecologically and medically important species, particularly in forensic entomology, where its developmental stages aid in minimum postmortem interval estimation. Microbial diversity in insects is known to fluctuate dynamically across developmental stages. However, the mechanisms governing microbial community assembly, symbiont transmission, and functional roles in H. ligurriens remain largely unexplored. This study utilized 16 S ribosomal RNA gene amplicon sequencing to characterize the microbiota structure and functional metabolic potential across all life stages of H. ligurriens. Microbial composition varied significantly across developmental stages, with distinct assemblages characterizing each stage. Proteobacteria (synonym Pseudomonadota), Firmicutes (synonym Bacillota), and Bacteroidota consistently dominated across all life stages and rearing media, suggesting their essential role in host development. Notably, natural strain flies exhibited significantly greater microbial diversity than laboratory-derived counterparts. While microbial diversity was comparable between male and female flies from both strains, sex-specific microbiota appeared exclusively in the natural strain. Functional metabolic profiling suggests that microbiota co-evolve with their host, playing vital roles in immune regulation and pathogen defense. This study provides the first comprehensive microbiota profile of H. ligurriens, offering novel insights into its potential applications in forensic entomology, maggot debridement therapy, and insect health management.

Indexed as

CalliphoridaeDipteraLife Cycle StagesMicrobiotaAnimalsFemaleForensic EntomologyMalePhylogenyRNA, Ribosomal, 16SRNA, Ribosomal, 16S16S ribosomal RNA geneBlow flyHemipyrellia ligurriensInsect microbiotaLife stages

Identifiers

PMID41286025
PMCPMC12645017

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LicenceCC BY-NC-ND
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Registered trials

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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.