Evidence map›Paper›PMID 40755398›Full record

ArticleMolecular ecology resources2025

An All-in-One Metabarcoding Approach to Mosquito and Arbovirus Xenosurveillance.

Brian J Johnson, Melissa C Graham, Elina Panahi, Carla Julia S P Vieira, Nisa Suraj Nath, Paul Mason, Jamie Gleadhill, Darran Thomas, Michael B Onn, Martin A Shivas and 3 more

Abstract read
In one paragraph

Article in Molecular ecology resources, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

13 authors.

Brian J JohnsonMosquito Control Laboratory, QIMR-Berghofer Medical Research Institute, Brisbane, Queensland, Australia.ORCID https://orcid.org/0000-0002-0545-4912
Melissa C GrahamMosquito Control Laboratory, QIMR-Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Elina PanahiMosquito Control Laboratory, QIMR-Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Carla Julia S P VieiraMosquito Control Laboratory, QIMR-Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Nisa Suraj NathMosquito Control Laboratory, QIMR-Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Paul MasonVector and Biosecurity Services Unit, Gold Coast, Queensland, Australia.
Jamie GleadhillVector and Biosecurity Services Unit, Gold Coast, Queensland, Australia.
Darran ThomasVector and Biosecurity Services Unit, Gold Coast, Queensland, Australia.
Michael B OnnEntomology Laboratory, Public Space Operations, Brisbane City Council, Brisbane, Queensland, Australia.
Martin A ShivasEntomology Laboratory, Public Space Operations, Brisbane City Council, Brisbane, Queensland, Australia.
Damien ShearmanMetro North Public Health Unit, Queensland Health, Brisbane, Queensland, Australia.
Jonathan M DarbroMetro North Public Health Unit, Queensland Health, Brisbane, Queensland, Australia.
Gregor J DevineMosquito Control Laboratory, QIMR-Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

Funding

Mosquito and Arbovirus Research Committee Inc.
6 · The paper itself

Abstract

Next-generation sequencing (NGS) has the potential to transform mosquito-borne disease surveillance but remains under-utilised. This study introduces a comprehensive multi-loci metabarcoding-based MX (molecular xenomonitoring) approach to mosquito and arbovirus surveillance, enabling parallel identification of mosquito vectors, circulating arboviruses, and vertebrate hosts from bulk mosquito collections. The feasibility of this approach was demonstrated through its application to a large set (n = 110) of bulk field collections. This set was complemented by a number (n = 28) of single-species mosquito pools that had previously been screened for viruses using quantitative reverse transcription PCR (RT-qPCR) and metatranscriptomics. Universal alphavirus and flavivirus primer sets were used to screen for arboviruses in the resulting metabarcoding library. Viral amplicons were then indexed and combined with mosquito-specific (ITS2), universal invertebrate (COI), and vertebrate (Cyt b) barcode amplicons prior to sequencing. This approach confirmed the presence of all previously identified mosquito species, as well as those commonly misidentified morphologically, and enabled a degree of quantification regarding their relative physical abundance in each collection. Additionally, the developed approach identified a diverse vertebrate host community (18 species), demonstrating its potential for defining host preferences and, in tandem with the viral screens and associated vector data, understanding disease transmission pathways. Importantly, metabarcoding detected a diversity of regionally prevalent arboviruses and insect-specific viruses, with all three viral diagnostics demonstrating a similar sensitivity and specificity in detecting Ross River virus and Barmah Forest virus, Australia's most common arboviruses. In summary, multi-loci metabarcoding is an affordable and efficient MX tool that enables complete mosquito-borne disease surveillance.

Indexed as

ArbovirusesBiosurveillanceCulicidaeDNA Barcoding, TaxonomicMetagenomicsMosquito VectorsAnimalsArbovirus InfectionsHigh-Throughput Nucleotide SequencingVertebratesarbovirusmetabarcodingmosquitomosquito‐borne diseasexenosurveillancezoonotic

Identifiers

PMID40755398
PMCPMC12550475

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.