Evidence map›Paper›PMID 26190638›Full record

ArticleJournal of virological methods2015

Development of multiplexed bead arrays for the simultaneous detection of nucleic acid from multiple viruses in bat samples.

Victoria Boyd, Ina Smith, Gary Crameri, Amy L Burroughs, Peter A Durr, John White, Christopher Cowled, Glenn A Marsh, Lin-Fa Wang

Abstract readEvaluation Study
In one paragraph

Article in Journal of virological methods, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Integrating metagenomics and metatranscriptomics intoThe Journal of general virology · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. The current landscape of nucleic acid tests for filovirus detection.Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2018
    Review
  9. Review
  10. 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

9 authors.

Victoria BoydCSIRO Biosecurity Flagship & Australian Animal Health Laboratory, Geelong, Victoria, Australia. Electronic address: Vicky.Boyd@csiro.au.
Ina SmithCSIRO Biosecurity Flagship & Australian Animal Health Laboratory, Geelong, Victoria, Australia. Electronic address: Ina.Smith@csiro.au.
Gary CrameriCSIRO Biosecurity Flagship & Australian Animal Health Laboratory, Geelong, Victoria, Australia. Electronic address: Gary.Crameri@csiro.au.
Amy L BurroughsCSIRO Biosecurity Flagship & Australian Animal Health Laboratory, Geelong, Victoria, Australia. Electronic address: amy_in_paris@hotmail.com.
Peter A DurrCSIRO Biosecurity Flagship & Australian Animal Health Laboratory, Geelong, Victoria, Australia. Electronic address: Peter.Durr@csiro.au.
John WhiteCSIRO Biosecurity Flagship & Australian Animal Health Laboratory, Geelong, Victoria, Australia. Electronic address: John.White@csiro.au.
Christopher CowledCSIRO Biosecurity Flagship & Australian Animal Health Laboratory, Geelong, Victoria, Australia. Electronic address: Chris.Cowled@csiro.au.
Glenn A MarshCSIRO Biosecurity Flagship & Australian Animal Health Laboratory, Geelong, Victoria, Australia. Electronic address: Glenn.Marsh@csiro.au.
Lin-Fa WangCSIRO Biosecurity Flagship & Australian Animal Health Laboratory, Geelong, Victoria, Australia; Program in Emerging Infectious Diseases, Duke-NUS Graduate Medical School Singapore, Singapore. Electronic address: Linfa.Wang@csiro.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Virus surveillance of wildlife populations is important for identifying, monitoring, and predicting the emergence of pathogens that pose a potential threat to animal and human health. Bats are identified as important wildlife hosts of many viruses capable of causing fatal human disease, including members of the henipaviruses, coronaviruses, rhabdoviruses and filoviruses. As global warming and habitat change are thought to impact upon pathogen transmission dynamics and increase the risk of spillover, virus surveillance in bat populations remains a significant component of efforts to improve the prediction and control of potential future disease outbreaks caused by bat-borne viruses. In this study we have developed two fluid bead array assays containing customized panels that target multiple bat-borne viruses. These assays detect up to 11 viral RNA's simultaneously in urine samples collected from wild bat populations in Australia and Bangladesh. The assays developed show high specificity for the target viruses and the analytical sensitivity compares favorably to qRT-PCR. These assays enhance the ability to monitor multi-pathogen dynamics and identify patterns of virus shedding from bat populations, thus informing key approaches to outbreak response and control.

Indexed as

AnimalsAustraliaBangladeshChiropteraMicrospheresMolecular Diagnostic TechniquesSensitivity and SpecificityUrineVirus DiseasesVirusesBatsLuminexMagPlex-TAGMultiplexVirus surveillance

Identifiers

PMID26190638
PMCPMC7113788

What OpenQuestion holds

Textmetadata
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.