Evidence map›Paper›PMID 40255978›Full record

ArticleACS nanoscience Au2025

Development of an Immunoassay for Highly Pathogenic Avian Influenza (H5N1) across Diverse Sample Matrices.

Josselyn Mata Calidonio, Arianna I Maddox, Dhruvi S Patel, Jonathan B Dain, Melba Torres Sosa, Nichola J Hill, Kimberly Hamad-Schifferli

Abstract read
In one paragraph

Article in ACS nanoscience Au, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. The emergence of highly pathogenic avian influenza H5N1 in dairy cattle: implications for public health, animal health, and pandemic preparedness.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical 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

7 authors.

Josselyn Mata CalidonioDepartment of Engineering, University of Massachusetts Boston, 100 Morrissey Blvd., Boston, Massachusetts 02125, United States.
Arianna I MaddoxDepartment of Biology, University of Massachusetts Boston, 100 Morrissey Blvd., Boston, Massachusetts 02125, United States.
Dhruvi S PatelDepartment of Biology, University of Massachusetts Boston, 100 Morrissey Blvd., Boston, Massachusetts 02125, United States.
Jonathan B DainDepartment of Biology, University of Massachusetts Boston, 100 Morrissey Blvd., Boston, Massachusetts 02125, United States.
Melba Torres SosaDepartment of Biology, University of Massachusetts Boston, 100 Morrissey Blvd., Boston, Massachusetts 02125, United States.
Nichola J HillDepartment of Biology, University of Massachusetts Boston, 100 Morrissey Blvd., Boston, Massachusetts 02125, United States.
Kimberly Hamad-SchifferliDepartment of Engineering, University of Massachusetts Boston, 100 Morrissey Blvd., Boston, Massachusetts 02125, United States.ORCID https://orcid.org/0000-0002-4839-3179

Funding

UMass Boston-DF/HCC U54 Partnership (2 of 2)U54CA156734 · NCI · UNIVERSITY OF MASSACHUSETTS BOSTON · PI Jan Mutchler · 2010 to 2026
$24.9M
NCI NIH HHS U54 CA156734
6 · The paper itself

Abstract

Avian influenza of the highly pathogenic subtype H5N1 has emerged as a global health concern, becoming endemic in wild birds and increasingly transmitting to poultry, livestock, and humans. This study aimed to develop a robust immunoassay for the rapid detection of the H5N1 highly pathogenic avian influenza virus across various sample matrices, including sera, milk, eggs, and bird samples. The assay targets the hemagglutinin (HA) protein, chosen for its abundance and accessibility on the virus surface. Utilizing gold nanospheres conjugated with α-HA IgG antibodies, the assay generated distinct colorimetric signals for both negative and positive samples. The test initially demonstrated an effective colorimetric response with a limit of detection (LOD) of 0.16 nM in human serum and was further optimized for running in whole milk, exhibiting an LOD of 1.72 nM. The assay exhibited versatility across different serum types and dairy products, although high-viscosity samples like heavy cream presented challenges. Furthermore, the immunoassay successfully detected HA of H5N1 in complex sample matrices such as oral, cloacal, and fecal samples from birds. This rapid and sensitive immunoassay represents a significant advance in HPAI surveillance tools, improving prospects for real-time detection to control outbreaks.

Identifiers

PMID40255978
PMCPMC12006854

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.