Evidence map›Paper›PMID 40680083›Full record

ArticlePLoS neglected tropical diseases2025

Enhanced rabies surveillance in roadkill specimens by real-time RT-PCR.

Crystal M Gigante, Claire Hartloge, Rene Edgar Condori, Jordona D Kirby, Lauren Hovis, Kathleen M Nelson, Ryan Wallace, Yu Li, Richard B Chipman

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 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. 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.

Crystal M GigantePoxvirus and Rabies Branch, Division of High-Consequence Pathogens and Pathology, United States of America Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.ORCID 0000-0002-2169-7156
Claire HartlogePoxvirus and Rabies Branch, Division of High-Consequence Pathogens and Pathology, United States of America Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Rene Edgar CondoriPoxvirus and Rabies Branch, Division of High-Consequence Pathogens and Pathology, United States of America Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Jordona D KirbyUSDA, APHIS, Wildlife Services, National Rabies Management Program, Concord, New Hampshire, United States of America.
Lauren HovisPoxvirus and Rabies Branch, Division of High-Consequence Pathogens and Pathology, United States of America Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Kathleen M NelsonUSDA, APHIS, Wildlife Services, National Rabies Management Program, Concord, New Hampshire, United States of America.
Ryan WallacePoxvirus and Rabies Branch, Division of High-Consequence Pathogens and Pathology, United States of America Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Yu LiPoxvirus and Rabies Branch, Division of High-Consequence Pathogens and Pathology, United States of America Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Richard B ChipmanUSDA, APHIS, Wildlife Services, National Rabies Management Program, Concord, New Hampshire, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Roadkill specimens are an important source of samples for enhanced rabies surveillance (ERS) in areas where other methods of sample collection may not be practical. However, the physical condition of roadkill specimens is unpredictable and, in many circumstances, unsatisfactory for rabies diagnostic testing by antigen detection methods. The high sensitivity of real-time reverse transcriptase PCR (RT-PCR) holds promise for rabies diagnostic testing of poor-quality samples. We conducted an evaluation of real-time RT-PCR to detect rabies virus RNA in roadkill samples. A total of 299 specimens were collected from raccoons (n = 232), skunks (n = 46), foxes (n = 17), coyotes (n = 2), a bobcat (n = 1), and a domestic cat (n = 1) across ten states during 2018 - 2021 in the United States. Eight samples (2.7%) were positive using the LN34 pan-lyssavirus real-time RT-PCR assay. These eight rabid animals in areas of high interest for wildlife rabies management would likely not have been identified otherwise. These findings support the use of real-time RT-PCR for samples that would typically be unsuitable for testing by widely used antigenic-based detection methods such as the direct fluorescent antibody test (DFA or FAT) and direct rapid immunohistochemistry test (DRIT).

Indexed as

RabiesRabies virusReal-Time Polymerase Chain ReactionAnimalsAnimals, WildCatsCoyotesEpidemiological MonitoringFoxesMephitidaeRaccoonsReverse Transcriptase Polymerase Chain ReactionRNA, ViralSensitivity and SpecificityUnited StatesRNA, Viral

Identifiers

PMID40680083
PMCPMC12324673

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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.