Evidence map›Paper›PMID 40108335›Full record

ArticleScientific reports2025

A novel method for estimating pathogen presence, prevalence, load, and dynamics at multiple scales.

John F Grider, Bradley J Udell, Brian E Reichert, Jeffrey T Foster, William L Kendall, Tina L Cheng, Winifred F Frick

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. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

John F GriderColorado Cooperative Fish and Wildlife Research Unit, Colorado State University, 1484 Campus Delivery, Fort Collins, CO, 80523, USA. jack.grider@state.co.us.
Bradley J UdellFort Collins Science Center, U.S. Geological Survey, 2150 Centre Avenue, Fort Collins, CO, 80526, USA.
Brian E ReichertFort Collins Science Center, U.S. Geological Survey, 2150 Centre Avenue, Fort Collins, CO, 80526, USA.
Jeffrey T FosterPathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ, 86011, USA.
William L KendallColorado Cooperative Fish and Wildlife Research Unit, U. S. Geological Survey, Colorado State University, 1484 Campus Delivery, Fort Collins, CO, 80523, USA.
Tina L ChengBat Conservation International, 500 North Capital of Texas Highway, Building 1, Austin, TX, 78746, USA.
Winifred F FrickBat Conservation International, 500 North Capital of Texas Highway, Building 1, Austin, TX, 78746, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of quantitative real-time PCR (qPCR) to monitor pathogens is common; however, quantitative frameworks that consider the observation process, dynamics in pathogen presence, and pathogen load are lacking. This can be problematic in the early stages of disease progression, where low level detections may be treated as 'inconclusive' and excluded from analyses. Alternatively, a framework that accounts for imperfect detection would provide more robust inferences. To better estimate pathogen dynamics, we developed a hierarchical multi-scale dynamic occupancy hurdle model (MS-DOHM). The model used data gathered during sampling for Pseudogymnoascus destructans (Pd), the causative agent of white-nose syndrome, a fungal disease that has cause severe declines in several species of hibernating bats in North America. The model allowed us to estimate initial occupancy, colonization, persistence and prevalence of Pd at bat hibernacula. Additionally, utilizing the relationship between cycle threshold and pathogen load, we estimated pathogen detectability and modeled expected colony and bat pathogen loads. To assess the ability of MS-DOHM to estimate pathogen dynamics, we compared MS-DOHM's results to those of a dynamic occupancy model and naïve detection/non-detection. MS-DOHM's estimates of site-level pathogen presence were up to 11.9% higher than estimates from the dynamic occupancy model and 35.7% higher than naïve occupancy. Including prevalence and load in our modeling framework resulted in estimates of pathogen arrival that were two to three years earlier compared to the dynamic occupancy and naïve detection/non-detection, respectively. Compared to naïve values, MS-DOHM predicted greater pathogen loads on colonies; however, we found no difference between model estimates and naïve values of prevalence. While the model predicted no declines in site-level prevalence, there were instances where pathogen load decreased in colonies that had been Pd positive for longer periods of time. Our findings demonstrate that accounting for pathogen load and prevalence at multiple scales changes our understanding of Pd dynamics, potentially allowing earlier conservation intervention. Additionally, we found that accounting for pathogen load and prevalence within hibernacula and among individuals resulted in a better fitting model with greater predictive ability.

Indexed as

AscomycotaChiropteraMycosesAnimalsPrevalenceReal-Time Polymerase Chain ReactionCycle threshold (Ct)Little brown BatMulti-scale modelingPathogen loadQuantitative polymerase chain reaction (qPCR)White-nose syndrome

Identifiers

PMID40108335
PMCPMC11923299

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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.