Evidence map›Paper›PMID 40139920›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2025

Jamestown Canyon Virus Seroprevalence in Endemic Regions and Implications for Diagnostic Testing.

Rebekah A Sutter, Amanda E Calvert, Kacie Grimm, Brad J Biggerstaff, Elisa Thrasher, Eric C Mossel, Stacey W Martin, Jennifer Lehman, Paula Saa, Rebecca Townsend and 12 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 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
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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

22 authors.

Rebekah A SutterEpidemic Intelligence Service, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.ORCID 0009-0006-6695-7421
Amanda E CalvertDivision of Vector-Borne Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado, USA.ORCID 0000-0002-8237-2654
Kacie GrimmAmerican Red Cross Scientific Affairs, Gaithersburg, Maryland, USA.
Brad J BiggerstaffDivision of Vector-Borne Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado, USA.ORCID 0000-0002-3105-3530
Elisa ThrasherDivision of Vector-Borne Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado, USA.
Eric C MosselDivision of Vector-Borne Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado, USA.ORCID 0000-0002-2315-4577
Stacey W MartinDivision of Vector-Borne Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado, USA.ORCID 0000-0003-1767-6042
Jennifer LehmanDivision of Vector-Borne Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado, USA.ORCID 0000-0001-7114-208X
Paula SaaAmerican Red Cross Scientific Affairs, Gaithersburg, Maryland, USA.ORCID 0000-0001-6077-4532
Rebecca TownsendAmerican Red Cross Scientific Affairs, Gaithersburg, Maryland, USA.
David KrysztofAmerican Red Cross Scientific Affairs, Gaithersburg, Maryland, USA.
Catherine M BrownBureau of Infectious Disease and Laboratory Sciences, Massachusetts Department of Public Health, Jamaica Plain, Massachusetts, USA.
Matthew OsborneBureau of Infectious Disease and Laboratory Sciences, Massachusetts Department of Public Health, Jamaica Plain, Massachusetts, USA.
Brandi HopkinsBureau of Infectious Disease and Laboratory Sciences, Massachusetts Department of Public Health, Jamaica Plain, Massachusetts, USA.
Rebecca OsbornDivision of Public Health, Wisconsin Department of Health Services, Madison, Wisconsin, USA.ORCID 0009-0004-1079-3558
Xia LeeDivision of Public Health, Wisconsin Department of Health Services, Madison, Wisconsin, USA.ORCID 0000-0001-9248-3940
Elizabeth K SchiffmanInfectious Disease Epidemiology, Prevention, and Control Division, Minnesota Department of Health, St. Paul, Minnesota, USA.ORCID 0000-0001-5153-7471
Aaron C BraultDivision of Vector-Borne Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado, USA.
Sridhar V BasavarajuDivision of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia.
Susan L StramerAmerican Red Cross Scientific Affairs, Gaithersburg, Maryland, USA.
J Erin StaplesDivision of Vector-Borne Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado, USA.
Carolyn V GouldDivision of Vector-Borne Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado, USA.ORCID 0000-0002-8216-0803

Funding

CDCIntramural CDC HHS CC999999Oak Ridge Institute for Science and EducationU.S. Department of Energy
6 · The paper itself

Abstract

backgroundJamestown Canyon virus, a mosquito-borne virus, can cause asymptomatic infection, febrile illness, or neuroinvasive disease in humans. Previous studies have found Jamestown Canyon virus-specific antibodies in a 4%-54% of people in various U.S. regions. To understand baseline seroprevalence in regions with the highest number of reported disease cases, we performed a serosurvey among blood donors.

methodsWe randomly selected blood donation specimens collected during December 2019-April 2020 from residents of counties reporting ≥2 disease cases in 2019 or 1 case in 2019 and ≥1 case during 2010-2018. Specimens were screened for Jamestown Canyon virus-specific neutralizing antibodies and, if positive, tested for immunoglobulin M (IgM) antibodies. We estimated county population seroprevalence by calibrating sample weights to population census data.

resultsFourteen counties in 3 states, Massachusetts, Minnesota, and Wisconsin, met the inclusion criteria. Within each state, average county seroprevalence ranged from 16.8% (95% confidence interval [CI], 9.3-27.0) to 18.8% (95% CI, 14.0-24.4) for Jamestown Canyon virus-neutralizing antibodies and from 7.6% (95% CI, 4.2-12.5) to 13.5% (95% CI, 9.6-18.3) for both neutralizing and IgM antibodies.

conclusionsEstimated Jamestown Canyon virus seroprevalence, including for IgM antibodies, is elevated in endemic areas, complicating the interpretation of serologic testing in diagnosing acute disease in symptomatic individuals. Diagnosing Jamestown Canyon virus disease requires a high degree of clinical suspicion, ruling out other possible causes of illness, and if possible, collecting acute and convalescent samples. New assays to detect acute infection could improve diagnosis and public health surveillance for Jamestown Canyon virus disease.

Indexed as

Antibodies, ViralEncephalitis, CaliforniaEncephalitis Virus, CaliforniaEndemic DiseasesAdolescentAdultAgedAntibodies, NeutralizingBlood DonorsFemaleHumansImmunoglobulin MMaleMiddle AgedSeroepidemiologic StudiesYoung AdultAntibodies, NeutralizingAntibodies, ViralImmunoglobulin Mblood donordiagnostic testingJamestown Canyon virusseroprevalenceserosurvey

Identifiers

PMID40139920
PMCPMC12955547

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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.