Evidence map›Paper›PMID 38885957›Full record

ArticleAmerican journal of epidemiology2025

SARS-CoV-2 incidence, seroprevalence, and antibody dynamics in a rural, population-based cohort: March 2020-July 2022.

Joshua G Petrie, David Pattinson, Jennifer P King, Gabriele Neumann, Lizheng Guan, Peter Jester, Melissa A Rolfes, Jennifer K Meece, Burney A Kieke, Edward A Belongia and 2 more

Abstract read
In one paragraph

Article in American journal of epidemiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Joshua G PetrieCenter for Clinical Epidemiology and Population Health, Marshfield Clinic Research Institute, Marshfield, WI 54449, USA.ORCID 0000-0002-5696-965X
David PattinsonDepartment of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, WI 53706, USA.ORCID 0000-0003-0001-8203
Jennifer P KingCenter for Clinical Epidemiology and Population Health, Marshfield Clinic Research Institute, Marshfield, WI 54449, USA.ORCID 0000-0003-4627-1378
Gabriele NeumannDepartment of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, WI 53706, USA.
Lizheng GuanDepartment of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, WI 53706, USA.
Peter JesterDepartment of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, WI 53706, USA.
Melissa A RolfesInfluenza Division, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.ORCID 0000-0002-0483-9941
Jennifer K MeeceCenter for Clinical Epidemiology and Population Health, Marshfield Clinic Research Institute, Marshfield, WI 54449, USA.
Burney A KiekeCenter for Clinical Epidemiology and Population Health, Marshfield Clinic Research Institute, Marshfield, WI 54449, USA.ORCID 0000-0002-7430-0570
Edward A BelongiaCenter for Clinical Epidemiology and Population Health, Marshfield Clinic Research Institute, Marshfield, WI 54449, USA.ORCID 0000-0001-7478-0415
Yoshihiro KawaokaDepartment of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, WI 53706, USA.ORCID 0000-0001-5061-8296
Huong Q NguyenCenter for Clinical Epidemiology and Population Health, Marshfield Clinic Research Institute, Marshfield, WI 54449, USA.ORCID 0000-0003-2725-6439

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

Studies of SARS-CoV-2 incidence are important for response to continued transmission and future pandemics. We followed a rural community cohort with broad age representation with active surveillance for SARS-CoV-2 identification from November 2020 through July 2022. Participants provided serum specimens at regular intervals and after SARS-CoV-2 infection or vaccination. We estimated the incidence of SARS-CoV-2 infection identified by study reverse transcriptase-polymerase chain reaction, electronic health record documentation or self-report of a positive test, or serology. We also estimated the seroprevalence of SARS-CoV-2 spike and nucleocapsid antibodies measured by ELISA. Overall, 65% of the cohort had ≥ 1 SARS-CoV-2 infection by July 2022, and 19% of those with primary infection were reinfected. Infection and vaccination contributed to high seroprevalence: 98% (95% CI, 95-99) of participants were spike or nucleocapsid seropositive at the end of follow-up. Among those seropositive, 82% were vaccinated. Participants were more likely to be seropositive to spike than nucleocapsid after infection. Infection among seropositive individuals could be identified by increases in nucleocapsid, but not spike, ELISA optical density values. Nucleocapsid antibodies waned more quickly after infection than spike antibodies. High levels of SARS-CoV-2 population immunity, as found in this study, are leading to changing epidemiology necessitating ongoing surveillance and policy evaluation.

Indexed as

Antibodies, ViralCOVID-19Rural PopulationSARS-CoV-2AdolescentAdultAgedCohort StudiesCOVID-19 VaccinesFemaleHumansIncidenceMaleMiddle AgedSeroepidemiologic StudiesSpike Glycoprotein, CoronavirusAntibodies, ViralCOVID-19 VaccinesSpike Glycoprotein, CoronaviruscohortCOVID-19ELISAincidenceruralSARS-CoV-2seroprevalencevaccine

Identifiers

PMID38885957
PMCPMC12442051

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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.