Evidence map›Paper›PMID 41980105›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

Distinct evolutionary patterns of endemic and emerging parvoviruses and the origin of a new pandemic virus.

Robert A López-Astacio, Brian R Wasik, Hyunwook Lee, Ian E H Voorhees, Wendy S Weichert, Oluwafemi F Adu, Laura B Goodman, Susan L Hafenstein, Uwe Truyen, Colin R Parrish

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Robert A López-Astacio *Baker Institute for Animal Health, Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853.ORCID 0000-0002-9049-7764
Brian R Wasik *Baker Institute for Animal Health, Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853.ORCID 0000-0001-5442-3883
Hyunwook LeeThe Hormel Institute, Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Medical Research Center, Austin, MN 55912.
Ian E H VoorheesBaker Institute for Animal Health, Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853.
Wendy S WeichertBaker Institute for Animal Health, Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853.
Oluwafemi F AduBaker Institute for Animal Health, Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853.ORCID 0000-0002-9914-6266
Laura B GoodmanBaker Institute for Animal Health, Department of Public and Ecosystems Health, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853.
Susan L HafensteinThe Hormel Institute, Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Medical Research Center, Austin, MN 55912.
Uwe TruyenInstitut für Tierhygiene und Öffentliches Veterinärwesen, Abteilung für Biochemie, Universität Leipzig, Leipzig 04103, Germany.ORCID 0000-0003-1275-9586
Colin R ParrishBaker Institute for Animal Health, Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853.ORCID 0000-0002-1836-6655

Funding

Structural Controls of Functional Receptor and Antibody Binding to Viral Capsids.R01AI092571 · NIAID · CORNELL UNIVERSITY · PI PARRISH, COLIN R. · 2011 to 2021
$4.0M
Feline Health Center at Cornell University I3554NIAID NIH HHS R01 AI092571NSF (NSF) DBI-2412389
6 · The paper itself

Abstract

Emergence of epidemic viruses in new hosts threatens both human and other animal populations, and often involves virus evolution to overcome barriers that normally prevent efficient infection and spread in that host. After transfer the separated viruses will evolve in parallel as they spread within the original and new hosts. Here we examine the details of a virus involved in such a host-jumping event, where we define the natural evolution of feline panleukopenia virus (FPV) over 60 y, clarify the origins of the new pandemic canine parvovirus (CPV) that arose in the 1970s, and compare the separate evolution of those viruses over 47 y in cats or dogs. Several live-attenuated FPV vaccine viruses originated from early-1960s isolates or were a recombinant of an early virus, and many sequences in databases proved to be vaccine-derived. The sequences of wild viruses showed that FPV-like strains evolved at less than one-third the rate observed for CPV in dogs, and the higher rate of CPV evolution has been consistent since 1979, when a genetic variant became widespread. The common ancestor of the CPV lineage was related to FPVs from Europe and contained several unique host-adaptive capsid changes associated with canine transferrin receptor type-1 binding. Although the FPV vaccine strains are around 60 y old, little selection for antigenic variation was observed. The distinct evolutionary patterns of these closely related viruses circulating for decades in different hosts emphasize the complex evolution associated with viral epidemic emergence and spread in endemic and new hosts.

Indexed as

Evolution, MolecularFeline PanleukopeniaFeline Panleukopenia VirusPandemicsParvoviridae InfectionsParvovirus, CanineAnimalsCatsDogsEndemic DiseasesHumansMolecular Sequence DataPhylogenyantibodiesemergenceparvovirusvaccinevirology

Identifiers

PMID41980105
PMCPMC13099694

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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.