Evidence map›Paper›PMID 40295797›Full record

ArticleNpj viruses2024

Reverse zoonosis of the 2022-2023 human seasonal H3N2 detected in swine.

Michael A Zeller, Daniel Carnevale de Almeida Moraes, Giovana Ciacci Zanella, Carine K Souza, Tavis K Anderson, Amy L Baker, Phillip C Gauger

Abstract read
In one paragraph

Article in Npj viruses, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

7 authors.

Michael A ZellerDepartment of Veterinary Diagnostic & Production Animal Medicine, Iowa State University, Ames, IA, 50011-1134, USA. mazeller@iastate.edu.
Daniel Carnevale de Almeida MoraesDepartment of Veterinary Diagnostic & Production Animal Medicine, Iowa State University, Ames, IA, 50011-1134, USA.
Giovana Ciacci ZanellaVirus and Prion Research Unit, National Animal Disease Center, USDA-ARS, Ames, IA, 50010, USA.
Carine K SouzaDepartment of Veterinary Diagnostic & Production Animal Medicine, Iowa State University, Ames, IA, 50011-1134, USA.
Tavis K AndersonVirus and Prion Research Unit, National Animal Disease Center, USDA-ARS, Ames, IA, 50010, USA.
Amy L BakerVirus and Prion Research Unit, National Animal Disease Center, USDA-ARS, Ames, IA, 50010, USA.
Phillip C GaugerDepartment of Veterinary Diagnostic & Production Animal Medicine, Iowa State University, Ames, IA, 50011-1134, USA.

Funding

NIAID Centers of Excellence for Influenza Research and Response: Universal Influenza Vaccine Research Activities75N93021C00015 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI HENSLEY, SCOTT · 2021 to 2025
$50.7M
Agricultural Research Service 0201-88888-003-000DAgricultural Research Service 5030-32000-231-000-DNIAID NIH HHS 75N93021C00015U.S. Department of Energy DE-SC0014664
6 · The paper itself

Abstract

The Iowa State University Veterinary Diagnostic Laboratory detected nineteen human-to-swine reverse zoonoses of the 2022-2023 human seasonal H3N2 between November 2022 and November 2023. Cases from seven U.S. locations were detected: 3 Colorado, 1 Illinois, 1 Indiana, 2 Missouri, 7 North Carolina, 1 Ohio, and 1 Pennsylvania. One additional case was detected in Mexico and two cases were identified from Chile. Case samples were comprised of 4 nasal swabs and 15 oral fluids. Virus was successfully isolated from two of four nasal swab samples, but isolation from oral fluids was unsuccessful. The swine detections of H3 human viruses were classified to one of two human-seasonal H3 clades, 3C.2a1b.2a.2b and 3C.2a1b.2a.2a.1. Phylogenetic inference indicated at minimum 7 reverse zoonotic events occurred, with possible swine-to-swine transmission following the initial spillover. Twelve neuraminidase genes were sequenced, and nine were classified as human-seasonal H3N2 lineage: the remaining were endemic swine IAV NA genes from the N2.2002B, N2.1998, or the N1.Classical lineage, suggesting reassortment. The two viral isolates obtained from nasal swab samples were sequenced and were entirely human-lineage viruses. Seven swine samples with human seasonal H3 were sequenced and revealed co-detections with H1 1A.3.3.3 (gamma), with internal gene segments from both the triple reassortant internal gene (TRIG) and pandemic 2009 lineages. Serologic investigation of samples from swine production systems provided evidence for infection with human seasonal H3N2. One farm in the United States and four farms in Mexico had concurrent virologic evidence. The swine-isolated 3C.2a1b.2a.2b H3N2 was antigenically distinct from endemic 1990.4.A, 2010.1, and 2010.2 swine H3N2 lineages, but retained antigenic similarity to a recent human seasonal H3N2 (A/Darwin/6/2021). Pigs experimentally inoculated with a representative isolate demonstrated replication in the nose and lungs and minimal to mild macroscopic and microscopic lung lesions, but primary pigs did not transmit the virus to indirect contacts. If sustained in the pig population, this human seasonal H3 would represent the first new lineage detected in pigs the 2020 decade and present an emerging threat to swine health and production.

Identifiers

PMID40295797
PMCPMC11721445

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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.