Literature detail

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

Michael A Zeller1,2 Daniel Carnevale de Almeida Moraes3 Giovana Ciacci Zanella4,5 Carine K Souza3,4 Tavis K Anderson4 Amy L Baker4 Phillip C Gauger3
Affiliations 5 institutions
  1. Department of Veterinary Diagnostic & Production Animal Medicine, Iowa State University, Ames, IA, 50011-1134, USA. [email protected].
  2. Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, 169857, Singapore. [email protected].
  3. Department of Veterinary Diagnostic & Production Animal Medicine, Iowa State University, Ames, IA, 50011-1134, USA.
  4. Virus and Prion Research Unit, National Animal Disease Center, USDA-ARS, Ames, IA, 50010, USA.
  5. Department of Veterinary Microbiology and Preventive Medicine, Iowa State University, Ames, IA, 50011-1134, USA.
PMID 40295797 2024 Npj Viruses eng epublish
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Article

Publication summary

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.

Structured evidence records

Evidence records

5 total
1 records
Extraction confidence 0.85
Key finding

Phylogenetic and sequencing analyses showed multiple human-to-swine H3N2 introductions with evidence of reassortment between human-seasonal H3N2 and endemic swine influenza virus lineages.

Virus
Host
Location
Not specified
Supporting text

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.

Genes or proteins
neuraminidase
Analysis methods
phylogenetic inference; sequencing analysis
1 records
Extraction confidence 0.75
Key finding

Experimental inoculation of pigs with human seasonal H3N2 resulted in viral replication in respiratory tissues and mild lesions but no transmission to contact pigs.

Virus
Location
Not specified
Supporting text

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.

Method
experimental inoculation
Sample type
nose; lungs
Experimental system
in vivo animal experiment
1 records
Extraction confidence 0.90
Key finding

Swine influenza viruses derived from reverse-zoonotic human seasonal H3N2 contained neuraminidase genes from endemic swine lineages, consistent with reassortment between human and swine influenza viruses.

Host
Not specified
Location
Not specified
Supporting text

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.

Event type
reassortment
Genes or segments
NA
1 records
Extraction confidence 0.80
Key finding

Swine sera showed antibodies indicating infection with human seasonal H3N2, supporting reverse zoonotic transmission on farms in the United States and Mexico.

Virus
Host
Location
Not specified
Supporting text

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.

Sample type
serum
1 records
Extraction confidence 0.98
Key finding

Nineteen human-to-swine reverse zoonotic transmission events of the human seasonal H3N2 virus were detected between November 2022 and November 2023.

Virus
Location
Supporting text

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.

Method
virus isolation; sequencing; phylogenetic analysis; serologic investigation
Study design
outbreak investigation
Transmission direction
human-to-animal
Geographic raw
United States, Mexico, Chile