Detection and characterization of H5N1 HPAIV in environmental samples from a dairy farm
The recent expansion of HPAIV H5N1 infections in terrestrial mammals in the Americas, most recently including the outbreak in dairy cattle, emphasizes the critical need for better epidemiological monitoring of zoonotic diseases. In this work, we detected, isolated, and characterized the HPAIV H5N1 f...
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| Published in: | Virus genes Vol. 60; no. 5; pp. 517 - 527 |
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| ISSN: | 0920-8569, 1572-994X, 1572-994X |
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| Abstract | The recent expansion of HPAIV H5N1 infections in terrestrial mammals in the Americas, most recently including the outbreak in dairy cattle, emphasizes the critical need for better epidemiological monitoring of zoonotic diseases. In this work, we detected, isolated, and characterized the HPAIV H5N1 from environmental swab samples collected from a dairy farm in the state of Kansas, USA. Genomic sequencing of these samples uncovered two distinctive substitutions in the PB2 (E249G) and NS1 (R21Q) genes which are rare and absent in recent 2024 isolates of H5N1 circulating in the mammalian and avian species. Additionally, approximately 1.7% of the sequence reads indicated a PB2 (E627K) substitution, commonly associated with virus adaptation to mammalian hosts. Phylogenetic analyses of the PB2 and NS genes demonstrated more genetic identity between this environmental isolate and the 2024 human isolate (A/Texas/37/2024) of H5N1. Conversely, HA and NA gene analyses revealed a closer relationship between our isolate and those found in other dairy cattle with almost 100% identity, sharing a common phylogenetic subtree. These findings underscore the rapid evolutionary progression of HPAIV H5N1 among dairy cattle and reinforces the need for more epidemiological monitoring which can be done using environmental sampling. |
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| AbstractList | The recent expansion of HPAIV H5N1 infections in terrestrial mammals in the Americas, most recently including the outbreak in dairy cattle, emphasizes the critical need for better epidemiological monitoring of zoonotic diseases. In this work, we detected, isolated, and characterized the HPAIV H5N1 from environmental swab samples collected from a dairy farm in the state of Kansas, USA. Genomic sequencing of these samples uncovered two distinctive substitutions in the PB2 (E249G) and NS1 (R21Q) genes which are rare and absent in recent 2024 isolates of H5N1 circulating in the mammalian and avian species. Additionally, approximately 1.7% of the sequence reads indicated a PB2 (E627K) substitution, commonly associated with virus adaptation to mammalian hosts. Phylogenetic analyses of the PB2 and NS genes demonstrated more genetic identity between this environmental isolate and the 2024 human isolate (A/Texas/37/2024) of H5N1. Conversely, HA and NA gene analyses revealed a closer relationship between our isolate and those found in other dairy cattle with almost 100% identity, sharing a common phylogenetic subtree. These findings underscore the rapid evolutionary progression of HPAIV H5N1 among dairy cattle and reinforces the need for more epidemiological monitoring which can be done using environmental sampling. The recent expansion of HPAIV H5N1 infections in terrestrial mammals in the Americas, most recently including the outbreak in dairy cattle, emphasizes the critical need for better epidemiological monitoring of zoonotic diseases. In this work, we detected, isolated, and characterized the HPAIV H5N1 from environmental swab samples collected from a dairy farm in the state of Kansas, USA. Genomic sequencing of these samples uncovered two distinctive substitutions in the PB2 (E249G) and NS1 (R21Q) genes which are rare and absent in recent 2024 isolates of H5N1 circulating in the mammalian and avian species. Additionally, approximately 1.7% of the sequence reads indicated a PB2 (E627K) substitution, commonly associated with virus adaptation to mammalian hosts. Phylogenetic analyses of the PB2 and NS genes demonstrated more genetic identity between this environmental isolate and the 2024 human isolate (A/Texas/37/2024) of H5N1. Conversely, HA and NA gene analyses revealed a closer relationship between our isolate and those found in other dairy cattle with almost 100% identity, sharing a common phylogenetic subtree. These findings underscore the rapid evolutionary progression of HPAIV H5N1 among dairy cattle and reinforces the need for more epidemiological monitoring which can be done using environmental sampling.The recent expansion of HPAIV H5N1 infections in terrestrial mammals in the Americas, most recently including the outbreak in dairy cattle, emphasizes the critical need for better epidemiological monitoring of zoonotic diseases. In this work, we detected, isolated, and characterized the HPAIV H5N1 from environmental swab samples collected from a dairy farm in the state of Kansas, USA. Genomic sequencing of these samples uncovered two distinctive substitutions in the PB2 (E249G) and NS1 (R21Q) genes which are rare and absent in recent 2024 isolates of H5N1 circulating in the mammalian and avian species. Additionally, approximately 1.7% of the sequence reads indicated a PB2 (E627K) substitution, commonly associated with virus adaptation to mammalian hosts. Phylogenetic analyses of the PB2 and NS genes demonstrated more genetic identity between this environmental isolate and the 2024 human isolate (A/Texas/37/2024) of H5N1. Conversely, HA and NA gene analyses revealed a closer relationship between our isolate and those found in other dairy cattle with almost 100% identity, sharing a common phylogenetic subtree. These findings underscore the rapid evolutionary progression of HPAIV H5N1 among dairy cattle and reinforces the need for more epidemiological monitoring which can be done using environmental sampling. |
| Author | Retallick, Jamie McDowell, Chester D. Matias-Ferreyra, Franco Richt, Juergen A. Noll, Lance Trujillo, Jessie D. Kafle, Sujan Kwon, Taeyong Fitz, Isaac Singh, Gagandeep Gaudreault, Natasha N. Morozov, Igor |
| AuthorAffiliation | 1 Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA 2 Kansas State Veterinary Diagnostic Laboratory (KSVDL), College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA |
| AuthorAffiliation_xml | – name: 1 Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA – name: 2 Kansas State Veterinary Diagnostic Laboratory (KSVDL), College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA |
| Author_xml | – sequence: 1 givenname: Gagandeep surname: Singh fullname: Singh, Gagandeep organization: Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University – sequence: 2 givenname: Jessie D. surname: Trujillo fullname: Trujillo, Jessie D. organization: Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University – sequence: 3 givenname: Chester D. surname: McDowell fullname: McDowell, Chester D. organization: Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University – sequence: 4 givenname: Franco surname: Matias-Ferreyra fullname: Matias-Ferreyra, Franco organization: Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University, Kansas State Veterinary Diagnostic Laboratory (KSVDL), College of Veterinary Medicine, Kansas State University – sequence: 5 givenname: Sujan surname: Kafle fullname: Kafle, Sujan organization: Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University – sequence: 6 givenname: Taeyong surname: Kwon fullname: Kwon, Taeyong organization: Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University – sequence: 7 givenname: Natasha N. surname: Gaudreault fullname: Gaudreault, Natasha N. organization: Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University – sequence: 8 givenname: Isaac surname: Fitz fullname: Fitz, Isaac organization: Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University – sequence: 9 givenname: Lance surname: Noll fullname: Noll, Lance organization: Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University, Kansas State Veterinary Diagnostic Laboratory (KSVDL), College of Veterinary Medicine, Kansas State University – sequence: 10 givenname: Igor surname: Morozov fullname: Morozov, Igor organization: Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University – sequence: 11 givenname: Jamie surname: Retallick fullname: Retallick, Jamie organization: Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University, Kansas State Veterinary Diagnostic Laboratory (KSVDL), College of Veterinary Medicine, Kansas State University – sequence: 12 givenname: Juergen A. surname: Richt fullname: Richt, Juergen A. email: jricht@vet.k-state.edu organization: Department of Diagnostic Medicine/Pathobiology (DMP), College of Veterinary Medicine, Kansas State University |
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| CitedBy_id | crossref_primary_10_1038_s41586_024_08063_y crossref_primary_10_3168_jds_2024_26222 crossref_primary_10_3390_v16091451 crossref_primary_10_3390_v17060811 crossref_primary_10_1016_j_ebiom_2025_105842 crossref_primary_10_2903_j_efsa_2025_9508 crossref_primary_10_3390_ijms25158550 crossref_primary_10_1093_nsr_nwaf262 crossref_primary_10_3390_v17030307 crossref_primary_10_1007_s10096_025_05147_z crossref_primary_10_3389_fvets_2025_1648878 |
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| Keywords | H5N1 Environmental Highly pathogenic avian influenza virus Bovine Mammalian |
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