Emergence of Pathogenic Coronaviruses in Cats by Homologous Recombination between Feline and Canine Coronaviruses
Type II feline coronavirus (FCoV) emerged via double recombination between type I FCoV and type II canine coronavirus (CCoV). In this study, two type I FCoVs, three type II FCoVs and ten type II CCoVs were genetically compared. The results showed that three Japanese type II FCoVs, M91-267, KUK-H/L a...
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Published in | PloS one Vol. 9; no. 9; p. e106534 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Public Library of Science
02.09.2014
Public Library of Science (PLoS) |
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Abstract | Type II feline coronavirus (FCoV) emerged via double recombination between type I FCoV and type II canine coronavirus (CCoV). In this study, two type I FCoVs, three type II FCoVs and ten type II CCoVs were genetically compared. The results showed that three Japanese type II FCoVs, M91-267, KUK-H/L and Tokyo/cat/130627, also emerged by homologous recombination between type I FCoV and type II CCoV and their parent viruses were genetically different from one another. In addition, the 3'-terminal recombination sites of M91-267, KUK-H/L and Tokyo/cat/130627 were different from one another within the genes encoding membrane and spike proteins, and the 5'-terminal recombination sites were also located at different regions of ORF1. These results indicate that at least three Japanese type II FCoVs emerged independently. Sera from a cat experimentally infected with type I FCoV was unable to neutralize type II CCoV infection, indicating that cats persistently infected with type I FCoV may be superinfected with type II CCoV. Our previous study reported that few Japanese cats have antibody against type II FCoV. All of these observations suggest that type II FCoV emerged inside the cat body and is unable to readily spread among cats, indicating that these recombination events for emergence of pathogenic coronaviruses occur frequently. |
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AbstractList | Type II feline coronavirus (FCoV) emerged via double recombination between type I FCoV and type II canine coronavirus (CCoV). In this study, two type I FCoVs, three type II FCoVs and ten type II CCoVs were genetically compared. The results showed that three Japanese type II FCoVs, M91-267, KUK-H/L and Tokyo/cat/130627, also emerged by homologous recombination between type I FCoV and type II CCoV and their parent viruses were genetically different from one another. In addition, the 3′-terminal recombination sites of M91-267, KUK-H/L and Tokyo/cat/130627 were different from one another within the genes encoding membrane and spike proteins, and the 5′-terminal recombination sites were also located at different regions of ORF1. These results indicate that at least three Japanese type II FCoVs emerged independently. Sera from a cat experimentally infected with type I FCoV was unable to neutralize type II CCoV infection, indicating that cats persistently infected with type I FCoV may be superinfected with type II CCoV. Our previous study reported that few Japanese cats have antibody against type II FCoV. All of these observations suggest that type II FCoV emerged inside the cat body and is unable to readily spread among cats, indicating that these recombination events for emergence of pathogenic coronaviruses occur frequently. Type II feline coronavirus (FCoV) emerged via double recombination between type I FCoV and type II canine coronavirus (CCoV). In this study, two type I FCoVs, three type II FCoVs and ten type II CCoVs were genetically compared. The results showed that three Japanese type II FCoVs, M91-267, KUK-H/L and Tokyo/cat/130627, also emerged by homologous recombination between type I FCoV and type II CCoV and their parent viruses were genetically different from one another. In addition, the 3'-terminal recombination sites of M91-267, KUK-H/L and Tokyo/cat/130627 were different from one another within the genes encoding membrane and spike proteins, and the 5'-terminal recombination sites were also located at different regions of ORF1. These results indicate that at least three Japanese type II FCoVs emerged independently. Sera from a cat experimentally infected with type I FCoV was unable to neutralize type II CCoV infection, indicating that cats persistently infected with type I FCoV may be superinfected with type II CCoV. Our previous study reported that few Japanese cats have antibody against type II FCoV. All of these observations suggest that type II FCoV emerged inside the cat body and is unable to readily spread among cats, indicating that these recombination events for emergence of pathogenic coronaviruses occur frequently.Type II feline coronavirus (FCoV) emerged via double recombination between type I FCoV and type II canine coronavirus (CCoV). In this study, two type I FCoVs, three type II FCoVs and ten type II CCoVs were genetically compared. The results showed that three Japanese type II FCoVs, M91-267, KUK-H/L and Tokyo/cat/130627, also emerged by homologous recombination between type I FCoV and type II CCoV and their parent viruses were genetically different from one another. In addition, the 3'-terminal recombination sites of M91-267, KUK-H/L and Tokyo/cat/130627 were different from one another within the genes encoding membrane and spike proteins, and the 5'-terminal recombination sites were also located at different regions of ORF1. These results indicate that at least three Japanese type II FCoVs emerged independently. Sera from a cat experimentally infected with type I FCoV was unable to neutralize type II CCoV infection, indicating that cats persistently infected with type I FCoV may be superinfected with type II CCoV. Our previous study reported that few Japanese cats have antibody against type II FCoV. All of these observations suggest that type II FCoV emerged inside the cat body and is unable to readily spread among cats, indicating that these recombination events for emergence of pathogenic coronaviruses occur frequently. |
Audience | Academic |
Author | Matsui, Nobutaka Terada, Yutaka Mochizuki, Masami Kuwata, Ryusei Noguchi, Keita Soma, Takehisa Maeda, Ken Shimoda, Hiroshi |
AuthorAffiliation | 1 Laboratory of Veterinary Microbiology, Joint Faculty of Veterinary Medicine, Yamaguchi University, Yamaguchi, Japan 2 Veterinary Diagnostic Laboratory, Marupi Lifetech Co. Ltd., Osaka, Japan 3 Laboratory of Emerging Infectious Diseases, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima, Japan University of Berne, Switzerland |
AuthorAffiliation_xml | – name: 3 Laboratory of Emerging Infectious Diseases, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima, Japan – name: 1 Laboratory of Veterinary Microbiology, Joint Faculty of Veterinary Medicine, Yamaguchi University, Yamaguchi, Japan – name: University of Berne, Switzerland – name: 2 Veterinary Diagnostic Laboratory, Marupi Lifetech Co. Ltd., Osaka, Japan |
Author_xml | – sequence: 1 givenname: Yutaka surname: Terada fullname: Terada, Yutaka – sequence: 2 givenname: Nobutaka surname: Matsui fullname: Matsui, Nobutaka – sequence: 3 givenname: Keita surname: Noguchi fullname: Noguchi, Keita – sequence: 4 givenname: Ryusei surname: Kuwata fullname: Kuwata, Ryusei – sequence: 5 givenname: Hiroshi surname: Shimoda fullname: Shimoda, Hiroshi – sequence: 6 givenname: Takehisa surname: Soma fullname: Soma, Takehisa – sequence: 7 givenname: Masami surname: Mochizuki fullname: Mochizuki, Masami – sequence: 8 givenname: Ken surname: Maeda fullname: Maeda, Ken |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25180686$$D View this record in MEDLINE/PubMed |
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Copyright | COPYRIGHT 2014 Public Library of Science 2014 Terada et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2014 Terada et al 2014 Terada et al |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Conceived and designed the experiments: KM. Performed the experiments: YT NM KN RK HS TS MM KM. Analyzed the data: YT KM. Contributed reagents/materials/analysis tools: MM TS KM. Contributed to the writing of the manuscript: YT NM KM. Competing Interests: The authors have declared that no competing interests exist. |
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Snippet | Type II feline coronavirus (FCoV) emerged via double recombination between type I FCoV and type II canine coronavirus (CCoV). In this study, two type I FCoVs,... |
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SubjectTerms | Animals Antibodies, Neutralizing - blood Antibodies, Viral - blood Biology and Life Sciences Cat Diseases - virology Cats Cell culture Comparative analysis Coronaviridae Coronavirus Infections - veterinary Coronavirus Infections - virology Coronavirus, Canine - classification Coronavirus, Canine - genetics Coronavirus, Canine - pathogenicity Coronavirus, Feline - classification Coronavirus, Feline - genetics Coronavirus, Feline - pathogenicity Coronaviruses COVID-19 Disease DNA, Viral - genetics Dogs Domestic cats Emergence Genes Genes, Viral Genomes Homologous Recombination Homology Infections Japan Laboratories Molecular Sequence Data Mutation Phylogeny Proteins Reassortant Viruses - genetics Reassortant Viruses - pathogenicity Sequence Homology, Nucleic Acid Veterinary medicine Viruses |
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Title | Emergence of Pathogenic Coronaviruses in Cats by Homologous Recombination between Feline and Canine Coronaviruses |
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