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      Pathogenicity and genetic characterisation of a novel reassortant, highly pathogenic avian influenza (HPAI) H5N6 virus isolated in Korea, 2017

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          Abstract

          We investigated influenza A(H5N6) viruses from migratory birds in Chungnam and Gyeonggi Provinces, South Korea following a reported die-off of poultry in nearby provinces in November 2017. Genetic analysis and virulence studies in chickens and ducks identified our isolate from December 2017 as a novel highly pathogenic avian influenza virus. It resulted from reassortment between the highly virulent H5N8 strain from Korea with the N6 gene from a low-pathogenic H3N6 virus from the Netherlands.

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          Novel Reassortant Influenza A(H5N8) Viruses, South Korea, 2014

          To the Editor: Highly pathogenic avian influenza (HPAI) viruses have caused considerable economic losses to the poultry industry and poses potential threats to animal and human health (www.oie.int/en/ and www.who.int/en/). Since 2003, influenza A(H5N1) viruses with a hemagglutinin (HA) gene derived from A/goose/Guandong/1/96–like viruses have become endemic to 6 countries (Bangladesh, China, Egypt, India, Indonesia, and Vietnam) ( 1 ) (www.cdc.gov/). Furthermore, HPAI viruses with an H5 subtype continue to undergo substantial evolution because of extensive genetic divergence and reassortment between other subtypes of influenza viruses. Especially in China, novel subtypes of H5 HPAI virus, such as influenza A(H5N2), influenza A(H5N5), and influenza A(H5N8) viruses, were reported during 2009–2011 ( 2 , 3 ). On January 16, 2014, clinical signs of HPAI, such as decreased egg production (60%) and slightly increased mortality rates, were detected in ducks on a breeder duck farm near the Donglim Reservoir in Jeonbuk Province, South Korea. On January 17, a farmer (5 km from the Donglim Reservoir) also reported clinical signs of HPAI in breeder ducks. In addition, 100 carcasses of Baikal teals were found in the Donglim Reservoir. RNAs extracted from organs (liver, pancreas, and trachea) of 3 dead birds (1 breeder duck, 1 broiler duck, and 1 Baikal teal) were positive for H5 subtype virus by reverse transcription PCR ( 4 ). We isolated viruses from suspected specimens by inoculation into embryonated specific pathogen–free chicken eggs. The H5N8 subtype was identified by using HA and neuraminidase (NA) inhibition assays. Three viruses isolated from domestic ducks and wild birds were designated A/breeder duck/Korea/Gochang1/2014 (H5N8) (Gochang1), A/duck/Korea/Buan2/2014 (H5N8) (Buan2), and A/Baikal Teal/Korea/Donglim3/2014 (H5N8) (Donglim3). All 8 RNA genome segments of these viruses were amplified by using segment-specific primers and directly sequenced ( 5 ). Sequences of the 8 RNA segments of each virus were submitted to GenBank under accession nos. KJ413831–KJ413854. Gochang1 virus has been shown to be highly pathogenic for chickens (intravenous pathogenicity index 3.0) ( 6 ). This finding was consistent with analysis of the HA gene, as shown by a series of deduced basic amino acid sequences (Gochang1, LREKRRKR/GLF, Buan2 and Donglim3, LRERRRKR/GLF) at cleavage sites of HA ( 6 ). This outbreak of influenza A(H5N8) infection in South Korea was reported to the World Organisation for Animal Health ( 7 ). Nucleotide identity analysis with BioEdit version 7.2.5 (http://bioedit.software.informer.com/) and ClustalW (www.ebi.ac.kr/Tolls/clustalw2) showed that 3 distinct novel influenza A(H5N8) viruses emerged in South Korea. Gochang1 virus had 87%–97% sequence identities in the 8 genome segments with sequences for Buan2 and Donglim3 viruses, which had high sequence identities (>99.5%) with each other. Conservative amino acid residues within receptor binding pockets of HA (including E190, R220, G225, Q226, and G228; H3 numbering) were present in all 3 viruses, which indicated that these viruses retained affinity for the avian (sialic acid-2,3-NeuAcGal) cell surface ( 8 ). Although there was an I314V mutation in the NA of the 3 viruses, other mutations that encode oseltamivir and zanamivir resistance were not detected ( 9 ). A BLAST (www.ncbi.nlm.nih.gov/genomes/FLU/FLU.html) search and phylogenetic analysis showed that these novel H5N8 subtype viruses likely originated from reassortment between A/duck/Jiangsu/k1203/2010 (H5N8) virus and other subtypes of avian influenza virus, all of which co-circulated in birds in eastern China during 2009–2012 ( 10 ). A phylogenetic tree of partial HA gene sequences for the 3 virus isolates from South Korea and other H5 subtype viruses (n = 72), showed that Gochang1, Buan2, and Donglime3 belong to the proposed H5 clade 2.3.4.6 (Figure) ( 10 ). Figure Phylogenetic tree of hemagglutin (HA) genes of influenza A(H5N8) viruses, South Korea, 2014. Triangles indicate viruses characterized in this study. Other viruses detected in South Korea are indicated in boldface. Subtypes are indicated in parentheses. A total of 72 HA gene sequences were ≥1,600 nt. Multiple sequence alignment was performed by using ClustalW (www.ebi.ac.kr/Tolls/clustalw2). The tree was constructed by using the neighbor-joining method with the Kimura 2-parameter model and MEGA version 5.2 (www.megasoftware.net/) with 1,000 bootstrap replicates. H5, hemagglutinin 5; Gs/Gd, Goose/Guangdong; LPAI, low pathogenic avian influenza; HPAI, highly pathogenic avian influenza. Scale bar indicates nucleotide substitutions per site. The H5 and N8 genes of the 3 viruses had high nucleotide identities with A/duck/Jiangsu/k1203/2010 (H5N8) (JQ97369691–98) (H5: Gochang1, 98.9%, Buan2 and Donglim3, 97.2%; N8: Gochang1, 98.5%, Buan2 and Donglim3, 98.1%). For Gochang1 virus, polymerase basic protein 2 (PB2) and nonstructural (NS) protein had the highest identities with A/environment/Jiangxi/28/2009 (H11N9) (PB2 98.6%, NS 97.7%). The other segments showed high genetic identities with A/duck/Jiangsu/k1203/2010 (H5N8) (>98.7%), which suggested that Gochang1 virus was generated by reassortment in which the PB2 and NS genes of A/duck/Jiangsu/k1203/2010 (H5N8) were replaced by those of influenza A(H11N9) viruses. For Buan2 and Donglim3 viruses, the PB2, HA, nucleoprotein, and NA genes were highly similar to those of A/duck/Jiangsu/k1203/2010 (H5N8) (>97.2%). However, the PB1, polymerase acidic protein, matrix protein, and NS genes of this virus had the highest genetic identities with A/duck/Eastern China/1111/2011 (H5N2) (>98.2%). Therefore, Buan2 and Donglim3 viruses might be reassortants that contain PB2, HA, nucleoprotein, and NA genes from A/duck/Jiangsu/k1203/2010 (H5N8) and PB1, polymerase acidic protein, NS, and matrix genes from A/duck/Eastern China/1111/2011 (H5N2) co-circulating in the same region of China ( 2 , 10 ). We characterized 3 distinct novel reassortant influenza A(H5N8) HPAI viruses during an influenza outbreak in South Korea. Buan2 and Donglim3 viruses showed high nucleotide identities, which suggested that the outbreak viruses in domestic ducks and Baikal teals might have an identical origin. Although research on the epidemiologic features of this outbreak is currently underway, it seems likely that on the basis of reassortant sequence features of the 8 genome segments, the 3 distinct viruses originated in eastern China. These influenza viruses are a potential threat to the poultry population in South Korea, including gallinaceous birds, during movement of domestic ducks through the distribution network of live bird markets.
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            Pathobiological features of a novel, highly pathogenic avian influenza A(H5N8) virus

            The endemicity of highly pathogenic avian influenza (HPAI) A(H5N1) viruses in Asia has led to the generation of reassortant H5 strains with novel gene constellations. A newly emerged HPAI A(H5N8) virus caused poultry outbreaks in the Republic of Korea in 2014. Because newly emerging high-pathogenicity H5 viruses continue to pose public health risks, it is imperative that their pathobiological properties be examined. Here, we characterized A/mallard duck/Korea/W452/2014 (MDk/W452(H5N8)), a representative virus, and evaluated its pathogenic and pandemic potential in various animal models. We found that MDk/W452(H5N8), which originated from the reassortment of wild bird viruses harbored by migratory waterfowl in eastern China, replicated systemically and was lethal in chickens, but appeared to be attenuated, albeit efficiently transmitted, in ducks. Despite predominant attachment to avian-like virus receptors, MDk/W452(H5N8) also exhibited detectable human virus-like receptor binding and replicated in human respiratory tract tissues. In mice, MDk/W452(H5N8) was moderately pathogenic and had limited tissue tropism relative to previous HPAI A(H5N1) viruses. It also induced moderate nasal wash titers in inoculated ferrets; additionally, it was recovered in extrapulmonary tissues and one of three direct-contact ferrets seroconverted without shedding. Moreover, domesticated cats appeared to be more susceptible than dogs to virus infection. With their potential to become established in ducks, continued circulation of A(H5N8) viruses could alter the genetic evolution of pre-existing avian poultry strains. Overall, detailed virological investigation remains a necessity given the capacity of H5 viruses to evolve to cause human illness with few changes in the viral genome.
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              Outbreaks among Wild Birds and Domestic Poultry Caused by Reassorted Influenza A(H5N8) Clade 2.3.4.4 Viruses, Germany, 2016

              In November 2016, an influenza A(H5N8) outbreak caused deaths of wild birds and domestic poultry in Germany. Clade 2.3.4.4 virus was closely related to viruses detected at the Russia–Mongolia border in 2016 but had new polymerase acidic and nucleoprotein segments. These new strains may be more efficiently transmitted to and shed by birds.
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                Author and article information

                Journal
                Euro Surveill
                Euro Surveill
                eurosurveillance
                Eurosurveillance
                European Centre for Disease Prevention and Control (ECDC)
                1025-496X
                1560-7917
                15 February 2018
                : 23
                : 7
                : 18-00045
                Affiliations
                [1 ]College of Medicine and Medical Research Institute, Chungbuk National University, Seowon-gu, Cheongju, South Korea
                [2 ]These authors contributed equally to this article
                [3 ]Avian Influenza Research and Diagnostic Division, Animal and Plant Quarantine Agency, Gimcheon-si, Gyeongsangbuk-do, South Korea
                Author notes

                Correspondence: Young Ki Choi ( choiki55@ 123456chungbuk.ac.kr ), Myoung-Heon Lee ( vetlee@ 123456korea.kr )

                Article
                18-00045 18-00045 18-00045
                10.2807/1560-7917.ES.2018.23.7.18-00045
                5824127
                29463346
                ce6ade9b-e31a-48e6-bb16-95832079f322
                This article is copyright of The Authors, 2018.

                This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) Licence. You may share and adapt the material, but must give appropriate credit to the source, provide a link to the licence, and indicate if changes were made.

                History
                : 30 January 2018
                : 14 February 2018
                Categories
                Rapid Communication
                Custom metadata
                2

                influenza a virus,h5n6,reassortant,highly pathogenic avian influenza (hpai),virulence,south korea

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