Volume 23, Number 4—April 2017
Characterization of Highly Pathogenic Avian Influenza Virus A(H5N6), Japan, November 2016
Highly pathogenic avian influenza viruses (HPAIVs) A(H5N6) were concurrently introduced into several distant regions of Japan in November 2016. These viruses were classified into the genetic clade 188.8.131.52c and were genetically closely related to H5N6 HPAIVs recently isolated in South Korea and China. In addition, these HPAIVs showed further antigenic drift.
Since their emergence in ≈2010–11 in China (1), highly pathogenic avian influenza viruses (HPAIVs) that have the hemagglutinin (HA) genes of the H5 subtype classified into the genetic clade 184.108.40.206 have threatened global bird species, including wild birds and poultry, as well as humans. Although the H5 HA genes of these viruses are closely related, the subtypes of their neuraminidase (NA) genes vary widely. These new H5 HPAIVs with NA genes of various subtypes, the so-called H5Nx viruses, have spread globally, most likely because of their host preference for waterfowl, similar to the previous H5N1 HPAIVs (2–4). During the winter season 2014–15, H5N8 HPAIVs were isolated from wild birds and chickens in western Japan (5–7). In November 2016, HPAIVs of the H5N6 subtype were isolated in 3 geographically distant regions of Japan. We report the genetic and antigenic characteristics of 6 H5N6 HPAIVs.
The first suspected case of an HPAI outbreak in Japan during winter 2016–17 was reported from Akita Prefecture in northern Japan (Figure 1). A black swan (Cygnus atratus) in a zoo that died on November 15, 2016, tested positive for influenza virus antigen by a rapid diagnostic test. While this bird’s specimens underwent further analysis, another influenza virus was isolated from a water sample collected at an overwintering site of migratory birds in Kagoshima Prefecture at the southern tip of Japan on November 14, 2016 (Table 1). This isolate, A/environment/Kagoshima/KU-ngr-I/2016 (H5N6), was confirmed to be an H5N6 subtype having multiple basic amino acid residues, PLRERRRKR/GLF, at the cleavage site in the HA protein, which is characteristic of HPAIVs, by conventional reverse transcription PCR and Sanger sequencing. Subsequently, an isolate from the first black swan, A/black swan/Akita/1/2016 (H5N6), also was confirmed to be an H5N6 HPAIV, showing that all 3 chickens inoculated intranasally with 108.4 of 50% egg infectious dose of the virus died within 2 days. In addition, a fecal sample of a common teal (Anas crecca) collected at an overwintering site of migratory birds in Tottori Prefecture in the middle of Japan on November 15, 2016, was reported to harbor an H5N6 HPAIV, A/teal/Tottori/1/2016 (H5N6) (Table 1). The isolation sites of these 3 H5N6 HPAIVs are distant (Figure 1), although the sample collection dates were close (Table 1). These 3 cases were followed by several reports of H5N6 HPAIVs, including A/black swan/Akita/2/2016 (H5N6), A/northern pintail/Tottori/b37/2016 (H5N6), and A/crane/Kagoshima/KU-4/2016 (H5N6), in Japan (Table 1). As of December 4, a total of 31 confirmed cases in wild birds had been reported to the Ministry of Environment (http://www.env.go.jp/nature/dobutsu/bird_flu/index.html), and 4 cases at poultry farms were confirmed in Japan (8).
To clarify the genetic background of the H5N6 HPAIVs concurrently introduced into several distant regions of Japan, we determined the complete genome sequences of 5 of our isolates: A/black swan/Akita/1/2016 (H5N6) (GenBank/DDBJ/EMBL accession nos. LC198525–LC198532), A/teal/Tottori/1/2016 (H5N6) (GenBank/DDBJ/EMBL accession nos. LC199865–LC199872), A/northern pintail/Tottori/b37/2016 (H5N6) (GenBank/DDBJ/EMBL accession nos. LC200414-LC200421), A/environment/Kagoshima/KU-ngr-I/2016 (H5N6) (GISAID EpiFlu [http://platform.gisaid.org/], GenBank/DDBJ/EMBL accession nos. EPI861582–EPI861589), and A/crane/Kagoshima/KU-4/2016 (H5N6) (GenBank/DDBJ/EMBL accession nos. EPI867577–EPI867584) by Sanger and/or Illumina Miseq next-generation sequencing. These 5 isolates were almost genetically identical. Even among the HA genes, which are the most frequently mutated ones among the 8 gene segments, only 3–8 nt mutations, including 3 nonsynonymous mutations, were detected compared with the earliest strain, A/northern pintail/Tottori/b37/2016 (H5N6) (Technical Appendix Table). Thus, the 5 isolates would share a close common ancestor.
The phylogenetic tree analysis of the HA gene revealed that our isolates are classified into the genetic clade 220.127.116.11c and clustered with the recent H5N6 HPAIV isolates from wild and domestic birds and humans in China, in addition to an isolate South Korea, A/Mandarin duck/Korea/K16-187-3/2016 (H5N6) (Figure 2, panel A), on the basis of a recent classification in clade 18.104.22.168 (9,10). The NA genes of our isolates also form a single cluster together with the H5N6 HPAIV isolates from China into group C in the phylogenetic tree (Figure 2, panel B). In addition, the remaining 6 genes were genetically close to the recent H5N6 HPAIV isolates from China in the corresponding phylogenetic trees (Technical Appendix Figure 1), except for the polymerase basic 1 genes, which are most closely related to the counterpart of A/duck/Guangdong/S4040/2011 (H4N2) that was isolated from a domestic duck at a live bird market in China (11). Thus, the H5N6 HPAIV isolates would be derived from a reassortant that arose between an H5N6 HPAIV recently circulating in wild birds, poultry, or both in East Asia and in low pathogenicity avian influenza virus circulating in poultry in China. The genetic background of the H5N6 HPAIV isolates in this study is similar to the recent South Korea H5N6 virus collected in October 2016 and clearly different from that of recent H5Nx HPAIVs in Russia (10), Western European countries, and Alaska (8).
Our putative amino acid sequence comparison revealed that a leucine residue at position 134 in the HA protein (H3 numbering) was deleted, unlike that with the closest relative A/feline/Guangdong/1/2015 (H5N6) (Technical Appendix Figure 2). Our isolates have the amino acid sequence QQG at positions 226–228, which are located at the receptor-binding site in the HA protein, although the corresponding amino acid sequences of the previous H5 viruses are QSG or QRG (Technical Appendix Figure 2). These findings suggest that the receptor specificity of our H5N6 HPAIV isolates might be altered from their parental viruses (12,13). We also found 11 aa deletions in the stalk region of the NA protein, unlike that of A/duck/Vietnam/HU1–1151/2014 (H5N6), a representative virus strain of an N6 NA gene-based group D (Technical Appendix Figure 3), which belongs to a different cluster of the clade 22.214.171.124.
For HA antigenic characterization, we investigated the reactivity of chicken antiserum raised against several H5 isolates to our H5N6 HPAIV isolates using the hemagglutination inhibition test (14). We selected 1 reference virus strain, A/black swan/Akita/1/2016 (H5N6), and prepared single immunized chicken antiserum against the virus because of the limited variation of the nucleotide sequences in the HA genes among our 6 H5N6 HPAIV isolates. Antibody titer of antiserum of A/black swan/Akita/1/2016 (H5N6) were 16–32-fold higher against homologous virus than against the other strains (Table 2). The reactivity of the antiserum of A/chicken/Kumamoto/1-7/2014 (H5N8), whose HA gene belongs to the genetic clade 126.96.36.199, to A/black swan/Akita/1/2016 (H5N6) was 4-fold lower than that of the antiserum to the homologous combination. Moreover, none of the antiserum samples tested reacted strongly with A/black swan/Akita/1/2016 (H5N6) except for the homologous antiserum. These results indicate that the HA antigenicity of the H5N6 HPAIVs recently introduced in Japan differ appreciably from those of the previous H5Nx viruses.
We isolated 6 H5N6 HPAIVs from dead birds, fecal samples of migratory birds, and environmental water sample in 3 distant regions of Japan in November 2016. A genetic analysis showed that these isolates were genetically closely related to H5N6 HPAIVs recently isolated in China except for the polymerase basic 1 gene segment. The HA antigenicity of our H5N6 HPAIVs was demonstrated to have drifted further than viruses belonging to the same genetic clade 188.8.131.52. To prevent the spread of HPAIVs by wild birds, prompt elimination of HPAIVs is urgently needed in countries in Asia.
Dr. Okamatsu is an associate professor at the Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan. His primary research interests are interspecies transmission and pathogenecity of influenza viruses.
We thank Mizuho Suzuki, Aiko Ohnuma, Junki Maruyama, Ayato Takada, Satoshi Saito, Hiroichi Ozaki, Toshiyuki Murase, Tsuyoshi Yamaguchi, Natsuko Nishi, Kaori Tokorozaki, Shigehisa Toda, Satoru Taura, Kotaro Kawabe, Atsushi Nishitani, and Naoko Maruta for their technical assistance. We thank the Ministry of the Environment, the Prefecture of Akita, the Prefecture of Tottori, and the City of Izumi for their kind cooperation.
This work was supported by a grant from the Project of the National Agriculture and Food Research Organization Bio-oriented Technology Research Advancement Institution (Integration Research for Agriculture and Interdisciplinary Fields) and by a grant for contracted research activity for crane conservation with the City of Izumi, Japan. This research was partially supported by the Japan Initiative for Global Research Network on Infectious Diseases from Japan’s Ministry of Education, Culture, Sport, Science and Technology, and Japan Agency for Medical Research and Development and by grants for Scientific Research on Innovative Areas from the Ministry of Education, Culture, Science, Sports and Technology of Japan (JP16H06431, JP16H06429, and JP16K21723). This research was commissioned by the Kagoshima Crane Conservation Committee.
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1These authors contributed equally to this article.
Table of Contents – Volume 23, Number 4—April 2017
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Yoshihiro Sakoda, Laboratory of Microbiology, Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, North 18, West 9, Kita-ku, Sapporo, Hokkaido 060-0818, Japan