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Volume 23, Number 4—April 2017

Dispatch

Outbreaks among Wild Birds and Domestic Poultry Caused by Reassorted Influenza A(H5N8) Clade 2.3.4.4 Viruses, Germany, 2016

Anne Pohlmann, Elke Starick, Timm Harder, Christian Grund, Dirk Höper, Anja Globig, Christoph Staubach, Klaas Dietze, Günter Strebelow, Reiner G. Ulrich, Jan Schinköthe, Jens P. Teifke, Franz J. Conraths, Thomas C. Mettenleiter, and Martin BeerComments to Author 
Author affiliations: Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany

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EID Pohlmann A, Starick E, Harder T, Grund C, Höper D, Globig A, et al. Outbreaks among Wild Birds and Domestic Poultry Caused by Reassorted Influenza A(H5N8) Clade 2.3.4.4 Viruses, Germany, 2016. Emerg Infect Dis. 2017;23(4):633-636. https://dx.doi.org/10.3201/eid2304.161949
AMA Pohlmann A, Starick E, Harder T, et al. Outbreaks among Wild Birds and Domestic Poultry Caused by Reassorted Influenza A(H5N8) Clade 2.3.4.4 Viruses, Germany, 2016. Emerging Infectious Diseases. 2017;23(4):633-636. doi:10.3201/eid2304.161949.
APA Pohlmann, A., Starick, E., Harder, T., Grund, C., Höper, D., Globig, A....Beer, M. (2017). Outbreaks among Wild Birds and Domestic Poultry Caused by Reassorted Influenza A(H5N8) Clade 2.3.4.4 Viruses, Germany, 2016. Emerging Infectious Diseases, 23(4), 633-636. https://dx.doi.org/10.3201/eid2304.161949.

Abstract

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.

During 2014–2015, after massive outbreaks of highly pathogenic avian influenza (HPAI) on the Korean Peninsula, subtype H5N8 viruses (group A clade 2.3.4.4) caused outbreaks among wild birds and domestic poultry in central Asia, Russia, and central Europe (1,2). Strains of this clade, and novel reassortants thereof, were transferred to North America (3). Transcontinental spread of these strains and an earlier HPAI virus (HPAIV) of the goose/Guangdong lineage of subtype H5N1 has been linked to dissemination by migratory wild birds (4). We describe a novel reassortant of HPAIV A(H5N8) within group B clade 2.3.4.4, which causes lethal infections in hundreds of wild birds and domestic poultry in Germany and elsewhere in Europe.

The Study

Figure 1

Thumbnail of Highly pathogenic avian influenza A(H5N8) cases in wild birds and outbreaks in poultry holdings (10 backyard holdings, 4 zoos or pet farms, and a few commercial operations) in Germany, November 2016. Circles indicate original locations of outbreaks and isolates.

Figure 1. Highly pathogenic avian influenza A(H5N8) cases in wild birds and outbreaks in poultry holdings (10 backyard holdings, 4 zoos or pet farms, and a few commercial operations) in Germany, November 2016....

In late May 2016, a group B clade 2.3.4.4 H5N8 virus was detected in dead and hunted wild birds at Lake Uvs-Nuur, at the Russia–Mongolia border (5). On November 7, 2016, many dead tufted ducks (Aythya fuligula) were found at Lake Plön in Schleswig-Holstein, northern Germany, and at Lake Constance in Baden-Württemberg, southern Germany (Figure 1); most were positive for H5N8. The epidemic among wild birds continued and spread toward the center of the country (Figure 1). As of December 2016, several backyard holdings, 4 zoos, and a few large commercial operations were also affected. Direct or indirect contact with wild birds was the most likely route of virus introduction into the backyard holdings and zoos. Despite the generally high standards of commercial operations, possible biosecurity gaps were identified.

Most affected birds were found dead or exhibited severe clinical signs such as apathy or sudden deaths (in some parts of the affected chicken breeder farms, up to 90% died before culling). Macroscopic changes commonly observed in tufted ducks and poultry included severe diffuse hepatic necrosis, multifocal petechiae, and variably hyperemic and edematous lungs. Light microscopy confirmed influenza A virus nucleoprotein (NP) antigen and variably distinct necrotizing lesions in liver, heart, lungs, brain, pancreas, spleen, and thymus (Technical Appendix [PDF - 661 KB - 4 pages] Figure 1). Some chickens also displayed severe diffuse catarrhal enterocolitis; influenza A virus NP antigen was present in the intestinal epithelium.

The spectrum of affected species of wild birds is broad and includes mainly diving ducks but also swans, grebes, gulls, buzzards, crows, and a white-tailed eagle (Table 1). As of November 30, 2016, ≈400 infected wild birds were detected in 13 federal states of Germany. H5N8 infections were also reported from Austria, Croatia, Denmark, Finland, France, Hungary, Poland, Romania, Sweden, Switzerland, and the Netherlands, indicating that the same subtype caused the recent outbreaks throughout Europe.

The high pathogenicity for gallinaceous poultry was confirmed; intravenous pathogenicity index for 1 isolate (A/tufted duck/Germany-SH/AR8444/2016) was 2.93, comparable to the 2.81 index for H5N8 circulating in 2014 (A/turkey/Germany-MV/AR2472/2014). However, deaths of wild birds of a variety of species, in particular diving ducks, and extended pathologic changes in dead wild birds suggested a marked shift of pathogenicity from the viruses in Germany in 2014 (1).

For genetic characterization, we analyzed virus sequences from several swab samples and the first 2 virus isolates from dead tufted ducks from Lake Plön and Lake Constance and compared them with sequences from H5N8-positive turkeys and chickens. We found few genetic differences between the analyzed strains from northern and southern Germany and only slight differences between sequences generated from wild bird or poultry samples. This finding clearly contrasts with those of the H5N1 clade 2.2 outbreaks in Germany in 2006, which showed similar distribution (6) but 2 distinct H5N1 northern and southern subclusters and a difference in timing during the first transcontinental wave; virus was found in Europe in October 2005 but not in Germany until early 2006.

Figure 2

Thumbnail of Proposed reassortment events leading to the novel central Europe HPAIV A(H5N8) clade 2.3.4.4 virus. The Russia–Mongolia reassortant clade 2.3.4.4 H5N8 virus acquired 2 new segments (polymerase acidic protein and nucleoprotein), leading to the novel central Europe clade 2.3.4.4 H5N8 in 2016. Similar segment origins are marked by similar colors. Dashed lines indicate putative precursors. HPAIV, highly pathogenic avian influenza virus; LPAIV, low pathogenicity avian influenza virus.

Figure 2. Proposed reassortment events leading to the novel central Europe HPAIV A(H5N8) clade 2.3.4.4 virus. The Russia–Mongolia reassortant clade 2.3.4.4 H5N8 virus acquired 2 new segments (polymerase acidic protein and nucleoprotein), leading...

All genome segments of the novel H5N8 clade 2.3.4.4 group B strains from Germany in 2016 differed significantly from the H5N8 clade 2.3.4.4 group A strains detected in 2014–2015 in Germany and other European countries (1). This finding is in accord with results of studies suggesting that there was no continued circulation of group A–like viruses among wild birds in the Netherlands from mid-November 2014 to January 2016 (7). Database searches identified H5N8 clade 2.3.4.4 viruses (first detected in wild birds at the Russia–Mongolia border at the end of May 2016) as closest relatives. Extended searches confirmed that the isolates from Germany in 2016 described in this study are novel reassortants, which can be clearly distinguished from the isolates from Russia–Mongolia in 2016 (e.g., A/great crested grebe/Uvs-Nuur Lake/341/2016) by 2 segments (Table 2; Technical Appendix [PDF - 661 KB - 4 pages] Figure 2). Six segments (polymerase basic [PB] 2, PB1, hemagglutinin, neuraminidase, matrix protein, nonstructural protein [NS]) were highly similar to those of clade 2.3.4.4 viruses from Russia in 2016 (99% for each surface protein; Table 2). The NS1 protein of the new 2016 isolate from Germany is truncated (217 aa) compared with the Russia–Mongolia viruses (230 aa), a also truncation found in other influenza virus strains. However, the nuclear export protein is not affected. Of note, the Russia–Mongolia virus proved to be a novel reassortant from earlier H5N8 clade 2.3.4.4 viruses within group B (Table 2; Figure 2) (5). These new H5N8 viruses are central Asia reassortants, which originated from strains circulating in eastern Asia. Genes of 3 segments (hemagglutinin, neuraminidase, and NS protein) cluster with segments of H5N8 clade 2.3.4.4 group B viruses identified in eastern China; the other 5 genes (PB1, PB2, polymerase acidic [PA], nucleoprotein [NP], and matrix protein) cluster with avian influenza viruses of low pathogenicity, which were identified in Mongolia, China, and Vietnam (5).

The viruses from Germany (2016) further evolved from the strains from Russia and harbor 2 new segments (PA, NP). The virus sequences are essentially identical to sequences from an H5N8 virus isolate found November 2016 in a dead wild duck in Poland near the Germany border (Table 2) but differ significantly from sequences of other currently circulating isolates (Technical Appendix [PDF - 661 KB - 4 pages] Figure 2). The new PA sequences cluster with sequences of viruses detected in eastern and central Asia. The NP segment sequences are similar to those of viruses frequently found in central and northwestern Europe. The PA and NP segments in question occurred concurrently in different avian influenza viruses before; namely, in H6N8 strains from Iceland in 2011 (e.g., A/greylag goose/Iceland/0921/2011) and in an H6N2 isolate from Georgia in 2011 (A/mallard/Republic of Georgia/13/2011) (Table 2; Technical Appendix [PDF - 661 KB - 4 pages] Figure 2). It is reasonable to suggest that the novel reassortant strain from Germany was generated by >1 reassortment event that occurred during June–November 2016 between central Asia (Mongolia) and central Europe (Poland/Germany).

Conclusions

A new reassortant influenza A(H5N8) virus is responsible for the recent HPAIV outbreak in Germany. The observed differences in pathogenicity for a broad spectrum of waterfowl compared with that of H5N8 viruses from 2014–2015 correlate with a new genome composition of these viruses. The novel NP and PA segments in the 2016 H5N8 viruses from Germany are candidates for future studies of the molecular basis of the biological differences. These new strains may be more efficiently transmitted by and shed to other wild and domestic birds, a hypothesis in line with the large number of cases among wild birds in November 2016. There is yet no indication that mammals (including humans) are infected by these novel strains. Future studies in mammalian models (e.g., ferrets, mice) will provide experimental data on the virulence for mammals.

Dr. Pohlmann is a microbiologist and senior scientist working at the Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Insel Riems, Germany. Her research interests are focused on influenza viruses, sequence analysis, phylogeny, and next-generation sequencing.

Acknowledgments

We gratefully acknowledge professional support from local veterinarians, diagnosticians in regional laboratories in Neumünster (Schleswig-Holstein), Rostock (Mecklenburg-Western Pomerania), Aulendorf and Freiburg (Baden-Wuerttemberg), and technical assistance by Diana Wessler, Aline Maksimov, Nicole Reimer, Kathrin Steffen, Patrick Zitzow, Bianka Hillmann, Jörn Gethmann, the Tierseuchennachrichtensystem (national animal disease notification system) team, and Cornelia Illing.

This work was financed in part by COMPARE, under the European Union Horizon 2020 program (grant agreement no. 643476.)

References

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Figures

Tables

Technical Appendix

Cite This Article

DOI: 10.3201/eid2304.161949

Table of Contents – Volume 23, Number 4—April 2017

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Martin Beer, Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Südufer 10, D-17493 Greifswald-Insel Riems, Germany


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