- Open Access
Host-specific exposure and fatal neurologic disease in wild raptors from highly pathogenic avian influenza virus H5N1 during the 2006 outbreak in Germany
- Judith MA van den Brand†1,
- Oliver Krone†2,
- Peter U Wolf3,
- Marco WG van de Bildt1,
- Geert van Amerongen1,
- Albert DME Osterhaus1 and
- Thijs Kuiken1Email author
© van den Brand et al.; licensee BioMed Central. 2015
- Received: 16 September 2014
- Accepted: 13 January 2015
- Published: 5 March 2015
Raptors may contract highly pathogenic avian influenza virus H5N1 by hunting or scavenging infected prey. However, natural H5N1 infection in raptors is rarely reported. Therefore, we tested raptors found dead during an H5N1 outbreak in wild waterbirds in Mecklenburg-Western Pomerania, Germany, in 2006 for H5N1-associated disease. We tested 624 raptors of nine species—common buzzard (385), Eurasian sparrowhawk (111), common kestrel (38), undetermined species of buzzard (36), white-tailed sea eagle (19), undetermined species of raptor (12), northern goshawk (10), peregrine falcon (6), red kite (3), rough-legged buzzard (3), and western marsh-harrier (1)—for H5N1 infection in tracheal or combined tracheal/cloacal swabs of all birds, and on major tissues of all white-tailed sea eagles. H5N1 infection was detected in two species: common buzzard (12 positive, 3.1%) and peregrine falcon (2 positive, 33.3%). In all necropsied birds (both peregrine falcons and the six freshest common buzzards), H5N1 was found most consistently and at the highest concentration in the brain, and the main H5N1-associated lesion was marked non-suppurative encephalitis. Other H5N1-associated lesions occurred in air sac, lung, oviduct, heart, pancreas, coelomic ganglion, and adrenal gland. Our results show that the main cause of death in H5N1-positive raptors was encephalitis. Our results imply that H5N1 outbreaks in wild waterbirds are more likely to lead to exposure to and mortality from H5N1 in raptors that hunt or scavenge medium-sized birds, such as common buzzards and peregrine falcons, than in raptors that hunt small birds and do not scavenge, such as Eurasian sparrowhawks and common kestrels.
- Reverse Transcriptase Polymerase Chain Reaction
- H5N1 Infection
- Cloacal Swab
- Peregrine Falcon
- Common Buzzard
Highly pathogenic avian influenza virus causes high mortality in poultry, but is rarely reported to cause clinical disease in wild waterbirds. However, since 2000 there have been several reported outbreaks of highly pathogenic avian influenza virus of the subtype H5N1 causing mortality in wild waterbirds. A major outbreak occurred in 2005 in western China, causing mortality of more than thousand birds, including bar-headed geese (Anser indicus), great black-headed gulls (Larus ichthyaetus), and brown-headed gulls (Larus brunnicephalus) [1,2]. Subsequently, H5N1 spread to Europe in 2005 and 2006, and caused mortality in a variety of wild birds. In Germany, H5N1 infection was detected by real-time reverse transcriptase polymerase chain reaction (RT-PCR) in several wild bird species, not only waterbirds such as whooper (Cygnus cygnus) and mute swans (Cygnus olor), Canada geese (Branta canadensis), tufted ducks (Aythya fuligula), greater black-backed gulls (Larus marinus), herring gulls (Larus argentatus), but also in raptors such as northern goshawks (Accipiter gentilis) and common buzzards (Buteo buteo) [3,4]. By histology, these birds showed meningitis and encephalitis, characterized by gliosis and inflammation of the grey matter, neuronal degeneration and necrosis, and perivascular cuffing. These brain lesions were associated with influenza virus antigen expression in neurons and cells of the glia, ependyma and choroid plexus . Additional lesions outside the brain were necrosis in liver, exocrine pancreas, adrenal glands and spleen, and hemorrhage in lungs and heart .
Since several raptor species selectively hunt moribund or otherwise conspicuous prey, including waterbirds, or scavenge on their carcasses, they may be assumed to have a high rate of exposure to H5N1 during outbreaks of this virus. However, there are only rare case reports of natural H5N1 infection in raptors: common buzzard [3,5,6], mountain hawk-eagle (Spizaetus nipalensis) [7,8], and saker falcon (Falco cherrug) , with limited information on virus distribution and associated lesions. Therefore, our goal was to determine whether raptors exposed to H5N1 during an outbreak in wild waterbirds suffered fatal disease, and—if so—how the H5N1-associated lesions compared to those in other avian species. To do so, we tested all raptors that were found dead in the region Mecklenburg-Western Pomerania during the H5N1 outbreak in 2006 for H5N1 by RT-PCR of tracheal and/or cloacal swabs, and performed full necropsies on a selection of these birds for the presence of H5N1-associated lesions.
RT-PCR results in swabs of wild raptor species found dead in Mecklenburg-Western Pomerania in 2006
Number of birds
Common buzzard (Buteo buteo)
Eurasian sparrow hawk (Accipiter nisus)
Common kestrel (Falco tinnunculus)
Buzzard, species undetermined (Buteo sp.)
White-tailed sea eagle (Haliaeetus albicilla)
Raptors, species undetermined
Northern goshawk (Accipiter gentilis)
Peregrine falcon (Falco peregrinus)
Red kite (Milvus milvus)
Rough-legged buzzard (Buteo lagopus)
Western marsh harrier (Circus aeruginosus)
Sex and age of selected raptor species found dead in Mecklenburg-Western Pomerania in 2006
White-tailed sea eagle
Both selection of carcasses for necropsy and level of sampling of necropsied carcasses differed between white-tailed sea eagles (Haliaeetus albicilla) and other raptor species. For white-tailed sea eagles, all 19 individuals underwent necropsy, regardless whether their swabs tested positive or negative for H5N1, and tissue samples of lung, liver, spleen, kidney, pancreas and brain were collected for virology and stored at −70 °C until analysis. Duplicate samples of the same tissues were collected for histopathology and immunohistochemistry and fixed in 10% neutral-buffered formalin until analysis. For other raptor species, only individuals with H5N1-positive swabs and either freshly dead or intact and expected to be in a mild state of autolysis underwent necropsy: six common buzzards (B1 to B6) and two peregrine falcons (Falco peregrinus) (F1 and F2). During this necropsy, tissue samples of nasal turbinate, air sac, trachea, bronchus, lung, heart, liver, spleen, kidney, adrenal gland, pancreas, stomach, jejunum, colon, cerebrum, cerebellum, reproductive tract and cloacal bursa (or cloacal area if cloacal bursa was not visible) were collected for virology and stored at −70 °C until analysis. Duplicate samples of the same tissues were collected for histopathology and immunohistochemistry and fixed in 10% neutral-buffered formalin until analysis. In addition, separate pharyngeal and cloacal swabs for virology were placed in Hank’s balanced salt solution containing 0.5% lactalbumin, 10% glycerol, 200 U/mL penicillin, 200 μg/mL streptomycin, 100 U/mL polymyxin B sulfate, 250 μg/mL gentamycin, and 50 U/mL nystatin (ICN Pharmaceuticals, Zoetermeer, The Netherlands), and stored at −70 °C until analysis.
Swabs were examined by testing extracted total RNA for the presence of influenza A virus matrix gene-fragment by RT-PCR. A positive result was followed by further subtype differentiation using real-time RT-PCR targeting fragments of the H5 and N1 genes . Tissue samples were weighed and subsequently homogenized with a FastPrep-24 (MP Biomedicals, Eindhoven, The Netherlands) in Hank’s balanced salt solution and centrifuged briefly before dilution. Quadruplicate 10-fold serial dilutions of tissue samples and swab supernatants (separate pharyngeal and cloacal swabs from common buzzards, B1 to B6, and peregrine falcons, F1 and F2, only) were used to determine the virus titers in confluent layers of Madin-Darby canine kidney cells as described previously .
Histopathology and immunohistochemistry
Formalin-fixed tissue samples from common buzzards, B1 to B6, and peregrine falcons, F1 and F2, were embedded in paraffin, sectioned at 4 μm, and stained with hematoxylin and eosin (HE) for histopathological examination by light microscopy. For immunohistochemical detection of influenza virus antigen, duplicate sections of the same tissue samples were stained with a primary antibody against the influenza A nucleoprotein as described previously . Peroxidase activity was revealed using 3-amino-9-ethylcarbazole (AEC) (Sigma, St Louis, MO, USA), resulting in a bright red precipitate. In each staining procedure an isotype control was included as a negative control and a lung section from an H5N1-infected cat was included as a positive control .
RT-PCR results and virus titers in swabs and organs of selected H5N1-infected wild raptors
RT-PCR values* (virus titers)**
By virus culture, pharyngeal swabs of necropsied common buzzards and peregrine falcons tested positive for H5N1 more frequently than cloacal swabs (Table 3). Far fewer tissue samples tested positive for H5N1 by virus culture than by RT-PCR (Table 3): H5N1 was consistently cultured only from brain and lung samples in both common buzzards and peregrine falcons, always with the highest titers in brain samples.
The nutritional state of the white-tailed sea eagles ranged from poor to good. All common buzzards and peregrine falcons were in poor nutritional state, lacking fat in the subcutis or body cavity, and showing mild to advanced atrophy of the breast muscles. Externally, no lesions were found. Internally, there were lesions in several organs: multifocal hemorrhage in the pancreas (B2 and B3); increased redness in the cerebrum (B1, B2, B3, B5, and F2); enlargement of the spleen (B1, B2 and B6) and kidneys (B1, B2, and B5); wet lungs (B4, B5, B6 and F2); many nematodes (most likely Serratospiculum sp.) in the abdominal air sac (F1 and F2), and multifocal hemorrhage in thorax or upper respiratory tract, suggestive of trauma (F1 and F2). Freeze-thaw artifacts and autolytic changes often hampered gross examination.
By immunohistochemistry, influenza virus antigen expression was visible as diffuse red staining mainly in the cytoplasm and occasionally in the nucleus of affected cells. Virus antigen expression was found in multiple tissues (Figure 1) and was associated with histopathological changes. Virus antigen expression was seen most frequently in the brain (all birds) and air sac (B1-3, B5, B6 and F1). In the brain there were multiple foci of positive cells in the cerebrum of all common buzzards and peregrine falcons and in the cerebellum of some birds. In the brain, many neurons and—in one peregrine falcon, F2—ependymal cells, and few glial cells expressed virus antigen. In the coelomic ganglion (B4 and F2), many neurons expressed virus antigen. In the air sac, oviduct (B1, B2 and F1), and bronchus (F2), few epithelial cells expressed virus antigen. In the heart (B2, B4 and B5), few myocardial cells expressed antigen. In multiple granulomas in the adrenal gland of one common buzzard (B5), many macrophages expressed antigen. In the pancreas (F1 and F2), moderate numbers of pancreatic acinar cells expressed antigen.
Our study shows that, during the 2006 H5N1 outbreak in wild waterbirds in Mecklenburg- Western Pomerania, Germany, both common buzzards and peregrine falcons were exposed to and suffered fatal disease from H5N1 infection, while seven other raptor species examined showed no evidence of H5N1 infection. In both species, H5N1 showed a distinct neurotropism associated with marked encephalitis, comparable to that observed in most other susceptible wild bird species.
The differences in diet and hunting or scavenging behavior among the nine raptor species was likely an important factor in their exposure to H5N1 in the 2006 outbreak in Germany. This outbreak affected mainly swans, geese, gulls, and diving ducks, all medium-sized birds  and the viruses of the waterbirds were closely related to the virus found in a common buzzard that tested positive for H5N1 in the same period and the same area . The Eurasian sparrowhawk and common kestrel do not eat carrion and hunt only small (passerine) birds [15,16] or small mammals ; this could explain why H5N1 was not detected in either raptor species, despite the relatively high number of individuals examined. In contrast, the common buzzard and peregrine falcon, both of which were found positive for H5N1, do hunt medium-sized birds—common buzzards up to the size of a pheasant (~1200 g) ; peregrine falcons mainly in the range 20 to 300 g for males, and 100–1000 g for females [18,19]—or feed on carrion (common buzzard) . (Interestingly, both H5N1-positive peregrine falcons were females.) The remaining five raptor species (white-tailed sea eagle, northern goshawk, red kite, rough-legged buzzard, and western marsh-harrier) all are known to hunt medium-sized birds and—except for the northern goshawk—to eat carrion, and therefore were at risk of exposure to H5N1 during the outbreak. Remarkably, the white-tailed sea eagles which feed on waterbirds up to the size of swans and also on carrion, were tested negative. The reason why H5N1 was not detected in any individuals of these five species may be due to the small sample size. Alternatively, it may be due to a species-specific resistance to disease from H5N1 infection, similar to that seen in other avian species. For example, in experimental H5N1 infection of six different duck species, tufted ducks (Aythya fuligula) and Eurasian pochards (A. ferina) showed clinical signs of disease, while the remaining four species, all dabbling ducks belonging to the genus Anas, were clinically unaffected .
The tissue tropism of H5N1 and the character of the associated lesions in these common buzzards and peregrine falcons correspond with those seen previously in other avian species (reviewed in [22,23], including naturally [3,5,6,24] and experimentally [25,26] H5N1 infected raptors. H5N1 in these common buzzards and peregrine falcons was clearly neurotropic and associated with marked encephalitis, similar to that seen in naturally infected common buzzards from Germany  and Sweden  and in experimentally infected American kestrels (Falco sparverius) . The detection of influenza virus antigen expression and associated lesions in the coelomic ganglion in our birds indicates neurotropism for both the peripheral and central nervous systems. Besides the nervous system, H5N1 in our common buzzards and peregrine falcons also had tropism for other organs, including pancreas, heart, lung, air sac and oviduct. Such pantropism corresponds with that found in other bird species (reviewed in [22,23]. The specific tropism of H5N1 for the pancreas in our peregrine falcons also has been noted in experimental H5N1 infection of American kestrels . In contrast to different swan species, where H5N1 exhibited endotheliotropism , no influenza virus antigen expression was seen in endothelial cells of any of these common buzzards or peregrine falcons.
The discrepancy between the results in the immunohistochemistry, RT-PCR and virus titration can most likely be attributed to the extended storage time in the −20 °C freezer and to the difference in sensitivity of the tests. Also, autolysis before storage and freezing artifacts hampered the necropsy and data analyses.
Although it is likely that these common buzzards and peregrine falcons became infected with H5N1 because of feeding on H5N1-contaminated carcasses, as has been shown experimentally in gulls , it is not clear by which of three potential portals of entry H5N1 gained entrance. The first possible portal of entry is the intestine, as proven by direct gastric inoculation of H5N1 in different experimental mammals [28-31]. A second possible portal of entry is the olfactory nerve: this was proven by intranasal inoculation of H5N1 in ferrets, in which viral replication in the olfactory mucosa was followed by spread to the olfactory bulb, and from there to the rest of the central nervous system . The third possible portal of entry is the respiratory tract. Because H5N1-contaminated meat in these common buzzards and peregrine falcons would have passed the throat, which is the cross-roads between digestive and respiratory tracts, this latter portal of entry cannot be excluded. More extensive sampling of H5N1-infected raptors at different time points after infection may elucidate the portal of entry and subsequent pathogenesis of H5N1 infection in raptors.
In conclusion, our study implies that the position of raptors at the top of the food pyramid puts them at risk of acquiring infectious pathogens such as H5N1 by eating sick or dead prey. Because of their broad geographic range and migratory nature, they may contribute to long-distance movement of such pathogens; however, this contribution is likely much smaller than that of more numerous species of migratory birds. Our data suggest that some raptor species, such as common buzzards and peregrine falcons, are more likely to eat sick or dead wild waterbirds and subsequently are more exposed to H5N1 infection than other species, such as Eurasian sparrowhawks and common kestrels. Whether there is species-specific resistance to disease from H5N1 infection in some raptor species, such as white-tailed sea eagles, remains to be determined.
We are grateful for the excellent technical assistance provided by D. de Meulder and P. van Run, and for the figure preparation by F. van der Panne.
- Liu J, Xiao H, Lei F, Zhu Q, Qin K, Zhang XW, Zhang XL, Zhao D, Wang G, Feng Y, Ma J, Liu W, Wang J, Gao GF (2005) Highly pathogenic H5N1 influenza virus infection in migratory birds. Science 309:1206View ArticlePubMedGoogle Scholar
- Chen H, Smith GJ, Zhang SY, Qin K, Wang J, Li KS, Webster RG, Peiris JS, Guan Y (2005) Avian flu: H5N1 virus outbreak in migratory waterfowl. Nature 436:191–192View ArticlePubMedGoogle Scholar
- Teifke JP, Klopfleisch R, Globig A, Starick E, Hoffmann B, Wolf PU, Beer M, Mettenleiter TC, Harder TC (2007) Pathology of natural infections by H5N1 highly pathogenic avian influenza virus in mute (Cygnus olor) and whooper (Cygnus cygnus) swans. Vet Pathol 44:137–143View ArticlePubMedGoogle Scholar
- Starick E, Beer M, Hoffmann B, Staubach C, Werner O, Globig A, Strebelow G, Grund C, Durban M, Conraths FJ, Mettenleiter T, Harder T (2008) Phylogenetic analyses of highly pathogenic avian influenza virus isolates from Germany in 2006 and 2007 suggest at least three separate introductions of H5N1 virus. Vet Microbiol 128:243–252View ArticlePubMedGoogle Scholar
- Brojer C, Agren EO, Uhlhorn H, Bernodt K, Jansson DS, Gavier-Widen D (2012) Characterization of encephalitis in wild birds naturally infected by highly pathogenic avian influenza H5N1. Avian Dis 56:144–152View ArticlePubMedGoogle Scholar
- Marinova-Petkova A, Georgiev G, Seiler P, Darnell D, Franks J, Krauss S, Webby RJ, Webster RG (2012) Spread of influenza virus A (H5N1) clade 126.96.36.199 to Bulgaria in common buzzards. Emerg Infect Dis 18:1596–1602View ArticlePubMed CentralPubMedGoogle Scholar
- Marjuki H, Wernery U, Yen HL, Franks J, Seiler P, Walker D, Krauss S, Webster RG (2009) Isolation of highly pathogenic avian influenza H5N1 virus from Saker falcons (Falco cherrug) in the Middle East. Adv Virol 2009:1View ArticlePubMedGoogle Scholar
- Van Borm S, Thomas I, Hanquet G, Lambrecht B, Boschmans M, Dupont G, Decaestecker M, Snacken R, van den Berg T (2005) Highly pathogenic H5N1 influenza virus in smuggled Thai eagles, Belgium. Emerg Infect Dis 11:702–705View ArticlePubMed CentralPubMedGoogle Scholar
- Landesamt für Landwirtschaft, Lebensmittelsicherheit und Fischerei Meckelenburg-Vorpommern: Jahrbuch 2006. 1.1 Aviäre influenza (Hausgeflügel, Wildvögel, Säugetiere). 2007, pp. 9–11.Google Scholar
- Spackman E, Senne DA, Myers TJ, Bulaga LL, Garber LP, Perdue ML, Lohman K, Daum LT, Suarez DL (2002) Development of a real-time reverse transcriptase PCR assay for type A influenza virus and the avian H5 and H7 hemagglutinin subtypes. J Clin Microbiol 40:3256–3260View ArticlePubMed CentralPubMedGoogle Scholar
- Rimmelzwaan GF, Baars M, Claas EC, Osterhaus AD (1998) Comparison of RNA hybridization, hemagglutination assay, titration of infectious virus and immunofluorescence as methods for monitoring influenza virus replication in vitro. J Virol Methods 74:57–66View ArticlePubMedGoogle Scholar
- van den Brand JM, Stittelaar KJ, Leijten LM, van Amerongen G, Simon JH, Osterhaus AD, Kuiken T (2012) Modification of the ferret model for pneumonia from seasonal human influenza A virus infection. Vet Pathol 49:562–568View ArticlePubMedGoogle Scholar
- Kuiken T, Rimmelzwaan G, van Riel D, van Amerongen G, Baars M, Fouchier R, Osterhaus A (2004) Avian H5N1 influenza in cats. Science 306:241View ArticlePubMedGoogle Scholar
- Globig A, Baumer A, Revilla-Fernandez S, Beer M, Wodak E, Fink M, Greber N, Harder TC, Wilking H, Brunhart I, Matthes D, Kraatz U, Strunk P, Fiedler W, Fereidouni SR, Staubach C, Conraths FJ, Griot C, Mettenleiter TC, Stärk KD (2009) Ducks as sentinels for avian influenza in wild birds. Emerg Infect Dis 15:1633–1636View ArticlePubMed CentralPubMedGoogle Scholar
- Thiollay JM (1994) Family Accipitridae. In: del Hoyo J, Elliot A, Sargatal J (ed) Handbook of the birds of the world. Volume 2. Barcelona, Spain, Lynx edicions, p 185Google Scholar
- Newton I (1986) The sparrowhawk. Staffordshire, England, Poyser MonographsGoogle Scholar
- Village A (2010) The kestrel. London, England, Poyser MonographsGoogle Scholar
- White CM, Olsen PD, Kiff LF (1994) Family Falconidae. In: del Hoyo J, Elliot A, Sargatal J (ed) Handbook of the birds of the world. Volume 2. Lynx Edicions, Barcelona, Spain, p 274Google Scholar
- Ratcliffe D (1993) The peregrine falcon. London, England, Poyser MonographsGoogle Scholar
- Melde M (1983) Der Mäusebussard. Magdenburg, Germany, Neue Brehm BüchereiGoogle Scholar
- Keawcharoen J, van Riel D, van Amerongen G, Bestebroer T, Beyer WE, van Lavieren R, Osterhaus AD, Fouchier RA, Kuiken T (2008) Wild ducks as long-distance vectors of highly pathogenic avian influenza virus (H5N1). Emerg Infect Dis 14:600–607View ArticlePubMed CentralPubMedGoogle Scholar
- Pantin-Jackwood MJ, Swayne DE (2009) Pathogenesis and pathobiology of avian influenza virus infection in birds. Rev Sci Tech 28:113–136PubMedGoogle Scholar
- Kuiken T, van den Brand J, van Riel D, Pantin-Jackwood M, Swayne DE (2010) Comparative pathology of select agent influenza a virus infections. Vet Pathol 47:893–914View ArticlePubMedGoogle Scholar
- Shivakoti S, Ito H, Otsuki K, Ito T (2010) Characterization of H5N1 highly pathogenic avian influenza virus isolated from a mountain hawk eagle in Japan. J Vet Med Sci 72:459–463View ArticlePubMedGoogle Scholar
- Hall JS, Ip HS, Franson JC, Meteyer C, Nashold S, TeSlaa JL, French J, Redig P, Brand C (2009) Experimental infection of a North American raptor, American Kestrel (Falco sparverius), with highly pathogenic avian influenza virus (H5N1). PLoS One 4:e7555View ArticlePubMed CentralPubMedGoogle Scholar
- Bertran K, Busquets N, Abad FX (2012) Garcia de la Fuente J, Solanes D, Cordon I, Costa T, Dolz R, Majo N: Highly (H5N1) and low (H7N2) pathogenic avian influenza virus infection in falcons via nasochoanal route and ingestion of experimentally infected prey. PLoS One 7:e32107View ArticlePubMed CentralPubMedGoogle Scholar
- Brown JD, Stallknecht DE, Beck JR, Suarez DL, Swayne DE (2006) Susceptibility of North American ducks and gulls to H5N1 highly pathogenic avian influenza viruses. Emerg Infect Dis 12:1663–1670View ArticlePubMed CentralPubMedGoogle Scholar
- Lipatov AS, Kwon YK, Pantin-Jackwood MJ, Swayne DE (2009) Pathogenesis of H5N1 influenza virus infections in mice and ferret models differs according to respiratory tract or digestive system exposure. J Infect Dis 199:717–725View ArticlePubMedGoogle Scholar
- Vahlenkamp TW, Teifke JP, Harder TC, Beer M, Mettenleiter TC (2010) Systemic influenza virus H5N1 infection in cats after gastrointestinal exposure. Influenza Other Respir Viruses 4:379–386View ArticlePubMedGoogle Scholar
- Reperant LA, van de Bildt MW, van Amerongen G, Leijten LM, Watson S, Palser A, Kellam P, Eissens AC, Frijlink HW, Osterhaus AD, Kuiken T (2012) Marked endotheliotropism of highly pathogenic avian influenza virus H5N1 following intestinal inoculation in cats. J Virol 86:1158–1165View ArticlePubMed CentralPubMedGoogle Scholar
- Shinya K, Makino A, Tanaka H, Hatta M, Watanabe T, Le MQ, Imai H, Kawaoka Y (2011) Systemic dissemination of H5N1 influenza A viruses in ferrets and hamsters after direct intragastric inoculation. J Virol 85:4673–4678View ArticlePubMed CentralPubMedGoogle Scholar
- Schrauwen EJ, Herfst S, Leijten LM, van Run P, Bestebroer TM, Linster M, Bodewes R, Kreijtz JH, Rimmelzwaan GF, Osterhaus AD, Fouchier RA, Kuiken T, van Riel D (2012) The multibasic cleavage site in H5N1 virus is critical for systemic spread along the olfactory and hematogenous routes in ferrets. J Virol 86:3975–3984View ArticlePubMed CentralPubMedGoogle Scholar
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