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Volume 15, Number 3—March 2009
Dispatch

Highly Pathogenic Avian Influenza Virus (H5N1) Outbreak in Captive Wild Birds and Cats, Cambodia

Author affiliations: Centre de Cooperation Internationale en Recherche Agronomique pour le Développement, Montpellier, France (S. Desvaux, N. Gaidet); WildAid, Phnom Penh, Cambodia (N. Marx, M. Hunt); Institut Pasteur du Cambodge, Phnom Penh (S. Ong, J.-M. Reynes); Institut Pasteur, Paris, France (J.-C. Manuguerra, S. Van der Werf); National Animal Health and Production Investigation Center, Phnom Penh (S. Sorn); University of Hong Kong and Queen Marie Hospital, Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China (M. Peiris)

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Abstract

From December 2003 through January 2004, the Phnom Tamao Wildlife Rescue Centre, Cambodia, was affected by the highly pathogenic influenza virus (H5N1). Birds from 26 species died. Influenza virus subtype H5N1 was detected in 6 of 7 species tested. Cats from 5 of 7 species were probably infected; none died.

On January 24, 2004, the first confirmed outbreak of highly pathogenic avian influenza virus (HPAIV) subtype H5N1 in Cambodia was reported to the Office International des Epizooties (1). During the previous month, an unusually high mortality rate had been noted among captive wild birds at the Phnom Tamao Wildlife Rescue Centre (PTWRC) in Takeo Province, 45 km South from Phnom Penh. We report the results of a retrospective investigation of this outbreak.

The Study

Figure

Thumbnail of Map of the 3 main sections of the Phnom Tamao Wildlife Rescue Centre, Cambodia, during outbreak of highly pathogenic avian influenza virus (H5N1), December 15, 2003–January 13, 2004. Shaded areas indicate contaminated cages (labeled with date of outbreak). NA, exact cage not available.

Figure. Map of the 3 main sections of the Phnom Tamao Wildlife Rescue Centre, Cambodia, during outbreak of highly pathogenic avian influenza virus (H5N1), December 15, 2003–January 13, 2004. Shaded areas indicate...

During the outbreak period, PTWRC housed 600–1,000 wild animals (70 species of mammals, birds, and reptiles). The center is divided into 3 main sections that cover 37 ha. Birds were kept in sections S1–1, S1–2, and S2, and the cats were in all sections (Figure). The information on bird deaths at PTWRC was systematically recorded by WildAid staff members who were at the Centre at the time of the outbreak. In June 2004, a complete investigation was conducted at PTWRC, and semistructured interviews of key informants were used to identify deaths of domestic poultry in the surrounding villages. Every bird death between December 15, 2003, through January 15, 2004, was defined as a suspected case of HPAIV (H5N1). For S1, the cumulative mortality rate could not be estimated because the exact bird population was not known and the birds were difficult to observe in that section (the semicaptive waterfowl population is able to mix with the wild population and disperse to breed). For S2, information was complete (Table 1).

The first case, in a crested serpent eagle (Spilornis cheela), was reported on December 15, 2003, in S2 (Figure). On December 19, the outbreak had reached every section and continued until January 12; a total of 86 birds, representing 8 taxonomic orders and 12 families, died (Table 1). Of 7 cat species, cats from 5 species were reported sick (16/39 total cats) (Table 2). In S2, 80% of the reported bird deaths were observed from December 15 to 21. Of the 29 wild bird species kept in S2 at the beginning of the outbreak, no birds from 12 species showed signs of disease (Table 1). Mortality rates varied among the orders, 0–100% (Table 1). The only mammals present in the aviaries in S2, slow lorises (Nycticebus sp.), did not become ill. None of the 27 animal keepers, who were 20–50 years of age, were reported to have gotten sick.

Most of the birds died within a few hours without showing any clinical signs of infection. A few birds died 1–2 days after onset of clinical signs (anorexia, extreme lethargy, occasional dark green diarrhea, respiratory distress, and neurologic abnormalities). The cats were sick for 5–7 days and exhibited anorexia and lethargy but no respiratory illness.

Laboratory investigations of the organs from 8 birds sampled in December 2003 were performed (Table 1). For those birds, West Nile virus infection was ruled out by reverse transcription–PCR (RT-PCR), according to the procedure described by Lanciotti et al. (2). All birds sampled, except a parakeet, were positive for influenza subtype H5N1 by RT-PCR (3) (Table 1). Molecular characterizations of hemagglutinin (H)5 and neuraminidase (N)1 were performed from the influenza virus (H5N1) strains from PTWRC as previously described (4). H5 amino acid sequences were identical in the coding region to the sequence of isolates obtained from poultry cases in Cambodia (ill poultry from a flock with high mortality rates) and similar (>96.5%) to HPAIV (H5N1) strain H5 sequences from Vietnam and Thailand in 2004 (data not shown). All belonged to the H5 clade 1 (4). Amino acid sequences from N1 from Cambodia were very close to each other (>97.12% identity) and to 2004 Vietnamese and Thai N1 sequences (>96%) (data not shown). The HA and NA sequences of the isolates were deposited in GenBank (accession nos. ISDN186319–ISN186324, ISDN186329, ISDN186330–ISDN186665, and ISDN242365).

Retrospective investigation of the villages surrounding the PTWRC and Phnom Penh showed that chickens from 2 flocks in which deaths had been reported in mid-December had been provided to the PTWRC, either for the restaurants or for the captive animal feeding. Furthermore, at the time of the outbreak, many wild crows were found dead in the forest surrounding the PTWRC.

The 4 cat serum samples, each from a different species, were positive for HPAIV (H5N1) with serum neutralization test (5); titers ranged from 10 to 40 (Table 2). None of the affected cats died.

Conclusions

The sources of introduction of HPAIV (H5N1) within the PTWRC were probably multiple: virus-infected chicken bought to feed the carnivorous species, infected live chickens brought to restaurants near S2 (i.e., the first place where deaths were detected), and contact between infected wild and captive birds. The introduction through infected chickens is supported by the absence of an outbreak at the PTWRC after the feeding of chickens to carnivorous species was discontinued; however, deaths in domestic poultry continued in the area. In addition, almost all carnivorous bird species in S2 died (93% of Falconiformes and 92% of Strigiformes) as did most species usually fed chicken meat in captivity (herons, storks, crows, great hornbill, pelican). Diet was also the origin of the outbreak among tigers and leopards in Thailand (6,7). The dispersion of the disease between PTWRD sections was probably due to poor biosecurity measures.

The clinical outcome of wild birds with suspected HPAIV (H5N1) infection at PTWRC ranged from severe illness and death to complete absence of clinical signs, as described (8). Several species from the orders Ciconiiformes, Galliformes, Passeriformes, Gruiformes, Coraciiformes, and Pelecaniformes were affected during the outbreak. This observation is consistent with data published earlier, except for Coraciiformes represented by 1 bird in our study (9). Only the carnivorous species (Corvus macrorynchos) among the 5 species of Passeriformes in the aviaries showed clinical signs and later was confirmed by RT-PCR to be positive for HPAIV (H5N1). This outbreak confirms that Falconiformes and Strigiformes are sensitive to HPAIV (H5N1) infection and disease (1012) and shows that numerous species of these orders can be affected by HPAIV (H5N1) (Table 1). Psittaciformes and Columbiformes were not visibly affected by the outbreak although they were kept in large numbers in S2, where large numbers of deaths occurred. As non–water-bird species, they do not belong to groups in which avian influenza is commonly reported (13). Anseriformes, represented in PTWRC by only 4 birds (Anas poecilorhyncha), did not show any clinical signs. Heterogeneity in the susceptibility of wild ducks to HPAIV (H5N1), including asymptomatic infection, has been demonstrated (14); this species also belongs to the group of wild ducks found asymptomatically infected with HPAIV (H5N1) in the People’s Republic of China during the winter of 2005 (15).

The serologic evidence of influenza virus (H5N1) infection in 4 species of wild cats is in agreement with previous infection in Thailand (6,7). The report of illness in the Asiatic golden cat (Catopuma temminckii) and the clouded leopard (Neofelis nebulosa) broadens the host range of the virus among mammals.

This report confirms the great variability of wild bird and mammal responses to HPAIV (H5N1) infection. It also confirms the broadening range of susceptible species that may be specific to this clade 1 virus.

Dr Desvaux is a veterinary epidemiologist working at the Centre de Cooperation Internationale en Recherche Agronomique pour le Développement. Her current research interests focus on HPAIV epidemiology and surveillance in Vietnam.

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References

  1. World Organisation for Animal Health. Update on highly pathogenic avian influenza in animals (type H5 and H7) [cited 2008 May 31]. Available from http://www.oie.int/downld/AVIAN%20INFLUENZA/A2004_AI.php
  2. Lanciotti  RS, Calisher  CH, Gubler  DJ, Chang  GJ, Vance-Vorndam  A. Rapid detection and typing of dengue viruses from clinical samples by using reverse transcriptase-polymerase chain reaction. J Clin Microbiol. 1992;30:54551.PubMedGoogle Scholar
  3. World Organisation for Animal Health. Recommended laboratory tests to identify influenza A/H5 virus in specimens from patients with an influenza-like illness. 19 February 2004 [cited 2005 Jun 12]. Available from http://www.who.int/csr/disease/avian_influenza/guidelines/en/avian_labtests1.pdf
  4. The World Health Organization Global Influenza Program Surveillance Network. Evolution of H5N1 avian influenza viruses in Asia. Emerg Infect Dis. 2005;11:151521.PubMedGoogle Scholar
  5. Choi  YK, Nguyen  TD, Ozaki  H, Webby  RJ, Puthavathana  P, Buranathal  C, Studies of H5N1 influenza virus infection of pigs by using viruses isolated in Vietnam and Thailand in 2004. J Virol. 2005;79:108215. DOIPubMedGoogle Scholar
  6. Keawcharoen  J, Oraveerakul  K, Kuiken  T, Fouchier  RAM, Amonsin  A, Payungporn  S, Avian influenza H5N1 in tigers and leopards. Emerg Infect Dis. 2004;10:218991.PubMedGoogle Scholar
  7. Thanawongnuwech  R, Amonsin  A, Tantilertcharoen  R, Damrongwatanapokin  S, Theamboonlers  A, Payungporn  S, Probable tiger-to-tiger transmission of avian influenza H5N1. Emerg Infect Dis. 2005;11:699701.PubMedGoogle Scholar
  8. Webster  RG, Hulse  DJ. Microbial adaptation and change: avian influenza. Rev Sci Tech. 2004;23:45365.PubMedGoogle Scholar
  9. Whitworth  D, Newman  SH, Mundkur  T, Harris  P, eds. Wild birds and avian influenza: an introduction to applied field research and disease sampling techniques. Rome (Italy): Food and Agriculture Organization, Animal Production and Health; 2007 [cited 2008 Jun 2]. Available from http://www.fao.org/avianflu/en/wildlife/info_res.htm
  10. World Organisation for Animal Health. Avian influenza in Hong Kong (Special Administrative Region of the People’s Republic of China) in a wild bird [in French]. Informations Sanitaires. 2004;17 [cited 2009 Jan 21]. Available from ftp://ftp.oie.int/infos_san_archives/fr/2004/fr_040130v17n05.pdf
  11. Van Borm  S, Thomas  I, Hanquet  G, Lambrecht  B, Boschmans  M, Dupont  G, Highly pathogenic H5N1 influenza virus in smuggled Thai eagles, Belgium. Emerg Infect Dis. 2005;11:7025.PubMedGoogle Scholar
  12. Sabirovic  M, Wilesmith  J, Hall  S, Coulson  N, Landeg  F. Outbreaks of HPAI H5N1 virus in Europe during 2005/2006. DEFRA, 2006 [cited 2009 Jan 21]. Available from http://collections.europarchive.org/tna/20080107205404/http://defra.gov.uk/animalh/diseases/monitoring/riskassess.htm
  13. Olsen  B, Munster  VJ, Wallensten  A, Waldenstrom  J, Osterhaus  AD, Fouchier  RA. Global patterns of influenza A virus in wild birds. Science. 2006;312:3848. DOIPubMedGoogle Scholar
  14. Brown  JD, Stallknecht  DE, Beck  JR, Suarez  DL, Swayne  DE. Susceptibility of North American ducks and gulls to H5N1 highly pathogenic avian influenza viruses. Emerg Infect Dis. 2006;12:166370.PubMedGoogle Scholar
  15. Chen  H, Smith  GJ, Li  KS, Wang  J, Fan  XH, Rayner  JM, Establishment of multiple sublineages of H5N1 influenza virus in Asia: implications for pandemic control. Proc Natl Acad Sci U S A. 2006;103:284550. DOIPubMedGoogle Scholar

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DOI: 10.3201/eid1503.071410

Table of Contents – Volume 15, Number 3—March 2009

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Stéphanie Desvaux, CIRAD, AGIRs, National Institute of Veterinary Research, 86 Truong Chinh, Hanoi, Vietnam;

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Page created: December 07, 2010
Page updated: December 07, 2010
Page reviewed: December 07, 2010
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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