Concurrent avian malaria and avipox virus infection in translocated South Island saddlebacks (Philesturnus carunculatus carunculatus)

Abstract CASE HISTORY: Outbreaks of mortality in South Island saddlebacks (Philesturnus carunculatus carunculatus) that had been translocated to two offshore islands in the Marlborough Sounds of New Zealand were investigated during the summer of 2002 and 2007. Both outbreaks were associated with a severe decrease in numbers of saddlebacks of up to 60% of approximately 200 birds. CLINICAL AND PATHOLOGICAL FINDINGS: Many of the surviving birds were in poor condition, and had skin lesions on the legs and head. Necropsy showed pale liver and lungs, and a swollen spleen. Histopathology revealed schizonts resembling Plasmodium spp. within the cytoplasm of many hepatocytes and splenic histiocytes. The skin lesions consisted of epithelial proliferations containing numerous Bollinger bodies typical of avipox virus (APV) infection. Two different APV were isolated, using PCR, from two different birds exhibiting skin lesions. Each isolate had 100% sequence homology with APV members from either Clade A or Clade B. In addition, PCR analysis revealed that the Plasmodium elongatum present in infected birdsbelonged to a strain that was endemic in the population of North Island saddlebacks (Philesturnus carunculatus rufusater). DIAGNOSIS: Concurrent infections with Plasmodium spp. haemoparasites and APV were identified as the likely cause of death in the birds examined. CONCLUSIONS AND CLINICAL RELEVANCE: Although the Plasmodium spp. identified is thought to be endemic to saddlebacks in New Zealand, the affected birds were likely to be immunocompromised by concurrent APV infection or through lack of genetic diversity. Both the introduced mosquito Culex quinquefasicatus and the native mosquito Culex pervigilans are likely vectors for both these diseases, and the provision of water supplies less favourable to mosquito-breeding is recommended.

[1]  G. Sironi,et al.  Molecular biological characterization of avian poxvirus strains isolated from different avian species. , 2010, Veterinary microbiology.

[2]  D. G. Martin,et al.  An outbreak of avian malaria in captive yellowheads/mohua (Mohoua ochrocephala) , 2008, New Zealand Veterinary Journal.

[3]  D. Phalen,et al.  Lymphatic and Hematopoietic System , 2008 .

[4]  S. Bensch,et al.  Polymerase chain reaction-based identification of Plasmodium (Huffia) elongatum, with remarks on species identity of haemosporidian lineages deposited in GenBank , 2008, Parasitology Research.

[5]  K. Hale Disease outbreak amongst South Island saddlebacks ( Philesturnus carunculatus carunculatus ) on Long Island , 2008 .

[6]  I. Jamieson,et al.  Historic and contemporary levels of genetic variation in two New Zealand passerines with different histories of decline , 2007, Journal of evolutionary biology.

[7]  D. Tompkins,et al.  Avian malaria (Plasmodium spp) in yellow-eyed penguins: Investigating the cause of high seroprevalence but low observed infection , 2007, New Zealand veterinary journal.

[8]  C. Atkinson,et al.  Infectious Diseases of Wild Birds , 2007 .

[9]  C. Riper Avian Malaria Parasites and Other Haemosporidia , 2007 .

[10]  K. Hale Population bottlenecks and the risk of parasitic and microbiological infections in the endangered saddleback (Philesturnus carunculatus) and South Island robin (Petroica a. australis) , 2007 .

[11]  J. Derraik,et al.  Anthropogenic Environmental Change, Mosquito-borne Diseases and Human Health in New Zealand , 2007, EcoHealth.

[12]  J. Meers,et al.  Evaluation of immune effects of fowlpox vaccine strains and field isolates. , 2006, Veterinary microbiology.

[13]  R. E. Gough,et al.  Avipoxvirus phylogenetics: identification of a PCR length polymorphism that discriminates between the two major clades. , 2006, The Journal of general virology.

[14]  D. Tompkins,et al.  Relationship between avian malaria distribution and an exotic invasive mosquito in New Zealand , 2006 .

[15]  S. Feldman,et al.  Phylogenetic Analysis of Avian Poxviruses Among Free-Ranging Birds of Virginia , 2005, Avian diseases.

[16]  G. Valkiūnas Avian Malaria Parasites and other Haemosporidia , 2004 .

[17]  H. Hafez,et al.  Differentiation of Avian Poxvirus Strains on the Basis of Nucleotide Sequences of 4b Gene Fragment , 2004, Avian diseases.

[18]  S. Bensch,et al.  A NEW PCR ASSAY FOR SIMULTANEOUS STUDIES OF LEUCOCYTOZOON, PLASMODIUM, AND HAEMOPROTEUS FROM AVIAN BLOOD , 2004, The Journal of parasitology.

[19]  T. Traavik,et al.  Analysis and comparison of the 4b core protein gene of avipoxviruses from wild birds: Evidence for interspecies spatial phylogenetic variation , 2004, Archives of Virology.

[20]  W. Suedmeyer Pathology of Pet and Aviary Birds , 2009 .

[21]  D. Phalen,et al.  Pathology of Pet and Aviary Birds , 2003 .

[22]  M. Alley Avian wildlife diseases in New Zealand: current issues and achievements , 2002, New Zealand veterinary journal.

[23]  H. Robertson,et al.  The Field Guide to the Birds of New Zealand , 1996 .

[24]  G. Speckmann,et al.  Zoo and Wild Animal Medicine. , 1986 .

[25]  M. Fowler Zoo and wild animal medicine , 1978 .

[26]  Griner La Some diseases of zoo animals. , 1974 .

[27]  R. Warner THE ROLE OF INTRODUCED DISEASES IN THE EXTINCTION OF THE ENDEMIC HAWAIIAN AVIFAUNA , 1968 .