Academic literature on the topic 'Bandicoot papillomatosis carcinomatosis viruses'

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Journal articles on the topic "Bandicoot papillomatosis carcinomatosis viruses"

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Chen, C. J., R. P. Kincaid, G. J. Seo, M. D. Bennett, and C. S. Sullivan. "Insights into Polyomaviridae MicroRNA Function Derived from Study of the Bandicoot Papillomatosis Carcinomatosis Viruses." Journal of Virology 85, no. 9 (February 23, 2011): 4487–500. http://dx.doi.org/10.1128/jvi.02557-10.

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Bennett, Mark D., Lucy Woolford, Amanda J. O'Hara, Kristin S. Warren, and Philip K. Nicholls. "In situ hybridization to detect bandicoot papillomatosis carcinomatosis virus type 1 in biopsies from endangered western barred bandicoots (Perameles bougainville)." Journal of General Virology 89, no. 2 (February 1, 2008): 419–23. http://dx.doi.org/10.1099/vir.0.83455-0.

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The western barred bandicoot (Perameles bougainville) is an endangered Australian marsupial species in which a papillomatosis and carcinomatosis syndrome occurs. Bandicoot papillomatosis carcinomatosis virus type 1 (BPCV1) is associated with the lesions of this progressively debilitating syndrome. Five digoxigenin-labelled DNA probes were generated for in situ hybridization (ISH) and the technique was optimized and performed on formalin-fixed paraffin-embedded (FFPE) biopsies. Staining of keratinocyte and sebocyte nuclei within lesions was achieved with all five probes. The sensitivity of ISH (76.9 %) surpassed that of PCR (30.8 %) for FFPE samples. The sensitivity of ISH varied from 81 % (papillomas) and 70 % (carcinoma in situ) to 29 % (squamous cell carcinomas). The specificity of the test was confirmed using an irrelevant probe and papillomas from other species. These results strengthen the association between BPCV1 and the western barred bandicoot papillomatosis and carcinomatosis syndrome and give insight into the biology of the virus–host interaction.
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Woolford, L., A. J. O'Hara, M. D. Bennett, M. Slaven, R. Swan, J. A. Friend, A. Ducki, et al. "Cutaneous Papillomatosis and Carcinomatosis in the Western Barred Bandicoot (Perameles bougainville)." Veterinary Pathology 45, no. 1 (January 2008): 95–103. http://dx.doi.org/10.1354/vp.45-1-95.

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O'hara, A. J., K. S. Warren, R. A. Swan, C. Simms, and J. A. Friend. "FC-17 Cutaneous papillomatosis and carcinomatosis in the highly endangered Western Barred Bandicoot." Veterinary Dermatology 15, s1 (August 2004): 25. http://dx.doi.org/10.1111/j.1365-3164.2004.411_17.x.

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Woolford, Lucy, Annabel Rector, Marc Van Ranst, Andrea Ducki, Mark D. Bennett, Philip K. Nicholls, Kristin S. Warren, Ralph A. Swan, Graham E. Wilcox, and Amanda J. O'Hara. "A Novel Virus Detected in Papillomas and Carcinomas of the Endangered Western Barred Bandicoot (Perameles bougainville) Exhibits Genomic Features of both the Papillomaviridae and Polyomaviridae." Journal of Virology 81, no. 24 (September 26, 2007): 13280–90. http://dx.doi.org/10.1128/jvi.01662-07.

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ABSTRACT Conservation efforts to prevent the extinction of the endangered western barred bandicoot (Perameles bougainville) are currently hindered by a progressively debilitating cutaneous and mucocutaneous papillomatosis and carcinomatosis syndrome observed in captive and wild populations. In this study, we detected a novel virus, designated the bandicoot papillomatosis carcinomatosis virus type 1 (BPCV1), in lesional tissue from affected western barred bandicoots using multiply primed rolling-circle amplification and PCR with the cutaneotropic papillomavirus primer pairs FAP59/FAP64 and AR-L1F8/AR-L1R9. Sequencing of the BPCV1 genome revealed a novel prototype virus exhibiting genomic properties of both the Papillomaviridae and the Polyomaviridae. Papillomaviral properties included a large genome size (∼7.3 kb) and the presence of open reading frames (ORFs) encoding canonical L1 and L2 structural proteins. The genomic organization in which structural and nonstructural proteins were encoded on different strands of the double-stranded genome and the presence of ORFs encoding the nonstructural proteins large T and small t antigens were, on the other hand, typical polyomaviral features. BPCV1 may represent the first member of a novel virus family, descended from a common ancestor of the papillomaviruses and polyomaviruses recognized today. Alternatively, it may represent the product of ancient recombination between members of these two virus families. The discovery of this virus could have implications for the current taxonomic classification of Papillomaviridae and Polyomaviridae and can provide further insight into the evolution of these ancient virus families.
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Bennett, Mark D., Andrea Reiss, Hans Stevens, Elisabeth Heylen, Marc Van Ranst, Adrian Wayne, Michael Slaven, et al. "The First Complete Papillomavirus Genome Characterized from a Marsupial Host: a Novel Isolate from Bettongia penicillata." Journal of Virology 84, no. 10 (March 3, 2010): 5448–53. http://dx.doi.org/10.1128/jvi.02635-09.

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ABSTRACT The first fully sequenced papillomavirus (PV) of marsupials, tentatively named Bettongia penicillata papillomavirus type 1 (BpPV1), was detected in papillomas from a woylie (Bettongia penicillata ogilbyi). The circular, double-stranded DNA genome contains 7,737 bp and encodes 7 open reading frames (ORFs), E6, E7, E1, E2, E4, L2, and L1, in typical PV conformation. BpPV1 is a close-to-root PV with L1 and L2 ORFs most similar to European hedgehog PV and bandicoot papillomatosis carcinomatosis virus types 1 and 2 (BPCV1 and -2). It appears that the BPCVs arose by recombination between an ancient PV and an ancient polyomavirus more than 10 million years ago.
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Dissertations / Theses on the topic "Bandicoot papillomatosis carcinomatosis viruses"

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au, M. Bennett@murdoch edu, and Mark Bennett. "Western barred bandicoots in health and disease." Murdoch University, 2008. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20090202.100128.

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For more than a decade, community groups, scientific organizations and government agencies have collaborated to repopulate the endangered western barred bandicoot (Perameles bougainville). While initially successful, the unexpected discovery of a papillomatosis and carcinomatosis syndrome in captive and wild populations of P. bougainville exposed a dearth of knowledge regarding their diseases. This dissertation addresses this issue through study of the clinical pathology, immunology, parasitology, and virology of P. bougainville. To facilitate the detection and understanding of diseases in P. bougainville, guidelines for interpreting haematology and clinical chemistry results were developed, including calculated species-specific reference intervals for plasma aspartate transaminase activity (20–283 U/L), haemoglobin (122-165 g/L), haematocrit (0.36-0.49 L/L), total leukocytes (2.9-14.9 x10^9/L), monocytes (0-0.6 x10^9/L), eosinophils (0-0.9 x10^9/L) and total protein (47-63 g/L) estimated by refractometry. P. bougainville immunoglobulin was also fractionated from plasma and inoculated into sheep to derive antiserum for serological screening assays. Arthropods, helminths and protozoa parasitic on P. bougainville were catalogued and Eimeria kanyana n. sp. was formally described. The pathogenic and zoonotic potential of bacteria detected in ticks parasitic on P. bougainville was also considered. The association between bandicoot papillomatosis carcinomatosis virus type 1 (BPCV1) and the western barred bandicoot papillomatosis and carcinomatosis syndrome was investigated using PCR, in situ hybridization and virus isolation. Optimized in situ hybridization techniques demonstrated BPCV1 DNA within keratinocyte and sebocyte nuclei, and BPCV1 mRNA within the cytoplasm. BPCV1 virions were isolated by ultracentrifugation and visualized with negative stain transmission electron microscopy revealing icosahedral, non-enveloped viral capsids ~47 nm in diameter, comparable to viruses classified within Papillomaviridae and Polyomaviridae. A novel virus, tentatively named bandicoot papillomatosis carcinomatosis virus type 2 (BPCV2) was discovered in papillomatous lesions from a southern brown bandicoot (Isoodon obesulus). It had a circular double-stranded DNA genome of 7277 bp, and encoded two papillomavirus-like structural proteins, L1 and L2, and two polyomavirus-like putative transforming proteins, large T antigen and small t antigen. DNA and RNA in situ hybridization confirmed the presence of BPCV2 nucleic acids within lesion biopsies. The discovery of the bandicoot papillomatosis carcinomatosis viruses has provoked reassessment of the established virus taxonomy paradigm, theories of virus-host co-speciation and bandicoot population management strategies.
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uk, L. Woolford@rvc ac, and Lucy Woolford. "Papillomatosis and carcinomatosis in the western barred bandicoot (Perameles bougainville)." Murdoch University, 2008. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20090512.53806.

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Conservation efforts to prevent the extinction of the endangered western barred bandicoot Perameles bougainville (WBB) are currently hindered by a debilitating progressive papillomatosis and carcinomatosis syndrome. Now extinct on mainland Australia, wild populations of the WBB are known only to exist on Bernier and Dorre Islands in Shark Bay, Western Australia. This thesis describes and analyses the pathological (gross, histological, ultrastructural) and immunohistochemical features of a papillomatosis and carcinomatosis syndrome in the WBB. The detection and characterisation of a novel virus, the bandicoot papillomatosis carcinomatosis virus type 1 (BPCV1), found in association with cutaneous and muco-cutaneous papillomas and carcinomas, is described. BPCV1 was found to exhibit genomic and morphological features of both the Papillomaviridae and the Polyomaviridae, and may represent the first member of a new family of viruses. The findings of this study provide evidence that BPCV1 is the causative agent of the papillomatosis and carcinomatosis syndrome. Clinical, pathological and molecular evidence of the syndrome and BPCV1 were found in the Bernier Island WBB population at Red Cliff and in captive populations comprising all or a proportion of founder WBBs from this site, but not at all in the WBB population on Dorre Island or Heirisson Prong. The papillomatosis and carcinomatosis syndrome in the western barred bandicoot is a pertinent example of a disease process hampering efforts to prevent the extinction of an endangered species.
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Woolford, Lucy. "Papillomatosis and carcinomatosis in the Western barred bandicoot (Perameles bougainville) /." Woolford, Lucy (2008) Papillomatosis and carcinomatosis in the western barred bandicoot (Perameles bougainville). PhD thesis, Murdoch University, 2008. http://researchrepository.murdoch.edu.au/673/.

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Conservation efforts to prevent the extinction of the endangered western barred bandicoot Perameles bougainville (WBB) are currently hindered by a debilitating progressive papillomatosis and carcinomatosis syndrome. Now extinct on mainland Australia, wild populations of the WBB are known only to exist on Bernier and Dorre Islands in Shark Bay, Western Australia. This thesis describes and analyses the pathological (gross, histological, ultrastructural) and immunohistochemical features of a papillomatosis and carcinomatosis syndrome in the WBB. The detection and characterisation of a novel virus, the bandicoot papillomatosis carcinomatosis virus type 1 (BPCV1), found in association with cutaneous and muco-cutaneous papillomas and carcinomas, is described. BPCV1 was found to exhibit genomic and morphological features of both the Papillomaviridae and the Polyomaviridae, and may represent the first member of a new family of viruses. The findings of this study provide evidence that BPCV1 is the causative agent of the papillomatosis and carcinomatosis syndrome. Clinical, pathological and molecular evidence of the syndrome and BPCV1 were found in the Bernier Island WBB population at Red Cliff and in captive populations comprising all or a proportion of founder WBBs from this site, but not at all in the WBB population on Dorre Island or Heirisson Prong. The papillomatosis and carcinomatosis syndrome in the western barred bandicoot is a pertinent example of a disease process hampering efforts to prevent the extinction of an endangered species.
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