Broad Tissue and Cell Tropism of Avian Bornavirus in Parrots with Proventricular Dilatation Disease

Author:

Rinder Monika1,Ackermann Andreas2,Kempf Hermann1,Kaspers Bernd3,Korbel Rüdiger1,Staeheli Peter2

Affiliation:

1. Clinic for Birds, University of Munich, Oberschleissheim, Germany

2. Department of Virology, University of Freiburg, Freiburg, Germany

3. Institute for Animal Physiology, University of Munich, Munich, Germany

Abstract

ABSTRACT Avian bornaviruses (ABV), representing a new genus within the family Bornaviridae , were recently discovered in parrots from North America and Israel with proventricular dilatation disease (PDD). We show here that closely related viruses are also present in captive European parrots of various species with PDD. The six ABV strains that we identified in clinically diseased birds are new members of the previously defined ABV genotypes 2 and 4. Viruses of both genotypes readily established persistent, noncytolytic infections in quail and chicken cell lines but did not grow in cultured mammalian cells in which classical Borna disease virus strains replicate very efficiently. ABV antigens were present in both the cytoplasm and nucleus of infected cells, suggesting nuclear replication of ABV. The genome organization of avian and mammalian bornaviruses is highly conserved except that ABV lacks a distinct control element in the 5′ noncoding region of the bicistronic mRNA encoding the viral proteins X and P. Reverse transcription-PCR analysis demonstrated the presence of virus in many, if not all, organs of birds with PDD. Viral nucleic acid was also found in feces of diseased birds, suggesting virus transmission by the fecal-oronasal route. Immunohistochemical analysis of organs from birds with PDD revealed that infection with ABV is not restricted to cells of the nervous system. Thus, ABV exhibits a broad tissue and cell tropism that is strikingly different from classical Borna disease virus.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference31 articles.

1. Berhane, Y., A. D. Smith, S. Newman, M. Taylor, E. Nagy, B. Binnington, and B. Hunter. 2001. Peripheral neuritis in psittacine birds with proventricular dilatation disease. Avian Pathol.30:653-670.

2. Boutette, J. B., and M. Taylor. 2004. Proventricular dilation disease: a review of research, literature, species differences, diagnostics, prognosis, and treatment, p. 175-181. In Proceedings of the Association of Avian Veterinarians, New Orleans, LA.

3. Carbone, K. M., B. D. Trapp, J. W. Griffin, C. S. Duchala, and O. Narayan. 1989. Astrocytes and Schwann cells are virus-host cells in the nervous system of rats with Borna disease. J. Neuropathol. Exp. Neurol.48:631-644.

4. Proventricular Impaction Associated with Nonsuppurative Encephalomyelitis and Ganglioneuritis in Two Canada Geese

5. de la Torre, J. C. 2002. Bornavirus and the brain. J. Infect. Dis.186(Suppl. 2):S241-S247.

Cited by 96 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3