» Articles » PMID: 1328671

Genetic Analysis of Simian Virus 40 from Brains and Kidneys of Macaque Monkeys

Overview
Journal J Virol
Date 1992 Nov 1
PMID 1328671
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

Simian virus 40 (SV40) was isolated from the brains of three rhesus monkeys and the kidneys of two other rhesus monkeys with simian immunodeficiency virus-induced immunodeficiency. A striking feature of these five cases was the tissue specificity of the SV40 replication. SV40 was also isolated from the kidney of a Taiwanese rock macaque with immunodeficiency probably caused by type D retrovirus infection. Multiple full-length clones were derived from all six fresh SV40 isolates, and two separate regions of their genomes were sequenced: the origin (ori)-enhancer region and the coding region for the carboxy terminus of T antigen (T-ag). None of the 23 clones analyzed had two 72-bp enhancer elements as are present in the commonly used laboratory strain 776 of SV40; 22 of these 23 clones were identical in their ori-enhancer sequences, and these had only a single 72-bp enhancer element. We found no evidence for differences in ori-enhancer sequences associated with tissue-specific SV40 replication. The T-ag coding sequence that was analyzed was identical in all clones from kidney. However, significant variation was observed in the carboxy-terminal region of T-ag in SV40 isolated from brain tissues. This sequence variation was located in a region previously reported to be responsible for SV40 host range in cultured cell lines. Thus, SV40 appears to be an opportunistic pathogen in the setting of simian immunodeficiency virus-induced immunodeficiency, similarly to JC virus in human immunodeficiency virus-infected humans, the enhancer sequence organization generally attributed to SV40 is not representative of natural SV40 isolates, and sequence variation near the carboxy terminus of T-ag may play a role in tissue-specific replication of SV40.

Citing Articles

How Simian Virus 40 Hijacks the Intracellular Protein Trafficking Pathway to Its Own Benefit … and Ours.

Toscano M, de Haan P Front Immunol. 2018; 9:1160.

PMID: 29892296 PMC: 5985306. DOI: 10.3389/fimmu.2018.01160.


Viral microRNA effects on persistent infection of human lymphoid cells by polyomavirus SV40.

McNees A, Harrigal L, Kelly A, Minard C, Wong C, Butel J PLoS One. 2018; 13(2):e0192799.

PMID: 29432481 PMC: 5809058. DOI: 10.1371/journal.pone.0192799.


Transcription enhancers as major determinants of SV40 polyomavirus growth efficiency and host cell tropism.

Schmidt K, Keiser S, Gunther V, Georgiev O, Hirsch H, Schaffner W J Gen Virol. 2016; 97(7):1597-1603.

PMID: 27100458 PMC: 5410105. DOI: 10.1099/jgv.0.000487.


Simian Virus 40 Infection in the Spinal Cord of Simian Immunodeficiency Virus-Immunosuppressed Rhesus Macaques.

Kaliyaperumal S, Wuthrich C, Westmoreland S, Koralnik I J Neuropathol Exp Neurol. 2015; 74(11):1071-6.

PMID: 26469249 PMC: 4610247. DOI: 10.1097/NEN.0000000000000252.


Frequent infection of neurons by SV40 virus in SIV-infected macaque monkeys with progressive multifocal leukoencephalopathy and meningoencephalitis.

Kaliyaperumal S, Dang X, Wuethrich C, Knight H, Pearson C, Mackey J Am J Pathol. 2013; 183(6):1910-1917.

PMID: 24095925 PMC: 5704577. DOI: 10.1016/j.ajpath.2013.08.007.


References
1.
Fiers W, Contreras R, Haegemann G, Rogiers R, Van de Voorde A, Van Heuverswyn H . Complete nucleotide sequence of SV40 DNA. Nature. 1978; 273(5658):113-20. DOI: 10.1038/273113a0. View

2.
Hsiung G, GAYLORD Jr W . The vacuolating virus of monkeys. I. Isolation, growth characteristics, and inclusion body formation. J Exp Med. 1961; 114:975-86. PMC: 2180415. DOI: 10.1084/jem.114.6.975. View

3.
SANGER F, Nicklen S, Coulson A . DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977; 74(12):5463-7. PMC: 431765. DOI: 10.1073/pnas.74.12.5463. View

4.
Tominaga T, Yogo Y, Kitamura T, Aso Y . Persistence of archetypal JC virus DNA in normal renal tissue derived from tumor-bearing patients. Virology. 1992; 186(2):736-41. DOI: 10.1016/0042-6822(92)90040-v. View

5.
Munholland J, Kelly J, Hassell J, Wildeman A . Cell specificity of transcription regulation by papovavirus T antigens and DNA replication. EMBO J. 1992; 11(1):177-84. PMC: 556438. DOI: 10.1002/j.1460-2075.1992.tb05040.x. View