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PMID: 9345433 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Characterization of JC virus DNA amplified from urine of chronic progressive multiple sclerosis patients.

Multiple sclerosis (Houndmills, Basingstoke, England) ·Vol. 1 ·No. 4 ·1996-02-00 ·Pages 193-9

Stoner GL, Agostini HT, Ryschkewitsch CF, Baumhefner RW, Tourtellotte WW

Abstract

Thirty-seven chronic progressive multiple sclerosis (MS) patients, 20 of whom were taking cyclosporine, were examined for excretion of JC virus (JCV) in the urine. Polymerase chain reaction (PCR) amplification of DNA in urinary cell extracts detected JCV in 30% of the MS urines. In the cyclosporine treated group four of 20 (20%) excreted JCV, whereas in the untreated group seven of 17 (41%) excreted JCV. Thus, cyclosporine treatment did not enhance urinary excretion of the virus. A control group consisting of an unselected series of 89 patients donating urine in a general medical clinic and 16 healthy volunteers showed 41% with detectable urinary JCV. Thirty-three percent of the control females excreted JCV (18/54), as did 49% of the control males (25/51). Although the percentage of MS patients excreting detectable virus was not increased compared to the control group, the presence of JCV in the urine provides a convenient source of the virus for further characterization. Genotyping of DNA fragments amplified from the VP1 region indicates mainly the presence of JCV Type 1 in these chronic progressive MS patients. This is also the type that predominates in the control group. An apparent recombinant between Type 1 and Type 3 (African) within the VP1 region, tentatively designated Type 1/3 (or Type 4), was found in both the MS group and the controls. A larger series of MS patients that includes relapsing/remitting disease will be required to determine whether the genotype profile of JCV excreted in the urine of MS patients differs significantly from controls.

MeSH Terms
Adult Amino Acid Sequence Base Sequence Case-Control Studies Chronic Disease Cyclosporine/adverse effects DNA, Viral/analysis Disease Progression Female Humans Immunosuppressive Agents/adverse effects JC Virus/isolation & purification Male Middle Aged Molecular Sequence Data Multiple Sclerosis/urine,virology Polymerase Chain Reaction
Chemicals
DNA, Viral Immunosuppressive Agents Cyclosporine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Stoner G L
Laboratory of Experimental Neuropathology, NINDS, National Institutes of Health, Bethesda, Maryland 20892, USA.
Agostini H T
Ryschkewitsch C F
Baumhefner R W
Tourtellotte W W
Article Info
Journal
Multiple sclerosis (Houndmills, Basingstoke, England)
Abbr.
Mult Scler
ISSN
1352-4585
Published
1996-02-00
Pages
193-9
Language
English
Region
England
NLM ID
9509185
Subset
IM
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