Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-12-01T00:29:37.887Z Has data issue: false hasContentIssue false
  • English
  • Français

2 Cytogenetic analysis of MSRV POL, GAG, ENV sequences and genome instability in multiple sclerosis

Published online by Cambridge University Press:  24 June 2014

M Zawada ,
I. Liwen ,
D. Januszkiewicz-Lewandowska ,
K. Nowicka ,
B. Jaworska-Kubica ,
J. Rembowska ,
H. Hertmanowska ,
M. Wender  and
J. Nowak
M Zawada
Affiliation:
Institute of Human Genetics Polish Academy of Sciences, Poznan, Poland
I. Liwen
Affiliation:
Institute of Human Genetics Polish Academy of Sciences, Poznan, Poland
D. Januszkiewicz-Lewandowska
Affiliation:
Institute of Human Genetics Polish Academy of Sciences, Poznan, Poland University of Medical Sciences, Poznan, Poland
K. Nowicka
Affiliation:
Institute of Human Genetics Polish Academy of Sciences, Poznan, Poland
B. Jaworska-Kubica
Affiliation:
Institute of Human Genetics Polish Academy of Sciences, Poznan, Poland
J. Rembowska
Affiliation:
Institute of Human Genetics Polish Academy of Sciences, Poznan, Poland
H. Hertmanowska
Affiliation:
Department of Neurology, State Hospital, Poznan, Poland, E-mail: [email protected]
M. Wender
Affiliation:
Neuroimunological Unit, Mossakowski Medical Research Centre Polish Academy of Sciences, Poznan, Poland
J. Nowak
Affiliation:
Institute of Human Genetics Polish Academy of Sciences, Poznan, Poland
Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content. As you have access to this content, full HTML content is provided on this page. A PDF of this content is also available in through the ‘Save PDF’ action button.
Type
Posters – Neurology
Information
Acta Neuropsychiatrica , Volume 21 , Issue S2: Special Issue: Abstracts of 49th Neuropsychiatric Pula Congress, 17-20 June 2009, Pula, Croatia , June 2009 , pp. 73
Copyright
Copyright © 2009 John Wiley & Sons A/S

Introduction/Objectives:

Among of the potential agents causing multiple sclerosis MSRV virus (multiple sclerosis-associated retrovirus) is often taken into consideration. Aims of the study were 1) an assessment of MSRV potential role in MS and 2) test of genome instability in MS patients.

Participants, Materials/Methods:

The material was peripheral blood lymphocytes from 92 patients with MS, 12 patients with myasthenia and 20 healthy persons. The FISH studies with labeled PCR products of pol, gag and env MSRV genes in nuclei, chromosomes and chromatin fibers were done. Classical cytogenetic techniques were introduced into karyotypes and micronuclei analyses. MSRV pol, gag and env sequences were found in both MS patients and controls.

Results:

The copy number of MSRV pol sequences was significantly greater in MS patients (6–24 copies on nucleus) than in myasthenia (4–5 copies) and normal individuals (3–6 copies). MSRV gag sequences was found in a range of 5–20, 4–5 and 2–4 copies in MS patients, patients with myasthenia and healthy donors, respectively. MSRV env was found in a range of 6–22, 4–5 and 2–4 copies in MS patients, patients with myasthenia and healthy donors, respectively. Moreover, the number of spontaneous micronuclei was significantly greater in MS patients compared to control. In patients with MS diversity of chromosome aberrations was observed.

Conclusions:

In conclusion, evident difference in MSRV pol, gag and env copy number between MS patients and control suggests that MSRV may play some role in the etiology of multiple sclerosis (latent viral infection). The presence of chromosome aberrations and high amount of micronuclei in MS patients shows that the instability in MS genome often occurs.