Genomic and template RNA transcription in a model of persistent enteroviral infection

References

• Archard L C, Bowles N E, Behan P O, Bell E J, Doyle D J. Postviral fatigue syndrome: persistence of enterovirus RNA in muscle and elevated creatine kinase. J Roy Soc Med 1988; 81: 326–329
   PubMed Web of Science ®Google Scholar
• Argo E, Gimenez B, Cash P. Non‐cytopathic infection of rhabdomyosarcoma cells by coxsackie B5 virus. Arch Virol 1992; 126: 215–229
   Google Scholar
• Behan P O, Behan W H M. Postviral fatigue syndrome. CRC Crit Rev Neurobiol 1988; 4: 157–178
   Google Scholar
• Behan W H M, Behan P O. The role of viral infection in polymyositis, dermatomyositis and chronic fatigue syndrome. Chapter 7. Inflammatory Myopathies, Bailliere's Clinical Neurology, F L Mastaglia. Bailliere Tindall, London, Philadelphia 1993; Vol 2: 637–658, No 3
   Google Scholar
• Borzakian S, Couderc T, Barbier Y, et al. Persistent poliovirus infection: establisment and maintenance involve distinct mechanisms. Virology 1992; 186: 398–408
   PubMed Web of Science ®Google Scholar
• Bowles N E, Olsen E G J, Richardson P J, Archard L C. Detection of coxsackie‐B‐virus specific RNA sequences in myocardial biopsy samples from patients with myocarditis and dilated cardiomyopathy. Lancet 1986; 1: 1120–1123
   PubMed Web of Science ®Google Scholar
• Bowles N E, Sewry C A, Dubowitz V, Archard L C. Dermatomyositis, polymyositis and coxsackie B virus infection. Lancet 1987; 1: 1004–1007
   PubMed Web of Science ®Google Scholar
• Cash E, Chamorro M, Brahic M. Minus‐strand RNA synthesis in the spinal cord of mice persistently infected with Theiler's virus. J Virol 1988; 62: 1824–1826
   Google Scholar
• Cash P. The application of two‐dimensional polyacrylamide gel electrophoresis to medical microbiology: molecular epidemiology of viruses and bacteria. Electrophoresis 1991; 12: 592–604
   Google Scholar
• Chomczynski P, Sacchi N. Single step method of RNA isolation by acid guanidium thiocyanate phenol chloroform extraction. Anal Biochem 1987; 162: 156–159
   PubMed Web of Science ®Google Scholar
• Cunningham L, Bowles N E, Love R J M, Dubowitz V, Archard L C. Persistence of enteroviral RNA in chronic fatigue syndrome is associated with the abnormal production of equal amounts of positive and negative strands of enteroviral RNA. J Gen Virol 1990; 71: 1399–1402
   PubMed Web of Science ®Google Scholar
• Dalakas M C. Enteroviruses and human neuromuscular diseases. Chapter 16. Human Enterovirus Infections, A Rotbart Harley. ASM Press, WashingtonUSA 1995; 387–398
   Google Scholar
• Davis L E, Bodian D, Price D. Chronic progressive poliomyelitis secondary to vaccination of an immunodeficient child. N Eng J Med 1977; 297: 2541–2545
   Google Scholar
• Evans D, Dunn G, Minor P, Schild G, Conn A, et al. Increased neurovirulence associated with a single nucleotide change in a non‐coding region of the Sabian type 3 poliovirus genome. Nature (London) 1985; 314: 548–544
   PubMed Web of Science ®Google Scholar
• Farquharson M, Harvie R, McNicol A M. Detection of messenger RNA using a digoxigenin end labelled oligodeoxynucleotide probe. J Clin Pathol 1990; 43: 424–428
   PubMed Web of Science ®Google Scholar
• Gow J W, Behan W M H, Clements G B, Woodall C, Riding M, Behan P O. Enteroviral RNA sequences detected by polymerase chain reaction in muscle of patients with postviral fatigue syndrome. Br Med J 1991; 302: 692–696
   PubMed Web of Science ®Google Scholar
• Gow J W, Cash P, Behan W M H, McGarry F, Simpson K, Behan P. Detection of picornavirus genomic and template RNA strands by a novel semi‐nested PCR technique and agarose gel electrophoresis. Electrophoresis 1995; 16: 338–340
   PubMed Web of Science ®Google Scholar
• Hillan K J. Detection of mRNA in fixed tissues using RNA probes. Nonradioactive Labelling and Detection of Biomolecules, C Kessler. Springer‐Verlag. 1990; 363–367
   Google Scholar
• Hohenadl C, Klingel K, Mertsching J, Hofschneider P H, Kandolf R. Strand‐specific detection of enteroviral RNA in myocardial tissue by in situ hybridisation. Mol Cell Probes 1991; 5: 11–20
   Google Scholar
• Jarousse N, Fiette L, Grant R A, Hogle J M, McAllister A, Michiels T, et al. Chimeric Theiler's virus with altered tropism for the central nervous system. J Virol 1994; 68: 2781–2786
   Google Scholar
• Kandolf R, Hofschneider P H. Viral Heart Disease. Springer Sem Immunpathol 1989; 11: 1–13
   PubMed Web of Science ®Google Scholar
• Kandolf R, Klingel K, Mertsching H, Canu A, et al. Molecular studies on enteroviral heart disease: patterns of acute and persistent infections. Europ Heart J 1991; 12(Suppl. D)49–55
   Google Scholar
• Klingel K, Hohenadl C, Canu A, Albrecht M, et al. Ongoing enterovirus‐induced myocarditis is associated with persistent heart muscle infection: quantitative analysis of virus replication, tissue damage and inflammation. Proc Nat Acad Sci USA 1992; 89: 314–318
   PubMed Web of Science ®Google Scholar
• Lipkin I W, Battenberg E L F, Bloom F E, Olstone M B A. Viral infection of neurones can depress neurotransmitter mRNA levels without histologic injury. Brain Res 1988; 451: 333–339
   Google Scholar
• Martino T A, Liu P, Petric M, Sole M J. Enteroviral myocarditis and dilated cardio‐myopathy: a review of clinical and experimental studies. Human Enterovirus Infections, H A Rotbert. ASM Press, Washington, DC 1995; 291–352
   Google Scholar
• Martyn C N, Barker D J, Osmond C. Motorneuron disease and past poliomyelitis in England and Wales. Lancet 1988; 1: 1319–1322
   Google Scholar
• Matloubian M, Somasundaram T, Kolhekar S R, Selvakumar R, Ahmed R. Genetic basis of viral persistence: single amino acid change in the viral glycoprotein affects ability of lymphocytic choriomenigitis virus to persist in adult mice. J Exp Med 1990; 172: 1043–1048
   Google Scholar
• McAllister R M, Melnyk J, Finkelstein J Z, Adams E C, Gardner M B. Cultivation in vitro of cells derived from a malignant human rhabdomyosarcoma. Cancer 1969; 24: 520–526
   PubMed Web of Science ®Google Scholar
• McKinney R E, Jr, Katz S L, Wilfert C M. Chronic enteroviral meningoencephalitis in agamma‐globulinaemic patients. Rev Infect Dis 1987; 9: 334–356
   PubMedGoogle Scholar
• McLaren J, Argo E, Cash P. Evolution of coxsackie B virus during in vitro persistent infection: detection of protein mutations using two‐dimensional polyacrylamide gel electrophoresis. Electrophoresis 1993; 14: 137–147
   Google Scholar
• Melchers W, Zoll T, van Kuppeveld F, Swanink C, Galama J. There is no evidence for persistent enterovirus infections in chronic medical conditions in humans. Rev Med Virol 1994; 4: 235–243
   Web of Science ®Google Scholar
• Muir P, Archard L C. There is evidence for persistent enterovirus infections in chronic medical conditions in humans. Rev Med Virol 1994; 4: 245–250
   Web of Science ®Google Scholar
• Oldstone M B A. Molecular anatomy of viral persistence. J Virol 1991; 65: 6381–6396
   PubMed Web of Science ®Google Scholar
• Oldstone M B A, Sinha Y N, Blount P, Tishon A, Rodriguez M, Wedel R, et al. Virus induced alterations in homeostasis: alterations in differentiated functions of infected cells in vivo. Science 1982; 218: 1125–1127
   PubMed Web of Science ®Google Scholar
• Patick A K, Oleszak E L, Leibowitz J L, Rodriguez M. Persistent infection of a glioma cell line generates a Theiler's virus variant which fails to induce demyelinating disease in SJL/J mice. J Gen Virol 1990; 71: 2122–2132
   Google Scholar
• Pelletier I, Couderc T, Borzakian S, et al. Characterisation of persistent poliovirus mutants selected in human neuroblastoma cells. Virology 1991; 180: 729–737
   Google Scholar
• Salvato M, Borrow P, Shimomaye E, Oldstone M A. Molecular basis of viral persistence: a single amino acid change in the glycoprotein of lymphocytic choriomeningitis virus is associated with suppression of the antiviral cytotoxic T‐lymphocyte response and establishment of persistence. J Virol 1991; 65: 1863–1869
   PubMed Web of Science ®Google Scholar
• Schnurr D P, Schmidt N J. Persistent infections. Coxsackie Viruses, a General Update, M Bendinelli, H Friedman. Plenum, New York 1989; 181–201
   Google Scholar
• Sharief M K, Hentges R, Ciardi M. Intrathecal immune response in patients with the post‐polio syndrome. New Engl J Med 1991; 324: 1206–1207
   Google Scholar
• Tracy S. The genome of the Group B coxsackieviruses. Chapter 2. Coxsackie viruses ‐ a general update, Mauro Bendinelli, Friedman Herman. Plenum Publishing Corporation, New York 1988; 19–33
   Google Scholar
• Tracy S, Chapman N M, McManus B M, Pallansch W A, Beck M A, et al. A molecular and serologic evaluation of enteroviral involvement in human myocarditis. J Mol Cell Cardiol 1990; 22: 403–414
   Google Scholar
• Webster A D, Rotbart H A, Warner T, et al. Diagnosis of enterovirus brain disease in hypogammaglobulinemic patients by polymerase chain reaction. Clin Infect Dis 1993; 17: 657–661
   Google Scholar
• Wilfert C M, Buckley R H, Mohanakumar T, Griffith S L, et al. Persistent and fatal central nervous system echovirus infections in patients with agammaglobulinaemia. N Engl J Med 1977; 296: 1485
   PubMedGoogle Scholar
• Woodall C J, Riding M H, Graham D I, Clemens G B. Sequences specific for entero‐viruses detected in spinal cord from patients with motor neuron disease. Br Med J 1994; 308: 1341–1343
   Google Scholar
• Woodruff J F. Viral myocarditis. Am J Pathol 1980; 101: 426–483
   Google Scholar
• Zoll G J, Melchers W G, Kopecka H, Jambroes G, et al. General primer‐mediated polymerase chain reaction for detection of enteroviruses: application for diagnostic routine and persistent infections. J Clin Microbiol 1992; 30: 160–165
   PubMed Web of Science ®Google Scholar