Establishing Evidence for Enterovirus Infection in Chronic Disease
Corresponding Author
M. STEVEN OBERSTE
Respiratory and Enteric Viruses Branch, Division of Viral and Rickettsial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA
Address for correspondence: M. Steven Oberste, Centers for Disease Control and Prevention, 1600 Clifton Road NE, Mailstop G-17, Atlanta, GA 30333. Voice: 404-639-5497; fax: 404-639-4011. [email protected]Search for more papers by this authorMARK A. PALLANSCH
Respiratory and Enteric Viruses Branch, Division of Viral and Rickettsial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA
Search for more papers by this authorCorresponding Author
M. STEVEN OBERSTE
Respiratory and Enteric Viruses Branch, Division of Viral and Rickettsial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA
Address for correspondence: M. Steven Oberste, Centers for Disease Control and Prevention, 1600 Clifton Road NE, Mailstop G-17, Atlanta, GA 30333. Voice: 404-639-5497; fax: 404-639-4011. [email protected]Search for more papers by this authorMARK A. PALLANSCH
Respiratory and Enteric Viruses Branch, Division of Viral and Rickettsial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA
Search for more papers by this authorAbstract
Abstract: Viruses have long been considered among potential environmental triggers of type 1 diabetes mellitus. Epidemiologic and seroprevalence studies have associated enterovirus infection with development of prediabetic autoimmunity and with the onset of clinical diabetes. Enterovirus infection has also been temporally correlated with disease onset by virus isolation or by detection of viral genome by reverse transcription-polymerase chain reaction (RT-PCR). For the large-scale prospective studies that are required to firmly establish a causal relationship between enterovirus infection and development of prediabetic autoimmunity or progression from autoimmunity to clinical diabetes, sensitive RT-PCR methods must be used to detect virus prior to the onset of diabetic symptoms. We have developed an RT-seminested PCR protocol to detect enteroviruses in clinical specimens. This method is approximately 10,000-fold more sensitive than conventional, single-amplification PCR. Further, we have developed molecular methods to rapidly and reliably identify enterovirus serotype, bypassing the cumbersome and often problematic neutralization test. The molecular serotyping approach will be valuable in examining the relationships between particular virus serotypes or genotypes and specific diseases.
REFERENCES
- 1 Yoon, J-W. 1990. The role of viruses and environmental factors in the induction of diabetes. Curr. Top. Microbiol. Immunol. 164: 95–123.
- 2 See, D.M. & J.G. Tilles. 1998. The pathogenesis of viral-induced diabetes. Clin. Diagn. Virol. 9: 85–88.
- 3 Leinikki, P. 1998. Viruses and type 1 diabetes: elusive problems and elusive answers. Clin. Diagn. Virol. 9: 65–66.
- 4 Hyöty, H. et al. 1998. Enterovirus infections and insulin dependent diabetes mellitus—evidence for causality. Clin. Diagn. Virol. 9: 77–84.
- 5 Karvonen, M. et al. 1993. A review of the recent epidemiological data on the worldwide incidence of type 1 (insulin-dependent) diabetes mellitus: World Health Organisation DIAMOND Project. Diabetologia 36: 883–892.
- 6 Hiltunen, M. et al. 1997. Islet cell antibody seroconversion in children is temporally associated with enterovirus infections. J. Infect. Dis. 175: 554–560.
- 7 Helfand, R.F. et al. 1995. Serologic evidence of an association between enteroviruses and the onset of type 1 diabetes mellitus: Pittsburgh Diabetes Research Group. J. Infect. Dis. 172: 1206–1211.
- 8 Yoon, J-W. et al. 1979. Isolation of a virus from the pancreas of a child with diabetic ketoacidosis. N. Engl. J. Med. 300: 1173–1179.
- 9 Andreoletti, L. et al. 1997. Detection of Coxsackie B virus RNA sequences in whole blood samples from adult patients at the onset of type I diabetes mellitus. J. Med. Virol. 52: 121–127.
- 10 Clements, G.B. et al. 1995. Coxsackie B virus infection and onset of childhood diabetes. Lancet 346: 221–223.
- 11 Morens, D.M. & M.A. Pallansch. 1995. Epidemiology. In Human Enterovirus Infections, pp. 3-23. ASM Press. Washington, D.C.
- 12 Pallansch, M.A. & R.P. Roos. 2001. Enteroviruses: polioviruses, coxsackieviruses, echoviruses, and newer enteroviruses. In Fields' Virology, pp. 723-775. Lippincott/Williams & Wilkins. Philadelphia/Baltimore.
- 13 Martino, T.A. et al. 1995. Enteroviral myocarditis and cardiomyopathy: a review of clinical and experimental studies. In Human Enterovirus Infections, pp. 291-351. ASM Press. Washington, D.C.
- 14 Kim, K-S. et al. 2001. The group B coxsackieviruses and myocarditis. Rev. Med. Virol. 11: 355–368.
- 15 Rewers, M. & M. Atkinson. 1995. The possible role of enteroviruses in diabetes mellitus. In Human Enterovirus Infections, pp. 353-385. ASM Press. Washington, D.C.
- 16 Dalakas, M.C. 1995. Enteroviruses and human neuromuscular diseases. In Human Enterovirus Infections, pp. 387-398. ASM Press. Washington, D.C.
- 17
Committee on Enteroviruses. 1962. Classification of human enteroviruses.
Virology
16: 501–504.
10.1016/0042-6822(62)90233-7 Google Scholar
- 18 Panel for Picornaviruses. 1963. Picornaviruses: classification of nine new types. Science 141: 153–154.
- 19 King, A.M.Q. et al. 2000. Picornaviridae. In Virus Taxonomy: Seventh Report of the International Committee on Taxonomy of Viruses, pp. 657-678. Academic Press. San Diego.
- 20 Lim, K.A. & M. Benyesh-Melnick. 1960. Typing of viruses by combinations of antiserum pools: application to typing of enteroviruses (Coxsackie and ECHO). J. Immunol. 84: 309–317.
- 21 Rotbart, H.A. & J.R. Romero. 1995. Laboratory diagnosis of enteroviral infections. In Human Enterovirus Infections, pp. 401-418. ASM Press. Washington, D.C.
- 22 Rotbart, H.A. et al. 1997. Diagnosis of enterovirus infection by polymerase chain reaction of multiple specimen types. Ped. Infect. Dis. J. 16: 409–411.
- 23 Yang, C-F. et al. 1992. Genotype-specific in vitro amplification of sequences of the wild type 3 polioviruses from Mexico and Guatemala. Virus Res. 24: 277–296.
- 24 Minor, P.D. 1990. Antigenic structure of picornaviruses. Curr. Top. Microbiol. Immunol. 161: 121–154.
- 25 Mateu, M.G. 1995. Antibody recognition of picornaviruses and escape from neutralization. Virus Res. 38: 1–24.
- 26 Oberste, M.S. et al. 1999. Molecular evolution of the human enteroviruses: correlation of serotype with VP1 sequence and application to picornavirus classification. J. Virol. 73: 1941–1948.
- 27 Kopecka, H. et al. 1995. Genotypic variation in coxsackievirus B5 isolates from three different outbreaks in the United States. Virus Res. 38: 125–136.
- 28 King, A.M.Q. 1988. Genetic recombination in positive strand RNA viruses. In RNA Genetics, pp. 149-165. CRC Press. Boca Raton, FL.
- 29 Santti, J. et al. 1999. Evidence of recombination among enteroviruses. J. Virol. 73: 8741–8749.
- 30 Oberste, M.S. et al. 1999. Typing of human enteroviruses by partial sequencing of VP1. J. Clin. Microbiol. 37: 1288–1293.
- 31 Oberste, M.S. et al. 2000. Comparison of classic and molecular approaches for the identification of “untypable” enteroviruses. J. Clin. Microbiol. 38: 1170–1174.
- 32 Vosloo, W. et al. 1992. Genetic relationships between southern African SAT-2 isolates of foot-and-mouth-disease virus. Epidemiol. Infect. 109: 547–558.
- 33 Oberste, M.S. et al. 2001. Molecular identification of new picornaviruses and characterization of a proposed enterovirus 73 serotype. J. Gen. Virol. 82: 409–416.
- 34 Hyypiä, T. et al. 1992. A distinct picornavirus group identified by sequence analysis. Proc. Natl. Acad. Sci. USA 89: 8847–8851.
- 35 Marvil, P. et al. 1999. Avian encephalomyelitis virus is a picornavirus and is most closely related to hepatitis A virus. J. Gen. Virol. 80: 653–662.
- 36 Niklasson, B. et al. 1999. A new picornavirus isolated from bank voles (Clethrionomys glareolus). Virology 255: 86–93.
- 37 Yamashita, T. et al. 1998. Complete nucleotide sequence and genetic organization of Aichi virus, a distinct member of the Picornaviridae associated with acute gastroenteritis in humans. J. Virol. 72: 8408–8412.