Literature DB >> 6300315

Diversity within a human isolate of coxsackie B4: relationship to viral-induced diabetes.

P C Hartig, G E Madge, S R Webb.   

Abstract

The ability of different strains of a single virus type to produce different pathogenic expressions is well documented within the picornavirus group. Coxsackievirus, group B, type 4 (CB4) has been associated with viral-induced diabetes in man, but expression of its potential to induce diabetes in experimental animals is variable. Evidence is presented here for one of the primary sources of this variability that could explain resulting contradictory reports offered in support or rejection of its diabetogenic potential. C57B1/6 and SWR mice were infected with the Edwards isolate of CB4 (CB4-Edw) and three of its plaque-purified virion "strains." These were designated Edwards isolate-1 (E1), E2, and E3. CB4-Edw, E1, E2, and E3 were serologically similar by infectivity neutralization tests, had identical plaque morphology, and replicated to a similar level in the pancreas. The most profound difference was the level of virus antigen accumulation in the islet cells as determined by immunoperoxidase localization. CB4-Edw had moderate antigen accumulation in most islet cells of SWR mice but was restricted to only a few specific cells within the periphery islets of C57B1/6 mice. Unlike CB4-Edw all three new isolates accumulated antigen in most islet cells of both mouse strains. Virus isolate (strain) E2 showed the most intense accumulation in islet cells. These observations suggest that the Edwards isolate of CB4, like other human isolates of CB4 virus, probably exists as a heterogeneous population of virion strains. The pathogenic consequences and expression of any diabetogenic potential is, therefore, dependent on virus strain selection. This diversity must be considered when evaluating the pathogenic nature of CB4 viruses in experimental animals and the possible role of the viruses in diabetes of man.

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Year:  1983        PMID: 6300315     DOI: 10.1002/jmv.1890110104

Source DB:  PubMed          Journal:  J Med Virol        ISSN: 0146-6615            Impact factor:   2.327


  7 in total

1.  Coxsackie B4 viruses with the potential to damage beta cells of the islets are present in clinical isolates.

Authors:  T M Szopa; T Ward; D M Dronfield; N D Portwood; K W Taylor
Journal:  Diabetologia       Date:  1990-06       Impact factor: 10.122

2.  Induction of the chemokine interferon-gamma-inducible protein-10 in human pancreatic islets during enterovirus infection.

Authors:  A-K Berg; O Korsgren; G Frisk
Journal:  Diabetologia       Date:  2006-09-13       Impact factor: 10.122

3.  Serum antibodies against Coxsackie B1-6 viruses in type 1 diabetics.

Authors:  A M Alberti; C Amato; A Candela; F Costantino; M E Grandolfo; F Lombardi; F Novello; M Orsini; R Santoro
Journal:  Acta Diabetol Lat       Date:  1985 Jan-Mar

4.  Differing cardiotropic and myocarditic properties of group B type 4 coxsackievirus strains.

Authors:  Y Cao; D P Schnurr; N J Schmidt
Journal:  Arch Virol       Date:  1984       Impact factor: 2.574

5.  Protection from lethal coxsackievirus-induced pancreatitis by expression of gamma interferon.

Authors:  M S Horwitz; T Krahl; C Fine; J Lee; N Sarvetnick
Journal:  J Virol       Date:  1999-03       Impact factor: 5.103

6.  WIN 54954 treatment of mice infected with a diabetogenic strain of group B coxsackievirus.

Authors:  D M See; J G Tilles
Journal:  Antimicrob Agents Chemother       Date:  1993-08       Impact factor: 5.191

7.  Humoral immunity against viral antigens in insulin-dependent diabetes mellitus (IDDM): altered IgA class immune response against mumps virus.

Authors:  H Hyöty; T Huupponen; P Leinikki
Journal:  Clin Exp Immunol       Date:  1985-04       Impact factor: 4.330

  7 in total

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