Literature DB >> 6089704

Influence of diabetes mellitus heredity on susceptibility to coxsackievirus B4.

R M Loria, L B Montgomery, L A Corey, V M Chinchilli.   

Abstract

Using the criteria of virus susceptibility as defined by the 50 percent lethal dose response and the percent cumulative mortality response it was shown that the diabetic mutation db, located on chromosome 4, exerted a particular influence on the host response to CB4 challenge. Neither the yellow obese mutation Ay on chromosome 2 nor the misty coat color mutation located one centimorgan from the db mutation had the same effect on CB4 response. The obese diabetic mutation ob located on chromosome 6 appeared to enhance susceptibility to CB4. However, the high susceptibility of the inbred C57BL/6J line on which the ob mutation is found was apparently a significant contributing factor to the ob mutant high virus susceptibility. The response to CB4 was also a useful criteria to discern differences in the genetic background of closely related inbred lines. Based on the CB4 LD50 values the C57BL/6J inbred line was the most susceptible while the C57BL/Ks inbred line was the most resistant. However, using the percent cumulative mortality response as an index of host resistance, the C57BL/KsJ was the most susceptible and the C57BL/Ks the least. These findings further support the thesis that genetic predisposition to diabetes mellitus, as characterized by the mutation db on chromosome 4 is associated with a particular susceptibility and host response to coxsackie-virus B4. It also illustrates that under specific conditions, comparison of the response to virus challenge can be used as an indicator of genetic differences between closely related inbred lines.

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Year:  1984        PMID: 6089704     DOI: 10.1007/bf01309997

Source DB:  PubMed          Journal:  Arch Virol        ISSN: 0304-8608            Impact factor:   2.574


  23 in total

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Authors:  C HELLERSTROM; B HELLMAN
Journal:  Metabolism       Date:  1963-06       Impact factor: 8.694

2.  Severe generalized disease (encephalohepatomyocarditis) occurring in the newborn period and due to infection with Coxsackie virus, group B; evidence of intrauterine infection with this agent.

Authors:  S KIBRICK; K BENIRSCHKE
Journal:  Pediatrics       Date:  1958-11       Impact factor: 7.124

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Authors:  G HOLLIFIELD; W PARSON
Journal:  Am J Physiol       Date:  1957-04

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Authors:  K J CARPENTER; J MAYER
Journal:  Am J Physiol       Date:  1958-06

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Authors:  D L Coleman; K P Hummel
Journal:  Diabetologia       Date:  1973-08       Impact factor: 10.122

6.  Effects of diet on pancreatic beta cell replication in mice with hereditary diabetes.

Authors:  W L Chick; A A Like
Journal:  Am J Physiol       Date:  1971-07

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Authors:  B M Wyse; W E Dulin
Journal:  Diabetologia       Date:  1970-06       Impact factor: 10.122

8.  Diabetes in the mouse due to two mutant genes - a bibliography.

Authors:  J Staats
Journal:  Diabetologia       Date:  1975-08       Impact factor: 10.122

9.  Host factors in Coxsackievirus B4-induced pancreopathy.

Authors:  S H Cook; R M Loria; G E Madge
Journal:  Lab Invest       Date:  1982-04       Impact factor: 5.662

10.  Diabetes, a new mutation in the mouse.

Authors:  K P Hummel; M M Dickie; D L Coleman
Journal:  Science       Date:  1966-09-02       Impact factor: 47.728

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  3 in total

1.  Immunomodulation of encephalomyocarditis virus-induced disease in A/J mice.

Authors:  M T Barger; J E Craighead
Journal:  J Virol       Date:  1991-05       Impact factor: 5.103

2.  Susceptibility to db gene and streptozotocin-induced diabetes in C57BL mice: control by gender-associated, MHC-unlinked traits.

Authors:  E H Leiter; P H Le; D L Coleman
Journal:  Immunogenetics       Date:  1987       Impact factor: 2.846

3.  Androstenediol regulates systemic resistance against lethal infections in mice.

Authors:  R M Loria; D A Padgett
Journal:  Arch Virol       Date:  1992       Impact factor: 2.574

  3 in total

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