scholarly journals Incomplete immune response to coxsackie B viruses associates with early autoimmunity against insulin

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Michelle P. Ashton ◽  
Anne Eugster ◽  
Denise Walther ◽  
Natalie Daehling ◽  
Stephanie Riethausen ◽  
...  
Keyword(s):  
Immune Response ◽  
Coxsackie B Viruses ◽  
Coxsackie B

Intratypic antigenic heterogeneity of Coxsackie B viruses

1963 ◽  
Vol 12 (1) ◽  
pp. 29-41 ◽  
Author(s):  
Reinhard Wigand ◽  
Albert B. Sabin
Keyword(s):  
Coxsackie B Viruses ◽  
Antigenic Heterogeneity ◽  
Coxsackie B

Coxsackie B viruses and autoimmune diabetes

1982 ◽  
Vol 101 (4) ◽  
pp. 647-648 ◽  
Author(s):  
C.S. Bartsocas ◽  
C.J. Papadatos ◽  
M. Lab ◽  
N. Spyrou ◽  
B. Krikelis ◽  
...  
Keyword(s):  
Autoimmune Diabetes ◽  
Coxsackie B Viruses ◽  
Coxsackie B

scholarly journals RNA Recombination Plays a Major Role in Genomic Change during Circulation of Coxsackie B Viruses

2004 ◽  
Vol 78 (6) ◽  
pp. 2948-2955 ◽  
Author(s):  
M. Steven Oberste ◽  
Silvia Peñaranda ◽  
Mark A. Pallansch
Keyword(s):  
Phylogenetic Trees ◽  
Clinical Isolates ◽  
Human Enterovirus ◽  
Rna Recombination ◽  
Genomic Change ◽  
Genome Region ◽  
Nontranslated Region ◽  
Frequent Event ◽  
Coxsackie B Viruses ◽  
Coxsackie B

ABSTRACT RNA recombination has been shown to occur during circulation of enteroviruses, but most studies have focused on poliovirus. To examine the role of recombination in the evolution of the coxsackie B viruses (CVB), we determined the partial sequences of four genomic intervals for multiple clinical isolates of each of the six CVB serotypes isolated from 1970 to 1996. The regions sequenced were the 5′-nontranslated region (5′-NTR) (350 nucleotides [nt]), capsid (VP4-VP2, 416 nt, and VP1, ∼320 nt), and polymerase (3D, 491 nt). Phylogenetic trees were constructed for each genome region, using the clinical isolate sequences and those of the prototype strains of all 65 enterovirus serotypes. The partial VP1 sequences of each CVB serotype were monophyletic with respect to serotype, as were the VP4-VP2 sequences, in agreement with previously published studies. In some cases, however, incongruent tree topologies suggested that intraserotypic recombination had occurred between the sequenced portions of VP2 and VP1. Outside the capsid region, however, isolates of the same serotype were not monophyletic, indicating that recombination had occurred between the 5′-NTR and capsid, the capsid and 3D, or both. Almost all clinical isolates were recombinant relative to the prototype strain of the same serotype. All of the recombination partners appear to be members of human enterovirus species B. These results suggest that recombination is a frequent event during enterovirus evolution but that there are genetic restrictions that may influence recombinational compatibility.

Association between group G chromosomes, especially chromosome G21, and susceptibility of human cells to coxsackie B viruses

1978 ◽  
Vol 86 (5) ◽  
pp. 1493-1496
Author(s):  
Ya. E. Khesin ◽  
A. M. Amchenkova ◽  
N. E. Gulevich ◽  
A. N. Narovlyanskii
Keyword(s):  
Human Cells ◽  
Coxsackie B Viruses ◽  
Coxsackie B

Echoviruses and Coxsackie B Viruses That Use Human Decay‐Accelerating Factor (DAF) as a Receptor Do Not Bind the Rodent Analogues of DAF

2000 ◽  
Vol 181 (1) ◽  
pp. 340-343 ◽  
Author(s):  
O. Brad Spiller ◽  
Ian G. Goodfellow ◽  
David J. Evans ◽  
Jeffrey W. Almond ◽  
B. Paul Morgan
Keyword(s):  
Decay Accelerating Factor ◽  
Coxsackie B Viruses ◽  
Coxsackie B

Coxsackie B viruses use multiple receptors to infect human cardiac cells

2004 ◽  
Vol 74 (2) ◽  
pp. 291-299 ◽  
Author(s):  
George Orthopoulos ◽  
Kathy Triantafilou ◽  
Martha Triantafilou
Keyword(s):  
Cardiac Cells ◽  
Multiple Receptors ◽  
Coxsackie B Viruses ◽  
Coxsackie B

An Incidence Peak of Juvenile Diabetes. Relation to Coxsackie B Virus Immune Response

1985 ◽  
Vol 74 (s320) ◽  
pp. 14-19 ◽  
Author(s):  
G. FRIMAN ◽  
J. FOHLMAN ◽  
G. FRISK ◽  
H. DIDERHOLM ◽  
U. EWALD ◽  
...  
Keyword(s):  
Immune Response ◽  
Juvenile Diabetes ◽  
B Virus ◽  
Coxsackie B Virus ◽  
Coxsackie B

Use of synthetic oligodeoxyribonucleotides for type-specific identification of coxsackie B viruses

1989 ◽  
Vol 3 (2) ◽  
pp. 103-108 ◽  
Author(s):  
Marianne Alksnis ◽  
Michael Lindberg ◽  
Per Stålhandske ◽  
Hans Hultberg ◽  
Ulf Pettersson
Keyword(s):  
Specific Identification ◽  
Coxsackie B Viruses ◽  
Coxsackie B
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