Literature DB >> 9504746

Characterisation of genomic RNA of Coxsackievirus B3 in murine myocarditis: reliability of direct sequencing of reverse transcription-nested polymerase chain reaction products.

H Zhang1, B Soteriou, S Knowlson, A Theodoridou, L C Archard.   

Abstract

SWR mice develop viral myocarditis histologically similar to the human disease following inoculation with a cardiovirulent Coxsackievirus B3 (CVB3), reactivated from a sequenced cDNA clone of Nancy strain. A sequence of 215 nucleotides, or 628 nucleotides in representative cases, of the 5'non-translated region (5'NTR) of CVB3 genome was amplified from myocardial samples of the infected mice by reverse transcription-nested polymerase chain reaction (RT-NPCR). In order to verify the viral nucleotide sequence and detect the mutation frequency of the viral RNA, the nucleotide sequence of NPCR products were determined by direct sequencing in both orientations. The amplified products from mouse heart on day 1-13 post-inoculation were sequenced and, in each case, the consensus sequence was identical to the published sequence of CVB3 (Nancy strain). To evaluate further the reproducibility of these techniques, three tissue samples from the same infected mouse heart were processed independently. Sequences of their RT-NPCR products were identical to each other as well as to the published sequence. When two attenuated CVB3 mutants were amplified and sequenced, single mutations were detected. To evaluate the overall fidelity of these two combined techniques, genomic RNA of a different CVB3 Nancy strain stock, Coxsackievirus A9 or poliovirus sabin 1 was amplified and the NPCR products sequenced. Each product showed 100% homology with its published sequence. These results demonstrate that the coupled technique of the enterovirus RT-NPCR with direct sequencing of NPCR products generates accurate consensus sequence data and this technique proved to be useful in verification of enteroviral amplicons and in detection of nucleotide mutations. In addition, a low mutation frequency was found in the 5'NTR of CVB3 detected in myocardial samples of immunocompetent mice up to 13 days.

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Year:  1997        PMID: 9504746     DOI: 10.1016/s0166-0934(97)00122-5

Source DB:  PubMed          Journal:  J Virol Methods        ISSN: 0166-0934            Impact factor:   2.014


  6 in total

1.  High prevalence of enteroviral genomic sequences in myocardium from cases of endemic cardiomyopathy (Keshan disease) in China.

Authors:  Y Li; T Peng; Y Yang; C Niu; L C Archard; H Zhang
Journal:  Heart       Date:  2000-06       Impact factor: 5.994

2.  Enterovirus related metabolic myopathy: a postviral fatigue syndrome.

Authors:  R J M Lane; B A Soteriou; H Zhang; L C Archard
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-10       Impact factor: 10.154

3.  Characterization of enterovirus isolates from patients with heart muscle disease in a selenium-deficient area of China.

Authors:  T Peng; Y Li; Y Yang; C Niu; P Morgan-Capner; L C Archard; H Zhang
Journal:  J Clin Microbiol       Date:  2000-10       Impact factor: 5.948

4.  Myocarditis.

Authors: 
Journal:  Curr Treat Options Cardiovasc Med       Date:  2000-10

5.  Myocarditis.

Authors:  Elaine Winkel; Joseph Parrillo
Journal:  Curr Treat Options Cardiovasc Med       Date:  2002-12

6.  Coxsackievirus B detection in cases of myocarditis, myopericarditis, pericarditis and dilated cardiomyopathy in hospitalized patients.

Authors:  Imed Gaaloul; Samira Riabi; Rafik Harrath; Timothy Hunter; Khaldoun B Hamda; Assia B Ghzala; Sally Huber; Mahjoub Aouni
Journal:  Mol Med Rep       Date:  2014-09-18       Impact factor: 2.952

  6 in total

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