Literature DB >> 12788033

Molecular sub-grouping of enterovirus reference and wild type strains into distinct genetic clusters using a simple RFLP assay.

Nikolaos Siafakas1, Panayotis Markoulatos, Constantin Vlachos, Glyn Stanway, Georgina Tzanakaki, Jenny Kourea-Kremastinou.   

Abstract

RFLP analysis and sequencing of RT-PCR amplicons in previous studies revealed the existence of intra-serotypic variability in the 5'-UTR of human enteroviruses, complicating the use of this method to serotype isolates. During the present study, the available sequences of many enterovirus reference and wild type strains were analysed in an attempt to discover restriction sites that would rapidly and reliably aid the classification of human enteroviruses into specific sub-groups on the basis of their 5'-UTR for diagnostic and/or epidemiological purposes. Despite intratypic genetic variability in the 5'-UTR, the results of the sequence analysis, as well as data from the RFLP analysis of 61 enterovirus reference strains from 60 different serotypes and 123 clinical isolates showed that one restriction endonuclease, HpaII, may contribute to a reliable sub-classification of CAVs and the rest of enteroviruses, on the basis of 5'-UTR, into five genetic groups, which could be particularly useful in clinical and epidemiological studies. Although more sequence data from enterovirus reference and wild type strains may be required for the elaboration of a precise molecular identification system, the more possible genotypic classification into distinct clusters, as shown with the restriction enzyme HpaII, and the determination of the biological significance of this grouping (pathogenesis, epidemiology) might constitute an alternative means of enterovirus identification against conventional classification into distinct serotypes.

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Year:  2003        PMID: 12788033     DOI: 10.1016/s0890-8508(03)00029-x

Source DB:  PubMed          Journal:  Mol Cell Probes        ISSN: 0890-8508            Impact factor:   2.365


  4 in total

1.  Nucleotide analysis and phylogenetic study of the homology boundaries of coxsackie A and B viruses.

Authors:  Eugenia Bolanaki; Christine Kottaridi; Panayotis Markoulatos; Lukas Margaritis; Theodoros Katsorchis
Journal:  Virus Genes       Date:  2005-12       Impact factor: 2.332

2.  Membrane adsorption with direct cell culture combined with reverse transcription-PCR as a fast method for identifying enteroviruses from sewage.

Authors:  D Papaventsis; N Siafakas; P Markoulatos; G T Papageorgiou; C Kourtis; E Chatzichristou; C Economou; S Levidiotou
Journal:  Appl Environ Microbiol       Date:  2005-01       Impact factor: 4.792

3.  Analysis of the serotype and genotype correlation of VP1 and the 5' noncoding region in an epidemiological survey of the human enterovirus B species.

Authors:  Inge Thoelen; Elien Moës; Philippe Lemey; Sara Mostmans; Elke Wollants; A Michael Lindberg; Anne-Mieke Vandamme; Marc Van Ranst
Journal:  J Clin Microbiol       Date:  2004-03       Impact factor: 5.948

4.  Echovirus 30, Jiangsu Province, China.

Authors:  Yan Na Zhao; Qing Wu Jiang; Ren Jie Jiang; Liang Chen; David S Perlin
Journal:  Emerg Infect Dis       Date:  2005-04       Impact factor: 6.883

  4 in total

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