2002Zhonghua jiehe he huxi zazhiRequires access

16S~23S rDNA internal transcribed spacer sequence analysis and its application in mycobacterial identification

LI Guo-li

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Abstract

Objective To study the applicability of the 16S~23S rDNA internal transcribed spacer(ITS)sequences in mycobacterial identification Methods The 16S~23S rDNA ITS sequences of 22 mycobacterial species(30 reference strains and 16 clinical isolates)were determined by PCR direct sequencing The sequences determined by this study and those reported in Genbank were analysed by Clustal program (MegAlign Package [Windows Version 4 01] ;DNASTAR,Madison,Wis). The percentage similarity of sequence pairs was calculated and a cluster analysis dendrogram was constructed by PHYLIP package Results The 16S~23S rDNA ITS sequences among mycobacterial species had highly polymorphism except that Mycobacterium tuberculosis complex(MTC) sequences were highly consistent The similarity between sequence pairs was 30 4% to 86 5% Mycobacterial species could be isolated by cluster analysis dendrogram The results showed that sequence analysis of the 16S~23S rDNA ITS can differentiate MTC from nontuberculous mycobacteria(NTM)and identify NTM at species level Conclusion 16S~23S rDNA ITS sequences can be used as target genes in mycobacterial identification

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Objective To study the applicability of the 16S~23S rDNA internal transcribed spacer(ITS)sequences in mycobacterial identification Methods The 16S~23S rDNA ITS sequences of 22 mycobacterial species(30 reference strains and 16 clinical isolates)were determined by PCR direct sequencing The sequences determined by this study and those reported in Genbank were analysed by Clustal program (MegAlign Package [Windows Version 4 01] ;DNASTAR,Madison,Wis). The percentage similarity of sequence pairs was calculated and a cluster analysis dendrogram was constructed by PHYLIP package Results The 16S~23S rDNA ITS sequences among mycobacterial species had highly polymorphism except that Mycobacterium tuberculosis complex(MTC) sequences were highly consistent The similarity between sequence pairs was 30 4% to 86 5% Mycobacterial species could be isolated by cluster analysis dendrogram The results showed that sequence analysis of the 16S~23S rDNA ITS can differentiate MTC from nontuberculous mycobacteria(NTM)and identify NTM at species level Conclusion 16S~23S rDNA ITS sequences can be used as target genes in mycobacterial identification

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Available abstract

Objective To study the applicability of the 16S~23S rDNA internal transcribed spacer(ITS)sequences in mycobacterial identification Methods The 16S~23S rDNA ITS sequences of 22 mycobacterial species(30 reference strains and 16 clinical isolates)were determined by PCR direct sequencing The sequences determined by this study and those reported in Genbank were analysed by Clustal program (MegAlign Package [Windows Version 4 01] ;DNASTAR,Madison,Wis). The percentage similarity of sequence pairs was calculated and a cluster analysis dendrogram was constructed by PHYLIP package Results The 16S~23S rDNA ITS sequences among mycobacterial species had highly polymorphism except that Mycobacterium tuberculosis complex(MTC) sequences were highly consistent The similarity between sequence pairs was 30 4% to 86 5% Mycobacterial species could be isolated by cluster analysis dendrogram The results showed that sequence analysis of the 16S~23S rDNA ITS can differentiate MTC from nontuberculous mycobacteria(NTM)and identify NTM at species level Conclusion 16S~23S rDNA ITS sequences can be used as target genes in mycobacterial identification

Key concepts: Internal transcribed spacer, Biology, GenBank, 16S ribosomal RNA, Genetics, Sequence analysis, Dendrogram, Ribosomal DNA

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