Multiplex 16S rRNA-derived geno-biochip for detection of 16 bacterial pathogens from contaminated foods

被引:8
作者
Shin, Hwa Hui [1 ]
Hwang, Byeong Hee [1 ,2 ]
Cha, Hyung Joon [1 ]
机构
[1] Pohang Univ Sci & Technol, Dept Chem Engn, Pohang 790784, South Korea
[2] Incheon Natl Univ, Div Bioengn, Inchon, South Korea
关键词
Direct RNA-detection; Foodborne pathogen; Food matrix; Multiple detection; Oligonucleotide microarray; ESCHERICHIA-COLI; SECONDARY STRUCTURE; SALMONELLA; HYBRIDIZATION; DNA; IDENTIFICATION; STABILIZATION; DISEASES; IMPACT; IONS;
D O I
10.1002/biot.201600043
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Foodborne diseases caused by various pathogenic bacteria occur worldwide. To prevent foodborne diseases and minimize their impacts, it is important to inspect contaminated foods and specifically detect many types of pathogenic bacteria. Several DNA oligonucleotide biochips based on 16S rRNA have been investigated to detect bacteria; however, a mode of detection that can be used to detect diverse pathogenic strains and to examine the safety of food matrixes is still needed. In the present work, a 16S rRNA gene-derived geno-biochip detection system was developed after screening DNA oligonucleotide specific capture probes, and it was validated for multiple detection of 16 pathogenic strains that frequently occur with a signature pattern. rRNAs were also used as detection targets directly obtained from cell lysates without any purification and amplification steps in the bacterial cells separated from eight food matrixes by simple pretreatments. Thus, the developed 16S rRNA-derived geno-biochip can be successfully used for the rapid and multiple detection of the 16 pathogenic bacteria frequently isolated from contaminated foods that are important for food safety.
引用
收藏
页码:1405 / 1414
页数:10
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