Detection of cesA mRNA from Bacillus cereus by RNA-specific amplification

被引:20
|
作者
Yasukawa, Kiyoshi [1 ]
Agata, Norio [2 ]
Inouye, Kuniyo [1 ]
机构
[1] Kyoto Univ, Grad Sch Agr, Div Food Sci & Biotechnol, Sakyo Ku, Kyoto 6068502, Japan
[2] Nagoya City Publ Hlth Res Inst, Mizuho Ku, Nagoya, Aichi 4678615, Japan
基金
日本学术振兴会;
关键词
Bacillus cereus; Cereulide; PCR; RNA-specific amplification; RT-PCR; MURINE LEUKEMIA-VIRUS; EMETIC TOXIN; MYCOBACTERIUM-TUBERCULOSIS; SEQUENCE AMPLIFICATION; REVERSE TRANSCRIPTASES; MYELOBLASTOSIS VIRUS; TEMPLATE-PRIMER; IDENTIFICATION; DODECADEPSIPEPTIDE; QUANTIFICATION;
D O I
10.1016/j.enzmictec.2009.12.009
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cereulide is the cyclic dodecadepsipeptide responsible for the emetic-type food-borne disease caused by Bacillus cereus. It is synthesized enzymatically by non-ribosomal peptide synthetases. In this study, we established an RNA-specific amplification assay for the detection of mRNA transcribed from the cesA gene, one of the 7 genes constituting the cereulide synthetase (ces) gene cluster of emetic-type B. cereus. The assay detected as few as 1000 copies of this RNA. Examination of the total RNAs extracted from 7 strains of cereulide-producing B. cereus, 6 strains of cereulide non-producing B. cereus, 6 strains of other Bacillus species, and 10 non-Bacillus strains showed that the assay specifically detected emetic-type B. cereus strains. RNA-specific amplification using RNA extracts provided comparable results to RT-PCR assays using RNA extracts and PCR assays using DNA extracts. The RNA-specific amplification assay is suitable for the detection of mRNA transcribed from the cesA gene. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:391 / 396
页数:6
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