## Abstract The reliability of varicella–zoster virus (VZV) loop‐mediated isothermal amplification (LAMP) was evaluated for rapid diagnosis of viral infection. VZV‐specific primers only amplified VZV DNA; no LAMP products were observed in reactions performed with other viral DNA templates. The spec
Sensitive and rapid detection of Alicyclobacillus acidoterrestris using loop-mediated isothermal amplification
✍ Scribed by Jing Chen; Xiaoyan Ma; Yaowu Yuan; Wei Zhang
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 182 KB
- Volume
- 91
- Category
- Article
- ISSN
- 0022-5142
No coin nor oath required. For personal study only.
✦ Synopsis
BACKGROUND: A loop-mediated isothermal amplification (LAMP) assay was developed for the rapid detection (within 2 h) of Alicyclobacillus acidoterrestris. The assay detected the species-specific DNA sequence of the 16S-23S rRNA internal transcribed spacer.
RESULTS:
The eight strains of A. acidoterrestris were successfully amplified, but six strains of other bacillus Acidocaldarius and 13 bacterial species other than bacillus Acidocaldarius were not. The sensitivity of the LAMP assay was at 4.50 × 10 -2 cfu per tube. This sensitivity is greater than that obtained by polymerase chain reaction (PCR) assay. The LAMP assay was examined further for its ability to detect A. acidoterrestris in juice samples. The results were compared with those of conventional PCR detection.
CONCLUSION: Results indicate that the proposed LAMP assay is a rapid, specific and sensitive method for detecting A. acidoterrestris. As the amplification has been conducted under isothermal conditions, only a water bath or heating block is needed to maintain the required temperature. Thus, the method can be generalised and popularised easily in the future.
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