Peer-reviewed veterinary case report
Rapid detection and identification of nontuberculous mycobacterial pathogens in fish by using high-resolution melting analysis.
- Journal:
- Applied and environmental microbiology
- Year:
- 2013
- Authors:
- Phung, Thu Nguyet et al.
- Affiliation:
- Institute of Biotechnology
Plain-English summary
In fish, infections caused by certain types of bacteria known as Mycobacterium can lead to a disease called piscine mycobacteriosis, which can be serious and sometimes even deadly. There are about 20 different species of Mycobacterium that can infect fish, with Mycobacterium marinum, M. fortuitum, and M. chelonae being the most common culprits. Researchers have been looking for a fast and affordable way to identify these bacteria, and they found that a method called high-resolution melting analysis (HRMA) can quickly tell apart 12 different Mycobacterium species at once. This method was able to detect very small amounts of the bacteria's genetic material and showed that it only works for Mycobacterium, not other types of bacteria. Overall, this new testing method could help diagnose fish infections more efficiently.
Abstract
Mycobacterial infections in fish are commonly referred to as piscine mycobacteriosis, irrespectively of the specific identity of the causal organism. They usually cause a chronic disease and sometimes may result in high mortalities and severe economic losses. Nearly 20 species of Mycobacterium have been reported to infect fish. Among them, Mycobacterium marinum, M. fortuitum, and M. chelonae are generally considered the major agents responsible for fish mycobacteriosis. As no quick and inexpensive diagnostic test exists, we tested the potential of high-resolution melting analysis (HRMA) to rapidly identify and differentiate several Mycobacterium species involved in fish infections. By analyzing both the melting temperature and melting profile of the 16S-23S rRNA internal transcribed spacer (ITS), we were able to discriminate 12 different species simultaneously. Sensitivity tests conducted on purified M. marinum and M. fortuitum DNA revealed a limit of detection of 10 genome equivalents per reaction. The primers used in this procedure did not lead to any amplification signal with 16 control non-Mycobacterium species, thereby demonstrating their specificity for the genus Mycobacterium.
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Search related cases →Original publication: https://pubmed.ncbi.nlm.nih.gov/24123734/