Loop-mediated isothermal amplification (LAMP) assay amplifies nucleic acid by use of six primers and strand-displacing DNA polymerase which requires only a single temperature. This technology has significant advantage in being of high sensitivity, specificity, rapidity and robust to use in the field by non-specialised personal. The high sensitivity of LAMP enables detection of the pathogens in sample material without time-consuming preparation thus being able to detect pathogens within 30 min.
SHEEP
CATTLE
EQUINE
HONEY BEES
eDNA IN WATERWAYS
AQUACULTURE
AQUACULTURE
Developing LAMP assays to detect pathogens affecting Australian aquaculture
Recently, there has been an increased demand for aquaculture animals over terrestrial meat due to growing awareness of their micronutrients and health benefits. However, pollution and intensive farming practices make these animals more vulnerable to diseases. The absence of effective vaccines and the risk of antibiotic resistance complicate the situation. To combat the spread of infections and prevent potential outbreaks, rapid pathogen detection is crucial. Most current methods rely heavily on polymerase chain reaction (PCR), requiring specialized equipment and expertise. In contrast, loop-mediated isothermal amplification (LAMP) offers a more cost-effective and accessible alternative, utilizing heat blocks or portable real-time LAMP devices. We have developed two LAMP assays to detect low concentrations of Yersinia ruckeri and Vagococcus salmoninarum, both significant threats to the Atlantic salmon industry in Tasmania, contributing approximately AUD 1 billion annually to Australia's economy. Additionally, a sensitive LAMP assay for abalone herpesvirus has been created, addressing severe economic losses in Victorian abalone farms over the past two decades. These assays are optimized for non-lethal sampling and in-field extraction, allowing farm personnel to conduct rapid testing and facilitating efficient management and control measures.
PhD Student: Hoda Abbas