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Reverse Transcription Loop-Mediated Isothermal Amplification RT-LAMP Assay for the Specific and Rapid Detection of Tilapia Lake Virus
Published on: May 18, 2020
Loop-mediated isothermal amplification (LAMP) assay for rapid detection and differentiation of selected Escherichia
Victor O Azuh1, Samia S Alkhalil2, Oludare Temitope Osuntokun3
1Biorespository and Clinical Virology Laboratory (BCVL), University College Hospital, Ibadan, Nigeria.
Background:
Escherichia coli is a bacterium that lives in both human and animal intestines and it is one of the first bacteria to infiltrate the intestine. The majority of E. coli strains are benign; however, some serotypes can infect people and animals with illnesses. The genomes of E. coli and Shigella spp. are closely related phenotypically, serotypically, biochemically, clinically and molecularly.
Methods:
Loop-mediated isothermal amplification (LAMP) assay was designed to accelerate E. coli detection and verify its specificity for different Shigella species and selected members of Enterobacteriaceae using specific LAMP primers designed along the E. colifliF gene region. For the E. coli sensitivity test, varying concentrations of betaine and MgSO4 were used to set up a LAMP reaction to detect 10 E. coli isolates and Enterobacteriaceae. The LAMP results interpretation was based on gel and colour change using SYBR green.
Results:
Results showed that for varying combinations of betaine and MgSO4 employed, 1.5 μL betaine and 1.0 μL MgSO4 gave the best amplification. The LAMP reaction amplified all E. coli strains used and did not amplify other Enterobacteriaceae indicating sensitivity and specificity.
Conclusion:
This study showed that this LAMP protocol can be used to detect E. coli among members of Enterobacteriaceae rapidly.
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