Idntification of Edwarsiella tarda Strains by Two-Temperature PCR
Xiaoli Yu
Abstract
Xiaoli Yu
Abstract
A pair of primer XZE15 and XZE16 was designed and synthesized according to the conserved gene sequences of 23S rDNA of Edwarsiella tarda,and then reaction parameters were optimized to develop two-temperature polymerase chain reaction(PCR)to simultaneously identify E.tarda.The results showed that only of 284pb-long DNA fragment for three E.tarda strains was amplified,and no DNA fragments for three Edwarsiella ictalur strains and other fish pathogenic viruses and bacteria were amplified by this two-temperature PCR.And 10 pg DNA of E.tarda was detected by this two-temperature PCR.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
A pair of primer XZE15 and XZE16 was designed and synthesized according to the conserved gene sequences of 23S rDNA of Edwarsiella tarda,and then reaction parameters were optimized to develop two-temperature polymerase chain reaction(PCR)to simultaneously identify E.tarda.The results showed that only of 284pb-long DNA fragment for three E.tarda strains was amplified,and no DNA fragments for three Edwarsiella ictalur strains and other fish pathogenic viruses and bacteria were amplified by this two-temperature PCR.And 10 pg DNA of E.tarda was detected by this two-temperature PCR.
Key concepts: Primer (cosmetics), Polymerase chain reaction, Biology, DNA, Molecular biology, Gene, Bacteria, Virology