Establishment of PCR for Detection of Mycoplasma gallisepticum
Qin Lu-lu
Abstract
Qin Lu-lu
Abstract
A pair of primers was designed based on fMG-2 sequences of avian Mycoplasma.The primers selectively amplified a 726 bp product from Mycoplasma gallisepticum(MG),but did not amplify the DNA or RNA of other bacteria or viruses.The detection threshold of PCR for MG was 3 pg.The samples detected by PCR,and isolation and identification.Using PCR,20.5% of field samples was positively detected,it was higher than that of isolation and identification.The results indicated that this technique is a useful screening assay for the detection of MG.
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 primers was designed based on fMG-2 sequences of avian Mycoplasma.The primers selectively amplified a 726 bp product from Mycoplasma gallisepticum(MG),but did not amplify the DNA or RNA of other bacteria or viruses.The detection threshold of PCR for MG was 3 pg.The samples detected by PCR,and isolation and identification.Using PCR,20.5% of field samples was positively detected,it was higher than that of isolation and identification.The results indicated that this technique is a useful screening assay for the detection of MG.
Key concepts: Mycoplasma gallisepticum, Biology, Isolation (microbiology), Mycoplasma, Virology, Polymerase chain reaction, Microbiology, DNA