The difficult problem of the
contamination of
cell cultured
mycoplasma and the
infection diagnosis of various
mycoplasma urgently need a reliable and effective kit.
Mycoplasma culture by a
fluorescent staining method is reliable but takes time and trouble, and culture
pollution is intensified. A direct PRC method for amplifying a
mycoplasma gene, which is used for the routine detection of the mycoplasma is easy for cross
contamination, and high false masculinity is only used as an auxiliary reference. The invention relates to a mycoplasma conservative
gene which across links a
plant arabidopsis LEY sequence into a reporting
gene DNA by a
hybridization probe and amplifies the indirect detection of a reporting gene. The mycoplasma conservative gene is characterized in that mycoplasma 16sRNA is hybridized with the head part and the
tail part of the LEY reporting gene
DNA whose head part and
tail part are provided with mycoplasma conservative sequence probes; the reporting gene
DNA is catalyzed into a ring by heat-proof ligase, and the annular reporting gene is reversely amplified by PCR so as to indirectly reflect the detection of the mycoplasma; by adjusting ligase reaction, the reporting gene is difficultly across linked by the cross
contamination, thereby reducing the false masculinity; and if a
system is contaminated, the reporting gene can be changed.