In order to establish a rapid detection method for
Mycoplasma ovipneumoniae
, this study used the loop-mediated isothermal amplification (LAMP) technique to carry out nucleic acid amplification and chromatographic visualization via a lateral flow dipstick (LFD) assay. The
M. ovipneumoniae
elongation factor
TU
gene (
EF-TU
) was detected using a set of specific primers designed for the
EF-TU
gene, and the
EF-TU
FIP was detected by biotin labeling, which was used in the LAMP amplification reaction. The digoxin-labeled probe specifically hybridized with LAMP products, which were visually detected by LFD. Here, we established the
M. ovipneumoniae
LAMP-LFD rapid detection method and tested the specificity, sensitivity, and clinical application of this method. Results showed that the optimized LAMP performed at 60 °C for 60 min, and LFD can specifically and visually detect
M. ovipneumoniae
with a minimum detectable concentration at 1.0 × 10
2
CFU/mL. The sensitivity of LAMP-LFD was 1000 times that of the conventional PCR detection methods, and the clinical lung tissue detection rate was 86% of 50 suspected sheep infected with
M. ovipneumoniae
. In conclusion, LAMP-LFD was established in this study to detect
M. ovipneumoniae
, a method that was highly specific, sensitive, and easy to operate, and provides a new method for the prevention and diagnosis of
M. ovipneumoniae
infection.
Electronic supplementary material
The online version of this article (10.1007/s11274-019-2601-5) contains supplementary material, which is available to authorized users.