Sensitive and Specific Detection of Mycoplasma species by Consensus Polymerase Chain Reaction and Dot Blot Hybridization.
10.5625/lar.2011.27.2.141
- Author:
Sunhwa HONG
1
;
Hyun A LEE
;
Sang Ho PARK
;
Okjin KIM
Author Information
1. Center for Animal Resources Development, Wonkwang University, Iksan, Republic of Korea. kimoj@wku.ac.kr
- Publication Type:Original Article
- Keywords:
Polymerase chain reaction;
Dot blot hybridization;
PCR/DBH;
Mycoplasma
- MeSH:
Animals;
Animals, Laboratory;
Bacteria;
Bacterial Infections;
Chimera;
Consensus;
Digoxigenin;
DNA;
Limit of Detection;
Mycoplasma;
Polymerase Chain Reaction;
Sensitivity and Specificity
- From:Laboratory Animal Research
2011;27(2):141-145
- CountryRepublic of Korea
- Language:English
-
Abstract:
Mycoplasmas are highly fastidious bacteria, difficult to culture and slow growing. Many species of mycoplasmas are important pathogens that cause respiratory infection in laboratory animals and that are known to affect experimental results obtained with contaminated animals. The aim of the present study was to develop a sensitive and specific assay for the detection of mycoplasma species. To this end, we developed a polymerase chain reaction and dot blot hybridization assay (PCR/DBH) for detecting mycoplasma DNA and evaluated it for its sensitivity and specificity. Mycoplasma consensus primer pairs were used for the amplification of target DNA. When PCR product was visually detected, the limit of detection of the PCR test was 10(2) pg of mycoplasma purified DNA. For DBH, the amplified DNA was labeled by incorporation of digoxigenin (DIG). This DIG-labeled probe was capable of detecting 10(4) pg of purified mycoplasma DNA by DBH. PCR/DBH was more sensitive than PCR or DBH alone and was also very specific. Our PCR/DBH assay can be applied efficiently to confirm the presence of mycoplasma species on clinical samples and to differentiate between mycoplasma species infection and other bacterial infections.
