DIFFERENTIATION OF MYCOPLASMA BOVIS AND UREAPLASMA DIVERSUM BY REAL TIME PCR

Author(s):  
S.A. Makavchik ◽  
◽  
A.A. Sukhinin ◽  
L.I. Smirnova ◽  
V.A. Kuzmin ◽  
...  
2019 ◽  
Vol 54 (2) ◽  
pp. 378-385
Author(s):  
A.D. Kozlova ◽  
◽  
N.S. Gorbacheva ◽  
R.F. Hayerova ◽  
M.S. Krasnikova ◽  
...  

2020 ◽  
Vol 32 (2) ◽  
pp. 182
Author(s):  
J. Peippo ◽  
N. Vähänikkilä ◽  
M. Mutikainen ◽  
H. Lindeberg ◽  
T. Pohjanvirta ◽  
...  

Mycoplasma bovis (Mbo) has been isolated from genital tracts of bulls, and it can survive in processed semen. Experimental studies have shown that Mbo inoculation into the uterus or insemination with Mbo-infected semen can cause bursitis, salpingitis, abortion, and infertility. The control of Mbo is very difficult because of latent carrier animals, increasing resistance to antibiotics, and unavailability of effective vaccines. The aim of this study was to follow the passage of Mbo infection from naturally contaminated semen to transferable embryos during bovine invitro embryo production (IVP). (Unless otherwise stated, all chemicals used were purchased from Sigma-Aldrich.) Two batches of slaughterhouse-derived oocytes were matured in tissue culture medium 199 (TCM-199) with glutamax-I (Gibco™; Invitrogen Corporation) supplemented with 0.25mM sodium pyruvate, 100IUmL−1 penicillin, 100µgmL−1 streptomycin, 2ngmL−1 FSH (Puregon, Organon), 1µgmL−1 β-oestradiol (E-2257), and 10% heat-inactivated fetal bovine serum (FBS; Gibco™) for 24h at 38.5°C in maximal humidity in 5% CO2 in air. Matured oocytes were fertilized for 20h in IVF-TL medium supplemented with 10µgmL−1 of heparin and 2mM of PHE at 38.5°C in maximal humidity in 5% CO2 in air, using spermatozoa per mL as a final concentration. The batches of oocytes were divided between uninfected IVP bull (N=205) and naturally Mbo-infected AI bull (N=690). Zygotes were cultured in G1/G2 media (Vitrolife) supplemented with bovine serum albumin, fatty acid free (4mgmL−1), at 38.5°C in maximal humidity in 5% O2, 5% CO2, and 90% N2. Blastocysts were collected for Mbo cultures on Days 7 and 8 (IVF=Day 0). Samples of washed semen, fertilization medium, cumulus cells, culture medium, all wash media, and transferable embryos (with and without zona pellucidae) were collected for Mbo cultures. Half of the embryos were treated with trypsin according to IETS standards after the collections. The Mbo cultures were performed in accordance with procedures previously described by Bölske (1988 Zentralbl. Bakteriol. Mikrobiol. Hyg. A 69, 331-340), followed by detection with real-time PCR. Infection with Mbo does not seem to have negative effects on fertilization (cleavage rates: 77.1% and 89.0% for IVP and Mbo AI bulls, respectively) or embryo development rates (blastocyst rate: 26.3% and 32.5% for IVP and Mbo AI bulls, respectively). Following Mbo cultures, only washed semen was found to be Mbo positive via real-time PCR. We conclude that M. bovis is not likely transmitted in bovine IVP when using naturally infected semen. We acknowledge Tiina Kortelainen for technical assistance and the Ministry of Agriculture and Forestry for funding.


Author(s):  
Jade Bokma ◽  
Nick Vereecke ◽  
Mathilde L. Pas ◽  
Laurens Chantillon ◽  
Marianne Vahl ◽  
...  

Rapid identification of Mycoplasma bovis infections in cattle is a key factor to guide antimicrobial therapy and biosecurity measures. Recently, nanopore sequencing became an affordable diagnostic tool for both clinically relevant viruses and bacteria, but the diagnostic accuracy for M. bovis identification is undocumented. Therefore, in this study nanopore sequencing was compared to rapid identification of M. bovis with MALDI-TOF MS (RIMM), and triplex real-time PCR in a Bayesian latent class model (BLCM) for M. bovis in bronchoalveolar lavage fluid (BALf) obtained from calves. In practice, pooling of samples is often used to save money, but the influence on diagnostic accuracy has not been described for M. bovis . Therefore, a convenience sample of 17 pooled samples containing 5 individual BALf samples per farm was analyzed as well. The results of the pooled samples were compared to the individual samples, to determine sensitivity (Se) and specificity (Sp). The BLCM showed a good Se (77.3%; 95% Credible Interval: 57.8%-92.8%) and high Sp (97.4%; 91.5%-99.7%) for nanopore sequencing compared to RIMM (Se: 93.0%; 76.8%-99.5%, Sp: 91.3; 82.5%-97.0%) and real-time PCR (Se: 94.6%; 89.7%-97.7%, Sp: 86.0%; 76.1-93.6%). Se and Sp of pooled analysis for M. bovis were 85.7% (95% confidence interval: 59.8-111.6%) and 90.0% (71.4-108.6%%) for nanopore sequencing and 100% (100%-100%) and 88.9% (68.4-109.4%) for RIMM, respectively. In conclusion, nanopore sequencing is a rapid, reliable tool for the identification of M. bovis . To reduce costs and increase the chance of M. bovis identification, pooling of 5 samples for nanopore sequencing and RIMM is possible.


2010 ◽  
Vol 24 (5) ◽  
pp. 321-323 ◽  
Author(s):  
Bigna C. Rossetti ◽  
Joachim Frey ◽  
Paola Pilo

2010 ◽  
Vol 186 (3) ◽  
pp. 299-303 ◽  
Author(s):  
Konrad Sachse ◽  
Hala S.H. Salam ◽  
Roland Diller ◽  
Evelyn Schubert ◽  
Bernd Hoffmann ◽  
...  

2018 ◽  
Vol 50 (4) ◽  
pp. 875-882 ◽  
Author(s):  
S. Behera ◽  
R. Rana ◽  
P. K. Gupta ◽  
D. Kumar ◽  
Sonal ◽  
...  

2005 ◽  
Vol 17 (6) ◽  
pp. 537-545 ◽  
Author(s):  
Hugh Y. Cai ◽  
Patricia Bell-Rogers ◽  
Lois Parker ◽  
John F. Prescott

A real-time polymerase chain reaction (PCR) assay using hybridization probes on a LightCycler platform was developed for detection of Mycoplasma bovis from individual bovine mastitis milk and pneumonic lung tissues. The detection limit was 550 colony forming units (cfu)/ml of milk and 650 cfu/25 mg of lung tissue. A panel of bovine Mycoplasma and of other bovine-origin bacteria were tested; only M. bovis strains were positive, with a melting peak of 66.6°C. Mycoplasma agalactiae PG2 was also positive and could be distinguished because it had a melting peak of 63.1°C. In validation testing of clinical samples, the relative sensitivity and specificity were 100% and 99.3% for individual milks and 96.6% and 100% for the lung tissue. Using M. bovis real-time PCR, the M. bovis culture-positive milk samples were estimated to contain between 5 × 104 and 7.7 × 108 cfu/ml and the M. bovis culture-positive lungs between 1 × 103 and 1 × 109 cfu/25 mg. Isolation, confirmed with the real-time PCR and colony fluorescent antibody test, showed that at the herd level, the proportion of samples positive for M. bovis isolation in mastitis milk samples submitted to the Mastitis Laboratory, Animal Health Laboratory, University of Guelph, Ontario, Canada, was 2.4% (5/201). We conclude that this probe-based real-time PCR assay is a sensitive, specific, and rapid method to identify M. bovis infection in bovine milk and pneumonic lungs.


2021 ◽  
Vol 8 ◽  
Author(s):  
Tarja Pohjanvirta ◽  
Nella Vähänikkilä ◽  
Vera Talvitie ◽  
Sinikka Pelkonen ◽  
Tiina Autio

Mycoplasma bovis is an important cattle pathogen affecting animal health, welfare, and productivity. The main disease syndromes are mastitis, pneumonia, and otitis media in young stock, as well as arthritis. Response to antibiotic treatment is poor and no effective vaccine is available. Asymptomatic carriers are common and usually harbor the organism in the airways or mammary glands. Purchase of carrier animals is a major risk for the introduction of infection into naive herds. Following the detection of M. bovis in Finland in 2012, a voluntary control program was established. It aims to prevent the spread of the infection and to help farms attain certification of a low M. bovis risk. Among the diagnostic tools in the program, nasal swabs (NS) from young calves have been tested for M. bovis to indicate the infection status of the herd. In this study, we assessed the suitability of this test method. We analyzed the effectiveness of NS and deep nasopharyngeal swabs (NP) to detect M. bovis in pneumonic and healthy calves in dairy herds recently infected with M. bovis. In pneumonic calves, NP sampling followed by culture and real-time PCR demonstrated a proportion of positive agreement (PPA) of 0.91 compared with bronchoalveolar lavage (BAL), whereas NS showed only 0.5 PPA compared with BAL. Among healthy dairy calves, overall M. bovis prevalence in NS was 29.6%. The highest rate of shedding (43%) occurred in calves 31–60 days old. At the calf level, M. bovis prevalence in NP samples was 47% compared with 33% in NS samples among the 284 studied calves. However, at the herd level, NS sampling classified 51 out of 54 herds with a positive infection status as infected, whereas in NP sampling, the respective figure was 43 out of 54 herds (p = 0.061). In conclusion, NS sampling from calves under 6 months of age and analyzed by real-time PCR is a cost-efficient method for a control program to detect M. bovis in dairy herds, even if no M. bovis mastitis has been detected in the herd. For pneumonic calves, we recommend only NP or BAL sampling.


Sign in / Sign up

Export Citation Format

Share Document