ArticleJournal of clinical microbiology2008
Real-time PCR assays to address genetic diversity among strains of Mycoplasma hyopneumoniae.
Article in Journal of clinical microbiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
30 citing papers in PubMed.
- Aoudad (Ammotragus lervia) as disease reservoirs for bighorn sheep (Ovis canadensis): experimental and epidemiological evidence.Scientific reports · 2026Article
- Comparative evaluation and validation of rapid quantification methods for Mycoplasma hyopneumoniae: development of a PMA-based viability qPCR assay.Scientific reports · 2026Article
- Longitudinal study of diagnostic sample matrices for respiratory pathogens on Irish farrow-to-finish pig herds.Irish veterinary journal · 2026Article
- Rationalizing the use of common parameters and technological tools to follow up Mycoplasma hyopneumoniae infections in pigs.Porcine health management · 2024Article
- Effect of pooled tracheal sample testing on the probability of Mycoplasma hyopneumoniae detection.Scientific reports · 2024Article
- Characterizing the detection of inactivated Mycoplasma hyopneumoniae DNA in the respiratory tract of pigs.Veterinary research · 2024Article
- Rapid detection ofFrontiers in cellular and infection microbiology · 2024Article
- Hijacking of Host Plasminogen byMicrobiology spectrum · 2023Article
- Regulatory functional role of NLRP3 inflammasome during Mycoplasma hyopneumoniae infection in swine.Journal of animal science · 2023Article
- Prevalence of three Mycoplasma sp. by multiplex PCR in cattle with and without respiratory disease in central Mexico.Tropical animal health and production · 2022Article
- Genotyping and biofilm formation of Mycoplasma hyopneumoniae and their association with virulence.Veterinary research · 2022Article
- Cough associated with the detection of Mycoplasma hyopneumoniae DNA in clinical and environmental specimens under controlled conditions.Porcine health management · 2022Article
- Seasonal Variation in Prevalence ofPathogens (Basel, Switzerland) · 2021Article
- Mycoplasma hyopneumoniae Surveillance in Pig Populations: Establishing Sampling Guidelines for Detection in Growing Pigs.Journal of clinical microbiology · 2021Article
- Evaluation of the clinical efficacy of a water soluble formulation of tylvalosin in the control of enzootic pneumonia associated with Mycoplasma hyopneumoniae and Pasteurella multocida in pigs.Porcine health management · 2020Article
- Diversity ofJournal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc · 2020Article
- Serum metabolite markers of early Mycoplasma hyopneumoniae infection in pigs.Veterinary research · 2019Article
- Genetic variation of Mycoplasma hyopneumoniae from Brazilian field samples.BMC microbiology · 2019Article
- Article
- Characterization of a PCV2d-2 isolate by experimental infection of pigs.Virology journal · 2018Article
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Mycoplasma hyopneumoniae is an important cause of pneumonia in pigs around the world, but confirming its presence in (or absence from) pigs can be difficult. Culture for diagnosis is impractical, and seroconversion is often delayed after natural infection, limiting the use of serology. Numerous PCR assays for the detection of M. hyopneumoniae have been developed, targeting several different genes. Recently, genetic diversity among strains of M. hyopneumoniae was demonstrated. The effect of this diversity on the accuracy and sensitivity of the M. hyopneumoniae PCR assays could result in false-negative results in current PCR tests. In this study, a panel of isolates of M. hyopneumoniae, M. flocculare, M. hyorhinis, and M. hyosynoviae were tested with a number of M. hyopneumoniae-specific PCR assays. Some M. hyopneumoniae PCR assays tested did not detect all isolates of M. hyopneumoniae. To increase the efficiency of PCR testing, two new real-time PCR assays that are specific and capable of detecting all of the M. hyopneumoniae isolates used in this study were developed.
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