ArticleJournal of clinical microbiology2009
Mycoplasma agalactiae p40 Gene, a novel marker for diagnosis of contagious agalactia in sheep by real-time PCR: assessment of analytical performance and in-house validation using naturally contaminated milk samples.
Article in Journal of clinical microbiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 23 citations in OpenAlex.
- Molecular Identification of Mycoplasma agalactiae in Iran Based on P30 Gene.Archives of Razi Institute · 2021Article
- Validation of Loop-Mediated Isothermal Amplification (LAMP) Field Tool for Rapid and Sensitive Diagnosis of Contagious Agalactia in Small Ruminants.Animals : an open access journal from MDPI · 2020Article
- Sensitivity of two methods to detect Mycoplasma agalactiae in goat milk.Irish veterinary journal · 2015Article
- Mycoplasma agalactiae, an Etiological Agent of Contagious Agalactia in Small Ruminants: A Review.Veterinary medicine international · 2014Review
- Mycoplasma conjunctivae in domestic small ruminants from high mountain habitats in Northern Spain.BMC veterinary research · 2013Article
- Molecular characterization of Mycoplasma agalactiae reveals the presence of an endemic clone in Spain.Journal of clinical microbiology · 2013Article
- A survey of Mycoplasma agalactiae in dairy sheep farms in Spain.BMC veterinary research · 2012Article
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Authors and funding
4 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
We evaluated the capacity of the Mycoplasma agalactiae p40 gene as a diagnostic marker for contagious agalactia in sheep by quantitative real-time PCR. The p40 gene encodes an immunodominant adhesin that plays a key role in cytoadhesion of M. agalactiae. The assay was 100% specific, with an analytical sensitivity of 1 genome equivalent (GE), a quantification that is highly linear (R(2) > 0.992) and efficient (PCR efficiency, >0.992) over a 6-log dynamic range, down to 10 GE. We evaluated the capacity of the assay to detect Mycoplasma agalactiae in 797 milk samples (373 raw sheep milk samples from refrigerated tanks of different farms and 424 milk samples from individual sheep of a flock positive for M. agalactiae). In parallel, we also tested the samples by using microbiological isolation coupled with microscopy identification and by a PCR method recommended by the World Organization for Animal Health. While our assay was able to detect 57 (15.28%) positive samples of the 373 milk samples from different farms, identification by microbiological isolation coupled with microscopy detected only 36 (9.65%) samples, and the conventional PCR detected 31 (8.31%) samples. These findings showed that our assay based on the p40 gene is more specific and sensitive for the detection of M. agalactiae in actual natural samples and, thus, can be a promising alternative tool for diagnosis and epidemiological studies of M. agalactiae infection.
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