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dc.contributor.authorGarcia-Morante, Beatriz
dc.contributor.authorDors, Arkadius
dc.contributor.authorLeón-Kempis, Rocio
dc.contributor.authorPérez de Rozas, Ana
dc.contributor.authorSegalés, Joaquim
dc.contributor.authorSibila, Marina
dc.contributor.otherProducció Animalca
dc.date.accessioned2018-10-23T10:24:08Z
dc.date.available2018-10-23T10:24:08Z
dc.date.issued2018-05-25
dc.identifier.citationGarcia-Morante, B., Dors, A., León-Kempis, R., Pérez de Rozas, A., Segalés, J., Sibila, M., 2018. Assessment of the in vitro growing dynamics and kinetics of the non-pathogenic J and pathogenic 11 and 232 Mycoplasma hyopneumoniae strains. Veterinary Research 49, 45.ca
dc.identifier.issn1297-9716ca
dc.identifier.urihttp://hdl.handle.net/20.500.12327/51
dc.description.abstractInformation on the in vitro growth of pathogenic and non-pathogenic Mycoplasma hyopneumoniae (M. hyopneumoniae) strains is scarce and controversial. Despite its limitations, the colour changing units (CCU) assay is still considered the golden standard titration technique for M. hyopneumoniae culture. Thus, the aims of the present study were: (1) to describe the growth dynamics and kinetics of pathogenic and non-pathogenic M. hyopneumoniae strains, and (2) to monitor the strains’ daily growth by ATP luminometry, CCU, colony forming units (CFU), and DNA quantification by real time quantitative PCR (qPCR) and by fluorescent double-stranded DNA (dsDNA) staining, to evaluate them as putative titration methodologies. The growth of the non-pathogenic J (ATCC®25934™) type strain and the pathogenic 11 (ATCC®25095™) reference strain and 232 strain was modelled by the Gompertz model. Globally, all three-strain cultures showed the same growing phases as well as similar maximal titres within a particular technique, but for CFU. However, the J strain displayed the fastest growing. During the logarithmic phase of growing, CCU, ATP and M. hyopneumoniae copy titres were strongly and linearly associated, and correlation between techniques could be reliably established. In conclusion, real-time culture titration by means of ATP or molecular assays was useful to describe the in vitro growth of the tested strains. Knowledge about the in vitro growth behaviour of a specific strain in a specific medium may provide several advantages, including information about the time required to reach maximal titres by the culture. Noteworthy, the obtained results refers to the three strains used, so extrapolation to other M. hyopneumoniae strains or culture conditions should be made cautiously.ca
dc.format.extent11ca
dc.language.isoengca
dc.publisherBioMed Centralca
dc.relation.ispartofVeterinary Researchca
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleAssessment of the in vitro growing dynamics and kinetics of the non-pathogenic J and pathogenic 11 and 232 Mycoplasma hyopneumoniae strainsca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.subject.udc619 - Veterinàriaca
dc.identifier.doihttps://doi.org/10.1186/s13567-018-0541-yca
dc.contributor.groupSanitat Animalca


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Attribution 4.0 International
Except where otherwise noted, this item's license is described as http://creativecommons.org/licenses/by/4.0/