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dc.contributor.authorSchäfer, Jenny
dc.contributor.authorKämpfer, Peter
dc.contributor.authorJäckel, Udo
dc.date.accessioned2023-06-12T07:58:38Z
dc.date.available2012-07-02T12:19:42Z
dc.date.available2023-06-12T07:58:38Z
dc.date.issued2011
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:hebis:26-opus-88678
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/17184
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-16562
dc.description.abstractThe thermophilic actinomycete species Saccharopolyspora rectivirgula has been associated with the exogen allergic alveolitis (EAA). EAA is caused by the inhalation of high amounts of airborne spores that can be found for example in environments of agricultural production, compost facilities, mushroom cultivation rooms, or rooms with technical air moistening. Because of the medical relevance of S. rectivirgula, a reliable detection system is needed. Therefore, a quantitative real-time polymerase chain reaction (qPCR) primer system was designed, targeting the 16S rRNA gene of the type strain S. rectivirgula DSM 43747T and six other S. rectivirgula reference strains. Our investigation showed that S. rectivirgula presumably own four operons of the 16S rRNA gene, which has to be considered for estimation of cell equivalents. Furthermore, the DNA recovery efficiency from these strains was tested in combination with bioaerosol or material sample as well as the influence of non-target DNA to the recovery rate. Results showed a recovery DNA efficiency of 7 55%. The recovery rate of DNA in a mixture with non-target DNA resulted in ~87%. In summary, a high amplification efficiency using real-time PCR was found, for which estimated concentrations revealed cell numbers of 2.7 × 105 cells m-3 in bioaerosol and 2.8 × 106 cells g-1 fw-1 in material samples from a duck house. The specificity of the new developed quantification system was shown by generation of two clone libraries from bioarosol samples, from a duck house, and from a composting plant. Totally, the results clearly show the specificity and practicability of the established qPCR assay for detection of S. rectivirgula.en
dc.language.isoende_DE
dc.rightsIn Copyright*
dc.rights.urihttp://rightsstatements.org/page/InC/1.0/*
dc.subjectSaccharopolyspora rectivirgulaen
dc.subjectexogen allergic alveolitis (EAA)en
dc.subjectdetection by quantitative rtPCRen
dc.subject16S rRNA geneen
dc.subject.ddcddc:570de_DE
dc.titleDetection of Saccharopolyspora rectivirgula by quantitative Real-Time PCRen
dc.typearticlede_DE
local.affiliationFB 09 - Agrarwissenschaften, Ökotrophologie und Umweltmanagementde_DE
local.opus.id8867
local.opus.instituteInstitut für Angewandte Mikrobiologiede_DE
local.opus.fachgebietAgrarwissenschaften, Ökotrophologie und Umweltmanagement fachübergreifendde_DE
local.source.freetextAnnals of Occupational Hygiene, 2011, 55(6), 612-619; doi:10.1093/annhyg/mer018de_DE


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