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1000 Titel
  • Serotyping and pathotyping of Glaesserella parasuis isolated 2012–2019 in Germany comparing different PCR-based methods
1000 Autor/in
  1. Schuwerk, Lukas |
  2. Hoeltig, Doris |
  3. Waldmann, Karl-Heinz |
  4. Strutzberg-Minder, Katrin |
  5. Valentin-Weigand, Peter |
  6. Rohde, Judith |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-11-17
1000 Erschienen in
1000 Quellenangabe
  • 51(1):137
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13567-020-00862-1 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673094/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Glaesserella parasuis is an important pathogen in swine production. It acts as a primary pathogen in systemic Glässer´s disease and as a secondary pathogen in Porcine Respiratory Disease Complex. In this study, a collection of 308 isolates from carrier animals and individuals with respiratory or Glässer´s disease isolated 2012–2019 in Germany was analysed. Isolates were characterized for serovar implementing two different PCR methods. Additionally, two different PCR methods for pathotyping isolates were applied to the collection and results compared. Serovar 6 (p < 0.0001) and 9 (p = 0.0007) were correlated with carrier isolates and serovar 4 was associated with isolates from animals with respiratory disease (p = 0.015). In systemic isolates, serovar 13 was most frequently detected (18.9%). Various other serovars were isolated from all sites and the ratio of serovar 5 to serovar 12 was approximately 1:2. These two serovars together represented 14.3% of the isolates; only serovar 4 was isolated more frequently (24.7%). The pathotyping method based on the leader sequence (LS = ESPR of vta) was easy to perform and corresponded well to the clinical background information. Of the carrier isolates 72% were identified as non-virulent while 91% of the systemic isolates were classified as virulent (p < 0.0001). Results of the pathotyping PCR based on 10 different marker genes overall were in good agreement with clinical metadata as well as with results of the LS-PCR. However, the pathotyping PCR was more complicated to perform and analyze. In conclusion, a combination of the serotyping multiplex-PCR and the LS-PCR could improve identification of clinically relevant G. parasuis isolates, especially from respiratory samples.
1000 Sacherschließung
lokal
lokal Serotyping/veterinary [MeSH]
lokal Swine [MeSH]
lokal pathotyping
lokal Polymerase Chain Reaction/veterinary [MeSH]
lokal Haemophilus Infections/microbiology [MeSH]
lokal Haemophilus Infections/veterinary [MeSH]
lokal Sus scrofa [MeSH]
lokal Animals [MeSH]
lokal Virulence/genetics [MeSH]
lokal Swine Diseases/microbiology [MeSH]
lokal serotyping
lokal Haemophilus parasuis/pathogenicity [MeSH]
lokal Germany [MeSH]
lokal virulence
lokal leader sequence
lokal Polymerase Chain Reaction/methods [MeSH]
lokal serovar
lokal Haemophilus parasuis/genetics [MeSH]
lokal Serogroup [MeSH]
lokal Research Article
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/U2NodXdlcmssIEx1a2Fz|https://frl.publisso.de/adhoc/uri/SG9lbHRpZywgRG9yaXM=|https://frl.publisso.de/adhoc/uri/V2FsZG1hbm4sIEthcmwtSGVpbno=|https://frl.publisso.de/adhoc/uri/U3RydXR6YmVyZy1NaW5kZXIsIEthdHJpbg==|https://frl.publisso.de/adhoc/uri/VmFsZW50aW4tV2VpZ2FuZCwgUGV0ZXI=|https://orcid.org/0000-0002-4671-2164
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1000 Erstellt am 2023-05-12T15:08:51.696+0200
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