Optimization and application of real-time qPCR assays in detection and identification of Chlamydiales in products of domestic ruminant abortion

dc.contributor.authorJonker, Annelize
dc.contributor.authorMichel, Anita Luise
dc.contributor.emailannelize.jonker@up.ac.zaen_US
dc.date.accessioned2024-09-10T12:06:53Z
dc.date.available2024-09-10T12:06:53Z
dc.date.issued2023-02-09
dc.descriptionDATA AVAILABILITY STATEMENT : Data are contained within the article.en_US
dc.descriptionSUPPLEMENTARY MATERIALS : TABLE S1: Synthetic controls; TABLES S2–S11: Limit of detection data; TABLE S12: Results of analysis of samples without placentitis or pneumonia.en_US
dc.description.abstractDomestic ruminant abortions due to infectious agents represent an important cause of economic losses in the agricultural industry. This study aimed to optimise and apply qPCR assays for detection of Chlamydiales in domestic ruminant abortion cases. Primers and probes for detection of the order Chlamydiales, Chlamydia abortus, Chlamydia pecorum, Parachlamydia acanthamoeba and Waddlia chondrophila were taken from the literature to create one singleplex and two duplex assays and the assays were optimised. Placentitis and pneumonia are pathological lesions associated with Chlamydiales infection. In a previous study, twenty-five clinical cases had pathological lesions of placentitis or pneumonia. These cases were investigated further by application of the qPCR assays in this study. Chlamydiales were detected in 16 cases. C. abortus, P. acanthamoeba and W. chondrophila were detected in bovine; and C. pecorum and W. chondrophila in ovine and caprine cases. Chlamydiales were detected in three previously inconclusive cases. Identification was improved from genus to species level (C. pecorum). Four cases remained inconclusive. In conclusion, detection of Chlamydiales and differentiation to species level was improved. This study reports the first detection of P. acanthamoeba and W. chondrophila in abortion cases in South Africa, indicating a potentially significant role in abortions in this country.en_US
dc.description.departmentVeterinary Tropical Diseasesen_US
dc.description.librarianam2024en_US
dc.description.sdgSDG-02:Zero Hungeren_US
dc.description.sdgSDG-03:Good heatlh and well-beingen_US
dc.description.sponsorshipAGRISeta and Red Meat Research and Development South Africa.en_US
dc.description.urihttps://www.mdpi.com/journal/pathogensen_US
dc.identifier.citationJonker, A.; Michel, A.L. Optimization and Application of Real-Time qPCR Assays in Detection and Identification of Chlamydiales in Products of Domestic Ruminant Abortion. Pathogens 2023, 12, 290. https://DOI.org/10.3390/pathogens12020290.en_US
dc.identifier.issn2076-0817 (online)
dc.identifier.other10.3390/pathogens12020290
dc.identifier.urihttp://hdl.handle.net/2263/98110
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.rights© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.en_US
dc.subjectChlamydialesen_US
dc.subjectAbortionen_US
dc.subjectRuminanten_US
dc.subjectChlamydiaen_US
dc.subjectParachlamydiaen_US
dc.subjectWaddliaen_US
dc.subjectSDG-03: Good health and well-beingen_US
dc.subjectSDG-02: Zero hungeren_US
dc.titleOptimization and application of real-time qPCR assays in detection and identification of Chlamydiales in products of domestic ruminant abortionen_US
dc.typeArticleen_US

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