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dc.contributor.authorFöldi, Dorottya
dc.contributor.authorNagy, Zsófia Eszter
dc.contributor.authorBelecz, Nikolett
dc.contributor.authorSzeredi, Levente
dc.contributor.authorFöldi, József
dc.contributor.authorKollár, Anna
dc.contributor.authorTenk, Miklós
dc.contributor.authorKreizinger, Zsuzsa
dc.contributor.authorGyuranecz, Miklós
dc.date.accessioned2024-09-27T10:25:31Z
dc.date.available2024-09-27T10:25:31Z
dc.date.issued2023
dc.identifier.citationFöldi D, Nagy ZE, Belecz N, Szeredi L, Földi J, Kollár A, Tenk M, Kreizinger Z, Gyuranecz M. Establishment of a Mycoplasma hyorhinis challenge model in 5-week-old piglets. Front Microbiol. 2023 Aug 4;14:1209119. doi: 10.3389/fmicb.2023.1209119en_US
dc.identifier.urihttp://hdl.handle.net/10832/4093
dc.description.abstractIntroduction: Mycoplasma hyorhinis is an emerging swine pathogen with high prevalence worldwide. The main lesions caused are arthritis and polyserositis, and the clinical manifestation of the disease may result in significant economic losses due to decreased weight gain and enhanced medical costs. We aimed to compare two challenge routes to induce M. hyorhinis infection using the same clinical isolate. Methods: Five-week-old, Choice hybrid pigs were inoculated on 2 consecutive days by intravenous route (Group IV-IV) or by intravenous and intraperitoneal routes (Group IV-IP). Mock-infected animals were used as control (control group). After the challenge, the clinical signs were recorded for 28 days, after which the animals were euthanized. Gross pathological and histopathological examinations, PCR detection, isolation, and genotyping of the re-isolated Mycoplasma sp. and culture of bacteria other than Mycoplasma sp. were carried out. The ELISA test was used to detect anti-M. hyorhinis immunoglobulins in the sera of all animals. Results: Pericarditis and polyarthritis were observed in both challenge groups; however, the serositis was more severe in Group IV-IV. Statistically significant differences were detected between the challenged groups and the control group regarding the average daily weight gain, pathological scores, and ELISA titers. Additionally, histopathological scores in Group IV-IV differed significantly from the scores in the control group. All re-isolated strains were the same or a close genetic variant of the original challenge strain. Discussion: Our results indicate that both challenge routes are suitable for modeling the disease. However, due to the evoked more severe pathological lesions and the application being similar to the hypothesized natural route of infection in Group IV-IV, the two-dose intravenous challenge is recommended by the authors to induce serositis and arthritis associated with M. hyorhinis infection.en_US
dc.language.isoenen_US
dc.titleEstablishment of a Mycoplasma hyorhinis challenge model in 5-week-old pigletsen_US
dc.typeArticleen_US
dc.identifier.doi10.3389/fmicb.2023.1209119


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