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Comparison of bacteriological culture method and multiplex real-time pcr for detection of mastitis

dc.contributor.buuauthorKAHYA DEMİRBİLEK, SERPİL
dc.contributor.buuauthorYildiz, Merve
dc.contributor.buuauthorAKKOÇ, AHMET
dc.contributor.buuauthorMUTLU, AYŞE
dc.contributor.buuauthorARDIÇLI, ÖZGE
dc.contributor.buuauthorAner, Havva
dc.contributor.departmentMikrobiyoloji Ana Bilim Dalı.
dc.contributor.departmentVeteriner Fakültesi
dc.contributor.departmentPatoloji Ana Bilim Dalı.
dc.contributor.orcid0009-0006-7709-182X
dc.date.accessioned2025-02-07T11:58:18Z
dc.date.available2025-02-07T11:58:18Z
dc.date.issued2024-03-30
dc.description.abstractThis study includes the evaluation of multiplex real-time PCR (rPCR) kit, which was developed to provide rapid diagnosis of mastitis infections, by working with milk samples of 2 different sources of mastitis and comparing the results with the classical bacteriological culture method (BC). A total of 273 bacteria were isolated in 226 samples (47.88%) out of 472 samples by BC. These were 139 (50.91%) Staphylococcus spp., 61 (22.34%) Streptococcus spp., 15 (5.49%) E. coli , 8 (2.93%) Enterococcus spp., 50 (18.31%) other bacteria. When we look at the multiplex rPCR results; 1052 positive were obtained for the gene regions of 14 different bacteria, 1 yeast, and 1 beta-lactamase gene examined in 472 samples. While no searched gene region was found by rPCR in 78 (16.5%) of the 472 samples studied, at least 1 gene was detected in 394 (83.5%) samples. These 1052 positive samples by rPCR were; 263 (28.43%) Staphylococcus spp. , 51 (5.51%) S. aureus, 57 (6.16%) Enterococcus spp. , 49 (5.29%) C. bovis, 16 (1.73%) S. dysgalactiae, 84 (9.08%) S. agalactiae, 71 (7.67%) S. uberis, 73 (7.89%) E. coli , 14 (1.51%) Prototheca spp. , 39 (4.21%) T. pyogenes/P. indolicus, 5 (0.54%) S. marcescens, 15 (1.62%) K. oxytoca/pneumonia, 117 (12.64%) Mycoplasma spp. , 31 (3.35%) M. bovis, 40 (4.32%) yeast , and 127 samples (26.90%) were beta-lactamase positive. When the antibiotic resistance of the isolates was evaluated, 78 (31.96%) tetracycline, 72 (29.5%) penicillin, and 60 (24.59%) clindamycin resistance were observed predominantly in Gram-positive isolates, while 6 (23.07%) tigecycline, 6 (23.07%) netilmicin, 6 (23.07%) pipercillin resistance was found in gram -negative isolates. While a bacteria and/or yeast gene was found by rPCR in 187 of 246 (76.01%) samples with no bacterial growth, a bacterium was isolated with BC in only 20 (8.84%) samples whose gene region was not found by rPCR. As a result, the multiplex rPCR system used in the diagnosis of mastitis has been found to be quite reliable as it can detect a large number of bacteria in a very short time compared to classical methods. Therefore, we advise the use of rPCR and/or culture for confirmation of clinical signs in mastitis and at routine mastitis surveillance.
dc.identifier.doi10.1016/j.rvsc.2024.105237
dc.identifier.issn0034-5288
dc.identifier.scopus2-s2.0-85189088719
dc.identifier.urihttps://doi.org/10.1016/j.rvsc.2024.105237
dc.identifier.urihttps://hdl.handle.net/11452/50210
dc.identifier.volume172
dc.identifier.wos001218537500001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherElsevier Sci Ltd
dc.relation.journalResearch In Veterinary Science
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectResistant staphylococcus-aureus
dc.subjectBovine mastitis
dc.subjectMolecular characterization
dc.subjectAntibiotic-resistance
dc.subjectMilk samples
dc.subjectPathogens
dc.subjectDairy
dc.subjectAssay
dc.subjectIdentification
dc.subjectPrevalence
dc.subjectMastitis
dc.subjectBacteriology
dc.subjectReal time pcr
dc.subjectAntibiotic resistance
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectVeterinary sciences
dc.titleComparison of bacteriological culture method and multiplex real-time pcr for detection of mastitis
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentVeteriner Fakültesi/Mikrobiyoloji Ana Bilim Dalı.
local.contributor.departmentVeteriner Fakültesi/Patoloji Ana Bilim Dalı.
local.indexed.atWOS
local.indexed.atScopus
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relation.isAuthorOfPublication77d6f8ff-e2a2-45b4-a991-48f59fee43a4
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relation.isAuthorOfPublication.latestForDiscoveryc131131a-7bfa-4fdb-a81a-f4b59c53a2d6

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