Publication:
The canonical Brucella species-host dependency is changing, however, the antibiotic susceptibility profiles remain unchanged

dc.contributor.authorÇelik, Elif
dc.contributor.authorKayman, Tuba
dc.contributor.authorBüyük, Fatih
dc.contributor.authorSaglam, Aliye Gülmez
dc.contributor.authorAbay, Seçil
dc.contributor.authorAkar, Mustafa
dc.contributor.authorKarakaya, Emre
dc.contributor.authorBozlak, Çiğdem Eda Balkan
dc.contributor.authorCoşkun, Mustafa Reha
dc.contributor.authorBüyük, Eray
dc.contributor.authorÇelebi, Özgür
dc.contributor.authorŞahin, Mitat
dc.contributor.authorSatıcıoğlu, İzzet Burçin
dc.contributor.authorDurhan, Seda
dc.contributor.authorBaykal, Atakan
dc.contributor.authorErsoy, Yaren
dc.contributor.authorOtlu, Salih
dc.contributor.authorAydın, Fuat
dc.contributor.buuauthorSATICIOĞLU, İZZET BURÇİN
dc.contributor.departmentVeteriner Fakültesi
dc.contributor.departmentSu Hayvanları Hastalıkları Ana Bilim Dalı
dc.contributor.researcheridAAD-4156-2019
dc.date.accessioned2024-11-26T06:14:23Z
dc.date.available2024-11-26T06:14:23Z
dc.date.issued2023-07-26
dc.description.abstractBrucellosis is a chronic disease caused by Brucella species with a wide range of hosts, from marine mammals to terrestrial species, but with strict host preferences. With the zoonotic character, the prevalence of human brucellosis cases is a reflection of animal infections. This study aimed to identify 192 Brucella isolates obtained from various sources by Bruce-ladder PCR and to determine their antibiotic susceptibilities by gradient diffusion method (E-test). As a result of the PCR, all human isolates (n = 57) were identified as B. melitensis. While 58 (82.9%) of the cattle isolates were identified as B. abortus, 59 (90.8%) of the sheep isolates were identified as B. melitensis. In addition, 12 (17.1%) of the cattle isolates and 6 (9.2%) of the sheep isolates were determined as B. melitensis and B. abortus, respectively. The primary host change behavior of B. melitensis was 1.9 times higher than that of B. abortus. While gentamicin and ciprofloxacin susceptibilities of Brucella isolates were 100%, tetracycline, doxycycline, streptomycin, trimethoprim/sulfamethoxazole and rifampicin susceptibilities were 99%, 99%, 97.4%, 91.7% and 83.9%, respectively. The lowest sensitivity of the isolates was determined against to cefoperazone as 26%. A triple-drug resistance was detected in 1 B. abortus isolate that included simultaneous resistance to cefoperazone, rifampicin, and trimethoprim/sulfamethoxazole. The high susceptibility profiles we found against to antibiotics such as tetracycline, doxycycline gentamicin and ciprofloxacin, used widely in treatment, are encouraging. However, the change in the canonical Brucella species-primary host preference suggests the need to reconsider eradication program, including updating vaccine formulations.
dc.identifier.doi10.1016/j.micpath.2023.106261
dc.identifier.issn0882-4010
dc.identifier.urihttps://doi.org/10.1016/j.micpath.2023.106261
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0882401023002942?via%3Dihub
dc.identifier.urihttps://hdl.handle.net/11452/48486
dc.identifier.volume182
dc.identifier.wos001049614900001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherAcademic Press Ltd- Elsevier Science Ltd
dc.relation.journalMicrobial Pathogenesis
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAntimicrobial resistance profiles
dc.subjectPcr assay
dc.subjectMelitensis
dc.subjectAbortus
dc.subjectHumans
dc.subjectProvince
dc.subjectAnimals
dc.subjectStrains
dc.subjectCattle
dc.subjectBruce-ladder pcr
dc.subjectCanonical brucella species
dc.subjectE -test
dc.subjectHuman
dc.subjectSheep
dc.subjectImmunology
dc.subjectMicrobiology
dc.titleThe canonical Brucella species-host dependency is changing, however, the antibiotic susceptibility profiles remain unchanged
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentVeteriner Fakültesi/Su Hayvanları Hastalıkları Ana Bilim Dalı
relation.isAuthorOfPublication039c73a6-fd48-4fbe-bd26-0fe99b40120f
relation.isAuthorOfPublication.latestForDiscovery039c73a6-fd48-4fbe-bd26-0fe99b40120f

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