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Prevalence of Salmonella serovars in chickens in Turkey

dc.contributor.authorCaner, Vildan
dc.contributor.buuauthorÇarlı, Kamil Tayfun
dc.contributor.buuauthorEyigör, Ayşegül
dc.contributor.departmentVeteriner Fakültesi
dc.contributor.departmentVeteriner Fakültesi
dc.contributor.departmentMikrobiyoloji Bölümü
dc.contributor.departmentBesin Hijyeni ve Teknolojisi Bölümü
dc.contributor.researcheridE-3867-2010
dc.contributor.researcheridAAI-1101-2021
dc.date.accessioned2021-07-05T07:46:46Z
dc.date.available2021-07-05T07:46:46Z
dc.date.issued2001-11
dc.description.abstractIn this study, 151 (18.6%) of 814 ceca obtained during in-line processing of 28 broiler (Hybro G, Avian, Arbor acres, and Cobb breeds) and 5 layer (Ross, Tetra SL, Isa Brown, and Brown Nick breeds) flocks in Turkey were found to be contaminated with four different Salmonella serovars. Only Salmonella enterica subsp. enterica Serovar Enteritidis (Salmonella Enteritidis) was recovered from layer birds, whereas Salmonella Enteritidis (81.5%), Salmonella Agona (7.6%), Salmonella Thompson (10.1%), and Salmonella Sarajane (0.8%) were isolated from broiler birds. Isolations of Salmonella Agona and Salmonella Thompson from poultry are reported for the first time in Turkey. The isolation of Salmonella Sarajane front Chickens is the first report in the world. The standard method of National Poultry Improvement Plan, U.S. Department of Agriculture, was used to detect Salmonella from chicken cecal samples. Primary and delayed secondary enrichments (PE and DSE) were done in tetrathionate-Hajna broth (TTHB). Two different agar media, xylose lysine tergitol 4 (XLT4) and brilliant green with novobiocin (BGN) were used to observe, and compared for their isolation and selective differentiation of, Salmonella-suspected colonies. Isolated salmonellae were then biotyped and serotyped. Ninety-one and 151 salmonellae were isolated with XLT4 agar after PE and DSE, respectively. From the same samples, BGN agar was able to detect only 50 and 131 Salmonella after PE and DSE, respectively. The isolation rate with XLT4 was 11.2% (P < 0.01) with PE, and this rate increased to 18.6% after DSE. Also, the RE isolation rate (11.2%) with XLT4 agar was significantly higher (P < 0.01) than PE with BGN agar (6.1%). Salmonella was isolated from 39.3% (11 of 28) of the broiler flocks and from 60.0% (3 of 5) of the layers. The detection sensitivity of the isolation method was determined as 1 CFU g(-1) experimentally. These data demonstrate the presence of Salmonella Enteritidis, Salmonella Thompson, Salmonella Agona, and Salmonella Sarajane in chicken flocks in Turkey.
dc.identifier.citationÇarlı, K. T. vd. (2001). "Prevalence of Salmonella serovars in chickens in Turkey". Journal of Food Protection, 64(11), 1832-1835.
dc.identifier.doi10.4315/0362-028X-64.11.1832
dc.identifier.endpage1835
dc.identifier.issn0362-028X
dc.identifier.issue11
dc.identifier.pubmed11726169
dc.identifier.scopus2-s2.0-0035543236
dc.identifier.startpage1832
dc.identifier.urihttps://doi.org/10.4315/0362-028X-64.11.1832
dc.identifier.urihttps://meridian.allenpress.com/jfp/article/64/11/1832/168174/Prevalence-of-Salmonella-Serovars-in-Chickens-in
dc.identifier.urihttp://hdl.handle.net/11452/21042
dc.identifier.volume34
dc.identifier.wos000172247800032
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherInt Assoc Food Protection
dc.relation.collaborationYurtiçi
dc.relation.journalJournal of Food Protection
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBiotechnology & applied microbiology
dc.subjectHens
dc.subjectLayer
dc.subjectPoultry
dc.subjectVaccination
dc.subjectFlocks
dc.subjectBroiler
dc.subjectEnteritidis
dc.subjectCompetitive-exclusion
dc.subjectFood science & technology
dc.subject.wosBiotechnology & applied microbiology
dc.subject.wosFood science & technology
dc.titlePrevalence of Salmonella serovars in chickens in Turkey
dc.typeArticle
dc.wos.quartileQ1 (Food science & technology)
dc.wos.quartileQ2 (Biotechnology & applied microbiology)
dspace.entity.typePublication
local.contributor.departmentVeteriner Fakültesi/Besin Hijyeni ve Teknolojisi Bölümü
local.contributor.departmentVeteriner Fakültesi/Mikrobiyoloji Bölümü
local.indexed.atPubMed
local.indexed.atScopus

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