Siriken Belgin, Ayaz Naim Deniz, Erol Irfan
Food Hygiene and Technology Department, Faculty of Veterinary Medicine, Kurupelit Campus, Ondokuz Mayis University, Samsun,Turkey.
Food Hygiene and Technology Department, Faculty of Veterinary Medicine, Ankara University, Ankara, Turkey.
Berl Munch Tierarztl Wochenschr. 2014 Jan-Feb;127(1-2):43-9.
The objectives of this study were, to find the prevalence and antimicrobial resistance of L. monocytogenes from a total of 116 chicken meat samples including 50 carcasses and 66 meat parts marketed in Turkey between 2008 and 2009 using immunomagnetic separation (IMS) based cultivation technique, to detect the hlyA gene for the verification of the isolates by PCR, and to identify the genoserotypes of the L. monocytogenes isolates by multiplex PCR assay. In the study, 51 L. monocytogenes colonies were isolated from 34 (29.3%) chicken meat samples (eleven [22.0%] carcasses and 23 [34.8%] pieces of meat) by IMS based cultivation technique and confirmed by PCR. According to the multiplex PCR results, all the 51 isolates were identified as genoserotype IIa (1/2a or 3a). L. monocytogenes isolates were also tested for their susceptibility to eight antibiotic (gentamicin, vancomycin, chloramphenicol, streptomycin, tetracycline, ampicillin, penicillin G, erythromycin) agents using the disk diffusion method. 14 isolates (27.45%) were susceptible to all eight antimicrobials drugs tested and the remaining 37 isolates (72.54%) were resistant to gentamicin (one isolate, 1.96%), vancomycin (four isolates, 7.84%), penicillin G (six isolates, 11.76%), streptomycin (nine isolates, 17.64%; resistant or intermediate), tetracycline (seven isolates, 13.72%) and ampicillin (six isolates, 11.76%). This study showed that antimicrobial resistance is not highly prevalent in L. monocytogenes isolated from chicken carcasses and pieces of meat. The presence of L. monocytogenes in chicken samples suggests an importance of this pathogen in chicken.
本研究的目的是,使用基于免疫磁珠分离(IMS)的培养技术,测定2008年至2009年在土耳其市场销售的总共116份鸡肉样本(包括50个鸡胴体和66个肉块)中单核细胞增生李斯特菌的流行率和抗菌药物耐药性,通过聚合酶链反应(PCR)检测hlyA基因以验证分离株,并通过多重PCR测定法鉴定单核细胞增生李斯特菌分离株的基因血清型。在该研究中,通过基于IMS的培养技术从34份(29.3%)鸡肉样本(11份[22.0%]鸡胴体和23份[34.8%]肉块)中分离出51个单核细胞增生李斯特菌菌落,并通过PCR进行了确认。根据多重PCR结果,所有51个分离株均被鉴定为基因血清型IIa(1/2a或3a)。还使用纸片扩散法检测了单核细胞增生李斯特菌分离株对八种抗生素(庆大霉素、万古霉素、氯霉素、链霉素、四环素、氨苄西林、青霉素G、红霉素)的敏感性。14个分离株(27.45%)对所有八种测试抗菌药物敏感,其余37个分离株(72.54%)对庆大霉素(1个分离株,1.96%)、万古霉素(4个分离株,7.84%)、青霉素G(6个分离株,11.76%)、链霉素(9个分离株,17.64%;耐药或中介)、四环素(7个分离株,13.72%)和氨苄西林(6个分离株,11.76%)耐药。本研究表明,从鸡胴体和肉块中分离出的单核细胞增生李斯特菌的抗菌药物耐药性并不十分普遍。鸡肉样本中存在单核细胞增生李斯特菌表明该病原体在鸡肉中具有重要性。