Department of Microbiology, College of Veterinary Medicine, Uludag University, Bursa, Turkey.
Foodborne Pathog Dis. 2013 Jul;10(7):608-17. doi: 10.1089/fpd.2012.1427. Epub 2013 May 2.
The objective of this study was to determine the prevalence and molecular typing of methicillin-susceptible Staphylococcus aureus (MSSA) and methicillin-resistant S. aureus (MRSA) in food-producing animals and retail meat in Fargo, North Dakota. A two-step enrichment followed by culture methods were used to isolate S. aureus from 167 nasal swabs from animals, 145 samples of retail raw meat, and 46 samples of deli meat. Positive isolates were subjected to multiplex polymerase chain reaction in order to identify the genes 16S rRNA, mecA, and Panton-Valentine Leukocidin. Pulsed-field gel electrophoresis and multilocus sequence typing were used for molecular typing of S. aureus strains. Antimicrobial susceptibility testing was carried out using the broth microdilution method. The overall prevalence of S. aureus was 37.2% (n=133), with 34.7% (n=58) of the animals positive for the organism, and the highest prevalence observed in pigs (50.0%) and sheep (40.6%) (p<0.05); 47.6% (n=69) of raw meat samples were positive, with the highest prevalence in chicken (67.6%) and pork (49.3%) (p<0.05); and 13.0% (n=6) of deli meat was positive. Five pork samples (7.0%) were positive for MRSA, of which three were ST398 and two were ST5. All exhibited penicillin resistance and four were multidrug resistant (MDR). The Panton-Valentine Leukocidin gene was not detected in any sample by multiplex polymerase chain reaction. The most common clones in sheep were ST398 and ST133, in pigs and pork both ST398 and ST9, and in chicken ST5. Most susceptible S. aureus strains were ST5 isolated from chicken. The MDR isolates were found in pigs, pork, and sheep. The presence of MRSA, MDR, and the subtype ST398 in the meat production chain and the genetic similarity between strains of porcine origin (meat and animals) suggest the possible contamination of meat during slaughtering and its potential transmission to humans.
本研究旨在确定北达科他州法戈市食用动物和零售肉中耐甲氧西林金黄色葡萄球菌(MSSA)和耐甲氧西林金黄色葡萄球菌(MRSA)的流行率和分子分型。采用两步富集加培养方法,从 167 份动物鼻腔拭子、145 份零售生肉和 46 份熟食中分离金黄色葡萄球菌。对阳性分离株进行多重聚合酶链反应,以鉴定 16S rRNA、mecA 和 Panton-Valentine Leukocidin 基因。脉冲场凝胶电泳和多位点序列分型用于金黄色葡萄球菌菌株的分子分型。采用肉汤微量稀释法进行抗菌药物敏感性试验。金黄色葡萄球菌的总流行率为 37.2%(n=133),其中 34.7%(n=58)的动物呈阳性,猪(50.0%)和羊(40.6%)的流行率最高(p<0.05);47.6%(n=69)的生肉样本呈阳性,其中鸡(67.6%)和猪肉(49.3%)的流行率最高(p<0.05);熟食样本中有 13.0%(n=6)呈阳性。5 份猪肉样本(7.0%)检测出耐甲氧西林金黄色葡萄球菌,其中 3 份为 ST398,2 份为 ST5。所有样本均对青霉素耐药,4 份为多药耐药(MDR)。多重聚合酶链反应未检测到任何样本携带 Panton-Valentine Leukocidin 基因。绵羊中最常见的克隆是 ST398 和 ST133,猪和猪肉中均为 ST398 和 ST9,鸡中为 ST5。最敏感的金黄色葡萄球菌菌株是从鸡中分离出的 ST5。MDR 分离株存在于猪、猪肉和绵羊中。在肉类生产链中发现了耐甲氧西林金黄色葡萄球菌、耐多药和亚型 ST398,以及猪源(肉和动物)菌株之间的遗传相似性,表明在屠宰过程中可能污染了肉类,并可能将其传播给人类。