Nemeghaire Stéphanie, Vanderhaeghen Wannes, Argudín M Angeles, Haesebrouck Freddy, Butaye Patrick
Department of General Bacteriology, Veterinary and Agrochemical Research Centre, Groeselenbergstraat 99, B-1180 Ukkel, Belgium Department of Pathology, Bacteriology and Avian Diseases, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium
Department of Reproduction, Obstetrics and Herd Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
J Antimicrob Chemother. 2014 Nov;69(11):2928-34. doi: 10.1093/jac/dku268. Epub 2014 Jul 25.
This study aimed at assessing the epidemiology and genetic diversity of methicillin-resistant Staphylococcus sciuri (MRSS) from different farm animal species.
Nasal swabs were collected from 200 pigs, 100 dairy cows, 100 beef cows, 150 veal calves and 200 broilers. Colonies were isolated on selective media containing cefoxitin and the mecA gene was detected by PCR. Antimicrobial resistance was determined by broth microdilution. The genetic diversity was assessed by PFGE and resistance and virulence genes were detected by microarray analysis.
The total MRSS prevalence at the animal level was estimated at 9.5%, varying from ∼10% in veal (13.3%), broilers (12.5%) and dairy cows (10.0%) to 6.5% in pigs and 3.0% in beef cows. mecA was detected in all isolates. SCCmec elements of type III and non-typeable ones were seen most frequently. More than 90% of isolates were non-wild-type (NWT) for gentamicin, penicillin, tiamulin, clindamycin and quinupristin/dalfopristin. The frequency of NWT isolates for fusidic acid and trimethoprim ranged between 78% and 87%. PFGE analysis allowed distinction between two major clusters. Most isolates tested by microarray carried erm and tet genes. Virulence genes were also detected, including an isa gene encoding an immune-evasion factor and the hsdS2 gene encoding a site-specific deoxyribonuclease.
This study shows that multiresistant MRSS is carried by different farm animal species. Although some animals shared the same strain, PFGE showed different patterns, indicating high diversity among the MRSS isolates recovered. The absence of clusters associated with a certain animal species suggests low host specificity.
本研究旨在评估来自不同农场动物物种的耐甲氧西林松鼠葡萄球菌(MRSS)的流行病学和遗传多样性。
从200头猪、100头奶牛、100头肉牛、150头犊牛和200只肉鸡中采集鼻拭子。在含有头孢西丁的选择性培养基上分离菌落,并通过PCR检测mecA基因。通过肉汤微量稀释法测定抗菌药物敏感性。通过脉冲场凝胶电泳(PFGE)评估遗传多样性,并通过微阵列分析检测耐药基因和毒力基因。
动物水平的MRSS总体流行率估计为9.5%,犊牛(13.3%)、肉鸡(12.5%)和奶牛(10.0%)中约为10%,猪中为6.5%,肉牛中为3.0%。在所有分离株中均检测到mecA。III型和不可分型的葡萄球菌盒式染色体mec(SCCmec)元件最为常见。超过90%的分离株对庆大霉素、青霉素、替米考星、克林霉素和奎奴普丁/达福普汀为非野生型(NWT)。对夫西地酸和甲氧苄啶的NWT分离株频率在78%至87%之间。PFGE分析可区分两个主要聚类。通过微阵列检测的大多数分离株携带erm和tet基因。还检测到毒力基因,包括编码免疫逃避因子的isa基因和编码位点特异性脱氧核糖核酸酶基因的hsdS2。
本研究表明,多种耐药的MRSS存在于不同的农场动物物种中。虽然一些动物携带相同菌株,但PFGE显示出不同模式,表明所分离的MRSS菌株具有高度多样性。未发现与特定动物物种相关的聚类,表明宿主特异性较低。